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Lisinopril

Brand namesPrinivilZestril

Lisinopril is an ACE inhibitor used to treat high blood pressure, heart failure, and improve survival after heart attack. It works by relaxing blood vessels and reducing strain on the heart.

Reviewed by Zimmer Medical GroupUpdated 9 min read

About Lisinopril

Lisinopril is an angiotensin-converting enzyme (ace) inhibitor also sold under brand names including Prinivil and Zestril. It is primarily used to is prescribed to treat: • High blood pressure (hypertension) • Heart failure • Improve survival after heart attack • Diabetic kidney disease (nephropathy) • Chronic kidney disease • Prevent cardiovascular events in high risk patients It helps protect the heart, kidneys, and blood vessels from damage. Lisinopril is available in oral tablet (2.5 mg, 5 mg, 10 mg, 20 mg, 30 mg, 40 mg) and oral solution (1 mg/ml) form. Healthcare providers commonly prescribe Lisinopril for conditions including Stroke.

Lisinopril at a Glance

Brand names
Prinivil, Zestril
Drug class
Angiotensin-Converting Enzyme (ACE) Inhibitor
Pregnancy category
FDA Category Category D — Drugs acting on the renin-angiotensin system during the second and third trimesters cause fetal renal dysfunction, oligohydramnios, skull hypoplasia, and death. Discontinue lisinopril as soon as pregnancy is detected. FDA Boxed Warning applies.
Available forms
Oral tablet (2.5 mg, 5 mg, 10 mg, 20 mg, 30 mg, 40 mg), Oral solution (1 mg/mL)
Therapeutic categories
Cardiovascular, ACE Inhibitors, Hypertension, Heart Failure
Conditions treated
1 related condition on this site

What Lisinopril Is Used For

Dosage Quick Reference

These are general dosage guidelines for Lisinopril. Your doctor will determine the appropriate dose for your specific situation.

ConditionStarting DoseMaintenance Dose
Hypertension (adults)10 mg once daily20–40 mg once daily; max 80 mg/day
Hypertension (children >= 6 years)0.07 mg/kg once daily (max 5 mg)Titrate up to 0.61 mg/kg or 40 mg/day
Heart failure2.5–5 mg once dailyTitrate every 1–2 weeks to target 20–40 mg once daily as tolerated
Acute MI (within 24 hours)5 mg once, then 5 mg after 24 hours10 mg once daily for at least 6 weeks
Diabetic nephropathy10 mg once dailyTitrate to maximum tolerated dose, typically 20–40 mg/day

Side Effects

Common side effects may include:

• Dry cough (most common) • Dizziness or lightheadedness • Headache • Fatigue • NauseaDiarrhea

Serious side effects (seek immediate medical attention):

• Angioedema (swelling of face, lips, tongue, throat) • Signs of high potassium (muscle weakness, irregular heartbeat) • Fainting • Difficulty breathing • Chest pain • Severe dizziness • Signs of kidney problems (change in urine amount, swelling) • Yellowing of skin or eyes

See also: Drug Interactions ↓

Drug Interactions

Lisinopril blocks the conversion of angiotensin I to angiotensin II and has interactions related to renin-angiotensin-aldosterone system effects.

  • ARBs (e.g., losartan, valsartan) or aliskiren: Dual RAAS blockade increases the risk of hyperkalemia, hypotension, and acute kidney injury without improving outcomes. Avoid combination, especially in patients with diabetes or chronic kidney disease (GFR < 60 mL/min).
  • Potassium-sparing diuretics (spironolactone, eplerenone, amiloride) or potassium supplements: Additive hyperkalemia risk. Monitor serum potassium regularly, particularly in patients with renal impairment, diabetes, or heart failure.
  • NSAIDs (ibuprofen, naproxen, celecoxib): Reduce the antihypertensive and renoprotective effects of lisinopril and increase the risk of acute kidney injury, particularly in volume-depleted or elderly patients. Use the lowest effective NSAID dose for the shortest duration.
  • Lithium: Lisinopril reduces lithium renal clearance, increasing the risk of lithium toxicity (tremor, confusion, renal damage). Monitor lithium levels closely if combination is necessary.
  • Sacubitril (Entresto): Concurrent use with lisinopril increases the risk of angioedema. Allow at least 36 hours between discontinuing lisinopril and starting sacubitril/valsartan.
  • Sulfonylureas and insulin: Lisinopril may enhance hypoglycemic effects, particularly during the first month. Patients with diabetes should monitor blood glucose more frequently when starting therapy.

