April 5, 2016
Mohenjo
Medical
amazon, Ambien, Belsomra, business, Business News, Dartmouth Medical College, FDA, Hotels, human-rights, Lunesta, medicine, mental-health, Merck, research, Science, Science News, technology, Technology News, travel, vacation

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One evening in the late summer of 2015, Lisa Schwartz was watching television at her Vermont home when an ad for a sleeping pill called Belsomra appeared on the screen. Schwartz, a longtime professor at Dartmouth Medical College, usually muted commercials, but she watched this one closely: a 90-second spot featuring a young woman and two slightly cute, slightly creepy fuzzy animals in the shape of the words “sleep” and “wake.”
Schwartz had a reason to be curious about this particular ad. Two years earlier, she had been a member of the advisory panel that reviewed Belsomra for the U.S. Food and Drug Administration—and the process had not gone well for the manufacturer, Merck. The company saw its new drug as a major innovation, emphasizing that the medication acted on an entirely different mechanism within the brain than the previous generation of insomnia medicines like Ambien and Lunesta. During the drug’s development, Merck had suggested that it could treat insomnia more effectively and produce fewer side effects than existing medications. In 2012, one Merck scientist described the science underlying Belsomra as a “sea change.”
But when Schwartz and her colleagues scrutinized data from the company’s own large-scale clinical trials, what they found was a lot less impressive. People taking Belsomra fell asleep, on average, only six minutes sooner than people taking a placebo and stayed asleep for a mere 16 minutes longer. Some test subjects experienced worrying side effects, like next-day drowsiness and temporary paralysis upon waking. For a number of people, these effects were so severe that the researchers halted their driving tests, fearing someone would get into an accident. Because of these safety concerns, the FDA ended up approving the drug at a lower starting dosage than the company had requested—a dosage so low that a Merck scientist admitted it was “ineffective.”
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Image: Breaking News and Opinion on The Huffington Post
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Click link below for article and video:
http://highline.huffingtonpost.com/articles/en/sleep-advertising/
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August 21, 2015
Mohenjo
Medical
"superbug" bacteria, amazon, business, Business News, FDA, Federal regulators, food and drug administration, hospital patients, Hotels, human-rights, manufacturer of medical scopes, medicine, mental-health, nbc news, Olympus, Olympus Corp., pseudomonas, research, Science, Science News, superbug Outbreak, technology, Technology News, travel, vacation

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Federal regulators have uncovered new violations by the manufacturer of medical scopes recently linked to outbreaks of deadly “superbug” bacteria at U.S. hospitals.
Olympus Corp. failed to alert regulators to a cluster of 16 infections in patients who underwent procedures with the company’s scope in 2012, according to a warning letter posted online Monday by the Food and Drug Administration. Olympus did not report the problems to the FDA until 2015, when the company was already under scrutiny for a more recent series of outbreaks.
Medical device manufacturers are required to report serious device problems to the FDA within 30 days of learning about them. The infections reported to the company involved a bacterial strain called pseudomonas, which can cause pneumonia, severe sickness and death in hospital patients.
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Click link below for article and video:
http://www.nbcnews.com/health/health-news/fda-says-endoscope-makers-failed-report-superbug-problems-n411241
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July 9, 2014
Mohenjo
Medical
acne, acne products, allergic reactions, amazon, Aveeno, benzoyl peroxide, business, Business News, Clean & Clear, dangerous reactions, FDA, food and drug administration, Health, Health officials, Hotels, human-rights, life-threatening allergic reactions, medicine, mental-health, Neutrogena, popular acne products, Proactiv, research, salicylic acid, Science, Science News, severe irritation, technology, Technology News, travel, vacation
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Health officials are warning that ingredients in some popular acne products including brands such as Proactiv, Neutrogena, Aveeno and Clean & Clear have been linked to potentially life-threatening allergic reactions.
Products containing benzoyl peroxide or salicylic acid can cause rare but potentially dangerous reactions or severe irritation, Food and Drug Administration said Wednesday.
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December 22, 2013
Mohenjo
Medical
amazon, Birth Control, Birth Control Blood Clots, birth control industry, Birth Control Safety, business, Business News, Carolyn Westhoff, David Grimes, FDA, Fda Birth Control, FDA NuvaRing, hormonal contraceptive vaginal ring, Hotels, huffingtonpost, human-rights, medicine, mental-health, Merck, Merck Nuvaring, Nuvaring, Nuvaring Blood Clots, Nuvaring Label, Nuvaring Litigation, Nuvaring Safety, Nuvaring Side Effects, Nuvaring Warning, obstetrics and gynecology, Organon, Organon Nuvaring, Ortho Evra, Politics News, research, Science, Science News, Slideshow, technology, Technology News, travel, vacation, Vaginal Ring, Video
FROM

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In the summer of 2002, the pharmaceutical company Organon unveiled what it believed would be a game-changer in the multibillion-dollar birth control industry. Its product, NuvaRing, was the first hormonal contraceptive vaginal ring in the world. An easy-to-use device that relieved women of the burden of taking a pill on a daily basis, it was hailed as the greatest advance in contraception since the introduction of the pill in 1960.
“We’ve never seen anything like this in my lifetime,” Dr. Carolyn Westhoff, a professor of obstetrics and gynecology who worked on NuvaRing’s clinical trials, told Newsday that August.
“It’s really an exciting time for contraceptive users,” Dr. David Grimes, a clinical professor of obstetrics and gynecology at the University of North Carolina, told The Washington Post. “It’s a new era.”
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NuvaRing prevents pregnancy while eliminating the inconvenience of taking a daily pill. (Getty photo)
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September 24, 2012
Mohenjo
Medical
business, climate, everyday health, FDA, FDA advisory committee, FDA advisory committee has voted 18-4, government, Health, lorcaserin hydrochloride (Lorqess), medicine, mental-health, myaol, new weight loss drug, politics, research, Science, technology, transportation, Video, weight loss
FROM

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An FDA advisory committee has voted 18-4, with one abstention, in favor of approving lorcaserin hydrochloride (Lorqess) as the first new weight loss drug in more than a decade.
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.Click link below for story and video:
http://www.everydayhealth.com/diet-nutrition/0510/fda-panel-gives-nod-to-new-diet-drug.aspx?xid=aol_eh-diet_7_20120507_&aolcat=APS&icid=maing-grid7|myaol|dl19|sec3_lnk1%26pLid%3D160095
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