Criticalkare Pharma

Strength	1 mg
Dosage Form	Capsule
Brand	Pomide
Usage/Application	Personal
Units per Pack	21 Units
Usage	Multiple Myeloma
Pack Type	Bottle
Compostion	Pomalidomide 1mg
Storage Condition	Store below 30 DegreeC
Prescription/Non prescription	Prescription
Country of Origin	Made in India

Pomide 1mg Capsule is a chemotherapy medicine containing the active constituent Pomalidomide. It belongs to the group of medications known as Immuno modulatory agents. It is used to treat multiple myeloma in adults. Multiple myeloma is a type of cancer mainly affecting certain white blood cells called the plasma cell. These cells grow uncontrolled and accumulate in the bone marrow, damaging the bones and kidneys. 

The common side effects that are likely to associate with Pomide 1mg Capsule are shortness of breath, tiredness, weakness, nausea, vomiting, diarrhea, constipation, back and bone pain, dizziness, tremor, upper respiratory tract infection, sleeping trouble, loss of appetite, lack of energy, muscle spasms, muscle weakness, numbness, tingling or burning sensation, the low potassium level in the blood and anemia. Inform your doctor if these side effects disturb or persist in you. 

Inform your medical professional if you are allergic to Pomide 1mg Capsule and its ingredients. Inform your doctor if you have high cholesterol levels, heart disorders, breathing problems, blood clot disorders, hepatitis B infection, neuropathy (Pain in hands or feet caused by nerve damage), or if you smoke before taking this chemotherapy medicine. It is not recommended for adolescents and children under 18 years of age. 

Uses of Pomide 1mg Capsule

• Treatment of Multiple myeloma.

 

More Information

• Keep Pomide 1mg Capsule out of sight and reach of children.
• Store at room temperature between 20°C to 25°C.

Safety Advices   Pregnancy  

Pomide 1mg Capsule is unsafe to use during pregnancy as it may cause harmful effects on the unborn baby. Inform your doctor if you are pregnant or planning to get pregnant before taking this medicine.  

Breast Feeding 

It is not recommended to use during breastfeeding as it is not known if Pomide 1mg Capsule passes into breast milk and harms the baby.  

Lungs  

It is unknown whether Pomide 1mg Capsule can be given to patients with lung disorders. Consult your doctor if you have any lung problems before starting the treatment.   

Liver  

Pomide 1mg Capsule is used with caution in severe liver disease patients. A dose adjustment is required. Your physician will perform blood tests to monitor your liver function during treatment with this medication.  

Alcohol  

No Data  

Driving  

Do not drive or operate heavy machines while taking Pomide 1mg Capsule, as it can cause tiredness, dizziness, and confusion. 

Side Effects

• Low white blood cells
• Bleeding or bruising
• Severe or bloody diarrhea
• Blood clots (chest or leg pain, swelling)
• Severe liver problems (yellowing of skin or eyes, dark-brow color urine, abdominal Pain)
• Severe allergic reactions (swelling of face, lips, tongue, or throat, difficulty breathing)

• Shortness of breath
• Tiredness, weakness
• Nausea, vomiting
• Dizziness, tremor
• Low potassium level in the blood (hypokalaemia)
• Back pain, bone pain
• Diarrhea, constipation
• Upper respiratory tract infection
• High blood sugar levels
• Loss of appetite, lack of energy
• Trouble sleeping
• Muscle spasms, muscle weakness
• Numbness, tingling, or burning sensation in the skin, Pain in hands or feet
• Anemia

Strength	4 mg
Dosage Form	Capsule
Brand	Pomalid
Usage/Application	Personal
Units per Pack	21 Units
Usage	Multiple Myeloma
Pack Type	Bottle
Compostion	Pomalidomide 4mg
Storage Condition	Store below 30 DegreeC
Prescription/Non prescription	Prescription
Country of Origin	Made in India

Pomalid 4mg Capsule is a chemotherapy medicine containing the active constituent Pomalidomide. It belongs to the group of medications known as Immuno modulatory agents. It is used to treat multiple myeloma in adults. Multiple myeloma is a type of cancer mainly affecting certain white blood cells called the plasma cell. These cells grow uncontrolled and accumulate in the bone marrow, damaging the bones and kidneys. 

The common side effects that are likely to associate with Pomalid 4mg Capsule are shortness of breath, tiredness, weakness, nausea, vomiting, diarrhea, constipation, back and bone pain, dizziness, tremor, upper respiratory tract infection, sleeping trouble, loss of appetite, lack of energy, muscle spasms, muscle weakness, numbness, tingling or burning sensation, the low potassium level in the blood and anemia. Inform your doctor if these side effects disturb or persist in you. 

Inform your medical professional if you are allergic to Pomalid 4mg Capsule and its ingredients. Inform your doctor if you have high cholesterol levels, heart disorders, breathing problems, blood clot disorders, hepatitis B infection, neuropathy (Pain in hands or feet caused by nerve damage), or if you smoke before taking this chemotherapy medicine. It is not recommended for adolescents and children under 18 years of age. 

Uses of Pomalid 4mg Capsule

• Treatment of Multiple myeloma.

 

More Information

• Keep Pomalid 4mg Capsule out of sight and reach of children.
• Store at room temperature between 20°C to 25°C.

Safety Advices  Pregnancy 

Pomalid 4mg Capsule is unsafe to use during pregnancy as it may cause harmful effects on the unborn baby. Inform your doctor if you are pregnant or planning to get pregnant before taking this medicine.  

Breast Feeding  

It is not recommended to use during breastfeeding as it is not known if Pomalid 4mg Capsule passes into breast milk and harms the baby.  

Lungs  

It is unknown whether Pomalid 4mg Capsule can be given to patients with lung disorders. Consult your doctor if you have any lung problems before starting the treatment.   

Liver  

Pomalid 4mg Capsule is used with caution in severe liver disease patients. A dose adjustment is required. Your physician will perform blood tests to monitor your liver function during treatment with this medication.  

Alcohol  

No Data  

Driving  

Do not drive or operate heavy machines while taking Pomalid 4mg Capsule, as it can cause tiredness, dizziness, and confusion. 

Side Effects

• Low white blood cells
• Bleeding or bruising
• Severe or bloody diarrhea
• Blood clots (chest or leg pain, swelling)
• Severe liver problems (yellowing of skin or eyes, dark-brow color urine, abdominal Pain)
• Severe allergic reactions (swelling of face, lips, tongue, or throat, difficulty breathing)

• Shortness of breath
• Tiredness, weakness
• Nausea, vomiting
• Dizziness, tremor
• Low potassium level in the blood (hypokalaemia)
• Back pain, bone pain
• Diarrhea, constipation
• Upper respiratory tract infection
• High blood sugar levels
• Loss of appetite, lack of energy
• Trouble sleeping
• Muscle spasms, muscle weakness
• Numbness, tingling, or burning sensation in the skin, Pain in hands or feet
• Anemia

Strength	4 mg
Dosage Form	Capsule
Brand	Bdpoma
Units per Pack	21 Units
Usage	Multiple Myeloma
Form	Tablet
Pack Type	Bottle
Storage Condition	Store at room temperature between 20 DegreeC to 25 DegreeC.
Prescription/Non prescription	Prescription
Country of Origin	Made in India

Bdpoma 4mg Capsule is a chemotherapy medicine containing the active constituent Pomalidomide. It belongs to the group of medications known as Immunomodulatory agents. It is used to treat multiple myeloma in adults. Multiple myeloma is a type of cancer mainly affecting certain white blood cells called the plasma cell. These cells grow uncontrolled and accumulate in the bone marrow, damaging the bones and kidneys.

Uses
Treatment of Multiple myeloma.

Storage 
Keep Bdpoma 4mg Capsule out of sight and reach of children.Store at room temperature between 20°C to 25°C.

Side Effects
Low white blood cellsBleeding or bruisingSevere or bloody diarrheaBlood clots (chest or leg pain, swelling)Severe liver problems (yellowing of skin or eyes, dark-brow color urine, abdominal Pain)Severe allergic reactions (swelling of face, lips, tongue, or throat, difficulty breathing)Shortness of breathTiredness, weaknessNausea, vomitingDizziness, tremorLow potassium level in the blood (hypokalaemia)Back pain, bone painDiarrhea, constipationUpper respiratory tract infectionHigh blood sugar levelsLoss of appetite, lack of energyTrouble sleepingMuscle spasms, muscle weaknessNumbness, tingling, or burning sensation in the skin, Pain in hands or feetAnemia

Strength	125mcg
Dosing Schedule	Once weekly
Pack Type	PFS
Route of Administration	SC
Brand	Plegridy
Indication	Multiple sclerosis
Usage/Application	Personal
Packaging Type	1 Prefilled Pen Device
Packaging Size	1 Prefilled Pen Device
Color	Beigene
Also Gives	Third Party Manufacturing
Composition	Pegylated Interferon Beta-1A 125mcg
Form	Injection
Manufacture By	EISAI PHARMACEUTICALS INDIA PVT LTD - JAPAN
Instruction	used to treat multiple sclerosis (MS)

Plegridy 125mcg injection contains active components as Pegylated Interferon Beta-1A. It is a medication used to treat multiple sclerosis (MS). Multiple sclerosis is a chronic autoimmune disease of the central nervous system characterized by inflammation, demyelination, and a wide range of neurological symptoms. One of the primary benefits of this medication is its ability to reduce the frequency of relapses in individuals with relapsing forms of MS. This can lead to a more stable disease course.: Modulating the immune response and reducing inflammation may slow down the progression of disability in people with MS. This can help individuals maintain a higher level of functioning for a longer period.

Individuals who have a known hypersensitivity or allergy to Plegridy 125mcg injection or any of its components should not use this medication. Suppose a patient has a history of severe depression, significant mood disorders, or suicidal ideation. In that case, the use of this medication should be carefully considered as it can have neuropsychiatric side effects. It can affect liver function, and individuals with severe liver disease or liver dysfunction should not use this medication. Although it primarily undergoes hepatic metabolism (in the liver), it is also partially excreted through the kidneys. Patients with severe renal impairment may require dose adjustments or alternative treatments. The safety and effectiveness of Plegridy 125mcg injection in pediatric patients have not been established, and it is generally not recommended for use in children.

Uses of Plegridy 125mcg Injection

• Multiple sclerosis (MS) treatment
• Relapse rate reduction
• Delaying disability progression
• Inflammation and immune modulation
• MRI lesion reduction
• Alternative disease-modifying therapy (DMT)

 

More Information

• Stored at room temperature from 2°C to 8°C
• Keep away from moisture, heat, and light.
• It should not be frozen.
• Keep away from children and pets.

Safety Advices  Pregnancy  

There is limited information on the safety of Plegridy 125mcg injection in pregnant women. It is, therefore, important to talk to your doctor before using it if you are pregnant. 

Breast Feeding  

It is not known whether Plegridy 125mcg injection passes into breast milk. It is, therefore, important to talk to your doctor before using it if you are breastfeeding.  

Lungs  

Plegridy 125mcg injection does not directly affect lung function. However, individuals with lung issues should consult a healthcare provider before using it.  

Liver  

Plegridy 125mcg injection can affect liver function, so it is important to consult a healthcare provider before taking this medication. 

Alcohol  

The interaction between alcohol and Plegridy 125mcg injection is not well-documented. However, alcohol can have its own effects on the liver and the central nervous system, and it's advisable to consume alcohol in moderation or as your healthcare provider recommends.  

Driving  

Plegridy 125mcg injection does do not cause any side effects that would affect your driving ability. However, if you experience dizziness or other unusual side effects, it's best to consult your healthcare provider.

Side Effects

• Liver problems
• Myelosuppression
• Neuropsychiatric effects
• Allergic reactions
• Anaphylaxis
• Cardiovascular issues
• Seizures
• Autoimmune disorders

• Flu-like symptoms
• Injection site reactions
• Headache
• Nausea
• Fatigue
• Mood changes

Strength	4 mg
Dosage Form	Capsule
Brand	Pomide
Usage/Application	Personal
Units per Pack	21 Units
Usage	Multiple Myeloma
Pack Type	Bottle
Compostion	Pomideomide 4mg
Storage Condition	Store below 30 DegreeC
Prescription/Non prescription	Prescription
Country of Origin	Made in India

Pomide 4mg Capsule is a chemotherapy medicine containing the active constituent Pomideomide. It belongs to the group of medications known as Immuno modulatory agents. It is used to treat multiple myeloma in adults. Multiple myeloma is a type of cancer mainly affecting certain white blood cells called the plasma cell. These cells grow uncontrolled and accumulate in the bone marrow, damaging the bones and kidneys. 

The common side effects that are likely to associate with Pomide 4mg Capsule are shortness of breath, tiredness, weakness, nausea, vomiting, diarrhea, constipation, back and bone pain, dizziness, tremor, upper respiratory tract infection, sleeping trouble, loss of appetite, lack of energy, muscle spasms, muscle weakness, numbness, tingling or burning sensation, the low potassium level in the blood and anemia. Inform your doctor if these side effects disturb or persist in you. 

Inform your medical professional if you are allergic to Pomide 4mg Capsule and its ingredients. Inform your doctor if you have high cholesterol levels, heart disorders, breathing problems, blood clot disorders, hepatitis B infection, neuropathy (Pain in hands or feet caused by nerve damage), or if you smoke before taking this chemotherapy medicine. It is not recommended for adolescents and children under 18 years of age. 

Uses of Pomide 4mg Capsule

• Treatment of Multiple myeloma.

 

More Information

• Keep Pomide 4mg Capsule out of sight and reach of children.
• Store at room temperature between 20°C to 25°C.

Safety Advices Pregnancy  

Pomide 4mg Capsule is unsafe to use during pregnancy as it may cause harmful effects on the unborn baby. Inform your doctor if you are pregnant or planning to get pregnant before taking this medicine.  

Breast Feeding  

It is not recommended to use during breastfeeding as it is not known if Pomide 4mg Capsule passes into breast milk and harms the baby.  

Lungs  

It is unknown whether Pomide 4mg Capsule can be given to patients with lung disorders. Consult your doctor if you have any lung problems before starting the treatment.   

Liver  

Pomide 4mg Capsule is used with caution in severe liver disease patients. A dose adjustment is required. Your physician will perform blood tests to monitor your liver function during treatment with this medication.  

Alcohol  

No Data  

Driving  

Do not drive or operate heavy machines while taking Pomide 4mg Capsule, as it can cause tiredness, dizziness, and confusion. 

Side Effects

• Low white blood cells
• Bleeding or bruising
• Severe or bloody diarrhea
• Blood clots (chest or leg pain, swelling)
• Severe liver problems (yellowing of skin or eyes, dark-brow color urine, abdominal Pain)
• Severe allergic reactions (swelling of face, lips, tongue, or throat, difficulty breathing)

• Shortness of breath
• Tiredness, weakness
• Nausea, vomiting
• Dizziness, tremor
• Low potassium level in the blood (hypokalaemia)
• Back pain, bone pain
• Diarrhea, constipation
• Upper respiratory tract infection
• High blood sugar levels
• Loss of appetite, lack of energy
• Trouble sleeping
• Muscle spasms, muscle weakness
• Numbness, tingling, or burning sensation in the skin, Pain in hands or feet
• Anemia

Strength	200 mg
Packaging Size	120 Tablets
Brand	Sorafekast
Manufacturer	Aprazer
Composition	Sorafenib
Form	Tablet
Storage Condition	Store below 30 DegreeC
Prescription/Non prescription	Prescription
Country of Origin	Made in India

Sorafekast 200mg Tablet belongs to the group of medicines called anti-cancer. It consists of the active ingredient Sorafenib which is indicated for advanced renal cell carcinoma (kidney cancer), advanced hepatocellular carcinoma (liver cancer) in patients ineligible for surgery, and differentiated thyroid carcinoma (thyroid cancer) in patients who are not responsive to radioactive iodine therapy. 

