Does TROFINETIDE Cause Off label use? 36 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 36 reports of Off label use have been filed in association with TROFINETIDE (Daybue). This represents 0.8% of all adverse event reports for TROFINETIDE.
36
Reports of Off label use with TROFINETIDE
0.8%
of all TROFINETIDE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Off label use From TROFINETIDE?
Of the 36 reports, 2 (5.6%) required hospitalization.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TROFINETIDE. However, 36 reports have been filed with the FAERS database.
What Other Side Effects Does TROFINETIDE Cause?
Diarrhoea (2,684)
Underdose (1,540)
Vomiting (870)
Product dose omission issue (710)
Seizure (603)
Constipation (523)
Product use complaint (472)
Weight decreased (433)
Drug ineffective (367)
Decreased appetite (331)
What Other Drugs Cause Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)
Which TROFINETIDE Alternatives Have Lower Off label use Risk?
TROFINETIDE vs TROFOSFAMIDE
TROFINETIDE vs TROPATEPINE
TROFINETIDE vs TROPICAMIDE
TROFINETIDE vs TROSPIUM
TROFINETIDE vs TROSPIUM\XANOMELINE