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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does SPIRONOLACTONE Cause Haemoglobin decreased? 113 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 113 reports of Haemoglobin decreased have been filed in association with SPIRONOLACTONE (spironolactone). This represents 0.5% of all adverse event reports for SPIRONOLACTONE.

113
Reports of Haemoglobin decreased with SPIRONOLACTONE
0.5%
of all SPIRONOLACTONE reports
8
Deaths
75
Hospitalizations

How Dangerous Is Haemoglobin decreased From SPIRONOLACTONE?

Of the 113 reports, 8 (7.1%) resulted in death, 75 (66.4%) required hospitalization, and 7 (6.2%) were considered life-threatening.

Is Haemoglobin decreased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SPIRONOLACTONE. However, 113 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 Haemoglobin decreased?

LENALIDOMIDE (4,031) RUXOLITINIB (3,297) ECULIZUMAB (3,028) ADALIMUMAB (2,459) CLOZAPINE (2,396) RITUXIMAB (1,803) APIXABAN (1,779) NIRAPARIB (1,759) METHOTREXATE (1,754) RIBAVIRIN (1,753)

Which SPIRONOLACTONE Alternatives Have Lower Haemoglobin decreased Risk?

SPIRONOLACTONE vs SPRYCEL SPIRONOLACTONE vs STALEVO SPIRONOLACTONE vs STANNOUS FLUORIDE SPIRONOLACTONE vs STANOZOLOL SPIRONOLACTONE vs STAVUDINE

Related Pages

SPIRONOLACTONE Full Profile All Haemoglobin decreased Reports All Drugs Causing Haemoglobin decreased SPIRONOLACTONE Demographics