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Table 4. Summary of Antimicrobial Dosing, Target Therapeutic Drug Monitoring Values, Adverse Effects, Drug Interactions, and Respective Management

Antimicrobial Dosing Therapeutic Drug Monitoring Targets Adverse Effects and Drug Interactions Suggested Monitoring and Management
Azithromycin 250–500 mg PO/IV daily; 500 mg 3x weekly Cmax: 0.2–0.7 µg/mL GI intolerance, reversible hearing loss, tinnitus, QTc prolongation, hypersensitivity, transient transaminitis Clinical evaluation, LFTs at baseline and every 1–2 months, ECG if QTc-prolonging agents used. Hold for significant adverse events.
Clarithromycin 500 mg PO twice daily Cmax: 2–5 µg/mL GI intolerance, reversible hearing loss, tinnitus, QTc prolongation, CYP3A4 inhibition, drug interactions, hepatotoxicity (rare) Clinical evaluation, LFTs at baseline and every 1–2 months, ECG if combined with QTc-prolonging agents. Adjust medications accordingly.
Rifampin 10 mg/kg PO daily (max 600 mg) Cmax: 8–24 µg/mL Hepatotoxicity, drug interactions (CYP inducer), thrombocytopenia, GI upset, orange discoloration of secretions Clinical evaluation, LFTs every 1–2 months. Monitor for drug interactions.
Rifabutin 300 mg PO daily (dose adjust with interactions) Cmax: 0.4–0.6 µg/mL Neutropenia, uveitis, hepatotoxicity, drug interactions, orange discoloration of secretions Clinical evaluation, CBC and LFTs every 1–2 months. Dose adjust with interacting agents.
Ethambutol 15–25 mg/kg PO daily Cmax: 2–6 µg/mL Optic neuritis, rash, arthralgia, hepatotoxicity Clinical evaluation, baseline and monthly visual acuity and color vision testing, LFTs every 1–2 months.
Amikacin (IV) 15–20 mg/kg IV daily or 3x weekly Peak: 35–45 µg/mL; Trough: <5 µg/mL Nephrotoxicity, ototoxicity, vestibular toxicity Clinical evaluation, baseline and periodic audiometry, renal function, monitor serum levels.
Amikacin (Inhaled) 590 mg nebulized daily Not applicable Ototoxicity, bronchospasm, oral candidiasis, dysphonia, hemoptysis Baseline spirometry, monitor oral cavity discomfort, rechallenge after 1-week holiday if tolerated.
Streptomycin 10–15 mg/kg IV daily or 3x weekly Peak: 20–30 µg/mL; Trough: <2 µg/mL Nephrotoxicity, ototoxicity, vestibular toxicity Baseline audiometry, renal function, monitor peaks/troughs, adjust dosing based on renal function.
Moxifloxacin 400 mg PO/IV daily Cmax: 3–5 µg/mL QTc prolongation, hepatitis, nausea, vomiting, tendinitis, aortic dissection (rare) Clinical evaluation, ECG at baseline and regularly, Cr and LFTs every 1–2 months, electrolyte management.
Bedaquiline 400 mg PO daily for 14 days, then 200 mg three times weekly QTc prolongation monitoring QTc prolongation, hepatitis, elevated amylase, nausea, rash, joint pain Clinical evaluation, ECG baseline and periodically, LFTs every 1–2 months, electrolyte management.
Linezolid 600 mg PO/IV twice daily Cmax: 12–26 µg/mL Myelosuppression, peripheral/optic neuropathy, serotonin syndrome Clinical evaluation, CBC weekly, monitor for neuropathy, monitor for serotonin syndrome if combined with serotonergic agents.
Clofazimine 100 mg PO daily Not established Skin discoloration, GI intolerance, QTc prolongation, hepatotoxicity Clinical evaluation, ECG baseline and periodically, LFTs every 1–2 months.
Trimethoprim-Sulfamethoxazole (TMP-SMX) 800/160 mg PO/IV twice daily Adjust based on renal function GI intolerance, cytopenias, hyperkalemia, renal injury, hypersensitivity, hepatitis Clinical evaluation, Cr, electrolytes, LFTs, and CBC monthly. Discontinue for severe adverse events.