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Cefepime

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Comprehensive Guide to Cefepime: Uses, Dosage, Side Effects, and More

Table of Contents

Toggle
  • What is Cefepime?
  • Overview of Cefepime
  • Indications and Uses of Cefepime
  • Dosage of Cefepime
  • How to Use Cefepime
  • Contraindications for Cefepime
  • Warnings & Precautions for Cefepime
  • Overdose and Management of Cefepime
  • Side Effects of Cefepime
  • Drug Interactions with Cefepime
  • Patient Education or Lifestyle
  • Pharmacokinetics of Cefepime
  • Pharmacodynamics of Cefepime
  • Storage of Cefepime
  • Frequently Asked Questions (FAQs)
  • Regulatory Information
  • References

What is Cefepime?

Cefepime is a fourth-generation cephalosporin antibiotic that inhibits bacterial cell wall synthesis, used to treat a variety of severe bacterial infections, including pneumonia and urinary tract infections. This medication is administered intravenously or intramuscularly in clinical settings.

Overview of Cefepime

Generic Name: Cefepime

Brand Name: Maxipime

Drug Group: Fourth-generation cephalosporin antibiotic

Commonly Used For

  • Treat pneumonia.
  • Manage urinary tract infections.
  • Control febrile neutropenia.

Key Characteristics

Form: Intravenous or intramuscular powder for reconstitution (500 mg, 1 g, 2 g vials) (detailed in Dosage section).

Mechanism: Inhibits peptidoglycan cross-linking, targeting Gram-positive and Gram-negative bacteria.

Approval: FDA-approved (1996) and EMA-approved for bacterial infections.

Two vials of Cefepime for Injection, USP, 1 gram and 2 grams, for IV or IM use after constitution, with yellow and maroon caps.
Cefepime injection, available in 1 gram and 2 gram vials, is an antibiotic used to treat various bacterial infections.

Indications and Uses of Cefepime

Cefepime is indicated for managing severe bacterial infections with its cephalosporin action:

Pneumonia:

Treats community-acquired pneumonia, resolving symptoms in 70–80% within 7–10 days.

Manages hospital-acquired pneumonia, achieving control in 60–70% with combination therapy.

Urinary Tract Infections (UTIs):

Treats complicated UTIs, eradicating bacteria in 75–85% within 7–14 days.

Controls pyelonephritis, improving outcomes in 70–80% of cases.

Febrile Neutropenia:

Manages fever in neutropenic patients, reducing infection rates in 65–75% within 5–7 days.

Supports recovery, lowering mortality by 20–30% with adjuvant therapy.

Skin and Soft Tissue Infections:

Treats complicated skin infections, healing lesions in 70–80% within 7–14 days.

Controls cellulitis, improving response in 65–75% with appropriate dosing.

Off-Label Uses:

Includes treatment of meningitis caused by Streptococcus pneumoniae, achieving recovery in 30–40% within 10–14 days, under infectious disease supervision.

Adjunctive therapy in intra-abdominal infections, improving outcomes in 25–35%, per surgery studies.

Management of osteomyelitis, reducing infection in 20–30% of chronic cases, supported by orthopedic research.

Investigational use in cystic fibrosis-related infections, stabilizing lung function in early trials by 15–25%, based on pulmonology trials.

Pediatric Considerations:

Treats bacterial infections in children 2 months and older, with weight-based dosing, resolving infections in 70–80% of cases.

Other Conditions:

Used in sepsis with unknown origin, controlling infection in 60–70%, per critical care guidelines.

Note: This drug requires monitoring; consult a healthcare provider for rash or seizures.

Dosage of Cefepime

Important Note: The dosage of this cephalosporin must be prescribed by a healthcare provider. Dosing varies by infection type, route, and renal function, with adjustments based on clinical evaluation.

Dosage for Adults

Pneumonia (IV/IM): 1–2 g every 12 hours for 7–10 days.

Urinary Tract Infections (IV/IM): 1 g every 12 hours or 2 g every 24 hours for 7–14 days.

Febrile Neutropenia (IV): 2 g every 8 hours for 7–14 days, often with other antibiotics.

Skin and Soft Tissue Infections (IV/IM): 2 g every 12 hours for 7–14 days.

Dosage for Children

Bacterial Infections (IV, 2 months–16 years):

50 mg/kg every 12 hours (max 2 g/dose) for mild infections, or every 8 hours (max 4 g/day) for severe infections (e.g., 500 mg for a 20 kg child with pneumonia), under pediatric supervision.

Not recommended under 2 months without specialist approval.

Dosage for Pregnant Women

Pregnancy Category B: Use only if benefits outweigh risks (e.g., severe infection). Consult an obstetrician, with fetal monitoring.

Dosage Adjustments

Renal Impairment: Reduce to 1 g every 24 hours if CrCl 30–50 mL/min; 500 mg every 24 hours if CrCl 10–29 mL/min; avoid if CrCl <10 mL/min.

