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  • ...e assembly of [[Boyle's machine]]s. Because India's Food & Drug Authority (FDA-India) rules state that transferring a drug from one container to another (
    61 KB (8,728 words) - 16:50, 27 September 2010
  • ...hough this use is in decline.<ref>{{cite web|author = FDA|url = http://www.fda.gov/Cber/vaccine/thimerosal.htm|title = Thimerosal in Vaccines|accessdate=O ...tivated influenza vaccine.<ref>{{cite web |date=2007-09-06 |url=http://www.fda.gov/cber/vaccine/thimerosal.htm |accessdate=2007-10-01 |title= Thimerosal i
    69 KB (10,077 words) - 21:35, 20 September 2010
  • ...uld later prove useful. Zidovudine (AZT) was approved for marketing by the FDA on March 20, 1987.<ref name="Cimons">{{cite news | last = Cimons | first = ...) approved the drug (via the then-new [[FDA Fast Track Development Program|FDA accelerated approval system]]) for use against HIV, AIDS, and ''AIDS Relate
    21 KB (3,049 words) - 16:51, 27 September 2010
  • ...ower than 2.5&nbsp;grams per day.<ref name="2009_FDA_support">"[http://www.fda.gov/downloads/AdvisoryCommittees/CommitteesMeetingMaterials/Drugs/DrugSafet ...[http://www.fda.gov/Drugs/DrugSafety/InformationbyDrugClass/ucm165107.htm "FDA: Drug Safety & Availability - Acetaminophen Information"]</ref>
    54 KB (7,376 words) - 16:52, 27 September 2010
  • ...Circuit|U.S. Court of Appeals for the Tenth Circuit]] in Denver upheld the FDA's final rule declaring all dietary supplements containing ephedrine alkaloi
    21 KB (2,906 words) - 16:51, 27 September 2010
  • ...as approved by the American [[Food and Drug Administration (United States)|FDA]] in January 2008. ...title=MiddleBrook Pharmaceuticals Launches MOXATAG(TM), the First and Only FDA-Approved Once-Daily Amoxicillin |year=2009 | month=March| url=http://www.mi
    11 KB (1,413 words) - 16:52, 27 September 2010
  • | work = FDA Poisonous Plant Database | url = http://vm.cfsan.fda.gov/~djw/pltx.cgi?QUERY=tephrosia
    3 KB (345 words) - 12:27, 7 July 2010
  • ...(United States)|U.S. Food and Drug Administration]] (FDA).<ref>[http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/EnforcementActi
    19 KB (2,832 words) - 12:27, 7 July 2010
  • ...is no antidote. Despite its [[toxicity]], colchicine is approved by the US FDA for the treatment of [[gout]] and [[Familial Mediterranean Fever]] and is a
    4 KB (471 words) - 12:27, 7 July 2010
  • ...ov/ohrms/dockets/dailys/03/jul03/070303/81N-0033P_emc-000001.txt Letter to FDA], Professor George T. Gallagher, [[Boston University]] [[Goldman School of | url = http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/EnforcementActivitiesbyFD
    14 KB (2,005 words) - 12:27, 7 July 2010
  • * [http://www.fda.gov/bbs/topics/NEWS/2003/NEW00941.html FDA Issues Advisory on Star Anise "Teas"]
    3 KB (449 words) - 12:28, 7 July 2010
  • ...d in the United States by the [[United States Food and Drug Administration|FDA]], that combines natural belladonna alkaloids in a specific, fixed ratio wi
    24 KB (3,421 words) - 12:28, 7 July 2010
  • ...with the use of temazepam. According to the [[Food and Drug Administration|FDA]], temazepam had an incidence of euphoria of 1.5%, much more rarely reporte
    45 KB (6,129 words) - 22:16, 19 September 2010
  • ...ght to [[chelate]] the bivalents [[calcium]] and [[magnesium]]. It is not FDA approved for human use as an antiarrhythmic agent, and it is not included i
    7 KB (891 words) - 09:44, 20 September 2010
  • It was withdrawn from FDA review by the manufacturer after [[clinical trials#Phase III|phase III clin
    2 KB (250 words) - 09:44, 20 September 2010
  • ...uesting that Solvay Pharmaceuticals provides additional information to the FDA.<ref>{{cite web |url=http://www.drugs.com/nda/pulzium_071213.html |title=Dr
    2 KB (270 words) - 09:44, 20 September 2010
  • ...w.fda.gov/NewsEvents/Newsroom/PressAnnouncements/2006/ucm108644.htm |title=FDA Approves First Generic Pravastatin |accessdate=2008-01-20 |format= |work=}}
    3 KB (359 words) - 09:44, 20 September 2010
  • ...ne, blood circulation, and the liver. It was approved by the United States FDA on 6 March 2007, and for use in Europe on 27 August 2007. Its trade name is
    5 KB (697 words) - 09:44, 20 September 2010
  • ...bination-medicine-comprehensive-846.html |title=Drugs.com, Abbott Receives FDA Approval for Simcor (Niaspan / simvastatin), a Novel Combination Medicine f
    1 KB (165 words) - 09:44, 20 September 2010
  • ...s by [[Acorda Therapeutics]] and will be available in March 2010.<ref name=FDA /><ref>http://www.nationalmssociety.org/news/news-detail/index.aspx?nid=258
    9 KB (1,146 words) - 09:44, 20 September 2010

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