Does SEMAGLUTIDE Cause Hypokalaemia? 111 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 111 reports of Hypokalaemia have been filed in association with SEMAGLUTIDE (WEGOVY). This represents 0.2% of all adverse event reports for SEMAGLUTIDE.
111
Reports of Hypokalaemia with SEMAGLUTIDE
0.2%
of all SEMAGLUTIDE reports
5
Deaths
79
Hospitalizations
How Dangerous Is Hypokalaemia From SEMAGLUTIDE?
Of the 111 reports, 5 (4.5%) resulted in death, 79 (71.2%) required hospitalization, and 15 (13.5%) were considered life-threatening.
Is Hypokalaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SEMAGLUTIDE. However, 111 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 Hypokalaemia?
FUROSEMIDE (2,503)
HYDROCHLOROTHIAZIDE (1,152)
CARBOPLATIN (1,118)
PREDNISONE (967)
DEXAMETHASONE (876)
CYCLOPHOSPHAMIDE (864)
OMEPRAZOLE (851)
RITUXIMAB (822)
AMLODIPINE (815)
PANTOPRAZOLE (811)
Which SEMAGLUTIDE Alternatives Have Lower Hypokalaemia 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