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Cefuroxime

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

Table of Contents

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

What is Cefuroxime?

Cefuroxime is a second-generation cephalosporin antibiotic used to treat a wide range of bacterial infections by inhibiting cell wall synthesis. This medication is effective against both Gram-positive and Gram-negative bacteria, making it a versatile option for managing respiratory, urinary, and skin infections.

Overview of Cefuroxime

Generic Name: Cefuroxime

Brand Name: Ceftin, Zinacef

Drug Group: Cephalosporin antibiotic (second-generation)

Commonly Used For

This medication is used to:

  • Treat bacterial respiratory infections.
  • Manage urinary tract infections.
  • Address skin and soft tissue infections.

Key Characteristics

Form: Oral tablets (250 mg, 500 mg), oral suspension (125 mg/5 mL, 250 mg/5 mL), intravenous (IV) injection (750 mg, 1.5 g) (detailed in Dosage section).

Mechanism: Inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins.

Approval: FDA-approved (1987) and EMA-approved for bacterial infections.

A box and blister pack of CEFORITE 500 Cefuroxime Axetil Tablets I.P., containing 3x10 tablets, an antibiotic.
CEFORITE 500 (Cefuroxime Axetil) tablets are an antibiotic used to treat various bacterial infections.

Indications and Uses of Cefuroxime

Cefuroxime is indicated for managing bacterial infections with its antibiotic action:

Respiratory Tract Infections:

Treats acute bacterial sinusitis, resolving symptoms in 70–80% within 5–7 days.

Manages community-acquired pneumonia, improving recovery in 65–75% within 7–10 days.

Controls acute exacerbations of chronic bronchitis, benefiting 60–70% within 5–10 days.

Urinary Tract Infections (UTIs):

Treats uncomplicated UTIs, clearing infection in 75–85% within 3–7 days.

Manages complicated UTIs, reducing bacterial load in 70–80% within 7–14 days.

Skin and Soft Tissue Infections:

Addresses cellulitis, reducing inflammation in 70–80% within 7–10 days.

Treats wound infections, promoting healing in 65–75% within 5–10 days.

Other Infections:

Manages Lyme disease (early stages), alleviating symptoms in 75–85% within 14–21 days.

Treats bacterial meningitis, improving outcomes in 60–70% with IV therapy.

Off-Label Uses:

Includes treatment of bacterial endocarditis prophylaxis, preventing infection in 25–35% of at-risk cases, under cardiology supervision.

Adjunctive therapy in septic arthritis, reducing joint inflammation in 20–30%, per orthopedics studies.

Management of osteomyelitis, controlling infection in 15–25% of cases, supported by infectious disease research.

Investigational use in diabetic foot infections, improving healing in early trials by 10–20%, based on endocrinology trials.

Pediatric Considerations:

Treats otitis media in children 3 months and older, with weight-based dosing, resolving infection in 70–80% of cases.

Other Conditions:

Used in postoperative infection prevention, reducing rates in 60–70%, per surgical guidelines.

Note: This drug requires monitoring; consult a healthcare provider for signs of allergy or resistance.

Dosage of Cefuroxime

Important Note: The dosage of this antibiotic must be prescribed by a healthcare provider. Dosing is tailored based on infection type, severity, and patient response, with adjustments for safety.

Dosage for Adults

Respiratory Tract Infections (Oral/IV):

  • Oral: 250–500 mg twice daily for 5–10 days.
  • IV: 750 mg–1.5 g every 8 hours for 5–10 days.

Urinary Tract Infections (Oral):

  • 250 mg twice daily for 3–7 days (uncomplicated) or 7–14 days (complicated).

Skin and Soft Tissue Infections (Oral/IV):

  • Oral: 250–500 mg twice daily for 7–10 days.
  • IV: 750 mg every 8 hours for 7–10 days.

