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Are FDA Regulators Prev... - Blogs - Revolution Health
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Most Recently Shared on May 23, 2008 at 7:31 pm By:
retweet @drval Senator and Congresswoman promote ACCESS Act for terminally ill use of investigational drugs: http://tinyurl.com/62ajpq
FDA strengthens international collaboration to ensure quality, safety of imported products | diabetes and more | Scoop.it
scoop.it — “The U.S. Food and Drug Administration Commissioner Margaret A. Hamburg, M.D. today released the agency’s “Global Engagement Report,” detailing the many activities and strategies FDA is using to transform from a domestic to a global public health agency. The report describes the steps the agency is taking to ensure that imported food, drugs, medical devices, and other regulated products meet the same rigorous standards for safety and quality as those manufactured domestically...” View full resource at scoop.it
Most Recently Shared on April 26, 2012 at 11:14 am By:
FDA strengthens international collaboration to ensure quality, safety of imported products | @scoopit http://t.co/fIaoJJ1b
Group asks for withdrawal of Victoza diabetes drug | Reuters
reuters.com — “WASHINGTON (Reuters) - Watchdog group Public Citizen urged U.S. regulators to withdraw approval of Novo Nordisk's diabetes drug Victoza, saying it increases the risk of serious health problems like thyroid” View full resource at reuters.com
Most Recently Shared on April 19, 2012 at 6:49 pm By:
Mark Hyman, M.D. Doctor and Physician
http://t.co/mIAI7FJd #FDA thinks this: $$$$>Your health. This is why we must take back our #health. New #diabetes #drug #victoza is danger
Medical App Developers Struggle To Prepare for Regulation From FDA - iHealthBeat
ihealthbeat.org — “Developers of mobile medical applications are facing difficulties preparing for FDA regulation. Many mobile app developers are used to working in the somewhat unregulated Internet sector and are worried that FDA oversight could hinder innovation in the creation of medical apps. Politico.” View full resource at ihealthbeat.org
Most Recently Shared on April 17, 2012 at 7:00 pm By:
iHealthBeat.org Health Organization
Medical App Developers Struggle To Prepare for Regulation From FDA - http://t.co/mNEw2VBu
FDA adds diabetes, memory loss warnings to statins | Reuters
reuters.com — “(Reuters) - U.S. health regulators will add warnings to the labels of widely used cholesterol lowering drugs, such as Lipitor, to indicate that they may raise levels of blood sugar and could cause memory” View full resource at reuters.com
Most Recently Shared on March 26, 2012 at 7:12 pm By:
FDA adds diabetes, memory loss warnings to statins http://t.co/K8LawBa8
FDA to end overuse of antibiotics in livestock - Atlanta natural health | Examiner.com
examiner.com — “Natural health community of Atlanta, the FDA has been ordered to regulate and end the overuse of antibiotics in livestock. The move comes in response to a rise” View full resource at examiner.com
Most Recently Shared on March 24, 2012 at 1:11 pm By:
Natural Health News! Health News
FDA to end overuse of antibiotics in livestock http://t.co/WvfA2lZa
FDA must act to cut antibiotics from animal feed - Health - Food safety - msnbc.com
msnbc.msn.com — “A federal judge on Thursday ordered U.S. regulators to start proceedings to withdraw approval for the use of common antibiotics in animal feed, citing concerns that overuse is endangering human health by creating antibiotic-resistant "superbugs".” View full resource at msnbc.msn.com
Most Recently Shared on March 23, 2012 at 9:00 pm By:
MSNBC: FDA must act to cut antibiotics from animal feed - http://t.co/vYjRRUGZ
FDA must act to remove antibiotics from animal feed: judge | Agricultural Commodities | Reuters
af.reuters.com — “NEW YORK, March 22 (Reuters) - A federal judge on Thursday ordered U.S. regulators to start proceedings to withdraw approval for the use of common antibiotics in animal feed, citing concerns that overuse” View full resource at af.reuters.com
Most Recently Shared on March 23, 2012 at 1:51 pm By:
Robyn O'Brien Health Executive
Federal judge urges FDA to remove antibiotics from animal feed, saying overuse endangers human health http://t.co/TfdgF0ux cc @Laurie_David
FDA must act to remove antibiotics from animal feed: judge - QualityPoint Technologies
