Does SEMAGLUTIDE Cause Dyspnoea? 809 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 809 reports of Dyspnoea have been filed in association with SEMAGLUTIDE (WEGOVY). This represents 1.4% of all adverse event reports for SEMAGLUTIDE.
809
Reports of Dyspnoea with SEMAGLUTIDE
1.4%
of all SEMAGLUTIDE reports
11
Deaths
211
Hospitalizations
How Dangerous Is Dyspnoea From SEMAGLUTIDE?
Of the 809 reports, 11 (1.4%) resulted in death, 211 (26.1%) required hospitalization, and 31 (3.8%) were considered life-threatening.
Is Dyspnoea Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SEMAGLUTIDE. However, 809 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 Dyspnoea?
ALBUTEROL (21,856)
TREPROSTINIL (16,348)
AMBRISENTAN (13,367)
PREDNISONE (12,830)
BUDESONIDE\FORMOTEROL (11,158)
TIOTROPIUM (10,863)
ADALIMUMAB (10,547)
DUPILUMAB (10,310)
FLUTICASONE\SALMETEROL (9,783)
MEPOLIZUMAB (9,192)
Which SEMAGLUTIDE Alternatives Have Lower Dyspnoea 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