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Cipla Xylistin 1MIU

Cipla Xylistin 1 MIU Injection contains streptokinase, a thrombolytic (clot-dissolving) medicine used to treat acute heart attacks, pulmonary embolism, and deep vein thrombosis. It works by breaking down blood clots in blood vessels, restoring normal blood flow. The injection is administered intravenously under strict medical supervision, usually in a hospital setting. Xylistin helps minimize tissue damage caused by blocked blood vessels. It must be used with caution due to the risk of serious bleeding and other complications.

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Description

Product Description

Xylistin 1 MIU Injection contains Colistimethate Sodium (1 Million International Units), a polymyxin-class antibiotic used for treating severe bacterial infections caused by multidrug-resistant Gram-negative organisms, such as Pseudomonas aeruginosa, Acinetobacter baumannii, and Klebsiella pneumoniae.

It is indicated for hospital-acquired pneumonia, bloodstream infections, urinary tract infections, intra-abdominal infections, and meningitis caused by susceptible bacteria.

Xylistin is available as a sterile powder for injection, which must be reconstituted with an appropriate diluent before intravenous or intramuscular administration. The product is intended for use under the supervision of a qualified healthcare professional.

Store below 25°C, protect from light and moisture, and use the reconstituted solution immediately or as directed on the label.


Product Specification

Parameter Specification
Brand Name Xylistin 1 MIU Injection
Generic Name Colistimethate Sodium Injection IP
Strength 1 Million International Units (1 MIU)
Composition Each vial contains: Colistimethate Sodium IP equivalent to 1 Million IU of Colistin Base Activity
Dosage Form Sterile Powder for Injection
Route of Administration Intravenous (IV) or Intramuscular (IM) use
Indications / Uses Treatment of serious infections caused by multidrug-resistant Gram-negative bacteria (e.g., Pseudomonas aeruginosa, Acinetobacter, Klebsiella spp.)
Mechanism of Action Colistimethate Sodium interacts with bacterial cell membranes, increasing permeability and leading to cell death
Packaging Type Glass vial (with sterile diluent if applicable)
Pack Size Single vial (1 MIU)
Manufacturer / Marketer Cipla Ltd.
Shelf Life 24 Months (Typical)
Storage Conditions Store below 25°C. Protect from moisture and light. Reconstituted solution should be used immediately or as per manufacturer’s instruction
Prescription Type Schedule H1 Drug – To be sold by retail on the prescription of a registered medical practitioner only
Common Side Effects Pain at injection site, tingling sensation, dizziness, mild kidney effects
Serious Side Effects Nephrotoxicity, neurotoxicity, muscle weakness (rare, dose-related)
Precautions Use with caution in patients with renal impairment or neuromuscular disorders. Dose adjustment may be required
Drug Interactions May increase toxicity when used with other nephrotoxic or neurotoxic agents (e.g., aminoglycosides, vancomycin)
Reconstitution Reconstitute with sterile water for injection or 0.9% sodium chloride solution before use
Mode of Administration Administer slowly by IV infusion or deep IM injection under medical supervision
Storage & Handling Keep out of reach of children. Handle aseptically during preparation and administration

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