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- ...fda.gov/BiologicsBloodVaccines/BloodBloodProducts/ Blood & Blood Products. Food and Drug Administration</ref>. As well as being a regulatory agency, it both does research and work | publisher = Food and Drug Administration}}</ref>Until her confirmation, the FDA was under the interim leadership of40 KB (5,751 words) - 04:07, 19 September 2013
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- *[[Food and Drug Administration/Catalogs/Therapeutic Equivalence Code|Therapeutic Equivalence Code]]113 bytes (12 words) - 04:31, 13 July 2010
- 139 bytes (20 words) - 04:08, 19 September 2013
- Auto-populated based on [[Special:WhatLinksHere/Food and Drug Administration]]. Needs checking by a human.4 KB (505 words) - 16:36, 11 January 2010
- * [http://www.fda.gov/ Food and Drug Administration Home Page] ...s.html Biologics Centennial: 100 Years of Biologics Regulation] — from the Food and Drug Administration Home Page524 bytes (76 words) - 04:08, 19 September 2013
- #REDIRECT [[Food and Drug Administration/Catalogs/Therapeutic Equivalence Code]]80 bytes (9 words) - 04:29, 13 July 2010
- ...uivalence Code for [[generic drug]]s by the [[United States of America]] [[Food and Drug Administration]]. The table is from: http://www.fda.gov/Drugs/DevelopmentApprovalProcess/F14 KB (1,981 words) - 13:19, 2 February 2023
Page text matches
- ...rchType=BasicSearch&Search_Button=Submit&searchTerm=079013 Drugs@FDA]. U S Food and Drug Administration</ref>1 KB (142 words) - 11:47, 2 February 2023
- ...rchType=BasicSearch&Search_Button=Submit&searchTerm=077451 Drugs@FDA]. U S Food and Drug Administration</ref>1 KB (142 words) - 14:35, 2 February 2023
- * [http://www.fda.gov/ Food and Drug Administration Home Page] ...s.html Biologics Centennial: 100 Years of Biologics Regulation] — from the Food and Drug Administration Home Page524 bytes (76 words) - 04:08, 19 September 2013
- #REDIRECT [[Food and Drug Administration/Catalogs/Therapeutic Equivalence Code]]80 bytes (9 words) - 04:29, 13 July 2010
- {{r|Food and Drug Administration}}428 bytes (54 words) - 18:09, 10 January 2010
- * [http://dailymed.nlm.nih.gov/ DailyMed]. Drug information approved by the [[Food and Drug Administration]].732 bytes (100 words) - 07:40, 8 September 2008
- ...Biomarkers in the Context of Approved Drug Labels. U.S. [[Food and Drug Administration]].423 bytes (56 words) - 13:18, 24 July 2008
- ...rchType=BasicSearch&Search_Button=Submit&searchTerm=075310 Drugs@FDA]. U S Food and Drug Administration</ref>1 KB (163 words) - 14:10, 9 October 2009
- ...gs@FDA |author= |authorlink= |coauthors= |date= |format= |work= |publisher=Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2009-02-02 KB (233 words) - 11:54, 2 February 2023
- ...gs@FDA |author= |authorlink= |coauthors= |date= |format= |work= |publisher=Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2009-01-2784 bytes (100 words) - 14:12, 2 February 2023
- *[[Food and Drug Administration/Catalogs/Therapeutic Equivalence Code|Therapeutic Equivalence Code]]113 bytes (12 words) - 04:31, 13 July 2010
- ...delayed release brand of omeprazole was approved for AstraZeneca by the [[Food and Drug Administration]] in the [[United States of America]] with a [http://www.fda.gov/Drugs/Deve2 KB (199 words) - 14:07, 2 February 2023
- ...rchType=BasicSearch&Search_Button=Submit&searchTerm=040422 Drugs@FDA]. U S Food and Drug Administration</ref>3 KB (410 words) - 11:51, 2 February 2023
- The U.S. regulatory process under which the [[Food and Drug Administration]] authorizes the marketing of new drugs, for which it has verified safety a298 bytes (42 words) - 14:43, 4 October 2008
- ...brand of rosuvastatin was approved for Merck and Schering-Plough by the [[Food and Drug Administration]] in the [[United States of America]] with a [http://www.fda.gov/Drugs/Deve2 KB (265 words) - 14:07, 2 February 2023
- ...|homeopathic physician]] and educator; drafted legislation creating U.S. [[Food and Drug Administration]] giving special exemptions to homeopathy320 bytes (39 words) - 13:58, 20 March 2023
- ...rchType=BasicSearch&Search_Button=Submit&searchTerm=076588 Drugs@FDA]. U S Food and Drug Administration</ref> ...this usage is approved by the [[United States of America|United States]] [[Food and Drug Administration]].<ref name="pmid18541820">{{cite journal| author=Cernik C, Gallina K, Br4 KB (502 words) - 14:34, 2 February 2023
- {{r|Food and Drug Administration}}764 bytes (100 words) - 16:05, 11 January 2010
- ...one-proguanil''', made by [[Smith Kline Glaxo]] and approved by the U.S. [[Food and Drug Administration]] in 2000, is a fixed-combination [[antimalarial]] drug for [[chemoprophyla1 KB (171 words) - 15:29, 27 May 2010
