Promotional Material	Visiting Cards, Calendars, Notepads, Pens, Bottle, Brochure, Working Bag, Writing Pads, Diaries, Visual Aids
Medicine Type	Allopathic
Form Of Medicine	Injection
Certification	WHO, GLP, GMP
Product List Available	Yes
Range of Products	Antibiotics, Antimicrobials
Pharmaceutical Experience	Above 5 Years

Flucloxacillin is a narrow-spectrum antibiotic that belongs to the penicillin class. It is commonly used to treat bacterial infections caused by susceptible organisms. Flucloxacillin is effective against certain types of bacteria, particularly those that produce beta-lactamase, an enzyme that can inactivate some antibiotics.

 

Flucloxacillin is available in various forms, including oral capsules and intravenous (IV) injections. The injection form is used when a rapid and direct delivery of the medication into the bloodstream is required, especially in more severe infections.

 

Here are some key points about Flucloxacillin:

 

Indications: Flucloxacillin is often prescribed to treat skin and soft tissue infections, such as cellulitis and abscesses. It is also used for bone and joint infections, respiratory tract infections, and other bacterial infections caused by susceptible organisms.

 

Mechanism of Action: Flucloxacillin works by inhibiting the formation of bacterial cell walls. It interferes with the synthesis of peptidoglycan, a key component of the bacterial cell wall, leading to the disruption of cell wall formation and ultimately causing bacterial cell death.

 

Administration: The injection form of Flucloxacillin is administered by a healthcare professional, usually in a hospital or clinical setting. The dosage and duration of treatment will depend on the specific infection being treated and the patient's individual factors.

 

Monitoring and Side Effects: Patients receiving Flucloxacillin should be monitored for any signs of allergic reactions, such as rash, itching, or swelling. Like any antibiotic, Flucloxacillin use may also be associated with gastrointestinal side effects, and patients should report any unusual symptoms to their healthcare provider.

 

Precautions: Inform your healthcare provider about any allergies, especially to penicillins or cephalosporins. It's crucial to complete the full course of treatment even if symptoms improve before the medication is finished.

 

As with any medication, it's important to use Flucloxacillin under the guidance and prescription of a qualified healthcare professional. If you have specific questions about Flucloxacillin or your treatment plan, it's best to consult with your healthcare provider.

Additional Information:

• Item Code: PCD03
• Production Capacity: 500000
• Delivery Time: Immediate in PCD Franchise & 40 to 60 Days in Third Party Manufacturing
• Packaging Details: Dry Powder Injection with SWFI

Promotional Material	Brochure, Visual Aids, Writing Pads, Diaries, Visiting Cards, Pens, Notepads, Bottle
Medicine Type	Allopathic
Form Of Medicine	Injection
Certification	GMP, GLP, WHO, ISO
Product List Available	Yes
Range of Products	Gastrointestinal
Pharmaceutical Experience	Above 5 Years

Pantoprazole is a proton pump inhibitor (PPI) that reduces the production of stomach acid. While pantoprazole is commonly available in oral form as tablets or capsules, there is also an intravenous (IV) formulation of pantoprazole, often referred to as pantoprazole injection.

 

Here are key points about pantoprazole injection:

 

Indications:

 

Pantoprazole injection is used for the short-term treatment of conditions where there is a need to reduce gastric acid secretion rapidly. This includes situations such as acute upper gastrointestinal bleeding, severe erosive esophagitis, and certain types of conditions requiring acid suppression.

Mechanism of Action:

 

Pantoprazole works by inhibiting the proton pump in the stomach lining, reducing the secretion of gastric acid. This results in a decrease in stomach acid production.

Administration:

 

Pantoprazole injection is administered intravenously. It is typically used in situations where oral administration is not feasible or when a rapid onset of action is required.

Indications for Use:

 

Common indications for the use of pantoprazole injection include the treatment of gastroesophageal reflux disease (GERD), erosive esophagitis, and conditions where there is an urgent need for acid suppression, such as upper gastrointestinal bleeding.

Dosage:

 

The dosage of pantoprazole injection is determined by healthcare providers based on the specific condition being treated. The dosage may vary for different indications.

Monitoring and Side Effects:

 

Patients receiving pantoprazole, whether in oral or intravenous form, may be monitored for potential side effects. Common side effects include headache, dizziness, nausea, and abdominal pain. Long-term use may be associated with certain risks, and healthcare providers may monitor for complications such as bone fractures or Clostridium difficile infection.

Precautions:

 

Pantoprazole should be used with caution in individuals with liver disease. It is important to inform healthcare providers about any pre-existing medical conditions and medications being taken.

Pregnancy and Lactation:

 

The use of pantoprazole during pregnancy and lactation should be carefully considered. Pregnant or breastfeeding individuals should discuss potential risks and benefits with their healthcare providers.

Duration of Treatment:

 

The duration of pantoprazole treatment depends on the specific condition being treated. In some cases, it may be prescribed for short-term use, while in others, it may be used for a more extended period.

As with any medication, pantoprazole should be used under the guidance of a qualified healthcare professional. If you have specific questions about pantoprazole injection or its use, it's best to consult with your healthcare provider, who can provide personalized information based on your medical history and condition.

Additional Information:

• Item Code: PCD020
• Production Capacity: 500000
• Delivery Time: Immediate in PCD Franchise & 40 to 60 Days in Third Party Manufacturing
• Packaging Details: Dry powder Injection with Diluent

Strength	1 gm
Quantity Unit	Vial
Country of Origin	Made in India
Form	Dry Powder Injection
Available in	PCD Franchise & in Third Party Manufacturing also

Cefepime is a broad-spectrum antibiotic that belongs to the cephalosporin class. It is commonly used to treat various bacterial infections. Cefepime is available in different formulations, including intravenous (IV) injections.

 

When you see "Cefepime Injection IP," the "IP" stands for "Indian Pharmacopoeia," indicating that the formulation complies with the standards set by the Indian Pharmacopoeia. The Indian Pharmacopoeia is a comprehensive book of standards for drugs in India.

 

Cefepime is used to treat infections caused by susceptible bacteria. It is often prescribed for conditions such as pneumonia, urinary tract infections, skin and soft tissue infections, intra-abdominal infections, and more. Like other antibiotics, it works by interfering with the bacteria's cell wall synthesis, leading to the disruption of their growth and eventual death.

 

As with any medication, it's important to use Cefepime under the supervision and prescription of a qualified healthcare professional. They will consider factors such as the specific type of infection, the patient's health status, and potential allergies or adverse reactions.

 

If you have been prescribed Cefepime or have questions about its use, it's crucial to follow your healthcare provider's instructions and inform them about any existing medical conditions or medications you are taking. Additionally, be aware of potential side effects and seek medical attention if you experience any adverse reactions.

Additional Information:

• Item Code: PCD01
• Production Capacity: 50000
• Delivery Time: Immediate in PCD Franchise & 40 to 60 Days in Third Party Manufacturing
• Packaging Details: Dry Injection Vial with 10 ml SWFI

Strength	60 mg
Packaging Size	20 ml Vial with SWFI
Prescription/Non prescription	Prescription
Country of Origin	Made in India
Available in	Third Party Manufacturing
Form	Dry Lyophilized Powder for Injection

Cerebroprotein Hydrolysate (Cerebrolysin) is a medication derived from porcine brain tissue that undergoes a complex process of enzymatic hydrolysis. It is commonly used in some countries as a nootropic agent and is believed to have neuroprotective and neurotrophic properties. However, it's essential to note that the use of Cerebroprotein Hydrolysate is not widely accepted or approved in all regions, and its efficacy is a subject of ongoing research.

