Antipsychotic

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Olanzapine, an example of a second-generation antipsychotic

Antipsychotics are a class of psychiatric medication primarily used to manage psychosis (including delusions, hallucinations, paranoia or disordered thought), principally in schizophrenia and bipolar disorder. They are increasingly being used in the management of non-psychotic disorders. Antipsychotics are usually effective in relieving symptoms of psychosis. However, their long term use is associated with significant side effects such as involuntary movement disorders and metabolic syndrome.

First-generation antipsychotics, known as typical antipsychotics, were discovered in the 1950s. Most second-generation drugs, known as atypical antipsychotics, have been developed more recently, although the first atypical antipsychotic, clozapine, was discovered in the 1960s and introduced clinically in the 1970s.[1] The terms neuroleptic and major tranquilizer were used for older antipsychotic drugs, but are gradually dropping from use.[2][3] Both generations of medication tend to block receptors in the brain's dopamine pathways, but atypicals tend to act on serotonin receptors as well. Neuroleptic, which originates from the Greek word νεῦρον neuron ("nerve") and λῆψις lepsis ("seizure" or "fit"), is a reference to neurological side effects.[4][5]

Medical uses[edit]

Antipsychotics are most frequently used for the following conditions:

  • Schizophrenia
  • Schizoaffective disorder most commonly in conjunction with either an antidepressant (in the case of the depressive subtype) or a mood stabiliser (in the case of the bipolar subtype).
  • Bipolar disorder (acute mania and mixed episodes) may be treated with either typical or atypical antipsychotics, although atypical antipsychotics are usually preferred because they tend to have more favourable adverse effect profiles[6] and, according to a recent meta-analysis, they tend to have a lower liability for causing conversion from mania to depression.[7]
  • Psychotic depression. In this indication it is a common practice for the psychiatrist to prescribe a combination of an atypical antipsychotic and an antidepressant as this practice is best supported by the evidence.[8]
  • Treatment-resistant (and not necessarily psychotic) major depression as an adjunct to standard antidepressant therapy.[8]

They are not recommended for dementia or insomnia unless other treatments have not worked.[9] They are not recommended in children unless other treatments are not effective or unless the child has psychosis.[9]

Schizophrenia[edit]

Main article: Schizophrenia

Antipsychotic drug treatment is a key component of schizophrenia treatment algorithms recommended by the National Institute of Health and Clinical Excellence (NICE),[10] the American Psychiatric Association,[11] and the British Society for Psychopharmacology.[12] The main effect of treatment with antipsychotics is to reduce the so-called "positive" symptoms, including delusions and hallucinations. There is mixed evidence to support a significant impact of antipsychotic use on negative symptoms (such as apathy, lack of emotional affect, and lack of interest in social interactions) or on the cognitive symptoms (disordered thinking, reduced ability to plan and execute tasks) of schizophrenia.[13][14] In general, the efficacy of antipsychotic treatment in reducing both positive and negative symptoms appears to increase with increasing severity of baseline symptoms.[15]

Applications of antipsychotic drugs in the treatment of schizophrenia include prophylaxis in those showing symptoms that suggest that they are at high risk of developing psychosis, treatment of first episode psychosis, maintenance therapy, and treatment of recurrent episodes of acute psychosis.[12]

Prevention of psychosis and symptom improvement[edit]

Test batteries such as the PACE (Personal Assessment and Crisis Evaluation Clinic) and COPS (Criteria of Prodromal Syndromes), which measure low level psychotic symptoms, and others focused on cognitive disturbances (Basic symptoms"), are used to evaluate people with early, low level symptoms of psychosis. Used in combination with family history information, these tests can identify a "high risk" group having a 20–40% risk of progression to frank psychosis within 2 years.[12] These patients are often treated with low doses of antipsychotic drugs with the goal of reducing their symptoms and preventing progression to frank psychosis. While generally useful for reducing symptoms, the clinical trials performed to date provide little evidence that early use of antipsychotics, alone or in combination with cognitive-behavioral therapy, provides improved long term outcomes in those with prodromal symptoms.[16]

First episode psychosis[edit]

NICE recommends that all persons presenting with a first episode of frank psychosis be treated with both an antipsychotic drug and cognitive-behavioral therapy (CBT). NICE further recommends that those expressing a preference for CBT alone be informed that combination treatment is more efficacious.[10] A diagnosis of schizophrenia is not normally made at this time, as up to 25% of those presenting with first episode psychosis are eventually found to suffer from bipolar disorder instead. The goals of treatment of these patients include reducing symptoms and potentially improving long-term treatment outcomes. Randomized clinical trials have provided strong evidence for the efficacy of antipsychotic drugs in achieving the former goal, with first-generation and second generation antipsychotics showing about equal efficacy. Evidence that early treatment has a favorable effect on long term outcomes is equivocal.[10][12]

Recurrent psychotic episodes[edit]

Placebo-controlled trials of both first and second generation antipsychotic drugs consistently demonstrate the superiority of active drug to placebo in suppressing psychotic symptoms.[12] A large meta analysis of 38 trials of antipsychotic drugs in schizophrenia acute psychotic episodes showed an effect size of about 0.5.[17] There is little or no difference in efficacy among approved antipsychotic drugs, including both first- and second-generation agents.[10][18] The efficacy of such drugs is suboptimal. Few patients achieve complete resolution of symptoms. Response rates, calculated using various cutoff values for symptom reduction, are low and their interpretation is complicated by high placebo response rates and selective publication of clinical trial results.[19]

Maintenance therapy[edit]

The majority of patients treated with an antipsychotic drug will experience a response within 4 weeks. The goals of continuing treatment are to maintain suppression of symptoms, prevent relapse, improve quality of life, and support engagement in psychosocial therapy.[12]

Maintenance therapy with antipsychotic drugs is clearly superior to placebo in preventing relapse, but is associated with weight gain, movement disorders, and high dropout rates.[20] A 3-year trial following persons receiving maintenance therapy after an acute psychotic episode found that 33% obtained long-lasting symptom reduction, 13% achieved remission, and only 27% experienced satisfactory quality of life. The effect of relapse prevention on long term outcomes is uncertain, as historical studies show little difference in long term outcomes before and after the introduction of antipsychotic drugs.[12]

A significant challenge in the use of antipsychotic drugs for the prevention of relapse is the poor rate of compliance. In spite of the relatively high rates of adverse effects associated with these drugs, some evidence, including higher dropout rates in placebo arms compared to treatment arms in randomized clinical trials, suggest that most patients who discontinue treatment do so because of suboptimal efficacy.[20][21]

Bipolar disorder[edit]

Main article: Bipolar disorder

Antipsychotics are routinely used, often in conjunction with mood stabilisers such as lithium/valproate, as a first-line treatment for manic and mixed episodes associated with bipolar disorder.[8][22] The reason for this combination is the therapeutic delay of the aforementioned mood stabilisers (for valproate therapeutic effects are usually seen around five days after treatment is commenced whereas lithium usually takes at least a week[22] before the full therapeutic effects are seen) and the comparatively rapid antimanic effects of antipsychotic drugs.[23] The antipsychotics have a documented efficacy when used alone in acute mania/mixed episodes.[6]

Three atypical antipsychotics (lurasidone,[24] olanzapine[25] and quetiapine[26]) have also been found to possess efficacy in the treatment of bipolar depression as a monotherapy. Whereas only olanzapine[27] and quetiapine[28][29] have been proven to be effective broad-spectrum (i.e. against all three types of relapse— manic, mixed and depressive) prophylactic (or maintenance) treatments in patients with bipolar disorder. A recent Cochrane review also found that olanzapine had a less favourable risk/benefit ratio than lithium as a maintenance treatment for bipolar disorder.[30]

The American Psychiatric Association and the UK National Institute for Health and Care Excellence recommend antipsychotics for managing acute psychotic episodes in schizophrenia or bipolar disorder, and as a longer-term maintenance treatment for reducing the likelihood of further episodes.[31][32] They state that response to any given antipsychotic can be variable so that trials may be necessary, and that lower doses are to be preferred where possible. A number of studies have looked at levels of "compliance" or "adherence" with antipsychotic regimes and found that discontinuation (stopping taking them) by patients is associated with higher rates of relapse, including hospitalization.

Dementia[edit]

As assessment for an underlying cause of behavior is needed before prescribing antipsychotic medication for symptoms of dementia.[33] Antipsychotics in old age dementia showed a modest benefit compared to placebo in managing aggression or psychosis, but this is combined with a fairly large increase in serious adverse events. Thus, antipsychotics should not be used routinely to treat dementia with aggression or psychosis, but may be an option in a few cases where there is severe distress or risk of physical harm to others.[34] Psychosocial interventions may reduce the need for antipsychotics.[35]

Unipolar depression[edit]

A number of atypical antipsychotics have some benefits when used in addition to other treatments in major depressive disorder.[36][37] Aripiprazole, quetiapine, and olanzapine (when used in conjunction with fluoxetine) have received the Food and Drug Administration (FDA) labelling for this indication.[38] There is, however, a greater risk of side effects with their use.[36]

Other[edit]

Besides the above uses antipsychotics may be used for obsessive-compulsive disorder, posttraumatic stress disorder, personality disorders, Tourette syndrome, autism and agitation in those with dementia.[39] Evidence however does not support the use of atypical antipsychotics in eating disorders or personality disorder.[40] Risperidone may be useful for obsessive compulsive disorder.[39] The use of low doses of antipsychotics for insomnia, while common, is not recommended as there is little evidence of benefit and concerns regarding adverse effects.[40][41] Low dose antipsychotics may also be used in treatment of impulse-behavioural and cognitive-perceptual symptoms of borderline personality disorder.[42]

In children they may be used in those with disruptive behavior disorders, mood disorders and pervasive developmental disorders or intellectual disability.[43] Antipsychotics are only weakly recommended for Tourette syndrome, because although they are effective, side effects are common.[44] The situation is similar for those on the autism spectrum.[45] Much of the evidence for the off-label use of antipsychotics (for example, for dementia, OCD, PTSD, Personality Disorders, Tourette's) was of insufficient scientific quality to support such use, especially as there was strong evidence of increased risks of stroke, tremors, significant weight gain, sedation, and gastrointestinal problems.[46] A UK review of unlicensed usage in children and adolescents reported a similar mixture of findings and concerns.[47] A survey of children with pervasive developmental disorder found that 16.5% were taking an antipsychotic drug, most commonly for irritability, aggression, and agitation. Risperidone has been approved by the US FDA for the treatment of irritability in autistic children and adolescents.[48]

Aggressive challenging behavior in adults with intellectual disability is often treated with antipsychotic drugs despite lack of an evidence base. A recent randomized controlled trial, however, found no benefit over placebo and recommended that the use of antipsychotics in this way should no longer be regarded as an acceptable routine treatment.[49]

Typicals versus atypicals[edit]

It is unclear whether the atypical (second-generation) antipsychotics offer advantages over older, first generation antipsychotics.[50][51] Amisulpride, olanzapine, risperidone and clozapine may be more effective but are associated with greater side effects.[52] Typical antipsychotics have equal drop-out and symptom relapse rates to atypicals when used at low to moderate dosages.[53]

Clozapine is an effective treatment for those who respond poorly to other drugs ("treatment-resistant" or "refractory" schizophrenia),[54] but it has the potentially serious side effect of agranulocytosis (lowered white blood cell count) in less than 4% of people.[55]

Due to bias in the research the accuracy of comparisons of atypical antipsychotics is a concern.[56]

In 2005, a US government body, the National Institute of Mental Health published the results of a major independent study (the CATIE project).[57] No other atypical studied (risperidone, quetiapine, and ziprasidone) did better than the typical perphenazine on the measures used, nor did they produce fewer adverse effects than the typical antipsychotic perphenazine, although more patients discontinued perphenazine owing to extrapyramidal effects compared to the atypical agents (8% vs. 2% to 4%).[58]

Compliance has not been shown to be different between the two types.[59]

Many researchers question the first-line prescribing of atypicals over typicals, and some even question the distinction between the two classes.[60][61][62] In contrast, other researchers point to the significantly higher risk of tardive dyskinesia and other extrapyramidal symptoms with the typicals and for this reason alone recommend first-line treatment with the atypicals, notwithstanding a greater propensity for metabolic adverse effects in the latter.[63] The UK government organization NICE recently revised its recommendation favoring atypicals, to advise that the choice should be an individual one based on the particular profiles of the individual drug and on the patient's preferences.

The re-evaluation of the evidence has not necessarily slowed the bias toward prescribing the atypicals.[64]

Adverse effects[edit]

For more detailed comparison of atypical antipsychotics, see Atypical antipsychotic § Adverse effects.

Generally, more than one antipsychotic drug should not be used at a time because of increased adverse effects.[65]

By rate[edit]

Common (≥ 1% and up to 50% incidence for most antipsychotic drugs) adverse effects of antipsychotics include
[66]
  • Sedation (particularly common in patients on clozapine, olanzapine, quetiapine, chlorpromazine and zotepine[67])
  • Headaches
  • Dizziness
  • Diarrhea
  • Anxiety
  • Extrapyramidal side effects (particularly common in patients on first-generation antipsychotics), which includes:
- Akathisia — an often distressing sense of inner restlessness.
- Dystonia
- Parkinsonism
- Tremor
  • Hyperprolactinaemia (rare for those on clozapine, quetiapine and aripiprazole[8][67]), which can cause:
- Galactorrhoea — unusual secretion of breast milk.
- Gynaecomastia
- Sexual dysfunction (in both sexes)
- Osteoporosis
  • Orthostatic hypotension
  • Weight gain (particularly prominent in patients on clozapine, olanzapine, quetiapine and zotepine[67])
  • Anticholinergic side-effects (common for olanzapine, clozapine; less likely on risperidone [68]) such as:
- Blurred vision
- Constipation
- Dry mouth (although hypersalivation may also occur)
- Reduced perspiration
  • Tardive dyskinesia appears to be more frequent in those on high-potency first-generation antipsychotics such as haloperidol and tends to appear after chronic and not acute treatment.[69] It is characterised by slow (hence the tardive) repetitive, involuntary and purposeless movements, most often of the face, lips, legs, or torso, which tend to resist treatment and are frequently irreversible. The rate of appearance of TD is about 5% per year of use of antipsychotic drug (whatever the drug used).
Rare/Uncommon (<1% incidence for most antipsychotic drugs) adverse effects of antipsychotics include
  • Blood dyscrasias (e.g., agranulocytosis, leukopaenia, and neutropaenia), which is more common in patients on clozapine.
  • Metabolic syndrome and other metabolic problems such as Type II diabetes mellitus — particularly common with clozapine, olanzapine and zotepine. In American studies African Americans appeared to be at a heightened risk for developing type II diabetes mellitus.[70] Evidence suggests that females are more sensitive to the metabolic side effects of first-generation antipsychotic drugs than males.[71] Metabolic adverse effects appears to be mediated by the following mechanisms:
- Causing weight gain by antagonising the histamine H1 and serotonin 5-HT2Creceptors[72] and perhaps by interacting with other neurochemical pathways in the central nervous system.[73]
- Autonomic instability, which can manifest itself with tachycardia, nausea, vomiting, diaphoresis, etc.
- Hyperthermia — elevated body temperature.
- Mental status change (confusion, hallucinations, coma, etc.)
- Muscle rigidity
- Laboratory abnormalities (e.g., elevated creatinine kinase, reduced iron plasma levels, electrolyte abnormalities, etc.)

Long term effects[edit]

Some studies have found decreased life expectancy associated with the use of antipsychotics, and argued that more studies are needed.[75][76] Antipsychotics may also increase the risk of early death in individuals with dementia.[77] Antipsychotics typically worsen symptoms in people who suffer from depersonalisation disorder.[78] Antipsychotic polypharmacy (prescribing two or more antipsychotics at the same time for an individual) is a common practice but not evidence-based or recommended, and there are initiatives to curtail it.[65][79] Similarly, the use of excessively high doses (often the result of polypharmacy) continues despite clinical guidelines and evidence indicating that it is usually no more effective but is usually more harmful.[65][80]

Loss of grey matter and other brain structural changes over time are observed in schizophrenia. Meta analyses of the effects of antipsychotic treatment on the course of grey matter loss and structural changes have reached conflicting conclusions. A 2012 meta analysis concluded that grey matter loss is greater in patients treated with first generation antipsychotics relative to those treated with atypicals, and hypothesized a protective effect of atypicals as one possible explanation.[81] A second meta analyses suggested that treatment with antipsychotics was associated with increased grey matter loss.[82]

Subtle, long-lasting forms of akathisia are often overlooked or confused with post-psychotic depression, in particular when they lack the extra pyramidal aspect that psychiatrists have been taught to expect when looking for signs of akathisia.[83]

Withdrawal[edit]

Withdrawal symptoms from antipsychotics may emerge during dosage reduction and discontinuation. Withdrawal symptoms can include nausea, emesis, anorexia, diarrhea, rhinorrhea, diaphoresis, myalgia, paresthesia, anxiety, agitation, restlessness, and insomnia. The psychological withdrawal symptoms can include psychosis, and can be mistaken for a relapse of the underlying disorder. Better management of the withdrawal syndrome may improve the ability of individuals to discontinue antipsychotics.[84]

Tardive dyskinesia may abate during withdrawal from the antispsychotic agent, or it may persist.[85]

Withdrawal effects may also occur when switching a person from one antipsychotic to another, (it is presumed due to variations of potency and receptor activity). Such withdrawal effects can include cholinergic rebound, an activation syndrome, and motor syndromes including dyskinesias. These adverse effects are more likely during rapid changes between antipsychotic agents, so making a gradual change between antipsychotics minimises these withdrawal effects.[86] The British National Formulary recommends a gradual withdrawal when discontinuing antipsychotic treatment to avoid acute withdrawal syndrome or rapid relapse.[87] The process of cross-titration involves gradually increasing the dose of the new medication while gradually decreasing the dose of the old medication.[69]

List of agents[edit]

Chlorpromazine.
Haloperidol.
Quetiapine.

Clinically used antipsychotic medications are listed below by drug group. Trade names appear in parentheses.

Notes:

† indicates drugs that are no longer marketed in English-speaking countries.

‡ denotes drugs that are no longer (or were never to begin with) marketed in the United States. Some antipsychotics are not firmly placed in either first-generation or second-generation classes.

# denotes drugs that have been withdrawn worldwide.

First-generation[edit]

Main article: Typical antipsychotic

Butyrophenones[edit]

Main article: Butyrophenones

Diphenylbutylpiperidine[edit]

Phenothiazines[edit]

Main article: Phenothiazines

Thioxanthenes[edit]

Main article: Thioxanthenes

Others[edit]

Disputed/unknown[edit]

This category is for drugs that have been called both first and second-generation, depending on the literature being used.

Second-generation[edit]

Main article: Atypical antipsychotic
  • Amisulpride‡– Selective dopamine antagonist. Higher doses (greater than 400 mg) act upon post-synaptic dopamine receptors resulting in a reduction in the positive symptoms of schizophrenia, such as psychosis. Lower doses, however, act upon dopamine autoreceptors, resulting in increased dopamine transmission, improving the negative symptoms of schizophrenia. Lower doses of amisulpride have also been shown to have antidepressant and anxiolytic effects in non-schizophrenic patients, leading to its use in dysthymia and social phobias.
  • Amoxapine, active metabolite of loxapine, that's most frequently used as a tricyclic antidepressant and has, in a few clinical trials, been found to possess atypical antipsychotic effects.[88][89][90]
  • Aripiprazole – Partial agonist at the D2 receptor unlike all other clinically-utilised antipsychotics.[91]
  • Asenapine is a 5-HT2A- and D2-receptor antagonist developed for the treatment of schizophrenia and acute mania associated with bipolar disorder.
  • Cariprazine a D3-preferring D2/D3 partial agonist.
  • Clozapine – Requires complete blood counts every one to four weeks due to the risk of agranulocytosis. It has unparalleled efficacy in the treatment of treatment-resistant schizophrenia.
  • Blonanserin † — an antipsychotic that is used in Japan and Korea. May have a beneficial effect on cognition via its antagonism of the 5-HT6 receptor.
  • Iloperidone – Approved by the US FDA in 2009, it is fairly well tolerated, although hypotension, dizziness, and somnolence were very common side effects. Has not received regulatory approval in other countries, however.
  • Lurasidone , approved by the US FDA for schizophrenia and bipolar depression. Given once daily, it has shown mixed Phase III efficacy results but has a relatively well-tolerated side effect profile. It is also licensed for use as schizophrenia treatment in Canada. Not yet licensed elsewhere, however. Has procognitive effects via its antagonism of the 5-HT7 receptor.
  • Melperone †, an atypical antipsychotic that is only used in a few European countries. No English-speaking country has licensed it to date.
  • Nemonapride †
  • Olanzapine – Used to treat psychotic disorders including schizophrenia, acute manic episodes, and maintenance of bipolar disorder. Used as an adjunct to antidepressant therapy, especially to fluoxetine treatment in the form of Symbyax.
  • Paliperidone – Primary Metabolite of risperidone that was approved in 2006, it offers a controlled release once-daily dose, or a once-monthly depot injection.
  • Perospirone † — has a higher incidence of extrapyramidal side effects than other atypical antipsychotics.[92]
  • Quetiapine – Used primarily to treat bipolar disorder and schizophrenia. Also used and licensed in a few countries (including Australia, the United Kingdom and the United States) as an adjunct to antidepressant therapy in patients with major depressive disorder. It's the only antipsychotic that's demonstrated efficacy as a monotherapy for the treatment of major depressive disorder. It indirectly serves as a norepinephrine reuptake inhibitor by means of its active metabolite, norquetiapine.
  • Remoxipride # has a risk of causing aplastic anaemia and, hence, has been withdrawn from the market worldwide. It has also been found to possess relatively low (virtually absent) potential to induce hyperprolactinaemia and extrapyramidal symptoms, likely attributable to its comparatively weak binding to (and, hence, rapid dissociation from) the D2 receptor.[93]
  • Risperidone – Divided dosing is recommended until initial titration is completed, at which time the drug can be administered once daily. Used off-label to treat Tourette syndrome and anxiety disorder.
  • Sertindole ‡. Sertindole was developed by the Danish pharmaceutical company H. Lundbeck. Like the other atypical antipsychotics, it is believed to have antagonist activity at dopamine and serotonin receptors in the brain.
  • Sultopride is an atypical antipsychotic of the benzamide chemical class used in Europe, Japan, and Hong Kong for the treatment of schizophrenia. It was launched by Sanofi-Aventis in 1976. Sultopride acts as a selective D2 and D3 receptor antagonist.
  • Trimipramine
  • Ziprasidone – Approved in 2004[94] to treat bipolar disorder. Side-effects include a prolonged QT interval in the heart, which can be dangerous for patients with heart disease or those taking other drugs that prolong the QT interval.
  • Zotepine – An atypical antipsychotic indicated for acute and chronic schizophrenia. It is still used in Japan and was once used in Germany but it was discontinued.†

Investigational agents[edit]

  • Brexpiprazole a D2/5-HT1A partial agonist.
  • ITI-007 a 5-HT2A antagonist, presynaptic D2 partial agonist, postsynaptic D2 antagonist, and SERT blocker.
  • Pimavanserin a 5-HT2A inverse agonist. Being investigated as an adjunct to antipsychotics in schizophrenia and as a monotherapy for Parkinson's disease psychosis.
  • RP5063 a D2/D3/D4/5-HT1A/5-HT2A partial agonist and 5-HT6/5-HT7 antagonist

Mechanism of action[edit]

All antipsychotic drugs tend to block D2 receptors in the dopamine pathways of the brain. This means that dopamine released in these pathways has less effect. Excess release of dopamine in the mesolimbic pathway has been linked to psychotic experiences. It has also been proven[citation needed] less dopamine released in the prefrontal cortex in the brain, and excess dopamine released from all other pathways, has also been linked to psychotic experiences, caused by abnormal dopaminergic function as a result of patients suffering from schizophrenia or bipolar disorder. Various neuroleptics such as haloperidol and chlorpromazine suppress dopamine chemicals throughout its pathways, in order for dopamine receptors to function normally.

In addition to the antagonistic effects of dopamine, antipsychotics (in particular atypical neuroleptics) also antagonize 5-HT2A receptors. Different alleles of the 5-HT2A receptor have been associated with schizophrenia and other psychoses, including depression.[95][96] Higher concentrations of 5-HT2A receptors in cortical and subcortical areas, in particular in the right caudate nucleus have been historically recorded.[95] This is the same receptor that psychedelic drugs agonize to various degrees, which explains the correlation between psychedelic drugs and schizophrenia.[97]

Typical antipsychotics are not particularly selective and also block dopamine receptors in the mesocortical pathway, tuberoinfundibular pathway, and the nigrostriatal pathway. Blocking D2 receptors in these other pathways is thought to produce some unwanted side effects that the typical antipsychotics can produce (see above). They were commonly classified on a spectrum of low potency to high potency, where potency referred to the ability of the drug to bind to dopamine receptors, and not to the effectiveness of the drug. High-potency antipsychotics such as haloperidol, in general, have doses of a few milligrams and cause less sleepiness and calming effects than low-potency antipsychotics such as chlorpromazine and thioridazine, which have dosages of several hundred milligrams. The latter have a greater degree of anticholinergic and antihistaminergic activity, which can counteract dopamine-related side-effects.

Atypical antipsychotic drugs have a similar blocking effect on D2 receptors, however, most also act on serotonin receptors, especially 5-HT2A and 5-HT2C receptors. Both clozapine and quetiapine appear to bind just long enough to elicit antipsychotic effects but not long enough to induce extrapyramidal side effects and prolactin hypersecretion.[98] 5-HT2A antagonism increases dopaminergic activity in the nigrostriatal pathway, leading to a lowered extrapyramidal side effect liability among the atypical antipsychotics.[98][99]

Comparison of medications[edit]

History[edit]

Advertisement for Thorazine (chlorpromazine) from the 1950s, reflecting the perceptions of psychosis, including the now-discredited perception of a tendency towards violence, from the time when antipsychotics were discovered[148]

The original antipsychotic drugs were happened upon largely by chance and then tested for their effectiveness. The first, chlorpromazine, was developed as a surgical anesthetic. It was first used on psychiatric patients because of its powerful calming effect; at the time it was regarded as a non-permanent "pharmacological lobotomy".[149] Lobotomy at the time was used to treat many behavioral disorders, including psychosis, although its effect was to markedly reduce behavior and mental functioning of all types. However, chlorpromazine proved to reduce the effects of psychosis in a more effective and specific manner than lobotomy, even though it was known to be capable of causing severe sedation. The underlying neurochemistry involved has since been studied in detail, and subsequent antipsychotic drugs have been discovered by an approach that incorporates this sort of information.

The discovery of chlorpromazine's psychoactive effects in 1952 led to greatly reduced use of restraint, seclusion, and sedation in the management of agitated patients,[149] and also led to further research that resulted in the development of antidepressants, anxiolytics, and the majority of other drugs now used in the management of psychiatric conditions. In 1952, Henri Laborit described chlorpromazine only as inducing indifference towards what was happening around them in nonpsychotic, nonmanic patients, and Jean Delay and Pierre Deniker described it as controlling manic or psychotic agitation. The former claimed to have discovered a treatment for agitation in anyone, and the latter team claimed to have discovered a treatment for psychotic illness.[150]

Until the 1970s there was considerable debate within psychiatry on the most appropriate term to use to describe the new drugs.[151] In the late 1950s the most widely used term was "neuroleptic", followed by "major tranquilizer" and then "ataraxic".[151] The first recorded use of the term tranquilizer dates from the early nineteenth century.[152] In 1953 Frederik F. Yonkman, a chemist at the Swiss-based Cibapharmaceutical company, first used the term tranquilizer to differentiate reserpine from the older sedatives.[153] The wordneuroleptic was derived from the Greek: "νεῦρον"(neuron, originally meaning "sinew" but today referring to the nerves) and "λαμβάνω" (lambanō, meaning "take hold of"). Thus, the word means taking hold of one's nerves. This may refer to common side effects such as reduced activity in general, as well as lethargy and impaired motor control. Although these effects are unpleasant and in some cases harmful, they were at one time, along with akathisia, considered a reliable sign that the drug was working.[149] The term "ataraxy" was coined by the neurologist Howard Fabing and the classicist Alister Cameron to describe the observed effect of psychic indifference and detachment in patients treated with chlorpromazine.[154] This term derived from the Greek adjective "ἀτάρακτος" (ataraktos), which means "not disturbed, not excited, without confusion, steady, calm".[151] In the use of the terms "tranquilizer" and "ataractic", medical practitioners distinguished between the "major tranquilizers" or "major ataractics", which referred to drugs used to treat psychoses, and the "minor tranquilizers" or "minor ataractics", which referred to drugs used to treat neuroses.[151] While popular during the 1950s, these terms are infrequently used today. They are being abandoned in favor of "antipsychotic", which refers to the drug's desired effects.[151] Today, "minor tranquilizer" can refer to anxiolytic and/or hypnotic drugs such as the benzodiazepines and nonbenzodiazepines, which have some antipsychotic properties and are recommended for concurrent use with antipsychotics, and are useful for insomnia or drug-induced psychosis.[155] They are powerful (and potentially addictive) sedatives.

Antipsychotics are broadly divided into two groups, the typical or first-generation antipsychotics and the atypical or second-generation antipsychotics. The typical antipsychotics are classified according to their chemical structure while the atypical antipsychotics are classified according to their pharmacological properties. These include serotonin-dopamine antagonists (see dopamine antagonist and serotonin antagonist), multi-acting receptor-targeted antipsychotics (MARTA, those targeting several systems), and dopamine partial agonists, which are often categorized as atypicals.[156]

Society and culture[edit]

Sales[edit]

Antipsychotics were once among the biggest selling and most profitable of all drugs, generating $22 billion in global sales in 2008.[157] By 2003 in the US, an estimated 3.21 million patients received antipsychotics, worth an estimated $2.82 billion. Over 2/3 of prescriptions were for the newer, more expensive atypicals, each costing on average $164 per year, compared to $40 for the older types.[158] By 2008, sales in the US reached $14.6 billion, the biggest selling drugs in the US by therapeutic class.[159]

Formulations[edit]

Antipsychotics are sometimes administered as part of compulsory psychiatric treatment via inpatient (hospital) commitment or outpatient commitment. They may be administered orally or, in some cases, through long-acting (depot) injections administered in the dorsgluteal, ventrogluteal or deltoid muscle.

Controversy[edit]

Joanna Moncrieff has argued that antipsychotic drug treatment is often undertaken as a means of control rather than to treat specific symptoms experienced by the patient.[160] Moncreiff has further argued that the evidence for antipsychotics from discontinuation-relapse studies may be flawed, because they do not take into account that antipsychotics may sensitize the brain and provoke psychosis if discontinued, which may then be wrongly interpreted as a relapse of the original condition.[161]

Use of this class of drugs has a history of criticism in residential care. As the drugs used can make patients calmer and more compliant, critics claim that the drugs can be overused. Outside doctors can feel under pressure from care home staff.[162] In an official review commissioned by UK government ministers it was reported that the needless use of antipsychotic medication in dementia care was widespread and was linked to 1800 deaths per year.[163][164] In the US, the government has initiated legal action against the pharmaceutical company Johnson & Johnson for allegedly paying kickbacks to Omnicare to promote its antipsychotic risperidone (Risperdal) in nursing homes.[165]

There has also been controversy about the role of pharmaceutical companies in marketing and promoting antipsychotics, including allegations of downplaying or covering up adverse effects, expanding the number of conditions or illegally promoting off-label usage; influencing drug trials (or their publication) to try to show that the expensive and profitable newer atypicals were superior to the older cheaper typicals that were out of patent. Following charges of illegal marketing, settlements by two large pharmaceutical companies in the US set records for the largest criminal fines ever imposed on corporations.[166] One case involved Eli Lilly and Company's antipsychotic Zyprexa, and the other involved Bextra. In the Bextra case, the government also charged Pfizer with illegally marketing another antipsychotic, Geodon.[166] In addition, Astrazeneca faces numerous personal-injury lawsuits from former users of Seroquel (quetiapine), amidst federal investigations of its marketing practices.[167] By expanding the conditions for which they were indicated, Astrazeneca's Seroquel and Eli Lilly's Zyprexa had become the biggest selling antipsychotics in 2008 with global sales of $5.5 billion and $5.4 billion respectively.[157]

Harvard medical professor Joseph Biederman conducted research on bipolar disorder in children that led to an increase in such diagnoses. A 2008 Senate investigation found that Biederman also received $1.6 million in speaking and consulting fees between 2000 and 2007 — some of them undisclosed to Harvard — from companies including makers of antipsychotic drugs prescribed for children with bipolar disorder. Johnson & Johnson gave more than $700,000 to a research center that was headed by Biederman from 2002 to 2005, where research was conducted, in part, on Risperdal, the company's antipsychotic drug. Biederman has responded saying that the money did not influence him and that he did not promote a specific diagnosis or treatment.[166]

Pharmaceutical companies have also been accused of attempting to set the mental health agenda through activities such as funding consumer advocacy groups.[168]

Special populations[edit]

It is recommended that persons with dementia who exhibit behavioral and psychological symptoms should not be given antipsychotics before trying other treatments.[169] When taking antipsychotics this population has increased risk of cerebrovascular effects, parkinsonism or extrapyramidal symptoms, sedation, confusion and other cognitive adverse effects, weight gain, and increased mortality.[169] Physicians and caretakers of persons with dementia should try to address symptoms including agitation, aggression, apathy, anxiety, depression, irritability, and psychosis with alternative treatments whenever antipsychotic use can be replaced or reduced.[169] Elderly persons often have their dementia treated first with antipsychotics and this is not best.[170]

Notes[edit]

  1. ^ Bolded drug names indicates drugs that are metabolites of clinically-marketed antipsychotics

References[edit]

