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Crestor (rosuvastatin, rosuvastatin) 10 mg, the recommended starting dose for is one 50mg tablet taken 1 hour before sexual activity.

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Rosuvastatin
Clinical data
Pronunciation/ r oʊ ˈ s uː v ə s t æ t ɪ n / roh- SOO -və-stat-in
Trade namesCrestor, Rosulip, Zuvamor
AHFS/Drugs.comMonograph
MedlinePlusa603033
Pregnancy categoryAU: D US: X (Contraindicated)
Routes of administrationBy mouth (tablets)
ATC codeC10AA07 ( WHO )
Legal status
Legal statusAU: S4 (Prescription only) UK: POM (Prescription only) US: ℞-only In general: ℞ (Prescription only)
Pharmacokinetic data
Bioavailability20% [1]
Protein binding88% [1]
MetabolismLiver: CYP2C9 (major) and CYP2C19-mediated; ~10% metabolized [1]
MetabolitesN -desmethyl rosuvastatin (major; 1/6–1/9 of rosuvastatin activity) [2]
Elimination half-life19 hours [1]
ExcretionFaeces (90%) [1]

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Atorvastatin, the generic version of lipitor, was approved by the FDA in November Side Effects Adverse reactions associated with the use of Lipitor may include, but are not limited to, the following: In patients with recent acute coronary syndrome, atorvastatin 80 mg daily reduced the risk of recurrent ischemia in the following 16 week period.

No post should be construed as medical advice and is not intended as such by the authors, editors, staff or by 2minutemedicine. Lipitor Atorvastatin is a statin class drug indicated for reducing high cholesterol levels in the blood, which helps in the prevention of cardiovascular diseases.

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When less cholesterol is produced, the liver takes up more cholesterol from the bloodstream, which results in lower levels of cholesterol circulating in the blood. The patent protection on Lipitor in the US expired in November There was no significant difference between the treatment groups for angina, revascularization procedures, and acute CHD death.

No works may be reproduced without expressed written consent from 2minutemedicine.

It is manufactured and marketed by Pfizer. Atorvastatin, the generic version of lipitor, was approved by the FDA in November Lipitor significantly reduced the rate of coronary events, both fatal coronary heart disease 46 events in click here placebo group vs.

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The FDA approval of Lipitor for Heterozygous Familial Hypercholesterolemia in pediatrics was based on a double-blind, placebo-controlled study, which was followed by an open-label phase. LDL is associated with cardiovascular diseases, whereas HDL helps in preventing thickening of artery atherosclerosis. The mean baseline LDL-C value was

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Crestor, 10 reviews:

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1010
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The results showed the drug reduced the rate of cardiovascular events to 83 when compared to in the placebo group.


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By blocking or inhibiting the action of HMG-CoA reductase, a link is broken in the chain of reactions that produces cholesterol. The difference in the primary endpoint was due to a reduction in the risk of recurrent symptomatic myocardial ischemia RR 0. In addition to diabetes, subjects had 1 or more risk factors.


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Lipitor significantly reduced the rate of coronary events, both fatal coronary heart disease 46 events in the placebo group vs. The primary endpoint was the time-to-first occurrence of any of the following major cardiovascular events MCVE:


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