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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does SIMEPREVIR Cause Incorrect drug administration duration? 31 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 31 reports of Incorrect drug administration duration have been filed in association with SIMEPREVIR. This represents 0.5% of all adverse event reports for SIMEPREVIR.

31
Reports of Incorrect drug administration duration with SIMEPREVIR
0.5%
of all SIMEPREVIR reports
1
Deaths
3
Hospitalizations

How Dangerous Is Incorrect drug administration duration From SIMEPREVIR?

Of the 31 reports, 1 (3.2%) resulted in death, 3 (9.7%) required hospitalization.

Is Incorrect drug administration duration Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SIMEPREVIR. However, 31 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 Incorrect drug administration duration?

ETONOGESTREL (1,796) POLYETHYLENE GLYCOL 3350 (1,722) NAPROXEN (1,272) DOCOSANOL (803) ETHINYL ESTRADIOL\ETONOGESTREL (740) NICOTINE (561) RANITIDINE (504) GUAIFENESIN (490) INSULIN LISPRO (367) ACETAMINOPHEN (340)

Which SIMEPREVIR Alternatives Have Lower Incorrect drug administration duration Risk?

SIMEPREVIR vs SIMPONI SIMEPREVIR vs SIMVASTATIN SIMEPREVIR vs SINGULAIR SIMEPREVIR vs SINTILIMAB SIMEPREVIR vs SIPONIMOD

Related Pages

SIMEPREVIR Full Profile All Incorrect drug administration duration Reports All Drugs Causing Incorrect drug administration duration SIMEPREVIR Demographics