Injections

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We are engaged in offering a wide range of  quality products  to our clients. Our range of all products is widely appreciated by our clients.

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Clarithromycin 500Mg Inj – A Potent Macrolide Antibiotic

Clarithromycin 500Mg Inj is a broad-spectrum macrolide antibiotic used to treat bacterial infections caused by susceptible organisms. It is particularly effective against respiratory tract infections, skin infections, and Helicobacter pylori-related gastric conditions. This intravenous (IV) formulation is often administered to patients who cannot take oral medications or require immediate, high-dose antibiotic therapy.

Composition and Mechanism of Action

• Clarithromycin 500 mg: A semi-synthetic macrolide antibiotic that inhibits bacterial protein synthesis, preventing bacterial growth and multiplication.

• Bacteriostatic Effect: At lower doses, it inhibits bacterial growth; at higher concentrations, it can be bactericidal against certain strains.

• Broad-Spectrum Activity: Effective against Gram-positive, Gram-negative, and atypical bacteria.

Indications and Uses

Clarithromycin 500Mg Inj is used to treat a variety of infections, including:
✔ Respiratory Tract Infections – Pneumonia, bronchitis, pharyngitis, and sinusitis.
✔ Skin and Soft Tissue Infections – Cellulitis, abscesses, and infected wounds.
✔ Helicobacter pylori Eradication – Used in combination therapy for peptic ulcers.
✔ Mycobacterial Infections – Effective against Mycobacterium avium complex (MAC) in HIV/AIDS patients.
✔ Legionnaire’s Disease – Atypical pneumonia caused by Legionella pneumophila.
✔ Otitis Media and Tonsillitis – Treats bacterial infections of the ear and throat.

Dosage and Administration

• Standard Dose: 500 mg IV every 12 hours, depending on the severity of the infection.

• Duration: Typically administered for 7-14 days, based on clinical response.

• Administration: Given as an intravenous infusion over 60 minutes, not as a direct IV push.

Pharmacokinetics

• Absorption: Rapidly distributed in the body after IV administration.

• Metabolism: Metabolized in the liver to its active form, 14-hydroxy clarithromycin.

• Excretion: Eliminated through urine and feces, requiring dose adjustment in renal impairment.

Side Effects and Adverse Reactions

While Clarithromycin 500Mg Inj is well tolerated, some patients may experience:
🔹 Common Side Effects: Nausea, vomiting, diarrhea, and abdominal discomfort.
🔹 Injection Site Reactions: Pain, redness, or swelling at the injection site.
🔹 Gastrointestinal Disturbances: Mild stomach upset, bloating, or taste disturbances.

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Heparin Sodium 5000 IU – A Potent Anticoagulant for Blood Clot Prevention

Heparin Sodium 5000 IU is a widely used anticoagulant (blood thinner) that helps prevent and treat blood clots in various medical conditions. It is primarily used in deep vein thrombosis (DVT), pulmonary embolism (PE), myocardial infarction (heart attack), and during surgeries requiring anticoagulation. This fast-acting injectable medication is crucial for maintaining blood flow in medical procedures and preventing life-threatening complications caused by clot formation.

Composition and Mechanism of Action

• Heparin Sodium 5000 IU – A naturally occurring anticoagulant that works by inhibiting thrombin and factor Xa, preventing clot formation.

• Immediate Action – Works within minutes after administration for rapid anticoagulation.

• Reversible Effect – Can be neutralized with protamine sulfate in case of excessive bleeding.

Indications and Uses

✔ Prevention & Treatment of Deep Vein Thrombosis (DVT) – Reduces the risk of clots in legs that can travel to the lungs.
✔ Pulmonary Embolism (PE) Management – Prevents clots from blocking lung arteries, a serious and potentially fatal condition.
✔ Myocardial Infarction (Heart Attack) & Stroke Prevention – Used in acute coronary syndrome to prevent further clotting.
✔ During Surgeries & Dialysis – Maintains blood fluidity in cardiovascular and renal procedures.
✔ Catheter Maintenance – Prevents clot formation in intravenous (IV) lines and dialysis machines.
✔ Disseminated Intravascular Coagulation (DIC) Management – Helps in conditions with excessive clotting and bleeding.

Dosage and Administration

• Intravenous (IV) Infusion or Subcutaneous (SC) Injection – Based on condition severity and doctor’s prescription.

• Prophylactic Use – 5000 IU every 8–12 hours to prevent clots in immobilized patients.

• Therapeutic Use – Initial IV bolus followed by continuous infusion for DVT, PE, or cardiac conditions.

• Monitoring – Regular activated partial thromboplastin time (aPTT) tests ensure optimal dosing.

Side Effects and Precautions

🔹 Common Side Effects – Minor bleeding, pain at injection site, and easy bruising.
🔹 Severe Risks – Excessive bleeding, heparin-induced thrombocytopenia (HIT), or osteoporosis with prolonged use.
🔹 Contraindications – Avoid in active bleeding disorders, recent surgeries, or uncontrolled hypertension.
🔹 Drug Interactions – Increased bleeding risk with aspirin, NSAIDs, and other anticoagulants.
🔹 Special Caution in Pregnancy – Safe for use but requires careful monitoring.

Why Choose Heparin Sodium 5000 IU?

✅ Fast-Acting & Effective in Preventing Life-Threatening Clots
✅ Versatile Use in Various Medical Conditions & Procedures
✅ Well-Established Safety Profile with Medical Supervision
✅ Essential for Critical Care, Surgery, and Dialysis

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Cefoperazone 1GM is a third-generation cephalosporin antibiotic used to treat various bacterial infections. It is often available as an injectable formulation and is commonly combined with sulbactam (a beta-lactamase inhibitor) to enhance its effectiveness against resistant bacteria.

Uses:

• Respiratory tract infections (e.g., pneumonia, bronchitis)

• Urinary tract infections (UTIs)

• Skin and soft tissue infections

• Intra-abdominal infections

• Septicemia

• Gynecological infections

• Bone and joint infections

Dosage & Administration:

• Adults: Typically 1–2 g IV/IM every 12 hours (depending on the severity of the infection).

• Children: Dose varies based on weight and severity.

• Renal Impairment: Dose adjustment may be required.

Side Effects:

• Nausea, vomiting, diarrhea

• Allergic reactions (rash, itching, anaphylaxis)

• Pain at the injection site

• Liver enzyme elevation

• Bleeding tendencies (due to vitamin K inhibition)

Precautions:

• Avoid in patients allergic to cephalosporins or penicillins.

• May increase bleeding risk, so monitor coagulation in at-risk patients.

• Use with caution in liver disease patients.

• Alcohol consumption may cause a disulfiram-like reaction (flushing, vomiting, headache).

 

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Cerebroprotein Hydrolysate is used in the treatment of Alzheimer's disease, stroke, dementia in Parkinson's disease, age related memory loss and head injury. Cerebroprotein Hydrolysate is a nerve repairing medicine. It works on the brain by repairing the nerve cells and improves their survival

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Meropenem 1GM Sulbactam 500MG Inj. is a powerful combination antibiotic used to treat severe and resistant bacterial infections. Meropenem 1GM Sulbactam 500MG Inj. combines a broad-spectrum carbapenem with a beta-lactamase inhibitor, making it effective against a wide range of pathogens. In critical care settings, Meropenem 1GM Sulbactam 500MG Inj. is often included in empiric therapy protocols. The use of Meropenem 1GM Sulbactam 500MG Inj. is common in treating hospital-acquired pneumonia, complicated urinary tract infections, and intra-abdominal infections. Meropenem 1GM Sulbactam 500MG Inj. offers enhanced protection against beta-lactamase-producing bacteria. Meropenem 1GM Sulbactam 500MG Inj. is administered intravenously and requires dilution prior to infusion. Dosage of Meropenem 1GM Sulbactam 500MG Inj. is adjusted based on renal function and infection severity. Meropenem 1GM Sulbactam 500MG Inj. is generally well tolerated, though side effects such as rash, GI upset, or altered liver enzymes can occur. Meropenem 1GM Sulbactam 500MG Inj. is frequently included in ICU infection management guidelines. In surgical prophylaxis for high-risk procedures, Meropenem 1GM Sulbactam 500MG Inj. may be recommended. Patients with multidrug-resistant infections benefit significantly from Meropenem 1GM Sulbactam 500MG Inj.. Pharmacy departments maintain strict protocols for the preparation of Meropenem 1GM Sulbactam 500MG Inj.. Meropenem 1GM Sulbactam 500MG Inj. should be used under the supervision of trained healthcare professionals. Pediatric dosing of Meropenem 1GM Sulbactam 500MG Inj. must be weight-adjusted. Meropenem 1GM Sulbactam 500MG Inj. is effective even in complex, polymicrobial infections. Regular monitoring is advised during prolonged Meropenem 1GM Sulbactam 500MG Inj. therapy. Meropenem 1GM Sulbactam 500MG Inj. plays a critical role in antimicrobial stewardship programs. Resistance patterns should be reviewed before initiating Meropenem 1GM Sulbactam 500MG Inj.

