Indications/Uses
Dosage/Direction for Use
For elderly and patients with renal or hepatic impairment: Initial dose of 0.5 mg two times a day and, if necessary increased to 1 mg to 2 mg two times a day. Or as prescribed by a physician.
Overdosage
In case of acute overdosage, establish and maintain an airway and ensure adequate oxygenation and ventilation. Gastric lavage (after intubation, if patient is unconscious) and administration of activated charcoal together with a laxative should be considered.
The possibility of obtundation, seizures, or dystonic reaction of the head and neck following overdose may create a risk of aspiration with induced emesis. Cardiovascular monitoring should commence immediately and should include continuous electrocardiographic monitoring to detect possible arrhythmias. Administration of antiarrhythmic agents (Disopyramide, Procainamide, and Quinidine) have a theoretical hazard of QT-prolonging effects that might be additive to those of Risperidone. Similarly, it is reasonable to expect that the alpha-blocking properties of Bretylium might be additive to those of Risperidone, resulting in problematic hypotension.
General supportive measures should immediately be instituted during overdose of Risperidone (Risdin) tablet. The possibility of multiple drug involvement should be considered. Hypotension and circulatory collapse should be treated with appropriate measures, such as intravenous fluids and/or sympathomimetic agents (epinephrine and dopamine should not be used, since beta stimulation may worsen hypotension in the setting of risperidone-induced alpha blockade). In cases of severe extrapyramidal symptoms, anticholinergic medication should be administered. Close medical supervision and monitoring should continue until the patient recovers.
Administration
Contraindications
Warnings
Special Precautions
Use In Pregnancy & Lactation
Nursing mothers receiving Risperidone (Risdin) tablet should discontinue breastfeeding because Risperidone is excreted in breast milk.
Adverse Reactions
Blood and lymphatic system disorders: neutropenia, decreased in white blood cell count thrombocytopenia, anemia, decreased in hematocrit, increased in eosinophil count, agranulocytosis.
Immune system disorders: hypersensitivity, anaphylactic reaction.
Endocrine disorders: hyperprolactinemia, inappropriate antidiuretic hormone secretion, presence of glucose in the urine.
Metabolism and nutrition disorders: weight increased, increased or decreased appetite, diabetes mellitus, hyperglycemia, polydipsia, weight decreased, anorexia, blood cholesterol increased, water intoxication, hypoglycemia, hyperinsulinemia, increased blood triglycerides, diabetic ketoacidosis.
Psychiatric disorders: insomnia, sleep disorder, agitation, depression, anxiety, mania, confusional state, decreased libido, nervousness, nightmare, catatonia, somnambulism, sleep-related eating disorder, blunted affect, anorgasmia.
Nervous system disorders: sedation/somnolence, parkinsonism, headache, akathisia, dystonia, dizziness, dyskinesia, tremor, tardive dyskinesia, cerebral ischemia, unresponsive to stimuli, loss of consciousness, depressed level of consciousness, convulsion, syncope, psychomotor hyperactivity, balance disorder, coordination abnormal, dizziness postural, disturbance in attention, dysarthria, dysgeusia, hypoesthesia, paresthesia, neuroleptic malignant syndrome, cerebrovascular disorder, diabetic coma, head titubation.
Eye disorders: vision blurred, conjunctivitis, photophobia, dry eye, increased lacrimation, ocular hyperemia, glaucoma, eye movement disorder, eye rolling, eyelid margin crusting, floppy iris syndrome (intraoperative).
Ear and labyrinth disorders: vertigo, tinnitus, ear pain.
Cardiac disorders: tachycardia, atrial fibrillation, atrioventricular block, conduction disorder, prolonged electrocardiogram OT, bradycardia, abnormal electrocardiogram, palpitations, sinus arrhythmia.
Vascular disorders: hypertension, hypotension, orthostatic hypotension, flushing, pulmonary embolism, venous thrombosis.
Respiratory, thoracic and mediastinal disorders: dyspnea, pharyngolaryngeal pain, cough, epistaxis, nasal congestion, pneumonia aspiration, pulmonary congestion, respiratory tract congestion, rales, wheezing, dysphonia, respiratory disorder, sleep apnea syndrome, hyperventilation.
Gastrointestinal disorders: abdominal pain, abdominal discomfort, vomiting, nausea, constipation, diarrhea, dyspepsia, dry mouth, toothache, fecal incontinence, fecaloma, gastroenteritis, dysphagia, flatulence, pancreatitis, intestinal obstruction, swollen tongue, cheilitis, ileus.
Skin and subcutaneous tissue disorders: rash, erythema, urticaria, pruritus, alopecia, hyperkeratosis, eczema, dry skin, skin discoloration, acne, seborrheic dermatitis, skin disorder, skin lesion, drug eruption, dandruff, angioedema.
Musculoskeletal and connective tissue disorders: muscle spasms, musculoskeletal pain, back pain, arthralgia, increased blood creatine phosphokinase, abnormal posture, joint stiffness, joint swelling, muscular weakness, neck pain, rhabdomyolysis.
Renal and urinary disorders: urinary incontinence, pollakiuria, urinary retention, dysuria.
Pregnancy, puerperium, and neonatal conditions: drug withdrawal syndrome neonatal.
Reproductive system and breast disorders: erectile dysfunction, ejaculation disorder, amenorrhea, menstrual disorder, gynecomastia, galactorrhea, sexual dysfunction, breast pain, breast discomfort, vaginal discharge, priapism, delayed menstruation, breast engorgement, breast enlargement, breast discharge.
General disorders and administration site conditions: edema, pyrexia, chest pain, asthenia, fatigue, pain, face edema, chills, increased or decreased body temperature, gait abnormal, thirst, chest discomfort, malaise, feeling abnormal, discomfort, hypothermia, peripheral coldness, drug withdrawal syndrome, induration.
Hepatobiliary disorders: increased transaminases, increased gamma-glutamyl transferase, increased hepatic enzyme, jaundice.
Injury, poisoning and procedural complications: fall, procedural pain.
Drug Interactions
Levodopa and Dopamine Agonists: Risperidone (Risdin) tablet may antagonize the effects of these agents.
H2-Receptor Antagonists (Cimetidine and Ranitidine): These drugs increase the bioavailability of Risperidone.
Clozapine: May decrease the clearance of Risperidone.
Valproate: Risperidone may increase peak plasma concentration of this drug.
Drugs that Inhibit CYP2D6 and Other CYP Isozymes: Drug interactions that reduce the metabolism of Risperidone to its active metabolite, 9-hydroxyrisperidone, would increase the plasma concentrations of Risperidone and lower the concentrations of 9-hydroxynsperidone.
Selective Serotonin Reuptake Inhibitors (Fluoxetine and Paroxetine): Increase plasma concentrations of Risperidone.
Storage
Action
Pharmacokinetics: Risperidone is readily absorbed after oral doses, peak plasma concentrations being reached within 1 to 2 hours. It is extensively metabolized in the liver by hydroxylation to its main active metabolite, 9-hydroxyrisperidone; oxidative N-dealkylation is a minor metabolic pathway. Hydroxylation is mediated by the cytochrome P450 isoenzyme CYP2D6 and is the subject of genetic polymorphism. Excretion is mainly in the urine and to a lesser extent, in the feces. Risperidone and 9-hydroxyrisperidone are about 88% and 77% bound to plasma proteins, respectively.
MedsGo Class
Features
- Risperidone