Gintarinė vaistinė nvaistine.lt (Lithuania) Phone: 880010008
Valga südameapteek (Estonia) Phone: +3727668005
Meness aptieka T. 8555, Open hours: Working days: 9.00-18.00. *Real final price may be varied.
Unreasonable use of drugs is harmful to your health! |
|
|
|||||||||||||||||||||||||||||
BRILIQUE TBL 90MG N56
Attention: Information on this site is provided for informational purposes and is not meant to substitute for the advice provided by your own physician or other medical professional. You should not use the information contained herein for treating a health problem or disease, or prescribing any medication. iDrugs24.com is not responsible for any damage to your health as the result of self treatment.
# On 2024-May-10
aproximate price on "BRILIQUE TBL 90MG N56 " in Riga city, Latvia is:86.65€ 93.09$ 74.59£ 10007Rub 1016.7SEK 373PLN 345.59₪
| Maximum allowed state defined price ( from ZVA webpage) Euro: | Recheck |
ATC code: B01AC24
Active substances: Ticagrelorum
Vendor, principal: Astra Ab.
BRILIQUE TBL 90MG N56 is compensated medicine in Latvia.
Prescription drug (℞)
* This table was compiled fully automatically, independently from any advertisers, transparently and without any modification relaying the open offers available on the mentioned dates.Only the distribution of over-the-counter remedies through the website is permitted in Latvia in accordance with national laws and regulations.
EUROPEAN MEDICINES AGENCY
SCIENCE MEDICINES HEALTH
EMA/214091/2016
EMEA/H/C/001241
EPAR summary for the public
Brilique
ticagrelor
This is a summary of the European public assessment report (EPAR) for Brilique. 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 Brilique.
What is Brilique?
Brilique is a medicine that contains the active substance ticagrelor. It is available as tablets (60 and 90 mg).
What is Brilique used for?
Brilique is used together with aspirin (acetylsalicylic acid) to prevent atherothrombotic events (problems caused by blood clots and hardening of the arteries) such as heart attacks or strokes. It is used in adults with acute coronary syndrome, a group of conditions in which blood flow in the vessels supplying the heart is blocked so heart tissue cannot work properly or dies, and which includes heart attack and unstable angina (a severe type of chest pain). Brilique is also used in adults who had a heart attack a year or more ago and are at a high risk of an atherothrombotic event.
The medicine can only be obtained with a prescription.
How is Brilique used?
For patients with acute coronary syndrome, the starting dose of Brilique is two 90-mg tablets taken at once, followed by a regular dose of one 90-mg tablet twice a day. They should take Brilique for a year unless the doctor asks them to stop it earlier. For longer treatment, the dose of Brilique should be reduced to one 60-mg tablet twice a day.
For patients who have had a heart attack a year or more ago (but less than 2 years ago) and are at high risk of an atherothrombotic event, the dose of Brilique is one 60-mg tablet twice a day—Patients
An agency of the European Union
30 Churchill Place • Canary Wharf • London E14 5EU • United Kingdom Telephone +44 (0)20 3660 6000 Facsimile +44 (0)20 3660 5555 Send a question via our website www.ema.europa.eu/contact
© European Medicines Agency, 2016. Reproduction is authorised provided the source is acknowledged.
taking Brilique should also be taking aspirin as directed by their doctor. The doctor may, for health reasons, tell them not to take aspirin. For further information, see the package leaflet.
How does Brilique work?
The active substance in Brilique, ticagrelor, is an inhibitor of platelet aggregation. This means that it helps to prevent blood clots from forming. When the blood clots, this is due to cell fragments in the blood called platelets aggregating (sticking together). Ticagrelor stops the platelets aggregating by blocking the action of a substance called ADP when it attaches to the surface of the platelets. This stops the platelets becoming sticky', reducing the risk of a blood clot forming and helping to prevent a stroke or another heart attack.
How has Brilique been studied?
Brilique was compared with clopidogrel (another inhibitor of platelet aggregation) in a main study involving over 18,000 adults who had had a heart attack or had unstable angina. The patients also took aspirin and were treated for up to a year.
In another main study, Brilique was compared with placebo (a dummy treatment) in over 21,000 adults who had a heart attack one to three years previously and were at high risk of an atherothrombotic event. Patients took Brilique twice a day in a dose of either 60 mg or 90 mg. The patients also took aspirin and were treated for up to 3 years.
The main measure of effectiveness for both studies was based on the number of patients having another heart attack, a stroke or dying from a cardiovascular disease.
What benefit has Brilique shown during the studies?
Brilique was shown to be beneficial to patients who have had a heart attack or unstable angina. In the first main study (in patients with acute coronary syndrome), 9.3% of the patients taking Brilique had another heart attack, stroke or died from a cardiovascular disease compared with 10.9% of patients taking clopidogrel.
In the second main study (in patients with a history of the heart attack), 7.8% of patients taking Brilique 60 mg twice a day had another heart attack, stroke or died from cardiovascular disease compared with 9.0% of patients taking placebo.
What is the risk associated with Brilique?
The most common side effects with Brilique (seen in more than 1 patient in 10) are dyspnoea (difficulty breathing), bleeding and raised uric acid level in the blood. For the full list of all side effects reported with Brilique, see the package leaflet.
Brilique must not be used in patients who have severe liver disease or are currently bleeding, or in patients who have had bleeding within the brain. It must also not be used in patients taking other medicines which have a strong blocking effect on one of the liver enzymes (CYP3A4). These are medicines such as ketoconazole (used to treat fungal infections), clarithromycin (an antibiotic), atazanavir and ritonavir (medicines used in HIV-positive patients) and nefazodone (used to treat depression). For the full list of restrictions with Brilique, see the package leaflet.
Why has Brilique been approved?
The CHMP decided that Brilique's benefits are greater than its risks and recommended that it be given marketing authorisation.
The CHMP considered that in patients with acute coronary artery syndrome, Brilique at a dose of 90 mg twice daily and given with aspirin, reduces the risk of atherothrombotic events such as heart attack, stroke and death from a cardiovascular event. Benefit regarding heart attack, stroke and death from a cardiovascular event has also been shown in patients who had a heart attack at least one year ago and have a high risk of an atherothrombotic event and a lower 60 mg dose twice daily dose is recommended for these patients.
Other information about Brilique
The European Commission granted a marketing authorisation valid throughout the European Union for Brilique on 3 December 2010.
The full EPAR for Brilique can be searched for on the Agency's website ema.europa.eu/Find medicine/Human medicines/European Public Assessment Reports. For more information about treatment with Brilique, read the package leaflet (also part of the EPAR) or contact your doctor or pharmacist.
This summary was last updated in 01-2016.
Brilique
EMA/214091/2016
Page 3/3
Instruction , annotation source: The European Medicines Agency
| ||
| For pharmacies & healthstores For advertisers About |
|
|