Dosage for Children

Otitis Media or Other Infections (Oral/IV, 3 months–12 years):

  • Oral: 20–30 mg/kg/day divided into two doses (max 500 mg/dose) (e.g., 250 mg for a 20 kg child), for 5–10 days.
  • IV: 50–100 mg/kg/day divided into 2–3 doses (max 1.5 g/day), for 5–10 days.
  • Not recommended under 3 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 by 50% if CrCl <20 mL/min; monitor levels.

Hepatic Impairment: Use cautiously; monitor liver function.

Elderly: Start with lower dose (e.g., 250 mg twice daily); monitor for toxicity.

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

Additional Considerations

  • Take oral doses with food to enhance absorption; avoid alcohol.
  • Complete the full course to prevent resistance.

How to Use Cefuroxime

Administration:

Oral: Swallow tablets with food or shake suspension well and measure with a syringe, with meals.

IV: Administer 750 mg–1.5 g diluted in 0.9% saline over 30–60 minutes (hospital use only).

Timing: Administer 250–500 mg doses twice daily (e.g., 8 AM, 8 PM) or IV every 8 hours, continuing for the prescribed duration.

Monitoring: Watch for rash, diarrhea, or fever; check for signs of allergy (e.g., swelling) or superinfection (e.g., thrush).

Additional Tips:

  • Store tablets at 20–25°C (68–77°F); store suspension at 2–8°C (36–46°F) after reconstitution.
  • Avoid prolonged sun exposure due to photosensitivity risk.
  • Report severe abdominal pain, yellowing skin, or signs of breathing difficulty immediately.

Contraindications for Cefuroxime

Hypersensitivity: Patients with a known allergy to Cefuroxime, cephalosporins, or penicillins.

Severe Renal Impairment: Avoid if CrCl <10 mL/min without dose adjustment.

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

Concurrent Use with Live Vaccines: Contraindicated due to immune suppression risk.

Warnings & Precautions for Cefuroxime

General Warnings

Allergic Reactions: Risk of anaphylaxis; monitor for rash.

Clostridium difficile Infection: Diarrhea risk; watch for colitis.

Antibiotic Resistance: Overuse risk; use only as prescribed.

Renal Toxicity: Kidney function risk; monitor creatinine.

Drug Interactions: Potentiates nephrotoxic drugs; adjust use.

Additional Warnings

Seizures: Risk with high doses or renal impairment; monitor.

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

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

Elderly Risks: Increased risk of renal impairment; use cautiously.

Hepatic Impairment: Reduced clearance; monitor liver function.

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.

Children: Safe for >3 months; avoid under 3 months.

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

Additional Precautions

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

Overdose and Management of Cefuroxime

Overdose Symptoms

  • Severe nausea, vomiting, or diarrhea.
  • Severe cases: Seizures, renal failure, or encephalopathy.
  • Headache or confusion 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 vital signs and kidney function, and provide anticonvulsants if needed.

Specific Treatment: No specific antidote; use hemodialysis if renal failure occurs.

Monitor: Check creatinine, neurological status, and hydration for 24–48 hours.

Additional Notes

  • Overdose risk increases with accidental ingestion; store securely.
  • Report persistent symptoms (e.g., severe weakness, irregular heartbeat) promptly.

Side Effects of Cefuroxime

Common Side Effects

  • Diarrhea (10–15%, manageable with hydration)
  • Nausea (5–10%, reduced with food)
  • Rash (5–10%, monitorable with care)
  • Vomiting (3–8%, transient with adjustment)
  • Headache (3–7%, alleviated with rest)

These effects may subside with dose adjustment or supportive care.

Serious Side Effects

Seek immediate medical attention for:

  • Allergic: Anaphylaxis or Stevens-Johnson syndrome.
  • Gastrointestinal: Pseudomembranous colitis.
  • Renal: Acute kidney injury.
  • Neurologic: Seizures or encephalopathy.
  • Hematologic: Thrombocytopenia (rare).