- ...rchType=BasicSearch&Search_Button=Submit&searchTerm=076436 Drugs@FDA]. U S Food and Drug Administration</ref>3 KB (403 words) - 13:22, 2 February 2023
- [[Drug toxicity]] includes arrhythmias. The [[United States of America]] [[Food and Drug Administration]] has issued a warning to not use higher doses because of use of the [[cyto1 KB (123 words) - 11:44, 2 February 2023
- {{r|Food and Drug Administration}}1 KB (150 words) - 19:29, 11 January 2010
- In the [[United States of America]], the [[Food and Drug Administration]] provides regulation:1 KB (179 words) - 11:46, 2 February 2023
- ...rchType=BasicSearch&Search_Button=Submit&searchTerm=016418 Drugs@FDA]. U S Food and Drug Administration</ref> ...rchType=BasicSearch&Search_Button=Submit&searchTerm=070103 Drugs@FDA]. U S Food and Drug Administration</ref>2 KB (236 words) - 14:07, 2 February 2023
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- Within the regulatory authority of the U.S. Food and Drug Administration, '''radiation-emitting product''' has a specific technical and legal meanin | author = Center for Diagnostics and Radiologic Health, [[Food and Drug Administration]], [[U.S. Department of Health and Human Services]]}}</ref>2 KB (318 words) - 06:05, 31 May 2009
- Viread brand of tenofovir was approved for Gilead Sciences by the [[Food and Drug Administration]] in the [[United States of America|United States]] with a [http://www.fda.2 KB (335 words) - 14:35, 2 February 2023
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- The drug is approved by the U.S. [[Food and Drug Administration]] for [[depression]], [[generalized anxiety disorder]], [[obsessive-compuls2 KB (279 words) - 11:00, 10 February 2010
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- ...rchType=BasicSearch&Search_Button=Submit&searchTerm=074047 Drugs@FDA]. U S Food and Drug Administration</ref>3 KB (394 words) - 07:05, 17 October 2009
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- ...uthor=Anonymous |authorlink= |coauthors= |date= |format= |work= |publisher=Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2009-02-0 ...ts |author= |authorlink= |coauthors= |date=2009 |format= |work= |publisher=Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2009-01-25 KB (657 words) - 23:50, 12 July 2010
- ...dication]] that is a [[antineoplastic agent]]. It is approved by the U.S. Food and Drug Administration for the palliative treatment [[chronic lymphocytic leukemia]] (CLL). It is638 bytes (88 words) - 02:54, 10 February 2010
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- Remeron brand of mirtazapine was approved for Organon USA by the [[Food and Drug Administration]] in the [[United States of America]] with a [http://www.fda.gov/Drugs/Deve3 KB (422 words) - 14:08, 2 February 2023
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- ...UMARATE&SponsorApplicant=MUTUAL%20PHARM&ProductMktStatus=3 Drugs@FDA]. U S Food and Drug Administration</ref>2 KB (313 words) - 14:09, 4 July 2009
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- ...rchType=BasicSearch&Search_Button=Submit&searchTerm=076747 Drugs@FDA]. U S Food and Drug Administration</ref> ...rchType=BasicSearch&Search_Button=Submit&searchTerm=076798 Drugs@FDA]. U S Food and Drug Administration</ref>6 KB (804 words) - 14:35, 2 February 2023
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- ...rchType=BasicSearch&Search_Button=Submit&searchTerm=020733 Drugs@FDA]. U S Food and Drug Administration</ref> ...rchType=BasicSearch&Search_Button=Submit&searchTerm=074137 Drugs@FDA]. U S Food and Drug Administration</ref>6 KB (820 words) - 11:49, 2 February 2023
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- ...artment of the Treasury]], and the Bureau of Drug Abuse Control, in the [[Food and Drug Administration]] in what was then the Department of Health, Education and Welfare (HEW). H5 KB (660 words) - 11:54, 24 August 2008
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- ...rchType=BasicSearch&Search_Button=Submit&searchTerm=076039 Drugs@FDA]. U S Food and Drug Administration</ref>4 KB (489 words) - 08:06, 27 June 2010
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- Dificid brand of fidaxomicin was approved for Optimer Pharms by the [[Food and Drug Administration]] in the [[United States of America]] with a [http://www.fda.gov/Drugs/Deve2 KB (243 words) - 13:18, 2 February 2023
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- Levetiracetam was approved by the [[United States of America]] [[Food and Drug Administration]] ...r=Anonymous |authorlink= |coauthors= |date=1999 |format= |work= |publisher=Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=}}</ref>5 KB (616 words) - 13:22, 2 February 2023
