The prescription of psychotropic medications for children continues to be a controversial area of medical practice. In the United States, academic medical centers, medical researchers, prescribers, and the FDA are all ostensibly committed to the common goal of disseminating accurate information and promoting treatment based on scientific evidence. In the United States, however, medical treatment takes place in the context of legal and pervasive direct-to-consumer advertising (DTCA). There are concerns about the potential for DTCA to affect public health negatively and to increase health care costs.1,2
In 2005, we wrote to the FDA regarding a perceived disconnect between widespread DTCA for attention-deficit/hyperactivity disorder (ADHD) medications and the peer-reviewed scientific literature.3 Such a disconnect is important because FDA regulations require that DTCA be consistent with the FDA-approved product label.4 The FDA notified us that it would further evaluate our concerns,5 but the advertisements continued. Three years later (on September 26, 2008), the FDA issued letters to 5 pharmaceutical companies that sell psychostimulants (eg, methylphenidate and mixed amphetamine salts), warning them to cease misleading promotion—including advertisements to both prescribers and consumers.6 The warning letters state that among other alleged infractions, the targeted advertisements overstate the efficacy of psychostimulants.
Some might question the delay in regulatory response. However, our central question is, where has the mainstream medical community been over the past 3 years while—as the FDA has now acknowledged—Americans were being misled about psychiatric drugs for children?
As anyone familiar with the treatment of children with an ADHD diagnosis already knows, psychostimulant medications represent but 1 type of intervention used with this population and are by no means a “magic bullet” treatment. Both the evidence-based literature and even the prescribing labels for psychostimulants acknowledge the need for a comprehensive treatment program in the treatment of ADHD.7,8 There is also a paucity of research demonstrating that the prescription of stimulants predictably results in enhanced socioemotional development.
Therefore, when we wrote to the FDA in 2005, we were concerned about a highly visible US advertising campaign for Adderall that featured smiling children and their parents. The advertisements were widely distributed in popular periodicals, such as People magazine, and they claimed that Adderall was a “trusted solution for ADHD” that would lead to “friends that ask him to join the group” and a “family hour that lasts for hours.” The Web site featured a celebrity endorsement by television personality Ty Pennington, in which he claimed that Adderall did not affect his appetite or sleep.9 All of these advertising claims exaggerated the positive impact of this medication as measured by scientific evidence.10
For instance, academic difficulties are often a precipitating factor in the diagnosis and treatment of ADHD, and thus parents may find claims that psychostimulants increase academic performance particularly compelling. For years, Adderall advertisements have used the slogan, “Schoolwork that matches his intelligence.”9 In 2005, we wrote to Shire Pharmaceuticals regarding this claim, pointing out that the experimental evidence was limited to improvement on a 10-minute math test, and questioning whether this was equivalent to the more global concept of “schoolwork.”11 At the time, Shire defended its advertising campaign.12 The FDA has subsequently clamped down on the gap between peer-reviewed scientific evidence and such claims, noting that an improvement on ADHD measures does not necessarily correlate with improved academic outcomes, and warning Shire directly that “improvement in attention, as evidenced by increased numbers of math problems answered correctly, has not been correlated with an improvement in academic performance throughout the day, an end point which has not been studied.”13
1. Mintzes B. Disease mongering in drug promotion: do governments have a regulatory role? PloS Med. 2006;3:e198. http://medicine.plosjournals.org/ archive/1549-1676/3/4/pdf/10.1371_journal. pmed.0030198-L.pdf. Accessed January 21, 2009.
2. Morgan S. Direct-to-consumer advertising and expenditure on prescription drugs: a comparison of experiences in the United States and Canada. Open Med. 2007;1:1. http://www.openmedicine.ca/article/view/23/26. Accessed January 21, 2009.
3. Lacasse JR, Leo J. Letter to T. Abrams, Director, Food and Drug Administration Division of Drug Marketing, Advertising, and Communications. http://www.public.asu.edu/~jlacass1/3_To_FDA_Sep_2005.pdf. Accessed January 26, 2009.
4. Food and Drug Administration. 21 CFR 202 Guidance for Industry: Consumer-Directed Broadcast Advertisements. Washington, DC: Food and Drug Administration; 1997.
5. Murphy JC. Letter to J Lacasse and J Leo: Promotional materials for Adderall XR® CII Capsules. http://www.public.asu.edu/~jlacass1/5_FDA_Response_Sep_2005.pdf. Accessed January 26, 2009.
6. Food and Drug Administration, Division of Drug Marketing, Advertising and Communications September 2008. [Warning letters issued to 5 manufacturers of psychostimulants]. http://www.accessdata.fda.gov/scripts/wlcfm/date.cfm?MONTH=9&YEAR=2008. Accessed January 26, 2009.
7. American Academy of Pediatrics. Clinical practice guideline: treatment of the school-aged child with attention-deficit/hyperactivity disorder. Pediatrics. 2001;108:1033-1044. http://aappolicy.aappublications.org/cgi/reprint/pediatrics;108/4/1033. Accessed January 21, 2009.
8. Shire Pharmaceticals. Adderall XR™ Prescribing Information. http://www.fda.gov/cder/foi/label/2004/ 021303s005lbl.pdf. Accessed January 21, 2009.
9. Shire Pharmaceuticals. Direct-to-consumer advertisement for Adderall XR™ [published in People magazine, August 22, 2005]. http://www.public.asu.edu/~jlacass1/Adderall_advertisement_2005.jpg. Accessed January 26, 2009. [see also http://www.public.asu.edu/~jlacass1/Adderall_advertisement_2_2005.pdf.]
10. Leo J, Lacasse JR. Consumer advertisements for ADHD. In: Timimi S, Leo J, eds. Rethinking ADHD: From Brain to Culture. New York: Palgrave Macmillan.In press.
11. Lacasse JR, Leo J.. Letter to G Flexter, Executive Vice-President and General Manager, North America, Shire Pharmaceuticals. http://www.public.asu.edu/~jlacass1/11_To_Shire_9_2005.pdf. Accessed January 26, 2009.
12. Casby J. Letter to J Lacasse and J Leo: Adderall XR™ Consumer Advertisements. http://www.public.asu.edu/~jlacass1/12_Shire_Response.pdf. Accessed January 26, 2009.
13. Food and Drug Administration. Warning Letter to Shire Pharmaceuticals. http://www.fda.gov/cder/ warn/2008/AdderallXR_Letter.pdf. Accessed January 26, 2009.
14. Harris G, Carey B. Researchers fail to reveal full drug pay. New York Times. June 8, 2008. http://www.nytimes.com/2008/06/08/us/08conflict.html?fta=y. Accessed January 26, 2009.
15. Jensen PS, Arnold LE, Swanson JM, et al. 3-year follow-up of the NIMH-MTA study. J Am Acad Child Adolesc Psychiatry. 2007;46:989-1002.
16. National Institute for Health and Clinical Excellence. Attention deficit hyperactivity disorder: diagnosis and management of ADHD in children, young people and adults. http://www.nice.org.uk/guidance/index.jsp?action=byID&o=12061. Accessed January 26, 2009.
17. Zito JM, Safer DJ, Berg LT, et al. A three-country comparison of psychotropic medication prevalence in youth. Child Adolesc Psychiatry Ment Health. 2008;2:26. http://www.capmh.com/content/pdf/ 1753-2000-2-26.pdf. Accessed January 21, 2009.