CRESTOR

OnDemand podcasts

An archive of commentary from leading experts on current topics around dyslipidemia management.



Managing the Broad Range of High-Risk Patients: A Case-Study Approach

Teleconference 3
This presentation reviews the key LDL-C treatment algorithm modifications for at-risk patients under ATP III. It uses a case-study approach to compare treatment outcomes from a variety of therapies appropriate to typical at-risk patients.

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Confronting the Challenge: Treating Patients to Their Dyslipidemia Goals

Teleconference 2
Since the NCEP ATP II LDL-C goals were established in 2001, seven major clinical end point trials with statin therapy have been published. These trials have provided a greater rationale for lowering target LDL-C levels, and for more intensive LDL-C-lowering therapy. This slide show will discuss challenges and identify potential strategies for treating at-risk patients in need of lower LDL-C targets.

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FDA Rejects Public Citizen's Petition

Teleconference 1
On March 11, 2005, the Food & Drug Administration formally denied a petition to remove CRESTOR from the market following a thorough analysis of clinical trial safety data and postmarketing data for CRESTOR. This presentation discusses the petition and the science behind its rejection.

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Important safety information about CRESTOR

1

CRESTOR is contraindicated in patients with a known hypersensitivity to any component of this product, in patients with active liver disease, which may include unexplained persistent elevations of hepatic transaminase levels, in women who are or may become pregnant, and in nursing mothers.



Please see full Prescribing Information for CRESTOR.

CRESTOR was licensed from SHIONOGI & CO. LTD, Osaka, Japan.

CRESTOR is a registered trademark of the AstraZeneca group of companies.
259343  3/08 ©2008 AstraZeneca Pharmaceuticals LP. All rights reserved.
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This product information is intended for
US health care professionals only.