- ...of Valid Genomic Biomarkers in the Context of Approved Drug Labels]. U.S. Food and Drug Administration</ref>.2 KB (230 words) - 12:47, 6 April 2009
- {{r|Food and Drug Administration}}923 bytes (113 words) - 21:25, 11 January 2010
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- ...or human-source research, such as the U.S. guidelines promulgated by the [[Food and Drug Administration]] (FDA).827 bytes (121 words) - 04:11, 21 February 2009
- Other participants in NACMCF include the [[Food and Drug Administration]] (FDA), the [[Centers for Disease Control]] (CDC), the [[National Marine F3 KB (446 words) - 10:25, 26 March 2024
- ...pplications/NewDrugApplicationNDA/default.htm New Drug Application] (NDA). Food and Drug Administration</ref> The NDA authorizes the drug to be advertised for specific '''indicat5 KB (808 words) - 15:51, 30 August 2009
- Pepcid brand of famotidine was approved by the [[Food and Drug Administration]] in the [[United States of America]]. It is available as a generic, and al4 KB (517 words) - 13:22, 2 February 2023
- {{r|Food and Drug Administration}}1 KB (132 words) - 17:56, 11 January 2010
- Inspra brand of eplerenone, submitted by GD Searle, was approved by the [[Food and Drug Administration]] in the [[United States of America]] with a [http://www.fda.gov/Drugs/Deve3 KB (447 words) - 13:22, 2 February 2023
- {{r|Food and Drug Administration}}1 KB (137 words) - 11:44, 11 January 2010
- {{r|Food and Drug Administration}}929 bytes (121 words) - 18:00, 1 April 2024
- ...eatment. Reich was convicted, and died in prison (1957), for violating a [[Food and Drug Administration]] 1954 injunction against him for fraud in claims for what were called "org1 KB (153 words) - 12:24, 16 September 2013
- {{r|Food and Drug Administration}}1 KB (145 words) - 10:57, 11 January 2010
- ...U.S. proprietary name is '''Fortaz'''. Indications approved by the U.S. [[Food and Drug Administration]] include: infections with [[Pseudomonas aeruginosa]], [[Escherichia coli]]2 KB (226 words) - 21:11, 21 August 2010
- {{r|Food and Drug Administration}}1 KB (146 words) - 21:45, 23 August 2010
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- | [[Food and Drug Administration]] || 177 || [[Food and Drug Administration Police]]<ref name=prisonpolicyFleo04/>5 KB (488 words) - 09:37, 26 October 2023
- ...uthor=Anonymous |authorlink= |coauthors= |date= |format= |work= |publisher=Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2009-01-1 ...uthor=Anonymous |authorlink= |coauthors= |date= |format= |work= |publisher=Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2009-01-15 KB (713 words) - 17:34, 10 February 2024
- {{r|Food and Drug Administration}}1 KB (151 words) - 23:49, 24 September 2010
- As defined by the U.S. [[Food and Drug Administration]], each 100 milliliters contains:951 bytes (133 words) - 03:09, 22 December 2010
- ...irus]]es. Four agents against influenza are currently approved by the US [[Food and Drug Administration]].1 KB (173 words) - 12:05, 21 January 2011
- Auto-populated based on [[Special:WhatLinksHere/Food and Drug Administration]]. Needs checking by a human.4 KB (505 words) - 16:36, 11 January 2010
- {{r|Food and Drug Administration}}1 KB (153 words) - 17:20, 11 January 2010
- Cellcept brand of mycophenolate mofetil was approved for Roche Palo by the [[Food and Drug Administration]] in the [[United States of America]] with a [http://www.fda.gov/Drugs/Deve Mycophenolate mofetil is approved by the [[Food and Drug Administration]] in the [[United States of America]] for:6 KB (836 words) - 14:09, 2 February 2023
- .../ref>, in which the precursors to the [[National Institutes of Health]], [[Food and Drug Administration]], the [[Social Security Administration]], and other well-known agencies, c2 KB (380 words) - 10:08, 10 February 2023
- In the [[United States of America]], the [[Food and Drug Administration]] has approved the use of aripiprazole for the treatment of [[schizophrenia2 KB (236 words) - 11:50, 2 February 2023
- ...|authorlink= |coauthors= |date=09/20/2010 8 |format= |work= |publisher=US Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2011-02-2 ...authorlink= |coauthors= |date=August 1, 1991 |format= |work= |publisher=US Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2009-01-16 KB (969 words) - 14:07, 2 February 2023
- ''Lexapro'' brand of escitalopram was approved by the [[Food and Drug Administration]] in the [[United States of America]] with a [http://www.fda.gov/Drugs/Deve4 KB (501 words) - 13:18, 2 February 2023
- Uses approved by the U.S. [[Food and Drug Administration]] are: ''[[Bacteroides]]'' brain sbscess, boutonneuse Fever, ''[[Hemophilus3 KB (358 words) - 23:20, 23 August 2010
- '''Effexor''' brand of venlafaxine was approved by the [[Food and Drug Administration]] in the [[United States of America|United States]] with a [http://www.fda.3 KB (390 words) - 14:34, 2 February 2023