 

Here are some key points about Cerebroprotein Hydrolysate injection:

 

Indications: Cerebroprotein Hydrolysate is often used in the management of various neurological disorders, including stroke, traumatic brain injury, Alzheimer's disease, and other conditions that involve neurodegeneration or neurological dysfunction.

 

Mechanism of Action: The exact mechanism of action is not fully understood, but it is believed to involve neurotrophic and neuroprotective effects. Cerebroprotein Hydrolysate is thought to stimulate the growth, survival, and repair of nerve cells, possibly through the promotion of neurotrophic factors.

 

Administration: Cerebroprotein Hydrolysate is typically administered by intramuscular or intravenous injection. The dosage and duration of treatment may vary based on the specific condition being treated and the healthcare provider's assessment.

 

Research Status: While there is some research suggesting potential benefits of Cerebroprotein Hydrolysate in certain neurological conditions, the evidence is not yet strong enough to establish it as a standard treatment. The use of Cerebroprotein Hydrolysate remains a subject of ongoing research and debate in the medical community.

 

Side Effects: Common side effects reported with Cerebroprotein Hydrolysate include local reactions at the injection site, as well as occasional mild allergic reactions. Serious adverse effects are rare but can occur.

 

Precautions: Individuals with a history of allergies, especially to proteins or peptides, should exercise caution. As with any medication, it's important to inform your healthcare provider about your medical history, current medications, and any existing health conditions.

 

It's crucial to emphasize that the use of Cerebroprotein Hydrolysate may not be approved or widely accepted in all countries, and its availability may vary. If you have been prescribed this medication or are considering its use, it's essential to discuss it thoroughly with your healthcare provider, who can provide guidance based on the latest medical knowledge and research.

Additional Information:

• Item Code: PCD08
• Production Capacity: 500000
• Delivery Time: Immediate in PCD Franchise & 40 to 60 Days in Third Party Manufacturing
• Packaging Details: Dry Lyophilized Powder for Injection

Strength	100 mcg
Packaging Size	1 ml
Packaging Type	Ampoule
Composition	Octreotide 100mcg
Shelf Life	24 Months
Prescription/Non-Prescription	Prescription
Country of Origin	Made in India
Also Gives	Third Party Manufacturing, PCD Pharma Franchise

Octreotide is a medication that belongs to a class of drugs called somatostatin analogs. It is a synthetic peptide that mimics the actions of somatostatin, a hormone produced naturally in the body. Octreotide has various uses, but it is most commonly known for its role in managing conditions related to hormonal imbalances.

 

Here are key points about Octreotide injection:

 

Indications:

 

Acromegaly: Octreotide is used to treat acromegaly, a condition characterized by the overproduction of growth hormone, often caused by a tumor in the pituitary gland.

Neuroendocrine Tumors: It is also used in the treatment of certain types of neuroendocrine tumors, including carcinoid tumors and gastrinomas.

Gastrointestinal Bleeding: Octreotide can be used to manage acute variceal bleeding in the gastrointestinal tract.

Symptomatic Treatment: In some cases, it may be used to alleviate symptoms associated with certain types of cancer or endocrine disorders.

Mechanism of Action:

 

Octreotide works by binding to somatostatin receptors, primarily subtype 2 (SST2). By doing so, it inhibits the release of several hormones, including growth hormone, insulin, glucagon, and others.

Administration:

 

Octreotide is available in various formulations, including short-acting subcutaneous injections and long-acting depot formulations. The injection is typically given subcutaneously, but in some cases, it may be administered intravenously.

Monitoring and Side Effects:

 

Patients receiving Octreotide may be monitored for hormonal levels, and adjustments to the dose may be made based on clinical response. Common side effects include pain or irritation at the injection site, gastrointestinal disturbances, and changes in blood glucose levels.

Precautions:

 

Octreotide should be used with caution in individuals with a history of gallstones, diabetes, or thyroid dysfunction. Close monitoring is necessary in patients with impaired renal or hepatic function.

Duration of Treatment:

 

The duration of treatment with Octreotide depends on the underlying condition being treated. It may be used as a long-term therapy for chronic conditions.

Pregnancy and Lactation:

 

The use of Octreotide during pregnancy should be carefully considered, and the potential benefits should outweigh the risks. It is not recommended during breastfeeding.

If you have been prescribed Octreotide or have questions about its use, it's important to discuss your concerns with your healthcare provider. They can provide specific information tailored to your medical condition and guide you through the treatment process.

Additional Information:

• Item Code: PCD09
• Production Capacity: 500000
• Delivery Time: Immediate in PCD Franchise & 40 to 60 Days in Third Party Manufacturing
• Packaging Details: 1 ml ampoule Tray Pack

Strength	5000 IU
Packaging Size	5 ml
Drug Type	Anticoagulant Drug
Prescription/ Non Prescription	Prescription
Shelf Life	24 Months

Heparin is an anticoagulant, which means it helps prevent the formation of blood clots. It is commonly used in medical settings for various conditions involving the risk of clot formation. Here are some key points about Heparin injection:

 

Indications:

 

Deep Vein Thrombosis (DVT): Heparin is often used to prevent and treat deep vein thrombosis.

Pulmonary Embolism: It may be used in the treatment and prevention of pulmonary embolism.

Atrial Fibrillation: Heparin may be used in some cases to prevent blood clots in individuals with atrial fibrillation.

Cardiac Surgery and Procedures: It is commonly used during and after certain cardiac surgeries and procedures to prevent clot formation.

Mechanism of Action:

 

Heparin acts as an anticoagulant by enhancing the activity of antithrombin III, a natural substance in the body that inhibits blood clot formation. It primarily inhibits the activity of clotting factors IIa (thrombin) and Xa.

Administration:

 

Heparin is usually administered by injection. It can be given subcutaneously or intravenously, depending on the clinical situation and the severity of the condition.

Monitoring and Dosage:

 

The dosage of heparin is carefully monitored based on laboratory tests, such as the activated partial thromboplastin time (aPTT). This helps ensure that the anticoagulant effect is within the therapeutic range.

Side Effects and Complications:

 

Common side effects may include bleeding, which can range from minor to serious. Other side effects may include heparin-induced thrombocytopenia (HIT), a condition characterized by a decrease in platelet count.

Reversal Agent:

 

Protamine sulfate is a reversal agent that can be used to counteract the anticoagulant effects of heparin if necessary.

Precautions:

 

Individuals with a history of bleeding disorders, severe hypertension, or a known hypersensitivity to heparin should use it with caution. It is also important to inform healthcare providers about all medications, including over-the-counter drugs and supplements.

Pregnancy and Lactation:

 

Heparin is generally considered safe during pregnancy, and it does not cross into breast milk in significant amounts.

Duration of Treatment:

 

The duration of heparin treatment depends on the specific condition being treated and the risk factors involved. It may be used for a short period during hospitalization or for more extended periods for certain medical conditions.

As with any medication, it is crucial to use heparin under the guidance and prescription of a qualified healthcare professional. If you have specific questions about heparin or your treatment plan, it's best to consult with your healthcare provider.

