» Articles » PMID: 38114758

Appeal for Increasing the Impact of Pharmacovigilance

Overview
Journal Drug Saf
Specialties Pharmacology
Toxicology
Date 2023 Dec 19
PMID 38114758
Authors
Affiliations
Soon will be listed here.
Citing Articles

Might We Come Together on a Paradigm Shift to Manage ICSRs with a Decentralized Data Model?.

Smith L, Glaser M, Kempf D, Roman X, Artlich C, Patel M Drug Saf. 2025; .

PMID: 40056291 DOI: 10.1007/s40264-025-01539-4.


Pharmacovigilance in the Community: A Special-Interest Group of the International Society of Pharmacovigilance.

Elhawary M, Noss R, Alj L, Younus M, Alkhakany M, Rostom H Drug Saf. 2025; 48(3):203-207.

PMID: 39779631 DOI: 10.1007/s40264-024-01513-6.


Views on the Development and Use of a New Digital Adverse Drug Event Reporting Platform in Australia: A Qualitative Study.

Gebreyohannes E, Thornton C, Thiessen M, de Vries S, Coombs G, Hwang I Drug Saf. 2024; 48(2):179-190.

PMID: 39487335 PMC: 11785647. DOI: 10.1007/s40264-024-01489-3.

References
1.
Patel T, Patel P, Bhalla H, Dwivedi P, Bajpai V, Kishore S . Impact of suspected adverse drug reactions on mortality and length of hospital stay in the hospitalised patients: a meta-analysis. Eur J Clin Pharmacol. 2022; 79(1):99-116. DOI: 10.1007/s00228-022-03419-7. View

2.
Pirmohamed M, James S, Meakin S, Green C, Scott A, Walley T . Adverse drug reactions as cause of admission to hospital: prospective analysis of 18 820 patients. BMJ. 2004; 329(7456):15-9. PMC: 443443. DOI: 10.1136/bmj.329.7456.15. View

3.
Lazarou J, Pomeranz B, Corey P . Incidence of adverse drug reactions in hospitalized patients: a meta-analysis of prospective studies. JAMA. 1998; 279(15):1200-5. DOI: 10.1001/jama.279.15.1200. View

4.
van Hunsel F, Gardarsdottir H, de Boer A, Kant A . Measuring the impact of pharmacovigilance activities, challenging but important. Br J Clin Pharmacol. 2019; 85(10):2235-2237. PMC: 6783581. DOI: 10.1111/bcp.14042. View

5.
Pacurariu A, Coloma P, van Haren A, Genov G, Sturkenboom M, Straus S . A description of signals during the first 18 months of the EMA pharmacovigilance risk assessment committee. Drug Saf. 2014; 37(12):1059-66. DOI: 10.1007/s40264-014-0240-1. View