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Claforan is a third-generation cephalosporin antibiotic containing cefotaxime sodium. It is used to treat a wide range of bacterial infections, including those resistant to first-line antibiotics. It works by inhibiting bacterial cell wall synthesis, leading to bacterial death. Supplied as a powder for solution in a 0.5 g vial, to be reconstituted with diluent before injection.
Active Ingredient: Cefotaxime sodium equivalent to 0.5 g cefotaxime
Excipients: None (sterile powder for reconstitution with sterile water or compatible diluent)
Antibiotic
Third-generation cephalosporin
Sterile powder in 1 vial (0.5 g)
To be reconstituted with 2 mL sterile water for intramuscular (IM) or intravenous (IV) injection
Claforan is indicated for treatment of infections caused by susceptible organisms, including:
Respiratory tract infections (pneumonia, bronchitis)
Urinary tract infections
Skin and soft tissue infections
Septicemia (bloodstream infections)
Bone and joint infections
Meningitis
Intra-abdominal infections (e.g., peritonitis)
Gynecological infections
Prophylaxis in surgical procedures
Adults: Typically 1–2 g every 8–12 hours IV or IM, depending on infection severity.
Severe infections: Up to 12 g/day in divided doses.
Children: 50–100 mg/kg/day divided every 6–12 hours.
Neonates: Adjusted lower dosing based on age/weight.
Dose must be tailored by physician based on severity, renal function, and organism sensitivity.
Symptoms: Neurological disturbances including seizures, encephalopathy, and risk of renal impairment.
Management: Symptomatic and supportive treatment. Hemodialysis may help remove cefotaxime.
Administer as soon as remembered.
If next dose is near, skip missed dose. Do not double dose.
Reconstitute powder in the vial with sterile water (usually 2 mL for IM or 10 mL for IV slow injection).
Ensure solution is clear, free of particles.
Administer as intravenous injection/infusion or intramuscular injection as directed.
Follow strict aseptic precautions.
Hypersensitivity to cefotaxime, other cephalosporins, or beta-lactam antibiotics (e.g., penicillins).
Previous severe allergic reactions (e.g., anaphylaxis) to beta-lactams.
Common:
Injection site pain, redness, swelling
Diarrhea, nausea, vomiting
Skin rash
Serious (rare):
Allergic reactions including anaphylaxis
Clostridium difficile-associated diarrhea
Hepatic dysfunction (elevated liver enzymes)
Blood disorders (leukopenia, thrombocytopenia)
Seizures (with very high doses or renal impairment)
Use cautiously in patients with history of beta-lactam allergy.
Adjust dose in renal or hepatic impairment.
Monitor complete blood count and liver/kidney function with prolonged therapy.
Risk of superinfection with prolonged use.
Pregnant and lactating women: use only if clearly needed and prescribed by physician.
Aminoglycosides & loop diuretics: ↑ risk of nephrotoxicity.
Warfarin & anticoagulants: may enhance anticoagulant effect.
Other antibiotics: avoid unnecessary combination unless indicated.
Alcohol: may cause disulfiram-like reaction (rare).
Store below 25°C, protected from light.
Use immediately after reconstitution or within manufacturer’s recommended time frame.
Discard unused reconstituted solution safely.
Follow hospital/clinic biomedical disposal regulations.
Prescription-only medicine
Must be used under medical supervision
Always complete the full course prescribed, even if symptoms improve early.
Do not self-inject; only a trained healthcare provider should administer.
Report any severe diarrhea, rash, or breathing difficulty immediately.
Inform your doctor about any kidney, liver, or seizure history before use.
Drink plenty of fluids during antibiotic therapy.
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