Does TENAPANOR Cause Hyperkalaemia? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Hyperkalaemia have been filed in association with TENAPANOR (IBSRELA). This represents 0.6% of all adverse event reports for TENAPANOR.
12
Reports of Hyperkalaemia with TENAPANOR
0.6%
of all TENAPANOR reports
2
Deaths
6
Hospitalizations
How Dangerous Is Hyperkalaemia From TENAPANOR?
Of the 12 reports, 2 (16.7%) resulted in death, 6 (50.0%) required hospitalization, and 1 (8.3%) 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 TENAPANOR. However, 12 reports have been filed with the FAERS database.
What Other Side Effects Does TENAPANOR Cause?
Diarrhoea (793)
Death (222)
Hospitalisation (138)
Inappropriate schedule of product administration (115)
Off label use (94)
Product use issue (72)
Nausea (59)
Abdominal distension (52)
Therapy interrupted (52)
Abdominal pain (50)
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 TENAPANOR Alternatives Have Lower Hyperkalaemia Risk?
TENAPANOR vs TENECTEPLASE
TENAPANOR vs TENELIGLIPTIN
TENAPANOR vs TENIPOSIDE
TENAPANOR vs TENOFOVIR
TENAPANOR vs TENOFOVIR ALAFENAMIDE