Does SEMAGLUTIDE Cause Intentional product misuse? 122 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 122 reports of Intentional product misuse have been filed in association with SEMAGLUTIDE (WEGOVY). This represents 0.2% of all adverse event reports for SEMAGLUTIDE.
122
Reports of Intentional product misuse with SEMAGLUTIDE
0.2%
of all SEMAGLUTIDE reports
3
Deaths
19
Hospitalizations
How Dangerous Is Intentional product misuse From SEMAGLUTIDE?
Of the 122 reports, 3 (2.5%) resulted in death, 19 (15.6%) required hospitalization, and 2 (1.6%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SEMAGLUTIDE. However, 122 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which SEMAGLUTIDE Alternatives Have Lower Intentional product misuse 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