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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 Respiration abnormal? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Respiration abnormal have been filed in association with TROFINETIDE (Daybue). This represents 0.2% of all adverse event reports for TROFINETIDE.

8
Reports of Respiration abnormal with TROFINETIDE
0.2%
of all TROFINETIDE reports
0
Deaths
4
Hospitalizations

How Dangerous Is Respiration abnormal From TROFINETIDE?

Of the 8 reports, 4 (50.0%) required hospitalization.

Is Respiration abnormal Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TROFINETIDE. However, 8 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 Respiration abnormal?

TREPROSTINIL (444) DUPILUMAB (387) ALBUTEROL (296) TIOTROPIUM (203) IVACAFTOR\LUMACAFTOR (191) MEPOLIZUMAB (182) AMBRISENTAN (174) FLUTICASONE\SALMETEROL (159) TADALAFIL (153) MONTELUKAST (146)

Which TROFINETIDE Alternatives Have Lower Respiration abnormal Risk?

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

Related Pages

TROFINETIDE Full Profile All Respiration abnormal Reports All Drugs Causing Respiration abnormal TROFINETIDE Demographics