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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 Underdose? 1,540 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 1,540 reports of Underdose have been filed in association with TROFINETIDE (Daybue). This represents 32.3% of all adverse event reports for TROFINETIDE.

1,540
Reports of Underdose with TROFINETIDE
32.3%
of all TROFINETIDE reports
2
Deaths
204
Hospitalizations

How Dangerous Is Underdose From TROFINETIDE?

Of the 1,540 reports, 2 (0.1%) resulted in death, 204 (13.2%) required hospitalization, and 1 (0.1%) were considered life-threatening.

Is Underdose Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TROFINETIDE. However, 1,540 reports have been filed with the FAERS database.

What Other Side Effects Does TROFINETIDE Cause?

Diarrhoea (2,684) Vomiting (870) Product dose omission issue (710) Seizure (603) Constipation (523) Product use complaint (472) Weight decreased (433) Drug ineffective (367) Decreased appetite (331) Intentional dose omission (324)

What Other Drugs Cause Underdose?

ADAPALENE (5,192) AVOBENZONE\OCTISALATE\OCTOCRYLENE (3,722) INSULIN LISPRO (3,156) ETANERCEPT (3,145) GALCANEZUMAB-GNLM (2,909) ENZALUTAMIDE (2,017) FLUTICASONE\SALMETEROL (1,600) ALBUTEROL (1,593) EXENATIDE (1,571) EVOLOCUMAB (1,398)

Which TROFINETIDE Alternatives Have Lower Underdose Risk?

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

Related Pages

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