Does SEMAGLUTIDE Cause Product prescribing error? 174 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 174 reports of Product prescribing error have been filed in association with SEMAGLUTIDE (WEGOVY). This represents 0.3% of all adverse event reports for SEMAGLUTIDE.
174
Reports of Product prescribing error with SEMAGLUTIDE
0.3%
of all SEMAGLUTIDE reports
0
Deaths
26
Hospitalizations
How Dangerous Is Product prescribing error From SEMAGLUTIDE?
Of the 174 reports, 26 (14.9%) required hospitalization, and 6 (3.4%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SEMAGLUTIDE. However, 174 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 prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which SEMAGLUTIDE Alternatives Have Lower Product prescribing error 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