Does SEMAGLUTIDE Cause Hyperkalaemia? 55 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 55 reports of Hyperkalaemia have been filed in association with SEMAGLUTIDE (WEGOVY). This represents 0.1% of all adverse event reports for SEMAGLUTIDE.
55
Reports of Hyperkalaemia with SEMAGLUTIDE
0.1%
of all SEMAGLUTIDE reports
6
Deaths
47
Hospitalizations
How Dangerous Is Hyperkalaemia From SEMAGLUTIDE?
Of the 55 reports, 6 (10.9%) resulted in death, 47 (85.5%) required hospitalization, and 25 (45.5%) were considered life-threatening.
Is Hyperkalaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SEMAGLUTIDE. However, 55 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 Hyperkalaemia?
METFORMIN (2,565)
SPIRONOLACTONE (2,518)
FUROSEMIDE (2,035)
RAMIPRIL (1,383)
SACUBITRIL\VALSARTAN (1,192)
SULFAMETHOXAZOLE\TRIMETHOPRIM (1,036)
LISINOPRIL (948)
POTASSIUM (944)
BISOPROLOL (850)
TACROLIMUS (713)
Which SEMAGLUTIDE Alternatives Have Lower Hyperkalaemia 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