Diarrhea, tiredness, stomach pain, nausea, weakness, rashes, flu-like illness, appetite loss, nausea, weight loss, and low blood calcium levels are common side effects of Sorafekast 200mg Tablet. Inform your doctor if any of these side effects disturb or persist with you. 

Inform your doctor if you are allergic to this Tablet and its ingredients. Before starting treatment with this tablet, you should tell your physician if you have heart problems, chest pain, bleeding problems, high blood pressure, or have had or are about to have surgery. Use effective contraception during the therapy and for 6 months after the last dose if you are a woman or 3 months after the last dose if you are a man. 

Uses of Sorafekast 200mg Tablet 120's

Sorafekast 200mg Tablet is used to treat:

• Advanced renal cell carcinoma
• Advanced hepatocellular carcinoma that cannot be surgically treated
• Advanced papillary and follicular Hurtle cell thyroid carcinoma

 

More Information

Store below 30°C in a dry place.

Safety Advices Pregnancy  

It is unsafe to use Sorafekast 200mg Tablet during pregnancy as it may harm the unborn baby. Inform your physician before starting this treatment if you are pregnant or think you might be pregnant. Your physician will conduct a pregnancy test before prescribing this medicine.   

Breast Feeding  

Do not breastfeed during treatment with Sorafekast 200mg Tablet and for two weeks after the last dose. It is vital to let your physician know if you are breastfeeding or planning to breastfeed before starting treatment with this drug.   

Lungs  

Sorafekast 200 mg tablet should be cautiously administered in patients with certain lung problems. Consult your doctor if you have any lung disorders.  

Liver  

Sorafekast 200 mg tablet should be taken with caution in patients with severe liver disease. Consult your doctor for advice.  

Alcohol  

Avoid drinking alcohol while taking Sorafekast 200mg Tablet as it can cause unpleasant side effects like drowsiness, dizziness, or difficulty in concentrating.  

Driving  

This medicine could cause peripheral sensory neuropathy that causes an impact on driving. Hence, avoid driving or doing things that require focus during this treatment period.

Side Effects

• Stevens Johnsons Syndrome and toxic epidermal necrosis
• Decreased blood flow to the heart
• Increased risk of bleeding (blood in urine, stool, vomit, cough, etc.)
• High BP
• Skin problems
• Liver problems
• Problems in wound healing

• Nausea, stomach pain, diarrhea
• Tiredness and weakness
• Infection
• Hair thinning and patchy hair loss
• Rash
• Weight loss
• Loss of appetite
• Low levels of calcium in the blood
• Flu-like illness

Dosage Form	Injection
Strength	800mg
Treatment	Non-Small Cell Lung Cancer
Packaging Type	Vial
Pack Type	Vial
Manufacturer	Sun Pharmaceutical Industries Ltd
Brand Name	Pexitaz
Pharmacopoeia Standard	IP
Usages	used in the treatment of non-small cell lung cancer and malignant pleural mesothelioma
Country of Origin	Made in India

Pexitaz 800mg injection is an anticancer medicine containing the active ingredient Pemetrexed.  It belongs to the medication class known as an antifolate agent. It is used to treat non-small cell lung cancer and malignant pleural mesothelioma (cancers of the lungs and chest). This medicine is given alone or in combination with another anticancer medicine, such as cisplatin. Your doctor may prescribe corticosteroids, folic acid, and vitamin B12 to limit the side effects.  Blood tests will be taken before each infusion to determine whether your kidney and liver functions are adequate and whether you have enough blood cells to receive this medicine. Before starting treatment with Pexitaz 800mg injection, it is very important to tell your physician if you currently or previously had any medical conditions of kidney problems, heart disorders, or fluid accumulation in the lungs. Report to your doctor if you recently had or currently having radiotherapy or any vaccination before taking this medication. Inform your doctor immediately if you are planning to get pregnant or think you may be pregnant. Use effective birth control during the treatment and at least six months after the last dose of Pexitaz 800mg injection. In men, it is recommended not to father a child during and up to 3 months after the treatment. So it is advised to get suggestions about fertility concerns from your doctor. This medication is not recommended for adolescents and children under 18 years of age. Uses of Pexitaz 800mg Infusion Malignant pleural mesotheliomaNon-small cell lung carcinoma More Information Keep the tablets away from light and moisture.Store refrigerated at 2°C to 8°C.Keep the tablets out of the reach of children and animals.Safety Advices   Pregnancy  Do not takePexitaz 800mg if you are pregnant because it may cause harm to the unborn baby. Consult your doctor before starting the treatment.   Breast Feeding  It is unsafe to breastfeed while taking Pexitaz 800mg because it can cause toxicity to the baby. If you are breastfeeding a baby, it has to be discontinued. Please consult your physician for more advice.  Lungs  Consult your doctor if you experience any symptoms like; shortness of breath, blockage, or inflammation in the lining of the lung while taking Pexitaz 800mg.   Liver  Inform your physician about any underlying liver disorders before taking Pexitaz 800mg, as this medication should be used with caution in liver disease patients. Alcohol  It is unknown whether consuming alcohol while taking a Pexitaz 800mg injection is safe. Please speak with your physician.  Driving  While taking Pexitaz 800mg, driving or using machines is unsafe because it may cause nausea, fatigue, vomiting, etc. Talk to your doctor for more information.Side Effects Blood infectionSevere allergic reactionBreathlessness, intense chest pain or cough with bloody sputumReduced neutrophil granulocytes (white blood cells)Kidney failurePharyngitis (a sore throat)Abnormal liver functionFatigueNausea, vomiting, diarrheaRedness, swelling or sores in the mouthLoss of appetite, sensationReduced hemoglobin levelIncreased skin pigmentationWatery and inflamed eyes, taste changeFeverMuscle weaknessDehydrationConstipationSkin rashHair loss

Strength	100 mg
Brand	Palbinas
Capsules per Pack	21 Capsules
Usage/Application	Personal
Usage	Breast Cancer
Form	Capsule
Pack Type	Bottle
Compostion	Palbociclib 100mg
Storage Condition	Store below 30 DegreeC
Country of Origin	Made in India

Palbinas 100 mg is a targeted therapy containing the active constituent palbociclib. It belongs to the group of anticancer medications known as cyclin-dependent kinase inhibitors. It is used in treating hormone receptor-positive, human epidermal growth factor 2 negative advanced or metastatic (has spread to other parts of the body) breast cancer. Cancer is a condition in which cells multiply in an uncontrolled and abnormal manner. It is given in combination with certain other anticancer medications. 

The common side effects that are likely to associate with Palbinas 100 mg capsule are nausea, vomiting, diarrhea, tiredness, hair loss, dry skin, rash, infections, nose bleed, decreased appetite, low blood cell counts, swelling of lips and mouth, changes in taste, dry eye, blurred vision, and increased tearing. Inform your doctor if these side effects disturb or persist in you.   

Inform your healthcare provider if you are allergic to Palbinas 100 mg capsule and its ingredients. Before taking this medicine, it is vital to inform your doctor if you have any signs of infections (fever, chills, or sore throat), liver disorders, kidney disorders, or intolerance to some sugars. Consult your physician immediately if you experience symptoms such as dry cough, chest pain, or difficulty breathing, as it could indicate lung inflammation. Make sure you inform your physician of all the medicines, including supplements and herbal medicines; you are taking before you start treatment with this medication. Use effective birth control during the treatment and at least three weeks after the last dose. It is not recommended for adolescents and children under 18 years of age.  

Uses

• Treatment of hormone receptor (HR)-positive, human epidermal growth factor 2 (HER2)-negative advanced or metastatic breast cancer.

 

More Information

• Store at 20°C to 25°C.

 Advices Pregnancy  

It is not recommended to take Palbinas 100 mg capsule during pregnancy as it can harm the unborn baby. Women with childbearing potential should use effective contraceptives during treatment and for at least three weeks after treatment.   

Breast Feeding  

It is not recommended to take Palbinas 100 mg capsule while breastfeeding as it is not known whether it passes into the breast milk.    

Lungs  

It is not unknown whether Palbinas 100 mg can be administered to patients with lung problems. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Inform your physician if you have any liver disorders before taking Palbinas 100 mg capsule, as it should be used with caution in liver disorder patients.  

Alcohol  

It is unknown whether it is safe to drink alcohol while taking Palbinas 100 mg capsule. Check with your doctor for advice.   

Driving  

Palbinas 100 mg capsule can cause tiredness. Avoid driving if you are unwell.

Side Effects

• Blood disorder (fever, chills, shortness of breath, weakness, bleeding, or bruising)
• Lung inflammation (chest pain, dry cough, or difficulty breathing)

• Tiredness
• Hair loss
• Dry skin, rash
• Infections
• Low blood cell counts
• Decreased of appetite
• Nausea, vomiting
• Diarrhea
• Swelling of lips and mouth
• Changes in taste
• Nose bleed
• Dry eye, blurred vision, increased tearing

Strength	100 mg
Brand	Palborest
Capsules per Pack	21 Capsules
Usage/Application	Personal
Usage	Breast Cancer
Form	Capsule
Pack Type	Blister
Compostion	Palbociclib 100mg
Storage Condition	Store below 30
Prescription/Non prescription	Prescription
Country of Origin	Made in India

Palborest 100 mg is a targeted therapy containing the active constituent palbociclib. It belongs to the group of anticancer medications known as cyclin-dependent kinase inhibitors. It is used in treating hormone receptor-positive, human epidermal growth factor 2 negative advanced or metastatic (has spread to other parts of the body) breast cancer. Cancer is a condition in which cells multiply in an uncontrolled and abnormal manner. It is given in combination with certain other anticancer medications. 

The common side effects that are likely to associate with Palborest 100 mg capsule are nausea, vomiting, diarrhea, tiredness, hair loss, dry skin, rash, infections, nose bleed, decreased appetite, low blood cell counts, swelling of lips and mouth, changes in taste, dry eye, blurred vision, and increased tearing. Inform your doctor if these side effects disturb or persist in you.   

Inform your healthcare provider if you are allergic to Palborest 100 mg capsule and its ingredients. Before taking this medicine, it is vital to inform your doctor if you have any signs of infections (fever, chills, or sore throat), liver disorders, kidney disorders, or intolerance to some sugars. Consult your physician immediately if you experience symptoms such as dry cough, chest pain, or difficulty breathing, as it could indicate lung inflammation. Make sure you inform your physician of all the medicines, including supplements and herbal medicines; you are taking before you start treatment with this medication. Use effective birth control during the treatment and at least three weeks after the last dose. It is not recommended for adolescents and children under 18 years of age.  

Uses of Palborest 100mg Capsule

• Treatment of hormone receptor (HR)-positive, human epidermal growth factor 2 (HER2)-negative advanced or metastatic breast cancer.

 

More Information

• Keep Palborest 100 mg capsule out of sight and reach of children.
• Store at 20°C to 25°C.

Safety Advices Pregnancy  

It is not recommended to take Palborest 100 mg capsule during pregnancy as it can harm the unborn baby. Women with childbearing potential should use effective contraceptives during treatment and for at least three weeks after treatment.   

Breast Feeding  

It is not recommended to take Palborest 100 mg capsule while breastfeeding as it is not known whether it passes into the breast milk.    

Lungs  

It is not unknown whether Palborest 100 mg can be administered to patients with lung problems. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Inform your physician if you have any liver disorders before taking Palborest 100 mg capsule, as it should be used with caution in liver disorder patients.  

Alcohol  

It is unknown whether it is safe to drink alcohol while taking Palborest 100 mg capsule. Check with your doctor for advice.   

Driving  

Palborest 100 mg capsule can cause tiredness. Avoid driving if you are unwell.

Side Effects

• Blood disorder (fever, chills, shortness of breath, weakness, bleeding, or bruising)
• Lung inflammation (chest pain, dry cough, or difficulty breathing)

• Tiredness
• Hair loss
• Dry skin, rash
• Infections
• Low blood cell counts
• Decreased of appetite
• Nausea, vomiting
• Diarrhea
• Swelling of lips and mouth
• Changes in taste
• Nose bleed
• Dry eye, blurred vision, increased tearing

Strength	125 mg
Brand	Palborest
Capsules per Pack	21 Capsules
Usage/Application	Personal
Usage	Breast Cancer
Form	Capsule
Pack Type	Blister
Compostion	Palbociclib 125mg
Storage Condition	Store below 30
Prescription/Non prescription	Prescription
Country of Origin	Made in India

Palborest 125mg is a targeted therapy containing the active constituent palbociclib. It belongs to the group of anticancer medications known as cyclin-dependent kinase inhibitors. It is used in treating hormone receptor-positive, human epidermal growth factor 2 negative advanced or metastatic (has spread to other parts of the body) breast cancer. Cancer is a condition in which cells multiply in an uncontrolled and abnormal manner. It is given in combination with certain other anticancer medications. 

The common side effects that are likely to associate with Palborest 125mg capsule are nausea, vomiting, diarrhea, tiredness, hair loss, dry skin, rash, infections, nose bleed, decreased appetite, low blood cell counts, swelling of lips and mouth, changes in taste, dry eye, blurred vision, and increased tearing. Inform your doctor if these side effects disturb or persist in you.   

Inform your healthcare provider if you are allergic to Palborest 125mg capsule and its ingredients. Before taking this medicine, it is vital to inform your doctor if you have any signs of infections (fever, chills, or sore throat), liver disorders, kidney disorders, or intolerance to some sugars. Consult your physician immediately if you experience symptoms such as dry cough, chest pain, or difficulty breathing, as it could indicate lung inflammation. Make sure you inform your physician of all the medicines, including supplements and herbal medicines; you are taking before you start treatment with this medication. Use effective birth control during the treatment and at least three weeks after the last dose. It is not recommended for adolescents and children under 18 years of age.  

Uses of Palborest 125mg Capsule

• Treatment of hormone receptor (HR)-positive, human epidermal growth factor 2 (HER2)-negative advanced or metastatic breast cancer.

More Information

• Keep Palborest 125mg capsule out of sight and reach of children.
• Store at 20°C to 25°C.

Safety Advices  Pregnancy  

It is not recommended to take Palborest 125mg capsule during pregnancy as it can harm the unborn baby. Women with childbearing potential should use effective contraceptives during treatment and for at least three weeks after treatment.   

Breast Feeding  

It is not recommended to take Palborest 125mg capsule while breastfeeding as it is not known whether it passes into the breast milk.    

Lungs  

It is not unknown whether Palborest 125mg can be administered to patients with lung problems. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Inform your physician if you have any liver disorders before taking Palborest 125mg capsule, as it should be used with caution in liver disorder patients.  

Alcohol  

It is unknown whether it is safe to drink alcohol while taking Palborest 125mg capsule. Check with your doctor for advice.   

Driving  

Palborest 125mg capsule can cause tiredness. Avoid driving if you are unwell.

Side Effects

• Blood disorder (fever, chills, shortness of breath, weakness, bleeding, or bruising)
• Lung inflammation (chest pain, dry cough, or difficulty breathing)

• Tiredness
• Hair loss
• Dry skin, rash
• Infections
• Low blood cell counts
• Decreased of appetite
• Nausea, vomiting
• Diarrhea
• Swelling of lips and mouth
• Changes in taste
• Nose bleed
• Dry eye, blurred vision, increased tearing

Strength	125 mg
Brand	Bdpalbo
Capsules per Pack	21 Capsules
Usage/Application	Personal
Usage	Breast Cancer
Form	Capsule
Pack Type	Bottle
Compostion	Palbociclib 125mg
Storage Condition	Store below 30 DegreeC
Prescription/Non prescription	Prescription
Country of Origin	Made in India

Bdpalbo 125mg is a targeted therapy containing the active constituent palbociclib. It belongs to the group of anticancer medications known as cyclin-dependent kinase inhibitors. It is used in treating hormone receptor-positive, human epidermal growth factor 2 negative advanced or metastatic (has spread to other parts of the body) breast cancer. Cancer is a condition in which cells multiply in an uncontrolled and abnormal manner. It is given in combination with certain other anticancer medications. 