Additional Information:

• Item Code: PCD010
• Production Capacity: 50000
• Delivery Time: Immediate in PCD Franchise or 40 to 60 Days in Third Party Manufacturing
• Packaging Details: 5 ml Vial

Strength	1 mg
Packaging Size	10 ml
Prescription/Non prescription	Prescription
Injectable Form	Liquid
Also Gives	PCD Pharma Franchise, Third Party Manufacturing
Country of Origin	Made in India

Terlipressin is a synthetic analog of vasopressin, also known as antidiuretic hormone (ADH). It is used as a medication for various medical conditions, primarily to manage certain complications related to liver cirrhosis and other conditions associated with low blood pressure.

 

Here are key points about Terlipressin injection:

 

Indications:

 

Hepatorenal Syndrome (HRS): Terlipressin is primarily used in the treatment of hepatorenal syndrome, a potentially serious complication of advanced liver cirrhosis where there is severe kidney dysfunction.

Mechanism of Action:

 

Terlipressin acts as a vasopressin analog and has vasoconstrictive effects. It works by constricting blood vessels, particularly in the splanchnic (abdominal) circulation. This vasoconstriction helps to improve blood flow to vital organs, including the kidneys.

Administration:

 

Terlipressin is usually administered by intravenous injection. The dosage and duration of treatment depend on the specific condition being treated, the severity of the condition, and the patient's response to the medication.

Monitoring and Side Effects:

 

Patients receiving Terlipressin may be monitored for changes in blood pressure, heart rate, and kidney function. Common side effects may include gastrointestinal symptoms (nausea, abdominal discomfort), changes in blood electrolytes, and fluid retention.

Duration of Treatment:

 

The duration of Terlipressin treatment depends on the individual patient's response and the underlying condition. It may be used as a short-term intervention to improve renal function in hepatorenal syndrome.

Precautions:

 

Terlipressin should be used with caution in individuals with cardiovascular diseases, as it can affect blood pressure and heart rate. It is also contraindicated in patients with known hypersensitivity to the drug.

Pregnancy and Lactation:

 

The safety of Terlipressin during pregnancy and lactation is not well established. It should be used with caution, and the potential risks and benefits should be carefully considered in consultation with a healthcare provider.

Reconstitution and Administration:

 

Terlipressin is typically supplied as a lyophilized powder and requires reconstitution before administration. Healthcare professionals should follow proper procedures for reconstitution and administration.

As with any medication, Terlipressin should be used under the supervision and prescription of a qualified healthcare professional. If you have been prescribed Terlipressin or have questions about its use, it's essential to discuss your concerns with your healthcare provider, who can provide specific information tailored to your medical condition.

Additional Information:

• Item Code: PCD012
• Production Capacity: 50000
• Delivery Time: Immediate in PCD Franchise & 40 to 60 Days in Third Party Manufacturing
• Packaging Details: 10 ml Ampoule Tray with Cover Pack

Strength	600 mg
Packaging Size	Dry powder Injetion along with SWFI
Packaging Type	Bottle
Also gives	PCD Pharma, Third Party Manufacturing
Dose	As directed by the Physician.
Country of Origin	Made in India
Available in	Third Party Manufacturing

Glutathione is a tripeptide molecule composed of three amino acids: glutamic acid, cysteine, and glycine. It is a vital antioxidant that plays a crucial role in various physiological processes, including the detoxification of harmful substances in the body.

 

While glutathione is naturally produced in the body and obtained through diet, there is a form of glutathione that is administered through injection for certain therapeutic or cosmetic purposes. This form is often referred to as "glutathione injection."

 

Here are some key points about glutathione injection:

 

Therapeutic Uses:

 

Antioxidant Therapy: Glutathione is a potent antioxidant that helps neutralize free radicals in the body. Some healthcare providers may use intravenous (IV) or intramuscular (IM) glutathione injections for individuals with certain medical conditions associated with oxidative stress.

Cosmetic Uses:

 

Skin Lightening: Glutathione injections have gained popularity in some regions for their purported skin-lightening effects. However, the use of glutathione for skin lightening is controversial, and its safety and efficacy for this purpose are not universally accepted.

Mechanism of Action:

 

Glutathione acts as an antioxidant by scavenging free radicals, which can help protect cells from damage. Additionally, it is involved in various metabolic and detoxification processes in the body.

Administration:

 

Glutathione injections can be administered through intravenous or intramuscular routes. The dosage and frequency of injections can vary based on the intended purpose and the recommendations of a healthcare professional.

Side Effects:

 

Side effects of glutathione injections may include local reactions at the injection site, allergic reactions, and rare cases of adverse effects. The safety of long-term or high-dose glutathione injections is not well established.

Precautions:

 

Individuals considering glutathione injections should consult with a qualified healthcare professional. It is important to be aware that the use of glutathione for skin lightening purposes is not supported by substantial scientific evidence, and potential risks should be carefully considered.

Pregnancy and Lactation:

 

The safety of glutathione injections during pregnancy and lactation has not been thoroughly studied. Pregnant and breastfeeding individuals should consult with their healthcare providers before using glutathione injections.

It's essential to note that the use of glutathione injections for cosmetic purposes, particularly skin lightening, is a controversial and debated practice. Before considering any form of glutathione injection, individuals should seek advice from qualified healthcare professionals who can provide personalized guidance based on the individual's health status and needs.

Additional Information:

• Item Code: PCD013
• Production Capacity: 50000
• Delivery Time: Immediate in PCD and 40 to 60 Days in Third Party Manufacturing
• Packaging Details: Dry powder injection along with SWFI

Strength	100mg
Packaging Type	Vial
Prescription/Non-Prescription	Prescription
Also Gives	Third Party Manufacturing, PCD Pharma Franchise
Country of Origin	Made in India

Hydrocortisone sodium succinate is a synthetic form of the naturally occurring hormone cortisol, which is produced by the adrenal glands. It belongs to the class of medications known as corticosteroids or glucocorticoids. Hydrocortisone sodium succinate is commonly administered as an injection for its anti-inflammatory and immunosuppressive properties.

 

Here are key points about hydrocortisone sodium succinate injection:

 

Indications:

 

Inflammatory Conditions: Hydrocortisone injection is used to treat various inflammatory conditions, including allergic reactions, rheumatoid arthritis, dermatitis, and inflammatory bowel diseases.

Shock: In emergency situations, hydrocortisone may be used to manage certain types of shock, such as septic shock.

Mechanism of Action:

 

Hydrocortisone has anti-inflammatory, immunosuppressive, and anti-allergic effects. It works by inhibiting the production of inflammatory mediators and suppressing the activity of immune cells.

Administration:

 

Hydrocortisone sodium succinate is usually administered intravenously (IV) or intramuscularly (IM) by healthcare professionals. The dosage and frequency of administration depend on the specific condition being treated.

Dosage:

 

The dosage of hydrocortisone depends on factors such as the severity of the condition, the patient's weight, and the response to treatment. It is important to follow the healthcare provider's prescribed dosage and administration instructions.

Monitoring and Side Effects:

 

Patients receiving hydrocortisone may be monitored for potential side effects, including changes in blood pressure, blood glucose levels, and electrolyte imbalances. Common side effects may include fluid retention, increased appetite, and mood changes.

Precautions:

 

Hydrocortisone should be used with caution in individuals with certain medical conditions, such as diabetes, hypertension, and peptic ulcer disease. Long-term use or abrupt discontinuation of the medication may require careful monitoring and adjustment of the dosage.

Pregnancy and Lactation:

 

The use of hydrocortisone during pregnancy and lactation should be carefully considered. The benefits and potential risks should be discussed with a healthcare provider.

Duration of Treatment:

 

The duration of hydrocortisone treatment depends on the specific condition being treated. Short courses are often used for acute inflammatory conditions, while chronic conditions may require long-term therapy.

