Results 61 to 70 of about 96 (70)
Objectives: This study aims to investigate adverse events (AEs) and adverse drug reactions (ADRs) associated with pirfenidone and nintedanib, two antifibrotic drugs used to treat idiopathic pulmonary fibrosis (IPF).Methods: Reporting odds ratio (ROR) and
Menglin He +4 more
doaj +1 more source
IntroductionAnti-EGFR monoclonal antibodies (mAbs)--cetuximab, panitumumab, and necitumumab--are cornerstone therapies for selected solid tumors but are frequently associated with cutaneous adverse drug reactions (ADRs).
Natalia Sauer +4 more
doaj +1 more source
Background: Anti-β-amyloid monoclonal antibodies provide a disease-modifying treatment approach for Alzheimer’s disease, but post-marketing safety concerns remain, particularly amyloid-related imaging abnormalities (ARIA).
Wei-Yang Xue +6 more
doaj +1 more source
IntroductionEnfortumab vedotin (EV) and Erdafitinib are effective therapeutic drugs for bladder cancer patients following post-chemotherapy and immunotherapy.
Yuanbin Huang +9 more
doaj +1 more source
Hepatocellular carcinoma (HCC) is one of the leading causes of cancer-related mortality, with limited therapeutic options available for advanced stages of the disease.
Zeyu Wang, Jiyao Sheng, Xuewen Zhang
doaj +1 more source
Adverse drug reaction profiles of histone deacetylase inhibitors
The safety and tolerability of histone deacetylase inhibitors (HDACIs) were always a matter of concern. This study aimed to explore the global observational adverse drug reaction (ADR) profiles of the HDACIs: vorinostat, belinostat, panobinostat ...
Ruqayyah Begum +2 more
doaj +1 more source
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Safety study on adverse events of zanubrutinib based on WHO-VigiAccess and FAERS databases
Expert Opinion on Drug Safetyexaly

