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. |