It's important for individuals receiving hydrocortisone to communicate openly with their healthcare providers about their medical history, other medications they are taking, and any concerns or side effects they may be experiencing. The use of corticosteroids should be under the guidance of a qualified healthcare professional.

Additional Information:

• Item Code: PCD015
• Production Capacity: 50000
• Delivery Time: Immediate in PCD Franchise & 40 to 60 Days in Third Party Manufacturing
• Packaging Details: Dry powder Injection with Diluent

Drug Type	Methylprednisolone Sodium Succinate Injection
Strength	1000mg
Packaging Size	10ml
Packaging Type	Vial
Injection Administration type	IV, IM
Shelf Life	24 Months
Also Gives	PCD Pharma Franchise, Third Party Manufacturing
Country of Origin	Made in India

Methylprednisolone Sodium Succinate is a corticosteroid medication that is commonly administered as an injection. It belongs to the class of drugs known as glucocorticoids, which are synthetic versions of the naturally occurring hormone cortisol. Methylprednisolone has anti-inflammatory and immunosuppressant properties, and it is used for various medical conditions to reduce inflammation and modulate the immune response.

 

Here are key points about Methylprednisolone Sodium Succinate Injection:

 

Indications: Methylprednisolone is used to treat a variety of conditions, including inflammatory and autoimmune disorders, allergic reactions, and certain types of cancers. Common indications include rheumatoid arthritis, asthma, severe allergic reactions, dermatitis, and inflammatory bowel diseases.

 

Mode of Action: Methylprednisolone works by suppressing the immune response and reducing inflammation. It inhibits the release of inflammatory mediators, such as prostaglandins and cytokines, and it also affects the function of white blood cells.

 

Dosage Forms: Methylprednisolone Sodium Succinate is available in various dosage forms, including intravenous (IV) injections. The IV form is often used for rapid and potent anti-inflammatory effects.

 

Administration: Methylprednisolone Sodium Succinate Injection is typically administered in a healthcare setting, such as a hospital or clinic, under the supervision of healthcare professionals. The dosage and duration of treatment depend on the specific condition being treated.

 

Dosage Adjustment: The dosage may be adjusted based on the severity of the condition, the patient's response to treatment, and individual patient factors. It is important to follow the healthcare provider's instructions regarding the dosage and administration schedule.

 

Precautions: Methylprednisolone should be used with caution in certain situations, including in individuals with infections, diabetes, hypertension, or a history of gastrointestinal bleeding. Long-term use or abrupt discontinuation may require careful monitoring and gradual dose reduction.

 

Side Effects: Common side effects may include increased blood sugar levels, fluid retention, increased blood pressure, and mood changes. Long-term use may be associated with more serious side effects, including bone loss and an increased risk of infections.

 

Pregnancy and Lactation: The use of Methylprednisolone during pregnancy and breastfeeding should be carefully considered, and the potential benefits should be weighed against the risks. It's important to consult with a healthcare provider in such situations.

 

It's crucial to use Methylprednisolone or any corticosteroid only under the guidance and prescription of a qualified healthcare professional. Self-medication or misuse of corticosteroids can lead to serious health risks. If prescribed Methylprednisolone, it's important to report any side effects or concerns to the healthcare provider promptly. Regular monitoring and follow-up appointments are typically recommended during the course of treatment.

Additional Information:

• Item Code: PCD019
• Production Capacity: 500000
• Delivery Time: Immediate in PCD Franchise & 40 to 60 in Third Party Manufacturing
• Packaging Details: Dry powder Injection along with SWFI

Strength	1.2 gm
Form	Injection
Packaging type	Vial
Country of Origin	Made in India
Available in	Third Party Manufacturing

Amoxicillin and clavulanate potassium combination is another antibiotic medication commonly used in veterinary medicine to treat bacterial infections. Amoxicillin is a penicillin-type antibiotic, and clavulanate potassium is a beta-lactamase inhibitor. The combination is often referred to as amoxicillin-clavulanate or co-amoxiclav.

 

This combination is effective against a broader range of bacteria compared to amoxicillin alone because clavulanate potassium helps prevent the breakdown of amoxicillin by bacterial beta-lactamase enzymes.

 

In veterinary medicine, amoxicillin and clavulanate potassium are often administered as an injection for more severe infections or when oral administration is not feasible. The injectable form allows for a more rapid and direct delivery of the medication.

 

 

The dosage and administration of amoxicillin-clavulanate in veterinary medicine depend on factors such as the type and severity of the infection, the species and weight of the animal, and the veterinarian's assessment. It is crucial to follow the veterinarian's instructions and prescription carefully.

 

As with any medication, there can be potential side effects and risks associated with the use of amoxicillin-clavulanate. It's essential to inform the veterinarian about the animal's medical history, any pre-existing conditions, and any other medications the animal may be taking.

 

If you have specific questions or concerns about the use of amoxicillin and clavulanate potassium for a particular veterinary case, it is recommended to consult with a veterinarian. They can provide tailored advice based on the individual needs and circumstances of the animal in question.

Additional Information:

• Item Code: PCD021
• Production Capacity: 500000
• Delivery Time: Immediate in PCD Franchise
• Packaging Details: Dry Powder Injection along with 20 ml SWFI

Strength	50 mg
Packaging Size	1ml
Packaging Type	Ampoule
Composition	Nandrolone Decanoate 50mg
Shelf Life	24 Months
Prescription/Non-Prescription	Prescription
Country of Origin	Made In India
Also Gives	PCD Pharma Franchise, Third Party Manufacturing

Nandrolone decanoate injection IP is a pharmaceutical product that contains the active ingredient nandrolone decanoate. It is an injectable form of nandrolone, which is an anabolic steroid. Nandrolone decanoate is commonly used in the treatment of various medical conditions such as anemia, certain types of breast cancer, and osteoporosis, among others.

 

As an anabolic steroid, nandrolone decanoate works by increasing the production of red blood cells and enhancing protein synthesis in the body, leading to increased muscle mass and strength. However, it's important to note that the use of nandrolone decanoate for non-medical purposes, such as athletic performance enhancement or bodybuilding, is illegal and can pose serious health risks.

 

Like any medication, nandrolone decanoate injection IP should only be used under the supervision of a qualified healthcare professional and according to prescribed dosage and instructions. It's crucial to be aware of potential side effects and risks associated with its use, including but not limited to liver damage, cardiovascular issues, and hormonal imbalances. Regular monitoring and follow-up with a healthcare provider are essential for those undergoing treatment with nandrolone decanoate.

Additional Information:

• Item Code: OU01
• Production Capacity: 500000
• Delivery Time: Immediate
• Packaging Details: 1 ml Ampoule along with syringe Dispo Pack

Strength	1.125 gm
Pack Type	Vial
Composition	Ceftriaxone 1 g + Tazobactam 125 mg
Shelf Life	24 Months
Usage	To treat various bacterial infections

Ceftriaxone and tazobactam are both medications used in combination to enhance the spectrum of bacterial coverage. Let's break down their pharmacology:

Ceftriaxone:

Class: Ceftriaxone is a third-generation cephalosporin antibiotic.

Mechanism of Action: It inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs), which are enzymes involved in the final steps of peptidoglycan synthesis in the bacterial cell wall. This leads to cell wall disruption and eventual bacterial cell death.

Spectrum of Activity: Ceftriaxone is effective against a broad range of Gram-positive and Gram-negative bacteria.

