Does SEMAGLUTIDE Cause Product use issue? 932 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 932 reports of Product use issue have been filed in association with SEMAGLUTIDE (WEGOVY). This represents 1.6% of all adverse event reports for SEMAGLUTIDE.
932
Reports of Product use issue with SEMAGLUTIDE
1.6%
of all SEMAGLUTIDE reports
3
Deaths
218
Hospitalizations
How Dangerous Is Product use issue From SEMAGLUTIDE?
Of the 932 reports, 3 (0.3%) resulted in death, 218 (23.4%) required hospitalization, and 9 (1.0%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SEMAGLUTIDE. However, 932 reports have been filed with the FAERS database.
What Other Side Effects Does SEMAGLUTIDE Cause?
Nausea (10,036)
Vomiting (6,518)
Off label use (5,425)
Diarrhoea (5,331)
Decreased appetite (4,317)
Constipation (4,036)
Weight decreased (3,518)
Impaired gastric emptying (2,622)
Product use in unapproved indication (2,613)
Wrong technique in product usage process (2,538)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which SEMAGLUTIDE Alternatives Have Lower Product use issue Risk?
SEMAGLUTIDE vs SEMUSTINE
SEMAGLUTIDE vs SENNA LEAF
SEMAGLUTIDE vs SENNA LEAF\SENNOSIDES\SENNOSIDES A AND B
SEMAGLUTIDE vs SENNOSIDES
SEMAGLUTIDE vs SENNOSIDES A AND B