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A pharmacovigilance study assessing risk of angioedema with angiotensin receptor blockers using the US FDA adverse event reporting system.

Kannan SridharanGowri Sivaramakrishnan
Published in: Expert opinion on drug safety (2024)
This pharmacovigilance study using AERS highlights potential higher risks of angioedema with losartan and irbesartan compared to other ARBs, warranting validation through prospective epidemiological studies to characterize individual ARB safety profiles.
Keyphrases
  • angiotensin converting enzyme
  • adverse drug
  • angiotensin ii
  • human health
  • drug induced
  • electronic health record
  • emergency department
  • risk assessment
  • binding protein