Tazobactam:

Class: Tazobactam is a beta-lactamase inhibitor.

Mechanism of Action: Beta-lactamase inhibitors, like tazobactam, protect the beta-lactam antibiotics (such as ceftriaxone) from degradation by beta-lactamase enzymes produced by some bacteria. Beta-lactamases are enzymes that can break the beta-lactam ring structure of antibiotics, rendering them ineffective. Tazobactam inhibits these enzymes, allowing ceftriaxone to remain active against a broader spectrum of bacteria.

Spectrum of Activity: Tazobactam does not have intrinsic antibacterial activity but enhances the effectiveness of beta-lactam antibiotics against beta-lactamase-producing bacteria.

Combination (Ceftriaxone + Tazobactam):

This combination is often used to treat infections caused by bacteria that produce beta-lactamase enzymes, which would otherwise inactivate ceftriaxone.

By combining ceftriaxone with tazobactam, the spectrum of activity is expanded, and the combination becomes effective against a broader range of bacteria, including those that produce beta-lactamases.

Administration:

The combination is usually administered as an intravenous (IV) injection or infusion.

Cautions:

As with any antibiotic, the use of ceftriaxone and tazobactam should be done under the supervision of a healthcare professional to ensure proper dosing, monitoring, and to minimize the risk of side effects.

It's important to note that specific dosages, indications, and contraindications may vary based on the specific product, regional guidelines, and the patient's individual health status. Always consult with a healthcare professional or pharmacist for detailed and personalized information.

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Additional Information:

• Item Code: PCD023
• Production Capacity: 500000
• Delivery Time: Immediate in PCD Franchise & 40 to 60 Days in Third Party Manufacturing
• Packaging Details: Dry powder Injection along with 10 ml SWFI

Strength	500 mg
Usage/Application	Hospital
Injectable Form	Lyophilized Powder
Packaging Size	500 mg
Also Gives	Third Party Manufacturing, PCD Pharma Franchise
Country of Origin	Made in India

Clarithromycin is a macrolide antibiotic that is used to treat various bacterial infections. It is available in different formulations, including oral tablets, oral suspension, and intravenous (IV) formulations. When you see "Clarithromycin for infusion," it means that the medication is prepared for intravenous administration, typically in a hospital or clinical setting.

 

Here are some key points about Clarithromycin for infusion:

 

Indications: Clarithromycin is commonly used to treat respiratory tract infections, skin and soft tissue infections, and certain other bacterial infections. It is effective against a variety of bacteria, including some types of Streptococcus, Staphylococcus, and Mycoplasma.

 

Mechanism of Action: Like other macrolide antibiotics, Clarithromycin works by inhibiting bacterial protein synthesis. It binds to the bacterial ribosome, preventing the synthesis of essential proteins needed for bacterial growth and reproduction.

 

Administration: Clarithromycin for infusion is administered directly into the bloodstream through an IV line. The dosage and duration of treatment will depend on the type and severity of the infection being treated, as well as the patient's individual factors.

 

Monitoring and Side Effects: Patients receiving Clarithromycin should be monitored for any signs of allergic reactions, such as rash, itching, or swelling. Common side effects may include gastrointestinal symptoms such as nausea, diarrhea, and abdominal pain. It's important to report any unusual or severe side effects to healthcare providers.

 

Precautions: Clarithromycin may interact with other medications, so it's essential to inform your healthcare provider about any other drugs you are taking. It should be used with caution in patients with pre-existing liver conditions, and dosage adjustments may be necessary in such cases.

 

Complete Course: It's important to complete the full course of Clarithromycin as prescribed by your healthcare provider, even if symptoms improve before the medication is finished. Stopping the antibiotic prematurely may result in incomplete treatment and the development of antibiotic-resistant bacteria.

 

As with any medication, it's crucial to use Clarithromycin for infusion under the guidance and prescription of a qualified healthcare professional. If you have specific questions about Clarithromycin or your treatment plan, it's best to consult with your healthcare provider.

Additional Information:

• Item Code: PCD04
• Production Capacity: 50000
• Delivery Time: Immediate in PCD Franchise & 40 to 60 Days in Third Party Manufacturing
• Packaging Details: Dry Powder Injection along with SWFI

Strength	1 gm
Pack Size	20 ml
Pack Type	Vial
Prescription/Non Prescription	Prescription
Shelf Life	24 Months
Also Gives	PCD Pharma Franchise, Third Party Manufacturing
Country of Origin	Made in India

Meropenem with Disodium Edetate (EDTA) and Sulbactam for Injection is a combination medication used to treat bacterial infections. Let's break down the components:

 

Meropenem: Meropenem is a broad-spectrum antibiotic belonging to the carbapenem class. It is effective against a wide range of bacteria, including both gram-positive and gram-negative bacteria. Meropenem works by inhibiting the synthesis of bacterial cell walls, leading to the death of susceptible bacteria.

 

Disodium Edetate (EDTA): Disodium edetate, also known as ethylenediaminetetraacetic acid, is a chelating agent. In this context, it may be added to the formulation to enhance the stability of meropenem. Chelating agents can bind to metal ions, preventing them from catalyzing reactions that may lead to the degradation of the antibiotic.

 

Sulbactam: Sulbactam is a beta-lactamase inhibitor. It is often combined with beta-lactam antibiotics, such as meropenem, to enhance their effectiveness against bacteria that produce beta-lactamase enzymes. Beta-lactamases are enzymes that can break down certain types of antibiotics, rendering them ineffective. Sulbactam helps protect meropenem from degradation by beta-lactamases, allowing it to exert its antibacterial effect.

 

Indications:

This combination medication is typically prescribed for the treatment of complicated intra-abdominal infections, complicated skin and soft tissue infections, and other severe infections caused by susceptible bacteria.

 

Administration:

Meropenem with Disodium Edetate and Sulbactam is usually administered intravenously (IV) by healthcare professionals. The dosage and duration of treatment depend on the specific type and severity of the infection, as well as the patient's individual factors.

 

Monitoring and Side Effects:

Patients receiving this medication should be monitored for signs of allergic reactions, as well as potential side effects related to the individual components. Common side effects may include gastrointestinal symptoms, skin reactions, and changes in laboratory parameters.

 

Precautions:

Inform your healthcare provider about any allergies, especially to beta-lactam antibiotics or other components of the medication. It's important to use the medication under the guidance of a qualified healthcare professional.

 

As with any antibiotic therapy, it's crucial to complete the full course of treatment as prescribed by your healthcare provider, even if symptoms improve before the medication is finished. Stopping the antibiotic prematurely may result in incomplete treatment and the development of antibiotic-resistant bacteria. If you have specific questions about this medication or your treatment plan, it's best to consult with your healthcare provider.

Additional Information:

• Item Code: PCD07
• Production Capacity: 5000000
• Delivery Time: Immediate in PCD Franchise & 40 to 60 Days in Third Party Manufacturing
• Packaging Details: As per Requirements.

