Promoting Collaboration of Regulators and Patients in Improving Drug Safety and Regulatory Decision Making

Author:

Khoo Yoong Khean,Lim John C. W.ORCID,Tan-Koi Wei Chuen,Kitikiti Nokuthula Sikhethiwe,Sim-Devadas Ai Ling

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Pharmacology,Toxicology

Reference43 articles.

1. World Health Organization. Regulations and laws promoting health and well-being goals (SDG3) in WHO South-East Asian countries. New Delhi, 2022. https://apps.who.int/iris/rest/bitstreams/1461864/retrieve. Accessed 2 Dec 2023.

2. Trifirò G, Crisafulli S. A new era of pharmacovigilance: future challenges and opportunities. Front Drug Saf Regul. 2022;2: 866898. https://doi.org/10.3389/fdsfr.2022.866898.

3. Sultana J, Cutroneo P, Trifirò G. Clinical and economic burden of adverse drug reactions”. J Pharmacol Pharmacother. 2013;4(1_Suppl):S73–7. https://doi.org/10.4103/0976-500X.120957.

4. US Centers for Disease Control and Prevention. About the Vaccine Adverse Event Reporting System (VAERS). https://wonder.cdc.gov/controller/datarequest/D8. Accessed 9 Jun 2023.

5. Medicine & Healthcare products Regulatory Agency (MHRA). The Yellow Card Scheme: MHRA. https://yellowcard.mhra.gov.uk/information. Accessed 8 Jun 2023.

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