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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does AVAPRITINIB Cause Product dose omission in error? 110 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 110 reports of Product dose omission in error have been filed in association with AVAPRITINIB (Ayvakit). This represents 1.1% of all adverse event reports for AVAPRITINIB.

110
Reports of Product dose omission in error with AVAPRITINIB
1.1%
of all AVAPRITINIB reports
0
Deaths
5
Hospitalizations

How Dangerous Is Product dose omission in error From AVAPRITINIB?

Of the 110 reports, 5 (4.5%) required hospitalization, and 1 (0.9%) were considered life-threatening.

Is Product dose omission in error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AVAPRITINIB. However, 110 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 in error?

DUPILUMAB (7,586) TOFACITINIB (2,461) LENALIDOMIDE (618) PALBOCICLIB (592) DIROXIMEL (481) ABALOPARATIDE (457) NIRAPARIB (428) RUXOLITINIB (425) TERIFLUNOMIDE (371) DIMETHYL (308)

Which AVAPRITINIB Alternatives Have Lower Product dose omission in error Risk?

AVAPRITINIB vs AVASTIN AVAPRITINIB vs AVATROMBOPAG AVAPRITINIB vs AVELOX AVAPRITINIB vs AVELUMAB AVAPRITINIB vs AVIBACTAM

Related Pages

AVAPRITINIB Full Profile All Product dose omission in error Reports All Drugs Causing Product dose omission in error AVAPRITINIB Demographics