Does PONATINIB Cause Wrong technique in product usage process? 28 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Wrong technique in product usage process have been filed in association with PONATINIB (Iclusig). This represents 0.3% of all adverse event reports for PONATINIB.
28
Reports of Wrong technique in product usage process with PONATINIB
0.3%
of all PONATINIB reports
10
Deaths
17
Hospitalizations
How Dangerous Is Wrong technique in product usage process From PONATINIB?
Of the 28 reports, 10 (35.7%) resulted in death, 17 (60.7%) required hospitalization, and 1 (3.6%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PONATINIB. However, 28 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which PONATINIB Alternatives Have Lower Wrong technique in product usage process Risk?
PONATINIB vs PONATINIB\PONATINIB
PONATINIB vs PONESIMOD
PONATINIB vs PORACTANT ALFA
PONATINIB vs PORFIMER
PONATINIB vs POSACONAZOLE