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Cephalexin is a first-generation cephalosporin antibiotic widely used for treating a variety of bacterial infections. It is valued for its effectiveness against Gram-positive bacteria and some Gram-negative organisms, as well as its availability in oral formulations. This article references the British National Formulary (BNF), Lippincott Textbook of Pharmacology, and Lange Basic & Clinical Pharmacology to provide a detailed overview of cephalexin, including its mechanism of action, clinical uses, dosing guidelines, side effects, precautions, drug interactions, and generic names.
Cephalexin exerts its bactericidal effect by inhibiting bacterial cell wall synthesis. According to the Lippincott Textbook of Pharmacology, cephalexin 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 highlights cephalexin’s activity against Gram-positive bacteria, including beta-lactamase-producing strains of Staphylococcus aureus. However, it is less effective against Gram-negative bacteria compared to later-generation cephalosporins.
Cephalexin is indicated for:
The BNF emphasizes its role as a first-line agent for mild to moderate infections caused by susceptible organisms.
Dosing varies by infection severity, patient age, and renal function:
Adults:
Children:
Renal Impairment:
Administration Tips:
Cephalexin is generally well-tolerated, but potential side effects include:
Key interactions per the BNF and Lange Basic & Clinical Pharmacology:
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