scholarly journals Analysis of Herbal-drug-associated Adverse Drug Reactions Using Data from Spontaneous Reporting System in Electronic Medical Records

2015 ◽  
Vol 36 (1) ◽  
pp. 45-60 ◽  
Author(s):  
Mikyung Kim ◽  
Chang-ho Han
Keyword(s):  
Electronic Medical Records ◽  
Adverse Drug Reactions ◽  
Medical Records ◽  
Spontaneous Reporting ◽  
Reporting System ◽  
Spontaneous Reporting System ◽  
Herbal Drug ◽  
Drug Reactions ◽  
Using Data

Adverse drug reactions with oral anticoagulants: data from sicilian spontaneous reporting system database

2021 ◽  
Author(s):  
Maria Antonietta Barbieri ◽  
Paola Maria Cutroneo ◽  
Chiara Baratelli ◽  
Giuseppe Cicala ◽  
Alessandro Battaglia ◽  
...  
Keyword(s):  
Adverse Drug Reactions ◽  
Spontaneous Reporting ◽  
Reporting System ◽  
Spontaneous Reporting System ◽  
Oral Anticoagulants ◽  
Drug Reactions ◽  
System Database

scholarly journals Determinants of signal selection in a spontaneous reporting system for adverse drug reactions

2001 ◽  
Vol 52 (5) ◽  
pp. 579-586 ◽  
Author(s):  
Eugène P. Van Puijenbroek ◽  
Kees Van Grootheest ◽  
Willem L Diemont ◽  
Hubert G. M. Leufkens ◽  
Antoine C. G. Egberts
Keyword(s):  
Adverse Drug Reactions ◽  
Spontaneous Reporting ◽  
Reporting System ◽  
Spontaneous Reporting System ◽  
Drug Reactions ◽  
Signal Selection

scholarly journals Severe Cutaneous Adverse Drug Reactions Associated with Allopurinol: An Analysis of Spontaneous Reporting System in Southern Italy

2019 ◽  
Vol 7 (1) ◽  
pp. 41-51 ◽  
Author(s):  
Cristina Scavone ◽  
Cristina Di Mauro ◽  
Rosanna Ruggiero ◽  
Francesca Futura Bernardi ◽  
Ugo Trama ◽  
...  
Keyword(s):  
Adverse Drug Reactions ◽  
Spontaneous Reporting ◽  
Reporting System ◽  
Southern Italy ◽  
Spontaneous Reporting System ◽  
Drug Reactions

scholarly journals Study of adverse drug reactions associated with antiepileptic drugs: a pharmacovigilance study using spontaneous reporting system

2021 ◽  
Vol 10 (9) ◽  
pp. 1125
Author(s):  
Sudha K. Mukhyaprana ◽  
Siddiraju Devipriya ◽  
Meenakshi Thirumalaiappan
Keyword(s):  
Antiepileptic Drugs ◽  
Adverse Drug Reactions ◽  
Spontaneous Reporting ◽  
Reporting System ◽  
Spontaneous Reporting System ◽  
Maculopapular Rash ◽  
Similar Efficacy ◽  
Drug Reactions ◽  
Post Marketing Surveillance ◽  
Post Marketing

Background: More than 25 antiepileptic drugs (AEDs) are available in the Indian market to treat epilepsy of which many have similar efficacy but differ in their tolerability and are associated with many adverse drug reactions (ADRs). ADRs are one of the most common causes of death and clinical trials are not sufficient to uncover all the ADRs, hence post-marketing surveillance or pharmacovigilance is necessary. The aim of the study was to analyze the ADRs of AEDs by spontaneous reporting system under Pharmacovigilance Program of India (PvPI).Methods: Suspected ADR reporting forms provided by PvPI were used to collect the data from healthcare professionals of Madras Medical College and Rajiv Gandhi Government General Hospital, Chennai.Results: A total of 77 ADRs from 61 reports were analysed of which 34 were male and 27 were female patients and maximum were in the middle-aged adult group (N=44). Majority of the ADRs were related to skin and subcutaneous disorders (N=55) and most implicated ADR was found to be maculopapular rash (N=12) associated with phenytoin. Most of the ADRs were non-serious (N=42) and were probable category (N=45) as per WHO-UMC scale.Conclusions: Monitoring ADRs in patients using antiepileptic drugs is a matter of importance; hence a robust pharmacovigilance practice is essential.

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