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Drugs You Don’t Need For Disorders You Don’t Have

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~~~~TheHuffingtonPostHighline1

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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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!!!!!BN2016-3-31YOU ARE GETTING SLEEPY. VERRRRY SLEEPY.1Image: Breaking News and Opinion on The Huffington Post

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http://highline.huffingtonpost.com/articles/en/sleep-advertising/

 

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FDA Says Endoscope Makers Failed to Report Superbug Problems

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~~~~NBCNews1

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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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http://www.nbcnews.com/health/health-news/fda-says-endoscope-makers-failed-report-superbug-problems-n411241

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Popular Acne Meds Can Cause Allergic Reactions: FDA

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~~~~NBCNews1
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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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Side Effects May Include Death: The Story Of The Biggest Advance In Birth Control Since The Pill

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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 blood clots

NuvaRing prevents pregnancy while eliminating the inconvenience of taking a daily pill. (Getty photo)
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FDA Panel Gives Nod to New Diet Drug

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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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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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