Antipsychotic abuse refers to the non-medical or inappropriate use of antipsychotic medications for purposes other than their intended therapeutic use. Antipsychotics, also known as neuroleptics, are a class of medications primarily used in treating psychiatric disorders such as schizophrenia, bipolar disorder, and certain types of depression. The misuse and abuse (MUA) of pharmaceuticals are typically linked to medications that elicit euphoria or other desirable effects, such as relaxation or increased alertness. Consequently, antipsychotics are not commonly categorized as significant substances prone to abuse. However, antipsychotics abuse may be attributed to its calming and sedative effects, and they have been exploited to either enhance the effects of illicit substances like cocaine and marijuana or counteract their adverse consequences. [1] Due to the potential of physical, social, and psychological consequences in patients using antipsychotics, the prevention and protection of these patient populations from the MUA of drugs has been implemented via various legislations worldwide which differ depending on the local jurisdiction.
Individuals may MUA antipsychotics for various reasons, including recreational purposes, self-medication, or attempting to alter their mental or emotional state. The most common forms of antipsychotic abuse may include non-prescribed use, which involves the use of antipsychotic medications without a valid legal prescription or the absence of medical supervision. This can involve obtaining medication from other individuals, sharing prescription drugs, or acquiring them through illicit means. Additionally, the misuse of prescribed medication can also involve using antipsychotics in a manner inconsistent with the prescribed indications. This includes taking higher dosages than recommended, increasing the dosing frequency, using them for longer durations than the prescribed treatment timespan as well as using medications prescribed to someone else. The combined or concurrent use of antipsychotics with other substances to enhance or alter the effects is also considered a form of abuse. This can involve combining them with alcohol, illicit drugs, or other prescription medications, which can have unpredictable and potentially dangerous interactions. [2]
There are two categories of oral antipsychotic drugs: typical; the first-generation antipsychotics and atypical; the new generation. Typical antipsychotics include Chlorpromazine, Fluphenazine, Haloperidol, and Trifluoperazine. Atypical antipsychotics include Amisulpride, Aripiprazole, Clozapine, Olanzapine, Paliperidone, and Quetiapine. [3] While both types of antipsychotic drugs are effective, the main differences are that atypical ones generally have fewer side effects compared to typical ones. These side-effects may include the onset of extrapyramidal motor symptoms which in the long term may cause a condition called tardive dyskinesia, which involves involuntary movements of the mouth, tongue, face, jaw, and sometimes other body parts. Atypical antipsychotics have also shown an increased risk of weight gain, diabetes, and cardiovascular disease.
The misuse of atypical antipsychotics can be attributed to various factors. From a pharmacological perspective, the involvement of neurotransmitter systems such as serotonin, histamine, and α-adrenergic systems is of significant importance. Quetiapine, a specific second-generation antipsychotic (SGAP), exhibits distinct pharmacological effects depending on the dosage administered. At lower doses, it primarily acts as an antagonist for histamine (H1) and serotonin receptors, resulting in an elevation of synaptic serotonin levels. [4] This mechanism contributes to the sedative effects associated with H1 antagonism and the anxiolytic effects mediated by α-blockade. These sedating and anxiolytic properties are considered to be the primary drivers of misuse.
Results from a study which analysed the WHO Global Individual Case Safety Report (ICSR) database VigiBase, a worldwide pharmacovigilance database on antipsychotic misuse, show that out of a total of 2096 ICSRs which fall under the subgroup of “Drug abuse, dependence and withdrawal”, 1683 involved SGAPs (80%), mainly quetiapine (1089 ICSRs) and olanzapine (209 ICSRs). [5] Further analysis showed that the major characteristics of quetiapine misuse mainly involved women with a mean age of 47 ± 15 years and olanzapine misuse mainly associated with men with a mean age of 43 ± 14 years. The study also noted that the trend in the misuse of SGAPs from 1993 to 2017 started to increase from 2009 with a peak in 2015 which confirms the significance of misuse in recent years.
