Does FEZOLINETANT Cause Wrong technique in product usage process? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Wrong technique in product usage process have been filed in association with FEZOLINETANT (VEOZAH). This represents 1.3% of all adverse event reports for FEZOLINETANT.
18
Reports of Wrong technique in product usage process with FEZOLINETANT
1.3%
of all FEZOLINETANT reports
0
Deaths
0
Hospitalizations
How Dangerous Is Wrong technique in product usage process From FEZOLINETANT?
Of the 18 reports.
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 FEZOLINETANT. However, 18 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 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 FEZOLINETANT Alternatives Have Lower Wrong technique in product usage process Risk?
FEZOLINETANT vs FIBRINOGEN HUMAN
FEZOLINETANT vs FIBRINOGEN HUMAN\HUMAN THROMBIN
FEZOLINETANT vs FIBRINOGEN HUMAN\THROMBIN HUMAN
FEZOLINETANT vs FIDAXOMICIN
FEZOLINETANT vs FILGOTINIB