The common side effects that are likely to associate with Bdpalbo 125mg capsule are nausea, vomiting, diarrhea, tiredness, hair loss, dry skin, rash, infections, nose bleed, decreased appetite, low blood cell counts, swelling of lips and mouth, changes in taste, dry eye, blurred vision, and increased tearing. Inform your doctor if these side effects disturb or persist in you.   

Inform your healthcare provider if you are allergic to Bdpalbo 125mg capsule and its ingredients. Before taking this medicine, it is vital to inform your doctor if you have any signs of infections (fever, chills, or sore throat), liver disorders, kidney disorders, or intolerance to some sugars. Consult your physician immediately if you experience symptoms such as dry cough, chest pain, or difficulty breathing, as it could indicate lung inflammation. Make sure you inform your physician of all the medicines, including supplements and herbal medicines; you are taking before you start treatment with this medication. Use effective birth control during the treatment and at least three weeks after the last dose. It is not recommended for adolescents and children under 18 years of age.  

Uses of Bdpalbo 125mg Capsule

• Treatment of hormone receptor (HR)-positive, human epidermal growth factor 2 (HER2)-negative advanced or metastatic breast cancer.

 

More Information

• Keep Bdpalbo 125mg capsule out of sight and reach of children.
• Store at 20°C to 25°C.

Safety Advices Pregnancy  

It is not recommended to take Bdpalbo 125mg capsule during pregnancy as it can harm the unborn baby. Women with childbearing potential should use effective contraceptives during treatment and for at least three weeks after treatment.   

Breast Feeding  

It is not recommended to take Bdpalbo 125mg capsule while breastfeeding as it is not known whether it passes into the breast milk.    

Lungs  

It is not unknown whether Bdpalbo 125mg can be administered to patients with lung problems. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Inform your physician if you have any liver disorders before taking Bdpalbo 125mg capsule, as it should be used with caution in liver disorder patients.  

Alcohol  

It is unknown whether it is safe to drink alcohol while taking Bdpalbo 125mg capsule. Check with your doctor for advice.   

Driving  

Bdpalbo 125mg capsule can cause tiredness. Avoid driving if you are unwell.

Side Effects

• Blood disorder (fever, chills, shortness of breath, weakness, bleeding, or bruising)
• Lung inflammation (chest pain, dry cough, or difficulty breathing)

• Tiredness
• Hair loss
• Dry skin, rash
• Infections
• Low blood cell counts
• Decreased of appetite
• Nausea, vomiting
• Diarrhea
• Swelling of lips and mouth
• Changes in taste
• Nose bleed
• Dry eye, blurred vision, increased tearing

Dosage Form	Solution for Injection
Brand	Benzz
Strength	45 mg
Packaging Type	Vial
Treatment	Chronic Lymphocytic Leukemia
Storage Temperature	2-8 degree c
Shelf Life	36 months
Prescription/Non Prescription	Prescription
Other Name	Benzz Bendamustine 45mg Injection
Injection Site	Benzz 45mg Injection is given as an injection into vein under the supervision of a doctor and shoul
Salt Name	Bendamustine 45mg
Generic Name	Bendamustine
Country of Origin	Made in India

Benzz 45mg Injection is an antineoplastic drug belonging to the class of alkylating agents, containing the active ingredient Bendamustine. It is used to prevent and treat chronic lymphocytic leukaemia (cancer of blood and bone marrow), non-Hodgkin’s lymphomas (cancer that forms in the lymph system, part of the immune system), and multiple myelomas (cancer of plasma cells, type of white blood cell).

The common side effects that are likely to occur with this medicine are headache, insomnia, fatigue, loss of appetite and rashes. Some serious side effects also include bone marrow suppression, tumor lysis syndrome, and Hepatotoxicity. Inform your healthcare provider if these side effects concern you or persist for longer than usual. It is often combined with rituximab, an immunotherapy drug, to treat various subtypes of non-Hodgkin's lymphoma, including follicular lymphoma, and mantle cell lymphoma. There may be an increased risk of certain types of skin cancer (non-melanoma skin cancer) with the use of this medicine. Consult your doctor immediately for more advice.

Uses

• Chronic lymphocytic leukaemia.
• Non-Hodgkin’s lymphomas
• Multiple myeloma

More Information

• Store Benzz 45mg Injection in the refrigerator (2°-8°C). Do not freeze.
• Keep it out of reach from children and pets.
• It is important to get the dose at the scheduled time. If you missed the schedule, contact your doctor and reschedule the dose.

Safety Advices Pregnancy  

Benzz 45mg Injection is not recommended for pregnant women as it may cause fetal harm. Consult your doctor if you are pregnant or planning for pregnancy during the treatment.  

Breast Feeding  

It is not known if Benzz 45mg Injection passes into your breast milk or if it will affect your baby. Please consult your doctor before breastfeeding.   

Lungs  

It is not known whether Benzz 45mg Injection can be administered to patients with lung problems. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Inform your doctor if you have any liver problems before taking Benzz 45mg Injection. Regular monitoring of liver function tests is recommended.  

Alcohol  

Consuming alcohol may affect the effectiveness of Benzz 45mg Injection. Stop consuming alcohol if you are taking this medicine.  

Driving  

It is unsafe to drive vehicles or operate heavy machinery after taking Benzz 45mg Injection, it may cause dizziness and impair your concentration.

Side Effects

• Severe allergic reactions
• Bone marrow suppression
• Abnormal liver function
• Tumor lysis syndrome

• Infection, fever
• Low blood cell count
• Headache, dizziness
• Nausea, vomiting
• Increased blood level of creatinine and urea (chemical waste products)
• Mucosal inflammation, sore mouth
• Insomnia, fatigue
• Hair loss, itching, rash
• Diarrhea, constipation
• Missed periods
• Dehydration, loss of appetite
• Low or high blood pressure

Strength	100 mg
Brand	Reditux
Strength per ml	10 mg/ml
Composition	Rituximab
Form	Injection
Packaging Type	Vial
Storage Condition	Store in a refrigerator (2 - 8 DegreeC). Do not freeze.
Manufacturer	Dr Reddy's Laboratories Ltd
Usage / Application	Personal
Storage Conditions	Store in a refrigerator (2 - 8 DegreeC). Do not freeze.
Shelf Life	48 months
Vial Volume	50 ml
Packaging Size	10 ml

Reditux 100mg injection contains the active constituent rituximab. It is used for several different disease conditions in adults. It is used alone or with other medications to treat non-hodgkin’s lymphoma (cancer affecting white blood cells called B-lymphocytes) and chronic lymphocytic leukemia (a most common form of cancer that affects B-cells). It is also indicated to treat moderate-to-severe rheumatoid arthritis (a type of disease where the immune system attacks the leukapheresis body cells of its own joints)  in combination with methotrexate in adults. Other uses include granulomatosis with polyangiitis or microscopic polyangiitis (inflammation of blood vessels that mainly affects the lungs and kidneys) in adults and children 2 years of age and older. It is also used to treat moderate to severe pemphigus vulgaris (an autoimmune condition that causes painful blisters on the skin and lining of the mouth, throat, nose, and genitals.  

Uses

• Non-hodgkin’s lymphoma (NHL)
• Chronic lymphocytic leukemia (CLL)
• Rheumatoid Arthritis
• Granulomatosis with polyangiitis or microscopic polyangiitis
• Pemphigus vulgaris

More Information

• Store Reditux 100mg injection  in the refrigerator (2°C to 8°C)
• Do not freeze
• keep the injection away from the reach of children and pets.
• If you have missed any dosing appointments, inform your doctor and schedule immediately.

Safety Advices Pregnancy  

Reditux 100mg injection is unsafe to administer in pregnant women because it may affect the fetus. Inform your physician if you are pregnant, suspect pregnancy, or planning to become pregnant. Using an effective birth control method during the treatment and for 12 months after your last dose is necessary.    

Breast Feeding  

Breastfeeding is not recommended in patients taking Reditux 100mg injection because the medicine passes into the breast milk in small amounts and may harm your baby.   

Lungs  

It is unknown whether Reditux 100mg injection can be used in patients with lung disorders. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Whether Reditux 100mg injection can be used in patients with liver impairment is unknown. Consult your doctor if you have or ever had liver disease or hepatitis B infection before starting the treatment. The reactivation of hepatitis viral infection can cause severe liver problems.   

Alcohol  

Consuming alcohol may affect the effectiveness of Reditux 100mg injection. Stop consuming alcohol if you are taking this medicine.   

Driving  

Caution is required while driving and operating machinery when you take Reditux 100mg injection because it may cause dizziness, sleepiness, tiredness, and risk of falling.

Side Effects

• Swelling in the face and body
• Diarrhea and nausea
• Itchy skin
• Anemia
• Muscle spasm
• Headache
• Urinary tract infection
• Fever, chills, and shivering
• Inflammation of nasal cavities
• Cough, sore throat
• Loss of hair

• Increased or decreased blood pressure
• Chest pain
• Hypersensitivity reactions
• Hepatitis B viral infection
• Memory loss, trouble thinking, difficulty in walking

Dosage Form	Injection
Brand	Rituxy
Strength	100 mg
Packaging Size	10 ml
Storage Temperature	2-8 degree c
Manufacturer	Glenmark Pharmaceuticals Ltd
Shelf Life	24 months
Also gives	Pharma Third party manufacturing
Packaging Type	Vial
Country of Origin	Made in India

Rituxy 100mg injection contains the active constituent rituximab. It is used for several different disease conditions in adults. It is used alone or with other medications to treat non-hodgkin’s lymphoma (cancer affecting white blood cells called B-lymphocytes) and chronic lymphocytic leukemia (a most common form of cancer that affects B-cells). It is also indicated to treat moderate-to-severe rheumatoid arthritis (a type of disease where the immune system attacks the leukapheresis body cells of its own joints)  in combination with methotrexate in adults. Other uses include granulomatosis with polyangiitis or microscopic polyangiitis (inflammation of blood vessels that mainly affects the lungs and kidneys) in adults and children 2 years of age and older. It is also used to treat moderate to severe pemphigus vulgaris (an autoimmune condition that causes painful blisters on the skin and lining of the mouth, throat, nose, and genitals.  

 

Uses

• Non-hodgkin’s lymphoma (NHL)
• Chronic lymphocytic leukemia (CLL)
• Rheumatoid Arthritis
• Granulomatosis with polyangiitis or microscopic polyangiitis
• Pemphigus vulgaris

More Information

• Store Rituxy 100mg injection  in the refrigerator (2°C to 8°C)
• Do not freeze
• keep the injection away from the reach of children and pets.
• If you have missed any dosing appointments, inform your doctor and schedule immediately.

Safety Advices  Pregnancy  

Rituxy 100mg injection is unsafe to administer in pregnant women because it may affect the fetus. Inform your physician if you are pregnant, suspect pregnancy, or planning to become pregnant. Using an effective birth control method during the treatment and for 12 months after your last dose is necessary.    

Breast Feeding  

Breastfeeding is not recommended in patients taking Rituxy 100mg injection because the medicine passes into the breast milk in small amounts and may harm your baby.   

Lungs  

It is unknown whether Rituxy 100mg injection can be used in patients with lung disorders. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Whether Rituxy 100mg injection can be used in patients with liver impairment is unknown. Consult your doctor if you have or ever had liver disease or hepatitis B infection before starting the treatment. The reactivation of hepatitis viral infection can cause severe liver problems.   

Alcohol  

Consuming alcohol may affect the effectiveness of Rituxy 100mg injection. Stop consuming alcohol if you are taking this medicine.   

Driving  

Caution is required while driving and operating machinery when you take Rituxy 100mg injection because it may cause dizziness, sleepiness, tiredness, and risk of falling.

Side Effects

• Swelling in the face and body
• Diarrhea and nausea
• Itchy skin
• Anemia
• Muscle spasm
• Headache
• Urinary tract infection
• Fever, chills, and shivering
• Inflammation of nasal cavities
• Cough, sore throat
• Loss of hair

• Increased or decreased blood pressure
• Chest pain
• Hypersensitivity reactions
• Hepatitis B viral infection
• Memory loss, trouble thinking, difficulty in walking

Strength	500 mg
Vial Volume	50 ml
Brand	Reditux
Packaging Size	50 ml
Strength per ml	10 mg/ml
Composition	Rituximab
Form	Injection
Packaging Type	Vial
Storage Condition	Store in a refrigerator (2 - 8 DegreeC). Do not freeze.
Manufacturer	Dr Reddy's Laboratories Ltd
Usage / Application	Personal
Storage Conditions	Store in a refrigerator (2 - 8 DegreeC). Do not freeze.
Shelf Life	48 months

Reditux 500mg injection contains the active constituent rituximab. It is used for several different disease conditions in adults. It is used alone or with other medications to treat non-hodgkin’s lymphoma (cancer affecting white blood cells called B-lymphocytes) and chronic lymphocytic leukemia (a most common form of cancer that affects B-cells). It is also indicated to treat moderate-to-severe rheumatoid arthritis (a type of disease where the immune system attacks the leukapheresis body cells of its own joints)  in combination with methotrexate in adults. Other uses include granulomatosis with polyangiitis or microscopic polyangiitis (inflammation of blood vessels that mainly affects the lungs and kidneys) in adults and children 2 years of age and older. It is also used to treat moderate to severe pemphigus vulgaris (an autoimmune condition that causes painful blisters on the skin and lining of the mouth, throat, nose, and genitals.  

 

Uses

• Non-hodgkin’s lymphoma (NHL)
• Chronic lymphocytic leukemia (CLL)
• Rheumatoid Arthritis
• Granulomatosis with polyangiitis or microscopic polyangiitis
• Pemphigus vulgaris

More Information

• Store Reditux 500mg injection  in the refrigerator (2°C to 8°C)
• Do not freeze
• keep the injection away from the reach of children and pets.
• If you have missed any dosing appointments, inform your doctor and schedule immediately.

Safety Advices   Pregnancy  

Reditux 500mg injection is unsafe to administer in pregnant women because it may affect the fetus. Inform your physician if you are pregnant, suspect pregnancy, or planning to become pregnant. Using an effective birth control method during the treatment and for 12 months after your last dose is necessary.    

Breast Feeding  

Breastfeeding is not recommended in patients taking Reditux 500mg injection because the medicine passes into the breast milk in small amounts and may harm your baby.  

Lungs  

It is unknown whether Reditux 500mg injection can be used in patients with lung disorders. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Whether Reditux 500mg injection can be used in patients with liver impairment is unknown. Consult your doctor if you have or ever had liver disease or hepatitis B infection before starting the treatment. The reactivation of hepatitis viral infection can cause severe liver problems.   

Alcohol  

Consuming alcohol may affect the effectiveness of Reditux 500mg injection. Stop consuming alcohol if you are taking this medicine.   

Driving  

Caution is required while driving and operating machinery when you take Reditux 500mg injection because it may cause dizziness, sleepiness, tiredness, and risk of falling.