- ...been raised about possible side effects of the medication, prompting the [[Food and Drug Administration|FDA]] to add a Boxed Warning for Chantix’s label listing depressed mood,3 KB (425 words) - 11:15, 13 March 2012
- Zetia brand of ezetimibe was approved for Merck and Schering-Plough by the [[Food and Drug Administration]] in the [[United States of America]] with a [http://www.fda.gov/Drugs/Deve6 KB (751 words) - 13:17, 2 February 2023
- The U.S. Food and Drug Administration (FDA) recognizes it as indicated for: [[glioma|glioblastoma multiforme]], m3 KB (376 words) - 14:53, 17 July 2010
- ...ntist]]. These medications are approved by national entities such as the [[Food and Drug Administration]] in the United States or by international entities such as the [[European United States [[Food and Drug Administration]] approved labels7 KB (977 words) - 08:20, 11 April 2024
- ...rchType=BasicSearch&Search_Button=Submit&searchTerm=075350 Drugs@FDA]. U S Food and Drug Administration</ref>7 KB (844 words) - 13:17, 2 February 2023
- ...nd superficial basal cell carcinoma; these indications are approved by the Food and Drug Administration. Other applications include actinic gheilitis, carcinoma in situ of the gla2 KB (318 words) - 02:18, 7 April 2024
- ...uses whose mothers had taken it during pregnancy. In response, the U.S. [[Food and Drug Administration]] banned its use in pregnancy.2 KB (233 words) - 11:16, 7 September 2008
- ...ively old drug, it is best known in the treatment of [[lymphoma]]s. U.S. [[Food and Drug Administration]] approved indications include: [[B-cell lymphoma]], [[Hodgkin's lymphoma]]3 KB (363 words) - 19:07, 1 July 2010
- [[Celecoxib]] remains marketed and according to the [[Food and Drug Administration]] is indicated for the treatment of acute pain, various types of arthritis,2 KB (265 words) - 09:16, 28 December 2010
- ...fatness to the point of health impairment is enough of a concern that "the Food and Drug Administration yesterday cleared Pfizer Inc. to market a drug called Slentrol for use in t3 KB (427 words) - 11:56, 8 June 2009
- ...s |authorlink= |coauthors= |date=November, 2003 |format= |work= |publisher=Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2009-02-0 ...authorlink= |coauthors= |date=August 1, 1991 |format= |work= |publisher=US Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2009-01-118 KB (2,553 words) - 13:17, 2 February 2023
- ...uivalence Code for [[generic drug]]s by the [[United States of America]] [[Food and Drug Administration]]. The table is from: http://www.fda.gov/Drugs/DevelopmentApprovalProcess/F14 KB (1,981 words) - 13:19, 2 February 2023
- *{{cite book| author=Food and Drug Administration (USA), Dockets Management Branch, Rockville, Maryland. Docket #82P-0316|tit2 KB (253 words) - 05:24, 2 August 2011
- The underlying problem is easy to identify: who gets to decide? The U. S. [[Food and Drug Administration]] is supposed to prevent companies or individuals from marketing drugs or f3 KB (483 words) - 01:52, 13 October 2019
- '''Labeled as approved uses''' by the U.S. [[Food and Drug Administration]]:<ref>{{citation3 KB (365 words) - 16:48, 30 July 2010
- ...r=Anonymous |authorlink= |coauthors= |date=2004 |format= |work= |publisher=Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2009-05-010 KB (1,452 words) - 14:10, 2 February 2023
- ...g for patients with impaired renal function.<ref name="fda-renalcategories>Food and Drug Administration, Guidance for Industry: [http://www.fda.gov/Drugs/DevelopmentApprovalProces7 KB (954 words) - 04:23, 12 January 2010
- ...r=Anonymous |authorlink= |coauthors= |date=2008 |format= |work= |publisher=Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2008-11-06 KB (776 words) - 14:13, 2 February 2023
- {{r|Food and Drug Administration}}2 KB (294 words) - 14:14, 6 April 2024
- ...e National Institute of Biomedical Imaging and Bioengineering (NIBIB), the Food and Drug Administration (FDA), private pharmaceutical companies and non-profit organizations, as a2 KB (343 words) - 09:59, 11 November 2009
- *[http://www.fda.gov/ Food and Drug Administration] (FDA)9 KB (1,270 words) - 09:48, 26 September 2007
- Cangrelor has not been approved for use in the United States by the [[Food and Drug Administration]]6 KB (873 words) - 12:25, 27 August 2013
- Rivaroxaban was approved by the [[Food and Drug Administration]] in the [[United States of America]] 7/2011.<ref>Anonymous (2011) [http://4 KB (500 words) - 14:12, 2 February 2023
- ...United States]] it was not approved for the treatment of insomnia by the [[Food and Drug Administration]] until 1981 when it came out under the brand name ''Restoril''. It quickly6 KB (893 words) - 14:32, 2 February 2023