In infectious disease units, Meropenem 1GM Sulbactam 500MG Inj. is often reserved for cases involving multidrug-resistant organisms. When culture results are pending, Meropenem 1GM Sulbactam 500MG Inj. serves as a strong empiric option. Meropenem 1GM Sulbactam 500MG Inj. is stable in solution for a limited period and should be administered promptly. Health professionals rely on Meropenem 1GM Sulbactam 500MG Inj. for its broad activity, especially in critically ill patients. Patients in post-operative care frequently receive Meropenem 1GM Sulbactam 500MG Inj. for prophylaxis and treatment. Dosing frequency of Meropenem 1GM Sulbactam 500MG Inj. is typically every 8 hours, adjusted by renal clearance. Meropenem 1GM Sulbactam 500MG Inj. should be reconstituted using sterile water or compatible IV fluids. In teaching hospitals, residents are trained in the proper administration of Meropenem 1GM Sulbactam 500MG Inj.. Combination therapy involving Meropenem 1GM Sulbactam 500MG Inj. and antifungals is sometimes used in febrile neutropenia. Meropenem 1GM Sulbactam 500MG Inj. is considered when initial treatment fails or the infection worsens. Meropenem 1GM Sulbactam 500MG Inj. has shown strong outcomes in treating peritonitis and pelvic infections. For elderly patients, careful monitoring is required while on Meropenem 1GM Sulbactam 500MG Inj.. Meropenem 1GM Sulbactam 500MG Inj. is often compared to other high-end antibiotics during drug selection. Pharmacokinetic properties of Meropenem 1GM Sulbactam 500MG Inj. allow for deep tissue penetration. Physicians must evaluate risk vs. benefit before starting Meropenem 1GM Sulbactam 500MG Inj. Meropenem 1GM Sulbactam 500MG Inj. can be part of step-down therapy when transitioning to o

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Meropenem 250mg Injection

Broad-Spectrum Power. Proven Efficacy. Trusted Protection.

Meropenem 250mg Injection is a high-performance, broad-spectrum carbapenem antibiotic designed for the rapid and reliable treatment of serious bacterial infections. With potent activity against a wide range of gram-positive, gram-negative, and anaerobic pathogens, Meropenem is your trusted choice in the fight against resistant infections.

Rapid Bactericidal Action – Targets and destroys tough pathogens with speed and precision
Broad Spectrum Coverage – Effective against ESBL-producing organisms and multidrug-resistant bacteria
Reliable in Critical Settings – Ideal for intra-abdominal infections, meningitis, pneumonia, and sepsis
Well-Tolerated – Excellent safety profile with low incidence of adverse effects
Flexible Dosing – Suitable for pediatric and adult use, with renal-adjusted dosing

 

 

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Methylcobalamin 1000 mcg + Thiamine HCl 100 mg + Pyridoxine HCl 100 mg + Nicotinamide 100 mg + D-Panthenol 50 mg + Benzyl Alcohol 2.0% v/v Inj. – Comprehensive Vitamin Support for Optimal Nerve and Metabolic Health

Product Overview:

Methylcobalamin 1000 mcg + Thiamine HCl 100 mg + Pyridoxine HCl 100 mg + Nicotinamide 100 mg + D-Panthenol 50 mg + Benzyl Alcohol 2.0% v/v Inj. is a highly effective injectable formulation designed to provide comprehensive nutritional support, particularly for individuals experiencing vitamin B deficiencies or nerve-related health concerns. This powerful combination of vitamins and essential nutrients plays a critical role in maintaining optimal nerve health, promoting energy production, and supporting overall metabolic processes within the body.

The formulation includes a potent blend of B vitamins, each contributing to specific metabolic and physiological functions, working synergistically to improve nerve function, energy metabolism, and cell regeneration.

Key Ingredients and Their Benefits:

1. Methylcobalamin (1000 mcg):
   Methylcobalamin is a bioavailable form of Vitamin B12, an essential nutrient for various bodily functions, including the production of red blood cells and the maintenance of the nervous system. It is especially beneficial for individuals suffering from Vitamin B12 deficiency, which can cause symptoms like fatigue, weakness, and nerve pain. This active form of B12 is involved in the synthesis of DNA and RNA and supports myelin formation, the protective sheath around nerves. Methylcobalamin also aids in cognitive function, mental clarity, and memory, making it a crucial component for overall neurological health.

2. Thiamine HCl (100 mg):
   Thiamine, also known as Vitamin B1, plays a vital role in converting carbohydrates into energy and supporting the function of the heart, muscles, and nervous system. It is critical for the proper functioning of the brain and nerves, helping to prevent neurological symptoms such as numbness, tingling, and pain. Thiamine deficiency can lead to serious health conditions, including nerve damage and cognitive impairment. By supplementing with Thiamine HCl, individuals can support their body's energy metabolism and protect against deficiencies that affect the nervous system.

3. Pyridoxine HCl (100 mg):
   Pyridoxine, or Vitamin B6, is involved in over 100 enzyme reactions related to protein metabolism and the synthesis of neurotransmitters, which are essential for proper nerve function. Pyridoxine plays a role in the production of hemoglobin, the protein in red blood cells responsible for transporting oxygen. Additionally, B6 is crucial for maintaining the health of the immune system, and it helps the body process and store carbohydrates and fats. Supplementing with Pyridoxine HCl helps to alleviate symptoms related to B6 deficiency, including irritability, confusion, and fatigue.

4. Nicotinamide (100 mg):
   Nicotinamide, also known as Niacinamide, is a form of Vitamin B3 (niacin) that contributes to cellular energy production and the repair of DNA. It helps regulate the body's energy levels, supports healthy skin, and contributes to the maintenance of healthy cholesterol levels. Nicotinamide is essential for the production of NAD+ (nicotinamide adenine dinucleotide), a coenzyme involved in many vital cellular processes, including energy metabolism, DNA repair, and cell survival. It also possesses anti-inflammatory properties and supports healthy brain function, making it an important nutrient for overall well-being.

5.  

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Enoxaparin 40mg is a medication commonly used to prevent and treat blood clots, particularly in individuals who are at an increased risk due to certain medical conditions or procedures. Enoxaparin is a low molecular weight heparin (LMWH), a class of anticoagulants that work by inhibiting specific clotting factors in the blood. It is often prescribed for patients undergoing surgery, especially orthopedic or abdominal surgery, to reduce the risk of deep vein thrombosis (DVT), a condition where blood clots form in the deep veins of the body, often in the legs. Enoxaparin 40mg is also used in the treatment of pulmonary embolism (PE), a serious condition where blood clots travel to the lungs, and for patients with acute coronary syndrome (ACS), such as those experiencing unstable angina or heart attacks.

The 40mg dose of Enoxaparin is typically administered by subcutaneous injection, often once or twice a day, depending on the specific condition being treated and the patient's health status. The dosage and frequency may vary based on individual needs, and it’s important to follow the healthcare provider’s instructions carefully to avoid complications such as bleeding or bruising. The injectable form of Enoxaparin allows for easy administration and effective absorption, offering rapid therapeutic action in the prevention and management of thromboembolic disorders.

Enoxaparin 40mg is well tolerated in many patients, but like all medications, it can have potential side effects. Common side effects include bleeding, bruising at the injection site, and, in rare cases, an allergic reaction. More serious but less frequent side effects can include low platelet counts or the development of a condition called heparin-induced thrombocytopenia (HIT), which requires immediate medical attention.

Before starting Enoxaparin, patients should inform their healthcare provider of any existing conditions, especially those related to the liver, kidneys, or bleeding disorders. It is also crucial to disclose any other medications being taken, as Enoxaparin can interact with certain drugs, including other anticoagulants and antiplatelet medications, increasing the risk of bleeding complications.

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Enoxaparin 60mg is a medication commonly used in the treatment and prevention of deep vein thrombosis (DVT), pulmonary embolism (PE), and to prevent clotting in individuals undergoing certain surgeries, such as hip or knee replacements. Enoxaparin is a low molecular weight heparin (LMWH) that works by inhibiting specific clotting factors in the blood, primarily factor Xa and to a lesser extent, thrombin. By doing so, it helps prevent the formation of abnormal blood clots that can lead to serious complications.

Enoxaparin 60mg is typically administered as an injection under the skin (subcutaneously), and the dosage may vary depending on the patient's medical condition, weight, and risk factors for clot formation. It is essential for individuals receiving Enoxaparin to follow their healthcare provider’s instructions closely to ensure proper dosing and to minimize the risk of bleeding, which is the most common side effect associated with blood thinners.

 

Patients may be prescribed Enoxaparin after major surgeries, especially orthopedic procedures like hip or knee replacement, where the risk of blood clots is heightened. Additionally, Enoxaparin is frequently used in the management of patients who are at risk for DVT or PE, including those with a history of these conditions, those undergoing long-term bed rest, or individuals with certain chronic illnesses such as cancer.