  1. ^ Hippius, H. (1989-03-01). "The history of clozapine". Psychopharmacology 99 (1): S3–S5. doi:10.1007/BF00442551. ISSN 0033-3158. 
  2. ^ Meyer, Jonathan M. (January 2011). "16. Pharmacotherapy of Psychosis and Mania". Goodman and Gilman's The Pharmacological Basis of Therapeutics, Twelfth Edition (12 ed.). McGraw-Hill Education / Medical. p. 417. ISBN 9780071624428. In the past, the term "neuroleptic" was also employed to refer to typical antipsychotic drugs, literally meaning to "take hold of the nerves" in Greek, but this has been dropped from contemporary usage (as has the term "major tranquilizer") in favor of "antipsychotic drug," a term that more accurately reflects the primary clinical use of those agents. 
  3. ^ Ayd, Frank J. (2000). "neuroleptic". Lexicon of Psychiatry, Neurology, and the Neurosciences. Lippincott Williams & Wilkins. p. 675. ISBN 9780781724685. 
  4. ^ Moby's Medical Dictionary. Elsevier. 
  5. ^ King, Caroline; Voruganti, Lakshmi N.P. (2002-05-01). "What's in a name? The evolution of the nomenclature of antipsychotic drugs". Journal of Psychiatry and Neuroscience 27 (3): 168–175. ISSN 1180-4882. PMC 161646. PMID 12066446. 
  6. ^ a b c d Leucht S, Corves C, Arbter D, Engel RR, Li C, Davis JM (January 2009). "Second-generation versus first-generation antipsychotic drugs for schizophrenia: a meta-analysis.". Lancet 373 (9657): 31–41. doi:10.1016/S0140-6736(08)61764-X. PMID 19058842. 
  7. ^ Goikolea JM, Colom F, Torres I, Capapey J, Valentí M, Undurraga J, Grande I, Sanchez-Moreno J, Vieta E (2013). "Lower rate of depressive switch following antimanic treatment with second-generation antipsychotics versus haloperidol". J Affect Disord 144 (3): 191–8. doi:10.1016/j.jad.2012.07.038. PMID 23089129. 
  8. ^ a b c d e f Taylor D, Paton C, Kapur S, Taylor D, South London and Maudsley NHS Trust. The Maudsley prescribing guidelines in psychiatry. Chichester, West Sussex: John Wiley & Sons; 2012. pp. 233-234 Cite error: Invalid <ref> tag; name "Maudsley" defined multiple times with different content (see the help page). Cite error: Invalid <ref> tag; name "Maudsley" defined multiple times with different content (see the help page).
  9. ^ a b "American Psychiatric Association Five Things Physicians and Patients Should Question". Choosing Wisely. Retrieved 23 September 2013. 
  10. ^ a b c d "Psychosis and schizophrenia in adults (CG178)". 
  11. ^ "PsychiatryOnline | Guidelines". 
  12. ^ a b c d e f g Barnes TR (May 2011). "Evidence-based guidelines for the pharmacological treatment of schizophrenia: recommendations from the British Association for Psychopharmacology". J. Psychopharmacol. (Oxford) 25 (5): 567–620. doi:10.1177/0269881110391123. PMID 21292923. 
  13. ^ Miyamoto S, Miyake N, Jarskog LF, Fleischhacker WW, Lieberman JA (December 2012). "Pharmacological treatment of schizophrenia: a critical review of the pharmacology and clinical effects of current and future therapeutic agents". Mol. Psychiatry 17 (12): 1206–27. doi:10.1038/mp.2012.47. PMID 22584864. 
  14. ^ Lisa Hartling, Ahmed M. Abou-Setta, Serdar Dursun, Shima S. Mousavi, Dion Pasichnyk & Amanda S. Newton (October 2012). "Antipsychotics in adults with schizophrenia: comparative effectiveness of first-generation versus second-generation medications: a systematic review and meta-analysis". Annals of Internal Medicine 157 (7): 498–511. doi:10.7326/0003-4819-157-7-201210020-00525. PMID 22893011. 
  15. ^ Toshi A. Furukawa, Stephen Z. Levine, Shiro Tanaka, Yair Goldberg, Myrto Samara, John M. Davis, Andrea Cipriani & Stefan Leucht (November 2014). "Initial Severity of Schizophrenia and Efficacy of Antipsychotics: Participant-Level Meta-analysis of 6 Placebo-Controlled Studies". JAMA psychiatry 72: 14. doi:10.1001/jamapsychiatry.2014.2127. PMID 25372935. 
  16. ^ "NICE Treatment Guideance 2014". Retrieved 2014-08-07. 
  17. ^ Leucht S, Arbter D, Engel RR, Kissling W, Davis JM (April 2009). "How effective are second-generation antipsychotic drugs? A meta-analysis of placebo-controlled trials". Mol. Psychiatry 14 (4): 429–47. doi:10.1038/sj.mp.4002136. PMID 18180760. 
  18. ^ Leucht S, Cipriani A, Spineli L, Mavridis D, Orey D, Richter F, Samara M, Barbui C, Engel RR, Geddes JR, Kissling W, Stapf MP, Lässig B, Salanti G, Davis JM (September 2013). "Comparative efficacy and tolerability of 15 antipsychotic drugs in schizophrenia: a multiple-treatments meta-analysis". Lancet 382 (9896): 951–62. doi:10.1016/S0140-6736(13)60733-3. PMID 23810019. 
  19. ^ Beitinger R, Lin J, Kissling W, Leucht S (October 2008). "Comparative remission rates of schizophrenic patients using various remission criteria". Prog. Neuropsychopharmacol. Biol. Psychiatry 32 (7): 1643–51. doi:10.1016/j.pnpbp.2008.06.008. PMID 18616969. 
  20. ^ a b Leucht S, Tardy M, Komossa K, Heres S, Kissling W, Davis JM (2012). "Maintenance treatment with antipsychotic drugs for schizophrenia". Cochrane Database Syst Rev 5: CD008016. doi:10.1002/14651858.CD008016.pub2. PMID 22592725. 
  21. ^ Kinon BJ, Ascher-Svanum H, Adams DH, Chen L (October 2008). "The temporal relationship between symptom change and treatment discontinuation in a pooled analysis of 4 schizophrenia trials". J Clin Psychopharmacol 28 (5): 544–9. doi:10.1097/JCP.0b013e318185e74a. PMID 18794651. 
  22. ^ a b Young LL, Kradjan WA, Guglielmo BJ, Corelli RL, Williams BR, Koda-Kimble MA (2009). Applied therapeutics: the clinical use of drugs (9th ed.). Philadelphia: Wolters Kluwer Health/Lippincott Williams & Wilkins. p. 3040. ISBN 0-7817-6555-2. 
  23. ^ Correll CU, Sheridan EM, DelBello MP (2010). "Antipsychotic and mood stabilizer efficacy and tolerability in pediatric and adult patients with bipolar I mania: a comparative analysis of acute, randomized, placebo-controlled trials". Bipolar Disord 12 (2): 116–41. doi:10.1111/j.1399-5618.2010.00798.x. PMID 20402706. 
  24. ^ Lowes R. "Lurasidone Approved for Bipolar Depression". Medscape. Retrieved 2013-10-02. 
  25. ^ Tohen M, Katagiri H, Fujikoshi S, Kanba S (2013). "Efficacy of olanzapine monotherapy in acute bipolar depression: a pooled analysis of controlled studies". J Affect Disord 149 (1-3): 196–201. doi:10.1016/j.jad.2013.01.022. PMID 23485111. 
  26. ^ Thase ME (2008). "Quetiapine monotherapy for bipolar depression". Neuropsychiatr Dis Treat 4 (1): 11–21. doi:10.2147/ndt.s1162. PMC 2515925. PMID 18728771. 
  27. ^ Tohen M, Greil W, Calabrese JR, Sachs GS, Yatham LN, Oerlinghausen BM, Koukopoulos A, Cassano GB, Grunze H, Licht RW, Dell'Osso L, Evans AR, Risser R, Baker RW, Crane H, Dossenbach MR, Bowden CL (2005). "Olanzapine versus lithium in the maintenance treatment of bipolar disorder: a 12-month, randomized, double-blind, controlled clinical trial". Am J Psychiatry 162 (7): 1281–90. doi:10.1176/appi.ajp.162.7.1281. PMID 15994710. 
  28. ^ Duffy A, Milin R, Grof P (2009). "Maintenance treatment of adolescent bipolar disorder: open study of the effectiveness and tolerability of quetiapine". BMC Psychiatry 9: 4. doi:10.1186/1471-244X-9-4. PMC 2644292. PMID 19200370. 
  29. ^ Weisler RH, Nolen WA, Neijber A, Hellqvist A, Paulsson B (2011). "Continuation of quetiapine versus switching to placebo or lithium for maintenance treatment of bipolar I disorder (Trial 144: a randomized controlled study)". J Clin Psychiatry 72 (11): 1452–64. doi:10.4088/JCP.11m06878. PMID 22054050. 
  30. ^ Cipriani A, Rendell JM, Geddes J (2009). Cipriani A, ed. "Olanzapine in long-term treatment for bipolar disorder". Cochrane Database of Systematic Reviews (1): CD004367. doi:10.1002/14651858.CD004367.pub2. PMID 19160237. 
  31. ^ Lehman AF, Lieberman JA, Dixon LB, McGlashan TH, Miller AL, Perkins DO, Kreyenbuhl J (February 2004). "Practice guideline for the treatment of patients with schizophrenia, second edition". Am J Psychiatry 161 (2 Suppl): 1–56. PMID 15000267. 
  32. ^ The Royal College of Psychiatrists & The British Psychological Society (2003).Schizophrenia. Full national clinical guideline on core interventions in primary and secondary care (PDF). London: Gaskell and the British Psychological Society.[page needed] Archived September 27, 2007, at the Wayback Machine.
  33. ^ AMDA – The Society for Post-Acute and Long-Term Care Medicine (February 2014), "Ten Things Physicians and Patients Should Question", Choosing Wisely: an initiative of the ABIM Foundation (AMDA – The Society for Post-Acute and Long-Term Care Medicine), retrieved 20 April 2015 .
  34. ^ Ballard C, Waite J (2006). Ballard CG, ed. "The effectiveness of atypical antipsychotics for the treatment of aggression and psychosis in Alzheimer's disease". Cochrane Database of Systematic Reviews (1): CD003476. doi:10.1002/14651858.CD003476.pub2. PMID 16437455. 
  35. ^ Richter T, Meyer G, Möhler R, Köpke S (Dec 12, 2012). Köpke S, ed. "Psychosocial interventions for reducing antipsychotic medication in care home residents". The Cochrane database of systematic reviews 12: CD008634. doi:10.1002/14651858.CD008634.pub2. PMID 23235663. 
  36. ^ a b Komossa K, Depping AM, Gaudchau A, Kissling W, Leucht S (2010). "Second-generation antipsychotics for major depressive disorder and dysthymia". Cochrane Database Syst Rev (12): CD008121. doi:10.1002/14651858.CD008121.pub2. PMID 21154393. 
  37. ^ Spielmans GI, Berman MI, Linardatos E, Rosenlicht NZ, Perry A, Tsai AC (2013). "Adjunctive atypical antipsychotic treatment for major depressive disorder: a meta-analysis of depression, quality of life, and safety outcomes". PLoS Med. 10 (3): e1001403. doi:10.1371/journal.pmed.1001403. PMC 3595214. PMID 23554581. 
  38. ^ Truven Health Analytics, Inc. DrugPoint® System (Internet) [cited 2013 Oct 2]. Greenwood Village, CO: Thomsen Healthcare; 2013.
  39. ^ a b Maher AR, Theodore G (June 2012). "Summary of the comparative effectiveness review on off-label use of atypical antipsychotics". J Manag Care Pharm 18 (5 Suppl B): S1–20. PMID 22784311. 
  40. ^ a b Maglione M, Maher AR, Hu J, Wang Z, Shanman R, Shekelle PG, Roth B, Hilton L, Suttorp MJ (2011). Off-Label Use of Atypical Antipsychotics: An Update. Comparative Effectiveness Reviews, No. 43. Rockville: Agency for Healthcare Research and Quality. PMID 22973576. 
  41. ^ Coe HV, Hong IS (May 2012). "Safety of low doses of quetiapine when used for insomnia". Annals of Pharmacotherapy 46 (5): 718–22. doi:10.1345/aph.1Q697. PMID 22510671. 
  42. ^ American Psychiatric Association and American Psychiatric Association. Work Group on Borderline Personality Disorder (2001). Practice Guideline for the Treatment of Patients With Borderline Personality Disorder. American Psychiatric Pub. p. 4. ISBN 0890423199. Retrieved June 5, 2013. 
  43. ^ Zuddas A, Zanni R, Usala T (August 2011). "Second generation antipsychotics (SGAs) for non-psychotic disorders in children and adolescents: a review of the randomized controlled studies". European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 21 (8): 600–20. doi:10.1016/j.euroneuro.2011.04.001. PMID 21550212. 
  44. ^ Pringsheim T, Doja A, Gorman D, McKinlay D, Day L, Billinghurst L, Carroll A, Dion Y, Luscombe S, Steeves T, Sandor P (March 2012). "Canadian guidelines for the evidence-based treatment of tic disorders: pharmacotherapy". Can J Psychiatry 57 (3): 133–43. PMID 22397999. 
  45. ^ McPheeters ML, Warren Z, Sathe N, Bruzek JL, Krishnaswami S, Jerome RN, Veenstra-Vanderweele J (May 2011). "A systematic review of medical treatments for children with autism spectrum disorders". Pediatrics 127 (5): e1312–21. doi:10.1542/peds.2011-0427. PMID 21464191. 
  46. ^ "Evidence Lacking to Support Many Off-label Uses of Atypical Antipsychotics" (Press release). Agency for Healthcare Research and Quality. January 17, 2007. Retrieved July 29, 2013. 
  47. ^ James AC (2010). "Prescribing antipsychotics for children and adolescents". Advances in Psychiatric Treatment 16 (1): 63–75. doi:10.1192/apt.bp.108.005652. 
  48. ^ Posey DJ, Stigler KA, Erickson CA, McDougle CJ (January 2008). "Antipsychotics in the treatment of autism". J. Clin. Invest. 118 (1): 6–14. doi:10.1172/JCI32483. PMC 2171144. PMID 18172517. 
  49. ^ Romeo R, Knapp M, Tyrer P, Crawford M, Oliver-Africano P (July 2009). "The treatment of challenging behaviour in intellectual disabilities: cost-effectiveness analysis". J Intellect Disabil Res 53 (7): 633–43. doi:10.1111/j.1365-2788.2009.01180.x. PMID 19460067. 
  50. ^ Kane JM, Correll CU (2010). "Pharmacologic treatment of schizophrenia". Dialogues Clin Neurosci 12 (3): 345–57. PMC 3085113. PMID 20954430. 
  51. ^ Hartling L, Abou-Setta AM, Dursun S, et al. (14 August 2012). "Antipsychotics in Adults With Schizophrenia: Comparative Effectiveness of First-generation versus second-generation medications: a systematic review and meta-analysis". Annals of Internal Medicine 157 (7): 498–511. doi:10.7326/0003-4819-157-7-201210020-00525. PMID 22893011. 
  52. ^ Barry SJ, Gaughan TM, Hunter R (2012). "Schizophrenia". BMJ Clinical Evidence 2012. PMC 3385413. PMID 23870705. 
