# Current Scenarios and Future Perspectives of Therapeutic Drug Monitoring in India: A Narrative Review

**Authors:** Joyeta Paul, Prasanjit Das, Alapan Das, Bisweswar Ojha, Krishnasish Das, Tirthankar Deb

PMC · DOI: 10.7759/cureus.102678 · Cureus · 2026-01-30

## TL;DR

This review discusses the current state and future potential of therapeutic drug monitoring in India, highlighting its underutilization and the need for policy and infrastructure support.

## Contribution

The paper provides a comprehensive overview of TDM in India, emphasizing barriers and suggesting strategies for improvement.

## Key findings

- TDM is underutilized in India due to systemic and infrastructural barriers.
- Special populations like children and the elderly require tailored TDM approaches.
- Adoption of point-of-care technologies and policy support can enhance TDM implementation.

## Abstract

Therapeutic drug monitoring (TDM) is a precision medicine tool that measures drug concentrations in biological fluids to guide individualized dosing. TDM has evolved into a multidisciplinary approach used across various therapeutic areas. In India, despite a growing clinical need, TDM remains underutilized due to systemic and infrastructural barriers. This narrative review aims to summarize the evolution, current status, analytical approaches, and future prospects of TDM in India and is based on published literature retrieved from databases, including PubMed, Scopus, and Google Scholar, and outlines TDM's utility in optimizing pharmacotherapy for drugs with narrow therapeutic windows or nonlinear pharmacokinetics. It compares analytical methods used for TDM and discusses challenges in the workflow of TDM. Special emphasis is placed on its relevance in children, pregnant women, the elderly, and critically ill patients. It also highlights barriers, including a lack of infrastructure, trained personnel, and standardized guidelines. TDM in India requires policy-level support, integration into national health programs, clinician education, and adoption of point-of-care technologies. Strengthening research in pharmacogenetics can help establish TDM as a cornerstone of individualized therapy.

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** epileptic drugs (MESH:D000069279), bipolar disorder (MESH:D001714), hypoalbuminemia (MESH:D034141), Tuberculosis (MESH:D014376), TDM (MESH:D000081015), inflammation (MESH:D007249), Hepatic disorders (MESH:D008107), epilepsy (MESH:D004827), thrombosis (MESH:D013927), Renal dysfunction (MESH:D007674), critically ill (MESH:D016638), bleeding (MESH:D006470), ototoxicity (MESH:D006311), toxicity (MESH:D064420), Haemolysis (MESH:D006461), sepsis (MESH:D018805), TB (MESH:D014390), HIV (MESH:D015658), uremic (MESH:D006463), liver or kidney dysfunction (MESH:D051437), fungal infections (MESH:D009181), seizure (MESH:D012640), infection (MESH:D007239), cancer drugs (MESH:D009369)
- **Chemicals:** tacrolimus (MESH:D016559), vancomycin (MESH:D014640), Lithium (MESH:D008094), cardiac glycosides (MESH:D002301), benzodiazepines (MESH:D001569), aminoglycosides (MESH:D000617), K+ (MESH:D011188), cyclosporine (MESH:D016572), carbamazepine (MESH:D002220), zinc (MESH:D015032), Na+ (MESH:D012964), digoxin (MESH:D004077), anti (-), metal (MESH:D008670), valproate (MESH:D014635), sirolimus (MESH:D020123), levetiracetam (MESH:D000077287), beta-lactams (MESH:D047090), lamotrigine (MESH:D000077213), warfarin (MESH:D014859), phenytoin (MESH:D010672), copper (MESH:D003300)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12951084/full.md

## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12951084/full.md

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Source: https://tomesphere.com/paper/PMC12951084