Does TROFINETIDE Cause Device dislocation? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Device dislocation have been filed in association with TROFINETIDE (Daybue). This represents 0.2% of all adverse event reports for TROFINETIDE.
8
Reports of Device dislocation with TROFINETIDE
0.2%
of all TROFINETIDE reports
0
Deaths
6
Hospitalizations
How Dangerous Is Device dislocation From TROFINETIDE?
Of the 8 reports, 6 (75.0%) required hospitalization.
Is Device dislocation 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 Device dislocation?
LEVONORGESTREL (13,757)
COPPER (6,955)
CARBIDOPA\LEVODOPA (2,937)
ETONOGESTREL (2,909)
TREPROSTINIL (1,626)
MIRENA (677)
BACLOFEN (492)
PARAGARD 380A (479)
ADALIMUMAB (372)
EPOPROSTENOL (358)
Which TROFINETIDE Alternatives Have Lower Device dislocation Risk?
TROFINETIDE vs TROFOSFAMIDE
TROFINETIDE vs TROPATEPINE
TROFINETIDE vs TROPICAMIDE
TROFINETIDE vs TROSPIUM
TROFINETIDE vs TROSPIUM\XANOMELINE