Obesity Drug Gets Green Light From FDA Advisory Panel

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Obesity Drug, Contrave Gets Green Light From FDA Advisory Panel

medicalnewstoday.com — “Experimental drug Contrave(R) (naltrexone SR/bupropion SR) for the treatment of obesity has been recommended for approval by the FDA's Endocrinologic and Metabolic Drugs Advisory Committee. The CoView full resource at medicalnewstoday.com

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Most Recently Shared on December 8, 2010 at 6:01 pm By:

medical_tweets medical_tweets Health News

Obesity Drug, Contrave Gets Green Light From FDA Advisory Panel Experimental drug Contrave(R) (naltrexone SR/bupropion .. http://dld.bz/9Ufx

1 year ago...

Firazyr For Hereditary Angioedema Gets Green Light From FDA Advisory Panel

medicalnewstoday.com — “An FDA Pulmonary-Allergy Drugs Advisory Committee voted in favor 11 to 1 (one abstention) of approving Firazyr (22150, icatibant solution), a medication for the treatment of hereditary angioedemaView full resource at medicalnewstoday.com

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Most Recently Shared on June 25, 2011 at 1:05 am By:

mnt_drugapprov MNT Drug Approvals Health News

Firazyr For Hereditary Angioedema Gets Green Light From FDA Advisory Panel http://mnt.to/3XFh #regulatory

11 months ago...

Epilepsy Drug Ezogabine Gets Green Light From FDA Advisory Panel - QualityPoint Technologies

qualitypointtech.net — “Ezogabine (Potiga) won a hearty endorsement by the FDA's Peripheral and Central Nervous System Drugs Advisory Committee for its efficacy as adjunctive treatment in partial-onset seizures. Medscape Medical NewsView full resource at qualitypointtech.net

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Most Recently Shared on August 12, 2010 at 4:48 pm By:

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Epilepsy Drug Ezogabine Gets Green Light From FDA Advisory Panel: Ezogabine (Potiga) won a hearty endorsement by t... http://bit.ly/cmqsKR

2 years ago...

Firazyr For Hereditary Angioedema Gets Green Light From FDA Advisory Panel - QualityPoint Technologies

qualitypointtech.net — “An FDA Pulmonary-Allergy Drugs Advisory Committee voted in favor 11 to 1 (one abstention) of approving Firazyr (22150, icatibant solution), a medication for the treatment of hereditary angioedema in patients aged 18+ years. Although the Committee's recommendations are not binding, the FDA nearly always goes along with what the Panel (Committee) advice. The FDA is expected to make its final decision on 25th August, 2011...View full resource at qualitypointtech.net

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Most Recently Shared on June 25, 2011 at 2:45 am By:

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Firazyr For Hereditary Angioedema Gets Green Light From FDA Advisory Panel: An FDA Pulmonary-Allergy Drugs Advisor... http://bit.ly/jdrn0l

11 months ago...

Seattle Genetics Lymphoma Drug Gets Second Green Light from FDA Panel | Xconomy

xconomy.com — “Seattle Genetics batted a clean 2-for-2 today in its appearances in front of an FDA advisory committee. The FDA's Oncologic Drugs Advisory Committee votedView full resource at xconomy.com

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Most Recently Shared on July 14, 2011 at 7:50 pm By:

ldtimmerman Luke Timmerman Health Communicator

Seattle Genetics gets 2nd green light from FDA panel for lymphoma drug. http://bit.ly/pTnPbZ

10 months ago...

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