FDA panel to review diet drugs | theheart.org

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FDA panel to review diet drugs | theheart.org

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The FDA's Endocrinologic and Metabolic Drugs Advisory Committee will review the CV outcomes data from SCOUT for sibutramine, and weigh the new drug application for lorcaserin.

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Tags: Metabolic, Obesity Medication, Diet and Nutrition, Drug, FDA, Lorcaserin

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Most Recently Shared on August 9, 2010 at 10:25 pm By:

theheartorg Shelley Wood

Sibutramine CV safety, lorcaserin, up for FDA review: The FDA's Endocrinologic and Metabolic Drugs Advisory Commit... http://bit.ly/bBPd6l

2 years ago...

Weight loss pill Qnexa wins panel vote and awaits approval

news-medical.net — “The drug was rejected in a 10-6 vote the first time it came before a Food and Drug Administration (FDA) advisory panel, in 2010, due to safety concerns. However when the medication returned for another review in February, the advisory committee gave it near-unanimous approval (20-2). Because the FDA often follows the advisory panel's advice, Qnexa is likely to get FDA approval, probably by mid-April.View full resource at news-medical.net

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Most Recently Shared on April 5, 2012 at 11:08 pm By:

Diet_News News-Medical.Net Health News

Diet News: Weight loss pill Qnexa wins panel vote and awaits approval: The drug was rejected in a 10-6 vote the ... http://t.co/rGbONdEq

2 weeks ago...

FDA notes concerns about Vivus diet pill safety ahead of panel - FierceBiotech

fiercebiotech.com — “U.S. regulators have cited concerns about the safety of Vivus’ ($VVUS) experimental diet pill Qnexa in review documents as the California drug developer pursues the first FDA approval of a Read more...View full resource at fiercebiotech.com

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Most Recently Shared on February 17, 2012 at 3:52 pm By:

FierceBiotech FierceBiotech Health News

FDA notes concerns about Vivus diet pill safety ahead of panel http://t.co/Z8Nc7jXR $VVUS

2 months ago...

theheart.org: trusted cardiology news and opinions

theheart.org — “The latest developments in cardiology and cardiovascular research, including breaking heartwire news and commentary by some of the world's most prominent cardiologists.View full resource at theheart.org

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Most Recently Shared on December 7, 2010 at 10:33 pm By:

theheartorg Shelley Wood Cardiology

Most FDA advisors say likely benefits of Contrave diet drug outweigh its cardiovascular risks: In all, 13 panel ... http://bit.ly/hHMhj8

1 year ago...

Orexigen ($OREX) braces for a brutal panel review - FierceBiotech

fiercebiotech.com — “Can Orexigen Therapeutics' ($OREX) diet drug Contrave survive the FDA's advisory panel review process? Analysts have been pondering that question now that the FDA is scheduled to release staff Read more...View full resource at fiercebiotech.com

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Most Recently Shared on December 1, 2010 at 3:30 am By:

FierceBiotech FierceBiotech Health News

Orexigen ($OREX) braces for a brutal panel review. http://bit.ly/hSZBo8

1 year ago...

Meridia risks warrant restrictions or withdrawal: FDA panel | theheart.org

theheart.org — “UPDATED // Six members of the FDA panel voted to recommend that the FDA severely restrict access to the weight-loss drug, and eight recommended the plug be pulled on it altogether. Only two on the panel reviewing the SCOUT trial concluded that the drug should remain on the market with a boxed warning only, and no members thought the drug could stay with no labeling changes.View full resource at theheart.org

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Most Recently Shared on September 15, 2010 at 8:58 pm By:

theheartorg Shelley Wood Cardiology

Full story on today's #Meridia / sibutramine FDA advisory meeting now @ theheart.org http://www.theheart.org/article/1122267.do

2 years ago...

Ticagrelor advisory panel | theheart.org

theheart.org — “FDA's Cardiovascular and Renal Drugs Advisory Committee will review AstraZeneca's new drug application for ticagrelor, the proposed new antiplatelet drug for patients with acute coronary syndrome.View full resource at theheart.org

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Most Recently Shared on July 28, 2010 at 11:57 am By:

theheartorg Shelley Wood Cardiology

#Brilinta. Waiting for the ticagrelor FDA advisory panel to begin. See our preview here: http://bit.ly/aQotet

2 years ago...

FDA Panel Votes Against New Diet Drug - ABC News

abcnews.go.com — “An initial review by the U.S. Food and Drug Administration has found the diet pill Qnexa to be safe and effective, according to an FDA report released Tuesday morning.View full resource at abcnews.go.com

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Most Recently Shared on July 16, 2010 at 11:47 am By:

F.D.A. Review of Diet Pill Relieves Investors - Prescriptions Blog - NYTimes.com

prescriptions.blogs.nytimes.com — “The regulatory agency released its examination of the safety and effectiveness of Qnexa, in advance of an advisory panel on Thursday.View full resource at prescriptions.blogs.nytimes.com

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Most Recently Shared on July 13, 2010 at 4:49 pm By:

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