Does VON WILLEBRAND FACTOR Cause Product dose omission issue? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Product dose omission issue have been filed in association with VON WILLEBRAND FACTOR. This represents 4.0% of all adverse event reports for VON WILLEBRAND FACTOR.
9
Reports of Product dose omission issue with VON WILLEBRAND FACTOR
4.0%
of all VON WILLEBRAND FACTOR reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product dose omission issue From VON WILLEBRAND FACTOR?
Of the 9 reports.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VON WILLEBRAND FACTOR. However, 9 reports have been filed with the FAERS database.
What Other Side Effects Does VON WILLEBRAND FACTOR Cause?
No adverse event (41)
Haemorrhage (23)
Product use issue (15)
Epistaxis (14)
Drug ineffective (13)
Haemarthrosis (12)
Off label use (12)
Gastrointestinal haemorrhage (10)
Product reconstitution quality issue (10)
Fall (8)
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)
Which VON WILLEBRAND FACTOR Alternatives Have Lower Product dose omission issue Risk?
VON WILLEBRAND FACTOR vs VON WILLEBRAND FACTOR HUMAN
VON WILLEBRAND FACTOR vs VONOPRAZAN
VON WILLEBRAND FACTOR vs VONOPRAZAN FUMURATE
VON WILLEBRAND FACTOR vs VORAPAXAR
VON WILLEBRAND FACTOR vs VORASIDENIB