Adherence to Antipsychotic Medications for Individuals
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Prochlorperazine 5Mg Tablets
Package leaflet: Information for the patient Prochlorperazine 5mg tablets Read all of this leaflet carefully before you start taking this • the person is a child. This is because children may develop unusual face and body medicine, because it contains important information for you. movements (dystonic reactions) • Keep this leaflet. You may need to read it again. • you are diabetic or have high levels of sugar in your blood (hyperglycaemia). Your doctor • If you have any further questions, ask your doctor or pharmacist. may want to monitor you more closely. • This medicine has been prescribed for you only. Do not pass it on to If you are not sure if any of the above apply to you, talk to your doctor or pharmacist before others. It may harm them, even if their signs of illness are the same taking Prochlorperazine Tablets. as yours. Other medicines and Prochlorperazine tablets • If you get any side effects, talk to your doctor or pharmacist. Tell your doctor or pharmacist if you are taking, have recently taken or might take any This includes any possible side effects not listed in this leaflet. other medicines. This includes medicines you buy without a prescription, including herbal See section 4. medicines. This is because Prochlorperazine Tablets can affect the way some other medicines work. What is in this leaflet: Also some medicines can affect the way Prochlorperazine Tablets work. 1 What Prochlorperazine tablets are and what they In particular, tell your doctor if you are taking any of the following: • medicines to help you sleep -
Treatment of Psychosis: 30 Years of Progress
Journal of Clinical Pharmacy and Therapeutics (2006) 31, 523–534 REVIEW ARTICLE Treatment of psychosis: 30 years of progress I. R. De Oliveira* MD PhD andM.F.Juruena MD *Department of Neuropsychiatry, School of Medicine, Federal University of Bahia, Salvador, BA, Brazil and Department of Psychological Medicine, Institute of Psychiatry, King’s College, University of London, London, UK phrenia. Thirty years ago, psychiatrists had few SUMMARY neuroleptics available to them. These were all Background: Thirty years ago, psychiatrists had compounds, today known as conventional anti- only a few choices of old neuroleptics available to psychotics, and all were liable to cause severe extra them, currently defined as conventional or typical pyramidal side-effects (EPS). Nowadays, new antipsychotics, as a result schizophrenics had to treatments are more ambitious, aiming not only to suffer the severe extra pyramidal side effects. improve psychotic symptoms, but also quality of Nowadays, new treatments are more ambitious, life and social reinsertion. We briefly but critically aiming not only to improve psychotic symptoms, outline the advances in diagnosis and treatment but also quality of life and social reinsertion. Our of schizophrenia, from the mid 1970s up to the objective is to briefly but critically review the present. advances in the treatment of schizophrenia with antipsychotics in the past 30 years. We conclude DIAGNOSIS OF SCHIZOPHRENIA that conventional antipsychotics still have a place when just the cost of treatment, a key factor in Up until the early 1970s, schizophrenia diagnoses poor regions, is considered. The atypical anti- remained debatable. The lack of uniform diagnostic psychotic drugs are a class of agents that have criteria led to relative rates of schizophrenia being become the most widely used to treat a variety of very different, for example, in New York and psychoses because of their superiority with London, as demonstrated in an important study regard to extra pyramidal symptoms. -
Standard Operating Procedure Initiation And
