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Cefdinir is a third-generation cephalosporin antibiotic widely prescribed for treating bacterial infections due to its broad-spectrum activity against both Gram-positive and Gram-negative pathogens. Known for its oral bioavailability and convenient dosing, cefdinir is a preferred choice for outpatient management of infections. This article references the British National Formulary (BNF), Lippincott Textbook of Pharmacology, and Lange Basic & Clinical Pharmacology to provide a detailed overview of cefdinir, including its mechanism of action, clinical uses, dosing guidelines, side effects, precautions, drug interactions, and generic names.
Cefdinir exerts its bactericidal effect by inhibiting bacterial cell wall synthesis. According to the Lippincott Textbook of Pharmacology, cefdinir binds to penicillin-binding proteins (PBPs) on the bacterial cell wall, disrupting peptidoglycan cross-linking. This weakens the cell wall, leading to osmotic instability and cell lysis.
The Lange Basic & Clinical Pharmacology emphasizes cefdinir’s stability against many beta-lactamases, enzymes produced by bacteria to inactivate earlier cephalosporins. However, it is less effective against Pseudomonas aeruginosa and methicillin-resistant Staphylococcus aureus (MRSA).
Cefdinir is indicated for:
The BNF highlights its role as a first-line option for mild to moderate infections in patients with penicillin allergies (non-severe).
Dosing is tailored to infection type, patient age, and renal function:
Adults and Adolescents (>12 years):
Children (6 months–12 years):
Renal Impairment:
Administration Tips:
Cefdinir is generally well-tolerated, but potential side effects include:
Key interactions per the BNF and Lange Basic & Clinical Pharmacology:
Brand Names: Omnicef®, Cefdinir Capsules/Oral Suspension
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