Spironolactone
Spironolactone is a potassium-sparing diuretic and aldosterone antagonist used to treat heart failure, high blood pressure, and fluid retention. It is also used to treat hormonal acne and hirsutism in women.
About Spironolactone
Spironolactone is an aldosterone receptor antagonist (potassium-sparing diuretic) also sold under brand names including Aldactone and CaroSpir. It is primarily used to is prescribed to treat: • Heart failure (reduces mortality and hospitalizations) • High blood pressure (hypertension) • Edema (fluid retention) from various causes • Primary hyperaldosteronism • Cirrhosis with ascites • Nephrotic syndrome • Hormonal acne in women (off label) • Polycystic ovary syndrome (PCOS) symptoms (off label) • Hirsutism (excessive hair growth in women) (off label) It helps remove excess fluid while retaining potassium. Spironolactone is available in oral tablet (25 mg, 50 mg, 100 mg) and oral suspension (carospir 25 mg/5 ml) form. Healthcare providers commonly prescribe Spironolactone for conditions including Acne, Cirrhosis, and Heart Failure Due to Coronary Artery Disease.
Spironolactone at a Glance
- Brand names
- Aldactone, CaroSpir
- Drug class
- Aldosterone Receptor Antagonist (Potassium-Sparing Diuretic)
- Pregnancy category
- FDA Category Category C — Spironolactone has anti-androgenic activity that can theoretically feminize a male fetus; animal data support this concern. Generally avoided in pregnancy unless no alternative is suitable. Patients with reproductive potential using spironolactone for acne or hirsutism should use effective contraception.
- Available forms
- Oral tablet (25 mg, 50 mg, 100 mg), Oral suspension (CaroSpir 25 mg/5 mL)
- Therapeutic categories
- Cardiovascular, Diuretics, Heart Failure, Dermatology, Hormonal
- Conditions treated
- 3 related conditions on this site
What Spironolactone Is Used For
is prescribed to treat:
• Heart failure (reduces mortality and hospitalizations) • High blood pressure (hypertension) • Edema (fluid retention) from various causes • Primary hyperaldosteronism • Cirrhosis with ascites • Nephrotic syndrome • Hormonal acne in women (off-label) • Polycystic ovary syndrome (PCOS) symptoms (off-label) • Hirsutism (excessive hair growth in women) (off-label)
It helps remove excess fluid while retaining potassium.
Dosage Quick Reference
These are general dosage guidelines for Spironolactone. Your doctor will determine the appropriate dose for your specific situation.
| Condition | Starting Dose | Maintenance Dose |
|---|---|---|
| Heart failure (HFrEF, NYHA Class II-IV) | 12.5–25 mg orally once daily | 25–50 mg once daily; monitor potassium and creatinine |
| Hypertension (resistant or as add-on) | 25 mg orally once daily | 25–100 mg/day in 1–2 divided doses |
| Edema (cirrhosis, nephrotic syndrome) | 100 mg orally daily in single or divided doses | 25–200 mg/day; titrate to clinical response |
| Primary hyperaldosteronism (preoperative or chronic) | 100–400 mg orally daily | Titrate to potassium and blood pressure response |
| Hormonal acne or hirsutism (off-label, women) | 25–50 mg orally daily | 50–200 mg/day; benefit usually evident at 3–6 months |
Side Effects
Common side effects may include:
• Increased urination • Dizziness or lightheadedness • Headache • Nausea or vomiting • Diarrhea or stomach cramps • Drowsiness • Irregular menstrual periods • Breast tenderness or enlargement (in both men and women)
Serious side effects (seek immediate medical attention):
• Signs of high potassium (muscle weakness, slow/irregular heartbeat, severe dizziness) • Severe dehydration (very dry mouth, extreme thirst, muscle cramps) • Signs of electrolyte imbalance • Severe allergic reactions • Unusual bleeding or bruising • Yellowing of skin or eyes (liver problems) • Confusion or mental changes
See also: Drug Interactions ↓
Drug Interactions
Spironolactone elevates potassium and modulates the renin-angiotensin-aldosterone system, producing several clinically critical interactions.
