MedPath
EMA Approval

Irbesartan Hydrochlorothiazide Zentiva (previously Irbesartan Hydrochlorothiazide Winthrop)

C09DA04

irbesartan and diuretics

Agents acting on the renin-angiotensin system

irbesartanhydrochlorothiazide

Basic Information

EMA regulatory identification and product classification information

EMA Identifiers

ATC CodeC09DA04
EMA European Classification

Overview Summary

Comprehensive product overview and regulatory summary

This is a summary of the European public assessment report (EPAR) for Irbesartan Hydrochlorothiazide Zentiva. It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the medicine to reach its opinion in favour of granting a marketing authorisation and its recommendations on the conditions of use for Irbesartan Hydrochlorothiazide Zentiva.

Authorisations (1)

EMEA/H/C/000783

sanofi-aventis groupe,sanofi-aventis groupe,54 rue La Boétie,,75008 Paris,France

Authorised

January 18, 2007

Active Substances (2)

irbesartan

hydrochlorothiazide

Documents (18)

Irbesartan Hydrochlorothiazide Zentiva : EPAR - Summary for the public

May 4, 2009

OVERVIEW_DOCUMENT

Irbesartan Hydrochlorothiazide Zentiva : EPAR - Product information

October 18, 2009

DRUG_PRODUCT_INFORMATION

Angiotensin-II-receptor antagonists (sartans) : Scientific conclusions - Impact of the Article 5(3) scientific opinion on nitrosamines

July 5, 2021

CHANGES_SINCE_INITIAL_AUTHORISATION

Irbesartan Hydrochlorothiazide Zentiva (previously Irbesartan Hydrochlorothiazide Winthrop)-H-C-PSUSA-00001653-201609 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisat...

November 6, 2017

CHANGES_SINCE_INITIAL_AUTHORISATION

Irbesartan Hydrochlorothiazide Winthrop : EPAR - Procedural steps taken before authorisation

February 4, 2007

CHANGES_SINCE_INITIAL_AUTHORISATION

Irbesartan Hydrochlorothiazide Winthrop : EPAR - Scientific Discussion

February 4, 2007

CHANGES_SINCE_INITIAL_AUTHORISATION

Irbesartan Hydrochlorothiazide Winthrop : EPAR - Procedural steps taken before authorisation

February 4, 2007

INITIAL_MARKETING_AUTHORISATION_DOCUMENTS

CHMP post-authorisation summary of positive opinion for Irbesartan Hydrochlorothiazide Zentiva

June 28, 2013

CHANGES_SINCE_INITIAL_AUTHORISATION

Irbesartan Hydrochlorothiazide Zentiva: EPAR - Procedural steps taken and scientific information after authorisation (archive)

October 25, 2009

CHANGES_SINCE_INITIAL_AUTHORISATION

Irbesartan Hydrochlorothiazide Zentiva : EPAR - All Authorised presentations

February 4, 2007

AUTHORISED_PRESENTATIONS

Angiotensin-II-receptor antagonists (sartans) Article 31 referral - CHMP assessment report

May 2, 2019

CHANGES_SINCE_INITIAL_AUTHORISATION

Angiotensin-II-receptor antagonists (sartans) Article 31 referral - CHMP assessment report - Impact of the Article 5(3) scientific opinion on nitrosamines

March 2, 2021

CHANGES_SINCE_INITIAL_AUTHORISATION

Irbesartan Hydrochlorothiazide Zentiva (previously Irbesartan Hydrochlorothiazide Winthrop)-H-C-A31-75 : EPAR - Assessment Report - Article 31

September 29, 2014

CHANGES_SINCE_INITIAL_AUTHORISATION

Irbesartan Hydrochlorothiazide Zentiva-H-C-783-II-69 : EPAR - Assessment Report - Variation

September 19, 2013

CHANGES_SINCE_INITIAL_AUTHORISATION

Irbesartan Hydrochlorothiazide Zentiva : EPAR - Scientific conclusions

May 23, 2019

CHANGES_SINCE_INITIAL_AUTHORISATION

Irbesartan Hydrochlorothiazide Zentiva: EPAR - Procedural steps taken and scientific information after authorisation

January 29, 2025

CHANGES_SINCE_INITIAL_AUTHORISATION

Irbesartan Hydrochlorothiazide Winthrop : EPAR - Scientific Discussion

February 4, 2007

INITIAL_MARKETING_AUTHORISATION_DOCUMENTS

Irbesartan Hydrochlorothiazide Zentiva (previously Irbesartan Hydrochlorothiazide Winthrop)-H-C-783-A31-75: EPAR - Scientific conclusions, grounds for variation to the terms of the marketing authorisations and detailed e...

September 29, 2014

CHANGES_SINCE_INITIAL_AUTHORISATION

Overview Q&A (9)

Question

Why has Irbesartan Hydrochlorothiazide Zentiva been approved?

Answer

The CHMP decided that Irbesartan Hydrochlorothiazide Zentiva’s benefits are greater than its risks and recommended that it be given marketing authorisation.

Question

How is Irbesartan Hydrochlorothiazide Zentiva used?