Strength	200 mg
Composition	200 MG
Prescription Required	Yes
Storage	STORE AT COOL DRY AND DARK PLACE
Manufactured By	WHO CERTIFIED CO
AVAILABLE	IN PCD FRANCHISE WITH MONOPOLY RIGHTS
ALSO PROVIDE	THIRD PARTY MAUFACTURING
INJECTION	VORICONAZOLE
FORM	DRY POWDER INJECTION

Voriconazole Injection 200 mg is a prescription antifungal medication used to treat serious, invasive fungal infections. Here's a concise overview:

Product Name: Voriconazole Injection 200 mg

Form: Intravenous (IV) solution

Generic Name: Voriconazole

Strength: 200 mg per vial

Route: Intravenous (IV)

ATC Code: J02AC03

Indications:

Voriconazole is used to treat:

• Invasive aspergillosis
• Candidemia in non-neutropenic patients
• Esophageal candidiasis
• Serious fungal infections caused by Scedosporium and Fusarium species

Mechanism of Action:

Voriconazole inhibits the fungal cytochrome P450–dependent enzyme lanosterol 14α-demethylase, interfering with ergosterol synthesis and damaging the fungal cell membrane.

Dosage (Adults, typical loading and maintenance):

• Loading Dose (IV): 6 mg/kg every 12 hours for the first 24 hours
• Maintenance Dose (IV): 4 mg/kg every 12 hours

Dose adjustments may be needed based on liver function and serum trough levels.

Preparation & Administration:

• Each vial contains 200 mg of voriconazole as a lyophilized powder.
• Must be reconstituted and diluted before IV infusion.
• Infuse over 1 to 2 hours to reduce the risk of infusion-related reactions.

Side Effects:

• Visual disturbances (common)
• Hepatotoxicity
• Hallucinations
• QT prolongation
• Rash or phototoxic reactions

Warnings & Precautions:

• Monitor liver function tests regularly.
• Avoid in patients with known hypersensitivity to voriconazole.
• Caution in patients with renal impairment (due to the IV vehicle, SBECD).
• Avoid or monitor drug interactions, especially with CYP3A4 substrates/inhibitors.

Storage:

• Store vials below 25°C (77°F).
• Use reconstituted and diluted solution within the recommended time frame as per manufacturer’s instructions.

If you're looking for more specific information (e.g., brand names, cost, or availability in a certain region), let me know!

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Additional Information:

• Item Code: IV012
• Production Capacity: 500000
• Delivery Time: IMMEDIATE
• Packaging Details: AS PER REQUIREMENTS

Injection Site	IV or IM
Form	Powder
Packaging Type	Vial
From	Dry Powder Injection
Available in	Third Party Manufacturing Also

Colistimethate is a medication used to treat certain bacterial infections, particularly those caused by multidrug-resistant strains of bacteria. It belongs to the class of antibiotics known as polymyxins. Colistimethate is often used as a last resort when other antibiotics have proven ineffective due to bacterial resistance.

 

Here are some key points about Colistimethate injection:

 

Indications: Colistimethate is primarily used to treat infections caused by gram-negative bacteria, including Pseudomonas aeruginosa and Klebsiella pneumoniae. It is often reserved for severe infections, especially when other antibiotic options are limited.

 

Mechanism of Action: Colistimethate disrupts the bacterial cell membrane, leading to leakage of cellular contents and ultimately causing bacterial cell death. It is particularly effective against gram-negative bacteria.

 

Administration: Colistimethate is typically administered intravenously (IV) or by inhalation. Intravenous administration is common for systemic infections, while inhalation is sometimes used for respiratory infections.

 

Monitoring and Side Effects: Patients receiving Colistimethate should be closely monitored for any signs of adverse reactions, including kidney problems and neurotoxicity. Common side effects may include kidney dysfunction, neurotoxicity (such as confusion or dizziness), and gastrointestinal symptoms. Regular monitoring of kidney function is essential during treatment.

 

Precautions: Colistimethate is a potent antibiotic and is usually reserved for serious infections due to the risk of adverse effects. It's important to use the medication under the guidance of a healthcare professional who will weigh the potential benefits against the risks.

 

Dosage: The dosage of Colistimethate depends on various factors, including the severity of the infection, the patient's weight, and kidney function. It is crucial to follow the prescribed dosage and administration schedule.

 

Complete Course: As with any antibiotic, it's important to complete the full course of treatment, even if symptoms improve before the medication is finished. Stopping the antibiotic prematurely may lead to incomplete treatment and the development of antibiotic-resistant bacteria.

 

If you have been prescribed Colistimethate or have questions about its use, it's important to discuss your concerns with your healthcare provider. They can provide specific information tailored to your medical condition and guide you through the treatment process.

Additional Information:

• Item Code: PCD05
• Production Capacity: 500000
• Delivery Time: Immediate in PCD & 40 to 60 Days in Third Party Manufacturing
• Packaging Details: Sterile Injectable Powder For IM IV USE

Strength	400 mg
Available in	Third Party Manufacturing also
Form	Dry Powder Injection
Packing	Dry Powder injection

Teicoplanin is an antibiotic that belongs to the glycopeptide class. It is commonly used to treat bacterial infections, particularly those caused by gram-positive bacteria. Teicoplanin is often reserved for serious infections, including those resistant to other antibiotics. The medication is administered intravenously (IV) or intramuscularly (IM), and it is commonly used in hospital settings.

 

Here are some key points about Teicoplanin injection:

 

Indications: Teicoplanin is used to treat infections caused by susceptible gram-positive bacteria, including Staphylococcus aureus (including methicillin-resistant strains), Streptococcus species, and other gram-positive bacteria. It is often used in the treatment of skin and soft tissue infections, respiratory tract infections, and bone and joint infections.

 

Mechanism of Action: Teicoplanin works by inhibiting the synthesis of bacterial cell walls. It interferes with the formation of peptidoglycan, an essential component of the bacterial cell wall, leading to cell wall damage and ultimately bacterial cell death.

 

Administration: Teicoplanin is typically administered by intravenous infusion or intramuscular injection. The choice of administration route depends on the specific indication, the severity of the infection, and the patient's condition.

 

Monitoring and Side Effects: Patients receiving Teicoplanin should be monitored for potential side effects, including kidney function, liver function, and hematologic parameters. Common side effects may include skin reactions at the injection site, as well as gastrointestinal symptoms. Rare but serious side effects may include allergic reactions and changes in kidney function.

 

Dosage: The dosage of Teicoplanin is determined based on factors such as the type and severity of the infection, the patient's weight, and renal function. It's essential to follow the prescribed dosage and administration schedule.

 

Precautions: Teicoplanin should be used with caution in patients with pre-existing kidney problems. It's important to inform your healthcare provider about any allergies, pre-existing medical conditions, or other medications you are taking.

 

Complete Course: As with any antibiotic, it's important to complete the full course of Teicoplanin as prescribed by your healthcare provider, even if symptoms improve before the medication is finished.

 

If you have been prescribed Teicoplanin or have questions about its use, it's important to discuss your concerns with your healthcare provider. They can provide specific information tailored to your medical condition and guide you through the treatment process.

Additional Information:

• Item Code: PCD06
• Production Capacity: 50000
• Delivery Time: Immediate in PCD Franchise & 40 to 60 Days in Third Party Manufacturing
• Packaging Details: Dry Powder injection

Strength	1500 mg
Shelf Life	24 Months
Available in	Third Party Manufacturing Also
Provide	PCD Franchise also

Cefuroxime is a second-generation cephalosporin antibiotic used to treat various bacterial infections. It is effective against a wide range of gram-positive and gram-negative bacteria. Cefuroxime is available in different formulations, including oral tablets, intravenous (IV) injections, and intramuscular (IM) injections.

 

Here are key points about Cefuroxime injection:

 

Indications:

 

Cefuroxime is commonly used to treat respiratory tract infections, urinary tract infections, skin and soft tissue infections, bone and joint infections, and other bacterial infections caused by susceptible organisms.