- ACE inhibitors, ARBs, and direct renin inhibitors (e.g., lisinopril, losartan, aliskiren): Additive hyperkalemia risk that can be life-threatening, especially in patients with reduced kidney function or diabetes. Routinely monitor serum potassium and creatinine 1 week after initiation, after dose changes, and periodically thereafter.
- Potassium supplements and salt substitutes containing potassium chloride: Avoid concurrent use unless serum potassium is closely monitored and clinically indicated (e.g., correcting documented hypokalemia).
- NSAIDs (e.g., ibuprofen, naproxen, celecoxib): Reduce diuretic and antihypertensive efficacy and increase the risk of hyperkalemia and acute kidney injury. Use the lowest NSAID dose for the shortest duration when needed.
- Digoxin: Spironolactone interferes with several digoxin assays and modestly raises digoxin levels. Monitor digoxin concentrations and clinical response.
- Lithium: Reduced renal clearance can elevate lithium levels into the toxic range. Monitor lithium concentrations carefully.
- Trimethoprim (including in TMP/SMX): Trimethoprim itself causes potassium retention and produces synergistic hyperkalemia with spironolactone, particularly in older adults. Several large studies have linked this combination to sudden death; avoid co-prescription when possible.
See also: Questions to Ask Your Doctor ↓
Key Considerations
Known drug interactions
Spironolactone has documented interactions with other medications, supplements, and certain foods. Review the Drug Interactions section below and tell your healthcare provider about every medication you take, including over-the-counter products. Jump to section →
Multiple forms available
Spironolactone comes in more than one form (Oral tablet (25 mg, 50 mg, 100 mg), Oral suspension (CaroSpir 25 mg/5 mL)). The right form for you depends on your condition, ease of use, and your provider's recommendation.
Additional Information
Spironolactone (Aldactone) is a mineralocorticoid receptor antagonist used in heart failure with reduced ejection fraction, in resistant hypertension, in cirrhosis with ascites, and — off-label but very widely — in acne and hirsutism in women, particularly with PCOS. It is a diuretic whose most important benefits are not diuretic at all.
Mechanism of Action
Spironolactone competitively blocks the mineralocorticoid receptor, preventing aldosterone from acting on the distal tubule and collecting duct. The immediate result is reduced sodium reabsorption and reduced potassium excretion — hence potassium-sparing diuresis, a weak natriuretic effect compared with a loop diuretic such as furosemide.
The diuretic effect, however, is not why it saves lives in heart failure. Aldosterone drives myocardial and vascular fibrosis, endothelial dysfunction, and adverse remodelling independent of its effect on sodium. Blocking that signal reduces mortality in heart failure with reduced ejection fraction at doses far below those needed for meaningful diuresis. This is why spironolactone appears in heart failure regimens at a low fixed dose rather than being titrated to urine output.
Spironolactone also binds androgen and progesterone receptors, which is a side effect in men and the entire therapeutic point in women treated for acne or hirsutism. Anti-androgen activity produces gynecomastia, breast tenderness, and erectile dysfunction in men — the most common reason male patients stop it. Eplerenone is more selective for the mineralocorticoid receptor and is the alternative when these effects are limiting, at higher cost.
Clinical Use
In heart failure with reduced ejection fraction, spironolactone is one of the four foundational therapies alongside a beta blocker, a renin-angiotensin agent, and an SGLT2 inhibitor. In resistant hypertension — blood pressure uncontrolled on three agents including a diuretic — it is the best-evidenced fourth-line drug and frequently the one that finally achieves control, because unrecognised aldosterone excess is a common underlying cause. A patient on three drugs with poor control deserves consideration of spironolactone before a fourth agent from another class.
In cirrhosis with ascites it is the diuretic of choice, because portal hypertension drives secondary hyperaldosteronism and blocking that axis directly addresses the mechanism.
The dermatologic and endocrine use in women is substantial and generally well tolerated: it reduces sebum production and hirsutism through androgen blockade. Effect takes several months, and patients told to expect improvement in weeks conclude it has failed. It is used with contraception given the teratogenic risk to a male fetus. Our cardiovascular team manages the heart failure and hypertension indications, and the MedlinePlus spironolactone entry covers prescribing detail.