  53. ^ Schultz SH, North SW, Shields CG (June 2007). "Schizophrenia: a review". Am Fam Physician 75 (12): 1821–9. PMID 17619525. 
  54. ^ Taylor DM (2000). "Refractory schizophrenia and atypical antipsychotics". J Psychopharmacol 14 (4): 409–418. doi:10.1177/026988110001400411. PMID 11198061. 
  55. ^ Essali A, Al-Haj Haasan N, Li C, Rathbone J (2009). "Clozapine versus typical neuroleptic medication for schizophrenia". Cochrane Database of Systematic Reviews (1): CD000059. doi:10.1002/14651858.CD000059.pub2. PMID 19160174. 
  56. ^ Heres S, Davis J, Maino K, Jetzinger E, Kissling W, Leucht S (February 2006). "Why olanzapine beats risperidone, risperidone beats quetiapine, and quetiapine beats olanzapine: an exploratory analysis of head-to-head comparison studies of second-generation antipsychotics". The American Journal of Psychiatry 163 (2): 185–94. doi:10.1176/appi.ajp.163.2.185. PMID 16449469. 
  57. ^ Lieberman JA, Stroup TS, McEvoy JP, Swartz MS, Rosenheck RA, Perkins DO, Keefe RS, Davis SM, Davis CE, Lebowitz BD, Severe J, Hsiao JK (September 2005). "Effectiveness of antipsychotic drugs in patients with chronic schizophrenia". N. Engl. J. Med. 353 (12): 1209–23. doi:10.1056/NEJMoa051688. PMID 16172203. 
  58. ^ Leucht S, Corves C, Arbter D, Engel RR, Li C, Davis JM (January 2009). "Second-generation versus first-generation antipsychotic drugs for schizophrenia: a meta-analysis". Lancet 373 (9657): 31–41. doi:10.1016/S0140-6736(08)61764-X. PMID 19058842. 
  59. ^ Voruganti LP, Baker LK, Awad AG (March 2008). "New generation antipsychotic drugs and compliance behaviour". Current Opinion in Psychiatry 21 (2): 133–9. doi:10.1097/YCO.0b013e3282f52851. PMID 18332660. 
  60. ^ Paczynski RP, Alexander GC, Chinchilli VM, Kruszewski SP (January 2012). "Quality of evidence in drug compendia supporting off-label use of typical and atypical antipsychotic medications". Int J Risk Saf Med 24 (3): 137–46. doi:10.3233/JRS-2012-0567. PMID 22936056. 
  61. ^ Owens, D. C. (2008). "How CATIE brought us back to Kansas: a critical re-evaluation of the concept of atypical antipsychotics and their place in the treatment of schizophrenia". Advances in Psychiatric Treatment 14 (1): 17–28. doi:10.1192/apt.bp.107.003970. 
  62. ^ Fischer-Barnicol D, Lanquillon S, Haen E, Zofel P, Koch HJ, Dose M, Klein HE (2008). "Typical and atypical antipsychotics--the misleading dichotomy. Results from the Working Group 'Drugs in Psychiatry' (AGATE)". Neuropsychobiology 57 (1–2): 80–7. doi:10.1159/000135641. PMID 18515977. 
  63. ^ Casey DE (March 1999). "Tardive dyskinesia and atypical antipsychotic drugs". Schizophr. Res. 35 (Suppl 1): S61–6. doi:10.1016/S0920-9964(98)00160-1. PMID 10190226. 
  64. ^ Makhinson M (January 2010). "Biases in medication prescribing: the case of second-generation antipsychotics". J Psychiatr Pract 16 (1): 15–21. doi:10.1097/01.pra.0000367774.11260.e4. PMID 20098227. 
  65. ^ a b c American Psychiatric Association (September 2013), "Five Things Physicians and Patients Should Question", Choosing Wisely: an initiative of the ABIM Foundation (American Psychiatric Association), retrieved 30 December 2013 , which cites
  66. ^ Muench J, Hamer AM (March 2010). "Adverse effects of antipsychotic medications". Am Fam Physician 81 (5): 617–22. PMID 20187598. 
  67. ^ a b c d e f g Leucht S, Cipriani A, Spineli L, Mavridis D, Orey D, Richter F, Samara M, Barbui C, Engel RR, Geddes JR, Kissling W, Stapf MP, Lässig B, Salanti G, Davis JM (September 2013). "Comparative efficacy and tolerability of 15 antipsychotic drugs in schizophrenia: a multiple-treatments meta-analysis.". Lancet 382 (9896): 951–962. doi:10.1016/S0140-6736(13)60733-3. PMID 23810019. 
  68. ^ Lieberman JA (2004). "Managing anticholinergic side effects". Prim Care Companion J Clin Psychiatry 6 (Suppl 2): 20–3. PMC 487008. PMID 16001097. 
  69. ^ a b Stahl, S. M. (2008). Stahl's Essential Psychopharmacology: Neuroscientific basis and practical applications. Cambridge University Press. [page needed]
  70. ^ Koller EA, Doraiswamy PM (July 2002). "Olanzapine-associated diabetes mellitus". Pharmacotherapy 22 (7): 841–52. doi:10.1592/phco.22.11.841.33629. PMID 12126218. 
  71. ^ Weston-Green K, Huang XF, Deng C (February 2010). "Sensitivity of the female rat to olanzapine-induced weight gain--far from the clinic?". Schizophr. Res. 116 (2–3): 299–300. doi:10.1016/j.schres.2009.09.034. PMID 19840894. 
  72. ^ a b c Brunton LL, Chabner B, Knollmann BC, eds. (2011). Goodman & Gilman's The Pharmacological Basis of Therapeutics (12th ed.). New York: McGraw-Hill. ISBN 978-0-07-162442-8. 
  73. ^ Weston-Green K, Huang XF, Deng C (2012). Chang AY, ed. "Alterations to melanocortinergic, GABAergic and cannabinoid neurotransmission associated with olanzapine-induced weight gain". PLoS ONE 7 (3): e33548. doi:10.1371/journal.pone.0033548. PMC 3306411. PMID 22438946. 
  74. ^ Koller EA, Cross JT, Doraiswamy PM, Malozowski SN (September 2003). "Pancreatitis associated with atypical antipsychotics: from the Food and Drug Administration's MedWatch surveillance system and published reports". Pharmacotherapy 23 (9): 1123–30. doi:10.1592/phco.23.10.1123.32759. PMID 14524644. 
  75. ^ Weinmann S, Read J, Aderhold V (August 2009). "Influence of antipsychotics on mortality in schizophrenia: systematic review". Schizophr. Res. 113 (1): 1–11. doi:10.1016/j.schres.2009.05.018. PMID 19524406. 
  76. ^ Joukamaa M, Heliövaara M, Knekt P, Aromaa A, Raitasalo R, Lehtinen V (February 2006). "Schizophrenia, neuroleptic medication and mortality". Br J Psychiatry 188 (2): 122–7. doi:10.1192/bjp.188.2.122. PMID 16449697. 
  77. ^ "American Geriatrics Society updated Beers Criteria for potentially inappropriate medication use in older adults". J Am Geriatr Soc 60 (4): 616–31. April 2012. doi:10.1111/j.1532-5415.2012.03923.x. PMC 3571677. PMID 22376048. 
  78. ^ Medford N, Sierra M, Baker D, David A (2005). "Understanding and treating depersonalisation disorder". Advances in Psychiatric Treatment (Royal College of Psychiatrists) 11 (2): 92–100. doi:10.1192/apt.11.2.92. 
  79. ^ Patrick V, Levin E, Schleifer S (July 2005). "Antipsychotic polypharmacy: is there evidence for its use?". J Psychiatr Pract 11 (4): 248–57. doi:10.1097/00131746-200507000-00005. PMID 16041235. 
  80. ^ Ito H, Koyama A, Higuchi T (September 2005). "Polypharmacy and excessive dosing: psychiatrists' perceptions of antipsychotic drug prescription". Br J Psychiatry 187 (3): 243–7. doi:10.1192/bjp.187.3.243. PMID 16135861. 
  81. ^ Vita A, De Peri L, Deste G, Sacchetti E (2012). "Progressive loss of cortical gray matter in schizophrenia: a meta-analysis and meta-regression of longitudinal MRI studies". Transl Psychiatry 2 (11): e190. doi:10.1038/tp.2012.116. PMC 3565772. PMID 23168990. 
  82. ^ Radua J, Borgwardt S, Crescini A, Mataix-Cols D, Meyer-Lindenberg A, McGuire PK, Fusar-Poli P (November 2012). "Multimodal meta-analysis of structural and functional brain changes in first episode psychosis and the effects of antipsychotic medication". Neurosci Biobehav Rev 36 (10): 2325–33. doi:10.1016/j.neubiorev.2012.07.012. PMID 22910680. 
  83. ^ Hirose S (2003). "The causes of underdiagnosing akathisia" (PDF). Schizophr Bull 29 (3): 547–58. doi:10.1093/oxfordjournals.schbul.a007027. PMID 14609248. 
  84. ^ Dilsaver SC, Alessi NE (March 1988). "Antipsychotic withdrawal symptoms: phenomenology and pathophysiology". Acta Psychiatr Scand 77 (3): 241–6. doi:10.1111/j.1600-0447.1988.tb05116.x. PMID 2899377. 
  85. ^ Glazer WM (2000). "Expected incidence of tardive dyskinesia associated with atypical antipsychotics". J Clin Psychiatry. 61 Suppl 4: 21–6. PMID 10739327. 
  86. ^ Lambert TJ (2007). "Switching antipsychotic therapy: what to expect and clinical strategies for improving therapeutic outcomes". J Clin Psychiatry. 68 Suppl 6: 10–3. PMID 17650054. 
  87. ^ Group B, ed. (March 2009). "4.2.1". British National Formulary (57 ed.). United Kingdom: Royal Pharmaceutical Society of Great Britain. p. 192. Withdrawal of antipsychotic drugs after long-term therapy should always be gradual and closely monitored to avoid the risk of acute withdrawal syndromes or rapid relapse. 
  88. ^ Chaudhry IB, Husain N, Khan S, Badshah S, Deakin B, Kapur S (2007). "Amoxapine as an antipsychotic: comparative study versus haloperidol". J Clin Psychopharmacol 27 (6): 575–81. doi:10.1097/jcp.0b013e31815a4424. PMID 18004123. 
  89. ^ Apiquian R, Fresan A, Ulloa RE, de la Fuente-Sandoval C, Herrera-Estrella M, Vazquez A, Nicolini H, Kapur S (2005). "Amoxapine as an atypical antipsychotic: a comparative study vs risperidone". Neuropsychopharmacology 30 (12): 2236–44. doi:10.1038/sj.npp.1300796. PMID 15956984. 
  90. ^ Apiquian R, Ulloa E, Fresan A, Loyzaga C, Nicolini H, Kapur S (2003). "Amoxapine shows atypical antipsychotic effects in patients with schizophrenia: results from a prospective open-label study". Schizophr. Res. 59 (1): 35–9. doi:10.1016/S0920-9964(01)00342-5. PMID 12413640. 
  91. ^ Swainston Harrison T, Perry CM (2004). "Aripiprazole: a review of its use in schizophrenia and schizoaffective disorder". Drugs 64 (15): 1715–36. doi:10.2165/00003495-200464150-00010. PMID 15257633. 
  92. ^ a b Onrust SV, McClellan K (2001). "Perospirone". CNS Drugs 15 (4): 329–37; discussion 338. doi:10.2165/00023210-200115040-00006. PMID 11463136. 
  93. ^ "Atypical Antipsychotics: Mechanism of Action" (PDF). FOCUS: the Journal of Lifelong Learning in Psychiatry 2 (1): 48–58. January 2004. 
  94. ^ Nemeroff CB, Lieberman JA, Weiden PJ, Harvey PD, Newcomer JW, Schatzberg AF, Kilts CD, Daniel DG (November 2005). "From clinical research to clinical practice: a 4-year review of ziprasidone". CNS Spectr 10 (11 Suppl 17): 1–20. PMID 16381088. 
  95. ^ a b McDonald C, Murphy KC (March 2003). "The new genetics of schizophrenia". The Psychiatric clinics of North America 26 (1): 41–63. doi:10.1016/S0193-953X(02)00030-8. PMID 12683259. 
  96. ^ Schmidt CJ, Sorensen SM, Kehne JH, Carr AA, Palfreyman MG (1995). "The role of 5HT2A receptors in antipsychotic activity". Life Sciences 56 (25): 2209–22. doi:10.1016/0024-3205(95)00210-W. PMID 7791509. 
  97. ^ Chattopadhyay eb (2007). Serotonin receptors in neurobiology. Boca Raton: CRC Press. ISBN 0-8493-3977-4. 
  98. ^ a b Stahl, SM (2003). "Describing an Atypical Antipsychotic: Receptor Binding and Its Role in Pathophysiology" (PDF). Prim Care Companion J Clin Psychiatry 5 (Suppl. 3): 9–13. 
  99. ^ Gross G, Geyer MA (2012). Current Antipsychotics. Springer. pp. 88–89. doi:10.1007/978-3-642-25761-2. ISBN 978-3-642-25761-2. 
  100. ^ Rossi, S, ed. (2013). Australian Medicines Handbook (2013 ed.). Adelaide: The Australian Medicines Handbook Unit Trust. ISBN 978-0-9805790-9-3. 
  101. ^ Joint Formulary Committee (2013). British National Formulary (BNF) (65 ed.). London, UK: Pharmaceutical Press. ISBN 978-0-85711-084-8. 
  102. ^ "Approximate relative frequency (not intensity) of common adverse effects of antipsychotics (Table 8.21) [NB1]". eTherapeutic Guidelines complete. Therapeutic Guidelines Limited. February 2013. Retrieved 2 November 2013. 
  103. ^ Isbister GK, Balit CR, Macleod D, Duffull SB (August 2010). "Amisulpride overdose is frequently associated with QT prolongation and torsades de pointes". Journal of Clinical Psychopharmacology 30 (4): 391–395. doi:10.1097/JCP.0b013e3181e5c14c. PMID 20531221. 
  104. ^ a b Deeks ED, Keating GM (January 2010). "Blonanserin A Review of its Use in the Management of Schizophrenia". CNS Drugs 24 (1): 65–84. doi:10.2165/11202620-000000000-00000. PMID 20030420. 
  105. ^ a b Tenjin T, Miyamoto S, Ninomiya Y, Kitajima R, Ogino S, Miyake N, Yamaguchi N (2013). "Profile of blonanserin for the treatment of schizophrenia". Neuropsychiatric Disease and Treatment 9: 587–594. doi:10.2147/NDT.S34433. PMC 3677929. PMID 23766647. 
  106. ^ "Clozapine". Martindale: The Complete Drug Reference. Royal Pharmaceutical Society of Great Britain. 30 January 2013. Retrieved 2 November 2013. 
  107. ^ Matar HE, Almerie MQ, Sampson S (July 2013). Matar HE, ed. "Fluphenazine (oral) versus placebo for schizophrenia (Review)" (PDF). Cochrane Database of Systematic Reviews 7: CD006352. doi:10.1002/14651858.CD006352.pub2. PMID 23861067. 
  108. ^ Chakrabarti A, Bagnall A, Chue P, Fenton M, Palaniswamy V, Wong W, Xia J (October 2007). Chakrabarti A, ed. "Loxapine for schizophrenia (Review)" (PDF). Cochrane Database of Systematic Reviews (4): CD001943. doi:10.1002/14651858.CD001943.pub2. PMID 17943763. 
  109. ^ Harvey PD, Ogasa M, Cucchiaro J, Loebel A, Keefe RS (April 2011). "Performance and interview-based assessments of cognitive change in a randomized, double-blind comparison of lurasidone vs. ziprasidone". Schizophrenia Research 127 (1–3): 188–194. doi:10.1016/j.schres.2011.01.004. PMID 21277745. 
  110. ^ Röhricht F, Gadhia S, Alam R, Willis M (2012). "Auditing Clinical Outcomes after Introducing Off-Licence Prescribing of Atypical Antipsychotic Melperone for Patients with Treatment Refractory Schizophrenia". Scientific World Journal 2012: 1–5. doi:10.1100/2012/512047. PMC 3330679. PMID 22566771. 
