Information for Healthcare Professionals: Pemoline Tablets and Chewable Tablets (marketed as Cylert)
FDA ALERT [10/2005]: Liver Injury Risk and Market Withdrawal
The Agency has concluded that the overall risk of liver toxicity from Cylert and generic pemoline products outweighs the benefits of this drug. In May 2005, Abbott chose to stop sales and marketing of Cylert in the U.S. All generic companies have also agreed to stop sales and marketing of this product (Pemoline tablets and chewable tablets). Cylert is a central nervous system stimulant indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD). This product is considered second line therapy for ADHD because of its association with life threatening hepatic failure (see BOXED WARNING in product label and patient package insert, available at Cylert Labeling Information (PDF - 60KB))
FDA intends to update this page when additional information or analyses become available.
Adverse reactions or quality problems experienced with the use of this Product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax, using the contact information at the bottom of this page.
Healthcare professionals who prescribe Cylert, or any of its generics, should transition their patients to an alternative therapy. Cylert will remain available through pharmacies and wholesalers until supplies are exhausted; no additional product will be available.
FDA is aware of 13 reports of liver failure resulting in liver transplant or death, usually within four weeks of onset of signs and symptoms of liver failure. Although the absolute number of reported cases of liver failure with pemoline is not large, the reporting rate for liver failure with pemoline is 10 to 25 times greater than the background rate of liver failure in the general population.
Despite diminished use of Cylert and generic pemoline products since the addition of the boxed warning in 1999 (about 1/5 the number of prescriptions now compared to before the boxed warning) and restrictive labeling (e.g., boxed warning, second line therapy, Medication Guide), a risk of liver failure remains (FDA is aware of 1 new case of pemoline-associated liver failure since the introduction of the boxed warning in 1999). Given the availability of multiple other drug treatments for ADHD, including 1 that is not scheduled and several products that can be given once a day, FDA has concluded that the risk of liver failure with this drug outweighs the potential benefits.