كويتياپين
البيانات السريرية | |
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النُطق | /kwᵻˈtaɪ.əpiːn/ kwi-TY-ə-peen |
الأسماء التجارية | Seroquel, Temprolide, others |
AHFS/Drugs.com | Monograph |
MedlinePlus | a698019 |
License data |
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فئة السلامة أثناء الحمل |
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مسارات الدواء | By mouth |
رمز ATC | |
الحالة القانونية | |
الحالة القانونية | |
بيانات الحركية الدوائية | |
التوافر الحيوي | 100%[1] |
ارتباط الپروتين | 83%[2] |
الأيض | Liver via CYP3A4-catalysed sulfoxidation to its active metabolite norquetiapine (N-desalkylquetiapine)[5] |
Elimination half-life | 7 hours (parent compound); 9–12 hours (active metabolite, norquetiapine)[2][3] |
الإخراج | Kidney (73%), faeces (20%)[1][2][3][4] |
المعرفات | |
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رقم CAS | |
PubChem CID | |
IUPHAR/BPS | |
DrugBank | |
ChemSpider | |
UNII | |
KEGG | |
ChEBI | |
ChEMBL | |
CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.131.193 |
Chemical and physical data | |
التركيب | C21H25N3O2S |
الكتلة المولية | 383.5099 g/mol |
3D model (JSmol) | |
Solubility in water | 3.29 mg/mL (20 °C) |
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كويتاپين، يُباع تحت الاسم التجاري سروكويل Seroquel، is an atypical antipsychotic used for the treatment of schizophrenia, bipolar disorder, and major depressive disorder.[6][7] Despite being widely used as a sleep aid due its sedating effect, the benefits of such use do not appear to generally outweigh the side effects.[8] It is taken by mouth.[6]
Common side effects include sleepiness, constipation, weight gain, and dry mouth.[6] Other side effects include low blood pressure with standing, seizures, a prolonged erection, high blood sugar, tardive dyskinesia, and neuroleptic malignant syndrome.[6] In older people with dementia, its use increases the risk of death.[6] Use in the third trimester of pregnancy may result in a movement disorder in the baby for some time after birth.[6] Quetiapine is believed to work by blocking a number of receptors including serotonin and dopamine.[6]
Quetiapine was developed in 1985 and approved for medical use in the United States in 1997.[6][9] It is available as a generic medication.[10] In the United States, the wholesale cost is about US$12 per month as of 2017.[11] In the United Kingdom, a month's supply costs the NHS about £60 as of 2017.[10] In 2016, it was the 86th most prescribed medication in the United States, with more than 8 million prescriptions.[12]
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الاستخدامات الطبية
Quetiapine is primarily used to treat schizophrenia or bipolar disorder.[13] Quetiapine targets both positive and negative symptoms of schizophrenia.[14]
الفصام
A 2013 Cochrane review compared quetiapine to typical antipsychotics:
Summary | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Quetiapine may not differ from typical antipsychotics in the treatment of positive symptoms, general psychopathology, and negative symptoms. However, it causes fewer adverse effects in terms of abnormal ECG, extrapyramidal effects, abnormal prolactin levels and weight gain.[15] | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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In a 2013 comparison of 15 antipsychotics in effectiveness in treating schizophrenia, quetiapine demonstrated standard effectiveness. It was 13-16% more effective than ziprasidone, chlorpromazine, and asenapine and approximately as effective as haloperidol and aripiprazole.[16]
There is tentative evidence of the benefit of quetiapine versus placebo in schizophrenia; however, definitive conclusions are not possible due to the high rate of attrition in trials (greater than 50%) and the lack of data on economic outcomes, social functioning, or quality of life.[17]
It is debatable whether, as a class, typical or atypical antipsychotics are more effective.[18] Both have equal drop-out and symptom relapse rates when typicals are used at low to moderate dosages.[19] While quetiapine has lower rates of extrapyramidal side effects, there is greater sleepiness and rates of dry mouth.[17]
A Cochrane review comparing quetiapine to other atypical antipsychotic agents tentatively concluded that it may be less efficacious than olanzapine and risperidone; produce fewer movement related side effects than paliperidone, aripiprazole, ziprasidone, risperidone and olanzapine; and produce weight gain similar to risperidone, clozapine and aripiprazole. They concluded that it produces suicide attempt, suicide; death; QTc prolongation, low blood pressure; tachycardia; sedation; gynaecomastia; galactorrhoea, menstrual irregularity and white blood cell count at a rate similar to first generation antipsychotics.[20]
الاضطراب ثنائي القطب
In those with bipolar disorder, quetiapine is used to treat depressive episodes; acute manic episodes associated with bipolar I disorder (as either monotherapy or adjunct therapy to lithium; valproate or lamotrigine); and maintenance treatment of bipolar I disorder (as adjunct therapy to lithium or divalproex).