  111. ^ a b Molindone Hydrochloride. Martindale: The Complete Drug Reference (The Royal Pharmaceutical Society of Great Britain). 30 January 2013. Retrieved 5 November 2013. 
  112. ^ Leucht S, Hartung B (April 2006). Leucht S, ed. "Perazine for schizophrenia" (PDF). Cochrane Database of Systematic Reviews (2): CD002832. doi:10.1002/14651858.CD002832.pub2. PMID 16625562. 
  113. ^ Onrust SV, McClellan K (April 2001). "Perospirone" (PDF). CNS Drugs 15 (4): 329–337. doi:10.2165/00023210-200115040-00006. PMID 11463136. 
  114. ^ a b Brayfield, A, ed. (23 September 2011). Perospirone. Martindale: The Complete Drug Reference (London, UK: Pharmaceutical Press). Retrieved 3 November 2013. 
  115. ^ Hartung B, Wada M, Laux G, Leucht S (January 2005). Hartung B, ed. "Perphenazine for schizophrenia" (PDF). The Cochrane Database of Systematic Reviews (1): CD003443. doi:10.1002/14651858.CD003443.pub2. PMID 15674907. 
  116. ^ Rathbone J, McMonagle T (July 2007). Rathbone J, ed. "Pimozide for schizophrenia or related psychoses" (PDF). The Cochrane Database of Systematic Reviews (3): CD001949. doi:10.1002/14651858.CD001949.pub2. PMID 17636692. 
  117. ^ Omori IM, Wang J (April 2009). Omori IM, ed. "Sulpiride versus placebo for schizophrenia" (PDF). Cochrane Database of Systematic Reviews (2): CD007811. doi:10.1002/14651858.CD007811. PMID 19370694. 
  118. ^ Fenton M, Rathbone J, Reilly J, Sultana A (July 2007). Reilly J, ed. "Thioridazine for schizophrenia" (PDF). Cochrane Database of Systematic Reviews (3): CD001944. doi:10.1002/14651858.CD001944.pub2. PMID 17636691. 
  119. ^ Fornaro P, Calabria G, Corallo G, Picotti GB (July 2002). "Pathogenesis of degenerative retinopathies induced by thioridazine and other antipsychotics: a dopamine hypothesis". Documenta Ophthalmologica 105 (1): 41–49. doi:10.1023/A:1015768114192. PMID 12152801. 
  120. ^ Marques LO, Lima MS, Soares BG (2004). Marques Ld, ed. "Trifluoperazine for schizophrenia" (PDF). Cochrane Database of Systematic Reviews (1): CD003545. doi:10.1002/14651858.CD003545.pub2. PMID 14974020. 
  121. ^ "Zotepine". Martindale: The Complete Drug Reference. Royal Pharmaceutical Society of Great Britain. 16 August 2013. Retrieved 2 November 2013. 
  122. ^ Cipriani A, Barbui C, Salanti G, Rendell J, Brown R, Stockton S, Purgato M, Spineli LM, Goodwin GM, Geddes JR (October 2011). "Comparative efficacy and acceptability of antimanic drugs in acute mania: a multiple-treatments meta-analysis". Lancet 378 (9799): 1306–1315. doi:10.1016/S0140-6736(11)60873-8. PMID 21851976. 
  123. ^ Citrome L (2013). "Addressing the need for rapid treatment of agitation in schizophrenia and bipolar disorder: focus on inhaled loxapine as an alternative to injectable agents". Therapeutics and Clinical Risk Management 9: 235–245. doi:10.2147/TCRM.S31484. PMID 23723707. 
  124. ^ Cruz N, Sanchez-Moreno J, Torres F, Goikolea JM, Valentí M, Vieta E (February 2010). "Efficacy of modern antipsychotics in placebo-controlled trials in bipolar depression: a meta-analysis". The International Journal of Neuropsychopharmacology 13 (1): 5–14. doi:10.1017/S1461145709990344. PMID 19638254. 
  125. ^ Popovic D, Reinares M, Goikolea JM, Bonnin CM, Gonzalez-Pinto A, Vieta E (May 2012). "Polarity index of pharmacological agents used for maintenance treatment of bipolar disorder". European Neuropsychopharmacology 22 (5): 339–346. doi:10.1016/j.euroneuro.2011.09.008. PMID 22000157. 
  126. ^ Vieta E, Günther O, Locklear J, Ekman M, Miltenburger C, Chatterton ML, Åström M, Paulsson B (September 2011). "Effectiveness of psychotropic medications in the maintenance phase of bipolar disorder: a meta-analysis of randomized controlled trials". The International Journal of Neuropsychopharmacology 14 (8): 1029–1049. doi:10.1017/S1461145711000885. PMID 21733231. 
  127. ^ Komossa K, Depping AM, Gaudchau A, Kissling W, Leucht S (December 2010). "Second-generation antipsychotics for major depressive disorder and dysthymia." (PDF). The Cochrane Database of Systematic Reviews (12): CD008121. doi:10.1002/14651858.CD008121.pub2. PMID 21154393. 
  128. ^ Kishi T, Iwata N (September 2013). "Efficacy and Tolerability of Perospirone in Schizophrenia: A Systematic Review and Meta-Analysis of Randomized Controlled Trials" (PDF). CNS Drugs 27 (9): 731–741. doi:10.1007/s40263-013-0085-7. PMID 23812802. 
  129. ^ Roth, BL; Driscol, J (12 January 2011). "PDSP Ki Database". Psychoactive Drug Screening Program (PDSP). University of North Carolina at Chapel Hill and the United States National Institute of Mental Health. Retrieved 11 November 2013. 
  130. ^ Shahid M, Walker GB, Zorn SH, Wong EH (2009). "Asenapine: a novel psychopharmacologic agent with a unique human receptor signature". J. Psychopharmacol. (Oxford) 23 (1): 65–73. doi:10.1177/0269881107082944. PMID 18308814. 
  131. ^ a b Ishiyama T, Tokuda K, Ishibashi T, Ito A, Toma S, Ohno Y (2007). "Lurasidone (SM-13496), a novel atypical antipsychotic drug, reverses MK-801-induced impairment of learning and memory in the rat passive-avoidance test". Eur. J. Pharmacol. 572 (2-3): 160–70. doi:10.1016/j.ejphar.2007.06.058. PMID 17662268. 
  132. ^ Deeks ED, Keating GM (2010). "Blonanserin: a review of its use in the management of schizophrenia". CNS Drugs 24 (1): 65–84. doi:10.2165/11202620-000000000-00000. PMID 20030420. 
  133. ^ Ishibashi T, Horisawa T, Tokuda K, Ishiyama T, Ogasa M, Tagashira R, Matsumoto K, Nishikawa H, Ueda Y, Toma S, Oki H, Tanno N, Saji I, Ito A, Ohno Y, Nakamura M (2010). "Pharmacological profile of lurasidone, a novel antipsychotic agent with potent 5-hydroxytryptamine 7 (5-HT7) and 5-HT1A receptor activity". J. Pharmacol. Exp. Ther. 334 (1): 171–81. doi:10.1124/jpet.110.167346. PMID 20404009. 
  134. ^ López-Muñoz F, Alamo C (2013). "Active Metabolites as Antidepressant Drugs: The Role of Norquetiapine in the Mechanism of Action of Quetiapine in the Treatment of Mood Disorders". Front Psychiatry 4: 102. doi:10.3389/fpsyt.2013.00102. PMC 3770982. PMID 24062697. 
  135. ^ "Medscape home page". Medscape. WebMD. 
  136. ^ "Therapeutic Goods Administration home page". Therapeutic Goods Administration. Department of Health (Australia). 
  137. ^ "Daily Med home page". Daily Med. United States National Library of Medicine. 
  138. ^ "electronic Medicines Compendium (eMC) home page". electronic Medicines Compendium. Datapharm. 
  139. ^ Wen YG, Shang DW, Xie HZ, Wang XP, Ni XJ, Zhang M, Lu W, Qiu C, Liu X, Li FF, Li X, Luo FT (March 2013). "Population pharmacokinetics of blonanserin in Chinese healthy volunteers and the effect of the food intake". Human Psychopharmacology 28 (2): 134–141. doi:10.1002/hup.2290. PMID 23417765. 
  140. ^ Borgström L, Larsson H, Molander L (1982). "Pharmacokinetics of parenteral and oral melperone in man". European Journal of Clinical Pharmacology 23 (2): 173–176. doi:10.1007/BF00545974. PMID 7140807. 
  141. ^ Callaghan JT, Bergstrom RF, Ptak LR, Beasley CM (September 1999). "Olanzapine. Pharmacokinetic and pharmacodynamic profile". Clinical Pharmacokinetics 37 (3): 177–193. doi:10.2165/00003088-199937030-00001. PMID 10511917. 
  142. ^ Vermeir M, Naessens I, Remmerie B, Mannens G, Hendrickx J, Sterkens P, Talluri K, Boom S, Eerdekens M, van Osselaer N, Cleton A (April 2008). "Absorption, Metabolism, and Excretion of Paliperidone, a New Monoaminergic Antagonist, in Humans" (PDF). Drug Metabolism and Disposition 36 (4): 769–779. doi:10.1124/dmd.107.018275. PMID 18227146. 
  143. ^ Álamo C, López-Muñoz F (January 2013). "The Pharmacological Role and Clinical Applications of Antipsychotics' Active Metabolites: Paliperidone versus Risperidone" (PDF). Clinical and Experimental Pharmacology 3 (1): 117. doi:10.4172/2161-1459.1000117. 
  144. ^ DeVane CL, Nemeroff CB (2001). "Clinical Pharmacokinetics of Quetiapine An Atypical Antipsychotic". Clinical Pharmacokinetics 40 (7): 509–522. doi:10.2165/00003088-200140070-00003. PMID 11510628. 
  145. ^ Wiesel FA, Alfredsson G, Ehrnebo M, Sedvall G (May 1980). "The pharmacokinetics of intravenous and oral sulpiride in healthy human subjects" (PDF). European Journal of Clinical Pharmacology 17 (5): 385–391. doi:10.1007/BF00558453. PMID 7418717. 
  146. ^ Prakash, A; Lamb, HM (January 1998). "Zotepine: A Review of its Pharmacodynamic and Pharmacokinetic Properties and Therapeutic Efficacy in the Management of Schizophrenia". CNS Drugs 9 (2): 153–175. doi:10.2165/00023210-199809020-00006. 
  147. ^ Product Information: Nipolept(R), zotepine. Klinge Pharma GmbH, Munich, 1996.
  148. ^ The text reads: "When the patient lashes out against 'them' - THORAZINE (brand of chlorpromazine) quickly puts an end to his violent outburst. 'Thorazine' is especially effective when the psychotic episode is triggered by delusions or hallucinations. At the outset of treatment, Thorazine's combination of antipsychotic and sedative effects provides both emotional and physical calming. Assaultive or destructive behavior is rapidly controlled. As therapy continues, the initial sedative effect gradually disappears. But the antipsychotic effect continues, helping to dispel or modify delusions, hallucinations and confusion, while keeping the patient calm and approachable. SMITH KLINE AND FRENCH LABORATORIES leaders in psychopharmaceutical research."
  149. ^ a b c Pieters T, Majerus B (2011). "The introduction of chlorpromazine in Belgium and the Netherlands (1951-1968); tango between old and new treatment features". Stud Hist Philos Biol Biomed Sci 42 (4): 443–52. doi:10.1016/j.shpsc.2011.05.003. PMID 22035718. 
  150. ^ Healy, D. 2005. Psychiatric Drugs Explained. 4th Ed. Britain:Elsevier Limited. P. 8, 17.
  151. ^ a b c d e King C, Voruganti LN (2002). "What's in a name? The evolution of the nomenclature of antipsychotic drugs". J Psychiatry Neurosci 27 (3): 168–75. PMC 161646. PMID 12066446. 
  152. ^ "tranquillizer, n". Oxford English Dictionary. 1989. Retrieved 2011-08-09. 
  153. ^ Healy D (2008). "The intersection of psychopharmacology and psychiatry in the second half of the twentieth century". In Wallace, Edwin R., Gach, John. History of Psychiatry and Medical Psychology. Boston, MA: Springer US. p. 421. ISBN 978-0-387-34707-3. Retrieved 9 August 2011. 
  154. ^ Owens DG (1999-04-13). A guide to the extrapyramidal side-effects of antipsychotic drugs. Cambridge University Press. p. 12. ISBN 978-0-521-63353-6. 
  155. ^ Tasman A. Psychiatry Volume 2. Saunders. p. 956. ISBN 0-7216-5257-3. 
  156. ^ Horacek J, Bubenikova-Valesova V, Kopecek M, Palenicek T, Dockery C, Mohr P, Höschl C (2006). "Mechanism of action of atypical antipsychotic drugs and the neurobiology of schizophrenia". CNS Drugs 20 (5): 389–409. doi:10.2165/00023210-200620050-00004. PMID 16696579. 
  157. ^ a b Pipelineantipsychotic drugs to drive next market evolution (2009). Healthcarefinancenews.com (7 August 2009).
  158. ^ Aparasu RR, Bhatara V (2006). "Antipsychotic use and expenditure in the United States". Psychiatr Serv 57 (12): 1693. doi:10.1176/appi.ps.57.12.1693. PMID 17158480. 
  159. ^ 2008 U.S. Sales and Prescription Information: Top Therapeutic Classes by U.S. Sales (PDF). Imshealth.com.
  160. ^ James, Adam (2 March 2008). "Myth of the antipsychotic". The Guardian. Guardian News and Media Limited. Retrieved 27 July 2012. 
  161. ^ Moncrieff J (2006). "Why is it so difficult to stop psychiatric drug treatment? It may be nothing to do with the original problem". Med. Hypotheses 67 (3): 517–23. doi:10.1016/j.mehy.2006.03.009. PMID 16632226. 
  162. ^ GPs under 'pressure' to issue neuroleptics, claims professor, Chemist + Druggist, 15 January 2009
  163. ^ Nick Triggle (12 November 2009). "Dementia drug use 'killing many'". BBC. Retrieved 2013-05-07. 
  164. ^ "UK study warns against antipsychotics for dementia". reuters. Nov 12, 2009. Retrieved 2013-05-07. 
  165. ^ Hilzenrath, David S. (16 January 2010). "Justice suit accuses Johnson & Johnson of paying kickbacks". The Washington Post. Retrieved 17 January 2010. 
  166. ^ a b c Wilson, Duff (October 2, 2010). "Side Effects May Include Lawsuits". New York Times. 
  167. ^ DUFF WILSON (27 February 2009). "Drug Maker's E-Mail Released in Seroquel Lawsuit". The New York Times (The New York Times Company). Retrieved 27 July 2012. 
  168. ^ Gosden R, Beder S (2001). "Pharmaceutical industry agenda setting in mental health policies". Ethical Human Sciences and Services : an International Journal of Critical Inquiry 3 (3): 147–59. PMID 15278977. 
  169. ^ a b c American Psychiatric Association (September 2013), "Five Things Physicians and Patients Should Question", Choosing Wisely: an initiative of the ABIM Foundation (American Psychiatric Association), retrieved 30 December 2013 , which cites
  170. ^ American Geriatrics Society, "Ten Things Physicians and Patients Should Question", Choosing Wisely: an initiative of the ABIM Foundation (American Geriatrics Society), retrieved August 1, 2013 , which cites

