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Adverse drug reactions in tuberculosis treatment: Incidence, duration and resolution pathways from a mixed-methods patient-centric study in India.

Title: Adverse drug reactions in tuberculosis treatment: Incidence, duration and resolution pathways from a mixed-methods patient-centric study in India.
Authors: Sodhi R; William J Clinton Foundation, New Delhi, India.; Kapoor T; William J Clinton Foundation, New Delhi, India.; Vatsyayan V; William J Clinton Foundation, New Delhi, India.; Seth I; Treemouse Research and Design Private Limited, New Delhi, India.; Chandra H; Treemouse Research and Design Private Limited, New Delhi, India.; Gill N; Treemouse Research and Design Private Limited, New Delhi, India.; Singh M; William J Clinton Foundation, New Delhi, India.; Pal A; William J Clinton Foundation, New Delhi, India.; Mannan S; William J Clinton Foundation, New Delhi, India.
Source: PLOS global public health [PLOS Glob Public Health] 2025 Dec 29; Vol. 5 (12), pp. e0004149. Date of Electronic Publication: 2025 Dec 29 (Print Publication: 2025).
Publication Type: Journal Article
Language: English
Journal Info: Publisher: Public Library of Science Country of Publication: United States NLM ID: 9918283779606676 Publication Model: eCollection Cited Medium: Internet ISSN: 2767-3375 (Electronic) Linking ISSN: 27673375 NLM ISO Abbreviation: PLOS Glob Public Health Subsets: PubMed not MEDLINE
Imprint Name(s): Original Publication: San Francisco, California : Public Library of Science, [2021]-
Abstract: Adverse drug reactions (ADRs) remain a major barrier to successful tuberculosis (TB) treatment. They undermine adherence, prolong morbidity, and increase the risk of treatment failures and mortality. Yet, evidence on their incidence, duration, and management across diverse patient groups remains limited. We conducted a mixed-methods study to address this gap, using a representative sample of patients from six states in India. Specifically, we combined ethnographic observations and interviews with patients and stakeholders (n = 40) across three districts with a quantitative survey of 2,124 randomly selected TB patients across eight districts. The ethnographic analysis revealed a novel taxonomy of ADRs, distinguishing active ADRs (acute, clinically urgent conditions), from passive ADRs (persistent, lower-intensity conditions) that quietly undermine adherence in later treatment phases. Passive ADRs such as skin darkening and fatigue typically warrant little clinical attention, yet their persistence makes them highly relevant for patient management strategies aimed at supporting adherence and achieving TB elimination. This finding was further contextualized and strengthened by quantitative analysis, which provided robust statistical insights into their incidence across diverse patient profiles. The quantitative analyses also reveal a near-universal burden of ADRs, with 86% of patients reporting at least one ADR (Mean = 3.1, SD 2.38). Women reported ADRs more frequently and for longer durations, particularly cutaneous ADRs, while elderly patients were more prone to gastrointestinal and musculoskeletal ADRs. Younger patients and women reported the highest prevalence of vomiting (41%), which emerged as the only independent predictor of unsuccessful treatment completion (OR = 0.39, 95% CI: 0.20-0.76). The overall number of ADRs was also strongly correlated with adverse treatment outcomes (OR = 0.88, 95% CI: 0.78-0.98). The active-passive taxonomy, along with risk-group profiling, offers a roadmap for differentiated counselling and pro-active patient-centric ADR management. We recommend embedding this approach into national TB protocols, with structured risk-based patient counselling at different stages of treatment, supported by adequate training for treatment coordinators and providers. While further research is warranted to assess scalability and cost-effectiveness, our findings demonstrate both the urgency and the feasibility of structured ADR management in high-burden TB settings.; (Copyright: © 2025 Sodhi et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.)
Competing Interests: The authors have declared that no competing interests exist.
