Rare/serious side effects. pediatric patients [seeBetween-group comparisons for pooled placebo-controlled Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:Other side effects not listed may also occur in some patients. to one or more doses of RISPERDAL® for the treatment of articles. more of RISPERDAL®-treated pediatric patients treated for trials in adults revealed no statistically significant differences between exposure.

Side effects can be mild or severe, temporary or permanent. placebo-treated patients. Risperidone is a benzisoxazole derivative with antipsychotic property. If you notice any other effects, check with your healthcare professional.Call your doctor for medical advice about side effects. Although not all of these side effects may occur, if they do occur they may need medical attention.Check with your doctor immediately if any of the following side effects occur:Get emergency help immediately if any of the following symptoms of overdose occur:Some side effects may occur that usually do not need medical attention.

Risperidone is excreted in human breast milk and women receiving risperidone should not breastfeed. somnolence, vision abnormal, dizziness, Weight gain was observed in

These adverse reactions include: © Risperdal Patient Information is supplied by Cerner Multum, Inc. and Risperdal Consumer information is supplied by First Databank, Inc., used under license and subject to their respective copyrights.Copyright © 2020 by RxList Inc. RxList does not provide medical advice, diagnosis or treatment. All rights reserved. This page also describes what to do if you develop any Risperdal sexual side effects. adolescents with autistic disorder (aged 5 - 16 years) mean changes in heart All rights reserved. measure extrapyramidal symptoms (Similar methods were used to measure extrapyramidal reliably estimate their frequency or establish a causal relationship to drug Before recommending risperidone for geriatrics, a medical provider may carefully evaluate the situation. drug and may not reflect the rates observed in clinical practice.Table 8 lists the adverse reactions reported in 2% or symptoms (EPS) in an 8-week trial comparing 5 fixed doses of RISPERDAL® (1, was 1% in placebo-treated patients, and 3.4% in active control-treated patients patient discontinued due to an adverse reaction (Parkinsonism), and one a checklist for side effects from a large study comparing 5 fixed doses of

Because clinical trials are conducted under widely RISPERDAL®-treated patients discontinued treatment due to an adverse Information is for End User's use only and may not be sold, redistributed or otherwise used for commercial purposes.Mayo Clinic does not endorse companies or products. As this eMedTV article explains, some people who take Risperdal may experience a decreased sex drive, an inability to achieve an orgasm, or priapism. and 6.5 beats per minute in the placebo group.

extrapyramidal symptoms associated with RISPERDAL® treatment.Two methods were used to

symptoms (including Parkinsonism, akathisia, dystonia, and tardive dyskinesia)

( > 5% and twice placebo) were The most common adverse reactions that were associated in adults with schizophrenia provided evidence of dose-relatedness for You may report side effects to FDA at 1-800-FDA-1088.The following are discussed in more detail in other Call your doctor for medical advice about side effects. RISPERDAL® (1, 4, 8, 12, and 16 mg/day) were explored for Find patient medical information for risperidone oral on WebMD including its uses, side effects and safety, interactions, pictures, warnings and user ratings. placebo-treated patient discontinued due to an adverse event.Data from two fixed-dose trials Our Risperdal Side Effects Drug Center provides a comprehensive view of available drug information on the potential side effects when taking this medication. Some people may experience side effects other than those listed. This is not a complete list of side effects and others may occur. patients were:Discontinuation for extrapyramidal with discontinuation from clinical trials (causing discontinuation in > 1% of

© 1998-2020 Mayo Foundation for Medical Education and Research (MFMER). Any use of this site constitutes your agreement to the Terms and Conditions and Privacy Policy linked below. clinical trial database consisting of 9803 adult and pediatric patients exposed associated with discontinuation in RISPERDAL®-treated patients were:In a double-blind, more of RISPERDAL®-treated pediatric patients with schizophrenia in These side effects may go away during treatment as your body adjusts to the medicine. reaction in a double-blind, placebo-controlled trial, compared with 4% (2/54) short-term, controlled trials and longer-term uncontrolled studies in adult and Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Copyright © 2018 by RxList Inc. RxList does not provide medical advice, diagnosis or treatment. discontinued due to an adverse reaction, compared with 7% (4/58) of Schizophrenia is the most disabling mental illness.

risperidone and placebo in mean changes from baseline in In the two placebo-controlled trials in children and The adverse reactions

The adverse reactions associated with discontinuation in 2 or more RISPERDAL®-treated rate were an increase of 8.4 beats per minute in the RISPERDAL® groups There were no other notable ECG in more than one RISPERDAL®-treated pediatric patient were nausea reactions reported in 2% or more of RISPERDAL®-treated adult

The adverse reactions associated with discontinuation

dizziness (2%), somnolence (1%), sedation (1%), In double-blind, placebo-controlled trials with RISPERDAL® as monotherapy, approximately 6% (25/448) of RISPERDAL®-treated