Indications |
Intravenous Urinary tract infections Adult: 0.5-1 g every 12 hr for 7-10 days. May be given via direct inj over 5 minutes or infuse over 30 minutes. Child: 2 mth - 16 yr: ≤40 kg: 50 mg/kg every 12 hr for 7-10 days. May be given via direct inj over 5 minutes or infuse over 30 minutes. Dose may also be given via IM inj for mild-moderate infections; for IM inj, it should be given via deep inj into large muscle mass. Renal impairment: Haemodialysis: 1 g on the 1st day of treatment, followed by 500 mg every 24 hr; dose should be given after haemodialysis on dialysis days and preferably at the same time each day. CAPD: Normal recommended doses every 48 hr.
Intravenous Empiric therapy for febrile neutropenic patients Adult: 2 g every 8 hr for 7 days or until resolution of neutrpenia. For patients who remain neutropenic for >7 days despite fever resolution, the need for continued anti-microbial treatment should be reviewed. May be given via direct inj over 5 minutes or infuse over 30 minutes. Child: 2 mth - 16 yr: ≤40 kg: 50 mg/kg every 8 hr for 7 days or until neutropenia resolves. May be given via direct inj over 5 minutes or infuse over 30 minutes. Renal impairment: Haemodialysis: 1 g every 24 hr, dose should be given after haemodialysis on dialysis days and preferably at the same time each day. CAPD: Normal recommended doses every 48 hr.
Intravenous Moderate to severe pneumonia Adult: 1-2 g every 12 hr for 10 days. May be given via direct inj over 5 minutes or infuse over 30 minutes. Child: 2 mth - 16 yr: ≤40 kg: 50 mg/kg every 12 hr for 10 days. May be given via direct inj over 5 minutes or infuse over 30 minutes. Renal impairment: Haemodialysis: 1 g on the 1st day of treatment, followed by 500 mg every 24 hr; dose should be given after haemodialysis on dialysis days and preferably at the same time each day. CAPD: Normal recommended doses every 48 hr.
Intravenous Complicated intra-abdominal infections Adult: 2 g every 12 hr for 7-10 days. Usually used in combination with metronidazole. May be given via direct inj over 5 minutes or infuse over 30 minutes. Renal impairment: Haemodialysis: 1 g on the 1st day of treatment, followed by 500 mg every 24 hr; dose should be given after haemodialysis on dialysis days and preferably at the same time each day. CAPD: Normal recommended doses every 48 hr.
Intravenous Uncomplicated skin and skin structure infections Adult: 2 g every 12 hr for 10 days. May be given via direct inj over 5 minutes or infuse over 30 minutes. Child: 2 mth - 16 yr: ≤40 kg: 50 mg/kg every 12 hr for 10 days. May be given via direct inj over 5 minutes or infuse over 30 minutes. Renal impairment: Haemodialysis: 1 g on the 1st day of treatment, followed by 500 mg every 24 hr; dose should be given after haemodialysis on dialysis days and preferably at the same time each day. CAPD: Normal recommended doses every 48 hr.
Incompatibility: Y-site admin: Acyclovir, amphotericin B, amphotericin B cholesteryl sulfate complex, chlordiazepoxide, chlorpromazine, cimetidine, famotidine, ciprofloxacin, filgrastim, floxuridine, ganciclovir, haloperidol, hydroxyzine, idarubicin, ifosfamide, magnesium sulfate, mannitol, mechlorethamine, meperidine, metoclopramide, mitomycin, mitoxantrone, morphine, nalbuphine, ofloxacin, ondansetron, plicamycin, prochlorperazine edisylate, promethazine, streptozocin, vancomycin, vinblastine, vincristine, cisplatin, dacarbazine, daunorubicin, diazepam, diphenhydramine, dobutamine, dopamine, doxorubicin, droperidol, enalaprilat, etoposide, etoposide phosphate. Admixture incompatibility: Metronidazole, vancomycin, gentamicin, tobramycin, netilmicin sulfate, aminophylline or solutions of ampicillin at concentrations >40 mg/ml. |
||||||||||||||||||||||||||||||||||||||||
Contraindications |
Hypersensitivity to cefepime or other cephalosporins. | ||||||||||||||||||||||||||||||||||||||||
Warnings / Precautions |
Renal impairment; history of penicillin or cephalosporin allergy; lactation, pregnancy. Caution when used in patients with history of GI diseases, especially colitis. May decrease prothrombin activity; monitor prothrombin time in patients with poor nutritional state, renal or hepatic impairment and those on prolonged treatment. Prolonged treatment may result in overgrowth of nonsusceptible organisms, resulting in superinfection. Consider the possibility of Clostridium difficile associated diarrhoea in patients who present with diarrhoea after treatment. Caution when used in patients with a history of seizures. | ||||||||||||||||||||||||||||||||||||||||
Adverse Reactions |
Positive Coombs' test without haemolysis; rash, pruritus; diarrhoea, nausea, vomiting; fever, headache; pain and erythema at inj site; agranulocytosis; anaphylactic shock; leucopenia; neutropenia; thrombocytopenia. | ||||||||||||||||||||||||||||||||||||||||
Overdose Reactions |
Symptoms include encephalopathy, myoclonus, seizures and neuromuscular excitability. Careful observation and supportive treatment are recommended. In the presence of renal insufficiency, haemodialysis may be used to remove cefepime from the body. | ||||||||||||||||||||||||||||||||||||||||
Drug Interactions |
Increased effect with high-dose probenecid; increased nephrotoxic potential with aminoglycosides. See Below for More cefepime Drug Interactions |
||||||||||||||||||||||||||||||||||||||||
Mechanism of Actions |
Cefepime is a 4th generation cephalosporin which inhibits the final transpeptidation step of peptidoglycan synthesis in bacterial cell wall by binding to one or more of the penicillin-binding proteins (PBPs). Absorption: IM admin: Rapid and almost complete absorption. Distribution: 16-19% bound to plasma proteins. Volume of distribution: 14-20 L; crosses the blood brain barrier. Penetrates into inflammatory fluid at concentrations of about 80% of serum levels. Metabolism: Minimally hepatic. Excretion: Plasma half-life: 2 hr. Excreted in urine with 85% as unchanged drug. |
||||||||||||||||||||||||||||||||||||||||
Storage Conditions |
Intravenous: In dry state: Store at 2-25°C and protected from light. After reconstitution: Cefepime solution is stable for 24 hr at controlled room temperature (2-25°C) and for 7 days under refridgeration (2-8°C). | ||||||||||||||||||||||||||||||||||||||||
ATC Classification |
J01DE01 - cefepime ; Belongs to the class of fourth generation cephalosporins. Used in the systemic treatment of infections. | ||||||||||||||||||||||||||||||||||||||||
Storage |
Intravenous: In dry state: Store at 2-25°C and protected from light. After reconstitution: Cefepime solution is stable for 24 hr at controlled room temperature (2-25°C) and for 7 days under refridgeration (2-8°C). | ||||||||||||||||||||||||||||||||||||||||
Available As |
|
Cefepime
Post Review about Cefepime Click here to cancel reply.
Cefepime Containing Brands
Cefepime is used in following diseases
Drug - Drug Interactions of Cefepime
Latest News
- FDA approves Ruconest for treatment of hereditary angioedema
- FDA recommend against aspirin to prevent First Heart Attacks
- FDA approves Pomalyst (pomalidomide) for advanced multiple myeloma
- FDA approves three new drug treatments for type 2 diabetes
- Long-term consequences of vaginal delivery on the pelvic floor
No comments yet.