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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 Hypersomnia? 100 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 100 reports of Hypersomnia have been filed in association with TROFINETIDE (Daybue). This represents 2.1% of all adverse event reports for TROFINETIDE.

100
Reports of Hypersomnia with TROFINETIDE
2.1%
of all TROFINETIDE reports
1
Deaths
14
Hospitalizations

How Dangerous Is Hypersomnia From TROFINETIDE?

Of the 100 reports, 1 (1.0%) resulted in death, 14 (14.0%) required hospitalization.

Is Hypersomnia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TROFINETIDE. However, 100 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 Hypersomnia?

PIMAVANSERIN (602) ADALIMUMAB (467) LENALIDOMIDE (401) QUETIAPINE (394) PREGABALIN (347) TREPROSTINIL (317) RISPERIDONE (302) ARIPIPRAZOLE (286) DULOXETINE (285) OXYCODONE (280)

Which TROFINETIDE Alternatives Have Lower Hypersomnia Risk?

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

Related Pages

TROFINETIDE Full Profile All Hypersomnia Reports All Drugs Causing Hypersomnia TROFINETIDE Demographics