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Evaluating Post-Market Adverse Events of The New Hepatitis C Therapies Using FEARS Data.

Majed Ahmed Algarni
Published in: Healthcare (Basel, Switzerland) (2022)
Depending on the FDA Adverse Events Reporting System (FAERS) database, most of the non-serious adverse effects were headache and fatigue. There was no significant difference in cases of death reported while using both drugs. Liver cancer was more reported while using Harvoni. Hospitalization was more reported while using Mavyret.
Keyphrases
  • adverse drug
  • electronic health record
  • health insurance
  • sleep quality
  • depressive symptoms
  • physical activity