ANCEF
What it isPBP-inhibiting first-generation cephalosporin; surgical prophylaxis and MSSA infection.
Why this oneThe standard surgical prophylaxis agent, and it outperforms vancomycin for susceptible staphylococcal bacteremia.
What limits itNo MRSA cover. Renally adjusted; poor CNS penetration.
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| FDA dosing | Population | Start | Target | Max |
|---|---|---|---|---|
| Moderate–severe infections | Adults (CrCl ≥55) | 500 mg–1 g q6–8h | 500 mg–1 g q6–8h | 12 g/day (rare) |
| Mild infections (gram-positive cocci) | Adults | 250–500 mg q8h | 250–500 mg q8h | |
| Acute uncomplicated UTI | Adults | 1 g q12h | 1 g q12h | |
| Pneumococcal pneumonia | Adults | 500 mg q12h | 500 mg q12h | |
| Severe life-threatening (endocarditis, septicemia) | Adults | 1–1.5 g q6h | 1–1.5 g q6h | 12 g/day (rare) |
| Perioperative prophylaxis | Adults | 1–2 g 0.5–1 h pre-op; 0.5–1 g intraop; 0.5–1 g q6–8h ×24 h post-op | ||
| Mild–moderate infections | Children ≥1 mo (CrCl ≥70) | 25–50 mg/kg/day divided into 3–4 doses | 25–50 mg/kg/day divided 3–4× | |
| Severe infections | Children ≥1 mo | up to 100 mg/kg/day divided into 3–4 doses | up to 100 mg/kg/day divided 3–4× |
Renal Adults CrCl <55: full dose q8h+ (35–54), half dose q12h (11–34), half dose q18–24h (≤10) after loading dose. Peds CrCl <70: 60% daily dose q12h (40–70), 25% q12h (20–40), 10% q24h (5–20)
Hepatic Undefined
Pregnancy No established drug-associated risk of birth defects/miscarriage; crosses placenta; animal studies without adverse developmental effects
Lactation Present in human milk but not expected to accumulate in the breastfed infant
NO BOXED WARNINGS
Principal riskNo MRSA cover
Cost, est. cash$20–$1,500/dose or month
Generic entry1985
Legacy pregnancy categoryB
Defining liabilityAllergy, gastrointestinal effects and agent-specific renal, hepatic, hematologic or interaction risks.

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