Abrea 0.075 g x 90 tablets, acetylsalicylic acid (Acidum Acetylsalicylicum)


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The drug Abrea contains acetylsalicylic acid at a dose of 75 mg in each tablet. The medicinal product ABREA 0.075 mg is indicated for use as a means of reducing the risk of blood clots formation, thus preventing, for example, heart attacks and strokes.

Composition of Abrea 0.075g:

Active substance: acetylsalicylic acid (Acidum Acetylsalicylicum). One gastro-resistant tablet contains 75 mg of acetylsalicylic acid and excipients: tablet core: lactose monohydrate, microcrystalline cellulose, colloidal anhydrous silica, potato starch. The composition of the first coating: talc, triacetin, methacrylic acid and ethyl acrylate copolymer (1: 1), 30% dispersion, sodium dodecyl sulfonate and polysobate 80. Composition of the second coating: polyvinyl alcohol (E1203), titanium dioxide (E171), macrogol 3350, talc , carmine (E120), sunset yellow (E110), aluminum lake

Action Abrea 0.075g:

Acetylsalicylic acid used in low doses is an antiplatelet drug. It prevents platelets from sticking together, which can cause blood clots, stopping blood flow and cutting off oxygen. As a result of such disorders, for example, a heart attack or a stroke can occur. Abrea 0.075 mg is also used to prevent blood clots following heart surgery to dilate or unblock blood vessels. The drug is intended for prophylactic use, it is not recommended to use it in cases that require emergency care.

The medicinal product Abrea 0.075g indicated for use to reduce the risk of blood clots and subsequent complications in the form of: heart attack, stroke, cardiovascular diseases in people with stable or unstable angina. The drug can be used to prevent blood clots following heart surgery.

Additional information:
Store the product out of reach of children, at room temperature. It is recommended to protect against moisture and light. Do not use as a pain reliever or antipyretic. Alcohol may increase the risk of gastrointestinal bleeding and prolong bleeding time. Use during pregnancy and breastfeeding: it is not recommended to use acetylsalicylic acid during this period, unless your doctor tells you otherwise. In the last three months of pregnancy, the daily dose should not exceed 100 mg of acetylsalicylic acid. The drug contains lactose - people with known intolerance to certain sugars should consult a doctor before using. The drug contains sunset yellow (E110) - this component may cause allergic reactions.

Do not use in case of hypersensitivity to any component of the drug. Do not use if you are allergic to other salicylates or non-steroidal anti-inflammatory drugs (NSAIDs). Do not use if you have ever had an asthma attack or swelling of certain parts of the body, e.g. face, lips, throat or tongue (angioedema) after taking salicylates or NSAIDs. Do not use if you have or have had a stomach ulcer or duodenal ulcer or any type of bleeding (e.g. stroke). Do not use in the case of blood coagulation disorders. Do not use in case of severe liver or kidney dysfunction. Do not use in cases of severe heart problems causing shortness of breath and ankle swelling. Do not use in the third trimester of pregnancy. Do not use when

Side effects:
Some people may experience side effects while taking the drug. If you experience any of the side effects listed below, stop taking this medicine immediately and seek medical attention: sudden wheezing, swelling of the lips, face or body, rash, fainting or difficulty swallowing (severe allergic reaction); reddening of the skin with blisters or peeling of the skin which may be associated with a high fever and joint pain (this may be erythema multiforme, Stevens-Johnson syndrome or Lyell's syndrome); unexpected bleeding (e.g. coughing up blood, blood in vomit or urine, tarry stools). Other side effects: common: nausea, vomiting, diarrhea; indigestion; increased bleeding tendency; uncommon: urticaria; runny nose; breathing difficulties; rare: severe bleeding in the stomach or intestines, cerebral bleeding; altered blood cell count; lower respiratory cramps, asthma attack; inflammation of the blood vessels; petechiae with purple spots (bleeding in the skin); severe skin reactions (rash known as erythema multiforme and its life-threatening forms, Stevens-Johnson syndrome and Lyell's syndrome); hypersensitivity reactions (swelling of e.g. lips, face or body, or shock); Rey's syndrome; abnormal heavy or prolonged menstruation; Not known: ringing in the ears (tinnitus) or impaired hearing; Headache; dizziness; stomach or duodenal ulcer or perforation; prolonged bleeding time; renal dysfunction, acute renal failure; liver problems, increased liver enzymes;

Dosage of Abrea 0.075g tablets:

Use as directed by your doctor or according to the instructions on the leaflet. Swallow the tablets whole, wash down with a sufficient amount of water (about 1/2 glass). Do not chew, crush or crush (tablets are coated which protects the contents against gastric juice). Adults, the elderly: prevention of myocardial infarction - the recommended dose is 75-160 mg once a day; prevention of stroke - the recommended dose is 75-325 mg once a day; prevention of cardiovascular disorders in patients with stabilized or unstable angina - the recommended dose is 75-160 mg once a day; prevention of blood clots after certain cardiac surgery - the recommended dose is 75-160 mg once a day. Maximum daily dose: 325 mg. Please note that the elderly are more prone to experiencing side effects, therefore caution is advised. The course of treatment should be reassessed regularly. It is not recommended to use the drug in children and adolescents under 16 years of age - unless your doctor tells you otherwise.