Does VONICOG ALFA Cause Product dose omission issue? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product dose omission issue have been filed in association with VONICOG ALFA. This represents 7.1% of all adverse event reports for VONICOG ALFA.
7
Reports of Product dose omission issue with VONICOG ALFA
7.1%
of all VONICOG ALFA reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product dose omission issue From VONICOG ALFA?
Of the 7 reports, 3 (42.9%) required hospitalization.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VONICOG ALFA. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does VONICOG ALFA Cause?
Off label use (27)
Epistaxis (17)
Haemorrhage (16)
Gastrointestinal haemorrhage (12)
No adverse event (11)
Fall (9)
Haemarthrosis (9)
Pain (8)
Drug ineffective (7)
Fatigue (7)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)