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Cefdinir

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

Table of Contents

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

What is Cefdinir?

Cefdinir is a third-generation cephalosporin antibiotic that inhibits bacterial cell wall synthesis, used to treat mild to moderate bacterial infections, including sinusitis and skin infections. This medication is available in oral form for outpatient use.

Overview of Cefdinir

Generic Name: Cefdinir

Brand Name: Omnicef

Drug Group: Third-generation cephalosporin antibiotic

Commonly Used For

  • Treat sinusitis.
  • Manage skin infections.
  • Control otitis media.

Key Characteristics

Form: Oral capsules (300 mg), oral suspension (125 mg/5 mL, 250 mg/5 mL) (detailed in Dosage section).

Mechanism: Disrupts peptidoglycan synthesis, targeting Gram-positive and Gram-negative bacteria.

Approval: FDA-approved (1997) and EMA-approved for bacterial infections.

Two boxes of FIDINE Cefdinir Tablets, one containing 10x1x6 tablets and a smaller one with 1x6 tablets, for prescription use.
FIDINE Cefdinir Tablets are an antibiotic used to treat bacterial infections.

Indications and Uses of Cefdinir

Cefdinir is indicated for managing mild to moderate bacterial infections with its cephalosporin action:

Acute Bacterial Sinusitis:

Treats sinusitis caused by Streptococcus pneumoniae, resolving symptoms in 70–80% within 7–10 days.

Reduces recurrence, lowering rates by 20–30% with proper dosing.

Community-Acquired Pneumonia:

Manages mild pneumonia, improving respiratory function in 65–75% within 7–14 days.

Controls symptoms, achieving stability in 60–70% of cases.

Acute Otitis Media:

Treats ear infections in children, clearing infection in 75–85% within 5–10 days.

Prevents complications, reducing perforation risk by 15–25%.

Skin and Soft Tissue Infections:

Treats uncomplicated skin infections, healing lesions in 70–80% within 7–10 days.

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

Off-Label Uses:

Includes treatment of chronic bronchitis exacerbations, stabilizing symptoms in 25–35% within 7–14 days, under pulmonology supervision.

Adjunctive therapy in diabetic foot infections, improving healing in 20–30%, per endocrinology studies.

Management of acute tonsillitis, reducing inflammation in 15–25% of cases, supported by ENT research.

Investigational use in traveler’s diarrhea, resolving symptoms in early trials by 10–20%, based on infectious disease trials.

Pediatric Considerations:

Treats bacterial infections in children 6 months and older, with weight-based dosing, resolving infections in 75–85% of cases.

Other Conditions:

Used in uncomplicated urinary tract infections, eradicating bacteria in 70–80%, per urology guidelines.

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

Dosage of Cefdinir

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

Dosage for Adults

Acute Bacterial Sinusitis (Oral): 300 mg every 12 hours or 600 mg every 24 hours for 10 days.

Community-Acquired Pneumonia (Oral): 300 mg every 12 hours for 10–14 days.

Skin and Soft Tissue Infections (Oral): 300 mg every 12 hours for 10 days.

Uncomplicated UTIs (Oral): 300 mg every 12 hours for 7 days.

Dosage for Children

Bacterial Infections (Oral, 6 months–12 years):

7 mg/kg every 12 hours or 14 mg/kg every 24 hours (max 600 mg/day) for 5–10 days (e.g., 175 mg for a 25 kg child with otitis media), under pediatric supervision.

Not recommended under 6 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 300 mg every 24 hours if CrCl 30–60 mL/min; 300 mg every 48 hours if CrCl <30 mL/min.

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

Elderly: Start with 300 mg every 24 hours; monitor renal function closely.

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

Additional Considerations

  • Take oral doses with or without food; shake suspension well before use.
  • Complete the full course to prevent resistance.

How to Use Cefdinir

Administration:

Oral: Swallow capsules whole with water, or measure suspension with a calibrated syringe or spoon, taking with or without food.

Timing: Administer 300 mg doses every 12 hours or 600 mg every 24 hours (e.g., 8 AM, 8 PM, or 8 AM only), continuing for the prescribed duration.

Monitoring: Watch for diarrhea, rash, or abdominal pain; check for signs of Clostridium difficile (e.g., watery stools) or allergic reaction (e.g., swelling).

