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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 Incorrect dose administered? 98 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 98 reports of Incorrect dose administered have been filed in association with TROFINETIDE (Daybue). This represents 2.1% of all adverse event reports for TROFINETIDE.

98
Reports of Incorrect dose administered with TROFINETIDE
2.1%
of all TROFINETIDE reports
0
Deaths
12
Hospitalizations

How Dangerous Is Incorrect dose administered From TROFINETIDE?

Of the 98 reports, 12 (12.2%) required hospitalization.

Is Incorrect dose administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TROFINETIDE. However, 98 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 Incorrect dose administered?

TIRZEPATIDE (23,301) ADALIMUMAB (14,000) DUPILUMAB (9,907) RANITIDINE (9,337) INSULIN LISPRO (8,318) ACETAMINOPHEN (5,316) DULAGLUTIDE (5,207) SECUKINUMAB (4,524) INSULIN GLARGINE (3,070) SOMATROPIN (2,772)

Which TROFINETIDE Alternatives Have Lower Incorrect dose administered Risk?

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

Related Pages

TROFINETIDE Full Profile All Incorrect dose administered Reports All Drugs Causing Incorrect dose administered TROFINETIDE Demographics