qualitypointtech.net — “NEW YORK (Reuters) - A federal judge on Thursday ordered regulators to start proceedings to withdraw approval for the use of common antibiotics in animal feed, citing concerns that overuse is endangering human health by creating antibiotic-resistant” View full resource at qualitypointtech.net
Most Recently Shared on March 23, 2012 at 5:45 am By:
FDA must act to remove antibiotics from animal feed: judge: NEW YORK (Reuters) - A federal judge on Thursday order... http://t.co/REYdS8CT
FDA must act to cut antibiotics from animal feed - TODAY Health - TODAY.com
today.msnbc.msn.com — “A federal judge on Thursday ordered U.S. regulators to start proceedings to withdraw approval for the use of common antibiotics in animal feed, citing concerns that overuse is endangering human health by creating antibiotic-resistant "superbugs".” View full resource at today.msnbc.msn.com
Most Recently Shared on March 23, 2012 at 4:02 am By:
This is huge: Judge: #FDA must act to cut antibiotics from animal feed http://t.co/1vIkyKx7 #foodsafety
FDA must act to remove antibiotics from animal feed: judge | Reuters
reuters.com — “NEW YORK (Reuters) - A federal judge on Thursday ordered regulators to start proceedings to withdraw approval for the use of common antibiotics in animal feed, citing concerns that overuse is endangering” View full resource at reuters.com
Most Recently Shared on March 23, 2012 at 4:01 am By:
FDA must act to remove antibiotics from animal feed: judge: NEW YORK (Reuters) - A federal judge o... http://t.co/qVsgvdr5 #health #news
FDA must act to cut antibiotics from animal feed - Health - Food safety - msnbc.com
msnbc.msn.com — “A federal judge on Thursday ordered U.S. regulators to start proceedings to withdraw approval for the use of common antibiotics in animal feed, citing concerns that overuse is endangering human health by creating antibiotic-resistant "superbugs".” View full resource at msnbc.msn.com
Most Recently Shared on March 23, 2012 at 3:46 am By:
msnbc.com - Health Health News
FDA must act to cut antibiotics from animal feed http://t.co/EeE07ndP
How FDA and FTC co-regulate health apps | mobihealthnews
mobihealthnews.com — “How FDA and FTC co-regulate health apps | mobihealthnews” View full resource at mobihealthnews.com
Most Recently Shared on March 22, 2012 at 12:43 pm By:
eyeonfda Pharma and Health Lawyer
How FDA and FTC co-regulate health apps http://t.co/KoxlftGU #mobileapps #hcsm
FDA says Merck's ridaforolimus meets study goal
health.yahoo.net — “WASHINGTON (Reuters) - Merck & Co Inc's ridaforolimus tablets met their primary research end-point of reducing by 25 percent the risk of progression or death in patients with metastatic soft tissue or bone sarcoma, U.S. health regulators said on Friday.” View full resource at health.yahoo.net
Most Recently Shared on March 16, 2012 at 3:40 pm By:
FDA says Merck's ridaforolimus meets study goal http://t.co/mspJf8V9
Votrient shows some cancer survival gains: FDA - Yahoo! News
news.yahoo.com — “From Yahoo! News: WASHINGTON (Reuters) - GlaxoSmithKline Plc's Votrient extended the lives of a significant number of patients suffering from an aggressive form of cancer without the disease getting worse, but the drug did not improve overall survival rates, U.S. health regulators said on Friday. Food and Drug Administration staff also said in a review document that the drug, known generically as pazopanib, has a safety profile for patients with soft-tissue sarcoma that is similar to indications” View full resource at news.yahoo.com
Most Recently Shared on March 16, 2012 at 2:46 pm By:
HealthTrendster Health Executive
Votrient shows some cancer survival gains: FDA - WASHINGTON (Reuters) - GlaxoSmithKline Plc's Votrient extended the ... http://t.co/3Ls1XTwd
FDA says Merck's ridaforolimus meets study goal - Yahoo! News
news.yahoo.com — “From Yahoo! News: WASHINGTON (Reuters) - Merck & Co Inc's ridaforolimus tablets met their primary research end-point of reducing by 25 percent the risk of progression or death in patients with metastatic soft tissue or bone sarcoma, U.S. health regulators said on Friday. A staff review document released by the Food and Drug Administration also said the treatment known by the brand name Taltorvic showed no new or unexpected safety signals in clinical research. The drug will come before an advisor” View full resource at news.yahoo.com
Most Recently Shared on March 16, 2012 at 2:46 pm By:
HealthTrendster Health Executive
FDA says Merck's ridaforolimus meets study goal - WASHINGTON (Reuters) - Merck & Co Inc's ridaforolimus tablets met ... http://t.co/olPZGSSo
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