Mechanism of Action:

 

Cefuroxime, like other cephalosporins, works by inhibiting bacterial cell wall synthesis. It interferes with the formation of the peptidoglycan layer in the bacterial cell wall, leading to cell wall disruption and bacterial cell death.

Administration:

 

Cefuroxime injection is administered intravenously or intramuscularly. The choice of administration route depends on the specific infection being treated, the severity of the infection, and the patient's condition.

Dosage:

 

The dosage of Cefuroxime varies based on the type and severity of the infection, as well as the patient's age, weight, and renal function. It's important to follow the prescribed dosage and administration schedule.

Monitoring and Side Effects:

 

Patients receiving Cefuroxime may be monitored for signs of allergic reactions, as well as potential side effects such as gastrointestinal symptoms (nausea, diarrhea), rash, and changes in blood counts. If any unusual or severe side effects occur, they should be reported to healthcare providers.

Precautions:

 

Individuals with a known allergy to cephalosporins or penicillins should use Cefuroxime with caution. It's important to inform healthcare providers about any allergies and pre-existing medical conditions.

Pregnancy and Lactation:

 

Cefuroxime is generally considered safe to use during pregnancy and lactation, but it's essential to discuss its use with a healthcare provider, considering the potential benefits and risks.

Complete Course:

 

As with any antibiotic, it's crucial to complete the full course of Cefuroxime as prescribed by the healthcare provider, even if symptoms improve before the medication is finished. Stopping the antibiotic prematurely may lead to incomplete treatment and the development of antibiotic-resistant bacteria.

If you have been prescribed Cefuroxime or have questions about its use, it's important to discuss your concerns with your healthcare provider. They can provide specific information tailored to your medical condition and guide you through the treatment process.

Additional Information:

• Item Code: PCD011
• Production Capacity: 50000
• Delivery Time: Immediate in PCD Franchise & 40 to 60 Days in Third Party Manufacturing
• Packaging Details: Dry Powder Injection along with SWFI

Packaging Size	1 ml
Usage/Application	Hospital
Injectable Form	Liquid
Also Gives	PCD Pharma Franchise, Third Party Manufacturing
Packaging Type	1*1 ml Tray Pack
Shelf Life	24 Months

asopressin, also known as antidiuretic hormone (ADH), is a naturally occurring hormone produced by the hypothalamus and released by the pituitary gland. In medical practice, a synthetic form of vasopressin is available and is often administered as an injection for various purposes. Here are key points about vasopressin injection:

 

Mechanism of Action:

 

Vasopressin acts primarily on the kidneys, promoting water reabsorption and reducing urine output. It also has vasoconstrictive effects on blood vessels, leading to an increase in blood pressure.

Indications:

 

Diabetes Insipidus: Vasopressin is commonly used in the treatment of diabetes insipidus, a condition characterized by excessive urination and thirst due to inadequate production or response to vasopressin.

Cardiac Arrest: In certain situations, vasopressin may be used during cardiac arrest as an alternative to epinephrine for its vasoconstrictive effects.

Gastrointestinal Bleeding: Vasopressin may be used to control bleeding from esophageal varices in cases of acute gastrointestinal bleeding.

Administration:

 

Vasopressin is typically administered as an intravenous (IV) injection. The dosage and rate of administration depend on the specific indication and the patient's condition.

Side Effects:

 

Side effects of vasopressin may include changes in blood pressure, fluid and electrolyte imbalances, and in rare cases, allergic reactions. Proper monitoring is essential during administration.

Contraindications:

 

Vasopressin is generally contraindicated in individuals with certain cardiovascular conditions, including coronary artery disease. It should be used with caution in patients with impaired renal function.

Duration of Treatment:

 

The duration of vasopressin treatment depends on the underlying condition being treated. In some cases, it may be used as a short-term intervention during specific medical procedures or emergencies.

Precautions:

 

Healthcare professionals should monitor patients closely for any adverse effects, especially changes in blood pressure and electrolyte balance. Individual patient factors, such as renal function, should be considered when determining the appropriate dosage.

Pregnancy and Lactation:

 

The safety of vasopressin during pregnancy and lactation is not well established. Pregnant or breastfeeding individuals should consult with their healthcare providers before receiving vasopressin.

It's important to note that vasopressin is a potent medication with specific indications and potential risks. Its use should be determined by healthcare professionals based on the individual patient's condition and needs. If you have questions about vasopressin or its use, it's best to consult with a qualified healthcare provider who can provide personalized guidance.

Additional Information:

• Item Code: PCD014
• Production Capacity: 500000
• Delivery Time: Immediate in PCD Franchise & 40 to 60 Days in Third Party Manufacturing
• Packaging Details: 1*1 ml Tray Pack

Pack Type	Vial
Quantity Unit	Vial
Shelf Life	24 Months
Usage	To treat bacterial infections caused by susceptible organisms.
Country of Origin	Made in India
Available in	Third Party Manufacturing

Ceftazidime-Sulbactam is a combination medication that consists of two active ingredients: ceftazidime, a third-generation cephalosporin antibiotic, and sulbactam, a beta-lactamase inhibitor. This combination is used to treat certain bacterial infections where the causative bacteria are resistant to standard antibiotics.

 

Here are some key points about Ceftazidime-Sulbactam injection:

 

Indications:

 

Ceftazidime-Sulbactam is typically used to treat infections caused by bacteria that produce beta-lactamase enzymes. This includes certain strains of gram-negative bacteria.

Mechanism of Action:

 

Ceftazidime: It inhibits the synthesis of bacterial cell walls, leading to cell death. Ceftazidime is effective against a broad spectrum of bacteria, particularly gram-negative organisms.

Sulbactam: It is a beta-lactamase inhibitor. Beta-lactamases are enzymes produced by some bacteria that can break down beta-lactam antibiotics. Sulbactam helps protect ceftazidime from beta-lactamase degradation, enhancing its effectiveness.

Administration:

 

Ceftazidime-Sulbactam is typically administered by intravenous (IV) infusion. The dosage and duration of treatment depend on the type and severity of the infection.

Indications:

 

Ceftazidime-Sulbactam is commonly used to treat complicated intra-abdominal infections, complicated urinary tract infections, lower respiratory tract infections, skin and soft tissue infections, and other infections caused by susceptible bacteria.

Monitoring and Side Effects:

 

Patients receiving this medication should be monitored for signs of an allergic reaction, changes in kidney function, and other potential side effects. Common side effects may include gastrointestinal symptoms, injection site reactions, and changes in laboratory parameters.

Precautions:

 

It's important to inform healthcare providers about any allergies, pre-existing medical conditions, and medications being taken. Ceftazidime-Sulbactam should be used with caution in individuals with a history of allergies to cephalosporins or other beta-lactam antibiotics.

Pregnancy and Lactation:

 

The safety of Ceftazidime-Sulbactam during pregnancy and lactation should be assessed by healthcare providers, and the potential benefits should be weighed against the risks.

Complete Course:

 

As with any antibiotic therapy, it's important to complete the full course of Ceftazidime-Sulbactam as prescribed by the healthcare provider, even if symptoms improve before the medication is finished.

If you have been prescribed Ceftazidime-Sulbactam or have questions about its use, it's essential to discuss your concerns with your healthcare provider. They can provide specific information tailored to your medical condition and guide you through the treatment process.

