Country: Jordan
Language: English
Source: JFDA (Jordan Food & Drug Administration - المؤسسة العامة للغذاء والدواء)
Rosuvastatin 10 mg
مستودع ادوية شاوي و رشيدات و مسنات - Shawi & Rushedat Drug Store
C10AA07
Rosuvastatin 10 mg
10 mg
28
اي بي ار فارماسيوتيكلز (امريكا)
11.96 :سعر الجمهور + الضريبة
1 Crestor 5 mg, 10 mg, 20 mg, 40 mg rosuvastatin calcium Film coated tablets Composition Each tablet contains 5 mg, 10 mg, 20 mg, or 40 mg of rosuvastatin (as calcium salt). Also contains glycerol. Pharmaceutical form Film-coated tablet. Round, yellow coloured (5 mg); round, pink coloured (10 mg and 20 mg); oval, pink coloured (40 mg). Therapeutic indications Treatment of hypercholesterolaemia Adults, adolescents and children aged 6 years or older with primary hypercholesterolaemia (type IIa including heterozygous familial hypercholesterolaemia) or mixed dyslipidaemia (type IIb) as an adjunct to diet when response to diet and other non-pharmacological treatments (e.g. exercise, weight reduction) is inadequate. Adults, adolescents and children aged 6 years or older with homozygous familial hypercholesterolaemia as an adjunct to diet and other lipid lowering treatments (e.g. LDL apheresis) or if such treatments are not appropriate. 2 Prevention of Cardiovascular Events Prevention of major cardiovascular events in patients who are estimated to have a high risk for a first cardiovascular event (see Pharmacodynamic properties), as an adjunct to correction of other risk factors. Posology and method of administration Before treatment initiation the patient should be placed on a standard cholesterol- lowering diet that should continue during treatment. The dose should be individualised according to the goal of therapy and patient response, using current consensus guidelines. Crestor may be given at any time of day, with or without food. Treatment of hypercholesterolaemia The recommended start dose is 5 mg or 10 mg orally once daily in both statin naïve or patients switched from another HMG-CoA reductase inhibitor. The choice of start dose should take into account the individual patient’s cholesterol level and future cardiovascular risk as well as the potential risk for adverse reactions (see below). A dose adjustment to the next dose level can be made after 4 weeks, if necessary (see Pharmacodynamic properties). In li Read the complete document