STANDARD OPERATING PROCEDURE Title: Procedure Document Version INITIATION AND PRESCRIBING OF PALIPERIDONE No: Replaced: LONG ACTING INJECTION (PLAI) Clinical N/A 2 SOP 03 Procedure Written By: Procedure Approved By: Approved Review Page Senior Pharmacist Gurj Bhella Date: Date: Deputy Chief Pharmacist Chief Pharmacist 22/05/2018 22/05/2020 1 of 3 Objective To ensure that all prescriptions for paliperidone are initiated by consultants on a named-patient basis and that a record of all patients is kept. Scope All BCPFT consultant teams, Pharmacy Team. Procedure 1. When a patient is identified as being a candidate for paliperidone LAI, the following criteria must be fulfilled: a. The prescribing of a typical antipsychotic depot injection first line has been tried to no effect or has not been tolerated, or is not considered clinically appropriate. b. PLAI to be initiated by Consultants only and be prescribed for its licensed indication only i.e. for maintenance treatment of schizophrenia in adult patients stabilised with risperidone (Oral or LAI) or have responded to it previously. In selected adult patients with schizophrenia and previous responsiveness to oral paliperidone or risperidone, it may be used without prior stabilisation with oral treatment if psychotic symptoms are mild to moderate and a long-acting injectable treatment is needed. Patients may now be switched from oral risperidone as well as risperidone LAI. c. PLAI must be prescribed in line with the treatment guidance for the use of long acting injections contained within NICE guideline CG178 ‘Psychosis and schizophrenia in adults: treatment and management’ issued February 2014. d. Paliperidone LAI must be prescribed once each calendar month i.e.12 times a year. -
Schizophrenia Care Guide
August 2015 CCHCS/DHCS Care Guide: Schizophrenia SUMMARY DECISION SUPPORT PATIENT EDUCATION/SELF MANAGEMENT GOALS ALERTS Minimize frequency and severity of psychotic episodes Suicidal ideation or gestures Encourage medication adherence Abnormal movements Manage medication side effects Delusions Monitor as clinically appropriate Neuroleptic Malignant Syndrome Danger to self or others DIAGNOSTIC CRITERIA/EVALUATION (PER DSM V) 1. Rule out delirium or other medical illnesses mimicking schizophrenia (see page 5), medications or drugs of abuse causing psychosis (see page 6), other mental illness causes of psychosis, e.g., Bipolar Mania or Depression, Major Depression, PTSD, borderline personality disorder (see page 4). Ideas in patients (even odd ideas) that we disagree with can be learned and are therefore not necessarily signs of schizophrenia. Schizophrenia is a world-wide phenomenon that can occur in cultures with widely differing ideas. 2. Diagnosis is made based on the following: (Criteria A and B must be met) A. Two of the following symptoms/signs must be present over much of at least one month (unless treated), with a significant impact on social or occupational functioning, over at least a 6-month period of time: Delusions, Hallucinations, Disorganized Speech, Negative symptoms (social withdrawal, poverty of thought, etc.), severely disorganized or catatonic behavior. B. At least one of the symptoms/signs should be Delusions, Hallucinations, or Disorganized Speech. TREATMENT OPTIONS MEDICATIONS Informed consent for psychotropic -
Management of Side Effects of Antipsychotics
Management of side effects of antipsychotics Oliver Freudenreich, MD, FACLP Co-Director, MGH Schizophrenia Program www.mghcme.org Disclosures I have the following relevant financial relationship with a commercial interest to disclose (recipient SELF; content SCHIZOPHRENIA): • Alkermes – Consultant honoraria (Advisory Board) • Avanir – Research grant (to institution) • Janssen – Research grant (to institution), consultant honoraria (Advisory Board) • Neurocrine – Consultant honoraria (Advisory Board) • Novartis – Consultant honoraria • Otsuka – Research grant (to institution) • Roche – Consultant honoraria • Saladax – Research grant (to institution) • Elsevier – Honoraria (medical editing) • Global Medical Education – Honoraria (CME speaker and content developer) • Medscape – Honoraria (CME speaker) • Wolters-Kluwer – Royalties (content developer) • UpToDate – Royalties, honoraria (content developer and editor) • American Psychiatric Association – Consultant honoraria (SMI Adviser) www.mghcme.org Outline • Antipsychotic side effect summary • Critical side effect management – NMS – Cardiac side effects – Gastrointestinal side effects – Clozapine black box warnings • Routine side effect management – Metabolic side effects – Motor side effects – Prolactin elevation • The man-in-the-arena algorithm www.mghcme.org Receptor profile and side effects • Alpha-1 – Hypotension: slow titration • Dopamine-2 – Dystonia: prophylactic anticholinergic – Akathisia, parkinsonism, tardive dyskinesia – Hyperprolactinemia • Histamine-1 – Sedation – Weight gain -