Side Effects

• Swelling in the face and body
• Diarrhea and nausea
• Itchy skin
• Anemia
• Muscle spasm
• Headache
• Urinary tract infection
• Fever, chills, and shivering
• Inflammation of nasal cavities
• Cough, sore throat
• Loss of hair

• Increased or decreased blood pressure
• Chest pain
• Hypersensitivity reactions
• Hepatitis B viral infection
• Memory loss, trouble thinking, difficulty in walking

Dosage Form	Solution for Infusion
Brand	Rituxem
Strength	500 mg
Packaging Size	50 ml
Storage Temperature	2-8 degree c
Manufacturer	Rituxem
Shelf Life	24 months
Also gives	Pharma Third party manufacturing
Packaging Type	Vial
Country of Origin	Made in India

Rituxem 500mg injection contains the active constituent rituximab. It is used for several different disease conditions in adults. It is used alone or with other medications to treat non-hodgkin’s lymphoma (cancer affecting white blood cells called B-lymphocytes) and chronic lymphocytic leukemia (a most common form of cancer that affects B-cells). It is also indicated to treat moderate-to-severe rheumatoid arthritis (a type of disease where the immune system attacks the leukapheresis body cells of its own joints)  in combination with methotrexate in adults. Other uses include granulomatosis with polyangiitis or microscopic polyangiitis (inflammation of blood vessels that mainly affects the lungs and kidneys) in adults and children 2 years of age and older. It is also used to treat moderate to severe pemphigus vulgaris (an autoimmune condition that causes painful blisters on the skin and lining of the mouth, throat, nose, and genitals.  

 

Uses

• Non-hodgkin’s lymphoma (NHL)
• Chronic lymphocytic leukemia (CLL)
• Rheumatoid Arthritis
• Granulomatosis with polyangiitis or microscopic polyangiitis
• Pemphigus vulgaris

More Information

• Store Rituxem 500mg injection  in the refrigerator (2°C to 8°C)
• Do not freeze
• keep the injection away from the reach of children and pets.
• If you have missed any dosing appointments, inform your doctor and schedule immediately.  

Safety Advices Pregnancy  

Rituxem 500mg injection is unsafe to administer in pregnant women because it may affect the fetus. Inform your physician if you are pregnant, suspect pregnancy, or planning to become pregnant. Using an effective birth control method during the treatment and for 12 months after your last dose is necessary.    

Breast Feeding 

Breastfeeding is not recommended in patients taking Rituxem 500mg injection because the medicine passes into the breast milk in small amounts and may harm your baby.   

Lungs  

It is unknown whether Rituxem 500mg injection can be used in patients with lung disorders. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Whether Rituxem 500mg injection can be used in patients with liver impairment is unknown. Consult your doctor if you have or ever had liver disease or hepatitis B infection before starting the treatment. The reactivation of hepatitis viral infection can cause severe liver problems.   

Alcohol  

Consuming alcohol may affect the effectiveness of Rituxem 500mg injection. Stop consuming alcohol if you are taking this medicine.   

Driving  

Caution is required while driving and operating machinery when you take Rituxem 500mg injection because it may cause dizziness, sleepiness, tiredness, and risk of falling.

Side Effects

• Swelling in the face and body
• Diarrhea and nausea
• Itchy skin
• Anemia
• Muscle spasm
• Headache
• Urinary tract infection
• Fever, chills, and shivering
• Inflammation of nasal cavities
• Cough, sore throat
• Loss of hair

• Increased or decreased blood pressure
• Chest pain
• Hypersensitivity reactions
• Hepatitis B viral infection
• Memory loss, trouble thinking, difficulty in walking

Salt Form	Methylprednisolone
Strength	125mg
Pack Size	Vial
Drug Type	Methylprednisolone Acetate Injection
Brand	Solu-Medrol
Route	IV
Form	Lyophilized powder
Usage	Pain and Inflammation
Manufacturer	Pfizer Ltd
Packaging Size	2ml
Packaging Type	Vial
Injection Administration type	IV
Shelf Life	24 Months
Composition	Methylprednisolone 125mg
Also Gives	Third Party Manufacturing

Solu medrol 125mg injection is an anti-inflammatory drug belonging to the class of glucocorticoids, containing the active ingredient methylprednisolone. It is used to treat inflammatory or allergic conditions affecting the brain (caused by tumor or meningitis), lungs (caused by asthma, hypersensitivity, tuberculosis, or breathing in vomit or stomach contents), gut, and bowel (Crohn’s disease and ulcerative colitis). It treats rheumatic, skin, eye, and endocrine disorders. It is also used for the palliative management of cancers (leukemia and lymphoma) and the reduction of pain after surgery. In higher doses, it is used to treat flare-ups of symptoms of multiple sclerosis. This injection should not be used if you have a fungal infection, swelling of the brain due to malaria, traumatic brain injury, or if you recently had vaccinated or about to have any vaccination. 

Uses

• Treatment of allergic conditions
• Rheumatic, blood, skin, eye, and endocrine disorders
• Leukemia and lymphomas (palliative management)
• Pain related to surgery (organ transplants)
• Multiple sclerosis
• Ulcerative colitis

More Information

• Store Solu medrol 125mg injection at controlled room temperature (20°-25°C).
• Protect from sunlight
• Keep it out of reach from children and pets.

Safety Advices Pregnancy  

Solu medrol 125mg injection is not recommended for pregnant women as it may cause fetal harm. Consult your doctor if you are pregnant or planning for pregnancy during the treatment. A dose adjustment is suggested.  

Breast Feeding  

Breastfeeding is not recommended in patients administered with a Solu medrol 125mg injection because it may harm your baby. Do not breastfeed during the treatment.  

Lungs  

It is not known whether Solu medrol 125mg injection can be administered to patients with lung problems. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Inform your doctor if you have any liver problems before taking Solu medrol 125mg injection. Regular monitoring of liver function tests is recommended.  

Alcohol  

Consuming alcohol may affect the effectiveness of Solu medrol 125mg injection. Stop consuming alcohol if you are taking this medicine.  

Driving  

It is unsafe to drive vehicles or operate heavy machinery after taking Solu medrol 125mg injection, it may cause dizziness and impair your concentration.

Side Effects

• Allergic reactions (wheezing, swelling of face, difficulty breathing)
• Stomach pain spreading to your back, accompanied by vomiting and loss of consciousness
• Bleeding ulcers
• Infections
• Blood clots in the lung (chest pain, coughing up blood, breathlessness)
• Raised pressure within the skull (lack of energy, drowsiness)
• Blood clots in the leg vein

• High blood pressure, headache
• Swelling
• Ulcers
• Vision problems
• Poor wound healing
• Round or moon-shaped face
• Slow growth in infants, children, and adolescents
• Muscle and bone weakness
• Feeling depressed or high, difficulty in thinking, memory loss
• Acne, bruising
• Thinning of skin

Strength	100 mg
Brand	Gliogrey
Capsules per Pack	Injection
Pack Type	Bottle
Form	Injection
Usage	Brain Tumor
Storage Condition	Store below 30 DegreeC
Manufacturer	Zee Laboratories
Prescription/Non prescription	Prescription
Shelf Life	24 Months
Storage Instruction	Store below 30 DegreeC
Usage/Application	Personal

Gliogrey 100mg Injection contains the active ingredient temozolomide. It belongs to the class of medications known as Antitumor agents. It is prescribed to treat brain cancer, such as glioblastoma multiforme in adults and malignant glioma, including glioblastoma multiforme or anaplastic astrocytoma in patients older than three years. Glioblastoma and anaplastic astrocytoma are the most common and aggressive brain cancers with low chances of survival. Anaplastic astrocytoma is treated with Gliogrey 100mg Injection or radiotherapy after biopsy, whereas Glioblastoma multiforme is treated with a combination of radiotherapy and Gliogrey 100mg Injection, and it is continued as maintenance therapy.

The common side effects that are likely to associate with Gliogrey 100mg Injection are nausea, vomiting, dizziness, diarrhea, constipation, hair loss, rashes, tiredness, frequent urination, vision and hearing problems, high blood sugar levels, muscle damage, pain in muscles and joints, memory loss, coordination problems, infections, sleep problems and loss of weight. Inform your doctor if any of these symptoms disturb you or persist

Uses

•  Treatment of newly diagnosed glioblastoma multiforme.
• Treatment of refractory anaplastic astrocytoma

More Information

• Keep Gliogrey 100mg Injection out of sight and reach of children.
• Store protected from light and moisture.
• Do not store above 25°C.

Safety Advices Pregnancy 

Gliogrey 100mg Injection is unsafe to use during pregnancy as it may cause fetal harm. It should not be used unless prescribed by your physician. Women with childbearing potential should use effective contraceptive precautions for at least 6 months following the completion of treatment.   

Breast Feeding  

Gliogrey 100mg Injection is unsafe to use during breastfeeding as it passes through breast milk and harm the baby. Consult your physician for advice before breastfeeding.  

Lungs  

Inform your physician before taking Gliogrey 100mg Injection if you have if you have any lung conditions.   

Liver  

Inform your physician before taking Gliogrey 100mg Injection if you have severe liver problems. Dose adjustment is required based on the condition.  

Alcohol  

Avoid consuming alcohol while taking Gliogrey 100mg Injection as it may cause unpleasant side effects. Consult our doctor for advice.  

Driving  

Do not drive or operate heavy machines while being treated with Gliogrey 100mg Injection as it may decrease alertness, affect your vision and make you dizzy and sleepy. 

Side Effects

• Secondary cancer like myelodysplastic syndrome and myeloid leukemia.
• Severe Allergic reactions
• Inflammation and fluid buildup in lungs
• Blood clot in lungs or legs
• Liver toxicity
• Convulsions
• Fever and chills
• Severe headache
• Uncontrolled bleeding

• Hair loss
• Rashes
• Tiredness
• Nausea, vomiting and diarrhea
• Constipation
• High blood sugar levels
• Dizziness, impaired sensation, tingling sensation, abnormal taste
• Vision and Hearing problem
• Frequent urination
• Muscle damage, pain in muscles and joints
• Weight changes
• Infections and wounds
• Amnesia
• Abnormal blood cell counts
• Loss of appetite
• Sleep problems
• Memory loss
• Difficulty concentrating, changes in mental status and alertness
• Coordination problems

Strength	15 mg
Route Of Administration	Intravenous
Brand	Thiopta
Packaging Type	Vial
Treatment	Brain Cancer
Manufacturer	Celon
Storage	Refrigerate (2-8°C)
Quality Standard	IP
Composition	Solution
Generic Name	Thiotepa
Dosage Form	Injection
Country of Origin	Made in India

Thiopta 15mg Injection belongs to the class of medication known as Antineoplastics. It contains the active ingredient Thiotepa. It is prescribed in combination with other anti-cancer drugs before stem cell transplantation for adult patients with cancer in the lymph nodes of the central nervous system. It is used as a Preparation before stem cell transplant to reduce the risk of graft rejection. It controls the outflow within the cavity due to cancer in serous membranes. It is also indicated for treating breast, ovarian, and bladder cancer.

The common side effects that are likely to be associated with Thiopta 15mg Injection are diarrhea, rashes, bleeding, blood in urine, and cytomegalovirus infection. Inform your doctor if these side effects disturb or persist in you. 

Inform your healthcare provider if you are allergic (hypersensitive) to Thiopta 15mg injection and its ingredients. It is contraindicated in patients using a live virus or bacterial vaccine, including the yellow fever vaccine. If you have a history of cardiac, liver, kidney, and pulmonary disease and profound myelosuppression (anemia, neutropenia, and thrombocytopenia), report to your doctor. Liver and cardiac function must be monitored regularly, and caution is advised in patients with cardiac disease and liver impairment. It is not recommended to use in pregnant and breastfeeding women.

Uses of Thiopta 15mg Injection

• Preparation for allogeneic hematopoietic stem cell transplantation in pediatric patients with class 3 beta-thalassemia
• Treatment of adenocarcinoma of breast and ovary.
• Treatment of superficial papillary cancer of the urinary bladder.

Therapeutic Effects of Thiopta 15mg Injection

Thiopta 15mg Injection acts by damaging the genetic material (DNA and RNA) of the cancer cells. It stops the growth and multiplication of cancer by directly attacking DNA. This causes the breakage of DNA strands. The process of cross-linking is crucial in exhibiting toxicity in cancer cells. This leads to the exertion of cytotoxic effect and death of tumor cells.

More Information

• Store between 2° to 8°C.
• Protect from light.
• Keep out of reach of children.

Safety Advices Pregnancy

Thiopta 15mg Injection is unsafe to use during pregnancy as it may cause fetal harm. Hence, Consult your doctor for advice.   

Breast Feeding

Breastfeeding while on treatment with Thiopta 15mg Injection is not recommended. Consult your physician for advice before breastfeeding.  

Lungs

It is unknown whether Thiopta 15 mg Injection can be administered in lung failure patients. Please consult the doctor for more advice.  

Liver

Inform your physician before taking Thiopta 15mg Injection if you have liver problems. Ensure that your physician monitors your liver functions regularly.  

Alcohol

It is unknown whether it is safe to consume alcohol while taking Thiopta 15mg Injection. Consult your doctor for advice.   

Driving

Thiopta 15mg Injection is used with caution while driving as it may cause convulsion, hallucination, delirium, dizziness, headache, and blurred vision. 

Side Effects

• Severe drop in blood cell count
• Heart problem
• Kidney damage
• Nerve damage
• Lung toxicity
• Liver toxicity

• Cytomegalovirus infection
• Hemorrhage
• Diarrhea
• Blood in urine
• Rashes

Strength	20 mg
Brand	Afatinib
Packaging Size	28 tablets
Composition	Afatinib Dimaleate
Dosage Form	Tablet
Form	Tablet
Prescription	Prescription
Storage Condition	Store below 25 DegreeC
Prescription/Non prescription	Prescription
Country of Origin	Made in India

Afzanna 20mg Tablet is an anticancer medicine containing Afatinib dimaleate as an active ingredient. It is used to treat patients with non-small cell lung cancer (NSCLC) whose tumors have certain (non-resistant) abnormal epidermal growth factor receptor (EGFR) genes and patients with metastatic, squamous NSCLC progressing after platinum-based chemotherapy. Cancer is a disorder in which cells multiply in an abnormal and uncontrolled manner. Talk to your doctor if you have kidney disorders, breathing problems, liver disorders, heart problems, intolerance to sugars, severe dry eye, or other eye problems before taking this medicine. 

Afzanna 20mg Tablet can delay disease progression and improve overall survival, it can also help patients maintain a better quality of life for a longer period of time. This includes improved physical functioning, reduced pain, and better mental and emotional health. Tell your doctor if you are wearing contact lenses or breastfeeding before taking this medication. Limit your time in the sun as this medicine may make your skin sensitive to the sun. It is not recommended for children and adolescents under the age of 18.  Do not stop taking this medicine without consulting your doctor.

Uses

• Non-small cell lung cancer (NSCLC)

 

More Information

• Afzanna 20mg Tablet should be stored at room temperature, between 20°C to 25°C (68°F to 77°F).
• Protected from light.
• Keep it in its original packaging until it is ready to be used.
• Keep out of the reach of children and pets.
• Should be disposed of properly.

Safety Advices Pregnancy  

Afzanna 20mg Tablet is unsafe during pregnancy as it can cause fetal harm. It is recommended to avoid this medication during pregnancy.  

Breast Feeding 

It is unknown, whether Afzanna 20mg Tablet is excreted in human milk or not, and the potential risks to a nursing infant are unknown. So nursing women should consult a healthcare provider before taking it.  

Lungs  

Afzanna 20mg Tablet is primarily used to treat non-small cell lung cancer (NSCLC). Patients should consult healthcare providers if they have any other lung disease before taking it.  

Liver  

Afzanna 20mg Tablet is primarily metabolized in the liver, so inform your healthcare provider if you have any liver problems or diseases. This medication may also increase liver enzymes, which can be a sign of liver damage or inflammation. Patients taking this medication require regular blood tests to monitor liver function.  

