Does SIMEPREVIR Cause Haemoglobin decreased? 385 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 385 reports of Haemoglobin decreased have been filed in association with SIMEPREVIR. This represents 6.4% of all adverse event reports for SIMEPREVIR.
385
Reports of Haemoglobin decreased with SIMEPREVIR
6.4%
of all SIMEPREVIR reports
10
Deaths
62
Hospitalizations
How Dangerous Is Haemoglobin decreased From SIMEPREVIR?
Of the 385 reports, 10 (2.6%) resulted in death, 62 (16.1%) required hospitalization, and 3 (0.8%) were considered life-threatening.
Is Haemoglobin decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SIMEPREVIR. However, 385 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)
Pruritus (341)
What Other Drugs Cause Haemoglobin decreased?
LENALIDOMIDE (4,031)
RUXOLITINIB (3,297)
ECULIZUMAB (3,028)
ADALIMUMAB (2,459)
CLOZAPINE (2,396)
RITUXIMAB (1,803)
APIXABAN (1,779)
NIRAPARIB (1,759)
METHOTREXATE (1,754)
RIBAVIRIN (1,753)
Which SIMEPREVIR Alternatives Have Lower Haemoglobin decreased Risk?
SIMEPREVIR vs SIMPONI
SIMEPREVIR vs SIMVASTATIN
SIMEPREVIR vs SINGULAIR
SIMEPREVIR vs SINTILIMAB
SIMEPREVIR vs SIPONIMOD