 

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Ferric carboxymaltose injection is an iron replacement product that is used to treat iron deficiency anemia (not enough iron in the blood) in patients with non-dialysis dependent chronic kidney disease (CKD), in patients who cannot take iron supplements or who are taking iron supplements that did not work well, and in patients with heart failure to improve the ability to exercise.

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Doxycycline 100mg injection is a broad-spectrum antibiotic used to treat a variety of bacterial infections. As a member of the tetracycline class of antibiotics, Doxycycline works by inhibiting bacterial protein synthesis. It does this by binding to the 30S ribosomal subunit of the bacteria, preventing the attachment of aminoacyl-tRNA to the ribosome, thereby inhibiting protein formation necessary for bacterial growth and replication.

This medication is commonly used for serious infections, particularly when oral administration is not an option or when a higher concentration in the bloodstream is required. The 100mg injectable form of Doxycycline is typically administered intravenously or intramuscularly, allowing for rapid absorption and higher drug concentrations in the bloodstream, making it effective in treating infections that require prompt therapeutic action.

Indications

Doxycycline 100mg injection is indicated for the treatment of various infections, including:

• Respiratory tract infections (such as pneumonia or bronchitis)

• Urinary tract infections (UTIs)

• Skin and soft tissue infections caused by susceptible organisms

• Sexually transmitted infections (STIs), including chlamydia, gonorrhea, and syphilis

• Rickettsial infections such as Rocky Mountain spotted fever and typhus

• Malaria prophylaxis and treatment of uncomplicated malaria

It is also used in the treatment of acne vulgaris and periodontitis, particularly when caused by susceptible organisms.

Dosage and Administration

The typical adult dose of Doxycycline 100mg injection is administered once or twice daily, depending on the severity of the infection and the clinical response. The drug is injected intravenously over a period of 1-2 hours, or intramuscularly if IV access is not available.

In cases of severe infection, the dosage may be adjusted according to the patient's condition, with the maximum dose not exceeding 200mg per day. Treatment duration depends on the infection being treated, but it is typically administered for 7-14 days.

Side Effects

Common side effects of Doxycycline 100mg injection include:

• Gastrointestinal discomfort: Nausea, vomiting, and diarrhea.

• Skin sensitivity: Increased sensitivity to sunlight, leading to a risk of sunburn.

• Allergic reactions: Skin rashes, itching, or more severe reactions such as anaphylaxis (rare).

• Esophageal irritation or ulceration: Especially if the drug is not adequately diluted or if the patient does not remain upright after administration.

More severe side effects can include liver toxicity, renal impairment, or severe allergic reactions. If any unusual symptoms occur, medical attention should be sought immediately.

Precautions and Contraindications

Doxycycline should be used with caution in patients with liver or kidney dysfunction, as dosage adjustments may be necessary. It is also contraindicated in pregnant women (especially during the second and third trimesters) and children under 8 years old due to the risk of permanent tooth discoloration and potential effects on bone growth.

Conclusion

Doxycycline 100mg injection is a highly effective antibiotic for the treatment of a range of infections, especially when oral administration is not feasible. With proper dosing and monitoring, it can provide rapid and effective treatment for conditions caused by susceptible bacteria. However, it should be used with caution in certain populations to minimize potential risks and side effects.

 

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Omeprazole 40mg is a medication that belongs to a class of drugs known as proton pump inhibitors (PPIs). The active salt in Omeprazole 40mg is Omeprazole, which works by reducing the amount of stomach acid produced. This action helps in managing various gastrointestinal conditions that are caused by excess acid production, such as acid reflux, ulcers, and gastroesophageal reflux disease (GERD).

Omeprazole is used for the treatment and prevention of conditions like gastric ulcers, duodenal ulcers, erosive esophagitis, and Helicobacter pylori infection when used as part of combination therapy. It is also commonly prescribed for the relief of symptoms associated with heartburn and acid reflux.

The 40mg dose is typically prescribed for more severe cases, such as for the treatment of GERD or Zollinger-Ellison syndrome, a condition in which the stomach produces excessive acid. Omeprazole 40mg may also be used to promote the healing of the esophagus and to prevent ulcers in individuals who are taking certain nonsteroidal anti-inflammatory drugs (NSAIDs).

The mechanism of action of Omeprazole involves the inhibition of the H+/K+ ATPase enzyme in the stomach lining, which is responsible for secreting gastric acid. By inhibiting this enzyme, Omeprazole reduces stomach acid production, thereby providing relief from the burning sensation, pain, and damage caused by excess stomach acid.

Omeprazole 40mg is usually taken once daily, preferably in the morning before a meal. It can be taken with or without food but should be swallowed whole without crushing or chewing the capsule. The exact dosage and duration of treatment should always be determined by a healthcare provider based on the specific condition being treated.

It is important to follow the prescribed dosage and not exceed the recommended amount, as taking higher doses than needed can lead to side effects such as headaches, dizziness, nausea, or diarrhea. Long-term use of Omeprazole may also increase the risk of certain health issues like bone fractures, kidney disease, and vitamin B12 deficiency, which is why it is crucial to monitor the treatment under medical supervision.

In conclusion, Omeprazole 40mg is an effective medication for treating acid-related gastrointestinal disorders, with the active salt being Omeprazole. It works by reducing stomach acid production, thereby alleviating symptoms and preventing complications related to acid reflux, ulcers, and other digestive disorders. However, it is important to take the medication as prescribed and consult a healthcare provider if any unusual symptoms or side effects occur.

 

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Ceftriaxone 1 g + Tazobactam 125 mg Injection

This combination of Ceftriaxone (1 g) and Tazobactam (125 mg) is a broad-spectrum injectable antibiotic used to treat a wide range of bacterial infections. The combination enhances the efficacy of Ceftriaxone against resistant bacteria by including a β-lactamase inhibitor, Tazobactam.

🧪 Composition:

• Ceftriaxone: 1 gram (third-generation cephalosporin antibiotic)

• Tazobactam: 125 mg (β-lactamase inhibitor)

⚡ Mechanism of Action:

• Ceftriaxone works by inhibiting bacterial cell wall synthesis, causing bacterial cell death.

• Tazobactam inhibits β-lactamase enzymes produced by resistant bacteria, preventing the breakdown of Ceftriaxone. This combination helps treat infections caused by β-lactamase-producing organisms.

✅ Uses:

This combination is effective against infections caused by susceptible bacteria, including:

• Respiratory tract infections (pneumonia, bronchitis, sinusitis)

• Urinary tract infections (UTIs)

• Skin and soft tissue infections

• Intra-abdominal infections

• Bone and joint infections

• Meningitis

• Sepsis

• Pelvic inflammatory disease (PID)

• Gonorrhea

💊 Dosage & Administration:

• Adults: Typically 1.5–3 grams daily, divided into 2 doses (1 gram every 12 hours), depending on infection severity.

• Children: Doses are weight-based and adjusted according to the type and severity of the infection.

• Route: Intravenous (IV) or intramuscular (IM) injection.

Note: Always follow the healthcare provider’s prescription for accurate dosing.

⚠️ Side Effects:

• Common: Diarrhea, nausea, vomiting, rash, pain at injection site.

• Serious (rare): Severe allergic reactions (anaphylaxis), liver dysfunction, blood disorders (e.g., thrombocytopenia), superinfection (e.g., candidiasis).

• Hypersensitivity Reactions: Risk of anaphylaxis, particularly in individuals with a history of allergy to β-lactam antibiotics.

🚫 Precautions:

• Allergies: Avoid in patients with hypersensitivity to cephalosporins, penicillins, or β-lactam antibiotics.

• Renal or Hepatic Impairment: Dose adjustments may be required.

• Neonates: Caution with calcium-containing IV solutions due to the risk of precipitation.

💊 Drug Interactions:

• Anticoagulants: Increased risk of bleeding.

• Calcium-containing IV solutions: Risk of precipitation, especially in neonates.

• Aminoglycosides: May enhance the antibacterial effect.

💾 Storage:

• Store at room temperature, away from moisture and light.

• Reconstituted solutions should be used promptly as per medical guidelines.

 

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Ceftriaxone 1 g + Sulbactam 500 mg Injection 

This combination of Ceftriaxone (1 g) and Sulbactam (500 mg) is a broad-spectrum injectable antibiotic used to treat a variety of bacterial infections. It combines the action of a third-generation cephalosporin with a β-lactamase inhibitor to enhance effectiveness against resistant bacteria.

�� Composition:

• Ceftriaxone: 1 gram (a third-generation cephalosporin antibiotic)

• Sulbactam: 500 mg (a β-lactamase inhibitor)

⚡ Mechanism of Action:

• Ceftriaxone works by inhibiting bacterial cell wall synthesis, leading to bacterial death.

• Sulbactam inhibits β-lactamase enzymes produced by resistant bacteria, which would otherwise break down ceftriaxone. This combination extends the range of Ceftriaxone’s activity, especially against β-lactamase-producing bacteria.

