Does TEDUGLUTIDE Cause Device breakage? 57 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 57 reports of Device breakage have been filed in association with TEDUGLUTIDE (Gattex). This represents 0.7% of all adverse event reports for TEDUGLUTIDE.
57
Reports of Device breakage with TEDUGLUTIDE
0.7%
of all TEDUGLUTIDE reports
2
Deaths
52
Hospitalizations
How Dangerous Is Device breakage From TEDUGLUTIDE?
Of the 57 reports, 2 (3.5%) resulted in death, 52 (91.2%) required hospitalization, and 1 (1.8%) were considered life-threatening.
Is Device breakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TEDUGLUTIDE. However, 57 reports have been filed with the FAERS database.
What Other Side Effects Does TEDUGLUTIDE Cause?
Vascular device infection (1,009)
Weight decreased (991)
Product dose omission issue (937)
Diarrhoea (779)
Abdominal pain (714)
Nausea (682)
Weight increased (631)
Dehydration (615)
Vomiting (585)
Death (527)
What Other Drugs Cause Device breakage?
COPPER (9,201)
SOMATROPIN (7,761)
ETONOGESTREL (4,140)
LEVONORGESTREL (2,726)
ETHINYL ESTRADIOL\ETONOGESTREL (741)
CARBIDOPA\LEVODOPA (634)
TREPROSTINIL (396)
ADALIMUMAB (375)
ALBUTEROL (256)
EPOPROSTENOL (240)
Which TEDUGLUTIDE Alternatives Have Lower Device breakage Risk?
TEDUGLUTIDE vs TEDUGLUTIDE\WATER
TEDUGLUTIDE vs TEGAFUR
TEDUGLUTIDE vs TEGAFUR\URACIL
TEDUGLUTIDE vs TEGASEROD
TEDUGLUTIDE vs TEGRETOL