Does VOXELOTOR Cause Product use complaint? 298 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 298 reports of Product use complaint have been filed in association with VOXELOTOR (OXBRYTA). This represents 1.4% of all adverse event reports for VOXELOTOR.
298
Reports of Product use complaint with VOXELOTOR
1.4%
of all VOXELOTOR reports
3
Deaths
62
Hospitalizations
How Dangerous Is Product use complaint From VOXELOTOR?
Of the 298 reports, 3 (1.0%) resulted in death, 62 (20.8%) required hospitalization, and 1 (0.3%) were considered life-threatening.
Is Product use complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VOXELOTOR. However, 298 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 use complaint?
TROFINETIDE (472)
ENZALUTAMIDE (336)
LIFITEGRAST (326)
CLASCOTERONE (285)
NIRMATRELVIR\RITONAVIR (248)
ABALOPARATIDE (224)
ESTRADIOL (208)
MOLNUPIRAVIR (206)
ACETAMINOPHEN (202)
DIMETHICONE\LOPERAMIDE (201)
Which VOXELOTOR Alternatives Have Lower Product use complaint Risk?
VOXELOTOR vs VUTRISIRAN
VOXELOTOR vs VX-770
VOXELOTOR vs VX-950
VOXELOTOR vs VYVANSE
VOXELOTOR vs WARFARIN