Does TROFINETIDE Cause Wrong technique in product usage process? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Wrong technique in product usage process have been filed in association with TROFINETIDE (Daybue). This represents 0.2% of all adverse event reports for TROFINETIDE.
9
Reports of Wrong technique in product usage process with TROFINETIDE
0.2%
of all TROFINETIDE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Wrong technique in product usage process From TROFINETIDE?
Of the 9 reports, 1 (11.1%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TROFINETIDE. However, 9 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which TROFINETIDE Alternatives Have Lower Wrong technique in product usage process Risk?
TROFINETIDE vs TROFOSFAMIDE
TROFINETIDE vs TROPATEPINE
TROFINETIDE vs TROPICAMIDE
TROFINETIDE vs TROSPIUM
TROFINETIDE vs TROSPIUM\XANOMELINE