Does VOXELOTOR Cause Product administration interrupted? 33 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 33 reports of Product administration interrupted have been filed in association with VOXELOTOR (OXBRYTA). This represents 0.2% of all adverse event reports for VOXELOTOR.
33
Reports of Product administration interrupted with VOXELOTOR
0.2%
of all VOXELOTOR reports
0
Deaths
17
Hospitalizations
How Dangerous Is Product administration interrupted From VOXELOTOR?
Of the 33 reports, 17 (51.5%) required hospitalization.
Is Product administration interrupted Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VOXELOTOR. However, 33 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 administration interrupted?
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (1,446)
SODIUM OXYBATE (1,272)
CANNABIDIOL (511)
ISOTRETINOIN (503)
APREMILAST (314)
TREPROSTINIL (295)
EPOPROSTENOL (205)
LENALIDOMIDE (146)
ETANERCEPT (142)
INTERFERON BETA-1A (115)
Which VOXELOTOR Alternatives Have Lower Product administration interrupted Risk?
VOXELOTOR vs VUTRISIRAN
VOXELOTOR vs VX-770
VOXELOTOR vs VX-950
VOXELOTOR vs VYVANSE
VOXELOTOR vs WARFARIN