hydrochlorothiazide/triamterene
Brand names: Dyazide, Maxzide
This medicine combines lisinopril and hydrochlorothiazide to lower high blood pressure. Lowering blood pressure reduces the risk of strokes and heart attacks.
What it does
This medicine is used to treat high blood pressure.
Common side effects
Dizziness, Headache, Cough
Key warnings
This medicine can harm your unborn baby.
How It Works
Lisinopril is an ACE inhibitor that widens blood vessels. Hydrochlorothiazide is a diuretic that helps your body get rid of extra salt and water. This combination helps to lower blood pressure.
How to Take It
Take this medicine exactly as your doctor tells you. Your doctor may start you on a low dose and increase it over time. You can take this medicine with or without food. Try to take it at the same time each day.
Pregnancy & Breastfeeding
This medicine can cause harm or death to an unborn baby. Do not take this medicine if you are pregnant. Talk to your doctor about other blood pressure medicines if you are breastfeeding.
Missed Dose
If you miss a dose, take it as soon as you remember. If it is close to your next dose, skip the missed dose and continue with your regular schedule.
Storage
Store this medicine at room temperature (68-77°F) away from light and moisture.
Side Effects (from patient reports)
Based on 79,221 FDA adverse event reports.
Serious Warnings
This medicine can harm your unborn baby. If you become pregnant, stop taking this medicine and tell your doctor right away. You should not take this medicine if you have ever had a severe allergic reaction (angioedema) to an ACE inhibitor or if you cannot urinate.
Known Drug Interactions
Monitor blood pressure, renal function, and electrolytes in patients on lisinopril and hydrochlorothiazide tablets and other agents that affect the RAS. Do not coadminister aliskiren with lisinopril and hydrochlorothiazide tablets in patients with diabetes. No meaningful clinically important pharmacokinetic interactions occurred when lisinopril was used concomitantly with propranolol, digoxin, or hydrochlorothiazide.
Mechanism: Both of these medicines can cause your body to lose too much water and salt, which can lead to dehydration or electrolyte imbalances.
What to do: Your doctor should monitor your blood pressure and salt levels closely to ensure they stay in a healthy range.
Dual Blockade of the Renin-Angiotensin System (RAS): Dual blockade of the RAS with angiotensin receptor blockers, ACE inhibitors, or direct renin inhibitors (such as aliskiren) is associated with increased risk of hypotension, syncope, hyperkalemia, and changes in renal function (including acute renal failure) compared to monotherapy. Do not coadminister aliskiren with lisinopril and hydrochlorothiazide tablets in patients with diabetes. Avoid use of aliskiren with PRINZIDE in patients with renal impairment (GFR <60 ml/min).
Mechanism: Using these two drugs together can put too much stress on your kidneys and cause your blood pressure to drop to unsafe levels.
What to do: Do not use these together if you have diabetes, and your doctor should check your kidney health if you use both.
Drug Interactions Lisinopril Hypotension - Patients on Diuretic Therapy: Patients on diuretics and especially those in whom diuretic therapy was recently instituted, may occasionally experience an excessive reduction of blood pressure after initiation of therapy with lisinopril. The possibility of hypotensive effects with lisinopril can be minimized by either discontinuing the diuretic or increasing the salt intake prior to initiation of treatment with lisinopril. If it is necessary to continue the diuretic, initiate therapy with lisinopril at a dose of 5 mg daily, and provide close medical...
Mechanism: Taking these two types of blood pressure medicines together can cause your blood pressure to drop too low, especially when you first start. This can make you feel very dizzy or lightheaded.
What to do: Your doctor may start you on a lower dose of the new medicine to keep your blood pressure steady. Be sure to stand up slowly and tell your doctor if you feel faint.
The VA NEPHRON trial enrolled 1448 patients with type 2 diabetes, elevated urinary-albumin-to-creatinine ratio, and decreased estimated glomerular filtration rate (GFR 30 to 89.9 ml/min), randomized them to lisinopril or placebo on a background of losartan therapy and followed them for a median of 2.2 years. Patients receiving the combination of losartan and lisinopril did not obtain any additional benefit compared to monotherapy for the combined endpoint of decline in GFR, end state renal disease, or death, but experienced an increased incidence of hyperkalemia and acute kidney injury comp...
Mechanism: Both of these medicines can cause your body to hold onto too much potassium. Having high potassium levels can be dangerous for your heart and may lead to kidney problems.
