Does SEMAGLUTIDE Cause Device malfunction? 598 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 598 reports of Device malfunction have been filed in association with SEMAGLUTIDE (WEGOVY). This represents 1.0% of all adverse event reports for SEMAGLUTIDE.
598
Reports of Device malfunction with SEMAGLUTIDE
1.0%
of all SEMAGLUTIDE reports
1
Deaths
20
Hospitalizations
How Dangerous Is Device malfunction From SEMAGLUTIDE?
Of the 598 reports, 1 (0.2%) resulted in death, 20 (3.3%) required hospitalization, and 2 (0.3%) were considered life-threatening.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SEMAGLUTIDE. However, 598 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 Device malfunction?
PEGFILGRASTIM (6,818)
EXENATIDE (3,273)
BUDESONIDE\FORMOTEROL (2,771)
ABATACEPT (2,459)
SOMATROPIN (2,311)
GOLIMUMAB (2,293)
SECUKINUMAB (2,259)
ALBUTEROL (2,257)
GUSELKUMAB (1,410)
MOMETASONE FUROATE (1,332)
Which SEMAGLUTIDE Alternatives Have Lower Device malfunction 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