Outcomes of abuse involved severe outcomes, such as hospitalisation or prolonged illness, mortality, life-threatening risks, and lasting effects. Within the VigiBase ICSRs, reasons for misuse included the off-label usage of SGAPs for sleeping disorders, and anxiety. Combining quetiapine or olanzapine with other medications included antidepressants, opioids, and anxiolytics. Additionally, both drugs have been found to be used in combination with illicit substances, primarily heroin and cocaine.
Indicators of the escalating street value of SGAPs is evident in the growing number of street names associated with the two drug, including quell, Susie Q, baby heroin, and squirrel for quetiapine and Zy for olanzapine. The black market value for quetiapine tablets are being sold illicitly at prices ranging from $3 to $8 per tablet. There has also been reports of both drugs extending past the traditional oral route of administration to using it intra-nasally (snorting) and injection also known as Q-ball which is the concomitant administration of cocaine with quetiapine. [6]
The wide variability in the toxic and lethal doses of antipsychotics is largely dependent on factors such as the actual drug compound, patient age, weight and the presence of co-intoxicants. However, the most frequent clinical presentations revolve around Central nervous system (CNS) effects, extrapyramidal side effects (EPS) and neuroleptic malignant syndrome which is more commonly seen in children. CNS side effects include: Miosis, rapid mood fluctuations (depression and agitation), seizures and coma. Anticholinergic side effects include: blurred vision, dry mouth, facial flushing and decreased sweating. Some cardiopulmonary side effects include: Tachycardia, palpitations, respiratory depression, and chest pain.
Weight gain | Parkinsonism | Tardive Dyskinesia | Sedation | Anticholinergic | QTc prolongation | |
---|---|---|---|---|---|---|
First-generation antipsychotics | ||||||
Chlorpromazine | ++ | ++ | +++ | +++ | +++ | +++ |
Fluphenazine | ++ | +++ | +++ | + | + | + |
Haloperidol | ++ | +++ | +++ | + | + | Oral: ++ IV: +++ |
Trifluoperazine | ++ | ++ | ++ | + | ++ | n/a |
Second-generation antipsychotic agents | ||||||
Aripiprazole | + | + | + | + | + | n/a |
Clozapine | +++ | + | + | +++ | +++ | ++ |
Olanzapine | +++ | ++ | + | +++ | ++ | ++ |
Paliperidone | ++ | ++ | ++ | + | + | + |
Quetiapine | ++ | + | + | +++ | ++ | ++ |
(+): Mild significance, (++): Moderate significance (+++): Strong significance |
The TDD is a tool used to assess potential antipsychotic misuse. It allows clinicians to calculate the total daily dosage of antipsychotic medications prescribed to patients based on guidelines from the British National Formulary (BNF). [9]
The calculator determines a patient's TDD by accounting for the specific antipsychotic drug(s), dosing frequency, and dosage amounts for both monotherapy (single drug) and polypharmacy (multiple drugs). [10] It then compares the calculated TDD to standard dosing recommendations in the BNF.
If the TDD exceeds guidelines outlined in the BNF or if the combination of individual drug dosages exceeds 100% of the maximum recommended daily amounts, the calculator flags this as a high dosage regimen which could indicate antipsychotic misuse or over prescription. By objectively quantifying total dosage levels, the TDD Calculator aims to help clinicians evaluate prescribing practices and identify situations where dosage reductions may be warranted to minimize health risks for patients.
Currently, there is no specific antidote for the treatment of antipsychotic overdose. The general protocol for the treatment of antipsychotic overdose involves primary supportive care, decontamination with enhanced elimination techniques such as using gastric lavage and activated charcoal. Specific anticholinergic side effects can be targeted by using anti-cholinergic agents. Every patient should be on continuous cardiac monitoring with an ECG done, intravenous (IV) access, and the constant reevaluation of changes in mental state.