Alcohol  

It is recommended to avoid consuming alcohol while taking Afzanna 20mg Tablet, as alcohol can increase the risk of certain side effects associated with the medication, such as stomach ulcers or gastrointestinal bleeding.  

Driving  

Patients receiving Afzanna 20mg Tablet should be advised to avoid driving or operating machinery if they experience side effects such as fatigue, dizziness, or blurred vision, impairing a patient's ability to drive or operate machinery safely.

Side Effects

• Interstitial lung disease (ILD)
• Severe diarrhea or dehydration
• Liver problems
• Eye problems, such as corneal erosion or ulceration
• Hemorrhage or bleeding problems
• Kidney problems
• Cardiac problems 

• Diarrhea
• Mouth sores
• Acne or skin rash
• Nausea and vomiting
• Fatigue
• Loss of appetite
• Abdominal pain
• Nail changes, such as nail bed infections or inflammation
• Dry skin or itching
• Eye irritation or dryness
• Respiratory infections

Strength	100 mg
Brand	Bdpalbo
Capsules per Pack	21 Capsules
Usage/Application	Personal
Usage	Breast Cancer
Form	Capsule
Pack Type	Bottle
Compostion	Palbociclib 100mg
Storage Condition	Store below 30 DegreeC
Prescription/Non prescription	Prescription
Country of Origin	Made in India

Bdpalbo 100 mg is a targeted therapy containing the active constituent palbociclib. It belongs to the group of anticancer medications known as cyclin-dependent kinase inhibitors. It is used in treating hormone receptor-positive, human epidermal growth factor 2 negative advanced or metastatic (has spread to other parts of the body) breast cancer. Cancer is a condition in which cells multiply in an uncontrolled and abnormal manner. It is given in combination with certain other anticancer medications. 

The common side effects that are likely to associate with Bdpalbo 100 mg capsule are nausea, vomiting, diarrhea, tiredness, hair loss, dry skin, rash, infections, nose bleed, decreased appetite, low blood cell counts, swelling of lips and mouth, changes in taste, dry eye, blurred vision, and increased tearing. Inform your doctor if these side effects disturb or persist in you.   

Inform your healthcare provider if you are allergic to Bdpalbo 100 mg capsule and its ingredients. Before taking this medicine, it is vital to inform your doctor if you have any signs of infections (fever, chills, or sore throat), liver disorders, kidney disorders, or intolerance to some sugars. Consult your physician immediately if you experience symptoms such as dry cough, chest pain, or difficulty breathing, as it could indicate lung inflammation. Make sure you inform your physician of all the medicines, including supplements and herbal medicines; you are taking before you start treatment with this medication. Use effective birth control during the treatment and at least three weeks after the last dose. It is not recommended for adolescents and children under 18 years of age.  

Uses of Bdpalbo 100mg Capsule

• Treatment of hormone receptor (HR)-positive, human epidermal growth factor 2 (HER2)-negative advanced or metastatic breast cancer.

 

More Information

• Keep Bdpalbo 100 mg capsule out of sight and reach of children.
• Store at 20°C to 25°C.

Safety Advices   Pregnancy  

It is not recommended to take Bdpalbo 100 mg capsule during pregnancy as it can harm the unborn baby. Women with childbearing potential should use effective contraceptives during treatment and for at least three weeks after treatment.   

Breast Feeding  

It is not recommended to take Bdpalbo 100 mg capsule while breastfeeding as it is not known whether it passes into the breast milk.    

Lungs  

It is not unknown whether Bdpalbo 100 mg can be administered to patients with lung problems. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Inform your physician if you have any liver disorders before taking Bdpalbo 100 mg capsule, as it should be used with caution in liver disorder patients.  

Alcohol  

It is unknown whether it is safe to drink alcohol while taking Bdpalbo 100 mg capsule. Check with your doctor for advice.   

Driving  

Bdpalbo 100 mg capsule can cause tiredness. Avoid driving if you are unwell.

Side Effects

• Blood disorder (fever, chills, shortness of breath, weakness, bleeding, or bruising)
• Lung inflammation (chest pain, dry cough, or difficulty breathing)

• Tiredness
• Hair loss
• Dry skin, rash
• Infections
• Low blood cell counts
• Decreased of appetite
• Nausea, vomiting
• Diarrhea
• Swelling of lips and mouth
• Changes in taste
• Nose bleed
• Dry eye, blurred vision, increased tearing

Strength	125 mg
Brand	Piclib
Capsules per Pack	21 Capsules
Usage/Application	Personal
Usage	Breast Cancer
Form	Capsule
Pack Type	Bottle
Compostion	Palbociclib 125mg
Storage Condition	Store below 30 DegreeC
Prescription/Non prescription	Prescription
Country of Origin	Made in India

Piclib 125mg is a targeted therapy containing the active constituent palbociclib. It belongs to the group of anticancer medications known as cyclin-dependent kinase inhibitors. It is used in treating hormone receptor-positive, human epidermal growth factor 2 negative advanced or metastatic (has spread to other parts of the body) breast cancer. Cancer is a condition in which cells multiply in an uncontrolled and abnormal manner. It is given in combination with certain other anticancer medications. 

The common side effects that are likely to associate with Piclib 125mg capsule are nausea, vomiting, diarrhea, tiredness, hair loss, dry skin, rash, infections, nose bleed, decreased appetite, low blood cell counts, swelling of lips and mouth, changes in taste, dry eye, blurred vision, and increased tearing. Inform your doctor if these side effects disturb or persist in you.   

Inform your healthcare provider if you are allergic to Piclib 125mg capsule and its ingredients. Before taking this medicine, it is vital to inform your doctor if you have any signs of infections (fever, chills, or sore throat), liver disorders, kidney disorders, or intolerance to some sugars. Consult your physician immediately if you experience symptoms such as dry cough, chest pain, or difficulty breathing, as it could indicate lung inflammation. Make sure you inform your physician of all the medicines, including supplements and herbal medicines; you are taking before you start treatment with this medication. Use effective birth control during the treatment and at least three weeks after the last dose. It is not recommended for adolescents and children under 18 years of age.  

Uses of Piclib 125mg Capsule

• Treatment of hormone receptor (HR)-positive, human epidermal growth factor 2 (HER2)-negative advanced or metastatic breast cancer.

 

More Information

• Keep Piclib 125mg capsule out of sight and reach of children.
• Store at 20°C to 25°C. 

Safety Advices Pregnancy  

It is not recommended to take Piclib 125mg capsule during pregnancy as it can harm the unborn baby. Women with childbearing potential should use effective contraceptives during treatment and for at least three weeks after treatment.   

Breast Feeding  

It is not recommended to take Piclib 125mg capsule while breastfeeding as it is not known whether it passes into the breast milk.    

Lungs  

It is not unknown whether Piclib 125mg can be administered to patients with lung problems. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Inform your physician if you have any liver disorders before taking Piclib 125mg capsule, as it should be used with caution in liver disorder patients.  

Alcohol  

It is unknown whether it is safe to drink alcohol while taking Piclib 125mg capsule. Check with your doctor for advice.   

Driving  

Piclib 125mg capsule can cause tiredness. Avoid driving if you are unwell.

Side Effects

• Blood disorder (fever, chills, shortness of breath, weakness, bleeding, or bruising)
• Lung inflammation (chest pain, dry cough, or difficulty breathing)

• Tiredness
• Hair loss
• Dry skin, rash
• Infections
• Low blood cell counts
• Decreased of appetite
• Nausea, vomiting
• Diarrhea
• Swelling of lips and mouth
• Changes in taste
• Nose bleed
• Dry eye, blurred vision, increased tearing

Dosage Form	Solution for Injection
Brand	Benzz
Strength	100 mg
Packaging Type	Vial
Treatment	Chronic Lymphocytic Leukemia
Storage Temperature	2-8 degree c
Shelf Life	36 months
Prescription/Non Prescription	Prescription
Other Name	Benzz Bendamustine 100mg Injection
Injection Site	Benzz 100mg Injection is given as an injection into vein under the supervision of a doctor and shoul
Salt Name	Bendamustine 100mg
Generic Name	Bendamustine
Country of Origin	Made in India

Benzz 100mg Injection is an antineoplastic drug belonging to the class of alkylating agents, containing the active ingredient Bendamustine. It is used to prevent and treat chronic lymphocytic leukaemia (cancer of blood and bone marrow), non-Hodgkin’s lymphomas (cancer that forms in the lymph system, part of the immune system), and multiple myelomas (cancer of plasma cells, type of white blood cell).

The common side effects that are likely to occur with this medicine are headache, insomnia, fatigue, loss of appetite and rashes. Some serious side effects also include bone marrow suppression, tumor lysis syndrome, and Hepatotoxicity. Inform your healthcare provider if these side effects concern you or persist for longer than usual. It is often combined with rituximab, an immunotherapy drug, to treat various subtypes of non-Hodgkin's lymphoma, including follicular lymphoma, and mantle cell lymphoma. There may be an increased risk of certain types of skin cancer (non-melanoma skin cancer) with the use of this medicine. Consult your doctor immediately for more advice.

Uses

• Chronic lymphocytic leukaemia.
• Non-Hodgkin’s lymphomas
• Multiple myeloma

More Information

• Store Benzz 100mg Injection in the refrigerator (2°-8°C). Do not freeze.
• Keep it out of reach from children and pets.
• It is important to get the dose at the scheduled time. If you missed the schedule, contact your doctor and reschedule the dose.

Safety Advices Pregnancy  

Benzz 100mg Injection is not recommended for pregnant women as it may cause fetal harm. Consult your doctor if you are pregnant or planning for pregnancy during the treatment.  

Breast Feeding  

It is not known if Benzz 100mg Injection passes into your breast milk or if it will affect your baby. Please consult your doctor before breastfeeding.   

Lungs  

It is not known whether Benzz 100mg Injection can be administered to patients with lung problems. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Inform your doctor if you have any liver problems before taking Benzz 100mg Injection. Regular monitoring of liver function tests is recommended.  

Alcohol  

Consuming alcohol may affect the effectiveness of Benzz 100mg Injection. Stop consuming alcohol if you are taking this medicine.  

Driving  

It is unsafe to drive vehicles or operate heavy machinery after taking Benzz 100mg Injection, it may cause dizziness and impair your concentration.

Side Effects

• Severe allergic reactions
• Bone marrow suppression
• Abnormal liver function
• Tumor lysis syndrome

• Infection, fever
• Low blood cell count
• Headache, dizziness
• Nausea, vomiting
• Increased blood level of creatinine and urea (chemical waste products)
• Mucosal inflammation, sore mouth
• Insomnia, fatigue
• Hair loss, itching, rash
• Diarrhea, constipation
• Missed periods
• Dehydration, loss of appetite
• Low or high blood pressure

Dosage Form	Solution for Injection
Brand	Benzz
Strength	180 mg
Packaging Type	Vial
Treatment	Chronic Lymphocytic Leukemia
Storage Temperature	2-8 degree c
Shelf Life	36 months
Prescription/Non Prescription	Prescription
Other Name	Benzz Bendamustine 180mg Injection
Injection Site	Benzz 180mg Injection is given as an injection into vein under the supervision of a doctor and shoul
Salt Name	Bendamustine 180mg
Generic Name	Bendamustine
Country of Origin	Made in India

Benzz 180mg Injection is an antineoplastic drug belonging to the class of alkylating agents, containing the active ingredient Bendamustine. It is used to prevent and treat chronic lymphocytic leukaemia (cancer of blood and bone marrow), non-Hodgkin’s lymphomas (cancer that forms in the lymph system, part of the immune system), and multiple myelomas (cancer of plasma cells, type of white blood cell).

The common side effects that are likely to occur with this medicine are headache, insomnia, fatigue, loss of appetite and rashes. Some serious side effects also include bone marrow suppression, tumor lysis syndrome, and Hepatotoxicity. Inform your healthcare provider if these side effects concern you or persist for longer than usual. It is often combined with rituximab, an immunotherapy drug, to treat various subtypes of non-Hodgkin's lymphoma, including follicular lymphoma, and mantle cell lymphoma. There may be an increased risk of certain types of skin cancer (non-melanoma skin cancer) with the use of this medicine. Consult your doctor immediately for more advice.

 

Uses

• Chronic lymphocytic leukaemia.
• Non-Hodgkin’s lymphomas
• Multiple myeloma

More Information

• Store Benzz 180mg Injection in the refrigerator (2°-8°C). Do not freeze.
• Keep it out of reach from children and pets.
• It is important to get the dose at the scheduled time. If you missed the schedule, contact your doctor and reschedule the dose.

Safety Advices   Pregnancy

Benzz 180mg Injection is not recommended for pregnant women as it may cause fetal harm. Consult your doctor if you are pregnant or planning for pregnancy during the treatment.  

Breast Feeding

It is not known if Benzz 180mg Injection passes into your breast milk or if it will affect your baby. Please consult your doctor before breastfeeding.   

Lungs

It is not known whether Benzz 180mg Injection can be administered to patients with lung problems. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver

Inform your doctor if you have any liver problems before taking Benzz 180mg Injection. Regular monitoring of liver function tests is recommended.  

Alcohol

Consuming alcohol may affect the effectiveness of Benzz 180mg Injection. Stop consuming alcohol if you are taking this medicine.  

Driving

It is unsafe to drive vehicles or operate heavy machinery after taking Benzz 180mg Injection, it may cause dizziness and impair your concentration.

Side Effects

• Severe allergic reactions
• Bone marrow suppression
• Abnormal liver function
• Tumor lysis syndrome

• Infection, fever
• Low blood cell count
• Headache, dizziness
• Nausea, vomiting
• Increased blood level of creatinine and urea (chemical waste products)
• Mucosal inflammation, sore mouth
• Insomnia, fatigue
• Hair loss, itching, rash
• Diarrhea, constipation
• Missed periods
• Dehydration, loss of appetite
• Low or high blood pressure

Strength	150 mg
Brand	Capmatinib
Packaging Size	60 Tablets
Dose Type	Oral
Form	Tablet
Pack Type	Blister
Storage Condition	Below 30 degree
Prescription/Non prescription	Prescription
Country of Origin	Made in India

Rahika 150mg tablet contains the active ingredient Capmatinib. It is an anti-cancer medicine that belongs to the class of medications called protein kinase inhibitors. It is used to treat adults with a type of lung cancer called non-small cell lung cancer (NSCLC) that has spread to other body parts or is caused by a change (mutation) in a gene that makes an enzyme called MET in adults.  

Do not take this medicine if you are allergic to Rahika 150mg tablet or any ingredients. Inform the physician if you have or have ever had lung or breathing problems other than your lung cancer, liver problems, or pancreatic problems. Inform your physician if you have any symptoms of an allergic reaction, including rash, hives, fever, difficulty breathing, or low blood pressure. This medicine is not recommended for children and adolescents below 18 years of age.  

Avoid getting pregnant and breastfeeding during the treatment. Use effective contraception to avoid pregnancy. The common side effects of Rahika 150mg tablet are swelling in the face, and body, nausea, tiredness, vomiting, shortness of breath, and decreased appetite. 

Uses of Rahika 150mg Tablet

• Non-small cell lung cancer (NSCLC)

Therapeutic Effects of Rahika 150mg Tablet

Rahika 150mg tablet is a kinase inhibitor that targets mesenchymal-epithelial transition (MET). It works by blocking the action of this abnormal protein that signals cancer cells to multiply. This helps slow or stop the spread of cancer cells.

  More Information

• Store at 20°C to 25°C
• Protect the medicine from light and excessive moisture.
• Keep the medicine out of reach of children and pets
• If you forgot to take the tablet, take your next dose at the scheduled time. Do not take a double dose to make up for a forgotten dose.