Additional Information:

• Item Code: PCD017
• Production Capacity: 500000
• Delivery Time: Immediate in Ready Brand & 40 to 60 Days in Third Party Manufacturing
• Packaging Details: Dry Powder Injection along with SWFI

Promotional Material	Notepads, Visual Aids, Calendars, Working Bag, Writing Pads, Visiting Cards, Pens, Bottle, Diaries, Brochure
Form Of Medicine	Injection
Certification	GMP, GLP, WHO, ISO
Product List Available	Yes
Range of Products	Neurological
Pharmaceutical Experience	Above 5 Years

Levetiracetam is an antiepileptic medication that is commonly used to manage seizures. While levetiracetam is typically available in oral formulations, there is also an intravenous (IV) formulation of levetiracetam for use in certain situations. Here are key points about levetiracetam injection:

 

Indications:

 

Seizure Management: Levetiracetam is indicated for the treatment of partial-onset seizures in adults and children. It is also used as an adjunctive therapy in the treatment of myoclonic seizures in juvenile myoclonic epilepsy and primary generalized tonic-clonic seizures in adults and children.

Mechanism of Action:

 

The precise mechanism of action of levetiracetam is not fully understood. It is believed to modulate neurotransmitter release by binding to synaptic vesicle protein 2A (SV2A) in the brain, which may contribute to its antiepileptic effects.

Administration:

 

Levetiracetam injection is administered intravenously. It is typically used in situations where oral administration is not feasible or when a rapid onset of action is required, such as in emergency or perioperative settings.

Dosage:

 

The dosage of levetiracetam injection depends on factors such as the patient's age, weight, and the specific type of seizure being treated. The dosage is determined by the healthcare provider based on individual patient needs.

Monitoring and Side Effects:

 

Patients receiving levetiracetam, whether in oral or intravenous form, may be monitored for potential side effects. Common side effects include somnolence, dizziness, asthenia (weakness), and infection. It's essential to report any unusual or severe side effects to healthcare providers.

Precautions:

 

Levetiracetam should be used with caution in patients with kidney impairment, as the drug is primarily eliminated through the kidneys. Dose adjustments may be necessary in individuals with renal dysfunction.

Pregnancy and Lactation:

 

The use of levetiracetam during pregnancy and lactation should be carefully considered. It's important for pregnant individuals to discuss the potential risks and benefits with their healthcare providers.

Complete Course:

 

If levetiracetam is prescribed as a long-term treatment for seizures, it is important to continue the medication as directed by the healthcare provider to maintain its effectiveness.

As with any medication, levetiracetam should be used under the guidance of a qualified healthcare professional. If you have specific questions about levetiracetam injection or its use, it's best to consult with your healthcare provider, who can provide personalized information based on your medical history and condition.

Additional Information:

• Item Code: PCD018
• Production Capacity: 500000
• Delivery Time: Immediate in PCD Franchise & 40 to 60 Days in Third Party Manufacturing
• Packaging Details: 5 ml Vials

Strength	150 mg
Packaging Size	3*2ml
Prescription/Non prescription	Prescription
Form	Injection
Usage / Application	Hospital
Product Type	Injectable
Shelf Life	24 Months
Country of Origin	Made in India

Arteether is an antimalarial medication used for the treatment of uncomplicated Plasmodium falciparum malaria. It belongs to the artemisinin class of drugs, which are known for their rapid and effective action against malaria parasites. Arteether is typically administered by injection.

 

Here are key points about Arteether injection:

 

Indications:

 

Arteether is primarily used for the treatment of uncomplicated malaria caused by Plasmodium falciparum, which is a common and severe form of malaria.

Mechanism of Action:

 

Arteether, like other artemisinin derivatives, has a unique mode of action against malaria parasites. It generates free radicals within the parasites, leading to damage and destruction of the parasites.

Administration:

 

Arteether is administered by intramuscular (IM) injection. The injection is typically given deep into the muscle.

Dosage:

 

The dosage of Arteether is determined based on factors such as the patient's weight and the severity of the malaria infection. It is important to follow the prescribed dosage and treatment duration.

Duration of Treatment:

 

Arteether is often used as a short-term treatment, typically for three days. The treatment duration may vary, and it is important to complete the full course as prescribed by the healthcare provider.

Monitoring and Side Effects:

 

Patients receiving Arteether may be monitored for any adverse effects or complications. Common side effects may include pain at the injection site, fever, and gastrointestinal symptoms. Severe adverse effects are rare but may include allergic reactions.

Precautions:

 

Arteether is generally well-tolerated, but it should be used with caution in individuals with a history of allergies or hypersensitivity to artemisinin derivatives. Patients should inform healthcare providers about any pre-existing medical conditions and medications being taken.

Pregnancy and Lactation:

 

The use of Arteether in pregnancy should be carefully considered, and the potential risks and benefits should be weighed. The safety of Arteether during lactation is not well established.

Resistance Considerations:

 

Artemisinin-based combination therapies (ACTs), which combine artemisinin derivatives with other antimalarial drugs, are recommended to prevent the development of resistance. Arteether is often used as part of a combination therapy.

It's important to note that the choice of antimalarial medication and its administration should be done under the supervision and prescription of qualified healthcare professionals. If you have been prescribed Arteether or have questions about its use, it's essential to discuss your concerns with your healthcare provider, who can provide specific information tailored to your medical condition.

Additional Information:

• Item Code: PCD022
• Production Capacity: 50000
• Delivery Time: Immediate in PCD Franchise
• Packaging Details: 3*2 ml Tray Pack

Packaging Size	20 ml & 60 ml
Prescription/Non prescription	Prescription
Country of Origin	Made in India
Available in	Third Party Manufacturing
USE	FOR IV USE ONLY

Piracetam is a nootropic medication that is often used to enhance cognitive function. It belongs to a class of drugs known as racetams. While piracetam is commonly available in oral forms such as tablets or capsules, there isn't a widely recognized or commonly used injectable form for intravenous (IV) use in many standard medical practices.

 

Here are some key points about piracetam:

 

Indications:

 

Piracetam is often used off-label to improve cognitive function and memory, particularly in conditions where cognitive impairment is a concern.

Mechanism of Action:

 

The exact mechanism of action of piracetam is not fully understood. It is believed to enhance cellular membrane fluidity, modulate neurotransmitter release, and improve blood flow to the brain.

Administration:

 

Piracetam is typically administered orally in the form of tablets or capsules. The recommended dosage can vary, and it is usually taken with meals.

Research Status:

 

While piracetam has been studied for its potential cognitive-enhancing effects, its use for cognitive improvement is not universally accepted, and the evidence supporting its efficacy is mixed.

Safety and Side Effects:

 

Piracetam is generally considered safe and well-tolerated when taken at recommended doses. Common side effects may include nervousness, insomnia, gastrointestinal discomfort, and headaches.

Precautions:

 

Individuals with a history of renal impairment should use piracetam with caution, and dosage adjustments may be necessary. It's important to inform healthcare providers about any pre-existing medical conditions or medications being taken.

IV Use:

 

While piracetam is not typically administered intravenously in standard medical practices, there may be some situations where healthcare professionals explore unconventional routes of administration based on individual patient needs. However, this would be an exception and not the norm.

It's crucial to note that the availability and use of injectable forms of piracetam for IV use may vary by region, and the use of such forms should only be done under the guidance of a qualified healthcare professional. If there are specific concerns or questions about the use of piracetam or its formulations, it's best to consult with a healthcare provider who can provide advice based on the latest medical knowledge and local regulations.

Additional Information:

• Item Code: PCD016
• Production Capacity: 50000
• Delivery Time: Immediate in Third Party Manufacturing
• Packaging Details: 20 ml 60 ml