Primary supportive care protocol involves the ABC approach which focuses on reversing any signs of airway obstruction (A), ensuring respiratory rate and breathing parameters are normal (B) and to assess the circulation of blood is normal to prevent hypovolemic shock (C). Whenever the patient is hemodynamically stable, a single dose of activated charcoal is recommended. [11] The onset of acute extrapyramidal symptoms due to antipsychotic overdose can be treated with anticholinergic agents, such as diphenhydramine or benztropine. Patients with neuroleptic malignant syndrome require supportive care, include active cooling to prevent overheating, benzodiazepines, bromocriptine, or neuromuscular blockade, depending upon the severity of symptoms. [12]
Antipsychotic abuse has grown increasingly more prevalent worldwide and has brought about various negative impacts to the society.
In the study examining 1683 patients with second-generation antipsychotic misuse extracted from WHO pharmacovigilance database, 24% were hospitalized. More importantly, the death rate was at 28%, which was higher than that of hospitalization by 4%. [5] This means that patients may risk of death before arriving at the hospital to receive any treatments with the misuse of SGAPs.
In addition to the high mortality rate, extra hospital services and medical resources were allocated to offset the negative effects of antipsychotic MUA. Research shows that non-adherence to antipsychotic medication would lead to increased number of relapses, being persistent psychotic and an enhanced risk of hospital admission in psychotic conditions. For instance, in a schizophrenic patient study group that assumes 90% of them comply to their medication at inclusion, more than 50% of the patients admitted to the hospital were non-compliant to their at-home antipsychotic dosage regimen. [13] By contrast, adherent patients tend to have better medical outcomes and improvements in Global Assessment of Functioning level across the two years.
In general, there were several issues posed by antipsychotic abuse with regards to their adverse reactions. [14]
Quetiapine-related emergency department visits increased by 90% from 2005 to 2011, according to Drug Abuse Warning Network (DAWN). [2]
About half of these admissions are due to MUA of antipsychotics whereas a quarter to a third of these visits are attributed to suicidal attempts or adverse reactions. The association of quetiapine with suicidal attempts is still unclear. Some propose higher dosage of quetiapine for those with suicidal intent. Some proposed the mix of substances causes more detrimental effects to patients. Some propose hospital stay is more likely for suicidal cause for patient stabilization or medication adjustment. However, following the adverse events, patients overall reported a significantly lower satisfaction of quality of life than asymptomatic patients. [15] This may be one potential reason of the suicidal attempt.
Canada has implemented several strategies to manage the use of antipsychotic medications:
From 2005, the indications of atypical antipsychotics medication for behavioral disease in elderly patient with dementia are removed. It is required for manufacturers in Canada to include a warning of this risk in their Product Monograph describing this risk and noting that these drugs (except for RISPERDAL) are not approved for treating behavioral disorders in elderly patients with dementia. [16]
RISPERDAL (Risperidone) is the exception among the atypical antipsychotics that still could be used for short-term symptomatic management of inappropriate behavior due to aggression and/or psychosis in patients with severe dementia. [16]
The programs are established in Canada to oversee prescription patterns and identify potential abuse. The universal database can keep track of the appropriateness of prescribing such as doses, refills frequencies and check if any overlapping prescription. [17]
Canadian law requires informed consent for the use of any medication, including antipsychotics, especially when used off-label or in populations like the elderly. [18]
The Mental Health Act 1983 is a legislation system which governs the administration of antipsychotic drugs to patients without their consent in certain circumstances. The Act is designed to protect the rights and well-being of individuals with mental disorders, ensuring that safety and appropriateness of treatments are maintained.
Under the Act, the Medicines and Healthcare products Regulatory Agency (MHRA) regulates the safety and efficacy of medications, including antipsychotics. The National Institute for Health and Care Excellence (NICE) provides comprehensive guidelines for the use of antipsychotic medications across different mental health conditions. [19]
Section 63: States that consent is not required for the treatment of a patient's mental disorder if it is given under the direction of the clinician in charge, except where treatments are specified under sections 57 or 58. [20]
Section 57: Specifies that certain treatments, like brain surgery, require consent from the patient and a second medical opinion. The Secretary of State can also specify other treatments through regulations. [21]
Section 58: Stipulates that some treatments require either patient consent or a second medical opinion if the patient cannot consent. The Secretary of State can specify which treatments are covered by this section. [22]
Patients under specific conditions that match with the sections mentioned above, then consent is not required for getting an optimal treatment.
