Risperdal®

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The growing concern with the large pharmaceutical companies is because of the influence exercised over safety regulations in pursuit of financial gain instead of patient safety. The worlds second biggest maker of medical products, Johnson & Johnsons, manufactures a schizophrenia drug Risperdal® which has annual global sales of $2.1 billion. While a J&J spokesperson claimed an update to the Risperdal® label is indeed being made, and we will be sending out letters to health care professionals soon, the company had already issued Risperdal® warning letters to Canadian doctors and pharmacists six months before announcing Risperdal® side effect risks in the U.S.

Clinical trials testing Risperdal® in Alzheimer patients heightened concerns that the occurrence of serious Risperdal® side effects is higher than previously thought. Among 764 Risperdal® patients, 29 cases of stroke and stroke-related events were seen, in addition to four deaths. A Public Citizen consumer watchdog group pharmacist and research analyst thinks that the recent Risperdal® studies should push U.S. regulators to examine more deeply if younger aged schizophrenia patients are also more prone to experiencing Risperdal® stroke and other side effects of Risperdal®.

Approved in the 1990s as a type of new atypical anti-psychotic drug and thought to initially have fewer unwanted side effects, Risperdal® uses upon approval only included schizophrenia treatment. Risperdal® is often prescribed to control behavioral disorders in elderly patients with dementia and Alzheimers disease, including delusions, aggression, and anxiety, but the recent Risperdal® stroke announcement shows there is an increased risk in prescribing Risperdal® to a wider range of patients.

Public Citizen consumer watchdog group pharmacist and research analyst Larry Sasich thinks, The Risperdal® label clearly states that there is no evidence this drug is safe or effective in treating dementia, and it looks like doctors are hurting people by prescribing it for this condition. Risperdal® labeling changes will be implemented according to J&J to more accurately warn of the increased risk of Risperdal® stroke and other Risperdal® side effects that can include blood clots, hemorrhages, and death.

For more information on Risperdal® side effects please contact us to confer with a Risperdal® lawyer.

Risperdal News

Sedatives Cause Early Death in Dementia Patients

March 30, 2007

Patients with Alzheimer’s Disease who are prescribed antipsychotic medications such as Risperdal are suffering early death as a result of … Full Story

Study: Multiple Antipsychotic Medications Not Useful

November 30, 1999

  -February 2, 2006 Recent studies have revealed that people with schizophrenia that are prescribed more than one medication, such … Full Story

Older Antipsychotics Not Safer than Newer Drugs

  -December 1, 2005   According to a study published in the New England Journal of Medicine , older antipsychotics … Full Story

Use of antipsychotic drugs increases among children

  August 2, 2004   According to a new study, the number of children with behavioral problems like ADHD being … Full Story

Federal lawsuit filed alleges children harmed by aggressive marketing

-July 6, 2004   A federal lawsuit was filed by a psychiatrist accusing drug companies of distorting statistics, violating regulations, … Full Story

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