Affiliation:
1. Viva Institute of Pharmacy, Thane, Maharashtra, India
Abstract
Adverse drug reactions (ADRs) are defined by the World Health Organization (WHO) as “a response to a medication that is noxious and unintended used in man to treat”. An adverse drug reaction (ADR) can be defined as ‘an appreciably harmful or unpleasant reaction resulting from an intervention related to the use of a medicinal product; adverse effects usually predict hazard from future administration and warrant prevention, or specific treatment, or alteration of the dosage regimen, or withdrawal of the product’.
Publisher
IP Innovative Publication Pvt Ltd
Reference29 articles.
1. Aronson JK, Ferner RE, Clarification of terminology in drug safety.Drug Saf 2005;28:851-70
2. Directive E, Directive 2011/62 - Amendment of Directive 2001/83/EC on the EC code relating to medicinal products for human use, as regards the prevention of the entry into the legal supply chain of falsified medicinal products..
3. Bates DW, Leape LL, Petrycki S, Incidence and preventability of adverse drug events in hospitalized adults.J Gen Intern Med 1993;8:289-94
4. Wester K, Jönsson AK, Spigset O, Druid H, Hägg S, Incidence of fatal adverse drug reactions: a population based study.Br J Clin Pharmacol 2008;65:573-82
5. Davies EC, Green CF, Taylor S, Adverse drug reactions in hospital in-patients: a prospective analysis of 3695 patient-episodes.PLoS One 2009;4:4439
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献