Does RESMETIROM Cause Condition aggravated? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Condition aggravated have been filed in association with RESMETIROM (REZDIFFRA). This represents 1.3% of all adverse event reports for RESMETIROM.
11
Reports of Condition aggravated with RESMETIROM
1.3%
of all RESMETIROM reports
0
Deaths
1
Hospitalizations
How Dangerous Is Condition aggravated From RESMETIROM?
Of the 11 reports, 1 (9.1%) required hospitalization.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RESMETIROM. However, 11 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 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 RESMETIROM Alternatives Have Lower Condition aggravated Risk?
RESMETIROM vs RESTASIS
RESMETIROM vs RETINOL
RESMETIROM vs REVATIO
RESMETIROM vs REVEFENACIN
RESMETIROM vs REVLIMID