References: PLoS One. 2011;6(5):e19566. (PMID: 21611117); Tuberc Res Treat. 2014;2014:412893. (PMID: 25506427); Indian J Med Res. 2011 May;133:529-34. (PMID: 21623039); BMJ Glob Health. 2024 Oct 30;9(10):. (PMID: 39477335); Int J Tuberc Lung Dis. 2007 Aug;11(8):868-75. (PMID: 17705952); Trop Med Infect Dis. 2021 Nov 30;6(4):. (PMID: 34941662); Clin Pharmacokinet. 2009;48(3):143-57. (PMID: 19385708); Ren Fail. 2024 Dec;46(2):2392883. (PMID: 39165235); Bull World Health Organ. 1997;75(6):569-81. (PMID: 9509630); PLOS Digit Health. 2024 Nov 21;3(11):e0000667. (PMID: 39570805); Drug Healthc Patient Saf. 2012;4:61-6. (PMID: 22826643); J Glob Health. 2024 Nov 22;14:04226. (PMID: 39575610); Tuber Lung Dis. 1996 Feb;77(1):37-42. (PMID: 8733412); Expert Rev Clin Pharmacol. 2015;8(4):449-60. (PMID: 26041035); Sci Rep. 2022 Jan 11;12(1):558. (PMID: 35017604); Pharm Pract (Granada). 2006;4(3):134-8. (PMID: 25214900); Pharmacoepidemiol Drug Saf. 2007 Oct;16(10):1104-10. (PMID: 17823987); Indian J Tuberc. 2019 Jul;66(3):358-363. (PMID: 31439180); Res Social Adm Pharm. 2024 Dec;20(12 Pt A):1102-1109. (PMID: 39218734); Biol Sex Differ. 2020 Jun 5;11(1):32. (PMID: 32503637); J Clin Pharm Ther. 2020 Feb;45(1):122-127. (PMID: 31486525); Am J Clin Dermatol. 2001;2(6):349-51. (PMID: 11770389); J Health Popul Nutr. 2018 Jan 5;37(1):1. (PMID: 29304840); Am J Mens Health. 2019 May-Jun;13(3):1557988319856739. (PMID: 31184245); Ther Adv Drug Saf. 2023 Sep 28;14:20420986231200746. (PMID: 37780667); Front Pharmacol. 2023 Jan 13;13:1029067. (PMID: 36712658); PLOS Digit Health. 2024 Sep 11;3(9):e0000421. (PMID: 39259731); BMJ Glob Health. 2019 Jan 24;4(1):e001029. (PMID: 30740248); Indian J Tuberc. 2019 Oct;66(4):520-532. (PMID: 31813444); PLoS One. 2020 Jan 15;15(1):e0227293. (PMID: 31940375); PLoS One. 2013 Jun 04;8(6):e65037. (PMID: 23750225); Indian J Tuberc. 2020 Jan;67(1):20-28. (PMID: 32192612); Drug Saf. 2009;32(1):19-31. (PMID: 19132802); PLoS Med. 2016 Sep 06;13(9):e1002119. (PMID: 27598345); PLoS One. 2023 Feb 7;18(2):e0269765. (PMID: 36749743); PLoS One. 2020 Jul 21;15(7):e0236109. (PMID: 32692774); J Pers Med. 2022 May 31;12(6):. (PMID: 35743692); J Korean Med Sci. 2024 Nov 25;39(45):e286. (PMID: 39592127); Indian J Tuberc. 2024;71 Suppl 1:S97-S100. (PMID: 39067964); Am J Respir Crit Care Med. 2003 Jun 1;167(11):1472-7. (PMID: 12569078); Psychol Health. 2012;27(5):570-87. (PMID: 21827288); Br J Clin Pharmacol. 2022 Jul;88(7):3434-3446. (PMID: 35128732); F1000Res. 2024 Jul 23;11:1388. (PMID: 39935535); Tuberculosis (Edinb). 2005 Sep-Nov;85(5-6):271-6. (PMID: 16253562); Drugs Aging. 2021 Jan;38(1):43-52. (PMID: 33145702); Health Technol Assess. 2011 May;15(20):1-234, iii-iv. (PMID: 21545758); BMC Infect Dis. 2023 Jun 21;23(1):421. (PMID: 37344775); BMJ Glob Health. 2023 Dec 9;8(12):. (PMID: 38070882)
Entry Date(s): Date Created: 20251229 Date Completed: 20251229 Latest Revision: 20260101
Update Code: 20260130
PubMed Central ID: PMC12747411
DOI: 10.1371/journal.pgph.0004149
PMID: 41460796
Database: MEDLINE

Journal Article