Does UNSPECIFIED INGREDIENT Cause Hyperkalaemia? 93 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 93 reports of Hyperkalaemia have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.4% of all adverse event reports for UNSPECIFIED INGREDIENT.
93
Reports of Hyperkalaemia with UNSPECIFIED INGREDIENT
0.4%
of all UNSPECIFIED INGREDIENT reports
12
Deaths
75
Hospitalizations
How Dangerous Is Hyperkalaemia From UNSPECIFIED INGREDIENT?
Of the 93 reports, 12 (12.9%) resulted in death, 75 (80.6%) required hospitalization, and 7 (7.5%) 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 UNSPECIFIED INGREDIENT. However, 93 reports have been filed with the FAERS database.
What Other Side Effects Does UNSPECIFIED INGREDIENT Cause?
Death (2,090)
Off label use (1,306)
Drug ineffective (1,227)
Completed suicide (1,190)
Nausea (1,041)
Fatigue (1,020)
Dyspnoea (934)
Pneumonia (903)
Asthenia (894)
Vomiting (877)
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 UNSPECIFIED INGREDIENT Alternatives Have Lower Hyperkalaemia Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN