CASE STUDIES OF ADVERSE DRUG REACTIONS (ADR) IN AYUSH

Authors

  • S.Heamavathi.,M.D(s) Junior Research Fellow, Peripheral Pharmacovigilance Centre GSMC Chennai
  • S.Shankar.,M.D(s) Co-ordinator, Peripheral Pharmacovigilance Centre GSMC Chennai
  • S.Karthi.,M.D House Officer, National institute of Siddha
  • K.Kanagavalli Principal, Government Siddha Medical College, Arumbakkam Chennai-106

Abstract

Background: AYUSH systems, including Ayurveda, Siddha, Sowgarigpa Unani, Yoga, and Naturopathy, have gained significant popularity worldwide. However, there is a growing concern about adverse drug reactions (ADRs) associated with AYUSH formulations.

Objective: This review aims to provide a comprehensive overview of ADRs reported in AYUSH systems, highlighting the challenges in ADR reporting and prevention.

Methods: A systematic review of literature was conducted using electronic databases to identify studies reporting ADRs in AYUSH. Relevant data on ADR types, frequency, severity, and associated factors were extracted.

Results: The review revealed a limited number of studies reporting ADRs in AYUSH systems. Common ADRs included gastrointestinal disturbances, skin reactions, and neurological symptoms. However, the underreporting of ADRs in AYUSH remains a significant challenge due to various factors, such as cultural beliefs, lack of awareness, and limited healthcare infrastructure.

Conclusion: While AYUSH systems offer potential benefits, it is essential to address the issue of ADRs to ensure their safe and effective use. Improved ADR reporting mechanisms, standardized pharmacovigilance practices, and further research are necessary to enhance the understanding of ADRs in AYUSH and to develop strategies for their prevention.

Keywords:

AYUSH, adverse drug reactions, pharmacovigilance, traditional medicine, safety

DOI

https://doi.org/10.70604/

References

1. WHO (2002). The importance of Pharmacovigilance. World Health Organization.

2. World Health Organization. Traditional Medicine Strategy 2014-2023. WHO; 2013.

3. WHO (2013). “Safety Monitoring of Herbal Medicines in Pharmacovigilance Systems.”

4. Ministry of AYUSH (2018), Government of India. “Operational Guidelines for Safety Monitoring & Pharmacovigilance in AYUSH Practices.”

5. Edwards, I.R., & Aronson, J.K. (2000). Adverse drug reactions: definitions, diagnosis, and management. The Lancet, 356(9237), 1255-1259.

6. Ministry of AYUSH, Government of India. (2018). National Pharmacovigilance Programme for AYUSH (available in ayush website).

7. PvPI, India. “Guidelines for Adverse Drug Reactions Monitoring in AYUSH Medicines.”

8. All India Institute of Ayurveda https://aiia.gov.in/pharmacovigilance/

9. ghttps://pib.gov.in/PressReleasePage.aspx?PRID=2043756government Reports and Databases:

Dr.S.Heamavathi.,M.D(s)

Published

2025-03-31
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How to Cite

S, H., S, S., S, K., & K, K. (2025). CASE STUDIES OF ADVERSE DRUG REACTIONS (ADR) IN AYUSH. International Journal of Zoology, Environment and Life Sciences , 2(1), 1-5. https://doi.org/10.70604/

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How to Cite

S, H., S, S., S, K., & K, K. (2025). CASE STUDIES OF ADVERSE DRUG REACTIONS (ADR) IN AYUSH. International Journal of Zoology, Environment and Life Sciences , 2(1), 1-5. https://doi.org/10.70604/