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  0%  461.  ATT Worldnet - Health
On Oct. 10, 2001, the Consumer Product Safety Commission (CPSC) announced that Ohio firm Evenflo Company Inc. is recalling more than 20,000 of its wooden baby gates. Model numbers: CPSC says only model numbers 1555/6 with manufacture dates before September 2001 are affected by the recall. You can see a photograph of the recalled gate on the CPSC web site.
Last modified 11-23-09    Size 22K
http://dailynews.att.net/cgi-bin/news?dt=071101&cat=alerts&st=alerts4050_134&src=webmd
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  0%  462.  ATT Worldnet - Health
On Oct. 10, 2001, the Consumer Product Safety Commission (CPSC) announced Dorel Juvenile Group of Indiana is recalling more than 100,000 Cosco playpens made between May 1995 and December 1997. See photographs of the recalled playpens on the CPSC web site. But only JC Penney sold the "Okie Dokie" playpen.
Last modified 11-23-09    Size 22K
http://dailynews.att.net/cgi-bin/news?dt=071101&cat=alerts&st=alerts4050_133&src=webmd
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  0%  463.  ATT Worldnet - Health
Oct. 12, 2001 -- Good news for everyone whose daily schedule includes putting in, taking out, and cleaning soft contact lenses. Ciba Vision announced Friday that the FDA has approved the company's contact lenses that allow wearers to use them continuously for up to 30 days and nights. Ciba says the new contacts have been worn by 250,000 people in 40 different countries outside the U.S. before the FDA approval.
Last modified 11-23-09    Size 22K
http://dailynews.att.net/cgi-bin/news?dt=071101&cat=alerts&st=alerts4050_131&src=webmd
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  0%  464.  ATT Worldnet - Health
On Aug. 20, 2001, the Consumer Product Safety Commission (CPSC) announced several recalls are being conducted for toys and safety helmets. Also on Aug. 20, 2001, CPSC announced the California firm World Industries, Inc., is recalling 10,000 of its skateboard helmets. A photograph of the recalled helmets also can be found on the CPSC web site.
Last modified 11-23-09    Size 26K
http://dailynews.att.net/cgi-bin/news?dt=071101&cat=alerts&st=alerts4050_121&src=webmd
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  0%  465.  ATT Worldnet - Health
May 21, 2002 -- The FDA has approved the use of the drug Bravelle for inducing ovulation in women with fertility problems. Bravelle is delivered by injection and is used in conjunction with another fertility treatment (human chorionic gonadotropin) to stimulate ovulation. One of these clinical trials compared Bravelle to a genetically engineered follicle-stimulating hormone treatment, follitropin beta.
Last modified 11-23-09    Size 21K
http://dailynews.att.net/cgi-bin/news?dt=071101&cat=alerts&st=alerts4048_145&src=webmd
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  0%  466.  ATT Worldnet - Health
On April 19, 2002,  the FDA and Danco Laboratories sent a letter detailing new safety information regarding the use of the abortion pill Mifeprex in combination with misoprostol, a medication that causes uterine contractions and is used along with Mifeprex to induce abortions. The FDA has been informed of rare cases of ectopic pregnancies in women who were treated with Mifeprex and misoprostol. The letter also stresses that there is no proof that Mifeprex and misoprostol actually ...
Last modified 11-23-09    Size 22K
http://dailynews.att.net/cgi-bin/news?dt=071101&cat=alerts&st=alerts4048_141&src=webmd
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  0%  467.  ATT Worldnet - Health
The study showed that Vioxx was associated with a 50% lower risk of serious digestive system side effects such as bleeding, perforation, and obstruction compared with naproxen. After reviewing the VIGOR study, the FDA agreed with a previous recommendation from the agency's Arthritis Advisory Committee that the label for Vioxx should include information about these heart, stomach, and digestive system risks. The committee also recommended that new information be included on the Vioxx label ...
Last modified 11-23-09    Size 23K
http://dailynews.att.net/cgi-bin/news?dt=071101&cat=alerts&st=alerts4048_140&src=webmd
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  0%  468.  ATT Worldnet - Health
The agency is not aware of any risks associated with use of powdered formulas in full-term infants at home or with the use of liquid formulas. The FDA says powdered infant formulas are not commercially sterile products. FDA recommends that healthcare providers avoid using powdered infant formulas in neonatal intensive care settings unless there is no alternative available.
Last modified 11-23-09    Size 22K
http://dailynews.att.net/cgi-bin/news?dt=071101&cat=alerts&st=alerts4048_139&src=webmd
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  0%  469.  ATT Worldnet - Health
Zerit is an antiviral drug used to treat people with HIV that works by blocking the reproduction of HIV in the body. It first affects the legs -- causing weakness -- and moves up the body, causing respiratory failure in some patients taking Zerit along with other antivirals. Officials say health care providers should closely monitor HIV patients on Zerit for signs of elevated lactic acid levels.
Last modified 11-23-09    Size 21K
http://dailynews.att.net/cgi-bin/news?dt=071101&cat=alerts&st=alerts4048_138&src=webmd
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  0%  470.  ATT Worldnet - Health
On Aug. 15, 2001, Perrigo Company announced it is recalling nearly 8,000 of the 4-oz bottles of its cherry-flavored liquid pain-reliever for children. It was sold under the Hy-Vee label at Hy-Vee stores in Illinois, Iowa, Kansas, Minnesota, Missouri, Nebraska and South Dakota. Perrigo reports that the pain reliever suspension liquid affected by the recall carries lot number 1AD0228.
Last modified 11-23-09    Size 22K
http://dailynews.att.net/cgi-bin/news?dt=071101&cat=alerts&st=alerts4048_112&src=webmd
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