Petition to the FDA to remove the Attention Deficit drug pemoline (CYLERT) from the market because of liver toxicity (HRG Publication #1731)
March 24, 2005
Lester Crawford, DVM, Acting Commissioner
Dear Dr. Crawford,
Public Citizen, representing more than 150,000 consumers nationwide, hereby petitions the Food and Drug Administration (FDA) pursuant to the Federal Food, Drug and Cosmetic Act 21 U.S.C. Section 355(e)(3), and 21 C.F.R. 10.30, to immediately remove from the market pemoline (CYLERT®-Abbott Laboratories, and all generic versions), a stimulant drug for the treatment of attention deficit hyperactivity disorder (ADHD). In addition to having no demonstrated unique therapeutic benefit over other ADHD drugs such as methylphenidate, pemoline is known to have caused at least 21 cases of liver failure, including 13 resulting in liver transplantation or death. The drug’s unfavorable risk to benefit ratio has led to its withdrawal in the United Kingdom and Canada, while the FDA instead opted for two separate changes to the pemoline label, in 1996 and 1999. A 2002 FDA study has clearly demonstrated that these labeling changes failed to increase monitoring for liver toxicity or ensure only second-line use of pemoline. In light of this evidence of unique liver toxicity without evidence of unique therapeutic benefit, we contend that the only responsible course of action is to remove this dangerous drug from the market.
We are joined in our petition by Dr. Fredric Solomon, Clinical Professor of Psychiatry and Behavioral Sciences at the George Washington University School of Medicine, who in the course of 42 years of clinical experience has evaluated and cared for hundreds of patients with ADHD.
Serious Liver Toxicity
Pemoline, a central nervous system stimulant, was approved by the FDA for the treatment of ADHD on January 27, 1975. Last year, there were approximately 117,000 pemoline prescriptions filled in the U.S. However, reports of liver abnormalities appeared in U.S. clinical trials even before approval., The first reports were identified in a 1973 prospective study of pemoline in which there were 2 cases of liver toxicity out of approximately 600 patients receiving chronic therapy. Fatty liver deposits were identified at biopsy, and in both cases liver toxicity diminished when treatment was discontinued but then reappeared after the drug was resumed.3 A 1974 pemoline trial enrolling 288 children reported a 3.1% rate of abnormal liver function tests. Incorporating data from this and previous studies, the authors estimated that drug-induced liver enzyme abnormalities occurred in 1% to 2% of patients taking pemoline. Between the 1975 approval and 1996, there were 193 adverse drug reactions involving the liver ascribed to pemoline reported to the FDA which concerned youths under the age of 20. As of May 1996, there were 13 cases acute liver failure due to pemoline, 11 of which resulted in death or liver transplantation.
Based on an analysis of three case reports of fatal liver failure, Berkovitch, et al. calculated in a 1995 study that pemoline caused a 45-fold increased risk for the development of fulminant liver failure in children (RR=45.3, 95% CI: 4.1-510, P<0.001). These findings prompted an FDA review by its Division of Pharmacovigilance and Epidemiology (DPE, now called the Office of Drug Safety) of the available case report data. While the DPE found flaws in the analysis by Berkovitch et al., its own analysis yielded an estimated 16.8-fold increased risk of acute liver failure due to pemoline compared to the general population, assuming no underreporting. Given that adverse events are reported to the FDA about 10% of the time, the relative risk for acute liver failure could be closer to 168-fold. The DPE’s medical officer who performed the analysis, Dr. David Graham, estimated an absolute risk of fulminant liver failure in pemoline users of 1 per 2,000, assuming that 10% of the actual cases had been reported.
In a letter to Abbott dated February 20, 1996, the FDA concluded that pemoline had “an unfavorable risk to benefit ratio,” and that it would be withdrawn from the market unless Abbott could provide a “satisfactory rationale” for keeping it on the market. Abbott responded by challenging the FDA’s analysis in an argument that, according to the DPE, “seriously underestimated the true relative and absolute risk of fulminant hepatic failure associated with pemoline use.”8 Nevertheless, Dr. Paul Leber, Director of the Division of Neuropharmacological Drug Products, allowed Abbott to continue marketing the drug. A black box warning was added to the labeling for pemoline in the United States in December 1996, and a “Dear Doctor” letter was mailed out from Abbott to all U.S. physicians. The warning stressed pemoline’s liver toxicity and recommended that it should no longer be considered a first-line therapy for ADHD.6 This decision to make pemoline a second-line therapy was made without any clinical trials showing that it actually worked in patients who had failed to respond to a first-line therapy.
