Fluid retention-associated adverse events in patients treated with BCR::ABL1 inhibitors based on FDA Adverse Event Reporting System (FAERS): a retrospective pharmacovigilance study
Conclusions
This pharmacovigilance study serves as a clinical reminder to physicians to be more vigilant for fluid retention-associated AEs with BCR::ABL inhibitors.
Source: BMJ Open - Category: General Medicine Authors: Huang, J., Cai, J., Ye, Q., Jiang, Q., Lin, H., Wu, L. Tags: Open access, Pharmacology and therapeutics Source Type: research
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