- ...are not approved for any medical use by the [[United States of America]] [[Food and Drug Administration]].<ref>Lisa Roazen, M.D., [http://www.quackwatch.org/01QuackeryRelatedTopic2 KB (377 words) - 11:46, 2 February 2023
- ....S. [[Centers for Disease Control]] (CDC) received an exception from the [[Food and Drug Administration]] to Artesunate in the United States, specifically for treatment of malari6 KB (877 words) - 21:22, 30 December 2009
- ...OL%20TARTRATE&SponsorApplicant=NOVARTIS&ProductMktStatus=1 Drugs@FDA]. U S Food and Drug Administration</ref> .../index.cfm?fuseaction=Search.Overview&DrugName=TOPROL%2DXL Drugs@FDA]. U S Food and Drug Administration</ref> According to drugstore.com, 30 days of 100 mg pills costs $52.99 in J7 KB (1,032 words) - 13:16, 2 February 2023
- ...rade name Pradaxa (Boehringer Ingelheim), Dabigatran was approved by the [[Food and Drug Administration]] in the [[United States of America]], in October 2010, <ref>{{citation | publisher = Food and Drug Administration}}</ref> "for the prevention of stroke and blood clots in patients with abn12 KB (1,732 words) - 11:47, 2 February 2023
- ...r=Anonymous |authorlink= |coauthors= |date=2008 |format= |work= |publisher=Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2008-11-06 KB (862 words) - 11:49, 2 February 2023
- ...us |authorlink= |coauthors= |date=2008 |format= |work= |publisher= U.S. Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=}}</ref>8 KB (1,138 words) - 02:03, 4 November 2010
- ...re general risk to the liver. In July 2009, an advisory committee to the [[Food and Drug Administration]] recommended that the maximum dose be reduced to 650 milligrams, from 1000 The Food and Drug Administration may reduce the recommended dose to 650 milligrams per dose and no more than10 KB (1,471 words) - 08:15, 15 March 2024
- ...f> [[Methylnaltrexone]], is approved by the [[United States of America]] [[Food and Drug Administration]] for the treatment of [[constipation]] due to [[opioid analgesic]]s, is an4 KB (491 words) - 14:08, 2 February 2023
- ...of liquid silicone for soft tissue augmentation is not approved by the US Food and Drug Administration (FDA).3 KB (546 words) - 21:31, 5 February 2010
- ...[[Foodborne Pathogenic Microorganisms and Natural Toxins Handbook.]] U.S. Food and Drug Administration. 4 April 2008.]</ref> The bacterium ''L. monocytogenes''is nearly found eve ...[[Foodborne Pathogenic Microorganisms and Natural Toxins Handbook.]] U.S. Food and Drug Administration. 4 April 2008. [http://vm.cfsan.fda.gov/~mow/chap6.html] </ref> The individ18 KB (2,585 words) - 23:08, 26 October 2013
- ...u/cite&retmode=ref&cmd=prlinks&id=16702591 }} </ref> In March, 2004. The [[Food and Drug Administration]] asked Novartis to revise the label for Aredia.<ref>[Aredia http://www.acc4 KB (599 words) - 09:12, 25 May 2010
- Aldactone brand (GD Searle) of spironolactone was approved by the [[Food and Drug Administration]] in the [[United States of America]] with a [http://www.fda.gov/Drugs/Deve9 KB (1,159 words) - 14:09, 2 February 2023
- Indications according to the [[United States of America]] [[Food and Drug Administration]] are:<ref>{{CZMed}}6 KB (806 words) - 11:51, 2 February 2023
- ...r=Anonymous |authorlink= |coauthors= |date=2008 |format= |work= |publisher=Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=}}</ref><9 KB (1,175 words) - 14:01, 29 April 2010
- ...g for patients with impaired renal function.<ref name="fda-renalcategories>Food and Drug Administration, Guidance for Industry: [http://www.fda.gov/Drugs/DevelopmentApprovalProces13 KB (1,800 words) - 07:59, 9 May 2012
- ...ics in treatment of adult insomnia: meta-analysis of data submitted to the Food and Drug Administration13 KB (1,809 words) - 16:36, 24 August 2014
- ...rchType=BasicSearch&Search_Button=Submit&searchTerm=018240 Drugs@FDA]. U S Food and Drug Administration</ref> According to drugstore.com, 90 days of generic 50 mg pills costs $17. ...rchType=BasicSearch&Search_Button=Submit&searchTerm=072303 Drugs@FDA]. U S Food and Drug Administration</ref>16 KB (2,243 words) - 11:52, 2 February 2023
- ...ement Industry. Washington, DC: Center for Food Safety and Administration, Food and Drug Administration; 1999.</ref>9 KB (1,254 words) - 01:42, 23 May 2009
- ...ed methamphetamine. After decades of reports of abuse, the [[United States Food and Drug Administration|FDA]] banned amphetamine inhalers, and limited the drug to prescription use16 KB (2,210 words) - 17:32, 10 February 2024
- ...p://www.cfsan.fda.gov/ Center for Food Safety & Applied Nutrition], U.S. [[Food and Drug Administration]]11 KB (1,506 words) - 17:00, 7 July 2011
