Does TROFINETIDE Cause Prescribed underdose? 253 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 253 reports of Prescribed underdose have been filed in association with TROFINETIDE (Daybue). This represents 5.3% of all adverse event reports for TROFINETIDE.
253
Reports of Prescribed underdose with TROFINETIDE
5.3%
of all TROFINETIDE reports
0
Deaths
38
Hospitalizations
How Dangerous Is Prescribed underdose From TROFINETIDE?
Of the 253 reports, 38 (15.0%) required hospitalization.
Is Prescribed underdose Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TROFINETIDE. However, 253 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 Prescribed underdose?
NATALIZUMAB (2,162)
SACUBITRIL\VALSARTAN (1,864)
APIXABAN (1,469)
ABATACEPT (1,192)
PIMAVANSERIN (1,165)
FINGOLIMOD (1,114)
RITUXIMAB (1,067)
METHOTREXATE (1,066)
ADALIMUMAB (1,010)
TOCILIZUMAB (1,002)
Which TROFINETIDE Alternatives Have Lower Prescribed underdose Risk?
TROFINETIDE vs TROFOSFAMIDE
TROFINETIDE vs TROPATEPINE
TROFINETIDE vs TROPICAMIDE
TROFINETIDE vs TROSPIUM
TROFINETIDE vs TROSPIUM\XANOMELINE