Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Pharmacology
Reference44 articles.
1. World Health Organization. The importance of pharmacovigilance. Safety monitoring of medicinal products. Geneva: World Health Organization; 2002.
2. Edwards IR, Aronson JK. Adverse drug reactions: definitions, diagnosis, and management. Lancet. 2000;356(9237):1255–9.
3. International Conference on Harmonization of technical requirements for registration of pharmaceuticals for human use. ICH harmonized tripartite guideline post-approval safety data management: definitions and standards for expedited reporting E2D. Current Step 4 version dated 12 November 2003.
https://www.ich.org/fileadmin/Public_Web_Site/ICH_Products/Guidelines/Efficacy/E2D/Step4/E2D_Guideline.pdf
. Accessed 10 Dec 2018.
4. Hazell L, Shakir SA. Under-reporting of adverse drug reactions: a systematic review. Drug Saf. 2006;29(5):385–96.
5. Kharkar M, Bowalekar S. Extent of under reporting of adverse drug reactions (ADRs) in India: evaluation using logistic regression analysis (LRA) model. J Clin Trials. 2014;4:1.
https://doi.org/10.4172/2167-0870.1000155
.
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