Connect to share and comment

FDA strengthens warnings on tanning beds to reduce cancer risk

By Toni Clarke Washington (Reuters) - Tanning beds and sunlamps will be required to carry stronger warning labels under new regulations proposed by the U.S. Food and Drug Administration, which is also recommending the machines not be used by people under the age of 18. The FDA said on Monday that it plans to reclassify sunbeds from low-risk to moderate-risk products, meaning they will need to be cleared by the agency before being allowed onto the market.

Baxter's Alzheimer's disease drug fails in late-stage trial

(Reuters) - Baxter International Inc said a late-stage study of its experimental drug to treat Alzheimer's disease failed to reduce the decline of cognitive functions and preserve functional abilities. The trial showed that after 18 months of treatment, patients with mild to moderate Alzheimer's disease taking Baxter's immunoglobulin treatment did not show a statistically significant difference in the rate of cognitive decline compared to a placebo.

Supplement builds strength in fibromyalgia trial

By Trevor Stokes NEW YORK (Reuters Health) - Creatine, a supplement favored by bodybuilders, modestly boosted muscle strength in patients with fibromyalgia, Brazilian researchers report. Apart from helping with muscle weakness, though, the treatment had little effect on other symptoms of the mysterious disorder, such as chronic pain, fatigue, memory loss, depression, anxiety and sleeplessness.

Sucking on your kid's pacifier: good idea or gross?

By Genevra Pittman NEW YORK (Reuters Health) - Toddlers are less likely to have asthma and itchy rashes if their parents "cleaned" their pacifiers by sucking on them when the kids were infants, a small new study suggests. The findings don't prove that technique protects kids against asthma, eczema or other allergies. But researchers said it's possible the transfer of mouth microbes from parents to baby may help boost the bacterial diversity of the young child's digestive system and foster immunity.

FDA advisers vote against Delcath's cancer therapy

(Reuters) - A panel of advisers to the U.S. health regulator said that risks outweighed the benefits in Delcath Systems Inc's cancer therapy for a rare form of eye cancer that spreads to the liver. The panel of independent experts voted 16-0 against the drug/device combination. The drug-device combination product consists of a chemotherapy drug, melphalan hydrochloride, and a device known as the Delcath Hepatic Delivery System. The two are combined in a single package known as the Melblez Kit.

Programs to reduce antibiotic use often work

By Andrew M. Seaman NEW YORK (Reuters Health) - Programs that attempt to encourage or force hospital doctors to cut back on prescribing antibiotics achieve that goal and help reduce the number of dangerous drug-resistant bacteria, says a review of past research.

Religious support tied to intensive end-of-life care

By Genevra Pittman NEW YORK (Reuters Health) - People with advanced cancer tend to get more aggressive care at the end of life and spend more time in the intensive care unit if they receive spiritual support from their religious communities, according to a new study. The report's lead researcher said that finding was "quite the opposite" of what her team was expecting - in part because of evidence that spiritual support coming from within a patient's medical team leads to less aggressive care and more use of hospice.

Insurance law tied to more breast reconstruction

By Kerry Grens NEW YORK (Reuters Health) - Many more breast cancer patients had breast reconstruction following a 1998 federal law mandating insurance coverage for the procedure, according to a new study. "I think it's the first large-scale study that shows that, slowly, legislation like the Women's Health and Cancer Rights Act is having an effect," said Dr. Evan Garfein, a plastic surgeon who has helped to draft a New York law aimed at improving access to breast reconstruction but who was not involved in the new research.

India regulators pull J&J plant license on baby powder concerns

(Reuters) - Health officials in India have revoked Johnson & Johnson's license to make cosmetics at a plant outside Mumbai after they discovered the company had used an unauthorized process for sterilizing its baby powder. J&J said in a statement on Friday that it is in "ongoing discussions" with Indian regulators.

MedEvac cost effective with modest use improvements

By Trevor Stokes NEW YORK (Reuters Health) - Emergency helicopter transport is expensive, but could become cost effective if it's used mainly for cases where it will make a measurable difference in trauma patients' survival or long-term disabilities, according to a new analysis.
Syndicate content