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For some personal reports of the effects of using risperidone for autism or [[Asperger's syndrome]] - occasionally beneficial especially at very low doses such as 0.5mg per day, but sometimes severely distressing even at low doses.{{cn}}


==Pharmacology==
==Pharmacology==

Revision as of 03:50, 29 November 2006

Risperidone
File:Risperidone.png
Clinical data
Pregnancy
category
  • C
Routes of
administration
Oral and extended-release intramuscular injection
ATC code
Legal status
Legal status
  • US: WARNING[1]
  • In general: ℞ (Prescription only)
Pharmacokinetic data
Bioavailability70% (oral)
MetabolismHepatic (CYP2D6-mediated)
Elimination half-life3–20 hours
ExcretionUrinary
Identifiers
  • 4-[2-[4-(6-fluorobenzo[d]isoxazol-3-yl)-
    1-piperidyl]ethyl]-3-methyl-
    2,6-diazabicyclo[4.4.0]deca-1,3-dien-5-one
CAS Number
PubChem CID
DrugBank
CompTox Dashboard (EPA)
ECHA InfoCard100.114.705 Edit this at Wikidata
Chemical and physical data
FormulaC23H27FN4O2
Molar mass410.485 g/mol g·mol−1

Risperidone (Belivon®, Rispen®, Risperdal® in the United States) is an atypical antipsychotic medication developed by Janssen Pharmaceutica. It was approved by the United States Food and Drug Administration (FDA) in 1993. It is most often used to treat delusional psychosis (including schizophrenia), but risperidone (like other atypical antipsychotics) is also used to treat some forms of bipolar disorder, psychotic depression and Tourette syndrome.

Generally lower doses are used for autistic spectrum disorders than are used for schizophrenia and other forms of psychosis; risperidone has received approval from the Food and Drug Administration (FDA) for symptomatic treatment of irritability in autistic children and adolescents.[2]

Risperidone is now the most commonly prescribed antipsychotic medication in the United States.

Side effects

File:Risperdal.gif
Risperdal Logo

Common side effects include nausea, anxiety, dizziness, insomnia, low blood pressure, muscle stiffness, muscle pain, sedation, tremors, increased salivation and weight gain (it is not uncommon for patients taking risperidone over long periods to gain upwards of 50 pounds or even more). It has also been known to cause sexual dysfunction.

Occasionally breast tenderness and eventually lactation in both genders may occur. Many antipsychotics are known to increase prolactin because they inhibit dopamine. However, Risperidone is known to increase prolactin to a greater extent than most other antipsychotics, such as quetiapine. It is thought that once Risperidone raises prolactin, it may cause tumors in the pituitary gland. This may recur even if the patient has switched to a different antipsychotic.[3]

Like all antipsychotics, Risperidone can potentially cause tardive dyskinesia (TD), extrapyramidal symptoms (EPS), and neuroleptic malignant syndrome (NMS), although the risk is generally less than for the older typical antipsychotics.

Also, like all atypical antipsychotics, risperidone can trigger diabetes and more serious conditions of glucose metabolism, including ketoacidosis and hyperosmolar coma.[4]

Pharmacology

Risperidone's receptor profile

Risperidone is a very strong dopamine blocker (antagonist); i.e., it inhibits functioning of postsynaptic dopamine receptors.

Risperidone also acts as a 5-HT2A antagonist, and can be used to quickly and effectively block the effects of 5-HT2A agonist drugs such as LSD.

It reaches peak plasma levels quickly regardless of whether it is administered as a liquid or pills. The strong dopamine-blocking reaction is known to make some people feel nauseated if they do things that normally trigger the dopamine response, such as eat a pleasing meal or experience orgasm. Risperidone is metabolised fairly quickly so this potential for nausea subsides usually in two to three hours.

References

  1. ^ "FDA-sourced list of all drugs with black box warnings (Use Download Full Results and View Query links.)". nctr-crs.fda.gov. FDA. Retrieved 22 Oct 2023.
  2. ^ "FDA Approves the First Drug to Treat Irritability Associated with Autism, Risperdal" (Press release). FDA. October 2 2006. Retrieved 2006-10-02. {{cite press release}}: Check date values in: |date= (help)
  3. ^ Szarfman A, Tonning J, Levine J, Doraiswamy P (2006). "Atypical antipsychotics and pituitary tumors: a pharmacovigilance study". Pharmacotherapy. 26 (6): 748–58. PMID 16716128.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  4. ^ "FDA Warning Letter" (Press release). FDA. April 19 2004. Retrieved 2006-10-02. {{cite press release}}: Check date values in: |date= (help)

External links