Does BOCEPREVIR Cause Haemoglobin decreased? 99 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 99 reports of Haemoglobin decreased have been filed in association with BOCEPREVIR. This represents 4.8% of all adverse event reports for BOCEPREVIR.
99
Reports of Haemoglobin decreased with BOCEPREVIR
4.8%
of all BOCEPREVIR reports
5
Deaths
20
Hospitalizations
How Dangerous Is Haemoglobin decreased From BOCEPREVIR?
Of the 99 reports, 5 (5.1%) resulted in death, 20 (20.2%) required hospitalization, and 1 (1.0%) 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 BOCEPREVIR. However, 99 reports have been filed with the FAERS database.
What Other Side Effects Does BOCEPREVIR Cause?
Anaemia (555)
Fatigue (316)
Nausea (283)
Neutropenia (201)
Rash (177)
Headache (158)
Thrombocytopenia (154)
Vomiting (153)
Dysgeusia (148)
Diarrhoea (137)
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 BOCEPREVIR Alternatives Have Lower Haemoglobin decreased Risk?
BOCEPREVIR vs BOCOCIZUMAB
BOCEPREVIR vs BONIVA
BOCEPREVIR vs BONVIVA
BOCEPREVIR vs BORAGE OIL
BOCEPREVIR vs BORIC ACID