In the United States, several measures are in place to prevent antipsychotic abuse:
Since 2005, Black Box Warnings established by the FDA that antipsychotic medications package requires to carry "black box" warnings, the most severe type of warning, about the risk of mortality in older adults with dementia-related psychosis. [23]
There is a list of preferred antipsychotics medications provided for the prescriber that the drug can be prescribed without prior authorization as long as the dose and frequency is within the recommendation of FDA. This helps to prevent the overdose of antipsychotic uses of patients. [24]
Antipsychotic peer review project is established to regulate the prescription of antipsychotics to children who aged beyond the FDA -approved age for that medication. Prior authorization by pediatric specialists to ensure appropriateness of prescription. To optimize the children’s care plan, evaluations and discussions are conducted between specialist and prescriber about the treatment choices, risks/benefits, monitoring needs, and non-medication alternatives, which this process is described as peer review. [25]
The approval processes and standards from regulatory bodies in the United Kingdom (UK) and United States (US) are different, therefore the drug approval varies. Variations in the following can impact the patterns of off-label and antipsychotic misuse between the two regions.
Some first-generation antipsychotics like haloperidol and chlorpromazine are approved down to children in the US, [26] but not in the UK. [27] Wider pediatric indications could increase misuse risks if not closely monitored.
Amisulpride is widely used in the UK [27] despite lacking US approval, where comparable alternatives would require off-label prescribing. [26] Unapproved status can hamper safety monitoring.
Variations in the indication of a drug may differ between two regions. Based on table 2, there is a broader indication of Olanzapine use in the US. [26] It is approved for treatment-resistant depression and agitation besides of bipolar and Schizophrenia. Whereas in UK, it is only for bipolar and schizophrenia. [27]
The tables below show the drugs approved with different indication and the indicated patient age group(s).
Drug Name | Indication | Age Group |
---|---|---|
Chlorpromazine | Schizophrenia, mania | Adults only |
Flupentixol | Schizophrenia, mania | Adults only |
Fluphenazine | Schizophrenia, mania | Adults only |
Haloperidol | Schizophrenia, mania | Adults only |
Pericyazine | Schizophrenia, mania | Adults only |
Pimozide | Tourette's syndrome | Adults and children |
Sulpiride | Schizophrenia, mania | Adults only |
Zuclopenthixol | Schizophrenia, mania | Adults only |
Drug Name | Indication | Age Group |
---|---|---|
Amisulpride | Schizophrenia, mania | Adults only |
Aripiprazole | Schizophrenia, mania, bipolar disorder | Adults and adolescents (15–17 years) |
Olanzapine | Schizophrenia, mania, bipolar disorder | Adults and adolescents (13–17 years) |
Paliperidone | Schizophrenia | Adults only |
Quetiapine | Schizophrenia, bipolar disorder, major depressive disorder | Adults and adolescents (13–17 years) |
Risperidone | Schizophrenia, bipolar disorder, irritability associated with autism | Adults and children/adolescents (13–17 years, 5–17 years) |
Ziprasidone | Schizophrenia, mania | Adults only |
Generic Name | Indications | Age Group for Which Approved |
---|---|---|
Chlorpromazine | Schizophrenia | Adults and children (1–12 years) |
Bipolar disorder (mania) | ||
Hyperactivity | ||
Severe behavioral problems | ||
Droperidol | Agitation | Adults and children |
Fluphenazine | Psychotic disorders | Adults |
Haloperidol | Schizophrenia | Adults |
Tourette syndrome | ||
Hyperactivity | ||
Severe childhood behavioral problems | ||
Loxapine | Schizophrenia | Adults and children ≥12 years |
Perphenazine | Schizophrenia | Adults and children ≥12 years |
Pimozide | Tourette syndrome | Adults and children ≥12 years |
Prochlorperazine | Schizophrenia | Adults and children >2 years and >20 pounds |
Generalized nonpsychotic anxiety | Adults | |
Thiothixene | Schizophrenia | Adults and children ≥12 years |
Thioridazine | Schizophrenia | Adults and children |
Trifluoperazine | Schizophrenia | Adults and children ≥6 years |
