{"id":7006,"date":"2009-09-17T13:20:00","date_gmt":"2009-09-17T13:20:00","guid":{"rendered":"http:\/\/www.pharma-mkting.com\/fda-reads-my-blog-declares-latisse-web\/"},"modified":"2019-02-21T01:22:37","modified_gmt":"2019-02-21T01:22:37","slug":"fda-reads-my-blog-declares-latisse-web","status":"publish","type":"post","link":"http:\/\/ec2-54-175-84-28.compute-1.amazonaws.com\/pharma-mkting.com\/blog\/fda-reads-my-blog-declares-latisse-web\/","title":{"rendered":"FDA Reads My Blog: Declares Latisse Web Site Misleading"},"content":{"rendered":"<p>On September 10, 2009, the FDA sent Allergan a notice that its Latisse Web site was misleading (see &#8220;<a href=\"http:\/\/www.forums.pharma-mkting.com\/showthread.php?t=20967\">FDA Says Allergan&#8217;s Web Site for Eyelash Thickener Is Misleading<\/a>&#8220;). The letter states:<\/p>\n<p>&#8220;the Division of Drug Marketing, Advertising, and Communications (DDMAC) has reviewed the \u201cFAQs\u201d and \u201cAbout Safety\u201d pages of a consumer website and a \u201cLaunch display timeline\u201d (timeline) (APC36ON09) for LatisseTM (bimatoprost ophthalmic solution) 0.03% (Latisse) submitted by Allergan, Inc. (Allergan) under cover of Form FDA-2253. These promotional materials are misleading because they <b>omit and minimize risks associated with Latisse<\/b>. Thus, the website and timeline misbrand Latisse in violation of the Federal Food, Drug, and Cosmetic Act&#8230;&#8221; [my emphasis]<\/p>\n<p>Latisse is Allergan&#8217;s product approved for hypotrichosis, a term dermatologists use to describe a condition of no hair growth. Allergan markets Latisse for increasing the growth of eyelashes. <\/p>\n<p>In a previous post dated June 1, 2009 &#8212; &#8220;<a href=\"http:\/\/pharma-mkting.com\/blog\/2009\/06\/will-latisse-turn-brooke-shields-blue.html\">Will Latisse Turn Brooke Shields&#8217; Blue Eyes Brown?<\/a>&#8221; &#8212; I noted that in the &#8220;About Safety&#8221; page of the Latisse web site, Allergan stated:<\/p>\n<p>&#8220;Increased brown iris pigmentation has occurred when similar medications were instilled directly into the eye to treat elevated intraocular pressure\/glaucoma. Although iris pigmentation was not reported in clinical studies with LATISSE\u2122, patients should be advised about the potential for increased brown iris pigmentation which is likely to be permanent.&#8221;<\/p>\n<p>I commented: <b>When Allergan says &#8220;similar medications,&#8221; it really should have said &#8220;this medication&#8221; because Latisse is just another name for Lumigan, Allergan&#8217;s anti-glacoma drug. Both are (bimatoprost ophthalmic solution) 0.03%.<\/b><\/p>\n<p>FDA, in its letter to Allergan, said (click on image to enlarge and read):<\/p>\n<div class=\"separator\" style=\"clear: both; text-align: center;\"><a href=\"http:\/\/3.bp.blogspot.com\/_ZiPiXEv_Q_g\/SrI2X2ur1YI\/AAAAAAAACs4\/FZDGLCxO2mc\/s1600-h\/FDALatisseStatement1.jpg\" imageanchor=\"1\" style=\"margin-left: 1em; margin-right: 1em;\"><img decoding=\"async\" border=\"0\" src=\"http:\/\/ec2-54-175-84-28.compute-1.amazonaws.com\/pharma-mkting.com\/wp-content\/uploads\/2009\/09\/FDALatisseStatement1.jpg\" \/><\/a><\/div>\n<p>\nOf course, I conclude from this that FDA reads Pharma Marketing Blog. Maybe it has also read my post about organic search &#8220;ads&#8221; (see &#8220;<a href=\"http:\/\/pharma-mkting.com\/blog\/2009\/09\/are-organic-search-results-next-on-fdas.html\">Are Organic Search Results Next on FDA&#8217;s Chopping Block?<\/a>&#8220;).<\/p>\n","protected":false},"excerpt":{"rendered":"<p>On September 10, 2009, the FDA sent Allergan a notice that its Latisse Web site was misleading (see &#8220;FDA Says Allergan&#8217;s Web Site for Eyelash Thickener Is Misleading&#8220;). The letter states: &#8220;the Division of Drug Marketing, Advertising, and Communications (DDMAC) has reviewed the \u201cFAQs\u201d and \u201cAbout Safety\u201d pages of a consumer website and a \u201cLaunch [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":9589,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[12],"tags":[89,243,527,44,902],"topic":[],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v22.0 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>FDA Reads My Blog: Declares Latisse Web Site Misleading - Pharma Marketing Network<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"http:\/\/ec2-54-175-84-28.compute-1.amazonaws.com\/pharma-mkting.com\/blog\/fda-reads-my-blog-declares-latisse-web\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"FDA Reads My Blog: Declares Latisse Web Site Misleading - Pharma Marketing Network\" \/>\n<meta property=\"og:description\" content=\"On September 10, 2009, the FDA sent Allergan a notice that its Latisse Web site was misleading (see &#8220;FDA Says Allergan&#8217;s Web Site for Eyelash Thickener Is Misleading&#8220;). The letter states: &#8220;the Division of Drug Marketing, Advertising, and Communications (DDMAC) has reviewed the \u201cFAQs\u201d and \u201cAbout Safety\u201d pages of a consumer website and a \u201cLaunch [&hellip;]\" \/>\n<meta property=\"og:url\" content=\"http:\/\/ec2-54-175-84-28.compute-1.amazonaws.com\/pharma-mkting.com\/blog\/fda-reads-my-blog-declares-latisse-web\/\" \/>\n<meta property=\"og:site_name\" content=\"Pharma Marketing Network\" \/>\n<meta property=\"article:published_time\" content=\"2009-09-17T13:20:00+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2019-02-21T01:22:37+00:00\" \/>\n<meta property=\"og:image\" content=\"http:\/\/ec2-54-175-84-28.compute-1.amazonaws.com\/pharma-mkting.com\/wp-content\/uploads\/2009\/09\/FDALatisseStatement1.jpg\" \/>\n\t<meta property=\"og:image:width\" content=\"400\" \/>\n\t<meta property=\"og:image:height\" content=\"140\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/jpeg\" \/>\n<meta name=\"author\" content=\"Pharma Guy\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Pharma Guy\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"1 minute\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"http:\/\/ec2-54-175-84-28.compute-1.amazonaws.com\/pharma-mkting.com\/blog\/fda-reads-my-blog-declares-latisse-web\/\",\"url\":\"http:\/\/ec2-54-175-84-28.compute-1.amazonaws.com\/pharma-mkting.com\/blog\/fda-reads-my-blog-declares-latisse-web\/\",\"name\":\"FDA Reads My Blog: Declares Latisse Web Site Misleading - 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