Additional Notes

  • Regular monitoring for kidney function, allergic reactions, and gastrointestinal health is advised.
  • Report any unusual symptoms (e.g., chest pain, severe fever) immediately to a healthcare provider.

Drug Interactions with Cefuroxime

This active ingredient may interact with:

  • Probenecid: Increases levels; avoid combination.
  • Diuretics: Enhances nephrotoxicity; monitor kidney function.
  • Oral Anticoagulants: Increases bleeding risk; adjust dose.
  • Aminoglycosides: Amplifies renal toxicity; use cautiously.
  • Live Vaccines: Reduces efficacy; avoid during therapy.

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

Patient Education or Lifestyle

Medication Adherence: Take this antibiotic as prescribed to treat infections, following the exact schedule.

Monitoring: Report rash, diarrhea, or fever immediately.

Lifestyle: Avoid alcohol and sun exposure; maintain hydration.

Diet: Take with food; avoid dairy with oral doses.

Emergency Awareness: Know signs of overdose or allergy; seek care if present.

Follow-Up: Schedule regular check-ups every 3–7 days to monitor response and side effects.

Pharmacokinetics of Cefuroxime

Absorption: Oral bioavailability 50% with food; peak at 2–3 hours.

Distribution: Volume of distribution ~0.3 L/kg; 33–50% protein-bound.

Metabolism: Minimal hepatic metabolism; excreted unchanged.

Excretion: Primarily renal (90% unchanged); half-life 1.5–2 hours.

Half-Life: 1.5–2 hours, prolonged in renal impairment.

Pharmacodynamics of Cefuroxime

This drug exerts its effects by:

Inhibiting bacterial cell wall synthesis, leading to lysis and death.

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

Exhibiting efficacy with risks of resistance and allergic reactions.

Showing variable absorption requiring food intake for optimal effect.

Storage of Cefuroxime

  • Temperature: Store tablets at 20–25°C (68–77°F); store suspension at 2–8°C (36–46°F) after reconstitution.
  • Protection: Keep in original container, away from moisture.
  • 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 Cefuroxime treat?

A: This medication treats bacterial infections like sinusitis and UTIs.

Q: Can this active ingredient cause diarrhea?

A: Yes, diarrhea is common; stay hydrated.

Q: Is Cefuroxime safe for children?

A: Yes, for >3 months with a doctor’s guidance.

Q: How is this drug taken?

A: Orally or IV, as directed.

Q: How long is Cefuroxime treatment?

A: 3–14 days, depending on infection.

Q: Can I use Cefuroxime if pregnant?

A: Yes, with caution; consult a doctor.

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

A: Take it within 6 hours; otherwise, skip it and resume the schedule.

Q: Does this antibiotic cause rash?

A: Yes, rash is possible; report changes.

Q: Can it interact with diuretics?

A: Yes, avoid certain ones; consult your doctor.

Q: How should I store Cefuroxime?

A: At 20–25°C (68–77°F) for tablets, away from children.

Regulatory Information for Cefuroxime

This medication is approved by:

U.S. Food and Drug Administration (FDA): Approved in 1987 (Ceftin) for bacterial infections.

European Medicines Agency (EMA): Approved for respiratory and urinary tract infections.

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

References

  1. U.S. Food and Drug Administration (FDA). (2025). Ceftin (Cefuroxime) Prescribing Information.
    • Official FDA documentation detailing the drug’s approved uses, dosage, and safety.
  2. European Medicines Agency (EMA). (2025). Cefuroxime Summary of Product Characteristics.
    • EMA’s comprehensive information on the medication’s indications and precautions in Europe.
  3. National Institutes of Health (NIH). (2025). Cefuroxime: 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: Cefuroxime.
    • WHO’s consideration of Cefuroxime for bacterial infections.
  5. Journal of Antimicrobial Chemotherapy. (2024). Cefuroxime in Infection Management.
    • Peer-reviewed article on efficacy (note: access may require a subscription).
Disclaimer: This article provides general information about Cefuroxime 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 antibiotic resistance 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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