Composition & Specifications
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Why we use Imipenem Cilastatin Injection I.P. - Vorilin-1000?
\nVorilin-1000 is an Imipenem Cilastatin Injection I.P., a highly effective carbapenem antibiotic combination used for treating severe and life-threatening bacterial infections. It provides broad-spectrum coverage against gram-positive, gram-negative, and anaerobic bacteria, including many resistant strains. This makes it a preferred choice in hospitals and intensive care units. \n
\nImipenem is a potent carbapenem antibiotic that works by inhibiting bacterial cell wall synthesis, leading to rapid bacterial death. However, Imipenem alone can be broken down by renal enzymes. Cilastatin is added to prevent this breakdown, increasing the stability and effectiveness of Imipenem in the body. Together, they ensure enhanced antibacterial activity and improved therapeutic outcomes. \n
Indications of Vorilin-1000 Injection
\nVorilin-1000 is indicated for: \n
- Complicated intra-abdominal infections
- Severe respiratory tract infections
- Urinary tract infections (UTIs)
- Skin and soft tissue infections
- Bone and joint infections
- Septicemia (bloodstream infections)
- Hospital-acquired infections
\nIts strong antimicrobial coverage makes it suitable for multidrug-resistant bacterial infections. \n
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- Broad-spectrum antibacterial coverage
- Effective against resistant organisms
- Rapid bactericidal action
- Suitable for critical and ICU patients
- Reliable hospital-grade antibiotic
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Dosage & Safety Information
\nVorilin-1000 is administered intravenously under strict medical supervision. The dosage depends on the severity of the infection and patient condition. Completing the full course of therapy is essential to prevent resistance and ensure optimal recovery. \n \nPatients with kidney disorders or a history of beta-lactam allergy should inform their healthcare provider before treatment. Proper monitoring ensures safe and effective use. \n \nVorilin-1000 offers powerful and dependable treatment for serious bacterial infections requiring advanced antibiotic therapy.
📋 Certificate of AnalysisBatch-specific CoA from NABL-accredited lab available for every product.
🏅 GMP Schedule MManufactured under Drugs & Cosmetics Act GMP Schedule M standards.
🔬 Third-Party TestedEvery batch independently tested by NABL-accredited laboratory before dispatch.
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Prescribing & Administration Information
⚠️ For Healthcare Professionals & Franchise Partners Only: This product is sold through licensed PCD franchise partners and authorised stockists. Prescribing, dosage, and administration information is available in the product literature and Patient Information Leaflet (PIL) supplied with each batch.
Dosage & Administration
As directed by the prescribing physician. Dosage varies by indication, patient age, and clinical condition. Full prescribing information included with product.
Storage Conditions
Store in a cool, dry place below 25°C, away from direct sunlight and moisture. Keep out of reach of children. Do not use after expiry date printed on the pack.
Available Documentation
📄Product Information Leaflet (PIL) — included with every batch
🔬NABL-accredited Certificate of Analysis (CoA) — available on request per batch
📋Drug License compliance documents — provided with franchise agreement
🏅WHO-GMP manufacturing certificate — available for regulatory submission
