Hydrochlorothiazide
Hct G.L. · ATC code C03AA03
Also known as: Hydrochlorothiazid, Hidroklorotiyazid
- Key facts
- Active substance
- Hydrochlorothiazide
- Drug class
- Thiazide
- ATC code
- C03AA03
- Authorisation
- authorised nationally; no central EU authorisation
- Information as of
- 2026-10-29
Key facts
Hydrochlorothiazide is, per the US prescribing information, a thiazide diuretic used to treat edema of various causes and hypertension, alone or with other antihypertensive drugs.
What it is used for
- Adjunctive therapy in edema associated with congestive heart failure, hepatic cirrhosis, and corticosteroid and estrogen therapy.
- Edema due to renal dysfunction such as nephrotic syndrome, acute glomerulonephritis and chronic renal failure.
- Hypertension, alone or to enhance other antihypertensive drugs.
Dosing
- Individualize therapy and use the smallest effective dose.
- Edema (adults): usually 25 mg to 100 mg daily as a single or divided dose; many patients respond to intermittent therapy (alternate days or 3 to 5 days each week).
- Hypertension (adults): start with 25 mg daily, may be increased to 50 mg daily; higher doses are often associated with marked reductions in serum potassium.
- Children: 1 to 2 mg/kg per day, not exceeding 37.5 mg per day up to 2 years or 100 mg per day in children 2 to 12 years; infants under 6 months may need up to 3 mg/kg per day.
Contraindications
- Anuria.
- Hypersensitivity to this product or other sulfonamide-derived drugs.
Important warnings
- Acute myopia and secondary angle-closure glaucoma within hours to weeks of starting; untreated, permanent vision loss can result.
- Caution in severe renal disease (azotemia, accumulation) and impaired hepatic function (fluid and electrolyte shifts may precipitate hepatic coma).
- Electrolyte disturbances such as hyponatremia, hypochloremic alkalosis, hypokalemia and hypomagnesemia; check electrolytes periodically.
- Hyperuricemia or acute gout, hyperglycemia (latent diabetes may become manifest), increased cholesterol and triglycerides.
- Increased risk of non-melanoma skin cancer; protect skin from the sun and have regular skin cancer screening.
- Possible exacerbation or activation of systemic lupus erythematosus.
Side effects
- No frequencies are given; reported reactions include weakness, (orthostatic) hypotension, pancreatitis, jaundice and gastrointestinal upset.
- Blood disorders such as aplastic anemia, agranulocytosis, thrombocytopenia.
- Hypersensitivity reactions, photosensitivity, Stevens-Johnson syndrome, toxic epidermal necrolysis.
- Dizziness, headache, muscle spasm, renal failure, interstitial nephritis, impotence.
Interactions
- Lithium should generally not be given with diuretics (high risk of lithium toxicity).
- Cholestyramine and colestipol reduce hydrochlorothiazide absorption (by up to 85 and 43 percent).
- Corticosteroids and ACTH intensify potassium loss; NSAIDs may reduce diuretic and antihypertensive effects.
- Alcohol, barbiturates and narcotics may potentiate orthostatic hypotension; antidiabetic doses may need adjustment.
Pregnancy and breastfeeding
- Routine use of diuretics in normal pregnancy is inappropriate; thiazides cross the placenta (risk of neonatal jaundice and thrombocytopenia, among others).
- Thiazides are excreted in breast milk.
Summary of the official product information, written with AI on 2026-10-29. Every number was checked automatically against the original text. Not reviewed by a physician – the full official text is authoritative.
Common questions – ask Medelix
For patients
Patient information (US)
This product has no separate US patient information.
Authorisation and brand names by country
Medicines with exactly this active-substance composition, as listed in the national registers – alphabetical and without ranking. Whether a product is currently available is not shown here.
Austria
- Hct G.L.G.L. Pharma Gmbh · 1 register entry
Source: EMA – Article 57 product data (EU/EEA), as of 2026-10-29
Germany
- Hct089pharm Gmbh, 1 A Pharma Gmbh, Ratiopharm Gmbh, Dexcel Pharma Gmbh, Hexal Ag, Puren Pharma Gmbh & Co. Kg, Betapharm Arzneimittel Gmbh, Abz-Pharma Gmbh · 8 register entries
Source: EMA – Article 57 product data (EU/EEA), as of 2026-10-29
Brand names in 21 more European countries
- Bulgaria
- Hypodehydra, Дехидразид, Дехидратин Нео
- Cyprus
- Didralin, Hydrochlorothiazide Remedica
- Czechia
- Hydrochlorothiazid Léčiva
- Denmark
- Hydrochlorothiazide Orifarm, Hydromed
- Estonia
- Hypothiazid
- Finland
- Hydrex
- France
- Esidrex, Hydrochlorothiazide Arrow, Hydrochlorothiazide Biogaran, Hydrochlorothiazide Eg, Hydrochlorothiazide Gerda, Hydrochlorothiazide Sfdb, Hydrochlorothiazide Substipharm
- Greece
- Diuren, Losazide
- Hungary
- Hypothiazid
- Iceland
- Hydromed
- Italy
- Esidrex, Idroclorotiazide Aurobindo
- Latvia
- Hypothiazid
- Lithuania
- Hypothiazid
- Netherlands
- Hydrochloorthiazide
- Norway
- Esidrex, Hydrochlorothiazide Orifarm, Hydromed
- Poland
- Hydrochlorothiazide Aurovitas, Hydrochlorothiazidum Polpharma
- Portugal
- Hidroclorotiazida Bluefish, Hidroclorotiazida Generis
- Romania
- Nefrix
- Slovakia
- Hydrochlorothiazid Léčiva
- Spain
- Drine, Esidrex, Hidroclorotiazida Aristo, Hidroclorotiazida Aurovitas, Hidroclorotiazida Cinfa, Hidroclorotiazida Gobens, Hidroclorotiazida Kern Pharma, Hidroclorotiazida Normon, Hidroclorotiazida Sandoz, Hidroclorotiazida Stada, Hidroclorotiazida Vir, Hidrosaluretil
- Sweden
- Esidrex, Hydrochlorothiazide Bluefish, Hydrochlorothiazide Orifarm, Hydroklortiazid Evolan
EMA – Article 57 product data (EU/EEA), 2026-10-29
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Sources
- U.S. Food and Drug Administration. Hydrochlorothiazide (Unichem Pharmaceuticals (USA), Inc.) – Prescribing Information, 2025-06-13. DailyMed (NLM), 2026-10-29. https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=33f3b980-b339-4dbf-99bd-05588c2a298c
- EMA – Article 57 product data (EU/EEA), 2026-10-29. https://www.ema.europa.eu/en/human-regulatory-overview/post-authorisation/data-medicines-iso-idmp-standards-post-authorisation/public-data-article-57-database
- EMA – Article 57 product data (EU/EEA), 2026-10-29. https://www.ema.europa.eu/en/human-regulatory-overview/post-authorisation/data-medicines-iso-idmp-standards-post-authorisation/public-data-article-57-database
- Wikidata (CC0): ATC C03AA.
Editorial: Medelix editorial team · last updated 2026-10-29 · How these pages are made · Report an error
Source: U.S. Food and Drug Administration (FDA), prescribing information, via DailyMed (NLM); public domain. Not advertising, not a treatment recommendation. For questions about your own treatment, ask your doctor or pharmacist.