الاكتئاب الحاد
Quetiapine is effective when used by itself[7] and when used along with other medications in major depressive disorder (MDD).[7][21] However, sedation is often an undesirable side effect.[7]
In the United States,[3] the United Kingdom[22] and Australia (while not subsidised by the Australian Pharmaceutical Benefits Scheme for treatment of MDD), quetiapine is licensed for use as an add-on treatment in MDD.[23]
مرض ألزايمر
Quetiapine does not decrease agitation among people with Alzheimer's. Quetiapine worsens intellectual functioning in the elderly with dementia and therefore is not recommended.[24]
أخرى
The use of low doses of quetiapine for insomnia, while common, is not recommended; there is little evidence of benefit and concerns regarding adverse effects.[25][26]
It is sometimes used off-label, often as an augmentation agent, to treat conditions such as Tourette syndrome,[27] musical hallucinations[28] and anxiety disorders.[29]
Quetiapine and clozapine are the most widely used medications for the treatment of Parkinson's disease psychosis due to their very low extrapyramidal side-effect liability. Owing to the risks associated with clozapine (e.g. agranulocytosis, diabetes mellitus, etc.), clinicians often attempt treatment with quetiapine first, although the evidence to support quetiapine's use for this indication is significantly weaker than that of clozapine.[30][31]
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الآثار الجانبية
Sources for incidence lists:[1][3][22][23][31][32]
- Very common (>10% incidence) adverse effects
- Dry mouth
- Dizziness
- Headache
- Somnolence (drowsiness; of 15 antipsychotics quetiapine causes the 5th most sedation. Extended release (XR) formulations tend to produce less sedation, dose-by-dose than the immediate release formulations)[16]
- Common (1–10% incidence) adverse effects
- High blood pressure
- Orthostatic hypotension
- High pulse rate
- High blood cholesterol
- Elevated serum triglycerides
- Abdominal pain
- Constipation
- Increased appetite
- Vomiting
- Increased liver enzymes
- Backache
- Asthenia
- Insomnia
- Lethargy
- Tremor
- Agitation
- Nasal congestion
- Pharyngitis
- Fatigue
- Pain
- Dyspepsia (Indigestion)
- Peripheral oedema
- Dysphagia
- Extrapyramidal disease: quetiapine and clozapine are noted for their relative lack of extrapyramidal side effects[16][22][31]
- Weight gain: SMD 0.43 kg when compared to placebo. Produces roughly as much weight gain as risperidone, less weight gain than clozapine, olanzapine and zotepine and more weight gain than ziprasidone, lurasidone, aripiprazole and asenapine.[16] As with many other atypical antipsychotics, this action is likely due to its actions at the H1 histamine receptor and 5-HT2C receptor.[5]
- Rare (<1% incidence) adverse effects
- Prolonged QT interval (had an odds ratio for prolonging the QT interval over placebo of 0.17)[16]
- Sudden cardiac death
- Syncope
- Diabetic ketoacidosis
- Restless legs syndrome
- Hyponatraemia, low blood sodium.
- Jaundice, yellowing of the eyes, skin and mucous membranes due to an impaired ability of the body to clear bilirubin, a by product of haem breakdown.
- Pancreatitis, pancreas swelling.
- Agranulocytosis, a potentially fatal drop in white blood cell count.
- Leukopenia, a drop in white blood cell count, not as severe as agranulocytosis.
