Does VOXELOTOR Cause Intentional product use issue? 80 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 80 reports of Intentional product use issue have been filed in association with VOXELOTOR (OXBRYTA). This represents 0.4% of all adverse event reports for VOXELOTOR.
80
Reports of Intentional product use issue with VOXELOTOR
0.4%
of all VOXELOTOR reports
0
Deaths
11
Hospitalizations
How Dangerous Is Intentional product use issue From VOXELOTOR?
Of the 80 reports, 11 (13.8%) required hospitalization, and 1 (1.3%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VOXELOTOR. However, 80 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which VOXELOTOR Alternatives Have Lower Intentional product use issue Risk?
VOXELOTOR vs VUTRISIRAN
VOXELOTOR vs VX-770
VOXELOTOR vs VX-950
VOXELOTOR vs VYVANSE
VOXELOTOR vs WARFARIN