Does SPIRONOLACTONE Cause Product dose omission issue? 99 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 99 reports of Product dose omission issue have been filed in association with SPIRONOLACTONE (spironolactone). This represents 0.5% of all adverse event reports for SPIRONOLACTONE.
99
Reports of Product dose omission issue with SPIRONOLACTONE
0.5%
of all SPIRONOLACTONE reports
3
Deaths
29
Hospitalizations
How Dangerous Is Product dose omission issue From SPIRONOLACTONE?
Of the 99 reports, 3 (3.0%) resulted in death, 29 (29.3%) required hospitalization, and 3 (3.0%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SPIRONOLACTONE. However, 99 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 dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which SPIRONOLACTONE Alternatives Have Lower Product dose omission issue Risk?
SPIRONOLACTONE vs SPRYCEL
SPIRONOLACTONE vs STALEVO
SPIRONOLACTONE vs STANNOUS FLUORIDE
SPIRONOLACTONE vs STANOZOLOL
SPIRONOLACTONE vs STAVUDINE