- Neutropenia, a drop in neutrophils, the cell of the immune cells that defends the body against bacterial infections.
- Eosinophilia
- Anaphylaxis, a potentially fatal allergic reaction.
- Seizure
- Hypothyroidism, underactive thyroid gland.
- Myocarditis, swelling of the myocardium.
- Cardiomyopathy
- Hepatitis, swelling of the liver.
- Suicidal ideation
- Priapism. A prolonged and painful erection.
- Stevens-Johnson syndrome. A potentially fatal skin reaction.
- Neuroleptic malignant syndrome a rare and potentially fatal complication of antipsychotic drug treatment. It is characterised by the following symptoms: tremor, rigidity, hyperthermia, tachycardia, mental status changes (e.g. confusion), etc.
- Tardive Dyskinesia. A rare and often irreversible neurological condition characterised by involuntary movements of the face, tongue, lips and rest of the body. Most commonly occurs after prolonged treatment with antipsychotics. It is believed to be particularly uncommon with atypical antipsychotics, especially quetiapine and clozapine[23][33]
Both typical and atypical antipsychotics can cause tardive dyskinesia.[34] According to one study, rates are lower with the atypicals at 3.9% as opposed to the typicals at 5.5%.[34] Although quetiapine and clozapine are atypical antipsychotics, switching to these atypicals is an option to minimize symptoms of tardive dyskinesia caused by other atypicals.[35]
Weight gain can be a problem for some, with quetiapine causing more weight gain than fluphenazine, haloperidol, loxapine, molindone, olanzapine, pimozide, risperidone, thioridazine, thiothixene, trifluoperazine, and ziprasidone, but less than chlorpromazine, clozapine, perphenazine, and sertindole.[36]
As with some other anti-psychotics, quetiapine may lower the seizure threshold,[37] and should be taken with caution in combination with drugs such as bupropion.
التوقف عن الاستخدام
The British National Formulary recommends a gradual withdrawal when discontinuing antipsychotics to avoid acute withdrawal syndrome or rapid relapse.[38] Symptoms of withdrawal commonly include nausea, vomiting, and loss of appetite.[39] Other symptoms may include restlessness, increased sweating, and trouble sleeping.[39] Less commonly there may be a feeling of the world spinning, numbness, or muscle pains.[39] Symptoms generally resolve after a short period of time.[39]
There is tentative evidence that discontinuation of antipsychotics can result in psychosis.[40] It may also result in reoccurrence of the condition that is being treated.[41] Rarely tardive dyskinesia can occur when the medication is stopped.[39]
الحمل والرضاة
Placental exposure is least for quetiapine compared to other atypical antipsychotics.[31] The evidence is insufficient to rule out any risk to the foetus but available data suggests it is unlikely to result in any major foetal malformations.[2][4][32] It is secreted in breast milk and hence quetiapine-treated mothers are advised not to breastfeed.[2][4][32]
الجرعة الزائدة
Most instances of acute overdosage result in only sedation, hypotension and tachycardia, but cardiac arrhythmia, coma and death have occurred in adults. Serum or plasma quetiapine concentrations are usually in the 1–10 mg/L range in overdose survivors, while postmortem blood levels of 10–25 mg/L are generally observed in fatal cases.[42] Non-toxic levels in postmortem blood extend to around 0.8 mg/kg, but toxic levels in postmortem blood can begin at 0.35 mg/kg.[43][44]