✅ Uses:

This combination is effective against infections caused by susceptible bacteria, including:

• Respiratory tract infections (pneumonia, bronchitis, sinusitis)

• Urinary tract infections (UTIs)

• Skin and soft tissue infections

• Intra-abdominal infections

• Bone and joint infections

• Meningitis

• Sepsis

• Gonorrhea

• Pelvic inflammatory disease (PID)

�� Dosage & Administration:

• Adults: Typically 1.5–3 grams daily, divided into 2 doses (1 gram every 12 hours) depending on infection severity.

• Children: Doses are weight-based and adjusted as per infection type and severity.

• Route: Intravenous (IV) or intramuscular (IM) injection.

Note: Always follow a healthcare provider's prescription for the exact dosage.

⚠️ Side Effects:

• Common: Diarrhea, nausea, vomiting, rash, pain at injection site.

• Serious (rare): Severe allergic reactions, liver dysfunction, blood disorders (e.g., thrombocytopenia), superinfection (e.g., candidiasis).

• Hypersensitivity Reactions: Anaphylaxis, especially in individuals allergic to β-lactam antibiotics.

�� Precautions:

• Allergies: Avoid if there’s a history of hypersensitivity to cephalosporins, penicillins, or β-lactam antibiotics.

• Renal or Hepatic Impairment: Dose adjustment may be needed.

• Neonates: Caution with calcium-containing IV solutions due to the risk of precipitation.

�� Drug Interactions:

• Anticoagulants: Increased bleeding risk.

• Calcium-containing IV solutions: Risk of precipitation, especially in neonates.

• Aminoglycosides: May have additive effects on bacteria.

�� Storage:

• Store at room temperature, away from light and moisture.

• Reconstituted solutions should be used promptly as per guidelines.

 

Approx. Rs 3,500 / PieceGet Latest Price

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Introduction: Imipenem 500 mg + Cilastatin Inj. is a potent antibiotic combination used in the treatment of severe infections caused by a variety of bacteria. This formulation consists of two active ingredients: Imipenem, a broad-spectrum carbapenem antibiotic, and Cilastatin, which is a renal dehydropeptidase I inhibitor. The combined effect of these two components ensures that Imipenem can be effectively utilized to combat a wide range of bacterial infections while minimizing potential side effects related to kidney function. This medication is administered parenterally, typically through intravenous (IV) injection or infusion.

Pharmacology:

• Imipenem: Imipenem belongs to the carbapenem class of antibiotics, which are characterized by their broad-spectrum activity against both gram-positive and gram-negative bacteria, including many that are resistant to other types of antibiotics. Imipenem works by inhibiting bacterial cell wall synthesis, leading to the death of the bacteria. It is especially effective against a range of pathogens including enterococci, Escherichia coli, Klebsiella, and Pseudomonas species, among others.

• Cilastatin: Cilastatin is not an antibiotic by itself but serves an important role in this combination. Imipenem is broken down in the kidneys by an enzyme called dehydropeptidase I. Cilastatin prevents the breakdown of Imipenem in the kidneys, allowing it to maintain its effectiveness throughout the body. Cilastatin thus enhances the action of Imipenem and reduces the likelihood of kidney-related side effects associated with the use of Imipenem alone.

Indications: Imipenem 500 mg + Cilastatin Inj. is indicated for the treatment of various serious infections caused by susceptible bacteria. It is particularly used when infections are caused by resistant organisms or when other antibiotics are ineffective. Some of the common indications for this combination include:

1. Pneumonia: This can include community-acquired pneumonia (CAP) and hospital-acquired pneumonia (HAP), which are often caused by bacteria such as Streptococcus pneumoniae, Haemophilus influenzae, and Pseudomonas aeruginosa.

2. Intra-abdominal Infections: These include infections such as peritonitis, abscesses, and cholecystitis caused by a broad spectrum of pathogens including both aerobic and anaerobic organisms.

3. Skin and Soft Tissue Infections: This includes infections such as cellulitis, wound infections, and diabetic foot infections, often caused by Gram-positive cocci, including Streptococcus and Staphylococcus species.

4. Urinary Tract Infections (UTIs): These can be complicated UTIs caused by resistant organisms, such as Klebsiella pneumoniae, Enterobacter species, and Pseudomonas aeruginosa.

5. Bone and Joint Infections: Imipenem + Cilastatin is effective in treating osteomyelitis and septic arthritis caused by various resistant organisms.

6. Sepsis: A life-threatening condition resulting from infection that can be caused by various pathogens. Imipenem + Cilastatin is utilized in treating sepsis when the causative organism is resistant to other antibiotics.

Dosage and Administration: Imipenem 500 mg + Cilastatin Inj. is administered intravenously, typically in hospital settings under the supervision of a healthcare provider. The exact dosage and frequency depend on the type of infection, the severity, and the patient's renal function. Generally, the adult dose is 500 mg of Imipenem combined with Cilastatin, administered every 6 to 8 hours for severe infections.

 

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Doripenem 1000mg is a potent broad-spectrum antibiotic used in the treatment of various serious bacterial infections. It belongs to a class of medications known as carbapenems, which are beta-lactam antibiotics. Known for its effectiveness against a wide range of both Gram-positive and Gram-negative bacteria, Doripenem offers clinicians a reliable and essential option for combating infections that may be resistant to other types of antibiotics.

Mechanism of Action

Doripenem works by inhibiting bacterial cell wall synthesis. It binds to specific proteins within the bacterial cell membrane, known as penicillin-binding proteins (PBPs), and prevents the bacteria from forming the protective cell wall structure. Without a proper cell wall, the bacteria lose their structural integrity and ultimately die. This bactericidal activity is highly effective against both fast-growing and more resistant bacterial strains.

Indications

Doripenem is typically indicated for the treatment of complicated infections, especially in hospital settings, where drug-resistant bacteria are more prevalent. The primary indications for Doripenem 1000mg include:

• Complicated Intra-abdominal Infections (cIAI): Doripenem is often used to treat infections such as peritonitis and abscesses, which may result from conditions like appendicitis, diverticulitis, or bowel perforations. Its ability to target a wide range of pathogens is crucial in these settings, especially in patients who may have underlying medical conditions.

• Complicated Urinary Tract Infections (cUTI): This includes infections like pyelonephritis, and Doripenem’s broad spectrum is especially useful in patients with multi-drug-resistant organisms or those who fail to respond to first-line treatments.

• Complicated Skin and Soft Tissue Infections (cSSTI): Doripenem is effective against a variety of Gram-positive and Gram-negative pathogens that cause deep skin infections, diabetic foot infections, and other soft tissue complications.

• Nosocomial Pneumonia: This refers to pneumonia acquired in hospital settings, including ventilator-associated pneumonia (VAP). Doripenem is particularly useful in treating pneumonia caused by resistant pathogens like Pseudomonas aeruginosa and Acinetobacter baumannii, both of which can be difficult to manage with other antibiotics.

Dosage and Administration

The typical dosage of Doripenem 1000mg is 1 gram intravenously every 8 hours. The duration of treatment usually depends on the severity and type of infection, but generally ranges from 7 to 14 days. It is important to administer Doripenem in a clinical setting under the supervision of a healthcare professional, especially in patients with renal impairment, as dose adjustments may be required.

The drug is usually delivered via intravenous infusion. Prior to administration, the powder in the vial is reconstituted with sterile water or saline to form a solution. It should then be further diluted and administered over the course of 60 minutes, to prevent rapid infusion-related side effects like hypotension.

Pharmacokinetics

Doripenem exhibits excellent tissue penetration, which makes it highly effective in treating infections in various organs such as the lungs, kidneys, and abdominal cavity. Its half-life is approximately 1 hour, and it is primarily excreted through the kidneys, which is important to consider when dosing patients with renal insufficiency.

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Vancomycin 500mg Injection is an antibiotic used in the treatment of severe bacterial infections in hospitalized patients. It is effective against infections of the respiratory tract (e.g. pneumonia), urinary tract, skin and soft tissues, bones and joints, heart, blood, and others.

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Vancomycin injection is used alone or in combination with other medications to treat certain serious infections such as endocarditis (infection of the heart lining and valves), peritonitis (inflammation of the lining of the abdomen), and infections of the lungs, skin, blood, and bones

Approx. Rs 135.63 / PieceGet Latest Price

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Levetiracetam 100mg Ml injection
Welcome to PCD Phara, where luxury meets wellness. Our franchise offers a divine fusion of French elegance and holistic health solutions. From skincare to supplements, our meticulously curated products embody sophistication and effectiveness. Pamper yourself with our exclusive line of rejuvenating creams, serums, and essential oils, crafted with the finest natural ingredients. Elevate your well-being with our nutritional supplements, designed to nourish both body and mind. Experience the epitome of self-care with PCD Phara, where every product is a testament to excellence and indulgence. Join us in the pursuit of beauty, inside and out.

Approx. Rs 562.91 / VialGet Latest Price

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Doxycycline 100 Mg Inj

Approx. Rs 250 / VialGet Latest Price

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Cefoperazone + Tazobactam (1g + 125mg) is a combination antibiotic used to treat various bacterial infections.