PRODUCT INFORMATION Perphenazine Item No
PRODUCT INFORMATION Perphenazine Item No. 20735 CAS Registry No.: 58-39-9 HO Formal Name: 4-[3-(2-chloro-10H-phenothiazin-10-yl) N propyl]-1-piperazineethanol N Synonyms: NSC 150866, SCH 3940 MF: C21H26ClN3OS FW: 404.0 Purity: ≥98% N Cl UV/Vis.: λmax: 257, 312 nm Supplied as: A crystalline solid Storage: -20°C S Stability: ≥2 years Information represents the product specifications. Batch specific analytical results are provided on each certificate of analysis. Laboratory Procedures Perphenazine is supplied as a crystalline solid. A stock solution may be made by dissolving the perphenazine in the solvent of choice, which should be purged with an inert gas. Perphenazine is soluble in organic solvents such as ethanol, DMSO, and dimethyl formamide. The solubility of perphenazine in these solvents is approximately 5, 20, and 30 mg/ml, respectively. Description 1 Perphenazine is a typical antipsychotic. It binds to dopamine D2, α1A-, α2A-, α2B-, and α2C-adrenergic, M3 muscarinic, and histamine H1 receptors (Kis = 1.4, 10, 1,848, 104.9, 85.2, 810.5 and 8 nM, respectively), as well as the serotonin (5-HT) receptor subtypes 5-HT1A, 5-HT2A, 5-HT2C, 5-HT6, and 5-HT7 (Kis = 421, 5.6, 132, 17, and 23 nM, respectively). Perphenazine (1, 5, and 10 mg/kg) enhances morphine-induced analgesia in the tail-flick and hot plate tests in rats.2 It reduces cannibalism in female mice when administered at doses of 2 and 4 mg/kg.3 Formulations containing perphenazine have been used in the treatment of schizophrenia and psychosis. References 1. -
Appendix 13C: Clinical Evidence Study Characteristics Tables
APPENDIX 13C: CLINICAL EVIDENCE STUDY CHARACTERISTICS TABLES: PHARMACOLOGICAL INTERVENTIONS Abbreviations ............................................................................................................ 3 APPENDIX 13C (I): INCLUDED STUDIES FOR INITIAL TREATMENT WITH ANTIPSYCHOTIC MEDICATION .................................. 4 ARANGO2009 .................................................................................................................................. 4 BERGER2008 .................................................................................................................................... 6 LIEBERMAN2003 ............................................................................................................................ 8 MCEVOY2007 ................................................................................................................................ 10 ROBINSON2006 ............................................................................................................................. 12 SCHOOLER2005 ............................................................................................................................ 14 SIKICH2008 .................................................................................................................................... 16 SWADI2010..................................................................................................................................... 19 VANBRUGGEN2003 .................................................................................................................... -
Sex-Specific Cannabidiol- and Iloperidone-Induced Neuronal Activity Changes in an in Vitro MAM Model System of Schizophrenia
International Journal of Molecular Sciences Article Sex-Specific Cannabidiol- and Iloperidone-Induced Neuronal Activity Changes in an In Vitro MAM Model System of Schizophrenia Rachel-Karson Thériault 1,2,†, Myles St-Denis 1,†, Tristen Hewitt 1,2, Jibran Y. Khokhar 2,3 , Jasmin Lalonde 1,2 and Melissa L. Perreault 2,3,* 1 Department of Molecular and Cellular Biology, University of Guelph, Guelph, ON N1G 2W1, Canada; [email protected] (R.-K.T.); [email protected] (M.S.