علم الأدوية
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الحركة الدوائية
Site | QTP | NQTP | Action | Ref |
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SERT | >10,000 | 927 | Blocker | [46] |
NET | >10,000 | 58 | Blocker | [46] |
DAT | >10,000 | >10,000 | ND | [46] |
5-HT1A | 320–432 | 45 | Partial agonist | [46][47] |
5-HT1B | 1,109–2,050 | 1,117 | ND | [46][47] |
5-HT1D | >10,000 | 249 | ND | [46][47] |
5-HT1E | 1,250–2,402 | 97 | ND | [46][47] |
5-HT1F | 2,240 | ND | ND | [47] |
5-HT2A | 96–101 | 48 | Antagonist | [46][47] |
5-HT2B | ND | 14 | Antagonist | [46] |
5-HT2C | 2,502 | 107 | Antagonist | [46] |
5-HT3 | >10,000 | 394 | Antagonist | [46] |
5-HT4 | ND | ND | ND | ND |
5-HT5A | 3,120 | 768 | ND | [46] |
5-HT6 | 1,865 | 503 | Antagonist | [46] |
5-HT7 | 307 | 76 | Antagonist | [46] |
α1A | 22 | 144 | Antagonist | [46] |
α1B | 39 | 95 | Antagonist | [46] |
α2A | 2,230–3,630 | 237 | Antagonist | [46][47] |
α2B | 90–747 | 378 | Antagonist | [46][47] |
α2C | 28.7–350 | 736 | Antagonist | [46][47] |
β1 | >10,000 | >10,000 | ND | [46][47] |
β2 | >10,000 | >10,000 | ND | [46][47] |
D1 | 712 | 214 | Antagonist | [46] |
D2 | 245 | 196 | Antagonist | [46] |
D2L | 700 | ND | Antagonist | [47] |
D2S | 390 | ND | Antagonist | [47] |
D3 | 340–483 | 567 | Antagonist | [46][47] |
D4 | 1,202 | 1,297 | Antagonist | [46] |
D4.2 | 1,600 | ND | Antagonist | [47] |
D5 | 1,738 | 1,419 | Antagonist | [46] |
H1 | 2.2–11 | 3.5 | Antagonist | [46][47] |
H2 | >10,000 | 298 | Antagonist | [46] |
H3 | >10,000 | >10,000 | ND | [46] |
H4 | >10,000 | 1,660 | ND | [46] |
M1 | 858 | 39 | Antagonist | [46] |
M2 | 1,339 | 453 | ND | [46] |
M3 | >10,000 | 23 | Antagonist | [46] |
M4 | 542 | 110 | ND | [46] |
M5 | 1,942 | 23 | Antagonist | [46] |
σ1 | 220–3,651 | >10,000 | ND | [46][47] |
σ2 | 1,344 | 1,050 | ND | [46] |
NMDA (PCP) |
>10,000 | ND | Antagonist | [46] |
VDCC | >10,000 | ND | ND | [46][47] |
hERG | ND | >10,000 (IC50) |
ND | [46] |
Values are Ki (nM), unless otherwise noted. The smaller the value, the more strongly the drug binds to the site. All data are for human cloned proteins, except σ1 (guinea pig), σ2 (rat), and VDCC (rat).[46][47] |
Quetiapine has the following pharmacological actions:[48][49][50][51][52][53][54][55]
- Dopamine D1, D2, D3, D4, and D5 receptor antagonist
- Serotonin 5-HT1A receptor partial agonist, 5-HT2A, 5-HT2B, 5-HT2C, 5-HT3, 5-HT6, and 5-HT7 receptor antagonist, and 5-HT1B, 5-HT1D, 5-HT1E, and 5-HT1F receptor ligand
- α1- and α2-adrenergic receptor antagonist
- Histamine H1 receptor antagonist
- Muscarinic acetylcholine receptor antagonist
This means quetiapine is a dopamine, serotonin, and adrenergic antagonist, and a potent antihistamine with some anticholinergic properties.[56] Quetiapine binds strongly to serotonin receptors; the drug acts as partial agonist at 5-HT1A receptors.[57] Serial PET scans evaluating the D2 receptor occupancy of quetiapine have demonstrated that quetiapine very rapidly disassociates from the D2 receptor.[58] Theoretically, this allows for normal physiological surges of dopamine to elicit normal effects in areas such as the nigrostriatal and tuberoinfundibular pathways, thus minimizing the risk of side-effects such as pseudo-parkinsonism as well as elevations in prolactin.[59] Some of the antagonized receptors (serotonin, norepinephrine) are actually autoreceptors whose blockade tends to increase the release of neurotransmitters.