Uses:

• Respiratory tract infections

• Urinary tract infections

• Intra-abdominal infections

• Skin and soft tissue infections

• Bone and joint infections

• Septicemia

Mechanism of Action:

• Cefoperazone: A third-generation cephalosporin that inhibits bacterial cell wall synthesis.

• Tazobactam: A beta-lactamase inhibitor that prevents bacterial resistance by inhibiting beta-lactamase enzymes.

Dosage & Administration:

• Typically administered intravenously (IV)

• Dosage depends on severity and type of infection (often 1.125g every 12 hours or as prescribed by a doctor).

Side Effects:

• Nausea, vomiting

• Diarrhea

• Allergic reactions (rash, itching)

• Liver enzyme elevation

Precautions:

• Use with caution in renal and hepatic impairment

• Monitor for superinfections (e.g., fungal infections)

• Avoid if allergic to cephalosporins or penicillins

Approx. Rs 120 / PieceGet Latest Price

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Methylprednisolone Acetate Injectable 80Mg is a long-acting corticosteroid widely used for its potent anti-inflammatory, immunosuppressive, and anti-allergic properties. It is commonly prescribed for inflammatory conditions, autoimmune disorders, severe allergies, and joint-related ailments. This injectable form provides sustained relief, making it an ideal choice for chronic inflammatory diseases, musculoskeletal disorders, and acute allergic reactions.

Methylprednisolone Acetate Injectable 80Mg is available in a sterile suspension formulation, designed for intramuscular (IM), intra-articular (IA), or soft tissue injection. It helps manage pain, swelling, and inflammation associated with various medical conditions, ensuring long-lasting therapeutic effects.

Composition & Mechanism of Action

🔹 Active Ingredient: Methylprednisolone Acetate 80Mg/ml
🔹 Pharmacological Class: Glucocorticoid / Corticosteroid
🔹 Mechanism of Action:
✔ Reduces Inflammation: Suppresses immune system activity to prevent excessive inflammatory responses.
✔ Immunosuppressive Effect: Controls autoimmune diseases by reducing overactive immune reactions.
✔ Anti-Allergic Properties: Provides rapid relief in cases of severe allergic reactions and anaphylaxis.
✔ Pain & Swelling Relief: Intra-articular administration helps reduce joint pain, stiffness, and swelling.

✅ Long-Acting Corticosteroid
✅ Effective in Arthritis, Autoimmune Disorders & Severe Allergies
✅ Administered via IM, IA, or Soft Tissue Injection
✅ Provides Extended Duration of Action

Indications & Uses

Methylprednisolone Acetate Injectable 80Mg is used in a wide range of medical conditions, including:

✔ Rheumatoid Arthritis & Osteoarthritis: Reduces joint inflammation and stiffness.
✔ Severe Allergic Reactions (Anaphylaxis): Controls life-threatening allergic responses.
✔ Asthma & Respiratory Disorders: Treats acute exacerbations of asthma and chronic obstructive pulmonary disease (COPD).
✔ Dermatological Conditions (Eczema, Psoriasis): Manages severe skin inflammation.
✔ Lupus & Autoimmune Diseases: Helps in conditions like systemic lupus erythematosus (SLE) and multiple sclerosis.
✔ Spinal Cord Injuries: Used as part of high-dose steroid therapy in trauma cases.
✔ Chronic Inflammatory Diseases: Effective for inflammatory bowel disease (IBD), ulcerative colitis, and Crohn’s disease.
✔ Tendonitis & Bursitis: Reduces pain and swelling in musculoskeletal conditions.

Dosage & Administration

📌 Route of Administration: Intramuscular (IM), Intra-articular (IA), or Soft Tissue Injection
📌 Recommended Dose:

• IM (Systemic Conditions): 40–80 mg every 1–2 weeks

• IA (Joint Injection for Arthritis): 10–80 mg depending on joint size

• Allergic Reactions & Respiratory Disorders: 80 mg IM as a single dose

• Severe Inflammatory Conditions: Up to 160 mg may be given as per physician’s recommendation

⚠ Must be administered by a healthcare professional under aseptic conditions.

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Methylcobalamin 2500mcg Inj. is a high-potency injectable formulation of Vitamin B12, designed to effectively support neurological function, red blood cell production, and overall metabolic health. As an active and bioavailable form of Vitamin B12, Methylcobalamin plays a crucial role in DNA synthesis, nerve regeneration, and energy metabolism. It is widely used for treating Vitamin B12 deficiency, peripheral neuropathy, anemia, and neurodegenerative disorders, making it an essential therapeutic option for individuals with increased B12 requirements.

What is Methylcobalamin 2500mcg Inj.?

Methylcobalamin 2500mcg Inj. is an injectable form of Vitamin B12, which is more readily absorbed and utilized by the body compared to other forms like cyanocobalamin. This injection provides a concentrated dose of 2500mcg, ensuring rapid replenishment of B12 levels and effective treatment for various health conditions associated with deficiency.

Key Benefits of Methylcobalamin 2500mcg Inj. 1. Supports Nerve Health and Neuropathy Treatment

• Methylcobalamin is vital for nerve cell repair and regeneration.

• Helps manage conditions such as diabetic neuropathy, peripheral neuropathy, and neuralgia.

• Reduces symptoms like tingling, numbness, and nerve pain.

2. Essential for Red Blood Cell Production and Anemia Prevention

• Boosts hemoglobin levels, reducing the risk of megaloblastic anemia.

• Improves oxygen transport and prevents symptoms like fatigue and weakness.

• Supports individuals with chronic anemia or Vitamin B12 malabsorption.

3. Enhances Brain Function and Cognitive Health

• Plays a crucial role in memory retention, focus, and mental clarity.

• Helps slow cognitive decline in elderly individuals and Alzheimer’s patients.

• Supports mood regulation, reducing the risk of depression and anxiety.

Approx. Rs 35,000 / VialGet Latest Price

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Critical Care Pcd Pharma Franchise in Tamil Nadu
Acyclovir Injection
Glutathione 600MG Injection
Amoxycillin 1GM Clavulanate Potass. 200MG Injection
Ascorbic acid 1.5GM/6ML Injection
Artesunate Injection
Aztreonam Injection
Cefuroxime Injection
Cefoperazone Injection
Ceftriaxone + Tazobactam Injection
Ceftriaxone + Sulbactam Injection
Cerebroprotein Hydrolysate 60 MG Injection
Cholecalciferol (Vit.D3)  (600000 I.U.) 15mg Injection
Citicoline Injection
Clarithromycin 500MG. Injection.
Clindamycin Injection
Colistimethate Injection
Doripenem Injection
Doxycycline 100MG Injection
ENOXAPARIN Injection
ETAMSYLATE 125MG Injection
Flucloxacillin 1GM Injection
Heparin Sodium Injection
Hydrocortisone Injection
Hydroxyprogesterone Injectionection
Imipenem 500MG.+Cilastatin 500MG. Injection
Iron Sucrose Injectionection
Ferric Carboxymaltose Injection
L Ornithine L Aspartate Injectionection 5gm
Labetalol HCL 5mg USP Injection
Levetiracetam 100mg/ML  Injection
Levosulpiride 2ML Injection
Levosulpiride 12.5 mg Injection
Meropenem 1GM Injection
Meropenem +Sulbactum Injection
Methylcobalamin 1500mcg Injection.
Methylcobalamin 1000 mcg + Thiamine HCl 100 MG + Pyridoxine HCl 100 MG + Nicotinamide 100 MG + D panthenol 50 MG + Benzyl Alcohol 2.0% v/v Injection.
Methylprednisolone sod. succinate Injectionection
Nandrolone decanoate Injectionection
Nicorandil 48MG Injectionection
Ondansetron Injectionection
Pantoprazole 40 MG Injection
Piperacillin + Tazobactam  Injection
PIRACETAM 15ML Injection
Polymixin B 5,00,000 Injection
Rabeprazole 20MG. Injection
Teicoplanin Injection
Thiamine 100MG Injection
Tigecycline 50MG Injectionection
Tranexamic Acid 500 Injectionection
Triamcinolone Acetonide Injectionection
Voriconazole 200MG Injection
Vancomycin Hydrochloride  Injection
Terlipressin 1mg Injection
Octreotide Injection
Milrinone 1mg Injection
Acetylcysteine Injection
Vasopressin Injection
Edaravone Injection
Granisetron Injection
Levocarnitine Injection
Drotaverine Injection
Piroxicam Injection
Cefepime 1GM Injection
Cefepime  + Sulbactum  Injection
Cefepime  + Tazobactum Injection
Cefotaxime Injection
Ceftazidime Injection
Ceftazidime + Tazobactum Injection
Esomeprazole 40MG Injection

Approx. Rs 157.17 / VialGet Latest Price

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Amoxycillin Clavulanate Potass. 1.2 GM – A Powerful Antibiotic Combination

Amoxycillin Clavulanate Potass. 1.2 GM is a broad-spectrum antibiotic widely used to treat bacterial infections caused by susceptible organisms. This combination drug consists of Amoxycillin (1 GM), a penicillin-class antibiotic that inhibits bacterial cell wall synthesis, and Clavulanate Potassium (200 MG), a beta-lactamase inhibitor that prevents bacterial resistance, enhancing the effectiveness of Amoxycillin.

