News tagged with food and drug administration
Related topics: drug , fda , centers for disease control and prevention , heart attack , patients
FDA approves once-a-day inhaler from Glaxo
The Food and Drug Administration says it has approved a new once-a-day inhaler drug from GlaxoSmithKline for patients with chronic lung disease.
Medications
May 10, 2013 |
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Wrigley takes new caffeinated gum off market
(AP)—A Food and Drug Administration investigation into the safety of caffeine-added foods has prompted Wrigley to take its new caffeinated gum off the market for the time being.
Health
May 09, 2013 |
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Turning Alzheimer's fuzzy signals into high definition
Scientists at the Virginia Tech Carilion Research Institute have discovered how the predominant class of Alzheimer's pharmaceuticals might sharpen the brain's performance.
Neuroscience
May 07, 2013 |
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Judge in NYC rips opposition to Plan B order
A federal judge, asked by the U.S. government on Tuesday to freeze his plan giving teenage girls broader access to morning-after birth control, instead seized the chance to accuse health officials of taking steps that would ...
Health
May 07, 2013 |
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Study demonstrates that once-a-day pill offers relief from ragweed allergy symptoms
An international team of researchers, led by physician-scientists at Johns Hopkins, reports that a once-daily tablet containing a high dose of a key ragweed pollen protein effectively blocks the runny noses, sneezes, nasal ...
Immunology
May 07, 2013 |
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Decades-old question: Is antibacterial soap safe?
It's a chemical that's been in U.S. households for more than 40 years, from the body wash in your bathroom shower to the knives on your kitchen counter to the bedding in your baby's basinet.
Health
May 07, 2013 |
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Bionic eye maker has vision of the future
Robert Greenberg got tired of hearing from senior engineers that it wasn't possible to build his product idea: a bionic eye that gives sight to the blind. "A lot of the folks straight out of school didn't know any better, ...
Medical research
May 06, 2013 |
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FDA warns pregnant women about migraine drugs
(HealthDay)—Pregnant women who struggle with migraine headaches should never use medicines containing the ingredient valproate because they can lower the IQ scores of their children, the U.S. Food and Drug ...
Medications
May 06, 2013 |
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FDA wants cancer warnings for tanning beds
Indoor tanning beds would carry new warnings about the risk of cancer and be subject to additional regulations, under a proposal unveiled by the Food and Drug Administration.
Health
May 06, 2013 |
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Oral drops can give kids needle-free relief from asthma, allergies
Allergy shots are commonly used to treat children with severe environmental allergies and asthma, but under-the-tongue drops may offer yet another beneficial—and stick-free—option for pediatric allergy sufferers, according ...
Immunology
May 06, 2013 |
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GPS-like technology helps diagnose prostate tumors
The lead investigator of a way to obtain images of prostate tumors and accurately diagnose them said Thursday that the new technology is the medical equivalent of a global positioning system for the prostate gland.
Cancer
May 03, 2013 |
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Caffeine in kids' foods 'dangerous', US regulator says
The US food and drug regulator on Friday called the addition of caffeine to children's foods like chewing gum and jelly beans "dangerous" and warned of a possible crackdown.
Health
May 03, 2013 |
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FDA warning against high dose antidepressant prescription may be unwarranted, study finds
The U.S. Food and Drug Administration's warning that high doses of the antidepressant citalopram can cause potentially serious abnormal heart rhythms might be doing more harm than good.
Psychology & Psychiatry
May 03, 2013 |
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FDA approves Procysbi for nephropathic cystinosis
(HealthDay)—Procysbi (cysteamine bitartrate) delayed-release capsules have been approved by the U.S. Food and Drug Administration to treat nephropathic cystinosis in children (6 years and up) and adults. ...
Medications
May 02, 2013 |
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FDA reports Samsca may cause liver damage
(HealthDay)—After reviewing data from recent large clinical trials, the U.S. Food and Drug Administration has determined that Samsca (tolvaptan) should not be used for longer than 30 days and should not ...
Medications
May 02, 2013 |
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