Does TEDUGLUTIDE\WATER Cause Intentional product use issue? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Intentional product use issue have been filed in association with TEDUGLUTIDE\WATER. This represents 0.2% of all adverse event reports for TEDUGLUTIDE\WATER.
9
Reports of Intentional product use issue with TEDUGLUTIDE\WATER
0.2%
of all TEDUGLUTIDE\WATER reports
0
Deaths
2
Hospitalizations
How Dangerous Is Intentional product use issue From TEDUGLUTIDE\WATER?
Of the 9 reports, 2 (22.2%) required hospitalization.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TEDUGLUTIDE\WATER. However, 9 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which TEDUGLUTIDE\WATER Alternatives Have Lower Intentional product use issue Risk?
TEDUGLUTIDE\WATER vs TEGAFUR
TEDUGLUTIDE\WATER vs TEGAFUR\URACIL
TEDUGLUTIDE\WATER vs TEGASEROD
TEDUGLUTIDE\WATER vs TEGRETOL
TEDUGLUTIDE\WATER vs TEICOPLANIN