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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does TROFINETIDE Cause Complication associated with device? 15 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Complication associated with device have been filed in association with TROFINETIDE (Daybue). This represents 0.3% of all adverse event reports for TROFINETIDE.

15
Reports of Complication associated with device with TROFINETIDE
0.3%
of all TROFINETIDE reports
0
Deaths
11
Hospitalizations

How Dangerous Is Complication associated with device From TROFINETIDE?

Of the 15 reports, 11 (73.3%) required hospitalization.

Is Complication associated with device Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TROFINETIDE. However, 15 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 Complication associated with device?

ETONOGESTREL (6,047) COPPER (1,083) BACLOFEN (525) TREPROSTINIL (422) EPOPROSTENOL (399) LEVONORGESTREL (344) ADALIMUMAB (269) CARBIDOPA\LEVODOPA (169) MACITENTAN (169) TEDUGLUTIDE (133)

Which TROFINETIDE Alternatives Have Lower Complication associated with device Risk?

TROFINETIDE vs TROFOSFAMIDE TROFINETIDE vs TROPATEPINE TROFINETIDE vs TROPICAMIDE TROFINETIDE vs TROSPIUM TROFINETIDE vs TROSPIUM\XANOMELINE

Related Pages

TROFINETIDE Full Profile All Complication associated with device Reports All Drugs Causing Complication associated with device TROFINETIDE Demographics