This antibiotic is particularly effective in treating respiratory tract infections, urinary tract infections, skin infections, and more. The intravenous (IV) form ensures rapid absorption and higher bioavailability, making it suitable for moderate to severe infections requiring immediate action.

Composition and Mechanism of Action

• Amoxycillin (1 GM) – A beta-lactam antibiotic that disrupts bacterial cell wall formation, causing bacterial cell death.

• Clavulanate Potassium (200 MG) – A beta-lactamase inhibitor that prevents bacterial enzymes from deactivating Amoxycillin, thus enhancing its antimicrobial effect.

Indications and Uses

🔹 Respiratory Tract Infections – Pneumonia, bronchitis, sinusitis, and tonsillitis.
🔹 Urinary Tract Infections (UTIs) – Cystitis, pyelonephritis, and complicated UTIs.
🔹 Skin and Soft Tissue Infections – Cellulitis, abscesses, and wound infections.
🔹 Bone and Joint Infections – Osteomyelitis, septic arthritis.
🔹 Gastrointestinal Infections – Infections due to Helicobacter pylori (used in combination therapy).
🔹 Gynecological Infections – Pelvic inflammatory disease, postpartum infections.
🔹 Sepsis and Septicemia – Bloodstream infections caused by susceptible bacteria.
🔹 Dental Infections – Severe tooth abscesses and post-extraction infections.
🔹 Surgical Prophylaxis – Used before surgery to prevent bacterial infections.

Dosage and Administration

• Route – Intravenous (IV) injection for faster absorption.

• Recommended Dosage – 1.2 GM every 8-12 hours (varies based on infection severity).

• Duration of Treatment – Typically 5-14 days, depending on clinical response.

• Renal Impairment – Requires dosage adjustment for kidney patients.

Side Effects and Precautions

⚠ Common Side Effects – Nausea, diarrhea, headache, and mild rash.
⚠ Serious Side Effects – Severe allergic reactions, Clostridium difficile-associated diarrhea, liver dysfunction.
⚠ Contraindications – Hypersensitivity to penicillins or cephalosporins.
⚠ Drug Interactions – Avoid alcohol and interactions with anticoagulants like warfarin.
⚠ Pregnancy & Lactation – Generally considered safe but should be taken under medical supervision.

Why Choose Amoxycillin Clavulanate Potass. 1.2 GM?

✅ Broad-spectrum coverage against a wide range of bacteria.
✅ Beta-lactamase inhibitor prevents antibiotic resistance.
✅ Effective for severe infections requiring IV administration.
✅ Rapid onset of action for quicker recovery.

Approx. Rs 690 / VialGet Latest Price

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L Ornithine L Aspartate is used to treat liver diseases such as acute and chronic hepatitis, chronic alcoholic liver damage, fatty liver, jaundice, liver cirrhosis, and non-alcoholic steatohepatitis (non-alcoholic fatty liver disease). Liver diseases lead to disturbance of vital liver functions.

Approx. Rs 447.3 / VialGet Latest Price

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composition of Piperacillin 4GM + Tazobactam 500Mg. The packing of Pipcrit 4.5GM is 20ML + WFI

Approx. Rs 690 / PieceGet Latest Price

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We are engaged in offering a wide range of  quality products  to our clients. Our range of all products is widely appreciated by our clients.

Aztreonam injection is a monobactam antibiotic used to treat serious Gram-negative bacterial infections. Aztreonam is especially effective against Pseudomonas aeruginosa and other resistant organisms. In hospital settings, Aztreonam is often used when patients are allergic to penicillins. Aztreonam works by inhibiting bacterial cell wall synthesis. The administration of Aztreonam is typically intravenous or intramuscular. Aztreonam has minimal cross-reactivity with other beta-lactams, making it safer for allergic patients. Dosage of Aztreonam depends on infection severity and renal function. Aztreonam is well tolerated, with few adverse reactions. Clinicians use Aztreonam in cases of urinary tract infections, sepsis, and lower respiratory tract infections. Aztreonam should be used according to culture and sensitivity results. Pharmacists prepare Aztreonam under sterile conditions. In ICU protocols, Aztreonam may be part of combination therapy. Aztreonam has limited activity against Gram-positive bacteria and anaerobes. Therefore, Aztreonam is often paired with other agents when needed. Aztreonam is excreted primarily by the kidneys. Care must be taken when administering Aztreonam to patients with renal impairment. Aztreonam dosing intervals may vary in such cases. Monitoring is important during extended Aztreonam therapy. Aztreonam is available in various vial sizes for flexible dosing. Overall, Aztreonam injection remains a reliable choice for treating resistant Gram-negative infections.

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AZETRONAM 250: A Broad-Spectrum Monobactam Antibiotic

AZETRONAM 250 is a monobactam antibiotic used for treating bacterial infections, particularly those caused by Gram-negative bacteria. It is commonly prescribed for infections where penicillin or cephalosporin antibiotics are ineffective or cannot be used due to allergies. AZETRONAM 250 works by targeting and disrupting bacterial cell wall synthesis, leading to bacterial death and infection resolution.

Mechanism of Action

AZETRONAM 250 binds to penicillin-binding proteins (PBPs) of Gram-negative bacteria, preventing them from forming a stable peptidoglycan layer in their cell walls. This weakens and ultimately destroys the bacteria, making AZETRONAM 250 highly effective in treating resistant infections.

Indications and Uses

AZETRONAM 250 is prescribed for treating infections such as:

✅ Respiratory Tract Infections – Pneumonia, bronchitis, and lung infections, particularly in cystic fibrosis patients.
✅ Urinary Tract Infections (UTIs) – Effective against E. coli, Klebsiella, and Pseudomonas species.
✅ Skin and Soft Tissue Infections – Used for cellulitis, abscesses, and infected wounds.
✅ Septicemia (Blood Infections) – Helps combat Gram-negative bacterial bloodstream infections.
✅ Intra-Abdominal Infections – Treats peritonitis, appendicitis, and post-surgical infections.
✅ Gynecological Infections – Used in cases of pelvic inflammatory disease (PID).

Dosage and Administration

• Standard Dosage: 250 mg (AZETRONAM 250) via intravenous (IV) or intramuscular (IM) injection.

• Frequency: Administered every 6 to 8 hours, based on the severity of infection.

• Duration: Typically 7 to 14 days, depending on medical guidance.

Side Effects

🔸 Nausea and vomiting
🔸 Diarrhea
🔸 Injection site pain or redness
🔸 Mild skin rash or itching
🔸 Liver enzyme changes (rare)

Precautions

⚠️ Not effective against Gram-positive bacteria or anaerobes.
⚠️ Dose adjustment needed in kidney disease patients.
⚠️ Monitor for allergic reactions, especially in patients with β-lactam allergies.

Conclusion

AZETRONAM 250 is a powerful and safe antibiotic for Gram-negative bacterial infections, especially for patients allergic to penicillins or cephalosporins. With high effectiveness and a well-tolerated profile, it is a valuable treatment option for various infections, ensuring faster recovery and better patient outcomes.

 

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AZETRONAM 500: A Broad-Spectrum Monobactam Antibiotic for Gram-Negative Infections

AZETRONAM 500 is a monobactam antibiotic used to treat a variety of Gram-negative bacterial infections. It is highly effective against Pseudomonas aeruginosa, Escherichia coli, Klebsiella, Proteus, and Enterobacter species. AZETRONAM 500 is often prescribed for patients with penicillin or cephalosporin allergies, as it has minimal cross-reactivity with other β-lactam antibiotics.

Mechanism of Action

AZETRONAM 500 works by inhibiting bacterial cell wall synthesis. It binds to penicillin-binding proteins (PBPs) in Gram-negative bacteria, preventing them from forming a strong peptidoglycan layer. This disruption weakens the bacterial cell wall, leading to bacterial death and stopping the spread of infection.

Indications and Uses

AZETRONAM 500 is commonly prescribed for the treatment of:

✅ Respiratory Tract Infections – Pneumonia, bronchitis, and infections in cystic fibrosis patients.
✅ Urinary Tract Infections (UTIs) – Effective against complicated and uncomplicated UTIs.
✅ Septicemia (Blood Infections) – Used for serious bloodstream infections caused by Gram-negative bacteria.
✅ Skin and Soft Tissue Infections – Treats cellulitis, abscesses, and wound infections.
✅ Intra-Abdominal Infections – Peritonitis, appendicitis, and post-surgical infections.
✅ Gynecological Infections – Pelvic inflammatory disease (PID) and post-operative infections.

Dosage and Administration

• Standard Dosage: 500 mg (AZETRONAM 500) via intravenous (IV) or intramuscular (IM) injection.

• Frequency: Every 6 to 8 hours, based on the severity of infection.

• Duration: Typically 7-14 days, depending on medical guidance.

