Does TEDUGLUTIDE Cause Wrong technique in product usage process? 68 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 68 reports of Wrong technique in product usage process have been filed in association with TEDUGLUTIDE (Gattex). This represents 0.8% of all adverse event reports for TEDUGLUTIDE.
68
Reports of Wrong technique in product usage process with TEDUGLUTIDE
0.8%
of all TEDUGLUTIDE reports
7
Deaths
38
Hospitalizations
How Dangerous Is Wrong technique in product usage process From TEDUGLUTIDE?
Of the 68 reports, 7 (10.3%) resulted in death, 38 (55.9%) required hospitalization, and 1 (1.5%) were considered life-threatening.
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 TEDUGLUTIDE. However, 68 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 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 TEDUGLUTIDE Alternatives Have Lower Wrong technique in product usage process Risk?
TEDUGLUTIDE vs TEDUGLUTIDE\WATER
TEDUGLUTIDE vs TEGAFUR
TEDUGLUTIDE vs TEGAFUR\URACIL
TEDUGLUTIDE vs TEGASEROD
TEDUGLUTIDE vs TEGRETOL