Drug Safety

Papers
(The H4-Index of Drug Safety is 26. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-12-01 to 2025-12-01.)
ArticleCitations
Correction to: Review of Over 15 Years Postmarketing Safety Surveillance Spontaneous Data for the Human Rotavirus Vaccine (Rotarix) on Intussusception166
Validation of a Natural Language Machine Learning Model for Safety Literature Surveillance109
Deliberate Self-Poisoning: Real-Time Characterization of Suicidal Habits and Toxidromes in the Food and Drug Administration Adverse Event Reporting System91
Authors’ Reply to Mungmunpuntipantip et al.’s Comment on “Description of Frequencies of Reported Adverse Events Following Immunization Among Four Different COVID-19 Vaccine Brands”83
Impact of Batoclimab Treatment on LDL-C with and Without Coadministration of Atorvastatin: Results from a Phase I Randomized Study in Healthy Participants77
Comment on “Performance and Reproducibility of Large Language Models in Named Entity Recognition: Considerations for the Use in Controlled Environments”63
Algorithms to Identify Major Congenital Malformations in Routinely Collected Healthcare Data: A Systematic Review59
Potential Risk Factors of Drug-Related Problems in Hospital-Based Mental Health Units: A Systematic Review47
Post-Marketing Safety Profile of Vortioxetine Using a Cluster Analysis and a Disproportionality Analysis of Global Adverse Event Reports45
Drug-Induced Liver Injury in the Elderly: Consensus Statements and Recommendations from the IQ-DILI Initiative44
Acknowledgement to Referees43
High-Dimensional Propensity Score-Adjusted Case-Crossover for Discovering Adverse Drug Reactions from Computerized Administrative Healthcare Databases42
Emergency Department Use of Heart Failure-Exacerbating Medications in Patients with Chronic Heart Failure42
A Comparison of Active Pharmacovigilance Strategies Used to Monitor Adverse Events to Antiviral Agents: A Systematic Review40
Comparison of the MOdified NARanjo Causality Scale (MONARCSi) for Individual Case Safety Reports vs. a Reference Standard39
Meeting Report: Herbal and Dietary Supplement Safety Surveillance Summit38
Use of Electrocardiogram Monitoring in Adult Patients Taking High-Risk QT Interval Prolonging Medicines in Clinical Practice: Systematic Review and Meta-analysis37
Early Detection of Hearing Impairment Signals Post-mRNA COVID-19 Vaccination: A Disproportionality Analysis Study on French Pharmacovigilance Database35
Incretin-Based Drugs and the Risk of Dementia Among Patients with Type 2 Diabetes35
21st ISoP Annual Meeting “A New Era of Pharmacovigilance: Challenges and Opportunities” 20–23 September 2022 Verona, Italy33
Uncovering the Hidden Hurdles: Exploring Challenges in Pediatric Pharmacovigilance in the Netherlands33
Sex Differences in Electrolyte Disturbances Among Diuretic Users According to Renal Function and Age32
Comment on "Drug–Drug Interaction of the Sodium Glucose Co-Transporter 2 Inhibitors with Statins and Myopathy: A Disproportionality Analysis Using Adverse Events Reporting Data"27
Preventable Deaths Involving Medicines: A Systematic Case Series of Coroners’ Reports 2013–2226
An Integrated Approach for Representing Knowledge on the Potential of Drugs to Cause Acute Kidney Injury26
Major Adverse Cardiovascular Events Related to JAK Inhibitors: A Disproportionality Analysis Using the WHO Global Individual Case Safety Database26
Mapping Strategies to Assess and Increase the Validity of Published Disproportionality Signals: A Meta-Research Study26
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