Does VOXELOTOR Cause Product dose omission? 151 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 151 reports of Product dose omission have been filed in association with VOXELOTOR (OXBRYTA). This represents 0.7% of all adverse event reports for VOXELOTOR.
151
Reports of Product dose omission with VOXELOTOR
0.7%
of all VOXELOTOR reports
1
Deaths
71
Hospitalizations
How Dangerous Is Product dose omission From VOXELOTOR?
Of the 151 reports, 1 (0.7%) resulted in death, 71 (47.0%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VOXELOTOR. However, 151 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?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which VOXELOTOR Alternatives Have Lower Product dose omission Risk?
VOXELOTOR vs VUTRISIRAN
VOXELOTOR vs VX-770
VOXELOTOR vs VX-950
VOXELOTOR vs VYVANSE
VOXELOTOR vs WARFARIN