Does VOXELOTOR Cause Product dose omission in error? 96 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 96 reports of Product dose omission in error have been filed in association with VOXELOTOR (OXBRYTA). This represents 0.4% of all adverse event reports for VOXELOTOR.
96
Reports of Product dose omission in error with VOXELOTOR
0.4%
of all VOXELOTOR reports
0
Deaths
36
Hospitalizations
How Dangerous Is Product dose omission in error From VOXELOTOR?
Of the 96 reports, 36 (37.5%) required hospitalization.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VOXELOTOR. However, 96 reports have been filed with the FAERS database.
What Other Side Effects Does VOXELOTOR Cause?
Sickle cell anaemia with crisis (11,023)
Product dose omission issue (5,122)
Diarrhoea (3,173)
Off label use (2,364)
Nausea (2,003)
Headache (1,683)
Abdominal pain upper (1,165)
Pain (1,059)
Therapy cessation (1,038)
Fatigue (1,004)
What Other Drugs Cause Product dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which VOXELOTOR Alternatives Have Lower Product dose omission in error Risk?
VOXELOTOR vs VUTRISIRAN
VOXELOTOR vs VX-770
VOXELOTOR vs VX-950
VOXELOTOR vs VYVANSE
VOXELOTOR vs WARFARIN