May 26, 2009

Seroquel Documents: Glucose Dysregulation In Kids

Next month, the FDA's psychopharmacology advisory committee takes up AstraZeneca's application to have its atypical antipsychotic Seroquel approved for the treatment of schizophrenia in kids aged 13 to 17 and for use in so-called pediatric bipolar disorder in kids aged 10 to 17. Seroquel is not currently approved for use in pediatric populations for any indication. The committee will make a recommendation to the FDA on whether to approve or not approve the drug for these disorders, but the agency is not bound by its recommendation.

AZ's submission to the FDA has not been made public yet, so it's not clear what kind of safety and efficacy data the committee will see, but from the recently-released Seroquel documents (all lawsuit-related) it is clear that the drug caused multiple cases of glucose dysregulation and potentially diabetes in some kids under the age of 18 who were given Seroquel off-label. There have also been reported cases of deaths in this population associated with use of Seroquel.

These details come from the following document dated Dec. 14, 2004 which is entitled "Review of all pediatric reports for Seroquel through 30 September 2004." It is an internal company document, labeled confidential and likely created in response to FDA queries. The document is sizable (13.8 MBs) and I respectfully request that you only download it if you have a serious research or journalistic need for it, as I do have bandwidth limits on this site.

On page 135 of the report, 27 cases of glucose dysregulation are identified with the majority of the reports involving patients aged 12 to 18. Several of these cases resolved into diabetes mellitus. How connected that is with Seroquel use is unclear, but what is clear is that the report identifies several cases of successful dechallenges--take away the Seroquel and away goes the glucose problem--and that's a clear indication of some kind of link between drug use and condition, at least in some of the patients.

Several of these children were being given Seroquel for pediatric bipolar disorder, conduct disorder, Asperger's and, in one case, ADHD. That's exactly the type of patient population that the advisory committee will be reviewing safety and efficacy data about in June and one hopes they pay attention to any glucose dysregulation data presented to them by the FDA and AZ. But there's only one problem: that data is almost certain to come from short-term clinical trials and glucose dysregulation doesn't usually happen immediately. So one hopes that members of the committee somehow gain access to the report I've made available above.

For itself, the AZ report notes that the company did not consider any of the data in the report to contain indications of safety problems in pediatric populations.

Posted by Philip Dawdy at May 26, 2009 12:01 AM
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Comments

Poor children!
There are 29 known physical causes of schizophrenia. mostly involving easily correctable imbalances - from vitamin B3 and zinc deficiencies to overload of copper, thyroid problems and infections. A proper workup is essential, so that the real cause is determined - not covered over with drugs that can disable and kill.
http://www.alternativementalhealth.com/articles/causesofschizophrenia.htm

Posted by: Lilly NC at May 26, 2009 07:26 AM

Unfortunately the deadline for written submission for this hearing is today. Any of you readers with personal experience with Seroquel, especially in kids, send something in ASAP. Here's the info direct from the FDA site:

Public Participation Information

Interested persons may present data, information, or views, orally or in writing, on issues pending before the committee.

Written submissions may be made to the contact person on or before May 26, 2009.
Oral presentations from the public will be scheduled between approximately 4 p.m. and 6 p.m. on June 9, 2009. Those desiring to make formal oral presentations should notify the contact person and submit a brief statement of the general nature of the evidence or arguments they wish to present, the names and addresses of proposed participants, and an indication of the approximate time requested to make their presentation on or before May 22, 2009.
Time allotted for each presentation may be limited. If the number of registrants requesting to speak is greater than can be reasonably accommodated during the scheduled open public hearing session, FDA may conduct a lottery to determine the speakers for the scheduled open public hearing session. The contact person will notify interested persons regarding their request to speak by May 26, 2009.

Contact Information

Diem-Kieu Ngo
Center for Drug Evaluation and Research (HFD-21)
Food and Drug Administration
5600 Fishers Lane (for express delivery, Fishers Lane, rm. 1093)
Rockville, MD 20857
Phone: 301-827-7001
Fax: 301-827-6776
E-mail: diem.ngo@fda.hhs.gov

Posted by: Sara at May 26, 2009 08:43 AM
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