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Janet Woodcock

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Available now: A 'female Viagra', but it comes with a warning

The first drug to treat low sexual desire in premenopausal women, dubbed "female Viagra", has been approved in the United States, but with a warning about potentially dangerous side effects such as......

Ranbaxy launches Lipitor's generic version in US

Drug major Ranbaxy Laboratories has launched its generic version of blockbuster cholesterol-lowering drug Lipitor in the US market.The launch came after final approval from the US health regulator......

US bans import of 30 generic drugs of Ranbaxy

The United States Food and Drug Administration on Tuesday banned the import of more than 30 generic drugs manufactured by Ranbaxy Laboratories Limited alleging that poor quality control at the......
  Web results for Janet Woodcock
FDA Advisory Committee Votes Against Approval of Eteplirsen; Coalition Duchenne Comments

PRWeb 2016-04-29 Coalition Duchenne Founder and Executive Director Catherine Jayasuriya Reflects on the Recent FDA Advisory Committee Meeting on... ...

http://www.bizwireexpress.com/showstoryPRWeb.php?storyid=512037
Jett Foundation on April 25th Advisory Committee Meeting

, /PRNewswire-USNewswire/ -- I want to thank the Duchenne Community for your effort, your time, and your strength. I want to thank all patients... ...

http://in.sys-con.com/node/3787168
Race to Yes Underscores Evidence Presented at FDAAdvisory Committee Meeting for Duchenne Muscular Dystrophy Drug Eteplirsen

GlobeNewswire 2016-04-27 We thank the scientific community from around the globe who came to Washington DC to stand with our community and defend... ...

http://www.bizwireexpress.com/showstoryGNW.php?storyid=116385
Sarepta Duchenne drug not proven effective

(Reuters) - An experimental drug to treat Duchenne muscular dystrophy, a devastating degenerative disease that mostly affects boys, has not been... ...

https://in.news.yahoo.com/u-panel-sarepta-duchenne-drug-not-proven-effective-010846244--finance.html
Sarepta shares sink as FDA staff stay sour on muscle drug

U.S. Food and Drug Administration staff reviewers stuck by their negative assessment of Sarepta Therapeutics Inc's rare muscle disorder drug,... ...

http://www.pharmafocusasia.com/news/sarepta-shares-sink-as-fda-staff-stay-sour-on-muscle-drug

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