Does FEZOLINETANT Cause Intentional product use issue? 19 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Intentional product use issue have been filed in association with FEZOLINETANT (VEOZAH). This represents 1.4% of all adverse event reports for FEZOLINETANT.
19
Reports of Intentional product use issue with FEZOLINETANT
1.4%
of all FEZOLINETANT reports
1
Deaths
1
Hospitalizations
How Dangerous Is Intentional product use issue From FEZOLINETANT?
Of the 19 reports, 1 (5.3%) resulted in death, 1 (5.3%) required hospitalization.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FEZOLINETANT. However, 19 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which FEZOLINETANT Alternatives Have Lower Intentional product use issue Risk?
FEZOLINETANT vs FIBRINOGEN HUMAN
FEZOLINETANT vs FIBRINOGEN HUMAN\HUMAN THROMBIN
FEZOLINETANT vs FIBRINOGEN HUMAN\THROMBIN HUMAN
FEZOLINETANT vs FIDAXOMICIN
FEZOLINETANT vs FILGOTINIB