In a letter to Abbott dated June 14, 1996, Dr. Leber wrote:
Despite this strongly conditional warning, we are not aware that Abbott has ever created such a registry. Certainly, there is no evidence that the registry’s findings have ever been published.
Recent Case Reports of Liver Toxicity
As liver failure cases continued to accumulate, the FDA addressed the issue with a stronger black box warning in June 1999. The 1999 warning label states that as of December 1998 there were 15 cases of acute liver failure due to pemoline reported to the FDA, 12 of which resulted in death or liver transplantation.Although pemoline use has declined significantly since that time, a review of the FDA Adverse Event Reporting System (AERS) database since December 1998 reveals 15 additional reports of liver toxicity in which pemoline was the primary suspect drug (See Table 1). These include 6 cases of liver failure including 1 liver transplant. This means that since pemoline was marketed, 21 cases of liver failure, including 13 deaths or liver transplants, have been reported to the FDA. Because only 10% or so of adverse events are reported to the FDA, these are clearly underestimates of the true number of such cases.
Table 1. Adverse drug reaction reports to FDA AERS database in which pemoline is the primary suspect for liver toxicity, 1/1999-9/2004. Searches of the database were conducted using adverse effect terms “liver” and “hepat-.”
Pemoline Withdrawn Abroad
While the United States has allowed Abbott to continue marketing the drug, other countries have taken more decisive action based on patient liver toxicity data collected predominantly from the U.S. In September 1997, the United Kingdom removed pemoline from the market. In its announcement that the drug would be banned, the Committee on Safe Medicines (CSM) wrote:
The UK decision was based entirely on case reports of liver toxicity from the United States. In September 1999, the Canadian government reached a similar conclusion and removed pemoline from the market, reasoning that the drug’s risks outweighed its benefits. According to Health Canada:
Pemoline’s FDA Labeling Proven Ineffective
In June 1999, as U.S. reports of liver toxicity due to pemoline continued to accumulate, Abbott sent another “Dear Healthcare Provider” letter to U.S. physicians describing the FDA’s newly revised black-box warning for pemoline. In addition to the 1996 warning that pemoline should be shifted from first-line to second-line therapy for ADHD, the 1999 recommendations specified baseline monitoring of liver enzymes, repeated every two weeks thereafter, and obtaining informed consent for treatment from the patient.
A 2002 study by the FDA itself measured adherence to the various black box labeling recommendations. The study used a large health care company’s administrative claims database, which included 1,308 patients who were newly prescribed pemoline from January 1998 to March 2000. While the recommendation that pemoline be used only as second-line therapy for ADHD had been in place since the 1996 label, only 237 patients (34%) were found to have received another ADHD drug prior to pemoline. Dividing the data into two six-month periods, before and after the June 1999 labeling change, the authors found that the new labeling had no measurable effect on liver enzyme testing rates. Twelve percent of pre-label change patients received baseline liver enzyme tests, compared to 11% of patients after the labeling change. The percentage of patients receiving any follow-up liver enzyme tests (the label recommended biweekly testing) was similarly low before and after the labeling change (9% pre-change vs. 12% post-change). The authors concluded that “labeling changes, including black-box warnings, had no measurable effect on compliance with the labeling recommendations for pemoline.”1
No Unique Therapeutic Role
Defenses of dangerous drugs such as pemoline often invoke arguments that there is some unique niche that the drug fills that justifies its remaining on the market. The main initial appeal of pemoline to clinicians was that it allowed once-a-day dosing, as opposed to multiple daily doses which might raise logistical problems especially for children in school during the day. However, due to the development of long-acting formulations of standard stimulant medications, this is no longer a unique characteristic.
Proponents of pemoline may claim that it has a lower abuse potential than other stimulant treatments for ADHD, and therefore, pemoline’s unique therapeutic role may be for the treatment of ADHD where substance abuse is a concern. In reality this argument breaks down to two separate potential scenarios, each of which we will discuss here.
The first scenario posits that exposure to stimulants results in increased neurological sensitivity to the effects of the drugs, thereby increasing the risk of generalized drug abuse. If this were true, a stimulant with lower abuse potential might be less likely to put patients at such risk. However, stimulant treatment for ADHD does not appear to adversely affect either co-occurring substance abuse or the likelihood of future substance abuse. Two randomized controlled trials, one studying methylphenidate treatment of patients with ADHD and cocaine-dependence and the other studying pemoline for ADHD in substance-abusing adolescents, have shown that neither methylphenidate nor pemoline had an effect on co-occurring substance-abuse behavior. Similarly, the weight of the evidence suggests that stimulant treatment for ADHD does not lead to substance use or abuse later in life.14 In fact, a 2003 meta-analysis of seven studies found that stimulant treatment of ADHD with methylphenidate or amphetamine actually reduced the risk of substance use disorders 1.9-fold, down to levels within normal population risks.