Safety Advices  Pregnancy  

Do not take Rahika 150mg tablet if you are pregnant because this may harm the unborn baby. Inform your physician if you are pregnant, suspecting, or planning to get pregnant during the treatment. Use effective contraception during the treatment and for 7 days after your last dose.  

Breast Feeding  

Breastfeeding is not recommended in patients taking Rahika 150mg tablet because the medicine passes into the breast milk in small amounts and may harm your baby. Do not breastfeed during the treatment.   

Lungs  

Rahika 150mg tablet should be cautiously administered in patients with lung problems other than lung cancer. Inform your physician if you have any lung diseases before initiating the therapy.  

Liver  

Rahika 150mg tablet should be used cautiously in patients with liver problems. Dose adjustments are necessary for liver failure patients. Inform your physician if you have any liver diseases before initiating the therapy.   

Alcohol  

It is unknown whether it is safe to consume alcohol with Rahika 150mg tablet. Please consult your doctor.  

Driving  

It is unknown whether Rahika 150mg tablet alters the ability to drive or operate heavy machinery. If you feel dizzy or sleepy, avoid driving and consult your doctor. 

Side Effects

• Swelling in the face, and body
• Decrease in appetite
• Nausea
• Cough
• Fatigue

• Vomiting
• Liver injury
• Muscle pain
• Shortness of breath
• Lung infection
• Respiratory disease

Strength	600 mg
Vial Volume	60 ml
Brand	Reditux
Packaging Size	60 ml
Strength per ml	10 mg/ml
Composition	Rituximab
Form	Injection
Packaging Type	Vial
Storage Condition	Store in a refrigerator (2 - 8 DegreeC). Do not freeze
Manufacturer	Dr Reddy's Laboratories Ltd
Usage / Application	Personal
Indication	CLL, RA, NHL
Storage Conditions	Store in a refrigerator (2 - 8 DegreeC). Do not freeze
Shelf Life	48 months

Reditux 600mg injection contains the active constituent rituximab. It is used for several different disease conditions in adults. It is used alone or with other medications to treat non-hodgkin’s lymphoma (cancer affecting white blood cells called B-lymphocytes) and chronic lymphocytic leukemia (a most common form of cancer that affects B-cells). It is also indicated to treat moderate-to-severe rheumatoid arthritis (a type of disease where the immune system attacks the leukapheresis body cells of its own joints)  in combination with methotrexate in adults. Other uses include granulomatosis with polyangiitis or microscopic polyangiitis (inflammation of blood vessels that mainly affects the lungs and kidneys) in adults and children 2 years of age and older. It is also used to treat moderate to severe pemphigus vulgaris (an autoimmune condition that causes painful blisters on the skin and lining of the mouth, throat, nose, and genitals.  

 

Uses

• Non-hodgkin’s lymphoma (NHL)
• Chronic lymphocytic leukemia (CLL)
• Rheumatoid Arthritis
• Granulomatosis with polyangiitis or microscopic polyangiitis
• Pemphigus vulgaris

More Information

• Store Reditux 600mg injection  in the refrigerator (2°C to 8°C)
• Do not freeze
• keep the injection away from the reach of children and pets.
• If you have missed any dosing appointments, inform your doctor and schedule immediately.

Safety Advices Pregnancy  

Reditux 600mg injection is unsafe to administer in pregnant women because it may affect the fetus. Inform your physician if you are pregnant, suspect pregnancy, or planning to become pregnant. Using an effective birth control method during the treatment and for 12 months after your last dose is necessary.    

Breast Feeding  

Breastfeeding is not recommended in patients taking Reditux 600mg injection because the medicine passes into the breast milk in small amounts and may harm your baby.   

Lungs  

It is unknown whether Reditux 600mg injection can be used in patients with lung disorders. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Whether Reditux 600mg injection can be used in patients with liver impairment is unknown. Consult your doctor if you have or ever had liver disease or hepatitis B infection before starting the treatment. The reactivation of hepatitis viral infection can cause severe liver problems.   

Alcohol  

Consuming alcohol may affect the effectiveness of Reditux 600mg injection. Stop consuming alcohol if you are taking this medicine.   

Driving  

Caution is required while driving and operating machinery when you take Reditux 600mg injection because it may cause dizziness, sleepiness, tiredness, and risk of falling.

Side Effects

• Swelling in the face and body
• Diarrhea and nausea
• Itchy skin
• Anemia
• Muscle spasm
• Headache
• Urinary tract infection
• Fever, chills, and shivering
• Inflammation of nasal cavities
• Cough, sore throat
• Loss of hair

• Increased or decreased blood pressure
• Chest pain
• Hypersensitivity reactions
• Hepatitis B viral infection
• Memory loss, trouble thinking, difficulty in walking

Salt Form	Methylprednisolone
Strength	125mg
Pack Size	Vial
Drug Type	Methylprednisolone Acetate Injection
Brand	Neo-Drol
Route	IV
Form	Lyophilized powder
Usage	Arthritis
Manufacturer	Neon Laboratories Ltd
Packaging Size	2ml
Packaging Type	Vial
Injection Administration type	IV
Shelf Life	24 Months
Composition	Methylprednisolone 125mg
Also Gives	Third Party Manufacturing

Neo-Drol 125mg injection is an anti-inflammatory drug belonging to the class of glucocorticoids, containing the active ingredient methylprednisolone. It is used to treat inflammatory or allergic conditions affecting the brain (caused by tumor or meningitis), lungs (caused by asthma, hypersensitivity, tuberculosis, or breathing in vomit or stomach contents), gut, and bowel (Crohn’s disease and ulcerative colitis). It treats rheumatic, skin, eye, and endocrine disorders. It is also used for the palliative management of cancers (leukemia and lymphoma) and the reduction of pain after surgery. In higher doses, it is used to treat flare-ups of symptoms of multiple sclerosis. This injection should not be used if you have a fungal infection, swelling of the brain due to malaria, traumatic brain injury, or if you recently had vaccinated or about to have any vaccination. The common side effects that are likely to occur with this medicine are headache, vision problems, poor wound healing, and bone weakness. Some serious side effects also include blood clots in the leg veins, lungs, and bleeding ulcers. Inform your healthcare provider if these side effects concern you or persist for longer than usual. Consult your doctor immediately for more advice.

 

Uses

• Treatment of allergic conditions
• Rheumatic, blood, skin, eye, and endocrine disorders
• Leukemia and lymphomas (palliative management)
• Pain related to surgery (organ transplants)
• Multiple sclerosis
• Ulcerative colitis 

More Information

• Store Neo-Drol 125mg injection at controlled room temperature (20°-25°C).
• Protect from sunlight
• Keep it out of reach from children and pets.

Safety Advices Pregnancy

Neo-Drol 125mg injection is not recommended for pregnant women as it may cause fetal harm. Consult your doctor if you are pregnant or planning for pregnancy during the treatment. A dose adjustment is suggested.  

Breast Feeding

Breastfeeding is not recommended in patients administered with a Neo-Drol 125mg injection because it may harm your baby. Do not breastfeed during the treatment.  

Lungs

It is not known whether Neo-Drol 125mg injection can be administered to patients with lung problems. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver

Inform your doctor if you have any liver problems before taking Neo-Drol 125mg injection. Regular monitoring of liver function tests is recommended.  

Alcohol

Consuming alcohol may affect the effectiveness of Neo-Drol 125mg injection. Stop consuming alcohol if you are taking this medicine.  

Driving

It is unsafe to drive vehicles or operate heavy machinery after taking Neo-Drol 125mg injection, it may cause dizziness and impair your concentration.

Side Effects

• Allergic reactions (wheezing, swelling of face, difficulty breathing)
• Stomach pain spreading to your back, accompanied by vomiting and loss of consciousness
• Bleeding ulcers
• Infections
• Blood clots in the lung (chest pain, coughing up blood, breathlessness)
• Raised pressure within the skull (lack of energy, drowsiness)
• Blood clots in the leg vein

• High blood pressure, headache
• Swelling
• Ulcers
• Vision problems
• Poor wound healing
• Round or moon-shaped face
• Slow growth in infants, children, and adolescents
• Muscle and bone weakness
• Feeling depressed or high, difficulty in thinking, memory loss
• Acne, bruising
• Thinning of skin

Salt Form	Methylprednisolone
Strength	500mg
Pack Size	Vial
Drug Type	Methylprednisolone Acetate Injection
Brand	Solu-Medrol
Route	IV
Form	Lyophilized powder
Usage	Arthritis
Manufacturer	Pfizer Ltd
Packaging Type	Vial
Injection Administration type	IV
Shelf Life	24 Months
Composition	Methylprednisolone 500mg
Also Gives	Third Party Manufacturing

Solu medrol 500mg injection is an anti-inflammatory drug belonging to the class of glucocorticoids, containing the active ingredient methylprednisolone. It is used to treat inflammatory or allergic conditions affecting the brain (caused by tumor or meningitis), lungs (caused by asthma, hypersensitivity, tuberculosis, or breathing in vomit or stomach contents), gut, and bowel (Crohn’s disease and ulcerative colitis). It treats rheumatic, skin, eye, and endocrine disorders. It is also used for the palliative management of cancers (leukemia and lymphoma) and the reduction of pain after surgery. In higher doses, it is used to treat flare-ups of symptoms of multiple sclerosis. This injection should not be used if you have a fungal infection, swelling of the brain due to malaria, traumatic brain injury, or if you recently had vaccinated or about to have any vaccination. The common side effects that are likely to occur with this medicine are headache, vision problems, poor wound healing, and bone weakness. Some serious side effects also include blood clots in the leg veins, lungs, and bleeding ulcers. Inform your healthcare provider if these side effects concern you or persist for longer than usual. Consult your doctor immediately for more advice.

 

Uses

• Treatment of allergic conditions
• Rheumatic, blood, skin, eye, and endocrine disorders
• Leukemia and lymphomas (palliative management)
• Pain related to surgery (organ transplants)
• Multiple sclerosis
• Ulcerative colitis

More Information

• Store Solu medrol 500mg injection at controlled room temperature (20°-25°C).
• Protect from sunlight
• Keep it out of reach from children and pets.

Safety Advices Pregnancy  

Solu medrol 500mg injection is not recommended for pregnant women as it may cause fetal harm. Consult your doctor if you are pregnant or planning for pregnancy during the treatment. A dose adjustment is suggested.  

Breast Feeding  

Breastfeeding is not recommended in patients administered with a Solu medrol 500mg injection because it may harm your baby. Do not breastfeed during the treatment.   

Lungs  

It is not known whether Solu medrol 500mg injection can be administered to patients with lung problems. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Inform your doctor if you have any liver problems before taking Solu medrol 500mg injection. Regular monitoring of liver function tests is recommended. 

Alcohol  

Consuming alcohol may affect the effectiveness of Solu medrol 500mg injection. Stop consuming alcohol if you are taking this medicine.  

Driving  

It is unsafe to drive vehicles or operate heavy machinery after taking Solu medrol 500mg injection, it may cause dizziness and impair your concentration.

Side Effects

• Allergic reactions (wheezing, swelling of face, difficulty breathing)
• Stomach pain spreading to your back, accompanied by vomiting and loss of consciousness
• Bleeding ulcers
• Infections
• Blood clots in the lung (chest pain, coughing up blood, breathlessness)
• Raised pressure within the skull (lack of energy, drowsiness)
• Blood clots in the leg vein

• High blood pressure, headache
• Swelling
• Ulcers
• Vision problems
• Poor wound healing
• Round or moon-shaped face
• Slow growth in infants, children, and adolescents
• Muscle and bone weakness
• Feeling depressed or high, difficulty in thinking, memory loss
• Acne, bruising
• Thinning of skin

Salt Form	Methylprednisolone
Strength	500mg
Pack Size	Vial
Drug Type	Methylprednisolone Acetate Injection
Brand	Methylprednisolone
Route	IV
Form	Lyophilized powder
Usage	Pain and Inflammation
Manufacturer	THEMIS MEDICARE
Packaging Type	Vial
Injection Administration type	IV
Shelf Life	24 Months
Composition	Methylprednisolone 500mg
Also Gives	PCD Pharma Franchise

Methnilon 500mg injection is an anti-inflammatory drug belonging to the class of glucocorticoids, containing the active ingredient methylprednisolone. It is used to treat inflammatory or allergic conditions affecting the brain (caused by tumor or meningitis), lungs (caused by asthma, hypersensitivity, tuberculosis, or breathing in vomit or stomach contents), gut, and bowel (Crohn’s disease and ulcerative colitis). It treats rheumatic, skin, eye, and endocrine disorders. It is also used for the palliative management of cancers (leukemia and lymphoma) and the reduction of pain after surgery. In higher doses, it is used to treat flare-ups of symptoms of multiple sclerosis. This injection should not be used if you have a fungal infection, swelling of the brain due to malaria, traumatic brain injury, or if you recently had vaccinated or about to have any vaccination. The common side effects that are likely to occur with this medicine are headache, vision problems, poor wound healing, and bone weakness. Some serious side effects also include blood clots in the leg veins, lungs, and bleeding ulcers. Inform your healthcare provider if these side effects concern you or persist for longer than usual. Consult your doctor immediately for more advice.

Uses

• Treatment of allergic conditions
• Rheumatic, blood, skin, eye, and endocrine disorders
• Leukemia and lymphomas (palliative management)
• Pain related to surgery (organ transplants)
• Multiple sclerosis
• Ulcerative colitis

More Information

• Store Methnilon 500mg injection at controlled room temperature (20°-25°C).
• Protect from sunlight
• Keep it out of reach from children and pets.

Safety Advices Pregnancy  

Methnilon 500mg injection is not recommended for pregnant women as it may cause fetal harm. Consult your doctor if you are pregnant or planning for pregnancy during the treatment. A dose adjustment is suggested.  

Breast Feeding  

Breastfeeding is not recommended in patients administered with a Methnilon 500mg injection because it may harm your baby. Do not breastfeed during the treatment.  

Lungs  

It is not known whether Methnilon 500mg injection can be administered to patients with lung problems. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Inform your doctor if you have any liver problems before taking Methnilon 500mg injection. Regular monitoring of liver function tests is recommended.  

Alcohol  

Consuming alcohol may affect the effectiveness of Methnilon 500mg injection. Stop consuming alcohol if you are taking this medicine.  

Driving  

It is unsafe to drive vehicles or operate heavy machinery after taking Methnilon 500mg injection, it may cause dizziness and impair your concentration.

Side Effects

• Allergic reactions (wheezing, swelling of face, difficulty breathing)
• Stomach pain spreading to your back, accompanied by vomiting and loss of consciousness
• Bleeding ulcers
• Infections
• Blood clots in the lung (chest pain, coughing up blood, breathlessness)
• Raised pressure within the skull (lack of energy, drowsiness)
• Blood clots in the leg vein

• High blood pressure, headache
• Swelling
• Ulcers
• Vision problems
• Poor wound healing
• Round or moon-shaped face
• Slow growth in infants, children, and adolescents
• Muscle and bone weakness
• Feeling depressed or high, difficulty in thinking, memory loss
• Acne, bruising
• Thinning of skin

Salt Form	Methylprednisolone
Strength	500mg
Pack Size	Vial
Drug Type	Methylprednisolone Acetate Injection
Brand	Methylprednisolone
Route	IV
Form	Lyophilized powder
Usage	Pain and Inflammation
Manufacturer	Neon Laboratories Ltd
Packaging Size	1ml
Packaging Type	Vial
Injection Administration type	IV
Shelf Life	24 Months
Composition	Methylprednisolone 500mg
Also Gives	PCD Pharma Franchise

Neo-Drol 500mg injection is an anti-inflammatory drug belonging to the class of glucocorticoids, containing the active ingredient methylprednisolone. It is used to treat inflammatory or allergic conditions affecting the brain (caused by tumor or meningitis), lungs (caused by asthma, hypersensitivity, tuberculosis, or breathing in vomit or stomach contents), gut, and bowel (Crohn’s disease and ulcerative colitis). It treats rheumatic, skin, eye, and endocrine disorders. It is also used for the palliative management of cancers (leukemia and lymphoma) and the reduction of pain after surgery. In higher doses, it is used to treat flare-ups of symptoms of multiple sclerosis. This injection should not be used if you have a fungal infection, swelling of the brain due to malaria, traumatic brain injury, or if you recently had vaccinated or about to have any vaccination. The common side effects that are likely to occur with this medicine are headache, vision problems, poor wound healing, and bone weakness. Some serious side effects also include blood clots in the leg veins, lungs, and bleeding ulcers. Inform your healthcare provider if these side effects concern you or persist for longer than usual. Consult your doctor immediately for more advice.

