Does TEDUGLUTIDE\WATER Cause Product dose omission? 20 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Product dose omission have been filed in association with TEDUGLUTIDE\WATER. This represents 0.5% of all adverse event reports for TEDUGLUTIDE\WATER.
20
Reports of Product dose omission with TEDUGLUTIDE\WATER
0.5%
of all TEDUGLUTIDE\WATER reports
1
Deaths
13
Hospitalizations
How Dangerous Is Product dose omission From TEDUGLUTIDE\WATER?
Of the 20 reports, 1 (5.0%) resulted in death, 13 (65.0%) required hospitalization, and 1 (5.0%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TEDUGLUTIDE\WATER. However, 20 reports have been filed with the FAERS database.
What Other Side Effects Does TEDUGLUTIDE\WATER Cause?
Nausea (347)
Abdominal pain (303)
Vomiting (207)
Dehydration (201)
Diarrhoea (200)
Weight decreased (189)
Weight increased (185)
Death (179)
Abdominal distension (165)
Drug dose omission (164)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which TEDUGLUTIDE\WATER Alternatives Have Lower Product dose omission Risk?
TEDUGLUTIDE\WATER vs TEGAFUR
TEDUGLUTIDE\WATER vs TEGAFUR\URACIL
TEDUGLUTIDE\WATER vs TEGASEROD
TEDUGLUTIDE\WATER vs TEGRETOL
TEDUGLUTIDE\WATER vs TEICOPLANIN