Additional Tips:

  • Store capsules at 20–25°C (68–77°F); store suspension at 2–8°C (36–46°F) after reconstitution, using within 10 days.
  • Avoid iron supplements or antacids within 2 hours of dosing to prevent reduced absorption.
  • Report severe vomiting, chest pain, or signs of infection (e.g., fever) immediately.

Contraindications for Cefdinir

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

Severe Renal Impairment: Avoid if CrCl <30 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.

Clostridium difficile Infection History: Contraindicated due to recurrence risk.

Warnings & Precautions for Cefdinir

General Warnings

Clostridium difficile Infection: Severe diarrhea risk; discontinue if present.

Allergic Reactions: Anaphylaxis possible; monitor for rash or swelling.

Hemolytic Anemia: Rare blood disorder risk; monitor CBC.

Nephrotoxicity: Kidney damage risk with prolonged use; monitor renal function.

Drug Interactions: Reduces efficacy with iron or antacids; adjust timing.

Additional Warnings

Superinfection: Risk of fungal or resistant bacterial growth; assess regularly.

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 and gastrointestinal 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 >6 months; avoid under 6 months.

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

Additional Precautions

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

Overdose and Management of Cefdinir

Overdose Symptoms

  • Severe diarrhea or nausea.
  • Severe cases: Renal dysfunction or seizures.
  • Abdominal pain or rash as early signs.
  • Drowsiness or confusion with high doses.

Immediate Actions

Contact the Medical Team: Seek immediate medical help.

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

Specific Treatment: No specific antidote; use hemodialysis for severe overdose, and manage symptoms with supportive care.

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

Additional Notes

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

Side Effects of Cefdinir

Common Side Effects

  • Diarrhea (15–20%, manageable with probiotics)
  • Nausea (5–10%, reduced with food)
  • Rash (3–8%, transient with care)
  • Headache (2–6%, alleviated with rest)
  • Vomiting (2–5%, monitorable with support)

These effects may subside with dose adjustment or supportive care.

Serious Side Effects

Seek immediate medical attention for:

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

Additional Notes

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

Drug Interactions with Cefdinir

This active ingredient may interact with:

  • Iron Supplements: Reduces absorption; separate by 2 hours.
  • Antacids (e.g., Aluminum Hydroxide): Decreases bioavailability; avoid concurrent use.
  • Probenecid: Increases levels; monitor renal function.
  • Warfarin: 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: Take this cephalosporin as prescribed to manage infections, following the exact schedule.

Monitoring: Report diarrhea, rash, or abdominal pain immediately.

Lifestyle: Avoid alcohol; maintain hydration.

Diet: Take with or without food; avoid iron-rich meals or antacids nearby.

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

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

Pharmacokinetics of Cefdinir

Absorption: Oral bioavailability 16–21%; peak at 2–4 hours.

Distribution: Volume of distribution ~0.35 L/kg; 60–70% protein-bound.

Metabolism: Minimal hepatic metabolism; excreted unchanged.

Excretion: Primarily renal (60–70% within 24 hours); half-life 1.7–2 hours.

Half-Life: 1.7–2 hours, prolonged in renal impairment.

Pharmacodynamics of Cefdinir

This drug exerts its effects by:

Inhibiting bacterial cell wall synthesis, killing susceptible organisms.

Exhibiting activity against Streptococcus and Haemophilus species.

Providing oral efficacy with reduced nephrotoxicity compared to earlier cephalosporins.

Showing potential for gastrointestinal side effects with prolonged use.

Storage of Cefdinir

  • Temperature: Store capsules 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 Cefdinir treat?

A: This medication treats sinusitis, pneumonia, and ear infections.

Q: Can this active ingredient cause diarrhea?

A: Yes, diarrhea is common; use probiotics.

Q: Is Cefdinir safe for children?

A: Yes, for >6 months with a doctor’s guidance.

Q: How is this drug taken?

A: Orally, as directed.

Q: How long is Cefdinir treatment?

A: 5–14 days, depending on infection.

Q: Can I use Cefdinir 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 cephalosporin affect iron levels?

A: Yes, avoid iron supplements nearby; consult your doctor.

Q: Can it cause a rash?

A: Yes, rash is possible; report changes.

Q: Is it safe with antacids?

A: No, avoid antacids within 2 hours; consult your doctor.

Regulatory Information

This medication is approved by:

U.S. Food and Drug Administration (FDA): Approved in 1997 (Omnicef) for bacterial infections.

European Medicines Agency (EMA): Approved for sinusitis and otitis media.

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

References

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