Article

Assessment of drug-induced adverse events reported for transgender population in India

2023-03-29

Abstract excerpt

<h4>Purpose: </h4> To assess the ADRs reported (2010-2020) for transgender population in India. <h4>Methods: </h4>: The study was based on the surveillance data received during the study period at Indian Pharmacopoeia Commission (IPC), as IPC is authorized for collating and analyzing ADRs submitted by healthcare professionals, marketing authorization holders and consumers under the Pharmacovigilance Programme of...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: 48e58849-9878-57be-a1c5-ac40b5424b23
DOI: 10.22541/au.168006432.24876719/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Assessment of drug-induced adverse events reported for transgender population in IndiaDOI 10.22541/au.168006432.24876719/v1Read

Evaluation of potential adverse effects of gender-affirming hormonal therapy; findings from the Spanish Pharmacovigilance System DatabaseSemantic proximity Read

Adverse drug reactions associated with the use of biological agentsSemantic proximity Read

An opportunity for clinical pharmacology trained physicians to improve patient drug safety: A retrospective analysis of adverse drug reactions in teenagersSemantic proximity Read

Research Progress on High-Risk Drugs for Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis with Insights from Adverse Drug Reaction Database MiningSemantic proximity Read

Real-world safety profile of Enfortumab Vedotin: A comprehensive pharmacovigilance analysis based on the FDA Adverse Event Reporting System (FAERS)Semantic proximity Read

Dolutegravir Reported Adverse Drug Reactions: A Systematic Review ProtocolSemantic proximity Read

Pharmacotherapy Associated with CYP2C19, CYP2C9, CYP2D6, and UGT1A1 Genes in Population Sample: Observational Cross Sectional Analytical StudySemantic proximity Read

Safety assessment of S-1: Real-world adverse event analysis from the FAERS databaseSemantic proximity Read

Common Causes and Characteristics of Adverse Drug Reactions in Older Adults: A Retrospective StudySemantic proximity Read

A real-world pharmacovigilance study of FDA adverse event reporting system (FAERS) events for TivozanibSemantic proximity Read

Real-world pharmacovigilance study of voclosporin based on FAERS and VigiBaseSemantic proximity Read

Evaluation of potential drug-drug interactions and associated factors among hospitalized pediatric patients in Adigrat general hospital, Tigrai, north Ethiopia: a retrospective cross-sectional studySemantic proximity Read