Side Effects

🔸 Nausea and vomiting
🔸 Diarrhea
🔸 Pain or redness at the injection site
🔸 Mild skin rash or itching
🔸 Liver enzyme abnormalities (rare)

Precautions

⚠️ Not effective against Gram-positive bacteria or anaerobes.
⚠️ Dose adjustment required for kidney disease patients.
⚠️ Monitor for allergic reactions, especially in those with β-lactam sensitivities.

Conclusion

AZETRONAM 500 is a highly effective antibiotic for Gram-negative bacterial infections, especially for penicillin-allergic patients. With its targeted antibacterial action, it is a vital option for treating severe infections while ensuring minimal resistance development.

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Cefuroxime 750 mg Injection

• Class: Second-generation cephalosporin antibiotic.

• Indication: Used to treat bacterial infections like respiratory tract infections, urinary tract infections, skin infections, bone and joint infections, and surgical prophylaxis.

• Dosage (Typical for Adults):

  • Usual dose: 750 mg IM or IV every 8 hours.

  • Severe infections: May increase to 1.5 g IV every 8 hours.

  • Surgical prophylaxis: Often 1.5 g IV at induction of anesthesia.

Approx. Rs 254.52 / PieceGet Latest Price

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Clindamycin 600Mg – A Potent Antibiotic for Severe Infections

Clindamycin 600Mg is a powerful lincosamide antibiotic used to treat a variety of bacterial infections caused by susceptible Gram-positive and anaerobic bacteria. It is particularly effective in treating severe respiratory infections, skin and soft tissue infections, bone infections, gynecological infections, and intra-abdominal infections. Its broad-spectrum antibacterial activity makes it an essential choice for serious infections where other antibiotics may not be effective.

Composition and Mechanism of Action

• Clindamycin 600 mg: Works by inhibiting bacterial protein synthesis at the 50S ribosomal subunit.

• Bacteriostatic or Bactericidal: Depending on the concentration and pathogen, Clindamycin can either inhibit bacterial growth or directly kill bacteria.

• Excellent Tissue Penetration: Can reach bone, joints, abscesses, and soft tissues, making it useful for deep-seated infections.

Indications and Uses

Clindamycin 600Mg is commonly prescribed for:
✔ Severe Skin and Soft Tissue Infections – Abscesses, cellulitis, wound infections.
✔ Respiratory Tract Infections – Pneumonia, bronchitis, lung abscesses.
✔ Bone and Joint Infections – Osteomyelitis, septic arthritis.
✔ Dental and Oral Infections – Severe tooth abscesses, periodontitis.
✔ Gynecological Infections – Pelvic inflammatory disease (PID), bacterial vaginosis.
✔ Intra-Abdominal Infections – Peritonitis, postoperative infections.
✔ Septicemia and Endocarditis – Used in severe bloodstream infections.
✔ Alternative for Penicillin Allergy – Suitable for patients allergic to penicillin-based antibiotics.

Approx. Rs 512.43 / VialGet Latest Price

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Acyclovir 250MG inj. is a highly effective antiviral medication commonly used to treat infections caused by herpes simplex virus (HSV) and varicella-zoster virus (VZV). Administered via injection, Acyclovir 250MG inj. works by inhibiting viral DNA replication, thereby reducing the spread of the virus within the body. This injectable formulation is particularly beneficial for patients requiring rapid therapeutic effects, such as those with severe HSV infections, herpes encephalitis, or herpes zoster (shingles).

Healthcare professionals often choose Acyclovir 250MG inj. for hospitalized patients or individuals who are unable to take oral medication. This treatment is crucial for managing conditions such as genital herpes, cold sores, and shingles, especially when symptoms are severe or complications arise. By preventing viral replication, Acyclovir 250MG inj. helps alleviate symptoms, promote healing, and reduce the risk of transmission.

Dosage and administration of Acyclovir 250MG inj. are carefully determined based on the patient’s medical condition, age, and renal function. The medication is usually administered intravenously under the supervision of healthcare providers to ensure accurate dosing and minimize potential side effects. It is essential to complete the prescribed course of Acyclovir 250MG inj. to achieve optimal therapeutic outcomes.

While generally well-tolerated, some patients may experience side effects such as local irritation at the injection site, nausea, headache, or, in rare cases, renal dysfunction. It is important to inform healthcare providers about any pre-existing conditions, allergies, or concurrent medications before receiving Acyclovir 250MG inj. to ensure safety and efficacy.

Acyclovir 250MG inj. plays a vital role in the management of viral infections, especially in immunocompromised patients or those with severe manifestations. By providing effective antiviral action, this injection helps control the progression of infections, thereby improving patient outcomes. Healthcare professionals trust Acyclovir 250MG inj. for its reliability, proven effectiveness, and targeted action against HSV and VZV infections.

In conclusion, Acyclovir 250MG inj. is a cornerstone in antiviral therapy, offering critical support in managing severe viral conditions. Its timely administration can significantly reduce complications, aid in faster recovery, and improve patients’ quality of life during the treatment process.

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Approx. Rs 71.98 / PieceGet Latest Price

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Tranexamic Acid 500 mg Injection  Overview:

Tranexamic Acid 500 mg Injection is an antifibrinolytic agent that helps prevent and control excessive bleeding. It works by blocking the breakdown of blood clots (fibrinolysis), making it effective in conditions involving heavy or abnormal bleeding.

Composition & Strength:

• Active Ingredient: Tranexamic Acid

• Strength: 500 mg per 5 mL vial

• Dosage Form: Injectable solution

• Route of Administration: Intravenous (IV) or Intramuscular (IM)

Indications & Uses:

Tranexamic Acid is used in the treatment and prevention of:

• Surgical bleeding (e.g., cardiac, liver, orthopedic, dental, and gynecological surgeries)

• Trauma-related bleeding (reduces risk of severe blood loss)

• Postpartum hemorrhage (PPH)

• Menorrhagia (heavy menstrual bleeding)

• Hemophilia-associated bleeding

• Epistaxis (nosebleeds)

• Disorders involving excessive fibrinolysis (e.g., leukemia, liver disease, prostate surgery)

Dosage & Administration:

• Surgical Bleeding Prevention:

  • Pre-operative: 10–15 mg/kg IV before surgery

  • Post-operative: 500–1000 mg IV every 6–8 hours

• Trauma/Acute Bleeding:

  • Loading dose: 1 g IV over 10 minutes

  • Maintenance dose: 1 g IV over 8 hours

• Menorrhagia: 500 mg IV/IM every 6–8 hours

Side Effects:

• Nausea, vomiting, diarrhea

• Dizziness, headache

• Hypotension (if administered too rapidly IV)

• Allergic reactions (rare)

• Increased risk of thrombosis in high-risk patients

Precautions & Warnings:

• Contraindicated in active thromboembolic conditions (e.g., DVT, PE, stroke)

• Use with caution in renal impairment (dose adjustment required)

• Avoid rapid IV infusion to prevent hypotension

• Monitor for visual disturbances (rare side effect)

 

Approx. Rs 3,500 / VialGet Latest Price

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Tigecycline 50 mg Injection  Overview:

Tigecycline 50 mg Injection is a broad-spectrum glycylcycline antibiotic, structurally related to tetracyclines. It is primarily used for treating serious bacterial infections, especially those caused by multidrug-resistant (MDR) organisms.

Composition & Strength:

• Active Ingredient: Tigecycline

• Strength: 50 mg per vial (lyophilized powder for reconstitution)

• Route of Administration: Intravenous (IV) infusion

Indications & Uses:

Tigecycline is indicated for the treatment of:

• Complicated Skin and Soft Tissue Infections (cSSTI)

• Complicated Intra-Abdominal Infections (cIAI)

• Community-Acquired Bacterial Pneumonia (CABP) (reserved for cases where alternatives are unsuitable)

• Infections caused by MDR pathogens, including MRSA, VRE, and ESBL-producing bacteria

Dosage & Administration:

• Loading Dose: 100 mg IV once

• Maintenance Dose: 50 mg IV every 12 hours

• Infusion Time: Administer over 30 to 60 minutes

• Duration: Usually 5–14 days, depending on infection severity

Side Effects:

• Common: Nausea, vomiting, diarrhea

• Less common: Liver enzyme elevation, dizziness, headache

• Rare but serious: Pancreatitis, hypersensitivity reactions, injection site reactions

Precautions & Warnings:

• Not recommended for bloodstream infections (low plasma concentration)

• Use with caution in hepatic impairment (dose adjustment may be needed)

• Avoid in pregnancy & breastfeeding (Category D – potential fetal harm)

• Higher mortality risk in certain infections (should be used only when other alternatives are not suitable

Approx. Rs 3,100 / PieceGet Latest Price

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                                                                                   Teicoplanin 400   Teicoplanin 400mg Injection - Description

Teicoplanin is an antibiotic used primarily to treat serious bacterial infections, especially those caused by Gram-positive bacteria. It belongs to the glycopeptide class of antibiotics, similar to vancomycin, and works by inhibiting the synthesis of bacterial cell walls, leading to bacterial death.