 

Uses

• Treatment of allergic conditions
• Rheumatic, blood, skin, eye, and endocrine disorders
• Leukemia and lymphomas (palliative management)
• Pain related to surgery (organ transplants)
• Multiple sclerosis
• Ulcerative colitis

More Information

• Store Neo-Drol 500mg injection at controlled room temperature (20°-25°C).
• Protect from sunlight
• Keep it out of reach from children and pets.

Safety Advices Pregnancy  

Neo-Drol 500mg injection is not recommended for pregnant women as it may cause fetal harm. Consult your doctor if you are pregnant or planning for pregnancy during the treatment. A dose adjustment is suggested.  

Breast Feeding  

Breastfeeding is not recommended in patients administered with a Neo-Drol 500mg injection because it may harm your baby. Do not breastfeed during the treatment.  

Lungs  

It is not known whether Neo-Drol 500mg injection can be administered to patients with lung problems. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Inform your doctor if you have any liver problems before taking Neo-Drol 500mg injection. Regular monitoring of liver function tests is recommended.  

Alcohol  

Consuming alcohol may affect the effectiveness of Neo-Drol 500mg injection. Stop consuming alcohol if you are taking this medicine.  

Driving  

It is unsafe to drive vehicles or operate heavy machinery after taking Neo-Drol 500mg injection, it may cause dizziness and impair your concentration.

Side Effects

• Allergic reactions (wheezing, swelling of face, difficulty breathing)
• Stomach pain spreading to your back, accompanied by vomiting and loss of consciousness
• Bleeding ulcers
• Infections
• Blood clots in the lung (chest pain, coughing up blood, breathlessness)
• Raised pressure within the skull (lack of energy, drowsiness)
• Blood clots in the leg vein

• High blood pressure, headache
• Swelling
• Ulcers
• Vision problems
• Poor wound healing
• Round or moon-shaped face
• Slow growth in infants, children, and adolescents
• Muscle and bone weakness
• Feeling depressed or high, difficulty in thinking, memory loss
• Acne, bruising
• Thinning of skin

Strength	100 mg
Brand	Temoget
Capsules per Pack	1 Capsule
Pack Type	Bottle
Form	Capsule
Usage	Brain Tumor
Storage Condition	Store below 30 DegreeC
Manufacturer	GLS Pharma Ltd.
Prescription/Non prescription	Prescription
Shelf Life	24 months
Storage Instruction	Store below 30 DegreeC
Usage/Application	Personal

Temoget 100mg Capsule contains the active ingredient temozolomide. It belongs to the class of medications known as Antitumor agents. It is prescribed to treat brain cancer, such as glioblastoma multiforme in adults and malignant glioma, including glioblastoma multiforme or anaplastic astrocytoma in patients older than three years. Glioblastoma and anaplastic astrocytoma are the most common and aggressive brain cancers with low chances of survival. Anaplastic astrocytoma is treated with Temoget 100mg Capsule or radiotherapy after biopsy, whereas Glioblastoma multiforme is treated with a combination of radiotherapy and Temoget 100mg Capsule, and it is continued as maintenance therapy.

The common side effects that are likely to associate with Temoget 100mg Capsule are nausea, vomiting, dizziness, diarrhea, constipation, hair loss, rashes, tiredness, frequent urination, vision and hearing problems, high blood sugar levels, muscle damage, pain in muscles and joints, memory loss, coordination problems, infections, sleep problems and loss of weight. Inform your doctor if any of these symptoms disturb you or persist

 

Uses

•  Treatment of newly diagnosed glioblastoma multiforme.
• Treatment of refractory anaplastic astrocytoma

More Information

• Keep Temoget 100mg Capsule out of sight and reach of children.
• Store protected from light and moisture.
• Do not store above 25°C.

Safety Advices Pregnancy  

Temoget 100mg Capsule is unsafe to use during pregnancy as it may cause fetal harm. It should not be used unless prescribed by your physician. Women with childbearing potential should use effective contraceptive precautions for at least 6 months following the completion of treatment.   

Breast Feeding  

Temoget 100mg Capsule is unsafe to use during breastfeeding as it passes through breast milk and harm the baby. Consult your physician for advice before breastfeeding.  

Lungs  

Inform your physician before taking Temoget 100mg Capsule if you have if you have any lung conditions.   

Liver  

Inform your physician before taking Temoget 100mg Capsule if you have severe liver problems. Dose adjustment is required based on the condition.  

Alcohol  

Avoid consuming alcohol while taking Temoget 100mg Capsule as it may cause unpleasant side effects. Consult our doctor for advice.  

Driving  

Do not drive or operate heavy machines while being treated with Temoget 100mg Capsule as it may decrease alertness, affect your vision and make you dizzy and sleepy. 

Side Effects

• Secondary cancer like myelodysplastic syndrome and myeloid leukemia.
• Severe Allergic reactions
• Inflammation and fluid buildup in lungs
• Blood clot in lungs or legs
• Liver toxicity
• Convulsions
• Fever and chills
• Severe headache
• Uncontrolled bleeding

• Hair loss
• Rashes
• Tiredness
• Nausea, vomiting and diarrhea
• Constipation
• High blood sugar levels
• Dizziness, impaired sensation, tingling sensation, abnormal taste
• Vision and Hearing problem
• Frequent urination
• Muscle damage, pain in muscles and joints
• Weight changes
• Infections and wounds
• Amnesia
• Abnormal blood cell counts
• Loss of appetite
• Sleep problems
• Memory loss
• Difficulty concentrating, changes in mental status and alertness
• Coordination problems

Strength	200mg
Pack Size	120 tablets
Brand	Bosutris
Brand Name	Bosutris
Composition	Bosutinib
Indication	CML
Prescription Type	Rx Only
Storage Condition	Store between 20 Degree to 25 DegreeC.
Prescription/Non prescription	Prescription
Form	Tablet
Treatment	CLL / SLL, Blood Cancer
Country of Origin	Made in India

Bosutris 100mg Tablet contains the active ingredient bosutinib. It belongs to the group of medications called Tyrosine kinase inhibitors. It is indicated to treat adult patients with a type of leukemia known as Philadelphia chromosome-positive (Ph-positive) Chronic Myeloid Leukaemia (CML) who have been newly diagnosed or for whom earlier CML treatments have either failed or have not worked or are not suitable. Philadelphia chromosome-positive chronic myelogenous leukemia is a blood cancer in which the body produces too many of a specific kind of white blood cell called granulocytes. 

Low white blood cell count (leukopenia), headache, shortness of breath, joint pain, dizziness, cough, back pain, decreased appetite, respiratory tract infection, raised blood pressure, ringing in the ears (tinnitus), itching, acne, dehydration, taste change, sensitivity to light and fluid on lungs are the common side effects of Bosutris 100mg Tablet. Inform your doctor if any of these symptoms disturb you or persist.

Uses
Treatment of Philadelphia chromosome-positive chronic myelogenous leukemia (Ph+ CML).

Storage
Keep Bosutris 100mg Tablet out of sight and reach of children.Store between 20° to 25°C.

Side Effects
Blood disorders (bleeding, fever, bruising)Stomach problems (stomach pain, vomiting, diarrhea, constipation, nausea)Hepatitis B reactivationSevere skin reactionsLiver problems (yellowing of white part of eyes and skin, tea-colored urine)Heart problems (loss of consciousness, irregular heartbeat)Low white blood cell count (leukopenia)Headache, dizzinessCough, shortness of breathJoint pain, back painDecreased appetiteRespiratory tract infectionIncrease in blood pressureRinging in the ears (tinnitus)Itching, acneDehydrationTaste changeSensitivity to lightFluid on lungs

Dose Ratio	100 mg + 224 mg
Packaging Size	10*14 Capsules
Capsules per Pack	10 Capsules
Brand	UFT
Strength	100 mg/224 mg
Composition	Tegafur + Uracil
Pack Type	Blister Pack
Usage	Colorectal Cancer
Storage Condition	Store below 30 DegreeC
Prescription/Non prescription	Prescription
Country of Origin	Made in India

Uratuf capsule is the combination of two medications called Tegafur +  Uracil. It is an anti-cancer medicine that belongs to the class of medication called pyrimidine analogs. It is indicated for the first-line treatment of metastatic colorectal cancer, along with other anti-cancer medications. Cancer is a condition in which cells multiply uncontrolled and abnormally. It is not recommended for adolescents and children. Avoid taking this medicine if you are pregnant or breastfeeding.   

Do not take Uratuf capsule if you are allergic to Tegafur +  Uracil or any other ingredients of this medicine. Inform your healthcare professional if you have liver diseases, kidney disorders, or other noncancerous conditions before initiating the treatment. This medicine may reduce fertility in men and women; discuss this with your doctor before starting the therapy. The most common side effects are diarrhea, nausea, vomiting, tiredness, and risk of infection. 

Uses of Uratuf Capsule

• Colorectal cancer

Therapeutic Effects of Uratuf Capsule

Uratuf capsule is a combination of two chemotherapy drugs: tegafur and uracil.  tegafur is absorbed into the bloodstream, converted into the active drug 5FU in the liver, and then absorbed by tumor cells. Within the cells is an enzyme that breaks down the 5FU. The uracil slows the breakdown of 5FU, which means that the 5FU stays in the cancer cells for longer.  It prevents the growth and multiplication of cancer cells and thus helps destroy the tumor.

More Information

• Store at temperatures not exceeding 25°C
• Keep the capsule away from the reach of children and pets.
• If you miss a dosage, take it as soon as you remember. If it is almost time for the next dose, skip the missing dose.
• Do not take a double dose to compensate for a missed dose.

Safety Advices Pregnancy  

Uratuf capsule is unsafe for pregnant women because it may cause birth defects. Inform your physician if you are pregnant, suspect pregnancy, or planning to become pregnant. Using effective contraception during the treatment.   

Breast Feeding  

Breastfeeding is not recommended in patients taking Uratuf capsule because the medicine passes into the breast milk in small amounts and may harm the baby. Uratuf   

Lungs  

It is unknown whether Uratuf capsule can be used in patients with lung disorders. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Uratuf capsule should be cautiously administered in patients with severe liver diseases. Dose adjustments are necessary for severe liver failure. Inform your physician if you have liver problems before initiating the therapy.    

Alcohol  

It is not known whether it is safe to consume alcohol with Uratuf capsule. Please consult your doctor.  

Driving  

Driving vehicles or operating machinery after taking Uratuf capsule is unsafe as you may develop dizziness, tiredness, and blurred vision. 

Side Effects

• Diarrhea
• Nausea, vomiting
• Tiredness
• Risk of infection
• Fever
• Bruising and bleeding
• Anemia
• Changes in skin and nail

• Swelling in the face, and body
• Severe skin rashes
• Severe diarrhea
• Liver injury

Strength	100 mg
Brand	Myzotem
Capsules per Pack	5 Capsules
Pack Type	Bottle
Form	Capsule
Usage	Brain Tumor
Storage Condition	Store below 30 DegreeC
Manufacturer	Mylan Pharmaceuticals Pvt Ltd - A Viatris Company
Prescription/Non prescription	Prescription
Shelf Life	24 Months
Storage Instruction	Store below 30 DegreeC
Usage/Application	Personal

Myzotem 100mg Capsule contains the active ingredient temozolomide. It belongs to the class of medications known as Antitumor agents. It is prescribed to treat brain cancer, such as glioblastoma multiforme in adults and malignant glioma, including glioblastoma multiforme or anaplastic astrocytoma in patients older than three years. Glioblastoma and anaplastic astrocytoma are the most common and aggressive brain cancers with low chances of survival. Anaplastic astrocytoma is treated with Myzotem 100mg Capsule or radiotherapy after biopsy, whereas Glioblastoma multiforme is treated with a combination of radiotherapy and Myzotem 100mg Capsule, and it is continued as maintenance therapy.

The common side effects that are likely to associate with Myzotem 100mg Capsule are nausea, vomiting, dizziness, diarrhea, constipation, hair loss, rashes, tiredness, frequent urination, vision and hearing problems, high blood sugar levels, muscle damage, pain in muscles and joints, memory loss, coordination problems, infections, sleep problems and loss of weight. Inform your doctor if any of these symptoms disturb you or persist

 

Uses

•  Treatment of newly diagnosed glioblastoma multiforme.
• Treatment of refractory anaplastic astrocytoma

More Information

• Keep Myzotem 100mg Capsule out of sight and reach of children.
• Store protected from light and moisture.
• Do not store above 25°C.

Safety Advices Pregnancy  

Myzotem 100mg Capsule is unsafe to use during pregnancy as it may cause fetal harm. It should not be used unless prescribed by your physician. Women with childbearing potential should use effective contraceptive precautions for at least 6 months following the completion of treatment.   

Breast Feeding  

Myzotem 100mg Capsule is unsafe to use during breastfeeding as it passes through breast milk and harm the baby. Consult your physician for advice before breastfeeding.  

Lungs  

Inform your physician before taking Myzotem 100mg Capsule if you have if you have any lung conditions.   

Liver  

Inform your physician before taking Myzotem 100mg Capsule if you have severe liver problems. Dose adjustment is required based on the condition.  

Alcohol  

Avoid consuming alcohol while taking Myzotem 100mg Capsule as it may cause unpleasant side effects. Consult our doctor for advice.  

Driving  

Do not drive or operate heavy machines while being treated with Myzotem 100mg Capsule as it may decrease alertness, affect your vision and make you dizzy and sleepy. 

Side Effects

• Secondary cancer like myelodysplastic syndrome and myeloid leukemia.
• Severe Allergic reactions
• Inflammation and fluid buildup in lungs
• Blood clot in lungs or legs
• Liver toxicity
• Convulsions
• Fever and chills
• Severe headache
• Uncontrolled bleeding

• Hair loss
• Rashes
• Tiredness
• Nausea, vomiting and diarrhea
• Constipation
• High blood sugar levels
• Dizziness, impaired sensation, tingling sensation, abnormal taste
• Vision and Hearing problem
• Frequent urination
• Muscle damage, pain in muscles and joints
• Weight changes
• Infections and wounds
• Amnesia
• Abnormal blood cell counts
• Loss of appetite
• Sleep problems
• Memory loss
• Difficulty concentrating, changes in mental status and alertness
• Coordination problems

Strength	100 mg
Brand	Temozol
Capsules per Pack	Injection
Pack Type	Bottle
Form	Injection
Usage	Brain Tumor
Storage Condition	Store below 30 DegreeC
Manufacturer	Getwell Pharma (I) Pvt Ltd
Prescription/Non prescription	Prescription
Shelf Life	24 Months
Storage Instruction	Store below 30 DegreeC
Usage/Application	Personal

Temzol 100mg Injection contains the active ingredient temozolomide. It belongs to the class of medications known as Antitumor agents. It is prescribed to treat brain cancer, such as glioblastoma multiforme in adults and malignant glioma, including glioblastoma multiforme or anaplastic astrocytoma in patients older than three years. Glioblastoma and anaplastic astrocytoma are the most common and aggressive brain cancers with low chances of survival. Anaplastic astrocytoma is treated with Temzol 100mg Injection or radiotherapy after biopsy, whereas Glioblastoma multiforme is treated with a combination of radiotherapy and Temzol 100mg Injection, and it is continued as maintenance therapy.