- ...r=Anonymous |authorlink= |coauthors= |date=1999 |format= |work= |publisher=Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=}}</ref>12 KB (1,573 words) - 13:22, 2 February 2023
- ...fda.gov/BiologicsBloodVaccines/BloodBloodProducts/ Blood & Blood Products. Food and Drug Administration</ref>. As well as being a regulatory agency, it both does research and work | publisher = Food and Drug Administration}}</ref>Until her confirmation, the FDA was under the interim leadership of40 KB (5,751 words) - 04:07, 19 September 2013
- ...maging (marketed as Magnevist, MultiHance, Omniscan, OptiMARK, ProHance)]. Food and Drug Administration</ref>10 KB (1,408 words) - 04:54, 21 March 2024
- ...tml Homeopathy:Real Medicine or Empty Promises?] by Isadora Stehlin , U.S. Food and Drug Administration.8 KB (1,105 words) - 09:43, 2 December 2010
- ...healthadvisories/ucm051136 Important Information on Chantix (varenicline)] Food and Drug Administration</ref>15 KB (2,047 words) - 13:29, 10 February 2023
- The American [[Food and Drug Administration]] defines severe effects as:<ref>{{cite web |url=http://www.fda.gov/medwatc ...dications to guide dosing for patients with impaired hepatic function.<ref>Food and Drug Administration, Guidance for Industry: [http://www.fda.gov/Drugs/DevelopmentApprovalProces39 KB (5,361 words) - 17:35, 10 February 2024
- *;[[Mercurochrome]]: Not recognized as safe and effective by the U.S. [[Food and Drug Administration]] (FDA) due to concerns about its [[Mercury (element)|mercury]] content. An9 KB (1,302 words) - 19:31, 11 February 2010
- ...r of growth hormone, glucagon, and insulin than the natural hormone. The [[Food and Drug Administration]] has approved the use of a form of this peptide ''octreotide acetate'', fo6 KB (912 words) - 17:45, 10 February 2024
- ...ials: An Analysis of Efficacy Comparing the Published Literature to the US Food and Drug Administration Database | journal = PLoS Med ...Bacchetti P, Bero L| title=Reporting bias in drug trials submitted to the Food and Drug Administration: review of publication and presentation. | journal=PLoS Med | year= 2008 |28 KB (3,923 words) - 14:09, 2 February 2023
- Because A.O.C. camemberts are aged less than 60 days, the Food and Drug Administration does not allow them to be imported into the United States; only those raw-m6 KB (973 words) - 12:38, 8 July 2011
- ...} </ref> can be taken once a day although this schedule is approved by the Food and Drug Administration only for tadalafil.9 KB (1,279 words) - 11:14, 28 August 2023
- ....S. [[Centers for Disease Control]] (CDC) received an exception from the [[Food and Drug Administration]] to Artesunate in the United States, specifically for treatment of malari15 KB (2,133 words) - 02:31, 27 October 2010
- [[Pregabalin]] (Lyrica) is approved for use in the United States by the [[Food and Drug Administration]] (FDA) for fibromyalgia. As compared to placebo, [[pregabalin]] benefits a ...ration antidepressant]], is approved for use in the United States by the [[Food and Drug Administration]] (FDA) for fibromyalgia. As compared to placebo, [[duloxetine]] 60 mg per25 KB (3,339 words) - 07:16, 2 July 2014
- *Aromatherapy products do not need approval by the U.S. Food and Drug Administration because there is no claim for treatment of specific diseases.9 KB (1,300 words) - 09:56, 28 January 2023
- ...ational Institutes of Health]], the [[Centers for Disease Control]], the [[Food and Drug Administration]], the [[American Medical Association]], the [[American College of Surgeons7 KB (1,096 words) - 18:30, 10 February 2010
- ...cts have not been evaluated (in the [[United States of America]]) by the [[Food and Drug Administration (United States)|FDA]], and their efficacy is questionable.<ref name="james"13 KB (1,912 words) - 11:48, 2 February 2023
- | title = Second breast cancer drug from yew tree - Food and Drug Administration approves Taxotere, or docetaxel17 KB (2,485 words) - 17:34, 10 February 2024
- ...was first given "generally recognized as safe" (GRAS) status by the [[U.S. Food and Drug Administration]] (FDA) in 2002 for use as a secondary packaging system, and does not requi17 KB (2,453 words) - 09:37, 6 March 2024
- * [[Citalopram]] (generic). The [[United States of America]] [[Food and Drug Administration]] has issued a warning to not use higher doses because of use of the [[cyto11 KB (1,448 words) - 14:12, 2 February 2023
- In the [[United States of America]], the [[Food and Drug Administration]] has issued warnings regarding combining PPIs with [[clopidogrel]].<ref>An26 KB (3,487 words) - 14:06, 2 February 2023
- In 2006 the U.S. [[Food and Drug Administration]] approved the use of [[Exubera]], the first inhalable insulin.<ref>[http:/21 KB (2,988 words) - 06:24, 9 October 2013