Formulation:

• Drug Name: Teicoplanin

• Strength: 400 mg

• Dosage Form: Injection (usually administered intravenously or intramuscularly)

• Packaging: Typically comes in vials for reconstitution with a diluent.

Indications:

Teicoplanin is used for the treatment of:

• Severe infections caused by Gram-positive bacteria, including:

  • Staphylococcus aureus (including MRSA)

  • Streptococcus species

  • Enterococcus species

• Bone and joint infections

• Pneumonia

• Endocarditis

• Skin and soft tissue infections

• Septicemia

Mechanism of Action:

Teicoplanin inhibits bacterial cell wall synthesis by binding to the D-Ala-D-Ala terminal of peptidoglycan precursors. This action disrupts the cell wall structure, making the bacteria vulnerable to lysis.

Dosage & Administration:

• Initial Dose: Typically 6–10 mg/kg IV every 12 hours for the first 3 doses.

• Maintenance Dose: 6–10 mg/kg IV once daily, depending on infection severity and patient response.

• Reconstitution: Requires dilution with sterile water or appropriate diluent.

Side Effects:

• Common: Fever, rash, headache, nausea, and injection site reactions.

• Serious: Nephrotoxicity, hepatotoxicity, thrombocytopenia, and allergic reactions.

Precautions:

• Renal Impairment: Dose adjustment may be needed.

• Allergy History: Caution in patients allergic to glycopeptides or similar antibiotics.

Drug Interactions:

• Nephrotoxic Drugs: Increased risk of kidney toxicity when combined with drugs like aminoglycosides or NSAIDs.

• Warfarin: Potential interaction affecting anticoagulation.

Storage:

• Store in a cool, dry place away from direct sunlight.

• After reconstitution, use promptly or as per manufacturer’s guidelines.

If you need more details about its clinical use, dosing protocols, or specific patient considerations, let me know!       

Approx. Rs 256.96 / VialGet Latest Price

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Artesunate 60: Powerful Antimalarial Treatment for Fast & Effective Recovery

Artesunate 60 is a highly effective antimalarial medication used to treat severe malaria infections caused by Plasmodium falciparum. This rapid-acting drug belongs to the artemisinin class of antimalarials and is known for its quick parasite clearance, making it a preferred choice for treating severe or complicated malaria cases.

Malaria remains a global health challenge, affecting millions of people worldwide. Artesunate 60 is widely recommended by healthcare professionals due to its high efficacy, safety, and fast action against malaria parasites. Whether used as a first-line treatment or in combination with other antimalarial drugs, Artesunate 60 plays a crucial role in saving lives.

What is Artesunate 60?

Artesunate 60 is an injectable antimalarial drug used primarily for the treatment of severe malaria. It is a water-soluble derivative of artemisinin, a natural compound extracted from the Artemisia annua plant. The medication works by producing reactive oxygen species (ROS) that damage the malaria parasite, leading to its rapid destruction.

This injectable formulation ensures fast absorption, making it ideal for treating patients with severe malaria who are unable to take oral medications. Artesunate 60 is recommended by the World Health Organization (WHO) for treating severe malaria cases in both adults and children.

Key Benefits of Artesunate 60

✔️ Rapidly Clears Malaria Parasites – Begins working immediately, reducing parasite load quickly.
✔️ Effective Against Drug-Resistant Malaria – Works even in areas with high resistance to traditional antimalarials.
✔️ Ideal for Severe Malaria Cases – Essential for treating life-threatening malaria complications.
✔️ Fast-Acting & Well-Tolerated – Provides immediate relief with minimal side effects.
✔️ WHO-Approved Treatment – Recommended by global health organizations.
✔️ Safe for Use in Pregnant Women & Children – Can be administered in emergency cases with proper medical supervision.

How Artesunate 60 Works

The mechanism of action of Artesunate 60 is based on its ability to rapidly kill malaria parasites at different stages of their lifecycle. Once administered, Artesunate 60 is converted into dihydroartemisinin (DHA), which produces free radicals that attack the parasite’s membranes and proteins, leading to its destruction. This results in a significant reduction of parasitemia, helping the patient recover quickly.

Unlike traditional antimalarial drugs, Artesunate 60 does not cause significant side effects, making it a safe and effective choice for treating severe malaria infections.

Dosage & Administration of Artesunate 60

Artesunate 60 is available as an injectable powder that must be reconstituted before administration. It is given through intravenous (IV) or intramuscular (IM) injection under medical supervision.

�� Recommended Dosage for Severe Malaria:
�� Adults & Children – 2.4 mg/kg at 0, 12, and 24 hours, followed by daily administration until the patient can tolerate oral therapy.
�� Newborns & Pregnant Women – Safe when administered under strict medical guidance.

Note: After completing the initial Artesunate 60 injections, patients should transition to oral antimalarial therapy, such as Artemisinin-Based Combination Therapy (ACT), for complete parasite clearance.

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Cefepime Tazobactam 281.25MG Injection is a powerful combination antibiotic used for the treatment of moderate to severe bacterial infections. It contains Cefepime (250MG), a fourth-generation cephalosporin, and Tazobactam (31.25MG), a β-lactamase inhibitor, which enhances the antibacterial activity by preventing resistance.

This combination is highly effective against gram-positive and gram-negative bacteria, including multi-drug resistant (MDR) strains, making it a preferred choice for pneumonia, septicemia, urinary tract infections (UTIs), intra-abdominal infections, and skin infections in hospital settings.

Composition & Mechanism of Action

🔹 Active Ingredients:
✔ Cefepime 250MG – A broad-spectrum cephalosporin that works by inhibiting bacterial cell wall synthesis, leading to bacterial destruction.
✔ Tazobactam 31.25MG – A β-lactamase inhibitor that prevents bacterial resistance, enhancing the effectiveness of Cefepime.

📌 Mechanism of Action:
✔ Prevents bacterial cell wall formation, leading to bacterial death.
✔ Effective against a wide range of bacteria, including drug-resistant strains.
✔ Inhibits β-lactamase enzymes, preventing bacterial resistance.
✔ Ideal for serious bacterial infections requiring hospital treatment.

✅ Effective against gram-positive and gram-negative bacteria
✅ Combats antibiotic resistance
✅ Rapid onset of action

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Ondansetron 4mg is a highly effective anti-nausea medication designed to prevent and treat nausea and vomiting caused by chemotherapy, radiation therapy, surgery, and gastrointestinal conditions. It belongs to the class of 5-HT3 receptor antagonists, which work by blocking serotonin, a chemical responsible for triggering nausea. Ondansetron 4mg provides fast relief, helping patients feel better and resume daily activities without discomfort.

Composition & Mechanism of Action

🔹 Ondansetron (4mg) – A Selective 5-HT3 Receptor Antagonist
✔ Blocks serotonin receptors in the brain and gut, preventing nausea and vomiting.
✔ Works quickly and effectively, making it a preferred choice for medical professionals.
✔ Can be used in multiple conditions, including chemotherapy and post-surgical recovery.

✅ Prevents Chemotherapy & Radiation-Induced Nausea – Helps cancer patients tolerate treatment better.
✅ Reduces Post-Surgical Nausea – Used in hospitals to prevent vomiting after anesthesia.
✅ Treats Gastrointestinal Disorders – Effective for food poisoning, stomach flu, and gastritis.
✅ Manages Motion Sickness & Pregnancy-Related Nausea – Provides relief from travel sickness and morning sickness.

Indications & Uses

Ondansetron 4mg is used for the following conditions:

✔ Cancer Treatment Support: Controls nausea caused by chemotherapy and radiation therapy.
✔ Post-Surgical Recovery: Prevents vomiting after surgeries involving anesthesia.
✔ Gastrointestinal Disorders: Used for vomiting caused by food poisoning, stomach flu, or infections.
✔ Pregnancy-Related Nausea: Helps with morning sickness (under medical supervision).
✔ Motion Sickness & Travel Nausea: Provides relief for those prone to vomiting while traveling.

Dosage & Administration

📌 Route of Administration: Oral tablets, IV injection, or IM injection
📌 Recommended Dose:

• Adults: 4mg every 6-8 hours as needed

• Children: Dose adjusted based on weight and condition

• Maximum Dose: 16mg per day unless prescribed otherwise

⚠ Must be taken under medical supervision for the best results.

Side Effects & Precautions

⚠ Common Side Effects: Mild headache, dizziness, constipation, or fatigue.
⚠ Serious Reactions: Rare cases of irregular heartbeat (QT prolongation), allergic reactions, or serotonin syndrome.
⚠ Contraindications: Not suitable for patients with liver disease or heart rhythm disorders.
⚠ Drug Interactions: Use with caution when combined with antidepressants, antibiotics, or heart medications.
⚠ Pregnancy & Lactation: Generally safe but should only be used under medical guidance.

Why Choose Ondansetron 4mg?

✔ Proven Effectiveness in Preventing Nausea & Vomiting
✔ Fast-Acting with Long-Lasting Relief
✔ Essential for Cancer Patients Undergoing Chemotherapy
✔ Safe for Post-Surgical & Gastrointestinal Use
✔ Minimal Side Effects and Well-Tolerated