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Tigecycline, an IV glycylcycline antibiotic, uses fixed dosing regardless of renal function: 100 mg loading dose, then 50 mg every 12 hours for most infections.[1]
No dose changes are needed in patients with renal impairment, including those on hemodialysis or continuous renal replacement therapy. Tigecycline's pharmacokinetics show minimal renal clearance—less than 20% of the dose is excreted unchanged in urine. Primary elimination occurs via biliary/fecal routes and metabolism.[1][2]
Pharmacokinetic trials confirm stable tigecycline exposure (AUC and Cmax) across creatinine clearance levels from normal (>80 mL/min) to severe (<30 mL/min). A study in end-stage renal disease patients on hemodialysis found no accumulation post-dialysis, as tigecycline is not significantly dialyzable.[2]
Renal function does not alter dosing, but hepatic issues do: reduce maintenance dose to 25 mg every 12 hours in Child-Pugh B/C cirrhosis (after 100 mg load).[1]
Monitor for superinfections or side effects like nausea, as tigecycline's broad-spectrum activity and fixed dosing apply uniformly. No loading dose adjustment needed even in acute kidney injury.[1][3] [1]: Tigecycline Prescribing Information (Pfizer) [2]: Clinical Pharmacology Review - NDA 21-821 (FDA) [3]: DrugPatentWatch.com - Tigecycline Patent Status
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