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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 product storage? 11 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Incorrect product storage have been filed in association with SIMEPREVIR. This represents 0.2% of all adverse event reports for SIMEPREVIR.

11
Reports of Incorrect product storage with SIMEPREVIR
0.2%
of all SIMEPREVIR reports
0
Deaths
0
Hospitalizations

How Dangerous Is Incorrect product storage From SIMEPREVIR?

Of the 11 reports.

Is Incorrect product storage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SIMEPREVIR. However, 11 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 product storage?

ETANERCEPT (2,149) INSULIN LISPRO (1,114) ABATACEPT (583) TERIPARATIDE (573) ADALIMUMAB (476) GOLIMUMAB (392) INSULIN GLARGINE (341) INSULIN HUMAN (336) USTEKINUMAB (299) ERYTHROPOIETIN (268)

Which SIMEPREVIR Alternatives Have Lower Incorrect product storage Risk?

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

Related Pages

SIMEPREVIR Full Profile All Incorrect product storage Reports All Drugs Causing Incorrect product storage SIMEPREVIR Demographics