Table 1.
Agent | Adult dosage (assuming normal renal and liver function) | Remarks | Major toxicities to consider |
---|---|---|---|
aAmpicillin-sulbactam | 3 g every 4 h if intolerance or toxicities preclude the use of higher dosages or for mild infections | Hepatotoxicity (1%) | |
aAmpicillin-Sulbactam |
9 g every 8 h, each dose given over 4 h 27-g continuous infusion over 24 h |
High dose, suitable for ampicillin-sulbactam-resistant CRAB | |
Cefiderocol | 2 g every 8 h infused over 3 h |
Elevated liver tests (2–16%) Hypokalemia (11%) |
|
Colistin | As per international consensus guidelinesb |
Nephrotoxicity (1–18%) Neurotoxicity (1–7%) |
|
Eravacycline | 1 mg/kg/dose every 12 h | GI (2–7%) | |
cImipenem-cilastatin | 500 mg every 6 h infused over 3 h | Seizures (1%) | |
cMeropenem | 2 g every 8 h infused over 3 h | Seizures (< 1%) | |
Minocycline | 200 mg every 12 h | CNS (1–3%) | |
Tigecycline | 200 mg once, then 100 mg every 12 h | High dose |
Hepatotoxicity (2–5%) Pancreatitis (< 1%), |
CRAB carbapenem-resistant Acinetobacter baumannii
aCurrently only ampicillin-sulbactam is considered appropriate for monotherapy; all other drugs should be used based on susceptibly as a combination with ampicillin sulbactam except in penicillin-allergic patients
bTsuji BT, Pogue JM, Zavascki AP, et al. International Consensus Guidelines for the Optimal Use of the Polymyxins: Endorsed by the American College of Clinical Pharmacy (ACCP), European Society of Clinical Microbiology and Infectious Diseases (ESCMID), Infectious Diseases Society of America (IDSA), International Society for Anti-infective Pharmacology (ISAP), Society of Critical Care Medicine (SCCM), and Society of Infectious Diseases Pharmacists (SIDP). Pharmacotherapy 2019; 39(1): 10–39
cCarbapenems may be considered as a third drug in combination regiments