Generalized nonpsychotic anxiety | Adults |
Generic Name | Indications | Age Group for Which Approved |
---|---|---|
Aripiprazole | Schizophrenia | Adults and adolescents (13–17 years) |
Bipolar disorder (manic/mixed) monotherapy or adjunctive to lithium or valproate | Adults and children (10–17 years) | |
Adjunctive treatment of major depressive disorder | Adults | |
Irritability Associated with autistic disorder | Children (6–17 years) | |
Acute treatment of agitation | Adults | |
Asenapine | Acute schizophrenia | Adults |
Bipolar disorder type 1 (manic/mixed) | ||
Clozapine | Treatment resistant schizophrenia | Adults |
Reduce the risk of suicidal behavior in younger patients with schizophrenia. | ||
Iloperidone | Acute schizophrenia | Adults |
Olanzapine | Schizophrenia Bipolar disorder (manic/mixed) | Adults and adolescents (13–17 years) |
Bipolar disorder | Adults | |
Treatment resistant depression | ||
Agitation associated with schizophrenia and bipolar I mania | ||
Paliperidone | Schizophrenia Schizoaffective disorder | Adults |
Quetiapine | Schizophrenia | Adults and adolescents (13–17 years) |
Bipolar disorder (acute manic) | Adults, children, and adolescents (10–17 years) | |
Bipolar disorder (depression) | Adults | |
Bipolar disorder (maintenance) | ||
Adjunctive therapy for major depressive disorder | ||
Risperidone | Schizophrenia | Adults and adolescents (13–17 years) |
Bipolar disorder (manic/mixed) | Adults and adolescents (10–17 years) | |
Irritability associated with autism | Children (5–16 years) | |
Ziprasidone | Schizophrenia | Adults |
Bipolar disorder (manic/mixed) | ||
Bipolar disorder (maintenance) | ||
Acute agitation in patients with schizophrenia |
Patients over the age of 50 has a higher chance of being prescribed antipsychotic medications. A study from Ghanna hospital presents that amid all the adult patients, elderly aged 50 and over presented a higher likelihood to have an antipsychotic prescription for either psychosis or off-label use, which may lead to the poly-pharmacy of antipsychotics, thus increasing the risk of exceeding the Total daily dose (TDD) and ultimately resulting in a greater risk of antipsychotic misuse [28]
Antipsychotic MUA displays disproportionality in different age groups with studies revealing that out of 1023 patients below the age of 18 with antipsychotic MUA, 70% of them were between the age of 12 to 17, mainly originating from the United States (30% of the total). [29] This disproportionality brings attention to the withdrawal symptoms in children under two years of age, deliberate misuse in children from 2 to 11 years old and abuse in adolescents from 12 to 17 years old. Such disproportionality may be attributed to the increase of off-label antipsychotic usage and the overdose issue. The intentional misuse of antipsychotics would usually result in addiction, aggressive behaviour and emotional problems within adolescents.
Several studies have found that the prevalence of antipsychotic prescription was higher among male teenagers in comparison to female teenagers. One study in Germany found that the prescription prevalence was over 3 times higher for boys than that in girls in 2011, and the rate of increase since 2008 was also higher for boys. [30] Other research in British Columbia presented similar findings and reported the highest rise in antipsychotic prescriptions occurring among males aged 13 to 18 years from 2003 to 2012. [31]
Age also appears to influence antipsychotic prescription rates, with older adolescents from 15–17 years showing the highest prescription levels across age groups in Germany each year based on that study's data. [30] Additionally, conditions like hyperkinetic disorder, which is more prevalent in male teenagers, may contribute to their higher antipsychotic prescription rates compared to females.
In summary, being a male teenager, as well as being in the older adolescent age range of 15–17 years, are factors that are associated with higher antipsychotic prescription prevalence according to the available research evidence.
Legislation in a number of provinces and the territories has codified the law on consent, including the reliance on maturity in assessing a young person's capacity to consent to or refuse medical treatment.
