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Group 52AM- Stem Cell Therapy – Video

Posted: Published on February 26th, 2013

Group 52AM- Stem Cell Therapy Group 52 (BIOL1103/11:00AM) clearly illustrates the topic of Stem Cell Therapy through a class project based on a member of their own group who is considering Stem Cell Therapy. By: Savannah Kelley … Continue reading

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How to Treat Facial Eczema [DermTV.com Epi #479] – Video

Posted: Published on February 26th, 2013

How to Treat Facial Eczema [DermTV.com Epi #479] Eczema can be uncomfortable and unsightly, but more importantly, difficult to treat. In this episode of DermTV, Dr. Schultz discusses one of the most common mistakes people make when treating eczema as well as one of the best ways to treat it. Subscribe to DermTV: http://www.youtube.com DermTV.com Connect with DermTV http://www.facebook.com http://www.twitter.com [TRANSCRIPT] Eczema is uncomfortable and unsightly. But here's the good news: if moisturizers and cortisone creams aren't giving you relief, help may be shockingly simple. The name Eczema just sounds uncomfortable... and it is. It's not exactly an onomatopoeia, but it's cacaphony tells you it's not something you want. Eczema's most immediate impact is discomfort, whether it's itching or burning or both, and even worse for many people, are the unsightly patches of redness, flaking and even crusting which, when on the face, just don't cover well with makeup. Eczema is often persistent, but when it does go away, just to make matters a little worse, it tends to be recurrent and come back for no apparent reason. While eczema can be anywhere on the body, it's the visual impact of … Continue reading

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DrugRisk Update: First Actos Lawsuit to Start This Week

Posted: Published on February 26th, 2013

Dallas, TX (PRWEB) February 25, 2013 The prescription drug resource center DrugRisk.com is alerting those patients whove taken the diabetes drug Actos of updated legal news on the site showing trial will commence this week in the first of thousands of lawsuits filed over bladder cancer. The goal of DrugRisk is to improve patient safety through education, including the latest drug warnings, recalls, studies and litigation news. By following the cases of others, patients can discuss options with their doctor and decide if they need legal advice, explains DrugRisk representative Ryan Mayer. The resource center has added Actos warnings by both the FDA* and European Medicines Agency** who indicated that long-term use of the drug may be associated with an increased risk of bladder cancer. The drug has also been banned in France and Germany.*** In DrugRisk legal news, more than 1,200 patients have filed an Actos lawsuit against drug maker Takeda Pharmaceuticals in a special multi-district federal court in Louisiana. The case is known as In Re: Actos Products Liability Litigation, MDL 2299, U.S. District Court, Western District of Louisiana (Lafayette). Now, the resource center is reporting that another group of Actos cases are set to kick off this … Continue reading

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DrugRisk Adding Latest Yaz Settlement Information from Bayer

Posted: Published on February 26th, 2013

Dallas, TX (PRWEB) February 25, 2013 The prescription drug resource center DrugRisk.com is alerting patients taking the birth control drugs Yaz or Yasmin of new information to be added to the site showing the latest Yaz settlement figures from Bayer. The mission of DrugRisk is to improve patient safety through education. This includes the latest warnings, recalls, studies and litigation news related to popular drugs like Yaz. Informed users can discuss options with their doctor and decide if they need legal advice, explains DrugRisk representative Ryan Mayer. The resource center had previously added studies from the British Medical Journal and U.S. FDA which warned birth control pills containing the hormone drospirenone, like Yaz and Yasmin, can increase the risk of blood clots, DVT and pulmonary embolism by as much as 74%.* DrugRisk has also uncovered information from Bayer, the maker of the drugs, indicating more than 12,000 women taking Yaz or Yasmin have filed a lawsuit over side effects like DVT and pulmonary embolism.** Due to the number of patients filing a Yaz lawsuit, cases were consolidated to a special federal Multi-District Litigation court in Illinois. The formal case is known as Yasmin and Yaz (Drospirenone) Marketing, Sales Practices and … Continue reading

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DrugRisk Report: Court Issues Latest Updates in Pradaxa Lawsuit

Posted: Published on February 26th, 2013

Orlando, FL (PRWEB) February 25, 2013 The prescription drug resource center DrugRisk.com is alerting patients taking the popular blood thinner Pradaxa of updated legal news information added to the site showing the federal court overseeing Pradaxa bleeding lawsuits has scheduled a new hearing for next month. DrugRisks mission is to improve the patient safety by providing the latest drug warnings, recalls, studies and litigation news. Patients informed of drug news can discuss side effect options with their doctor and decide if they need legal advice, explains DrugRisk representative Ryan Mayer. The resource center contains information from health organizations showing experts have differing opinions about the safety of Pradaxa. The FDA recently updated an advisory to indicate the drug carries the same risks as warfarin.* However, the American College of Cardiology has warned Pradaxa can significantly increase the risk of bleeding complications compared to warfarin.** DrugRisk has also obtained a report from the Institute for Safe Medication Practices ranking anticoagulants like Pradaxa among the highest risk outpatient drugs. In reviewing adverse event reports of hemorrhaging submitted to the FDA, the institute found bleeding from Pradaxa almost 5 times as likely to result in death than with warfarin.*** Due to the number … Continue reading

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DrugRisk Update: Pradaxa Maker Pays for Study to Dispute Risks

