Does RESMETIROM Cause Unevaluable event? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Unevaluable event have been filed in association with RESMETIROM (REZDIFFRA). This represents 1.4% of all adverse event reports for RESMETIROM.
12
Reports of Unevaluable event with RESMETIROM
1.4%
of all RESMETIROM reports
0
Deaths
0
Hospitalizations
How Dangerous Is Unevaluable event From RESMETIROM?
Of the 12 reports.
Is Unevaluable event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RESMETIROM. However, 12 reports have been filed with the FAERS database.
What Other Side Effects Does RESMETIROM Cause?
Diarrhoea (182)
Nausea (162)
Pruritus (147)
Alanine aminotransferase increased (98)
Aspartate aminotransferase increased (97)
Fatigue (72)
Abdominal pain upper (69)
Dizziness (68)
Vomiting (60)
Weight decreased (47)
What Other Drugs Cause Unevaluable event?
ADALIMUMAB (4,242)
ETANERCEPT (3,902)
LENALIDOMIDE (3,331)
OXYCODONE (3,145)
AMBRISENTAN (2,336)
SODIUM OXYBATE (2,328)
CARBIDOPA\LEVODOPA (1,632)
DUPILUMAB (1,410)
MORPHINE (1,161)
ACETAMINOPHEN\HYDROCODONE (1,118)
Which RESMETIROM Alternatives Have Lower Unevaluable event Risk?
RESMETIROM vs RESTASIS
RESMETIROM vs RETINOL
RESMETIROM vs REVATIO
RESMETIROM vs REVEFENACIN
RESMETIROM vs REVLIMID