Does PEXIDARTINIB Cause Product administration error? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product administration error have been filed in association with PEXIDARTINIB (Turalio). This represents 0.5% of all adverse event reports for PEXIDARTINIB.
5
Reports of Product administration error with PEXIDARTINIB
0.5%
of all PEXIDARTINIB reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product administration error From PEXIDARTINIB?
Of the 5 reports, 1 (20.0%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEXIDARTINIB. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does PEXIDARTINIB Cause?
Fatigue (378)
Product dose omission issue (335)
Hair colour changes (327)
Nausea (213)
Pruritus (186)
Aspartate aminotransferase increased (134)
Rash (131)
Off label use (130)
Alanine aminotransferase increased (124)
Diarrhoea (106)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which PEXIDARTINIB Alternatives Have Lower Product administration error Risk?
PEXIDARTINIB vs PHENACETIN
PEXIDARTINIB vs PHENAZOPYRIDINE
PEXIDARTINIB vs PHENCYCLIDINE
PEXIDARTINIB vs PHENELZINE
PEXIDARTINIB vs PHENOBARBITAL