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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 Condition aggravated? 92 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 92 reports of Condition aggravated have been filed in association with SIMEPREVIR. This represents 1.5% of all adverse event reports for SIMEPREVIR.

92
Reports of Condition aggravated with SIMEPREVIR
1.5%
of all SIMEPREVIR reports
8
Deaths
14
Hospitalizations

How Dangerous Is Condition aggravated From SIMEPREVIR?

Of the 92 reports, 8 (8.7%) resulted in death, 14 (15.2%) required hospitalization, and 1 (1.1%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SIMEPREVIR. However, 92 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 Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which SIMEPREVIR Alternatives Have Lower Condition aggravated Risk?

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

Related Pages

SIMEPREVIR Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated SIMEPREVIR Demographics