Metolazone 5mg tablets
Requires a prescription from a doctor or prescriber
A quinazoline-sulfonamide that is considered a thiazide-like diuretic which is long-acting so useful in chronic renal failure.
Official documents, adverse reaction reporting, and safety monitoring
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Official medicine documents
Safety monitoring data
Yellow Card reports
The MHRA Yellow Card scheme collects reports of suspected side effects from healthcare professionals and patients. View the Drug Analysis Profile (iDAP) for real-world adverse reaction data.
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Suspected adverse reactions reported for Metolazone
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Submit a Yellow Card report to the MHRA
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.
EudraVigilance
The European Medicines Agency (EMA) collects suspected adverse reaction reports from across the EU/EEA through the EudraVigilance system. Search for safety data on this medicine.
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Suspected adverse reactions reported for Metolazone
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EudraVigilance data is published by the European Medicines Agency (EMA). A suspected adverse reaction is not necessarily caused by the medicine.
4 branded products available
MHRA licensed products
View all licensed products for Metolazone on the MHRA register
Xaqua 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.
WHO defined daily dose (DDD)
5 mg
Not a recommended dose. The DDD is the assumed average maintenance dose per day for a drug used for its main indication in adults. It is a statistical measure used for research and comparison purposes only.
Source: WHO Collaborating Centre for Drug Statistics Methodology, distributed via the NHS dm+d supplementary BNF/ATC mapping files (NHSBSA). 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.
NHS prescribing volume and spending trends
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Supply & safety information
Official UK regulator monitoring and safety alerts
Pharmacy links redirect to the retailer's own search and do not represent real-time stock levels. Shortage and safety information sourced from MHRA drug safety updates (gov.uk, Crown Copyright under OGL v3.0).
Codes for healthcare professionals and prescribing systems
These codes are used by healthcare IT systems and prescribers to identify this medicine.
NHS UK identifiers
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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. BNF code shown is the factual mapping value distributed by NHS Business Services Authority (NHSBSA) in the dm+d supplementary file under OGL v3.0; it is not affiliated with, nor licensed from, the publishers of the British National Formulary. 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: 9 · Randomised trials: 1 · Trials: 3 · 1988–2026
Showing the 50 most relevant studies, sorted by most relevant.
D. Shrestha, Y. Sedhai, S. Gaire, et al.
Health Sciences Review, 2023
Tunuguntla MN, Chanti P, Nelogal SS, et al.
2024
Acute decompensated heart failure (ADHF) often necessitates combination diuretic therapy when patients develop resistance to loop diuretics alone. Understanding baseline characteristics predictive of successful decongestion is essential for tailoring treatment strategies. This systematic review aimed to identify baseline characteristics associated with successful decongestion in ADHF patients undergoing combination diuretic therapy and to evaluate the effectiveness and risks of these therapies. A systematic review was conducted following Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines, with a literature search spanning 2019 to 2024 across PubMed and other databases. Studies included randomized controlled trials (RCTs) and clinical trials focusing on combination diuretic therapy, including thiazide diuretics and acetazolamide. Inclusion criteria emphasized studies reporting baseline characteristics and decongestion outcomes. From 43 initially identified articles, four studies met inclusion criteria. Combination diuretic therapy improved diuretic response and congestion resolution, with specific therapies such as metolazone, hydrochlorothiazide, and tolvaptan showing varying levels of effectiveness. Patients with lower baseline congestion scores, preserved renal function (estimated glomerular filtration rate (eGFR) ≥41 ± 20 mL/min/1.73m²), and higher ejection fractions (≥35%) were more likely to experience favorable outcomes. Risks such as renal impairment occurred more frequently in patients with pre-existing chronic kidney disease (CKD), highlighting the importance of careful monitoring. Notably, metolazone led to greater weight loss (e.g., -6 kg vs. -3 kg) and enhanced diuretic response (940 ± 149 mL/40 mg furosemide/day vs. 541 ± 314 mL). Combination diuretic therapy is effective for improving fluid management in resistant ADHF, but baseline patient characteristics significantly influence outcomes. This review provides novel insights into the role of individualized treatment strategies in optimizing therapy. Future research should focus on validating biomarkers, risk stratification tools, and promising but understudied combinations to improve safety and efficacy.
Abstract licence: CC BY
Kido K, Shimizu M, Shiga T, et al.
2025
A. Jaleel, V. Varughese, Cara Joseph, et al.
Journal of the American College of Cardiology, 2025
Matthew Kaye, Mohamad A. Kalot, Ronak Bahuva, et al.
Journal of Cardiac Failure, 2024
Taylor D. Steuber, Kristin M. Janzen, Meredith L. Howard
Pharmacotherapy The Journal of Human Pharmacology and Drug Therapy, 2020
- Chlorothiazide
- Diuretics
- Heart Failure
D. Shrestha, S. Gaire, B. Aryal, et al.
Circulation Research, 2022
M. Salahudin, H. Shah, M. Jan, et al.
JPMA. The Journal of the Pakistan Medical Association, 2019
- Diuretics
- Furosemide
- Indapamide
Su Ern Yeoh, Joanna Osmanska, Mark C. Petrie, et al.
European Heart Journal, 2023
- Heart Failure
- Metolazone
- Diuretics
Jens Rosenberg, Finn Gustafsson, Søren Galatius, et al.
Cardiovascular Drugs and Therapy, 2005
- Blood Pressure
- Body Weight
- Bumetanide
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.
Pharmacology and chemical data from DrugBank
Key facts
Drug status
Approved
Major interactions
52 found
Half-life
14 hours
Mechanism
The actions of metolazone result from interference with the renal tubular mechanism of electrolyte reabsorption.
Food interactions
1 warning
Human targets
1 target
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
2 to 4 hours
Half-life
14 hours
Protein binding
50-70%
Metabolism
70-95%
Elimination
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
Known interactions with other medications. Always consult a healthcare professional.
Showing 50 of 1556 interactions
How the body processes this drug — absorption, distribution, metabolism, and elimination
Proteins and enzymes this drug interacts with in the body
PMID:18270262 PMID:21613606 PMID:22009145 PMID:36351028 PMID:36792826
Also acts as a receptor for the pro-inflammatory cytokine IL18, thereby contributing to IL18-induced cytokine production, including IFNG, IL6, IL18 and CCL2 (By similarity). May act either independently of IL18R1, or in a complex with IL18R1 (By similarity)
Involved compounds
ATC C03EA12
ATC G01AE10
ATC C03BA08
Chemical identifiers
CAS, UNII, InChI Key and database cross-references
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Chemical identifiers
CAS, UNII, InChI Key and database cross-references
Linked compound data from DrugBank Open Data (CC BY-NC 4.0)
Metolazone
Additional database identifiers
Drugs Product Database (DPD)
8133
ChemSpider
4026
BindingDB
25899
HUGO Gene Nomenclature Committee (HGNC)
HGNC:10912
GenAtlas
SLC12A3
GeneCards
SLC12A3
GenBank Gene Database
U44128
GenBank Protein Database
1172161
UniProt Accession
S12A3_HUMAN
DrugBank citations
If you use DrugBank data in your research, please cite the following publications:
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Structured knowledge from the free knowledge base
ATC classifications (Wikidata)
Linked open data from Wikidata (Q1169561), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication. WHO INN from the World Health Organization.