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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 CATEQUENTINIB Cause Product use issue? 12 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Product use issue have been filed in association with CATEQUENTINIB. This represents 3.7% of all adverse event reports for CATEQUENTINIB.

12
Reports of Product use issue with CATEQUENTINIB
3.7%
of all CATEQUENTINIB reports
1
Deaths
9
Hospitalizations

How Dangerous Is Product use issue From CATEQUENTINIB?

Of the 12 reports, 1 (8.3%) resulted in death, 9 (75.0%) required hospitalization, and 1 (8.3%) were considered life-threatening.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CATEQUENTINIB. However, 12 reports have been filed with the FAERS database.

What Other Side Effects Does CATEQUENTINIB Cause?

Myelosuppression (84) Off label use (37) Diarrhoea (33) Hypertension (26) Nausea (26) Vomiting (26) Rash (25) Thrombocytopenia (24) Fatigue (23) Anaemia (22)

What Other Drugs Cause Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Which CATEQUENTINIB Alternatives Have Lower Product use issue Risk?

CATEQUENTINIB vs CC-4047 CATEQUENTINIB vs CEDAZURIDINE\DECITABINE CATEQUENTINIB vs CEDIRANIB CATEQUENTINIB vs CEFACLOR CATEQUENTINIB vs CEFADROXIL

Related Pages

CATEQUENTINIB Full Profile All Product use issue Reports All Drugs Causing Product use issue CATEQUENTINIB Demographics