At very low doses, quetiapine acts primarily as a histamine receptor blocker (antihistamine) and α1-adrenergic blocker. When the dose is increased, quetiapine activates the adrenergic system and binds strongly to serotonin receptors and autoreceptors. At high doses, quetiapine starts blocking significant amounts of dopamine receptors.[49][60] Off-label prescriptions, e.g. for chronic insomnia, of low-dose quetiapine is not recommended due to the harmful side-effects.[61]
When treating schizophrenia, antagonism of D2 receptor by quetiapine in the mesolimbic pathway relieves positive symptoms and antagonism of the 5HT2A receptor in the frontal cortex of the brain relieves negative symptoms.[14][62][63] Quetiapine has fewer extrapyramidal side effects and is less likely to cause hyperprolactinemia when compared to other drugs used to treat schizophrenia, so is used as a first line treatment.[64][65]
الكيمياء
Quetiapine is a tetracyclic compound and is closely related structurally to clozapine, olanzapine, loxapine, and other tetracyclic antipsychotics.
التحضير
The synthesis of quetiapine begins with a dibenzothiazepinone. The lactam is first treated with phosphoryl chloride to produce a dibenzothiazepine. A nucleophilic substitution is used to introduce the sidechain.[66]
التاريخ
المجتمع والثقافة
الوضع التنظيمي
التكلفة
In the United States as of 2015, the branded extended-release 400 mg pills cost between US$9.68 and US$23.16 each.[67] In 2017, the short-acting version had a wholesale cost of about US$12 per month.[11]
In the United Kingdom, a month's supply, as of 2017, costs the NHS approximately £107.45.[10] This is following an increase of 30 to 70 fold in 2017/2018.[68]
الدعاوى القضائية
In April 2010, the U. S. Department of Justice fined Astra-Zeneca $520 million for the company's aggressive marketing of Seroquel for off-label uses.[69] According to the Department of Justice, "the company recruited doctors to serve as authors of articles that were ghostwritten by medical literature companies and about studies the doctors in question did not conduct. AstraZeneca then used those studies and articles as the basis for promotional messages about unapproved uses of Seroquel."[69]
Multiple lawsuits have been filed in relation to quetiapine's side-effects, in particular, diabetes.[70][71][72][73]
Approximately 10,000[74] lawsuits[75] have been filed against AstraZeneca, alleging that quetiapine caused problems ranging from slurred speech and chronic insomnia to deaths.
جدل
In 2004, a young man named Dan Markingson committed suicide in a controversial Seroquel clinical trial at the University of Minnesota while under an involuntary commitment order.[76] A group of University of Minnesota bioethicists charged that the trial involved an alarming number of ethical violations.[77]
حالة تلاعب نيوروفن پلس
In August 2011, the UK's Medicines and Healthcare products Regulatory Agency (MHRA) issued a class-4 drug alert following reports that some batches of Nurofen plus contained Seroquel XL instead.[78]
Following the issue of the Class-4 Drug Alert, Reckitt Benckiser (UK) Ltd received further reports of rogue blister strips in cartons of two additional batches of Nurofen Plus tablets. One of the new batches contained Seroquel XL 50 mg tablets and one contained the Pfizer product Neurontin 100 mg capsules.
Following discussions with the MHRA's Defective Medicines Report Centre (DMRC), Reckitt Benckiser (UK) Ltd decided to recall all remaining unexpired stock of Nurofen Plus tablets in any pack size, leading to a Class-1 Drug Alert.[79] The contamination was later traced to in-store tampering by a customer.[80]
المصادر
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<ref>
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وصلات خارجية
- "Quetiapine". MedlinePlus. The American Society of Health-System Pharmacists, Inc. 2008-09-01.
- NAMI summary
- Internet Drug List summary
- Compound #1802: Quetiapine[dead link] ChemBank
- U.S. National Library of Medicine: Drug Information Portal - Quetiapine
- Australian Public Assessment Report for Quetiapine (as fumarate)
- CS1 maint: unflagged free DOI
- CS1 errors: unsupported parameter
- Template:drugs.com link with non-standard subpage
- ECHA InfoCard ID from Wikidata
- Infobox-drug molecular-weight unexpected-character
- Pages using infobox drug with unknown parameters
- Drugboxes which contain changes to watched fields
- Articles with dead external links from July 2016
- Alpha blockers
- مضادات اكتئاب
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