-D.); [email protected] (T.H.); [email protected] (J.L.) 2 Collaborative Program in Neuroscience, University of Guelph, Guelph, ON N1G 2W1, Canada; [email protected] 3 Department of Biomedical Sciences, University of Guelph, Guelph, ON N1G 2W1, Canada * Correspondence: [email protected]; Tel.: +1-(519)-824-4120 (ext. 52013) † These authors contributed equally to this work. Abstract: Cortical circuit dysfunction is thought to be an underlying mechanism of schizophrenia (SZ) pathophysiology with normalization of aberrant circuit activity proposed as a biomarker for antipsychotic efficacy. Cannabidiol (CBD) shows potential as an adjunctive antipsychotic therapy; however, potential sex effects in these drug interactions remain unknown. In the present study, we sought to elucidate sex effects of CBD coadministration with the atypical antipsychotic iloperidone (ILO) on the activity of primary cortical neuron cultures derived from the rat methylazoxymethanol Citation: Thériault, R.-K.; St-Denis, acetate (MAM) model used for the study of SZ. Spontaneous network activity measurements were M.; Hewitt, T.; Khokhar, J.Y.; Lalonde, J.; Perreault, M.L. Sex-Specific obtained using a multielectrode array at baseline and following administration of CBD or ILO Cannabidiol- and Iloperidone- alone, or combined. -
Washington State Health Care Authority
Washington State Health Care Authority Prescription Drug Program 626 8th Ave SE, Olympia, WA 98501 ● 206-521-2029 https://www.hca.wa.gov/about-hca/prescription-drug-program February 17, 2021 Dear Interested Party, Based on recommendations by the Washington State Pharmacy and Therapeutics Committee, the Health Care Authority, Uniform Medical Plan (UMP), and the Department of Labor & Industries (L&I) have named the following drugs as preferred in their respective therapeutic classes on the Washington State Preferred Drug List (PDL), effective immediately: Antiplatelet reviewed 8/15/2018 Agency Coverage Ingredient Name Label Name of Preferred Product L&I UMP clopidogrel bisulfate clopidogrel tablet Not participating Yes The effect of this recommendation is no change to the Washington PDL. Second Generation Antipsychotics reviewed 12/18/2019 Agency Coverage Ingredient Name Label Name of Preferred Products L&I UMP aripiprazole Abilify Maintena® suspension reconstituted No Yes aripiprazole solution Yes Yes aripiprazole tablet Yes Yes aripiprazole ODT tablet dispersible Yes Yes aripiprazole lauroxil Aristada® injectable No Yes Aristada Initio® injectable No Yes asenapine maleate Saphris® sublingual Yes Yes brexpiprazole Rexulti® tablet Yes Yes cariprazine HCL Vraylar® capsule Yes Yes clozapine clozapine tablet Yes Yes clozapine ODT tablet dispersible Yes Yes iloperidone Fanapt® tablet Yes Yes Fanapt Titration Pack® tablet Yes Yes lurasidone HCL Latuda® tablet Yes Yes olanzapine olanzapine injectable No Yes olanzapine tablet Yes Yes olanzapine -
Management of Major Depressive Disorder Clinical Practice Guidelines May 2014
Federal Bureau of Prisons Management of Major Depressive Disorder Clinical Practice Guidelines May 2014 Table of Contents 1. Purpose ............................................................................................................................................. 1 2. Introduction ...................................................................................................................................... 1 Natural History ................................................................................................................................. 2 Special Considerations ...................................................................................................................... 2 3. Screening ........................................................................................................................................... 3 Screening Questions .......................................................................................................................... 3 Further Screening Methods................................................................................................................ 4 4. Diagnosis ........................................................................................................................................... 4 Depression: Three Levels of Severity ............................................................................................... 4 Clinical Interview and Documentation of Risk Assessment............................................................... -
