Does SEMAGLUTIDE Cause Presyncope? 135 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 135 reports of Presyncope have been filed in association with SEMAGLUTIDE (WEGOVY). This represents 0.2% of all adverse event reports for SEMAGLUTIDE.
135
Reports of Presyncope with SEMAGLUTIDE
0.2%
of all SEMAGLUTIDE reports
0
Deaths
45
Hospitalizations
How Dangerous Is Presyncope From SEMAGLUTIDE?
Of the 135 reports, 45 (33.3%) required hospitalization, and 5 (3.7%) were considered life-threatening.
Is Presyncope Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SEMAGLUTIDE. However, 135 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 Presyncope?
TREPROSTINIL (585)
BISOPROLOL (485)
LEVONORGESTREL (429)
ADALIMUMAB (420)
AMBRISENTAN (407)
ASPIRIN (370)
TAMSULOSIN (361)
FUROSEMIDE (348)
SERTRALINE (337)
ETANERCEPT (334)
Which SEMAGLUTIDE Alternatives Have Lower Presyncope 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