See also: Questions to Ask Your Doctor ↓

Key Considerations

Known drug interactions

Lisinopril 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

Lisinopril comes in more than one form (Oral tablet (2.5 mg, 5 mg, 10 mg, 20 mg, 30 mg, 40 mg), Oral solution (1 mg/mL)). The right form for you depends on your condition, ease of use, and your provider's recommendation.

Additional Information

Lisinopril (Prinivil, Zestril) is an angiotensin-converting enzyme inhibitor used for high blood pressure, heart failure, and kidney protection in diabetes. Within the ACE inhibitor class it is distinguished by a long half-life allowing once-daily dosing, by not requiring hepatic activation — unlike enalapril or ramipril, it is administered in its active form — and by being cleared unchanged by the kidneys.

Mechanism of Action

Lisinopril blocks angiotensin-converting enzyme, interrupting the renin-angiotensin-aldosterone system. Less angiotensin II is produced, which means less direct arterial vasoconstriction and less aldosterone release, so the body retains less sodium and water. Both effects lower blood pressure, and the reduction in aldosterone also limits the fibrotic remodelling that aldosterone drives in the heart and kidney.

The same enzyme also degrades bradykinin, so inhibiting it raises bradykinin levels. This contributes usefully to vasodilation, but it is also the mechanism behind the class's two characteristic adverse effects: the dry, persistent cough that affects roughly one in ten patients, and angioedema, which is far rarer but potentially life-threatening.

In the kidney, angiotensin II preferentially constricts the efferent arteriole leaving the glomerulus. Removing that constriction lowers intraglomerular pressure. This is why ACE inhibitors slow the progression of chronic kidney disease and proteinuria — and also why serum creatinine typically rises slightly after starting one. A rise of up to about 30 percent that then stabilises is expected and reflects the drug working, not kidney injury.

Clinical Use

Lisinopril is a first-line antihypertensive and is particularly favoured in patients who also have diabetes with albuminuria, chronic kidney disease, heart failure with reduced ejection fraction, or a history of myocardial infarction, because the benefit in those settings goes beyond blood pressure lowering. In heart failure it reduces mortality, an effect established across the class.

Population response varies. ACE inhibitors are somewhat less effective as monotherapy in Black patients and in older adults, groups whose hypertension tends to be more volume- and salt-driven; a calcium channel blocker such as amlodipine or a thiazide diuretic such as hydrochlorothiazide is often more effective first, and combination therapy works well. Patients who develop the ACE inhibitor cough are usually switched to an angiotensin receptor blocker such as losartan, which blocks the receptor rather than the enzyme and therefore does not raise bradykinin. The American Heart Association publishes accessible background on how these classes compare.

One combination to avoid: ACE inhibitors and ARBs together. Dual blockade increases hyperkalemia and kidney injury without improving outcomes, and it is no longer recommended.

Monitoring and Follow-Up

Check basic metabolic panel — creatinine, eGFR, and potassium — before starting and again one to two weeks after initiation or any dose increase. The two things being watched for are an excessive creatinine rise and hyperkalemia, since reduced aldosterone means the kidney holds onto potassium. Risk of high potassium climbs with reduced kidney function, in diabetes, and with concurrent potassium-sparing diuretics, potassium supplements, or salt substitutes, which are usually potassium chloride and are an underappreciated cause.

Home blood pressure monitoring gives a far better picture than isolated office readings, and the home monitoring guide covers correct technique. Our cardiovascular team reviews readings alongside overall risk. Once stable, kidney function and potassium are typically rechecked every six to twelve months. The blood pressure numbers article explains what the targets mean.

Adherence deserves explicit attention in a symptomless condition. Hypertension causes no symptoms until it causes organ damage, so patients frequently stop when they feel well, and roughly half of people prescribed antihypertensives are no longer taking them consistently a year later. Once-daily dosing, fixed-dose combination pills, and home monitoring that lets patients see their own numbers all improve persistence more than repeated warnings do. The MedlinePlus lisinopril entry is a useful reference for patients who want the full prescribing picture.

