Intravenous dosing for adults | Intravenous dosing for children and adolescents (age ≥1 month through 17 years) | Comments | |
FIRST-LINE ANTIBIOTICS: Empiric regimen consists of a combination of 2 bactericidal agents and 1 protein-synthesis inhibitor | |||
First-line bactericidal agents | |||
Meropenem | 2 g every 8 hours |
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Ciprofloxacin | 400 mg every 8 hours |
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Levofloxacin | 500 mg every 12 hours |
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Penicillin G | 4 million units every 4 hours |
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Ampicillin | 2 g every 4 hours |
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Imipenem-cilastatin | 1 g every 6 hours |
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Ampicillin-sulbactam | 3 g every 6 hours |
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First-line protein-synthesis inhibitors | |||
Minocycline | 200 mg once then 100 mg every 12 hours |
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Doxycycline | 200 mg once then 100 mg every 12 hours |
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ALTERNATIVE ANTIBIOTICS (reserve for when first-line agents cannot be used or are unavailable, as in a crisis setting; listed in descending order of preference) | |||
Alternative bactericidal agents | |||
Piperacillin-tazobactam | 3.375 g every 4 hours |
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Moxifloxacin | 400 mg every 24 hours |
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Vancomycin | 15 mg/kg over 1 to 2 hours every 12 hours |
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Alternative protein-synthesis inhibitors | |||
Omadacycline | 200 mg once then 100 mg every 12 hours |
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Eravacycline | 1 mg/kg every 12 hours |
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Clindamycin | 900 mg every 8 hours |
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Linezolid | 600 mg every 12 hours |
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Rifampin | 600 mg every 12 hours |
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Systemic anthrax includes anthrax meningitis and inhalation, injection, and gastrointestinal anthrax; patients often have temperature abnormalities, tachycardia, tachypnea, hypotension, or leukocytosis or leukopenia.
In addition to antibiotic therapy, antitoxin therapy (raxibacumab, obiltoxaximab, or anthrax immunoglobulin) should also be given for systemic anthrax. Refer to other UpToDate content for details.
Duration of the intravenous antibiotic is at least 2 to 3 weeks or until clinically stable, whichever is longer. Subsequently, selected patients exposed to aerosolized Bacillus anthracis spores warrant post-exposure prophylaxis. Refer to other UpToDate content on prevention of anthrax.
The doses recommended above are intended for patients with normal kidney function; the doses of some of these agents must be adjusted in patients with kidney insufficiency.
These recommendations are consistent with those from the Centers for Disease Control and Prevention (CDC) in the United States. For dosing in neonates, refer directly to CDC documents.