Antipsychotics, previously known as neuroleptics and major tranquilizers, are a class of psychotropic medication primarily used to manage psychosis, principally in schizophrenia but also in a range of other psychotic disorders. They are also the mainstay, together with mood stabilizers, in the treatment of bipolar disorder. Moreover, they are also used as adjuncts in the treatment of treatment-resistant major depressive disorder.
Hypnotic, or soporific drugs, commonly known as sleeping pills, are a class of psychoactive drugs whose primary function is to induce sleep and to treat insomnia (sleeplessness).
A mood stabilizer is a psychiatric medication used to treat mood disorders characterized by intense and sustained mood shifts, such as bipolar disorder and the bipolar type of schizoaffective disorder.
A psychiatric or psychotropic medication is a psychoactive drug taken to exert an effect on the chemical makeup of the brain and nervous system. Thus, these medications are used to treat mental illnesses. These medications are typically made of synthetic chemical compounds and are usually prescribed in psychiatric settings, potentially involuntarily during commitment. Since the mid-20th century, such medications have been leading treatments for a broad range of mental disorders and have decreased the need for long-term hospitalization, thereby lowering the cost of mental health care. The recidivism or rehospitalization of the mentally ill is at a high rate in many countries, and the reasons for the relapses are under research.
Neuroleptic malignant syndrome (NMS) is a rare but life-threatening reaction that can occur in response to antipsychotic (neuroleptic) medications. Symptoms include high fever, confusion, rigid muscles, variable blood pressure, sweating, and fast heart rate. Complications may include rhabdomyolysis, high blood potassium, kidney failure, or seizures.
Typical antipsychotics are a class of antipsychotic drugs first developed in the 1950s and used to treat psychosis. Typical antipsychotics may also be used for the treatment of acute mania, agitation, and other conditions. The first typical antipsychotics to come into medical use were the phenothiazines, namely chlorpromazine which was discovered serendipitously. Another prominent grouping of antipsychotics are the butyrophenones, an example of which is haloperidol. The newer, second-generation antipsychotics, also known as atypical antipsychotics, have largely supplanted the use of typical antipsychotics as first-line agents due to the higher risk of movement disorders with typical antipsychotics.
The atypical antipsychotics (AAP), also known as second generation antipsychotics (SGAs) and serotonin–dopamine antagonists (SDAs), are a group of antipsychotic drugs largely introduced after the 1970s and used to treat psychiatric conditions. Some atypical antipsychotics have received regulatory approval for schizophrenia, bipolar disorder, irritability in autism, and as an adjunct in major depressive disorder.
Quetiapine, sold under the brand name Seroquel among others, is an atypical antipsychotic medication used for the treatment of schizophrenia, bipolar disorder, and major depressive disorder. Despite being widely used as a sleep aid due to its sedating effect, the benefits of such use may not outweigh its undesirable side effects. It is taken orally.
Ziprasidone, sold under the brand name Geodon among others, is an atypical antipsychotic used to treat schizophrenia and bipolar disorder. It may be used by mouth and by injection into a muscle (IM). The IM form may be used for acute agitation in people with schizophrenia.
Olanzapine, sold under the brand name Zyprexa among others, is an atypical antipsychotic primarily used to treat schizophrenia and bipolar disorder. For schizophrenia, it can be used for both new-onset disease and long-term maintenance. It is taken by mouth or by injection into a muscle.
Aripiprazole, sold under the brand names Abilify and Aristada, among others, is an atypical antipsychotic. It is primarily used in the treatment of schizophrenia and bipolar disorder; other uses include as an add-on treatment in major depressive disorder and obsessive compulsive disorder (OCD), tic disorders, and irritability associated with autism. Aripiprazole is taken by mouth or via injection into a muscle. A Cochrane review found low-quality evidence of effectiveness in treating schizophrenia.
A dopamine antagonist, also known as an anti-dopaminergic and a dopamine receptor antagonist (DRA), is a type of drug which blocks dopamine receptors by receptor antagonism. Most antipsychotics are dopamine antagonists, and as such they have found use in treating schizophrenia, bipolar disorder, and stimulant psychosis. Several other dopamine antagonists are antiemetics used in the treatment of nausea and vomiting.
