This handout is for tuberculosis (active drug-susceptible, mdr-tb, ltbi). Your care team identified this based on: cough ≥2 weeks + weight loss + drenching night sweats + fever ± hemoptysis — who 4-symptom screen (sens ~70-90% for active pulmonary tb; lower in hiv) (who tb module 4 2022).
Other reasons your team may use this plan: upper-lobe / apical / cavitary / miliary infiltrate on cxr or ct — cavitation raises pretest probability and predicts relapse (ats/cdc/idsa 2016 pmid 27516382); positive xpert mtb/rif ultra or afb smear / mycobacterial culture from sputum — xpert ultra overall sens ~88% vs culture (dorman lancet id 2018 pmid 29198911); close contact with infectious tb or birth/extended residence in a high-burden country — sets the pretest prior (cdc ltbi 2020).
Take these medications exactly as prescribed. Do not stop or change a dose without talking to your provider.
| Medication | Starting dose | How | When | What it does |
|---|---|---|---|---|
| isoniazid | 5 mg/kg PO daily (max 300 mg) | PO | daily × 6 months (intensive + continuation) | Early-bactericidal backbone. Hepatotoxicity + dose-dependent peripheral neuropathy (pyridoxine MANDATORY). RxCUI corrected 1011→6038 RxNav-verified IN 2026-05-16 (1011 was anti-thymocyte globulin — SAFETY-CRITICAL) (ATS/CDC/IDSA 2016 PMID 27516382) |
| rifampin | 10 mg/kg PO daily (max 600 mg) | PO | daily on empty stomach × 6 months | Sterilising backbone enabling the 6-month course. STRONG CYP3A4/P-gp inducer — collapses PI/NNRTI, DOAC, warfarin, hormonal-contraceptive, methadone, azole, steroid levels; substitute rifabutin (RxCUI 55672) for PI-based ART. Orange body fluids — counsel. RxCUI 9384 RxNav-verified IN 2026-05-16 |
| pyrazinamide | 25 mg/kg PO daily (max 2000 mg) | PO | daily × 2 months (intensive phase only) | Sterilising in the acidic intracellular milieu — its 2-month use is what permits a 6-month total. Hepatotoxic; hyperuricemia/arthralgia; renal interval-extension to 3×/week if CrCl <30. RxCUI 8987 RxNav-verified IN 2026-05-16 |
| ethambutol | 15-25 mg/kg PO daily | PO | daily × 2 months (until pan-susceptibility confirmed) | Companion drug preventing resistance amplification until INH/RIF susceptibility confirmed — DROP once DST shows full susceptibility. Dose-dependent optic neuritis — baseline + monthly Snellen/Ishihara; renal interval-extension if CrCl <30. RxCUI 4110 RxNav-verified IN 2026-05-16 |
| pyridoxine | 25-50 mg PO daily | PO | daily for the entire INH-containing course | MANDATORY with INH to prevent peripheral neuropathy — risk amplified in diabetes, HIV, alcohol, pregnancy, malnutrition, CKD. RxCUI 684879 RxNav-verified IN 2026-05-16 |
Plan: TB treatment by phenotype — DS-TB 6-month (2HRZE/4HR) vs 4-month rifapentine-moxifloxacin (Study 31) vs LTBI (3HP/4R/3HR/9H); DR-TB routed to id.tb_drug_resistant.v1
Use these zones to know what to do based on how you feel.
Call 911 or go to the nearest emergency room right away if you have:
End-of-treatment CURE assessment per WHO/ATS (clinical + microbiological — culture-negative at end of therapy; treatment completed if doses verified). Close-contact investigation → IGRA/TST + symptom screen + LTBI evaluation/treatment. Mandatory public-health reporting and case closure. Adherence/relapse education; relapse usually within 6-12 mo (highest if cavitary + positive month-2 culture). Long-term follow-up for late toxicity and post-TB lung function (ATS/CDC/IDSA 2016 PMID 27516382; CDC LTBI 2020)
Guideline: WHO Consolidated Guidelines on TB Module 4: Treatment — drug-susceptible TB & patient care (2022) + ATS/CDC/IDSA Treatment of Drug-Susceptible Tuberculosis (Nahid CID 2016; PMID 27516382) + CDC 2022 4-month rifapentine-moxifloxacin update (Study 31/A5349) + CDC/NTCA LTBI Treatment Guidelines 2020 + WHO LTBI consolidated guidelines 2024