专题:Pharmacovigilance and Adverse Drug Reactions

This cluster of papers focuses on the study, detection, monitoring, and reporting of adverse drug reactions (ADRs) through pharmacovigilance. It covers various aspects such as signal detection, drug safety surveillance, data mining techniques, patient reporting, regulatory actions, causality assessment, and the impact of ADRs on hospital admissions.
最新文献
Age and Sex Differences in Adverse Events Associated With Antipsychotics: An Analysis of the FDA Adverse Events Database

article Full Text OpenAlex

Patient‐Reported Adverse Drug Events on Nirmatrelvir–Ritonavir: A Prospective Observational Study of a Pharmacist‐Led Follow‐Up and Monitoring Service

article Full Text OpenAlex

Safety evaluation of tucatinib: Adverse event signal mining and analysis based on the FAERS database.

article Full Text OpenAlex

Safety evaluation of deucravacitinib: a real-world analysis based on the FDA adverse event reporting system database

article Full Text OpenAlex

Adverse drug reaction to tremelimumab and durvalumab in hepatocellular carcinoma patients: an analysis of the food and drug administration adverse event reporting system database

article Full Text OpenAlex

Possible Association Between Concomitant Use of SSRIs with NSAIDs and an Increased Risk of Adverse Events Among People with Depressive Disorders: Data Mining of FDA Adverse Event Reporting System

article Full Text OpenAlex

Higher risk of gastrointestinal stenosis and obstruction in clozapine-treated individuals with schizophrenia: a pharmacovigilance study based on the FDA adverse event reporting system database

article Full Text OpenAlex

Adverse Drug Reactions

book-chapter Full Text OpenAlex

Exploring potential associations between GLP-1RAs and depressive disorders: a pharmacovigilance study based on FAERS and VigiBase data

article Full Text OpenAlex

Penicillin allergy assessment pathway versus usual clinical care for primary care patients with a penicillin allergy record in the UK (ALABAMA): an open-label, multicentre, randomised controlled trial

article Full Text OpenAlex

近5年高被引文献
Vaccines safety case studies

book-chapter Full Text OpenAlex 332 FWCI87.844

Frequency and Factors Associated With Adverse Events Among Multi-Drug Resistant Tuberculosis Patients in Pakistan: A Retrospective Study

article Full Text OpenAlex 310 FWCI34.69

Artificial Intelligence and Machine Learning for Drug Safety

book-chapter Full Text OpenAlex 215 FWCI56.887

Characterising the background incidence rates of adverse events of special interest for covid-19 vaccines in eight countries: multinational network cohort study

article Full Text OpenAlex 199 FWCI12.065

Detection algorithms and attentive points of safety signal using spontaneous reporting systems as a clinical data source

article Full Text OpenAlex 191 FWCI22.628

Adverse drug reactions in older adults: a narrative review of the literature

review Full Text OpenAlex 174 FWCI4.805

Technology for Drug Safety: Challenges

book-chapter Full Text OpenAlex 145 FWCI38.366

Injection fears and COVID-19 vaccine hesitancy

article Full Text OpenAlex 143 FWCI18.808

Real-World Evidence: A Primer

review Full Text OpenAlex 141 FWCI12.353

Real‐World Evidence in EU Medicines Regulation: Enabling Use and Establishing Value

article Full Text OpenAlex 141 FWCI21.261