The second scenario refers specifically to the potential for the abuse of the stimulants themselves. Pemoline, like the other stimulant treatments for ADHD, is a controlled substance. While the potential for the abuse and diversion of methylphenidate and amphetamines is better established, pemoline is not devoid of risk for abuse. The FDA-approved labeling for pemoline (CYLERT) warns that “the pharmacologic similarity of pemoline to other psychostimulants with known dependence liability suggests that psychological and/or physical dependence might also occur with CYLERT.” Furthermore, concerns about abuse and diversion with older immediate-release stimulant tablets have been eased with the arrival of newer stimulant preparations. Concerta, for example, is a once-daily extended-release form of methylphenidate in the form of a paste, which cannot be ground up or snorted. The American Academyof Child and Adolescent Psychiatry recommends these newer preparations, not pemoline, as the most suitable for adolescents with ADHD who are at risk for abusing or diverting their stimulant medications.
Relatively safe and effective drug treatments exist for ADHD. Methylphenidate and dextroamphetamine are generally considered the drugs of choice, and patients with ADHD who fail to respond to one of these two drugs are rare., There is no good evidence from appropriate clinical trials that pemoline has a unique therapeutic benefit for the treatment of ADHD, or that it is effective in patients who have failed to respond to first-line drugs. Indeed, parameters for stimulant treatment of ADHD issued by the American Academy of Child and Adolescent Psychiatry do not recommend the use of pemoline under any circumstances.20
In the late 1990’s, as evidence of pemoline’s liver toxicity mounted, the UK and Canada made the decision that it was in the interest of public health to withdraw pemoline from the market because its risk outweighed its benefit. The FDA gave strong consideration to the withdrawal of the drug, but instead elected to allow sales of pemoline as long as the sponsor made a good faith effort to gather more safety data and the label was changed. However, Abbott does not appear to have carried out the prospective patient registry that was a condition for the drug’s continued marketing, and the labeling changes made have had no measurable effect on ensuring safe use of pemoline. Proponents have never submitted any compelling evidence that pemoline is effective in patients for whom alternative drugs for ADHD are not effective. In the absence of data demonstrating that pemoline has any unique therapeutic benefit over other, safer drugs for the treatment of ADHD, there is no responsible basis for keeping this unacceptably dangerous drug on the market.
ENVIRONMENTAL IMPACT STATEMENT
Nothing requested in this petition will have an impact on the environment.
We certify that, to the best of our knowledge and belief, this petition includes all information and views on which this petition relies, and that it includes representative data and information known to the petitioners which are unfavorable to the petition.
Peter Lurie, MD, MPH
Sidney M. Wolfe, MD
Public Citizen’s Health Research Group
Fredric Solomon, MD*
*Dr. Solomon practices Child, Adolescent and Adult Psychiatry in Washington, DC. He is Clinical Professor of Psychiatry and Behavioral Sciences at the George Washington University School of Medicine. His former positions include: Director, Division of Mental Health and Behavioral Medicine at the Institute of Medicine of the National Academy of Sciences; Associate Professor of Psychiatry and Neurology at Howard University College of Medicine; and Consultant to the National Institute of Mental Health. He was elected by child psychiatrists in the Washington, DC area for three terms as their delegate to the Assembly of the American Academy of Child and Adolescent Psychiatry. In the course of 42 years of clinical experience, Dr. Solomon has evaluated and cared for hundreds of patients who suffered from ADHD.
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Leber PD. Letter from Director, Division of Neuropharmacologic Drug Products, FDA, to Abbott Laboratories, February 20, 1996. (Referenced in Leber, PD. Decision on Cylert Hepatotoxicity Action. Memorandum from Director, Division of Neuropharmacologic Drug Products (HFD-120). October 29, 1996. Accessed January 12, 2005, at http://www.fda.gov/cder/foi/nda/96/1996-016832a_s014.pdf.
Leber PD. Letter from Director, Division of Neuropharmacologic Drug Products, FDA, to Abbott Laboratories. June 14, 1996. Accessed January 12, 2005, at http://www.fda.gov/cder/foi/nda/96/1996-016832a_s013.pdf.
Pizzuti D. Dear Health Care Professional Letter, Cylert. Abbott Laboratories, Abbot Park, IL, June 1999.
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