- ...000]], a device holding a telescopic camera during MIS was approved by the Food and Drug Administration (FDA).<br />9 KB (1,299 words) - 06:23, 14 January 2024
- The [[Food and Drug Administration]] released an advisory<ref>{{cite web |url=http://www.fda.gov/cder/drug/adv13 KB (1,859 words) - 17:44, 10 February 2024
- - [[Food and Drug Administration]] -9 KB (1,506 words) - 08:22, 28 April 2024
- ...chType=BasicSearch&Search_Button=Submit&searchTerm= 019655 Drugs@FDA]. U S Food and Drug Administration</ref>20 KB (2,873 words) - 11:51, 2 February 2023
- ...their use has not been approved, for acute radiation syndrome, by the U.S. Food and Drug Administration. It is also rational, especially if the patient has survived for an appreci9 KB (1,365 words) - 14:05, 31 March 2024
- ...od and Drug Administration itself does not make a recommendation<ref>U. S. Food and Drug Administration [http://www.fda.gov/fdac/features/1997/797_salt.html A Pinch of Controversy ...atement is required if the food exceeds 480mg of sodium per 'serving.'<ref>Food and Drug Administration [http://www.cfsan.fda.gov/~dms/flg-6a.html A Food Labeling Guide--Appendix35 KB (5,116 words) - 08:31, 11 September 2023
- Within the first few days of the Obama administration, the [[Food and Drug Administration]] gave the go-ahead to an embryonic stem cell research program aimed at fin31 KB (4,594 words) - 08:40, 28 April 2024
- ...M170188.pdf| publisher = Center for Drug Evaluation and Research (CDER), [[Food and Drug Administration]] (FDA)42 KB (5,794 words) - 14:08, 2 February 2023
- *[[DHHS]], [[Food and Drug Administration]] (FDA) - evaluates human health risk if the plant is intended for human co22 KB (3,139 words) - 14:32, 2 February 2023
- In the United States, glucosamine is not approved by the [[Food and Drug Administration]] for medical use in humans. Since glucosamine is classified as a dietary22 KB (3,050 words) - 05:38, 2 August 2011
- | publisher = [[Food and Drug Administration]]}}</ref> and iron dextran, as opposed to [[iron sucrose]], provided ferrou14 KB (1,989 words) - 13:18, 2 February 2023
- ===='''How does the U.S. Food and Drug Administration (FDA) regulate homeopathic remedies?'''==== U.S. Food and Drug Administration (FDA)39 KB (5,723 words) - 06:28, 31 May 2009
- ...chotic agents are less effective uses that have not been approved by the [[Food and Drug Administration]].<ref name="pmid21954480">{{cite journal| author=Maher AR, Maglione M, Bag15 KB (2,004 words) - 12:39, 28 February 2012
- ...is a question; I happened to look at the list of externals, and spotted [[Food and Drug Administration]] listed there; I know I'd worked on it in the past but never noticed that13 KB (2,279 words) - 19:01, 3 February 2009
- ...ogically incompatible with conventional medicine, to say the least. The US Food and Drug Administration strictly patrols claims made for herbal medicine, to prevent medical claims29 KB (4,262 words) - 10:07, 28 February 2024
- ...metabolic syndrome]]” is not a disease, regulatory agencies (such as the [[Food and Drug Administration]]) do not approve drugs to treat metabolic syndrome, as a specific indicate22 KB (3,243 words) - 08:33, 17 April 2024
- ...bined use since 2000, but in 2016, the [[United States of America|U.S.]] [[Food and Drug Administration]] (FDA), deeming the two drugs proven safe by hundreds of medical studies a46 KB (7,085 words) - 08:52, 26 July 2023
- ...i=|url=http://www.annals.org/cgi/content/full/146/1/52}}</ref> by the U.S. Food and Drug Administration of the drug NitroMed has led to the concept of race-based therapeutics.<ref ...|title=BiDil for heart failure in black patients: implications of the U.S. Food and Drug Administration approval |journal=Ann. Intern. Med. |volume=146 |issue=1 |pages=52–6 |yea73 KB (10,150 words) - 21:46, 20 August 2014
- ...y official recommendations at this time, in March 2009 was approved by the Food and Drug Administration and seems to be more tolerable than JE-VAX. It also only requires 2 inject17 KB (2,632 words) - 01:36, 22 April 2014
- ...10 | volume= 61 | pages= 63-75 | pmid=19686083 | }} </ref> The American [[Food and Drug Administration]] "highlights the opportunity for healthcare providers to use genetic tests52 KB (7,136 words) - 22:53, 6 April 2014
- ...effectiveness of amantadine against BDV. Amantadine was approved by the US Food and Drug Administration for use as a prophylactic against influenza in the 1960s and was shortly th28 KB (4,083 words) - 03:50, 14 February 2010
- |last=[[Food and Drug Administration]]26 KB (3,927 words) - 13:35, 11 May 2011
- ...States of America]], a number of HIV test kits have been approved by the [[Food and Drug Administration]] for diagnosis, [[prognosis|prognostic determination]], patient monitoring26 KB (3,990 words) - 13:22, 2 February 2023
