Basic Information
C09CA07
telmisartan
Angiotensin II antagonists, plain
Therapeutic indication
Hypertension
Treatment of essential hypertension in adults.
Cardiovascular prevention
Reduction of cardiovascular morbidity in patients with:
- manifest atherothrombotic cardiovascular disease (history of coronary heart disease or peripheral arterial disease) or;
- type 2 diabetes mellitus with documented target organ damage.
Overview Summary
This is a summary of the European public assessment report (EPAR) for Tolura. 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 Tolura.
Active Substances (2)
Telmisartan
Telmisartan
Documents (11)
Tolura : EPAR - Public assessment report
June 21, 2010
INITIAL_MARKETING_AUTHORISATION_DOCUMENTS
Tolura : EPAR - Procedural steps taken and scientific information after authorisation
July 20, 2011
CHANGES_SINCE_INITIAL_AUTHORISATION
CHMP positive summary of opinion for Tolura
March 18, 2010
INITIAL_MARKETING_AUTHORISATION_DOCUMENTS
Tolura : EPAR - All Authorised presentations
June 21, 2010
AUTHORISED_PRESENTATIONS
Tolura : EPAR - Procedural steps taken and scientific information after authorisation
March 19, 2025
CHANGES_SINCE_INITIAL_AUTHORISATION
Tolura : EPAR - Public assessment report
June 21, 2010
CHANGES_SINCE_INITIAL_AUTHORISATION
Tolura : EPAR - Summary for the public
June 21, 2010
OVERVIEW_DOCUMENT
Tolura-H-C-1196-A31-0013 : EPAR - Scientific conclusions, grounds for variation to the terms of the marketing authorisations and detailed explanation of the scientific grounds for the differences from the PRAC recommenda...
September 25, 2014
CHANGES_SINCE_INITIAL_AUTHORISATION
Tolura : EPAR - Product Information
June 21, 2010
DRUG_PRODUCT_INFORMATION
Tolura : EPAR - Procedural steps taken and scientific information after authorisation (archive)
July 20, 2011
CHANGES_SINCE_INITIAL_AUTHORISATION
CHMP positive summary of opinion for Tolura
March 18, 2010
CHANGES_SINCE_INITIAL_AUTHORISATION
Overview Q&A (8)
Question
How is Tolura used?
Answer
For the treatment of essential hypertension, the recommended dose of Tolura is 40 mg once a day, but some patients may benefit from using a 20-mg dose. If the target blood pressure is not reached, the dose can be increased to 80 mg, or another medicine for hypertension can be added, such as hydrochlorothiazide.
For the prevention of cardiovascular problems, the recommended dose is 80 mg once a day. The doctor should monitor the patient’s blood pressure closely when starting Tolura, and may decide to adjust the patient’s blood pressure-lowering medication.
Question
How does Tolura work?
Answer
The active substance in Tolura, telmisartan, 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, telmisartan stops the hormone having an effect, allowing the blood vessels to widen. This allows the blood pressure to drop, reducing the risks associated with high blood pressure, such as having a heart attack. It also allows the heart to pump blood more easily, which can help to reduce the risk of future cardiovascular problems.
Question
Other information about Tolura
Answer
The European Commission granted a marketing authorisation valid throughout the EU for Tolura to Krka, d.d., Novo mesto on 4 June 2010. The marketing authorisation is valid for five years, after which it can be renewed.
For more information about treatment with Tolura, read the package leaflet (also part of the EPAR) or contact your doctor or pharmacist.
Question
Why has Tolura been approved?
Answer
The CHMP concluded that, in accordance with EU requirements, Tolura has been shown to have comparable quality and to be bioequivalent to Micardis. Therefore, the CHMP’s view was that, as for Micardis, the benefit outweighs the identified risk. The Committee recommended that Tolura be given marketing authorisation.
Question
What is Tolura?
Answer
Tolura is a medicine that contains the active substance telmisartan. It is available as white tablets (round: 20 mg; oval: 40 mg; capsule-shaped: 80 mg).
Tolura is a ‘generic medicine’. This means that Tolura is similar to a ‘reference medicine’ already authorised in the European Union (EU) called Micardis.
Question
What is Tolura used for?
Answer
Tolura is used to treat essential hypertension (high blood pressure) in adults. ‘Essential’ means that the hypertension has no obvious cause.
Tolura is also used to prevent cardiovascular problems (problems with the heart and blood vessels) such as heart attacks. It is used in patients who have had problems due to blood clots in the past (such as heart disease or artery disease) or who have type 2 diabetes that has damaged an organ (such as the eyes, heart or kidneys).
The medicine can only be obtained with a prescription.
Question
How has Tolura been studied?
Answer
Because Tolura is a generic medicine, studies in patients have been limited to tests to determine that it is bioequivalent to the reference medicine, Micardis. Two medicines are bioequivalent when they produce the same levels of the active substance in the body.
Question
What are the benefit and risk of Tolura?
Answer
Because Tolura is a generic medicine and is bioequivalent to the reference medicine, its benefit and risk are taken as being the same as the reference medicine’s.