Does PONATINIB Cause Product prescribing error? 51 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 51 reports of Product prescribing error have been filed in association with PONATINIB (Iclusig). This represents 0.5% of all adverse event reports for PONATINIB.
51
Reports of Product prescribing error with PONATINIB
0.5%
of all PONATINIB reports
2
Deaths
7
Hospitalizations
How Dangerous Is Product prescribing error From PONATINIB?
Of the 51 reports, 2 (3.9%) resulted in death, 7 (13.7%) required hospitalization.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PONATINIB. However, 51 reports have been filed with the FAERS database.
What Other Side Effects Does PONATINIB Cause?
Death (1,735)
Off label use (1,071)
Product dose omission issue (817)
Fatigue (687)
Rash (639)
Headache (553)
Pyrexia (542)
Nausea (466)
Hospitalisation (459)
Constipation (435)
What Other Drugs Cause Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which PONATINIB Alternatives Have Lower Product prescribing error Risk?
PONATINIB vs PONATINIB\PONATINIB
PONATINIB vs PONESIMOD
PONATINIB vs PORACTANT ALFA
PONATINIB vs PORFIMER
PONATINIB vs POSACONAZOLE