Treatment-resistant depression (TRD) is a term used in psychiatry to describe people with major depressive disorder (MDD) who do not respond adequately to a course of appropriate antidepressant medication within a certain time. Definitions of treatment-resistant depression vary, and they do not include a resistance to psychotherapy. Inadequate response has most commonly been defined as less than 50% reduction in depressive symptoms following treatment with at least one antidepressant medication, although definitions vary widely. Some other factors that may contribute to inadequate treatment are: a history of repeated or severe adverse childhood experiences, early discontinuation of treatment, insufficient dosage of medication, patient noncompliance, misdiagnosis, cognitive impairment, low income and other socio-economic variables, and concurrent medical conditions, including comorbid psychiatric disorders. Cases of treatment-resistant depression may also be referred to by which medications people with treatment-resistant depression are resistant to. In treatment-resistant depression adding further treatments such as psychotherapy, lithium, or aripiprazole is weakly supported as of 2019.
Extrapyramidal symptoms (EPS) are symptoms that are archetypically associated with the extrapyramidal system of the brain's cerebral cortex. When such symptoms are caused by medications or other drugs, they are also known as extrapyramidal side effects (EPSE). The symptoms can be acute (short-term) or chronic (long-term). They include movement dysfunction such as dystonia, akathisia, parkinsonism characteristic symptoms such as rigidity, bradykinesia, tremor, and tardive dyskinesia. Extrapyramidal symptoms are a reason why subjects drop out of clinical trials of antipsychotics; of the 213 (14.6%) subjects that dropped out of one of the largest clinical trials of antipsychotics, 58 (27.2%) of those discontinuations were due to EPS.
Asenapine, sold under the brand name Saphris among others, is an atypical antipsychotic medication used to treat schizophrenia and acute mania associated with bipolar disorder as well as the medium to long-term management of bipolar disorder.
Olanzapine/fluoxetine is a fixed-dose combination medication containing olanzapine (Zyprexa), an atypical antipsychotic, and fluoxetine (Prozac), a selective serotonin reuptake inhibitor (SSRI). Olanzapine/fluoxetine is primarily used to treat the depressive episodes of bipolar I disorder as well as treatment-resistant depression.
Lurasidone, sold under the brand name Latuda among others, is an antipsychotic medication used to treat schizophrenia and bipolar disorder. It is taken by mouth.
Pomaglumetad (LY-404,039) is an amino acid analog drug that acts as a highly selective agonist for the metabotropic glutamate receptor group II subtypes mGluR2 and mGluR3. Pharmacological research has focused on its potential antipsychotic and anxiolytic effects. Pomaglumetad is intended as a treatment for schizophrenia and other psychotic and anxiety disorders by modulating glutamatergic activity and reducing presynaptic release of glutamate at synapses in limbic and forebrain areas relevant to these disorders. Human studies investigating therapeutic use of pomaglumetad have focused on the prodrug LY-2140023, a methionine amide of pomaglumetad (also called pomaglumetad methionil) since pomaglumetad exhibits low oral absorption and bioavailability in humans.
Evenamide is a selective voltage-gated sodium channel blocker, including subtypes Nav1.3, Nav1.7, and Nav1.8, which is described as an antipsychotic and is under development by Newron Pharmaceuticals as an add-on therapy for the treatment of schizophrenia. The drug has shown efficacy in animal models of psychosis, mania, depression, and aggression. It has completed phase I clinical trials, and phase II clinical trials will be commenced in the third quarter of 2015.
Antipsychotic switching refers to the process of switching out one antipsychotic for another antipsychotic. There are multiple indications for switching antipsychotics, including inadequate efficacy and drug intolerance. There are several strategies that have been theorized for antipsychotic switching, based upon the timing of discontinuation and tapering of the original antipsychotic and the timing of initiation and titration of the new antipsychotic. Major adverse effects from antipsychotic switching may include supersensitivity syndromes, withdrawal, and rebound syndromes.