Does SEMAGLUTIDE Cause Product dispensing error? 379 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 379 reports of Product dispensing error have been filed in association with SEMAGLUTIDE (WEGOVY). This represents 0.6% of all adverse event reports for SEMAGLUTIDE.
379
Reports of Product dispensing error with SEMAGLUTIDE
0.6%
of all SEMAGLUTIDE reports
0
Deaths
32
Hospitalizations
How Dangerous Is Product dispensing error From SEMAGLUTIDE?
Of the 379 reports, 32 (8.4%) required hospitalization, and 1 (0.3%) were considered life-threatening.
Is Product dispensing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SEMAGLUTIDE. However, 379 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 dispensing error?
INSULIN GLARGINE (1,048)
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (692)
ADALIMUMAB (386)
PREGABALIN (323)
NIRMATRELVIR\RITONAVIR (310)
ETANERCEPT (305)
SECUKINUMAB (300)
APIXABAN (299)
PALBOCICLIB (299)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (296)
Which SEMAGLUTIDE Alternatives Have Lower Product dispensing 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