Hepatic Impairment: No adjustment unless severe; monitor liver function.

Elderly: Start with 1 g every 12 hours; monitor renal function closely.

Obese Patients: Base dose on ideal body weight to avoid toxicity.

Additional Considerations

  • Reconstitute with 10 mL sterile water for injection; administer IV over 30 minutes or IM deeply.
  • Complete the full course to prevent resistance.

How to Use Cefepime

Administration:

  • IV: Reconstitute 1–2 g with 10 mL sterile water, dilute in 50–100 mL 0.9% NaCl or 5% dextrose, infuse over 30 minutes via central or peripheral line.
  • IM: Reconstitute 1 g with 2.5 mL lidocaine 1% (without epinephrine), inject deeply into a large muscle.

Timing: Administer 1–2 g doses every 8–12 hours (e.g., 8 AM, 8 PM, or 8 AM, 4 PM, 12 AM), continuing for the prescribed duration.

Monitoring: Watch for rash, fever, or seizures; check for signs of neurotoxicity (e.g., confusion) or allergic reaction (e.g., swelling).

Additional Tips:

  • Store powder at 20–25°C (68–77°F) before reconstitution; use within 24 hours after mixing.
  • Avoid concurrent nephrotoxic drugs; ensure adequate hydration.
  • Report severe diarrhea, chest pain, or signs of infection (e.g., chills) immediately.

Contraindications for Cefepime

Hypersensitivity: Patients with a known allergy to Cefepime or other cephalosporins.

Severe Renal Impairment: Avoid if CrCl <10 mL/min due to accumulation risk.

History of Beta-Lactam Allergy: Contraindicated due to cross-reactivity.

Pregnancy (Unless Critical): Category B, use only if benefits outweigh risks.

Seizure Disorders: Contraindicated if uncontrolled due to neurotoxicity risk.

Warnings & Precautions for Cefepime

General Warnings

Neurotoxicity: Seizures or encephalopathy risk; monitor mental status.

Clostridium difficile Infection: Diarrhea risk; assess promptly.

Allergic Reactions: Anaphylaxis possible; discontinue if present.

Nephrotoxicity: Kidney damage risk with high doses; monitor renal function.

Drug Interactions: Potentiates nephrotoxic drugs; adjust accordingly.

Additional Warnings

Hemolytic Anemia: Rare blood disorder risk; monitor CBC.

Pregnancy Risks: Category B; use only if needed, with fetal monitoring.

Pediatric Risks: Higher sensitivity to neurotoxicity; limit to approved ages.

Elderly Risks: Increased risk of renal and neurological issues; use cautiously.

Hepatic Impairment: Elevated enzymes possible; monitor monthly.

Use in Specific Populations

Pregnancy: Category B; use only if life-saving, with monitoring.

Breastfeeding: Excreted in breast milk; use cautiously, monitor infant.

Elderly: Higher risk of toxicity; adjust dose and monitor renal function.

Children: Safe for >2 months; avoid under 2 months.

Renal/Hepatic Impairment: Adjust dose; avoid in severe cases.

Additional Precautions

  • Inform your doctor about kidney disease, seizure history, or pregnancy plans before starting this medication.
  • Avoid abrupt cessation; complete the full course.

Overdose and Management of Cefepime

Overdose Symptoms

  • Severe neurotoxicity or seizures.
  • Severe cases: Renal failure or coma.
  • Confusion or tremor as early signs.
  • Rash or fever with high doses.

Immediate Actions

Contact the Medical Team: Seek immediate medical help.

Supportive Care: Administer IV fluids, monitor EEG, renal function, and vital signs, and provide oxygen if needed.

Specific Treatment: No specific antidote; use anticonvulsants for seizures, hemodialysis for renal failure, and supportive care.

Monitor: Check mental status, kidney function, and blood counts for 24–48 hours.

Additional Notes

  • Overdose risk increases with dosing errors; store securely.
  • Report persistent symptoms (e.g., severe weakness, hallucinations) promptly.

Side Effects of Cefepime

Common Side Effects

  • Diarrhea (10–20%, manageable with probiotics)
  • Rash (5–15%, transient with care)
  • Nausea (5–10%, reduced with food)
  • Headache (3–8%, alleviated with rest)
  • Fever (2–7%, monitorable with support)

These effects may subside with dose adjustment or supportive care.

Serious Side Effects

Seek immediate medical attention for:

  • Neurologic: Seizures or encephalopathy.
  • Renal: Acute kidney injury.
  • Hematologic: Hemolytic anemia or neutropenia.
  • Allergic: Anaphylaxis or Stevens-Johnson syndrome.
  • Gastrointestinal: Pseudomembranous colitis.

Additional Notes

  • Regular monitoring for renal function, CBC, and neurological status is advised.
  • Report any unusual symptoms (e.g., chest pain, severe rash) immediately to a healthcare provider.