External links[edit]

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Antipsychotics (neuroleptics) (N05A)
Typical
Benzamides
Levosulpiride
Sulpiride
Veralipride‡
Butyrophenones
Azaperone
Benperidol
Bromperidol
Droperidol
Fluanisone
Haloperidol#
Lenperone
Moperone
Pipamperone
Spiperone
Timiperone
Trifluperidol
Diphenylbutylpiperidines
Clopimozide
Fluspirilene
Penfluridol
Pimozide
Phenothiazines
Acepromazine
Acetophenazine
Butaperazine
Carphenazine (carfenazine)
Chloracizine
Chlorproethazine
Chlorpromazine
Cyamemazine
Dixyrazine
Fluacizine
Fluphenazine
Levomepromazine/Methotrimeprazine
Mesoridazine
Perazine
Periciazine
Perphenazine
Perphenazine 4-aminobutyrate
Piperacetazine
Pipotiazine
Prochlorperazine
Promazine
Promethazine
Sulforidazine
Thiethylperazine
Thiopropazate
Thioproperazine
Thioridazine
Trifluoperazine
Triflupromazine
Thioxanthenes
Chlorprothixene
Clopenthixol
Clothixamide
Flupentixol
Fluprothixene
Piflutixol
Teflutixol
Thiothixene
Zuclopenthixol
Tricyclics
Fluotracen
Loxapine
Trimipramine
Others
Butaclamol
Prothipendyl
Atypical
Others
Gastrointestinal tract/
metabolism (A)
Blood and blood
forming organs (B)
Cardiovascular
system (C)
Skin (D)
Genitourinary
system (G)
Endocrine
system (H)
Infections and
infestations (J, P, QI)
Malignant disease
(L01-L02)
Immune disease
(L03-L04)
Muscles, bones,
and joints (M)
Brain and
nervous system (N)
Respiratory
system (R)
Sensory organs (S)
Other ATC (V)
History
Symptoms
Spectrum
Treatment
Non-pharmaceutical
Authority control
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