Does SEMAGLUTIDE Cause Device leakage? 374 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 374 reports of Device leakage have been filed in association with SEMAGLUTIDE (WEGOVY). This represents 0.6% of all adverse event reports for SEMAGLUTIDE.
374
Reports of Device leakage with SEMAGLUTIDE
0.6%
of all SEMAGLUTIDE reports
0
Deaths
4
Hospitalizations
How Dangerous Is Device leakage From SEMAGLUTIDE?
Of the 374 reports, 4 (1.1%) required hospitalization.
Is Device leakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SEMAGLUTIDE. However, 374 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 leakage?
SOMATROPIN (9,113)
LEUPROLIDE (5,861)
EXENATIDE (5,115)
PEGFILGRASTIM (1,380)
ALBIGLUTIDE (1,195)
SECUKINUMAB (910)
RISPERIDONE (878)
TREPROSTINIL (874)
DEVICE (795)
GUSELKUMAB (712)
Which SEMAGLUTIDE Alternatives Have Lower Device leakage 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