Cefozopran Injection powder for solution


Product Details
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Name Of Product(Genric Name) :

Cefozopran Injection powder for solution

Dosage :

500mg/1g

Product Description :

CEFOZOPRAN INJECTION
Sterile Powder for Solution for Intravenous Administration

1. COMPOSITION
Each vial contains:
• Cefozopran Hydrochloride, equivalent to Cefozopran, in the labelled strength.
• Excipients: As applicable.

2. PHARMACEUTICAL FORM
Sterile, white to off-white powder for solution for intravenous administration.

3. THERAPEUTIC CLASS
Fourth-Generation Cephalosporin Antibiotic.

4. INDICATIONS
Cefozopran Injection is indicated for the treatment of susceptible bacterial infections, including:
• Respiratory tract infections.
• Urinary tract infections.
• Intra-abdominal infections.
• Skin and soft-tissue infections.
• Bone and joint infections.
• Biliary tract infections.
• Septicemia and other serious bacterial infections.
Treatment should be guided by the susceptibility of the causative organism and applicable antimicrobial guidelines.

5. CONTRAINDICATIONS
• Hypersensitivity to cefozopran, cephalosporins, or any component of the formulation.
• History of severe immediate hypersensitivity reactions to beta-lactam antibiotics.

6. DRUG INTERACTIONS
• Concomitant nephrotoxic medicines may increase the risk of renal toxicity.
• Probenecid may affect renal elimination of cefozopran.
• Anticoagulants may require appropriate monitoring.
• Other medicines affecting renal function should be used with caution.
The treating physician should review all concomitant medications before administration.

7. ADMINISTRATION
For intravenous administration after reconstitution with a compatible diluent under aseptic conditions. Administer according to the approved product information and institutional protocol.

8. STORAGE
Store according to the storage conditions stated on the approved product label. Protect from excessive heat, moisture and light. After reconstitution, use within the period specified in the approved product information. Do not use if the reconstituted solution shows visible particles, precipitation or unexpected discoloration.