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- [[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
- {{r|Food and Drug Administration}}994 bytes (123 words) - 16:54, 11 January 2010
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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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