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FDA Warns Antipsychotic Geodon May Cause Fatal Skin Reaction

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The U.S. Food and Drug Administration issued a safety announcement and required a new warning label for the antipsychotic drug Geodon – also known as ziprasidone – after it found evidence that medication can cause a potentially fatal skin reaction. The serious side effect may affect up to 2.5 million Americans who were prescribed the popular drug.

The FDA warned patients and doctors in December that Pfizer’s Geodon can cause a condition called Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS).

Symptoms of DRESS begin as a rash that can spread all over the body, and also include swollen lymph nodes, fever and damage to organs such as heart, liver, pancreas or kidneys.

The FDA said no fatalities reported in the cases that it reviewed, but some patients required hospitalization. Symptoms surfaced anywhere from 11 days to a month after taking the drug. Though the FDA states DRESS is rare, its severity prompted the agency to require Pfizer to add a new warning to the medication’s label.

“Patients who have a fever with a rash and/or swollen lymph glands should seek urgent medical care. Health care professionals should immediately stop treatment with ziprasidone if DRESS is suspected,” the FDA said.

Geodon belongs to a class of medications called second-generation atypical antipsychotics that the FDA approved to treat schizophrenia and bipolar disorder. Doctors also prescribed the medication to treat seniors and children even if though it was not proven safe for children and has a black box warning for increased risk of death for seniors.

Along with DRESS, side effects of the drug include movement disorders such as tardive dyskinesia, weight gain, high cholesterol, diabetes, dizziness seizures, and suicidal thoughts.

Pfizer maintains that its medication is safe, though it complied with the FDA’s request.

Pfizer Pays Billions to Settle Federal Charges

Not only does this latest warning call the safety of the drug into question, it may also trigger litigation from patients or families affected by the drug. As a class, antipsychotics like Geodon are frequently the center of legal claims brought brought by the government and injured patients.

The Department of Justice sued Pfizer in 2009 for illegally marketing the powerful drug to children even if it is not approved for this use.

The $2.3 billion fine is one of the largest in DOJ history. Court documents accused the company of hiring 250 child psychiatrists to push the drug to children. Pfizer paid a fine to settle the case and denied any wrongdoing.

A new whistleblower lawsuit filed in 2010 accused the drug maker of marketing Geodon to improve cognition. Pfizer tried to have the case thrown out, but in 2014 U.S. District Judge Douglas P. Woodlock denied the motion to dismiss.

Antipsychotics’ Benefits ‘Greatly Exaggerated’

Second generation atypical antipsychotics like Geodon, Abilify and Risperdal grew popular because they caused fewer physical symptoms such as tics, compared to first generation drugs like Haldol and Thorazine. But benefits of the drugs are debatable.

Claims that the new generation of antipsychotics is better are “greatly exaggerated” and “may have been encouraged by an overly expectant community of clinicians and patients eager to believe in the power of new medications,” Columbia University psychiatry department chairman, Dr. Jeffrey A Lieberman told the New York Times.

While they cause less movement disorders, new drugs come with a host of new side effects which are at the center of lawsuits.

For instance, Abilify generated more in $6 billion in sales for Japanese Otsuka Pharmaceutical Co. It faces a growing number of lawsuits for side effects such as compulsive gambling.

Meanwhile, Johnson & Johnson’s Risperdal – also tagged by the feds for $2.2 billion for illegal marketing – faces lawsuits brought by young men, boys and their families because of gynecomastia, a condition where males grow breasts.

“They sold the story they’re more safe, when they aren’t,” journalist Robert Whitaker, who wrote two books about the pharmaceutical industry, told The New York Times. “They had to cover up the problems. Right from the start, we got this false story.”

Last modified: November 16, 2017

Author

Michelle Y. Llamas is a senior content writer. She is also the host of Drugwatch Podcast where she interviews medical experts as well as patients affected by drugs and medical devices. She has written medical and legal content for several years — including an article in The Journal of Palliative Medicine and an academic book review for Nova Science Publishers. With Drugwatch, she has developed relationships with legal and medical professionals as well as with several patients and support groups. Prior to writing for Drugwatch, she spent several years as a legal assistant for a personal injury law firm in Orlando. She obtained her English – Technical Communication degree from the University of Central Florida. She is a committee member with the American Medical Writers Association.

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  2. Grover, N. (2014, December 11). FDA warns Pfizer's antipsychotic could cause fatal skin reaction. Retrieved from http://www.reuters.com/article/2014/12/11/pfizer-fda-antipsychotic-idUSL3N0TV4MH20141211
  3. Wilson, D. (2010, October 2). Side effects may include lawsuits. The New York Times. Retrieved from http://www.nytimes.com/2010/10/03/business/03psych.html?pagewanted=all&_r=0
  4. McAffe, D. (2014, March 26). Pfizer fails to get Geodon off-label use case tossed. Retrieved from http://www.law360.com/articles/522337/pfizer-fails-to-get-geodon-off-label-use-case-tossed