Postmarketing surveillance of simeprevir and sofosbuvir using FDA adverse event database (FAERS).

Trial Profile

Postmarketing surveillance of simeprevir and sofosbuvir using FDA adverse event database (FAERS).

Completed
Phase of Trial: Phase IV

Latest Information Update: 14 Dec 2015

At a glance

  • Drugs Simeprevir (Primary) ; Sofosbuvir (Primary)
  • Indications Hepatitis C
  • Focus Adverse reactions
  • Most Recent Events

    No Data Available
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