How to Identify and Manage Non-Response to Clozapine? T ⁎ Mujeeb U
Asian Journal of Psychiatry 45 (2019) 50–52 Contents lists available at ScienceDirect Asian Journal of Psychiatry journal homepage: www.elsevier.com/locate/ajp Short communication How to identify and manage non-response to clozapine? T ⁎ Mujeeb U. Shada,b,c, , Emma Felziena, Kamalika Roya,b, Simrat Sethib a School of Medicine, Oregon Health & Science University, Portland, Oregon, United States b Department of Psychiatry, Oregon State Hospital, Salem, Oregon, United States c Samaritan Mental Healthcare System, Corvallis, Oregon, United States ARTICLE INFO ABSTRACT Keywords: Clozapine is the only approved treatment for Treatment-Refractory Schizophrenia. Here we describe a case series Clozapine of three hospitalized patients with clozapine nonresponse. One of them responded to clozapine after dose ad- Non-response justments were made for an interaction between clozapine and ciprofloxacin. The other two cases remained Identify clozapine nonresponders despite optimizing clozapine treatment. However, both these patients responded to Manage other antipsychotic medications (APMs) with better tolerability than observed with clozapine treatment. This case series focuses on diagnosing a genuine from a pseudo-nonresponse to clozapine and to consider other APMs in genuine nonresponse before switching to invasive interventions, such as ECT. 1. Introduction medications (APMs), except in situations where bone marrow toxicity warrants clozapine discontinuation. Although augmentation strategies Since clozapine provides the only evidence-based treatment for with APMs, glutamate modulators and mood stabilizers have been patients with treatment-refractory schizophrenia (TRS) (Manu and proposed in ultra-treatment resistant schizophrenia (Naguy and Grudnikoff, 2016; Mukku et al., 2018), optimal efforts are warranted to Alamiri, 2019), a recent metanalysis reported a low quality of sup- confirm a true clozapine non-response before giving up on clozapine porting evidence for these clozapine augmentation strategies with the treatment. -
Clinical Guideline Drug/Drug Class: Antipsychotics Prepared By
MassHealth Drug Utilization Review Program Commonwealth Medicine University of Massachusetts Medical School P.O. Box 2586 Worcester MA, 01613-2586 Clinical Guideline Drug/Drug Class: Antipsychotics Prepared by: Drug Utilization Review Program Prepared for: MassHealth Pharmacy Program Purpose: The purpose of this guideline is to clarify the procedures for approving and denying prior authorization (PA) requests for: Polypharmacy with two or more antipsychotics for members ≥ 18 years old (including first- generation [typical] and second-generation [atypical]) for greater than 60 days (excluding clozapine and injectable formulations) Orally disintegrating dosage forms and Versacloz® (clozapine) oral suspension Medication exceeding defined quantity limits Fanapt® (iloperidone), Invega® (paliperidone), Latuda® (lurasidone), Rexulti® (brexpiprazole), Saphris® (asenapine), and Vraylar® (cariprazine) for members of all ages and all quantities Abilify® (aripiprazole) and Seroquel XR® (quetiapine extended-release) for members 18 years of age and older and all quantities Background: Since 2003, MassHealth has determined that oral second-generation (atypical) antipsychotics (with the exception of clozapine and injectables) would require prior authorization for polypharmacy, defined as two or more second-generation (atypical) antipsychotics for greater than 60 days. Clozapine is excluded from the polypharmacy requirement because the guidelines for the treatment of schizophrenia recognize that combinations including clozapine have been reported. 1 In 2016, the adult antipsychotic polypharmacy criteria was updated and the PA restriction was expanded to include first-generation (typical), and second-generation (atypical) antipsychotics, excluding clozapine and injectable formulations. Orally disintegrating tablets (ODT) of aripiprazole, clozapine, olanzapine and risperidone, as well as Versacloz® (clozapine) oral suspension also require PA since there are more cost-effective alternatives available.