What to do: Your doctor will need to monitor your potassium levels and kidney health with regular blood tests. Seek medical help if you feel muscle weakness or notice a change in your heartbeat.
Use of lisinopril with potassium-sparing diuretics (e.g., spironolactone, eplerenone, triamterene, or amiloride), potassium supplements, or potassium-containing salt substitutes may lead to significant increases in serum potassium.
Mechanism: Both drugs stop the kidneys from getting rid of potassium. This can cause potassium to build up to unsafe levels in your blood.
What to do: Your doctor should monitor your blood potassium levels closely. You may need to avoid this combination or have your doses adjusted.
Common Questions
Can I stop taking this medicine if my blood pressure is normal?
What should I do if I feel dizzy after taking this medicine?
Can I drink alcohol while taking this medicine?
Will this medicine cure my high blood pressure?
Can I take other medicines with this one?
How long does it take for this medicine to work?
What if I have kidney problems?
Can this medicine cause allergic reactions?
Does this medicine interact with NSAIDs like ibuprofen?
Can I use salt substitutes with this medication?
What are the common side effects of hydrochlorothiazide/triamterene?
Does hydrochlorothiazide/triamterene interact with other medications?
What drug class is hydrochlorothiazide/triamterene?
Is hydrochlorothiazide/triamterene safe during pregnancy?
Related Medications in Thiazide / Potassium-Sparing Diuretic Combination
Other drugs grouped near hydrochlorothiazide/triamterene — same-class peers and common alternatives.
acebutolol
Sectral
Acebutolol is a medicine that helps lower blood pressure and control irregular heartbeats.
Compare with hydrochlorothiazide/triamterene →
aliskiren
Tekturna
Tekturna is a medicine used to treat high blood pressure.
Compare with hydrochlorothiazide/triamterene →
amiloride
Midamor
Amiloride is a water pill that helps your body hold onto potassium.
Compare with hydrochlorothiazide/triamterene →
amlodipine
Norvasc
Amlodipine (Norvasc) is a drug that lowers blood pressure and treats chest pain.
Compare with hydrochlorothiazide/triamterene →
amlodipine/benazepril
Lotrel
Lotrel is a combination medicine that contains amlodipine and benazepril.
Compare with hydrochlorothiazide/triamterene →
Compare hydrochlorothiazide/triamterene vs acebutolol side-by-side →
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What the FDA Data Shows for hydrochlorothiazide/triamterene
The FDA label for hydrochlorothiazide/triamterene (sold under brand names such as Dyazide, Maxzide) classifies it as a prescription-only medication in the Thiazide / Potassium-Sparing Diuretic Combination class. This medicine is used to treat high blood pressure. Official labeling lists 5 commonly reported side effects, including Dizziness, Headache, Cough.
Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 79,221 voluntary reports. The database also lists 13 documented drug interactions derived from FDA labeling, with the top-flagged interaction rated major severity. Acquisition-cost data is surveyed weekly by CMS and updated as manufacturers report changes.
Report counts do not establish causation — a FAERS entry documents a temporal association, not proof that the drug produced the outcome. Widely prescribed medications naturally accumulate more reports than niche therapies, so raw totals must be interpreted alongside total exposure. Shortage status, recall history, and patent information further shape supply and switching decisions. This page summarizes public FDA data for educational purposes only and is not a substitute for professional medical advice — always consult a licensed healthcare provider before starting, stopping, or changing any medication.
Data Sources
Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS).
FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. Always consult a healthcare professional before making medication decisions.
Last updated: June 29, 2023
Read our methodology — how this data is sourced, computed, and verified.
All federal data sources used on this page
- FDA Orange Book — approved drug products with therapeutic equivalence. accessdata.fda.gov/cder/ob
- FDA DailyMed — NIH-hosted drug labeling for FDA-approved meds. dailymed.nlm.nih.gov
- FDA Adverse Event Reporting System (FAERS) — post-marketing safety surveillance. fda.gov/drugs/faers
- NLM RxNorm — standardized clinical drug nomenclature. nlm.nih.gov/research/umls/rxnorm
- CMS Medicare Part B Drug Average Sales Price Files — federal drug pricing data. cms.gov/medicare/part-b-drugs/asp
- FDA Drug Shortages Database — current and resolved drug shortage tracking. accessdata.fda.gov/drugshortages