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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 PONATINIB Cause Full blood count abnormal? 21 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Full blood count abnormal have been filed in association with PONATINIB (Iclusig). This represents 0.2% of all adverse event reports for PONATINIB.

21
Reports of Full blood count abnormal with PONATINIB
0.2%
of all PONATINIB reports
5
Deaths
11
Hospitalizations

How Dangerous Is Full blood count abnormal From PONATINIB?

Of the 21 reports, 5 (23.8%) resulted in death, 11 (52.4%) required hospitalization, and 1 (4.8%) were considered life-threatening.

Is Full blood count abnormal Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PONATINIB. However, 21 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 Full blood count abnormal?

ALBUTEROL (3,060) PREDNISONE (2,230) BUDESONIDE\FORMOTEROL (1,786) TIOTROPIUM (1,754) MONTELUKAST (1,529) MEPOLIZUMAB (1,440) BUDESONIDE (1,339) PALBOCICLIB (1,146) CICLESONIDE (916) PANTOPRAZOLE (776)

Which PONATINIB Alternatives Have Lower Full blood count abnormal Risk?

PONATINIB vs PONATINIB\PONATINIB PONATINIB vs PONESIMOD PONATINIB vs PORACTANT ALFA PONATINIB vs PORFIMER PONATINIB vs POSACONAZOLE

Related Pages

PONATINIB Full Profile All Full blood count abnormal Reports All Drugs Causing Full blood count abnormal PONATINIB Demographics