DIPYRIDAMOLE is a brand name for Dipyridamole. The medicine, its uses, side effects and dosage are the same regardless of brand.
Used for: As an adjunct to oral anti-coagulation for prophylaxis of thromboembolism associated with prosthetic heart valves.
Verbatim from this product's MHRA label. Tap a section to expand.
Posology Adults: 300-600 mg daily in three or four doses.
Paediatric population:
Dipyridamole is not recommended for children.
Elderly:
As for adults. Method of administration Dipyridamole is taken by mouth, and should usually be taken before meals.
Adverse effects at therapeutic doses are usually mild and transient The following side effects have been reported frequencies have been assigned based on a clinical trial (ESPS-2) in which 1654 patients received dipyridamole alone.
Very common (≥10), Common (≥ 1/100 < 1/10), Uncommon (≥1/1,000 < 1/100), Rare (≥1/10,000 < 1/1,000), Very rare (<1/10,000) Not Known – cannot be estimated from the available data. 4 Special warnings and precautions for use). Reporting of suspected adverse reactions Reporting suspected adverse reactions after authorisation of the medicinal product is important.
It allows continued monitoring of the benefit/risk balance of the medicinal product. uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.
Among other properties, Dipyridamole acts as a vasodilator. g. decompensated heart failure) . Patients being treated with regular oral doses of Dipyridamole should not receive additional intravenous Dipyridamole. Clinical experience suggests that patients being treated with oral dipyridamole who also require pharmacological stress testing with intravenous dipyridamole, should discontinue drugs containing oral dipyridamole for twenty-four hours prior to stress testing.
5). Dipyridamole tablets should be used with caution in patients with coagulation disorders. A small number of cases have been reported in which unconjugated dipyridamole was shown to be incorporated into gallstones to a variable extent (up to 70% by dry weight of stone).
These patients were all elderly, had evidence of ascending cholangitis and had been treated with oral dipyridamole for a number of years. There is no evidence that dipyridamole was the initiating factor in causing gallstones to form in these patients.
It is possible that bacterial deglucuronidation of conjugated dipyridamole in the bile may be the mechanism responsible for the presence of dipyridamole in gallstones. Dipyridamole contains lactose and sucrose. Patients with rare hereditary conditions of fructose intolerance, galactose intolerance, the Lapp lactase deficiency, glucose/galactose malabsorption or sucrase-isomaltase insufficiency should not take this medicine.
1. In case of rare hereditary conditions that may be incompatible with an excipient of the product (please refer to Special warnings and precautions for use) the use of the product is contraindicated.
Not medical advice. Always read the patient information leaflet and follow your prescriber or pharmacist.
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