Disproportionality analysis of post-marketing safety concerns associated with selumetinib in the FDA adverse event reporting system. [PDF]
Liu F, Su H, Wei W.
europepmc +1 more source
Pharmacovigilance for Vaccines Used in Pregnancy: A Gap Analysis From Uganda. [PDF]
Nambasa VP+9 more
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Knowledge, Attitude, Practice, and Barriers of Adverse Drug Reaction Reporting Among Healthcare Professionals in Timor-Leste: A Cross-Sectional Survey. [PDF]
da Costa J+3 more
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Comparative Analysis of Neuropsychiatric Adverse Reactions Associated with Remdesivir and Nirmatrelvir/Ritonavir in COVID-19 Treatment: Insights from EudraVigilance Data. [PDF]
Pacnejer AM+8 more
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Incidence of Adverse Drug Reactions Among HIV Patients on Antiretroviral Drugs in Ethiopia: A Systematic Review and Meta-Analysis. [PDF]
Endalamew SG+6 more
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Reply: [Post-marketing safety concerns with Lecanemab: a disproportionality analysis using the FDA adverse event reporting system]. [PDF]
Xing X, Wang K, Dong X.
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Adverse events associated with hepatic arterial infusion chemotherapy and its combination therapies in hepatocellular carcinoma: a systematic review. [PDF]
Wu Y+5 more
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Risk comparison of adverse reactions between gemcitabine monotherapy and gemcitabine combined with albumin-bound paclitaxel in pancreatic cancer: insights from the FDA Adverse Event Reporting System (FAERS) database. [PDF]
Jiang P, Zong K, Peng D, Zhou B, Wu Z.
europepmc +1 more source
Exploring the influencing factors of adverse drug reaction reporting among medical personnel: a COM-B model-based study. [PDF]
Cheng W+8 more
europepmc +1 more source
Post-marketing safety surveillance of vortioxetine hydrobromide: a pharmacovigilance study leveraging FAERS database. [PDF]
Zhang Y, Sun S, Ning Y.
europepmc +1 more source