Methods to Compare Adverse Events in Twitter to FAERS, Drug Information Databases, and Systematic Reviews: Proof of Concept with Adalimumab

Author:

Smith Karen,Golder Su,Sarker AbeedORCID,Loke Yoon,O’Connor Karen,Gonzalez-Hernandez Graciela

Funder

U.S. National Library of Medicine

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Pharmacology,Toxicology

Reference93 articles.

1. Kongkaew C, Noyce PR, Ashcroft DM. Hospital admissions associated with adverse drug reactions: a systematic review of prospective observational studies. Ann Pharmacother. 2008;42(7):1017–25.

2. FDA Adverse Event Reporting System (FAERS). http://www.fda.gov/Drugs/InformationOnDrugs/ucm135151.htm . Accessed 6 Jan 2016.

3. Heinrich J. Adverse drug events: Substantial problem but magnitude uncertain: United States General Accounting Office; 2000. p. 6. http://www.gao.gov/new.items/he00053t.pdf . Accessed 10 Aug 2018.

4. World Health Organization. Safety of medicines—a guide to detecting and reporting adverse drug reactions—why health professionals need to take action: World Health Organization; 2017. http://apps.who.int/medicinedocs/en/d/Jh2992e/3.html . Accessed Apr 2017.

5. Lahue BJ, Pyenson B, Iwasaki K, Blumen HE, Forray S, Rothschild JM. National burden of preventable adverse drug events associated with inpatient injectable medications: healthcare and medical professional liability costs. Am Health Drug Benefits. 2012;5(7):1–10.

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