Answer

The dose of Irbesartan Hydrochlorothiazide Zentiva to be used depends on the dose of irbesartan or hydrochlorothiazide that the patient was taking before. Doses higher than 300 mg irbesartan and 25 mg hydrochlorothiazide once a day are not recommended. Irbesartan Hydrochlorothiazide Zentiva may be added to some other treatments for hypertension.

Question

How does Irbesartan Hydrochlorothiazide Zentiva work?

Answer

Irbesartan Hydrochlorothiazide Zentiva contains two active substances, irbesartan and hydrochlorothiazide.

Irbesartan is an ‘angiotensin-II-receptor antagonist’, which means that it blocks the action of a hormone in the body called angiotensin II. Angiotensin II is a powerful vasoconstrictor (a substance that narrows blood vessels). By blocking the receptors to which angiotensin II normally attaches, irbesartan stops the hormone having an effect, allowing the blood vessels to widen.

Hydrochlorothiazide is a diuretic, which is another type of treatment for hypertension. It works by increasing urine output, reducing the amount of fluid in the blood and lowering the blood pressure.

The combination of the two active substances has an additive effect, reducing the blood pressure more than either medicine alone. By lowering the blood pressure, the risks associated with high blood pressure, such as having a stroke, are reduced.

Question

Other information about Irbesartan Hydrochlorothiazide Zentiva

Answer

The European Commission granted a marketing authorisation valid throughout the European Union for Irbesartan Hydrochlorothiazide Winthrop on 19 January 2007. The name of the medicine was changed to Irbesartan Hydrochlorothiazide Zentiva on 6 February 2012.

For more information about treatment with Irbesartan Hydrochlorothiazide Zentiva, read the package leaflet (also part of the EPAR) or contact your doctor or pharmacist.

Question

What is the risk associated with Irbesartan Hydrochlorothiazide Zentiva?

Answer

The most common side effects with Irbesartan Hydrochlorothiazide Zentiva (seen in between 1 and 10 patients in 100) are dizziness, nausea (feeling sick) or vomiting, abnormal urination, fatigue (tiredness), and increases in blood urea nitrogen (BUN, a breakdown product of protein), creatinine (a breakdown product of muscle) and creatine kinase (an enzyme found in muscles). For the full list of all side effects reported with Irbesartan Hydrochlorothiazide Zentiva, see the package leaflet.

Irbesartan Hydrochlorothiazide Zentiva must not be used in people who are hypersensitive (allergic) to irbesartan, hydrochlorothiazide, sulfonamides, or any of the other ingredients. It must not be used in women who are more than three months pregnant. Its use during the first three months of pregnancy is not recommended. Irbesartan Hydrochlorothiazide Zentiva must also not be used in patients who have severe liver, kidney or bile problems, blood potassium levels that are too low or blood calcium levels that are too high.

Irbesartan Hydrochlorothiazide Zentiva in combination with aliskiren-containing medicines (used to treat essential hypertension) must not be used in patients with diabetes, or moderate or severe kidney impairment. Care must be taken when using Irbesartan Hydrochlorothiazide Zentiva with other medicines that have an effect on blood potassium levels. The full list of these medicines is given in the package leaflet.

Question

What is Irbesartan Hydrochlorothiazide Zentiva?

Answer

Irbesartan Hydrochlorothiazide Zentiva is a medicine that contains two active substances, irbesartan and hydrochlorothiazide. It is available as tablets (150 mg or 300 mg irbesartan and 12.5 mg hydrochlorothiazide; 300 mg irbesartan and 25 mg hydrochlorothiazide).

This medicine is the same as CoAprovel, which is already authorised in the European Union (EU). The company that makes CoAprovel has agreed that its scientific data can be used for Irbesartan Hydrochlorothiazide Zentiva.

Question

How has Irbesartan Hydrochlorothiazide Zentiva been studied?

Answer

Irbesartan on its own has been approved in the EU since 1997 under the names Karvea and Aprovel. It can be used with hydrochlorothiazide to treat hypertension. The studies of Karvea / Aprovel used with hydrochlorothiazide as separate tablets were used to support the use of Irbesartan Hydrochlorothiazide Zentiva. Further studies were also carried out with doses of 300 mg irbesartan in combination with 25 mg hydrochlorothiazide. The main measure of effectiveness was the reduction in diastolic blood pressure (the blood pressure measured between two heartbeats).

Question

What is Irbesartan Hydrochlorothiazide Zentiva used for?

Answer

Irbesartan Hydrochlorothiazide Zentiva is used in adults who have essential hypertension (high blood pressure) that is not adequately controlled by irbesartan or hydrochlorothiazide alone. ‘Essential’ means that the hypertension has no obvious cause.

The medicine can only be obtained with a prescription.

Question

What benefit has Irbesartan Hydrochlorothiazide Zentiva shown during the studies?

Answer

Irbesartan Hydrochlorothiazide Zentiva was more effective than placebo (a dummy treatment) and than hydrochlorothiazide alone in reducing diastolic blood pressure. Increasing the dose to 300 mg irbesartan and 25 mg hydrochlorothiazide may give a further decrease in blood pressure.

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.

Irbesartan Hydrochlorothiazide Zentiva (previously Irbesartan Hydrochlorothiazide Winthrop) - EMA Approval | MedPath