Does VOXELOTOR Cause Wrong technique in product usage process? 50 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 50 reports of Wrong technique in product usage process have been filed in association with VOXELOTOR (OXBRYTA). This represents 0.2% of all adverse event reports for VOXELOTOR.
50
Reports of Wrong technique in product usage process with VOXELOTOR
0.2%
of all VOXELOTOR reports
0
Deaths
13
Hospitalizations
How Dangerous Is Wrong technique in product usage process From VOXELOTOR?
Of the 50 reports, 13 (26.0%) required hospitalization, and 2 (4.0%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VOXELOTOR. However, 50 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which VOXELOTOR Alternatives Have Lower Wrong technique in product usage process Risk?
VOXELOTOR vs VUTRISIRAN
VOXELOTOR vs VX-770
VOXELOTOR vs VX-950
VOXELOTOR vs VYVANSE
VOXELOTOR vs WARFARIN