Drug Guide
Cefdinir
Classification
Therapeutic: Antibacterial
Pharmacological: Third-generation cephalosporin
FDA Approved Indications
- Uncomplicated skin and skin structure infections
- Pharyngitis and tonsillitis caused by Streptococcus pyogenes
- Otitis media (middle ear infections)
- Sinusitis
Mechanism of Action
Cefdinir inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins, leading to cell lysis and death.
Dosage and Administration
Adult: 300 mg every 12 hours or 600 mg once daily for 5-10 days, depending on infection severity.
Pediatric: 14 mg/kg/day in divided doses every 12 hours; maximum dose typically not exceeding adult doses.
Geriatric: Adjust dose based on renal function; no specific dose reduction required in absence of renal impairment.
Renal Impairment: Dose adjustment needed; typically reduce frequency or dose depending on severity.
Hepatic Impairment: No specific adjustment required but caution advised.
Pharmacokinetics
Absorption: Well absorbed orally, with bioavailability around 50-70%.
Distribution: Widely distributed in body tissues and fluids.
Metabolism: Minimal hepatic metabolism, predominantly excreted unchanged.
Excretion: Primarily renal excretion via glomerular filtration and tubular secretion.
Half Life: Approximately 1.7 hours.
Contraindications
- Hypersensitivity to cephalosporins or penicillins.
Precautions
- History of allergic reactions to beta-lactam antibiotics, renal impairment, antibiotic-associated colitis.
Adverse Reactions - Common
- Diarrhea (Common)
- Nausea (Common)
- Rash (Uncommon)
Adverse Reactions - Serious
- Anaphylaxis (Rare)
- Clostridioides difficile-associated diarrhea (Rare)
Drug-Drug Interactions
- Probenecid (may increase cefdinir levels)
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Assess for allergies to penicillins or cephalosporins; monitor renal function.
Diagnoses:
- Risk for allergic reaction
- Impaired comfort related to gastrointestinal symptoms
Implementation: Administer with or without food; encourage adequate hydration; observe for allergic reactions.
Evaluation: Assess infection resolution and monitor for adverse reactions.
Patient/Family Teaching
- Take medication exactly as prescribed and complete the full course.
- Report signs of allergic reactions such as rash, itching, swelling, or difficulty breathing.
- Notify healthcare provider if diarrhea worsens or persists.
Special Considerations
Black Box Warnings:
- None currently for cefdinir.
Genetic Factors: None specific.
Lab Test Interference: May cause false-positive urine glucose tests with glucose oxidase methods.
Overdose Management
Signs/Symptoms: Nausea, vomiting, diarrhea, stomach pain.
Treatment: Supportive care; hemodialysis may be considered in severe cases.
Storage and Handling
Storage: Store at room temperature, 20°C to 25°C (68°F to 77°F).
Stability: Stable up to the expiration date printed on the packaging.