Special Populations

Lisinopril is contraindicated in pregnancy. ACE inhibitors cause fetal injury — kidney damage, oligohydramnios, and skull hypoplasia — particularly in the second and third trimesters, and should be stopped as soon as pregnancy is recognised or planned. Women of reproductive age should understand this before starting.

Anyone with a prior history of angioedema on an ACE inhibitor must never receive one again. Angioedema can occur after years of uneventful use, not just at initiation, and it disproportionately affects Black patients. Bilateral renal artery stenosis is a contraindication, since these kidneys depend on angiotensin II to maintain filtration pressure. In older adults, start low and re-check kidney function promptly, as age-related decline may not be visible in the creatinine alone. Volume-depleted patients — those on high-dose diuretics or with poor intake — can drop their pressure sharply with the first dose.

Cough deserves a note of its own because it is so often mismanaged. The ACE inhibitor cough is dry, tickling, and persistent; it can begin within days or after more than a year of treatment, and it does not respond to cough suppressants because it is not driven by mucus or infection. It resolves within one to four weeks of stopping, though occasionally it lingers longer. Patients are frequently investigated for asthma, reflux, or postnasal drip before anyone revisits the medication list, so it is worth naming the possibility early. Switching to an ARB resolves it in the large majority of cases while preserving the same cardiovascular and kidney protection.

When to Contact Your Doctor

Swelling of the lips, tongue, face, or throat, or any difficulty breathing or swallowing, is a medical emergency: stop the drug and seek immediate care, because airway angioedema can progress quickly. A persistent dry cough is not dangerous but is a good reason to change agents rather than endure it. Report lightheadedness on standing, which may mean the dose is too high or you are volume depleted. Muscle weakness, palpitations, or an irregular heartbeat can signal high potassium and warrant prompt lab work. Reduced urine output or unusual swelling should also be reported.

To review your blood pressure control, kidney function, and whether your regimen still fits your risk profile, contact us or schedule a visit.

Frequently Asked Questions

A persistent dry cough affects 5 to 20 percent of patients on ACE inhibitors and is caused by accumulation of bradykinin and substance P in the airways — a class effect, not a sign of allergy. The cough usually begins within weeks to months of starting therapy and resolves within 1 to 4 weeks of stopping. If bothersome, ask your provider about switching to an ARB, which works similarly without the cough.
Angioedema is sudden swelling of the face, lips, tongue, or throat that can compromise the airway. It occurs in less than 1 percent of patients on ACE inhibitors but can be life-threatening. It can develop after years of uneventful use. Stop lisinopril immediately and seek emergency care if you experience swelling — particularly of the tongue or throat — and inform all future providers of the reaction.
In diabetic kidney disease, the angiotensin-mediated constriction of the efferent arteriole increases pressure within the glomerulus, accelerating kidney damage. Lisinopril dilates this arteriole, reducing intraglomerular pressure and slowing the progression of nephropathy. This benefit is independent of blood pressure lowering and is the main reason ACE inhibitors are preferred in diabetic patients with hypertension.
Lisinopril reduces aldosterone production, which can raise serum potassium, and it lowers pressure within the glomerulus, which can transiently elevate creatinine. A small rise in creatinine (less than 30 percent above baseline) is expected and acceptable. Larger increases or significant hyperkalemia may indicate the need to lower the dose or evaluate for renal artery stenosis.
Yes. Food does not significantly affect the absorption of lisinopril. Take it at the same time each day to maintain consistent blood pressure control. Avoid salt substitutes containing potassium chloride, as these can contribute to hyperkalemia.

Questions to Ask Your Doctor About Lisinopril

Consider discussing these topics at your next appointment:

  • How will we monitor my kidney function and potassium after starting lisinopril?
  • What blood pressure readings at home should prompt me to call you?
  • If I develop a cough or swelling, what is the plan?
  • Are any of my other medications likely to interact with lisinopril?
  • If lisinopril alone is not enough, what is the next step in my treatment plan?

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.