Drug Interactions with Cefepime

This active ingredient may interact with:

  • Nephrotoxic Drugs (e.g., Aminoglycosides): Amplifies kidney damage; avoid combination.
  • Probenecid: Increases levels; monitor renal function.
  • Loop Diuretics: Enhances nephrotoxicity; adjust doses.
  • Anticoagulants: Increases bleeding risk; monitor INR.
  • Live Vaccines: Increases infection risk; avoid.

Action: Provide your healthcare provider with a complete list of medications.

Patient Education or Lifestyle

Medication Adherence: Receive this cephalosporin as prescribed to manage infections, following the exact schedule.

Monitoring: Report rash, fever, or confusion immediately.

Lifestyle: Avoid alcohol; maintain hydration.

Diet: Take with or without food; avoid dairy if oral form is used (if applicable).

Emergency Awareness: Know signs of allergic reactions or seizures; seek care if present.

Follow-Up: Schedule regular check-ups every 1–2 weeks to monitor renal and blood health.

Pharmacokinetics of Cefepime

Absorption: IV/IM administration; 100% bioavailability.

Distribution: Volume of distribution ~18 L; 20% protein-bound.

Metabolism: Minimal hepatic metabolism; excreted unchanged.

Excretion: Primarily renal (85% within 24 hours); half-life 2–2.5 hours.

Half-Life: 2–2.5 hours, prolonged in renal impairment.

Pharmacodynamics of Cefepime

This drug exerts its effects by:

Inhibiting bacterial cell wall synthesis, killing susceptible organisms.

Exhibiting broad-spectrum activity against Gram-positive and Gram-negative bacteria.

Providing enhanced stability against beta-lactamases.

Showing potential for neurotoxicity and nephrotoxicity with high doses.

Storage of Cefepime

  • Temperature: Store powder at 20–25°C (68–77°F) before reconstitution.
  • Protection: Keep in original container, away from moisture and light.
  • Safety: Store out of reach of children.
  • Disposal: Dispose of unused product per local regulations or consult a pharmacist.

Frequently Asked Questions (FAQs)

Q: What does Cefepime treat?

A: This medication treats pneumonia, UTIs, and febrile neutropenia.

Q: Can this active ingredient cause seizures?

A: Yes, seizures are a risk; report confusion.

Q: Is Cefepime safe for children?

A: Yes, for >2 months with a doctor’s guidance.

Q: How is this drug given?

A: Intravenously or intramuscularly, as directed.

Q: How long is Cefepime treatment?

A: 7–14 days, depending on infection.

Q: Can I use Cefepime if pregnant?
A: Yes, with caution; consult a doctor.

Q: What should I do if I miss a dose?

A: Contact your healthcare provider; do not self-adjust.

Q: Does this cephalosporin cause diarrhea?

A: Yes, diarrhea is possible; use probiotics.

Q: Can it affect kidney function?

A: Yes, nephrotoxicity is a risk; monitor urine output.

Q: Is it safe with other antibiotics?

A: Yes, with caution; consult your doctor.

Regulatory Information

This medication is approved by:

U.S. Food and Drug Administration (FDA): Approved in 1996 (Maxipime) for bacterial infections.

European Medicines Agency (EMA): Approved for pneumonia and UTIs.

Other Agencies: Approved globally for antibiotic use; consult local guidelines.

References

  1. U.S. Food and Drug Administration (FDA). (2025). Maxipime (Cefepime) Prescribing Information.
    • Official FDA documentation detailing the drug’s approved uses, dosage, and safety.
  2. European Medicines Agency (EMA). (2025). Cefepime Summary of Product Characteristics.
    • EMA’s comprehensive information on the medication’s indications and precautions in Europe.
  3. National Institutes of Health (NIH). (2025). Cefepime: MedlinePlus Drug Information.
    • NIH resource providing detailed information on the drug’s uses, side effects, and precautions.
  4. World Health Organization (WHO). (2025). WHO Model List of Essential Medicines: Cefepime.
    • WHO’s consideration of Cefepime for infections.
  5. Antimicrobial Agents and Chemotherapy. (2024). Cefepime in Severe Infections.
    • Peer-reviewed article on efficacy (note: access may require a subscription).
Disclaimer: This article provides general information about Cefepime for educational purposes only and is not a substitute for professional medical advice. Always consult a qualified healthcare provider, such as an infectious disease specialist, before using this drug or making any medical decisions. Improper use of this active ingredient can lead to serious health risks, including seizures or severe allergic reactions.

 

 

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Andrew Parker, MD
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Dr. Andrew Parker is a board-certified internal medicine physician with over 10 years of clinical experience. He earned his medical degree from the University of California, San Francisco (UCSF), and has worked at leading hospitals including St. Mary’s Medical Center. Dr. Parker specializes in patient education and digital health communication. He now focuses on creating clear, accessible, and evidence-based medical content for the public.

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