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Singulair Side Effects Possibly Include Suicide

FDA has started to look into the additional side effects of Merck's Singulair drug for Asthma treatment as reports link suicidal thoughts to Singulair.

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FDA to impose restrictions on Aranesp and Procrit drugs

Anemia drugs made by Amgen and Johnson & Johnson may raise the risk of death among those suffering from cancerous diseases, a new study says.

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FDA approves Nexium for children aged 1-11

A drug related to the class of proton pump inhibitors, most effective in reducing gastric acid secretion, was approved for the use in children.

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FDA inspects wrong heparin facility

A mere mistake in records may lead to unexpected things. For example, the Food and Drug Administration's Center for Drug Evaluation and Research mistakenly cleared the heparin facility belonging to another company with a similar name.

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Too Many Deaths Caused by Trasylol: 22,000 People

At least one critic of the US Food and Drug Administration (FDA) says the organization acted too slowly when it learned of the dangers of Trasylol. According to Dr. Dennis Mangano, approximately 22,000 lives could have been saved if the FDA had removed Trasylol from the market when it received evidence that the drug was linked to thousands of deaths. The FDA received that information two years ago from Dr. Mangano.

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Call For FDA Accountability

A poor man's lobbying effort.

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FDA recalls Duragesic patches

The FDA recalled Tuesday all the patches (25-microgram-per-hour patches with expiration dates on or before December 2009) containing fentanyl, because it can have a serious defect.

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FDA concerned with skin-harming tattoo inks

FDA, the Federal Drug Administration, has launched a study to review chemicals used in tattoo parlors. The US government initiated the research against the background of numerous incidents of skin problems, which particularly include rashes, blistering and swelling. The chemicals are used for tattoos which can be seen on various body parts of about 45 million American citizens.

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Physicians for Provenge

Open letter to Chairman Dingell and Ranking Member Barton, Subcommittee Chairman Pallone and Ranking Member Deal, and Chairman Stupak and Ranking Member Shimkus:

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FDA fines Red Cross 4.6 million for poor blood products

Food and Drug Administration fined the Red Cross $4.6 million after the latter did not make it to test blood donations and questioning donors.

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New FDA-approved asthma inhaler helps children under 4

The Food and Drug Administration has approved new inhaled steroid treatment for preventing asthma attacks in young children produced by Schering-Plough Corp.

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FDA concerned about sedation caused by Eli Lilly & Co's Zyprexa

Is Zyprexa safe for a schizophrenic? FDA tries to give answers.

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