| | | US FDA nod for Helixate FS for routine prophylaxis in children with haemophilia A |  | Advertisements: |
|  08/18/09 CSL Behring announced that Helixate FS, Antihemophilic Factor (Recombinant), has been approved by the US Food and Drug Administration (FDA) for routine prophylaxis in children with haemophilia A who are 16 years old or younger and do not have pre-existing joint damage. READ FULL SOURCE |
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Other news07/18/11 The U.S. Food and Drug Administration announced today that it has approved the influenza vaccine formulation for the 2011-2012 vaccine that will be used by the six manufacturers licensed to produce and distribute influenza vaccine for the United States.
07/18/11 A foodborne illness outbreak associated with raw milk from Tucker Adkins Dairy of York, South Carolina involves three confirmed and five probable cases of campylobacteriosis seen in North Carolina, the U.S. Food and Drug Administration (FDA) just announced. According to the FDA, raw milk is unpasteurized milk from hoofed mammals, such as cows, sheep, [...]
07/18/11 The U.S. Food and Drug Administration (FDA) just issued a notification to the medical imaging community and the public concerning the potential for inadvertent, increased radiation exposure in patients who underwent or will undergo cardiac positron emission tomography (PET) scans with rubidium (Rb)-82 chloride injection from CardioGen-82, a device manufactured by Bracco Diagnostics, Inc. The ... Hot themes this week:
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