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ANTIINFECTIVES FOR SYSTEMIC USE › ANTIBACTERIALS FOR SYSTEMIC USE › OTHER BETA-LACTAM ANTIBACTERIALS › Second-generation cephalosporins
cefamandole
J01DC03
Forms & Strengths
- Injectable powder for reconstitution: 1 g, 2 g, 10 g vials
Adult Dosing
- General infections: 500 mg to 1 g every 4 to 8 hours intramuscularly or intravenously
- Severe infections: 1 g to 2 g every 4 to 6 hours
- Surgical prophylaxis: 1 to 2 g IV 30-60 minutes before surgery, then 1 to 2 g every 6 hours for up to 24-48 hours
Pediatric Dosing
- Neonates (over 1 week) and infants/children: 50 to 100 mg/kg/day divided into equally spaced doses every 4 to 8 hours
- Severe infections: Up to 150 mg/kg/day (not to exceed maximum adult doses)
Indications
- Treatment of respiratory tract infections caused by susceptible organisms
- Urinary tract infections
- Peritonitis, septicemia, skin and skin structure infections, bone and joint infections
- Perioperative surgical prophylaxis
Mechanism of Action
- Second-generation cephalosporin beta-lactam antibiotic
- Inhibits bacterial cell wall synthesis by binding to one or more penicillin-binding proteins (PBPs)
- Bactericidal activity against a broad spectrum of gram-positive and gram-negative bacteria
Contraindications
- Hypersensitivity to cefamandole, other cephalosporins, or penicillin class antibiotics
- History of cephalosporin-associated jaundice or hepatic dysfunction
Adverse Reactions
- Hypersensitivity reactions including anaphylaxis, urticaria, rash
- Hematologic effects: hypoprothrombinemia, bleeding diathesis, positive direct Coombs' test, neutropenia
- Gastrointestinal: pseudomembranous colitis, diarrhea, nausea, vomiting
- Local reactions: thrombophlebitis at injection site, pain and induration with IM administration
- Transient elevations in liver function tests and BUN/creatinine
Drug Interactions
- Disulfiram-like reaction (flushing, nausea, vomiting, tachycardia) when co-administered with ethanol
- Increased risk of bleeding when combined with anticoagulants, thrombolytic agents, or long-term NSAIDs due to N-methylthiotetrazole side chain causing hypoprothrombinemia
- Antagonism of bactericidal activity possible with concurrent bacteriostatic antibiotics (e.g., tetracyclines, erythromycin)
- Potential nephrotoxicity enhancement when used concomitantly with aminoglycosides or potent loop diuretics
Curated Content: Needs Vetting Before Put to Clinical Use