Posted: Published on February 26th, 2013

Los Angeles, CA (PRWEB) February 26, 2013 The prescription drug resource center DrugRisk.com is alerting patients taking the popular blood thinner Pradaxa of updated information added to the site showing the maker of Pradaxa, Boehringer Ingelheim, has funded a study which disputes prior warnings over bleeding risks. DrugRisks mission is to improve the patient safety by providing the latest drug warnings, recalls, studies and litigation news. In the case of research, it is important for patients to know whether it is independent or funded by drug makers with a financial stake in the outcome, explains DrugRisk representative Ryan Mayer. The resource center contains information from health organizations showing experts have differing opinions about the safety of Pradaxa. The FDA recently updated an advisory to indicate the drug carries the same risks as warfarin.* However, the American College of Cardiology has warned Pradaxa can significantly increase the risk of bleeding complications compared to warfarin.** DrugRisk has also obtained a recent study from the Institute for Safe Medication Practices which again ranks blood thinners like Pradaxa among the most dangerous drugs. In reviewing nearly 18,000 adverse events reported to the FDA, the institute found those patients with bleeding from Pradaxa are nearly … Continue reading

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DrugRisk Update: Latest Yaz Settlement Amounts Released This Week

Posted: Published on February 26th, 2013

Dallas, TX (PRWEB) February 26, 2013 The birth control safety advocates at DrugRisk.com are alerting those who have taken the oral contraceptives Yaz or Yasmin that new information will be added this week showing how many Yaz lawsuits Bayer has settled, how much they have paid, and what type of cases they are settling. DrugRisks goal is to improve consumer safety through education of the latest drug warnings, recalls, studies and litigation news. We receive calls every day from patients concerned over blood clot side effects and whether Bayer is still compensating victims, explains DrugRisk representative Ryan Mayer. The resource center contains studies from the British Medical Journal and FDA which warned birth control pills containing the hormone drospirenone, like Yaz and Yasmin, can increase the risk of blood clots, DVT and pulmonary embolism by as much as 74%.* In previous financial information uncovered by DrugRisk, Bayer admitted more than 12,000 women taking Yaz or Yasmin had filed a Yaz lawsuit over side effects like DVT and pulmonary embolism.** Due to the number of patients filing a claim, they were consolidated to a special federal Multi-District Litigation court in Illinois. The case is known as Yasmin and Yaz (Drospirenone) Marketing, … Continue reading

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AED for Kids Escaping Drugs – Video

Posted: Published on February 26th, 2013

AED for Kids Escaping Drugs Three residential treatment facilities for adults working to break the grip of chemical dependency are better equipped to respond to life-threatening emergencies, thanks to a Univera Healthcare donation of automated external defibrillator units. The three sites are in the city of Buffalo and are associated with Alcohol and Drug Dependency Services Foundation, Inc., more familiar to Western New Yorkers as Kids Escaping Drugs. Univera Healthcare has placed more than 150 AED units into service across upstate New York, including AEDs donated to the Erie, Wyoming and Chautauqua County Sheriff's Departments. By: UniveraHealthcare … Continue reading

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Reckitt hurt as rivals steal heroin march

Posted: Published on February 26th, 2013

Shares in Reckitt Benckiser took a tumble yesterday on news that its competitors will be able to make heroin-dependency drugs to compete with the consumer goods group. Reckitt had been trying to slow down competitors' plans to make rival drugs after it lost US patent protection for its heroin-dependency treatment drug Suboxone in 2009. But yesterday investors reacted to news that the US Food and Drug Administration had rejected Reckitt's petition to force rivals to take more precautions with the drugs packaging. Reckitt's shares took a hit and ended 135p lower at 4,381p. Not only has Reckitt lost its plea, but two generic drug makers have been given the go-ahead to enter the Suboxone tablet market with drugs that contain its key buprenorphine ingredient. The Dettol-to-Durex maker introduced a film-strip version of Suboxone that is less likely to be taken accidentally by children. It will stop producing Suboxone in tablet form next month. It had hoped packaging for the opiate substitute would become regulated to make it more expensive for rivals to produce. But the FDA decided that data presented by Reckitt did not necessitate the regulation that the company had suggested, which had included educational campaigns and child-resistant packaging. … Continue reading

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Reckitt Benckiser Says FDA Rejects Suboxone Safeguard Petition

Posted: Published on February 26th, 2013

Feb. 25 (Bloomberg) -- Reckitt Benckiser Group Plc faces competition in pharmaceuticals for the first time after the U.S. Food and Drug Administration approved two generic variants of its Suboxone heroin-dependency drug, thwarting the companys attempts to keep rivals away from its most profitable business. The company said today that two manufacturers have FDA approval to produce generic Suboxone tablets in the U.S. Competition could arrive within a month, according to Alex Howson, an analyst at Jefferies International in London. Reckitt Benckiser shares fell as much as 4.4 percent, also hurt by the FDAs rejection in a Feb. 22 letter of the companys September petition asking that makers of similar medicines implement more safeguards. The FDA also asked the Federal Trade Commission to look into claims by generic drug makers of anti- competitive business practices on Reckitt Benckisers part. The shadow of competition to Suboxone has hung over the Slough, England-based company since it lost U.S. patent protection in 2009. The pharmaceuticals unit generated 21 percent of profit last year, and analysts today reduced their 2013 profit estimates by as much as 4 percent. The market has been waiting for this news since October 2009, when Suboxones orphan drug status … Continue reading

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