Description
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.
Ingredients
Drug Class
Dosage Form
Uses / Indications
Claforan is indicated for treatment of infections caused by susceptible organisms, including:
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Respiratory tract infections (pneumonia, bronchitis)
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Urinary tract infections
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Skin and soft tissue infections
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Septicemia (bloodstream infections)
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Bone and joint infections
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Meningitis
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Intra-abdominal infections (e.g., peritonitis)
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Gynecological infections
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Prophylaxis in surgical procedures
Dosage
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Adults: Typically 1–2 g every 8–12 hours IV or IM, depending on infection severity.
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Severe infections: Up to 12 g/day in divided doses.
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Children: 50–100 mg/kg/day divided every 6–12 hours.
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Neonates: Adjusted lower dosing based on age/weight.
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Dose must be tailored by physician based on severity, renal function, and organism sensitivity.
In Case of Overdose
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Symptoms: Neurological disturbances including seizures, encephalopathy, and risk of renal impairment.
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Management: Symptomatic and supportive treatment. Hemodialysis may help remove cefotaxime.
Missed Dose
How To Use / Administration Instructions
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Reconstitute powder in the vial with sterile water (usually 2 mL for IM or 10 mL for IV slow injection).
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Ensure solution is clear, free of particles.
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Administer as intravenous injection/infusion or intramuscular injection as directed.
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Follow strict aseptic precautions.
When Not to Use / Contraindications
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Hypersensitivity to cefotaxime, other cephalosporins, or beta-lactam antibiotics (e.g., penicillins).
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Previous severe allergic reactions (e.g., anaphylaxis) to beta-lactams.
Side Effects / Adverse Reactions
Common:
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Injection site pain, redness, swelling
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Diarrhea, nausea, vomiting
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Skin rash
Serious (rare):
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Allergic reactions including anaphylaxis
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Clostridium difficile-associated diarrhea
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Hepatic dysfunction (elevated liver enzymes)
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Blood disorders (leukopenia, thrombocytopenia)
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Seizures (with very high doses or renal impairment)
Precautions & Warnings
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Use cautiously in patients with history of beta-lactam allergy.
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Adjust dose in renal or hepatic impairment.
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Monitor complete blood count and liver/kidney function with prolonged therapy.
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Risk of superinfection with prolonged use.
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Pregnant and lactating women: use only if clearly needed and prescribed by physician.
Drug Interactions
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Aminoglycosides & loop diuretics: ↑ risk of nephrotoxicity.
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Warfarin & anticoagulants: may enhance anticoagulant effect.
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Other antibiotics: avoid unnecessary combination unless indicated.
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Alcohol: may cause disulfiram-like reaction (rare).
Storage / Disposal
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Store below 25°C, protected from light.
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Use immediately after reconstitution or within manufacturer’s recommended time frame.
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Discard unused reconstituted solution safely.
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Follow hospital/clinic biomedical disposal regulations.
Control Drug / Prescription Status
Quick Tips
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Always complete the full course prescribed, even if symptoms improve early.
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Do not self-inject; only a trained healthcare provider should administer.
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Report any severe diarrhea, rash, or breathing difficulty immediately.
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Inform your doctor about any kidney, liver, or seizure history before use.
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Drink plenty of fluids during antibiotic therapy.