Does SIMEPREVIR Cause Product quality issue? 26 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 26 reports of Product quality issue have been filed in association with SIMEPREVIR. This represents 0.4% of all adverse event reports for SIMEPREVIR.
26
Reports of Product quality issue with SIMEPREVIR
0.4%
of all SIMEPREVIR reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product quality issue From SIMEPREVIR?
Of the 26 reports, 1 (3.8%) required hospitalization.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SIMEPREVIR. However, 26 reports have been filed with the FAERS database.
What Other Side Effects Does SIMEPREVIR Cause?
Off label use (1,166)
Anaemia (999)
Platelet count decreased (833)
White blood cell count decreased (581)
Hepatitis c (537)
Blood bilirubin increased (467)
Drug ineffective (440)
Pyrexia (429)
Rash (388)
Haemoglobin decreased (385)
What Other Drugs Cause Product quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which SIMEPREVIR Alternatives Have Lower Product quality issue Risk?
SIMEPREVIR vs SIMPONI
SIMEPREVIR vs SIMVASTATIN
SIMEPREVIR vs SINGULAIR
SIMEPREVIR vs SINTILIMAB
SIMEPREVIR vs SIPONIMOD