Does SPIRONOLACTONE Cause Product prescribing error? 173 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 173 reports of Product prescribing error have been filed in association with SPIRONOLACTONE (spironolactone). This represents 0.8% of all adverse event reports for SPIRONOLACTONE.
173
Reports of Product prescribing error with SPIRONOLACTONE
0.8%
of all SPIRONOLACTONE reports
0
Deaths
150
Hospitalizations
How Dangerous Is Product prescribing error From SPIRONOLACTONE?
Of the 173 reports, 150 (86.7%) required hospitalization, and 6 (3.5%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SPIRONOLACTONE. However, 173 reports have been filed with the FAERS database.
What Other Side Effects Does SPIRONOLACTONE Cause?
Acute kidney injury (3,273)
Hyperkalaemia (2,518)
Hypotension (1,583)
Dyspnoea (1,468)
Drug ineffective (1,379)
Hyponatraemia (1,166)
Dizziness (991)
Fatigue (990)
Fall (947)
Off label use (899)
What Other Drugs Cause Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which SPIRONOLACTONE Alternatives Have Lower Product prescribing error Risk?
SPIRONOLACTONE vs SPRYCEL
SPIRONOLACTONE vs STALEVO
SPIRONOLACTONE vs STANNOUS FLUORIDE
SPIRONOLACTONE vs STANOZOLOL
SPIRONOLACTONE vs STAVUDINE