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Risnia, the generic form of the brand name drug Risperdal, is in a class of medications called atypical antipsychotics.
It works by changing the activity of dopamine and other naturally occurring chemicals in the brain.
Janssen Pharmaceuticals makes risperidone, and the Food and Drug Administration (FDA) first approved Risperdal in 2002 to treat schizophrenia in adults and youths at least 13 years old.
Schizophrenia is a mental illness that can cause people to lose interest in life and develop abnormal thoughts and emotions.
In 2003, the FDA also approved Risperdal for the short-term treatment of adults and children 10 and older with bipolar disorder who experience mania, or episodes of unusually excited moods.
Doctors can also prescribe the drug to treat mixed episodes that cause people to experience symptoms of both mania and depression.
The FDA approved the first generic forms of Risperdal, risperidone tablets, in 2008.
Doctors can also prescribe risperidone for children 5 to 16 years old with autism, a condition that causes repetitive behavior and difficulty communicating and interacting with others.
The drug can alleviate symptoms that include aggression, self-injury, and sudden mood changes.
Medical evidence does not indicate whether the drug is safe and effective in younger children.
Janssen, however, also marketed Risperdal as a treatment for older people with agitation from dementia, which is not an FDA-approved use of the medication.
In fact, it can be dangerous for older adults with dementia to take antipsychotics, including Risperdal, and Janssen had to pay a fine for misbranding the drug.
The combined criminal plea agreement with the Justice Department and a civil settlement totaled more than $1.67 billion.
In This Section: What Are the Key Things I Need to Know About Risnia (Risperdal)? Before taking risperidone, you should be aware of several important warnings: Anyone with dementia should not take risperidone.
Older adults with dementia who take risperidone or other medications for mental illness are at greater risk for death during treatment.
They also face an increased risk for stroke or mini-stroke.
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