Adverse drug reactions monitoring: prospects and impending challenges for pharmacovigilance

Author:

Sahu Ram Kumar,Yadav Rajni,Prasad Pushpa,Roy Amit,Chandrakar Shashikant

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Reference91 articles.

1. Aeries N: Consumer reporting of ADRs. WHO Drug Information 1995, 14: 211-215.

2. Arnott J, Hesselgreaves H, Nunn AJ, Peak M, Pirmohamed M: What can we learn from parents about enhancing participation in Pharmacovigilance? British J Clin Pharmacol 2012, 78(2):312-322.

3. Arora D: Pharmacovigilance obligations of the pharmaceutical companies in India. Indian J Pharmacol 2008, 40: 13-16.

4. Bahri P, Tsintis P: Pharmacovigilance–related topics at the level of the International Conference on Harmonisation (ICH). Pharmacoepidemiol Drug Saf 2005, 14: 377-387. 10.1002/pds.1043

5. Bates DW, Cullen DJ, Laird N: Incidence of adverse drug events and potential adverse drug events. JAMA 1995, 274: 29-34. 10.1001/jama.1995.03530010043033

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