The common side effects that are likely to associate with Temzol 100mg Injection are nausea, vomiting, dizziness, diarrhea, constipation, hair loss, rashes, tiredness, frequent urination, vision and hearing problems, high blood sugar levels, muscle damage, pain in muscles and joints, memory loss, coordination problems, infections, sleep problems and loss of weight. Inform your doctor if any of these symptoms disturb you or persist

 

Uses

•  Treatment of newly diagnosed glioblastoma multiforme.
• Treatment of refractory anaplastic astrocytoma

More Information

• Keep Temzol 100mg Injection out of sight and reach of children.
• Store protected from light and moisture.
• Do not store above 25°C.

Safety Advices Pregnancy  

Temzol 100mg Injection is unsafe to use during pregnancy as it may cause fetal harm. It should not be used unless prescribed by your physician. Women with childbearing potential should use effective contraceptive precautions for at least 6 months following the completion of treatment.   

Breast Feeding  

Temzol 100mg Injection is unsafe to use during breastfeeding as it passes through breast milk and harm the baby. Consult your physician for advice before breastfeeding.  

Lungs  

Inform your physician before taking Temzol 100mg Injection if you have if you have any lung conditions.   

Liver  

Inform your physician before taking Temzol 100mg Injection if you have severe liver problems. Dose adjustment is required based on the condition.  

Alcohol  

Avoid consuming alcohol while taking Temzol 100mg Injection as it may cause unpleasant side effects. Consult our doctor for advice.  

Driving  

Do not drive or operate heavy machines while being treated with Temzol 100mg Injection as it may decrease alertness, affect your vision and make you dizzy and sleepy. 

Side Effects

• Secondary cancer like myelodysplastic syndrome and myeloid leukemia.
• Severe Allergic reactions
• Inflammation and fluid buildup in lungs
• Blood clot in lungs or legs
• Liver toxicity
• Convulsions
• Fever and chills
• Severe headache
• Uncontrolled bleeding

• Hair loss
• Rashes
• Tiredness
• Nausea, vomiting and diarrhea
• Constipation
• High blood sugar levels
• Dizziness, impaired sensation, tingling sensation, abnormal taste
• Vision and Hearing problem
• Frequent urination
• Muscle damage, pain in muscles and joints
• Weight changes
• Infections and wounds
• Amnesia
• Abnormal blood cell counts
• Loss of appetite
• Sleep problems
• Memory loss
• Difficulty concentrating, changes in mental status and alertness
• Coordination problems

Strength	100 mg
Brand	Temother
Capsules per Pack	Injection
Pack Type	Bottle
Form	Injection
Usage	Brain Tumor
Storage Condition	Store below 30 DegreeC
Prescription/Non prescription	Prescription
Manufacturer	Therdose Pharma Pvt Ltd
Shelf Life	24 Months
Storage Instruction	Store below 30 DegreeC
Usage/Application	Personal

Temother 100mg Injection contains the active ingredient temozolomide. It belongs to the class of medications known as Antitumor agents. It is prescribed to treat brain cancer, such as glioblastoma multiforme in adults and malignant glioma, including glioblastoma multiforme or anaplastic astrocytoma in patients older than three years. Glioblastoma and anaplastic astrocytoma are the most common and aggressive brain cancers with low chances of survival. Anaplastic astrocytoma is treated with Temother 100mg Injection or radiotherapy after biopsy, whereas Glioblastoma multiforme is treated with a combination of radiotherapy and Temother 100mg Injection, and it is continued as maintenance therapy.

The common side effects that are likely to associate with Temother 100mg Injection are nausea, vomiting, dizziness, diarrhea, constipation, hair loss, rashes, tiredness, frequent urination, vision and hearing problems, high blood sugar levels, muscle damage, pain in muscles and joints, memory loss, coordination problems, infections, sleep problems and loss of weight. Inform your doctor if any of these symptoms disturb you or persist

 

Uses

•  Treatment of newly diagnosed glioblastoma multiforme.
• Treatment of refractory anaplastic astrocytoma

More Information

• Keep Temother 100mg Injection out of sight and reach of children.
• Store protected from light and moisture.
• Do not store above 25°C.

Safety Advices  Pregnancy

Temother 100mg Injection is unsafe to use during pregnancy as it may cause fetal harm. It should not be used unless prescribed by your physician. Women with childbearing potential should use effective contraceptive precautions for at least 6 months following the completion of treatment.   

Breast Feeding

Temother 100mg Injection is unsafe to use during breastfeeding as it passes through breast milk and harm the baby. Consult your physician for advice before breastfeeding.  

Lungs

Inform your physician before taking Temother 100mg Injection if you have if you have any lung conditions.   

Liver

Inform your physician before taking Temother 100mg Injection if you have severe liver problems. Dose adjustment is required based on the condition.  

Alcohol

Avoid consuming alcohol while taking Temother 100mg Injection as it may cause unpleasant side effects. Consult our doctor for advice.  

Driving

Do not drive or operate heavy machines while being treated with Temother 100mg Injection as it may decrease alertness, affect your vision and make you dizzy and sleepy. 

Side Effects

• Secondary cancer like myelodysplastic syndrome and myeloid leukemia.
• Severe Allergic reactions
• Inflammation and fluid buildup in lungs
• Blood clot in lungs or legs
• Liver toxicity
• Convulsions
• Fever and chills
• Severe headache
• Uncontrolled bleeding

• Hair loss
• Rashes
• Tiredness
• Nausea, vomiting and diarrhea
• Constipation
• High blood sugar levels
• Dizziness, impaired sensation, tingling sensation, abnormal taste
• Vision and Hearing problem
• Frequent urination
• Muscle damage, pain in muscles and joints
• Weight changes
• Infections and wounds
• Amnesia
• Abnormal blood cell counts
• Loss of appetite
• Sleep problems
• Memory loss
• Difficulty concentrating, changes in mental status and alertness
• Coordination problems

Dose Ratio	100 mg + 224 mg
Packaging Size	10*14 Capsules
Capsules per Pack	10 Capsules
Brand	UFT
Strength	100 mg/224 mg
Composition	Tegafur + Uracil
Pack Type	Blister Pack
Usage	Colorectal Cancer
Storage Condition	Store below 30 DegreeC
Prescription/Non prescription	Prescription
Form	Tablet
Country of Origin	Made in India

Tegafi capsule is the combination of two medications called Tegafur +  Uracil. It is an anti-cancer medicine that belongs to the class of medication called pyrimidine analogs. It is indicated for the first-line treatment of metastatic colorectal cancer, along with other anti-cancer medications. Cancer is a condition in which cells multiply uncontrolled and abnormally. It is not recommended for adolescents and children. Avoid taking this medicine if you are pregnant or breastfeeding.   

Do not take Tegafi capsule if you are allergic to Tegafur +  Uracil or any other ingredients of this medicine. Inform your healthcare professional if you have liver diseases, kidney disorders, or other noncancerous conditions before initiating the treatment. This medicine may reduce fertility in men and women; discuss this with your doctor before starting the therapy. The most common side effects are diarrhea, nausea, vomiting, tiredness, and risk of infection. 

Uses of Tegafi Capsule

• Colorectal cancer

Therapeutic Effects of Tegafi Capsule

Tegafi capsule is a combination of two chemotherapy drugs: tegafur and uracil.  tegafur is absorbed into the bloodstream, converted into the active drug 5FU in the liver, and then absorbed by tumor cells. Within the cells is an enzyme that breaks down the 5FU. The uracil slows the breakdown of 5FU, which means that the 5FU stays in the cancer cells for longer.  It prevents the growth and multiplication of cancer cells and thus helps destroy the tumor.

More Information

• Store at temperatures not exceeding 25°C
• Keep the capsule away from the reach of children and pets.
• If you miss a dosage, take it as soon as you remember. If it is almost time for the next dose, skip the missing dose.
• Do not take a double dose to compensate for a missed dose.

Safety Advices Pregnancy  

Tegafi capsule is unsafe for pregnant women because it may cause birth defects. Inform your physician if you are pregnant, suspect pregnancy, or planning to become pregnant. Using effective contraception during the treatment.   

Breast Feeding  

Breastfeeding is not recommended in patients taking Tegafi capsule because the medicine passes into the breast milk in small amounts and may harm the baby. Tegafi   

Lungs  

It is unknown whether Tegafi capsule can be used in patients with lung disorders. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Tegafi capsule should be cautiously administered in patients with severe liver diseases. Dose adjustments are necessary for severe liver failure. Inform your physician if you have liver problems before initiating the therapy.    

Alcohol  

It is not known whether it is safe to consume alcohol with Tegafi capsule. Please consult your doctor.  

Driving  

Driving vehicles or operating machinery after taking Tegafi capsule is unsafe as you may develop dizziness, tiredness, and blurred vision. 

Side Effects

• Diarrhea
• Nausea, vomiting
• Tiredness
• Risk of infection
• Fever
• Bruising and bleeding
• Anemia
• Changes in skin and nail

• Swelling in the face, and body
• Severe skin rashes
• Severe diarrhea
• Liver injury

Dose Ratio	100 mg + 224 mg
Capsules per Pack	14 Capsules
Strength	100 mg
Brand	Tegafur Uracil
Brand Name	Bdficil
Composition	Tegafur Uracil
Packaging Size	10 Capsules
Pack Type	Blister Pack
Usage	Colorectal Cancer
Storage Condition	Store below 30 DegreeC
Prescription/Non prescription	Prescription
Form	Tablet
Manufacturer	Natco Pharma
Country of Origin	Made in India

Bdfucil capsule is the combination of two medications called Tegafur +  Uracil. It is an anti-cancer medicine that belongs to the class of medication called pyrimidine analogs. It is indicated for the first-line treatment of metastatic colorectal cancer, along with other anti-cancer medications. Cancer is a condition in which cells multiply uncontrolled and abnormally. It is not recommended for adolescents and children. Avoid taking this medicine if you are pregnant or breastfeeding.   

Do not take Bdfucil capsule if you are allergic to Tegafur +  Uracil or any other ingredients of this medicine. Inform your healthcare professional if you have liver diseases, kidney disorders, or other noncancerous conditions before initiating the treatment. This medicine may reduce fertility in men and women; discuss this with your doctor before starting the therapy. The most common side effects are diarrhea, nausea, vomiting, tiredness, and risk of infection. 

Uses of Bdfucil Capsule

• Colorectal cancer

Therapeutic Effects of Bdfucil Capsule

Bdfucil capsule is a combination of two chemotherapy drugs: tegafur and uracil.  tegafur is absorbed into the bloodstream, converted into the active drug 5FU in the liver, and then absorbed by tumor cells. Within the cells is an enzyme that breaks down the 5FU. The uracil slows the breakdown of 5FU, which means that the 5FU stays in the cancer cells for longer.  It prevents the growth and multiplication of cancer cells and thus helps destroy the tumor.

More Information

• Store at temperatures not exceeding 25°C
• Keep the capsule away from the reach of children and pets.
• If you miss a dosage, take it as soon as you remember. If it is almost time for the next dose, skip the missing dose.
• Do not take a double dose to compensate for a missed dose.

Safety Advices   Pregnancy  

Bdfucil capsule is unsafe for pregnant women because it may cause birth defects. Inform your physician if you are pregnant, suspect pregnancy, or planning to become pregnant. Using effective contraception during the treatment.   

Breast Feeding  

Breastfeeding is not recommended in patients taking Bdfucil capsule because the medicine passes into the breast milk in small amounts and may harm the baby. Bdfucil  

Lungs  

It is unknown whether Bdfucil capsule can be used in patients with lung disorders. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Bdfucil capsule should be cautiously administered in patients with severe liver diseases. Dose adjustments are necessary for severe liver failure. Inform your physician if you have liver problems before initiating the therapy.    

Alcohol  

It is not known whether it is safe to consume alcohol with Bdfucil capsule. Please consult your doctor.  

Driving  

Driving vehicles or operating machinery after taking Bdfucil capsule is unsafe as you may develop dizziness, tiredness, and blurred vision. 

Side Effects

• Diarrhea
• Nausea, vomiting
• Tiredness
• Risk of infection
• Fever
• Bruising and bleeding
• Anemia
• Changes in skin and nail

• Swelling in the face, and body
• Severe skin rashes
• Severe diarrhea
• Liver injury

Dose Ratio	100 mg + 224 mg
Packaging Size	10*14 Capsules
Capsules per Pack	14 Capsules
Brand	Uracel
Strength	100 mg/224 mg
Composition	Tegafur + Uracil
Pack Type	Blister Pack
Usage	Colorectal Cancer
Storage Condition	Store below 30 DegreeC
Prescription/Non prescription	Prescription
Country of Origin	Made in India

Uracel capsule is the combination of two medications called Tegafur +  Uracil. It is an anti-cancer medicine that belongs to the class of medication called pyrimidine analogs. It is indicated for the first-line treatment of metastatic colorectal cancer, along with other anti-cancer medications. Cancer is a condition in which cells multiply uncontrolled and abnormally. It is not recommended for adolescents and children. Avoid taking this medicine if you are pregnant or breastfeeding.   

Do not take Uracel capsule if you are allergic to Tegafur +  Uracil or any other ingredients of this medicine. Inform your healthcare professional if you have liver diseases, kidney disorders, or other noncancerous conditions before initiating the treatment. This medicine may reduce fertility in men and women; discuss this with your doctor before starting the therapy. The most common side effects are diarrhea, nausea, vomiting, tiredness, and risk of infection. 

Uses of Uracel Capsule

• Colorectal cancer

Therapeutic Effects of Uracel Capsule

Uracel capsule is a combination of two chemotherapy drugs: tegafur and uracil.  tegafur is absorbed into the bloodstream, converted into the active drug 5FU in the liver, and then absorbed by tumor cells. Within the cells is an enzyme that breaks down the 5FU. The uracil slows the breakdown of 5FU, which means that the 5FU stays in the cancer cells for longer.  It prevents the growth and multiplication of cancer cells and thus helps destroy the tumor.

More Information

• Store at temperatures not exceeding 25°C
• Keep the capsule away from the reach of children and pets.
• If you miss a dosage, take it as soon as you remember. If it is almost time for the next dose, skip the missing dose.
• Do not take a double dose to compensate for a missed dose.

Safety Advices Pregnancy  

Uracel capsule is unsafe for pregnant women because it may cause birth defects. Inform your physician if you are pregnant, suspect pregnancy, or planning to become pregnant. Using effective contraception during the treatment.   

Breast Feeding  

Breastfeeding is not recommended in patients taking Uracel capsule because the medicine passes into the breast milk in small amounts and may harm the baby. Uracel  

Lungs  

It is unknown whether Uracel capsule can be used in patients with lung disorders. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Uracel capsule should be cautiously administered in patients with severe liver diseases. Dose adjustments are necessary for severe liver failure. Inform your physician if you have liver problems before initiating the therapy.    

Alcohol  

It is not known whether it is safe to consume alcohol with Uracel capsule. Please consult your doctor. 

Driving  

Driving vehicles or operating machinery after taking Uracel capsule is unsafe as you may develop dizziness, tiredness, and blurred vision. 

Side Effects

• Diarrhea
• Nausea, vomiting
• Tiredness
• Risk of infection
• Fever
• Bruising and bleeding
• Anemia
• Changes in skin and nail 

• Swelling in the face, and body
• Severe skin rashes
• Severe diarrhea
• Liver injury