- In August, 2006 the [[United States Food and Drug Administration]] (FDA) approved using bacteriophages on certain ready-to-eat meats to kill25 KB (3,809 words) - 14:09, 8 March 2024
- ...]|| Parke-Davis|| "stimulating off-label prescribing despite the lack of [[Food and Drug Administration|FDA]] approval"<ref name="pmid16908919">{{cite journal| author=Steinman MA,32 KB (4,430 words) - 08:23, 27 September 2012
- In August, 2006 the [[United States Food and Drug Administration]] (FDA) approved using bacteriophages on certain ready-to-eat meats to kill25 KB (3,752 words) - 13:50, 8 March 2024
- In January, the [[U.S. Food and Drug Administration]] gave the go-ahead to a stem cell research program that had been on hold s38 KB (5,883 words) - 16:13, 19 April 2024
- ...chType=BasicSearch&Search_Button=Submit&searchTerm= 019655 Drugs@FDA]. U S Food and Drug Administration</ref>31 KB (4,264 words) - 13:22, 2 February 2023
- ...drugs can be administered by injection. For the 2009 pandemic, the U.S. [[Food and Drug Administration]] issued an emergency authorization for the use of intravenous peramavir, w37 KB (5,103 words) - 13:22, 2 February 2023
- ...r=Anonymous |authorlink= |coauthors= |date=2003 |format= |work= |publisher=Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2009-05-081 KB (10,863 words) - 17:35, 10 February 2024
- | [[Food and Drug Administration]] New Drug Approvals<ref name="pmid11980521"/>|| 8% acquire a new black box | [[Food and Drug Administration]] New Drug Approvals<ref name="pmid11980521"/>|| 3% withdrawn. Half occur w63 KB (8,790 words) - 06:57, 2 March 2021
- ...requirements. In some, acupuncturists must work with an MD. In 1996, the [[Food and Drug Administration]] changed the status of acupuncture needles from [[Medical devices#Classifi31 KB (4,744 words) - 10:07, 28 February 2024
- ...mith necktie." In Stein's reading, The Wealth of Nations could justify the Food and Drug Administration, The Consumer Product Safety Commission, mandatory employer health benefits22 KB (3,614 words) - 06:30, 13 September 2013
- ...r [[Royal Copeland]] (a former homeopathic medical school dean) gave the [[Food and Drug Administration]] (FDA) the power to regulate drugs, and gave legal recognition to the ''Ho50 KB (7,299 words) - 08:34, 6 March 2024
- ...[[United States of America]], Good Clinical Practices is overseen by the [[Food and Drug Administration]] (http://www.fda.gov/ScienceResearch/SpecialTopics/RunningClinicalTrials/) ...62334 |doi=}}</ref> Many scientists and ethicists consider that the U.S. [[Food and Drug Administration]], by demanding placebo-controlled trials, encourages the systematic violat79 KB (10,925 words) - 14:12, 2 February 2023
- * U.S. Food and Drug Administration (November 2002) [http://www.fda.gov/fdac/features/995_snakes.html "For Good34 KB (5,336 words) - 14:21, 8 March 2024
- ...uthor=Anonymous |authorlink= |coauthors= |date= |format= |work= |publisher=Food and Drug Administration |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=}}</ref>70 KB (9,828 words) - 17:34, 10 February 2024
- ...[[United States of America]], Good Clinical Practices is overseen by the [[Food and Drug Administration]] (http://www.fda.gov/ScienceResearch/SpecialTopics/RunningClinicalTrials/) ...62334 |doi=}}</ref> Many scientists and ethicists consider that the U.S. [[Food and Drug Administration]], by demanding placebo-controlled trials, encourages the systematic violat87 KB (12,105 words) - 14:08, 2 February 2023
- ...became the first breast cancer predictor to win formal approval from the [[Food and Drug Administration]]. This is a new gene test to help predict whether women with early stage b ...[bevacizumab]], has filed a supplemental biological application with the [[Food and Drug Administration]] for approval of [[bevacizumab]] in the setting of [[metastatic]] breast c101 KB (14,716 words) - 09:04, 5 April 2024
- For years the [[Food and Drug Administration]] (FDA) was in contention with the Life Extension Foundation, including thr54 KB (8,078 words) - 09:18, 1 July 2023
- ...veloped in the 1870s. The federal government created the new regulatory [[Food and Drug Administration]]. [[Ida M. Tarbell]] exposed the greed of the [[Standard Oil]] monopoly, w41 KB (6,136 words) - 10:39, 5 March 2024
- ...sperdal) is the only anti-psychotic agent currently approved by the U.S. [[Food and Drug Administration]] to treat children and adolescents with autism.<ref name="pmid18172517">{{49 KB (7,285 words) - 04:27, 20 January 2011
- Various disease-modifying treatments have been approved by the USA's [[Food and Drug Administration]] (FDA); as well as in other countries; for multiple sclerosis. More treatm52 KB (7,594 words) - 17:09, 21 March 2024