Lisinopril 10mg / Hydrochlorothiazide 12.5mg tablets
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Data from the MHRA Yellow Card scheme. A reported reaction does not necessarily mean the medicine caused it. Contains public sector information licensed under the Open Government Licence v3.0.
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24 branded products available
Part of the Zestoretic brand family (generic: Lisinopril + Hydrochlorothiazide)
MHRA licensed products
View all licensed products for Lisinopril + Hydrochlorothiazide on the MHRA register
Lisoretic 10mg/12.5mg tablets
Zestoretic 10 tablets
Zestoretic 10 tablets
Zestoretic 10 tablets
Lisinopril 10mg / Hydrochlorothiazide 12.5mg tablets
Lisinopril 10mg / Hydrochlorothiazide 12.5mg tablets
Lisinopril 10mg / Hydrochlorothiazide 12.5mg tablets
Lisinopril 10mg / Hydrochlorothiazide 12.5mg tablets
Lisinopril 10mg / Hydrochlorothiazide 12.5mg tablets
Lisinopril 10mg / Hydrochlorothiazide 12.5mg tablets
Lisinopril 10mg / Hydrochlorothiazide 12.5mg tablets
This is the NHS Drug Tariff indicative price used for reimbursement purposes. It may not reflect the price paid by patients or pharmacies.
View full Drug TariffSource: NHS Drug Tariff via NHSBSA. Derived from dm+d VMPP (Virtual Medicinal Product Pack) pricing data. Contains public sector information licensed under the Open Government Licence v3.0.
Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
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SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 4 · Randomised trials: 10 · 1994–2026
Showing the 50 most relevant studies, sorted by most relevant.
Nish Chaturvedi
The Lancet, 1997
Jean L Rouleau, Marc A Pfeffer, Duncan J Stewart, et al.
The Lancet, 2000
Ian R Reid, Ruth W Ames, Brandon J Orr-Walker, et al.
The American Journal of Medicine, 2000
Michal Fishel Bartal, S. Blackwell, C. Pedroza, et al.
American journal of obstetrics and gynecology, 2023
Ishani A, Hau C, Raju S, et al.
2024
- Hypertension
- Chlorthalidone
- Hydrochlorothiazide
ImportanceHypertension is a risk factor for the development and progression of chronic kidney disease (CKD). It is unclear whether different thiazide diuretics have a differential impact on kidney outcomes.ObjectiveTo compare kidney outcomes in patients with hypertension taking chlorthalidone and hydrochlorothiazide.Design, setting, and participantsThis prespecified secondary analysis of the Diuretic Comparison Project, a randomized clinical trial comparing chlorthalidone and hydrochlorothiazide for the treatment of hypertension, was conducted between June 1, 2016, and June 1, 2022, through Veterans Affairs facilities nationwide. This analysis extended follow-up to December 31, 2023. Veterans 65 years or older with hypertension who were taking hydrochlorothiazide were included.InterventionThe Diuretic Comparison Project randomized 13 523 participants to continue hydrochlorothiazide or switch to chlorthalidone.Main outcome and measuresThe main kidney outcome was CKD progression, defined as doubling of serum creatinine level from baseline, a terminal estimated glomerular filtration rate (eGFR) less than 15 mL/min, or dialysis initiation.ResultsAnalysis included 12 265 participants (90.7%) with a baseline and 1 or more follow-up creatinine measurements (median [IQR] age, 71 [69-75] years; 3.2% female and 96.8% male). The mean (SD) study duration was 3.9 (1.3) years. Chlorthalidone was not superior to hydrochlorothiazide at preventing kidney outcomes (369 of 6118 [6.0%] vs 396 of 6147 [6.4%]; hazard ratio [HR], 0.94; 95% CI, 0.81-1.08; P = .37). Similar results were observed when a 40% or greater reduction of eGFR was substituted for doubling of creatinine in the above outcome, as well as any of the components of the primary composite outcome. There was no difference in the incidence of CKD (961 of 4520 [21.3%] for chlorthalidone vs 939 of 4518 [20.8%] for hydrochlorothiazide; P = .59) or acute kidney injury requiring hospitalization (391 [6.4%] for chlorthalidone vs 379 [6.2%] for hydrochlorothiazide; P = .63) between groups. However, a statistically significant increased incidence of hypokalemia for chlorthalidone vs hydrochlorothiazide was observed (545 [8.9%] vs 426 [6.9%]; P Conclusions and relevanceChlorthalidone was not superior to hydrochlorothiazide for kidney outcomes but was associated with an increased risk for hypokalemia. Given these findings, clinicians should feel confident using either agent for the treatment of hypertension and kidney outcomes.Trial registrationClinicalTrials.gov Identifier: NCT02185417.
Abstract licence: CC BY
Nish Chaturvedi, Anne-Katrin Sjolie, Judith M Stephenson, et al.
The Lancet, 1998
Allan I. Goldberg, Mary C. Dunlay, Charles S. Sweet
The American Journal of Cardiology, 1995
Susan C. Brozena, Maryl R. Johnson, Hector Ventura, et al.
Journal of the American College of Cardiology, 1996
M. Schram, F. V. van Ittersum, A. S. Spoelstra-de Man, et al.
Journal of Human Hypertension, 2005
E. Reisin, M. Weir, B. Falkner, et al.
Hypertension, 1997
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Scientific data (pharmacology, interactions, ADME) is not yet available for this medicine. Clinical sections are sourced from the NHS dm+d database.