Does AVUTOMETINIB\DEFACTINIB Cause Product dose omission issue? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product dose omission issue have been filed in association with AVUTOMETINIB\DEFACTINIB. This represents 9.2% of all adverse event reports for AVUTOMETINIB\DEFACTINIB.
7
Reports of Product dose omission issue with AVUTOMETINIB\DEFACTINIB
9.2%
of all AVUTOMETINIB\DEFACTINIB reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product dose omission issue From AVUTOMETINIB\DEFACTINIB?
Of the 7 reports.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AVUTOMETINIB\DEFACTINIB. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does AVUTOMETINIB\DEFACTINIB Cause?
Nausea (17)
Fatigue (13)
Diarrhoea (10)
Off label use (9)
Vomiting (9)
Visual impairment (8)
Vision blurred (7)
Blood creatine phosphokinase increased (6)
Peripheral swelling (5)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)