Does TROFINETIDE Cause Product use complaint? 472 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 472 reports of Product use complaint have been filed in association with TROFINETIDE (Daybue). This represents 9.9% of all adverse event reports for TROFINETIDE.
472
Reports of Product use complaint with TROFINETIDE
9.9%
of all TROFINETIDE reports
1
Deaths
42
Hospitalizations
How Dangerous Is Product use complaint From TROFINETIDE?
Of the 472 reports, 1 (0.2%) resulted in death, 42 (8.9%) required hospitalization.
Is Product use complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TROFINETIDE. However, 472 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)
Weight decreased (433)
Drug ineffective (367)
Decreased appetite (331)
Intentional dose omission (324)
What Other Drugs Cause Product use complaint?
ENZALUTAMIDE (336)
LIFITEGRAST (326)
VOXELOTOR (298)
CLASCOTERONE (285)
NIRMATRELVIR\RITONAVIR (248)
ABALOPARATIDE (224)
ESTRADIOL (208)
MOLNUPIRAVIR (206)
ACETAMINOPHEN (202)
DIMETHICONE\LOPERAMIDE (201)
Which TROFINETIDE Alternatives Have Lower Product use complaint Risk?
TROFINETIDE vs TROFOSFAMIDE
TROFINETIDE vs TROPATEPINE
TROFINETIDE vs TROPICAMIDE
TROFINETIDE vs TROSPIUM
TROFINETIDE vs TROSPIUM\XANOMELINE