Does TROFINETIDE Cause Intentional dose omission? 324 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 324 reports of Intentional dose omission have been filed in association with TROFINETIDE (Daybue). This represents 6.8% of all adverse event reports for TROFINETIDE.
324
Reports of Intentional dose omission with TROFINETIDE
6.8%
of all TROFINETIDE reports
0
Deaths
39
Hospitalizations
How Dangerous Is Intentional dose omission From TROFINETIDE?
Of the 324 reports, 39 (12.0%) required hospitalization.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TROFINETIDE. However, 324 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 Intentional dose omission?
DUPILUMAB (2,269)
CERTOLIZUMAB PEGOL (1,253)
ADALIMUMAB (845)
TOFACITINIB (845)
INFLIXIMAB (815)
ABALOPARATIDE (623)
ETANERCEPT (615)
AMBRISENTAN (595)
SODIUM OXYBATE (580)
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)
Which TROFINETIDE Alternatives Have Lower Intentional dose omission Risk?
TROFINETIDE vs TROFOSFAMIDE
TROFINETIDE vs TROPATEPINE
TROFINETIDE vs TROPICAMIDE
TROFINETIDE vs TROSPIUM
TROFINETIDE vs TROSPIUM\XANOMELINE