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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 FEZOLINETANT Cause Condition aggravated? 34 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 34 reports of Condition aggravated have been filed in association with FEZOLINETANT (VEOZAH). This represents 2.4% of all adverse event reports for FEZOLINETANT.

34
Reports of Condition aggravated with FEZOLINETANT
2.4%
of all FEZOLINETANT reports
0
Deaths
0
Hospitalizations

How Dangerous Is Condition aggravated From FEZOLINETANT?

Of the 34 reports.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for FEZOLINETANT. However, 34 reports have been filed with the FAERS database.

What Other Side Effects Does FEZOLINETANT Cause?

Drug ineffective (184) Alanine aminotransferase increased (139) Hepatic enzyme increased (129) Aspartate aminotransferase increased (104) Off label use (84) Headache (78) Hot flush (77) Insomnia (75) Liver function test increased (70) Nausea (65)

What Other Drugs Cause Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which FEZOLINETANT Alternatives Have Lower Condition aggravated Risk?

FEZOLINETANT vs FIBRINOGEN HUMAN FEZOLINETANT vs FIBRINOGEN HUMAN\HUMAN THROMBIN FEZOLINETANT vs FIBRINOGEN HUMAN\THROMBIN HUMAN FEZOLINETANT vs FIDAXOMICIN FEZOLINETANT vs FILGOTINIB

Related Pages

FEZOLINETANT Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated FEZOLINETANT Demographics