Monitoring and Follow-Up
Potassium and kidney function are the monitoring priorities and the checks are not optional. Measure both at baseline, within one week of starting or any dose increase, again at one month, and periodically thereafter.
Hyperkalemia is the serious risk and can be fatal. It becomes far more likely with reduced kidney function, in diabetes, in older adults, and — critically — when spironolactone is combined with an ACE inhibitor or ARB, which is exactly the combination heart failure guidelines recommend. That combination is correct and beneficial, but it makes monitoring mandatory rather than advisory. Potassium supplements and salt substitutes, which are potassium chloride, should be stopped.
Gynecomastia and breast tenderness in men are dose-related and often develop over months. Menstrual irregularity is common in women. Both are worth asking about directly, since patients frequently stop the drug rather than report them. The heart failure early signs article covers what decompensation looks like, and the American Heart Association provides patient background.
Resistant hypertension deserves a closer look before a fourth drug is chosen at random. True resistance — uncontrolled pressure on three agents at adequate doses including a diuretic — should prompt a check for the common mimics first: white coat effect, poor adherence, NSAIDs, excess salt, alcohol, and untreated sleep apnea. Once those are excluded, primary aldosteronism is far more common than historically assumed, and spironolactone addresses it directly. The white coat and masked hypertension article covers why office readings alone mislead, and confirming resistance with home or ambulatory readings before escalating avoids treating a measurement artefact with a fourth medication.
Special Populations
In older adults, hyperkalemia risk is substantially higher and kidney function is often worse than creatinine suggests; start low and check potassium sooner. In significant kidney impairment spironolactone is generally avoided, and it is contraindicated in severe impairment, anuria, and pre-existing hyperkalemia.
In pregnancy it is avoided because of anti-androgen effects on a male fetus. Any woman of reproductive potential taking it for acne or hirsutism needs reliable contraception and an explicit conversation about why. NSAIDs blunt the effect and add to hyperkalemia and kidney injury risk, particularly alongside an ACE inhibitor or ARB. Trimethoprim, including in trimethoprim-sulfamethoxazole, raises potassium independently and is a recognised precipitant of dangerous hyperkalemia in patients on spironolactone — a common outpatient antibiotic pairing worth checking before prescribing.
Timing helps with one common complaint. Spironolactone is a weak diuretic, but it still increases urine output, and an evening dose disrupts sleep in some patients. Taking it in the morning generally solves this. Its onset is also slow relative to a loop diuretic, taking days rather than hours to reach full effect, so it should not be judged on the first day.
When to Contact Your Doctor
Report muscle weakness, fatigue, palpitations, an irregular or slow heartbeat, or tingling around the mouth or in the extremities — these can indicate hyperkalemia and warrant same-day potassium testing rather than waiting.
Any illness causing vomiting, diarrhea, or reduced fluid intake is a reason to ask whether spironolactone and other diuretics should be held temporarily, since dehydration and kidney injury drive potassium up quickly. Report breast tenderness or enlargement, menstrual changes, or sexual dysfunction rather than stopping the drug silently — there are alternatives. Confirm before starting any new antibiotic or NSAID.
To review your potassium, your heart failure regimen, or side effects that are making treatment hard to continue, contact us or schedule a visit.
Frequently Asked Questions
Questions to Ask Your Doctor About Spironolactone
Consider discussing these topics at your next appointment:
- How often will my potassium and kidney function be checked while I am on spironolactone?
- Are any of my other medications likely to interact with spironolactone to raise my potassium?
- What symptoms of high potassium should make me call you immediately?
- For long-term use, what would prompt us to switch to eplerenone or another agent?
- How will we know whether spironolactone is achieving the goal we set — better blood pressure, fluid control, or skin response?
Medical Disclaimer: This information is for educational purposes only and should not be considered medical advice. Always consult with your healthcare provider before starting, stopping, or changing any medication. Your doctor can provide personalized recommendations based on your specific health condition and medical history.