Does AVAPRITINIB Cause Product dose omission? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product dose omission have been filed in association with AVAPRITINIB (Ayvakit). This represents 0.1% of all adverse event reports for AVAPRITINIB.
6
Reports of Product dose omission with AVAPRITINIB
0.1%
of all AVAPRITINIB reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product dose omission From AVAPRITINIB?
Of the 6 reports.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AVAPRITINIB. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does AVAPRITINIB Cause?
Fatigue (1,527)
Off label use (1,138)
Nausea (1,033)
Diarrhoea (886)
Swelling face (481)
Memory impairment (467)
Dizziness (458)
Vomiting (456)
Headache (454)
Asthenia (433)
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 AVAPRITINIB Alternatives Have Lower Product dose omission Risk?
AVAPRITINIB vs AVASTIN
AVAPRITINIB vs AVATROMBOPAG
AVAPRITINIB vs AVELOX
AVAPRITINIB vs AVELUMAB
AVAPRITINIB vs AVIBACTAM