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SEROQUEL-GENERIC

(generic name: Quetiapine )
Reviews
BMJ. 2005 Feb 18.
Quetiapine and rivastigmine and cognitive decline in Alzheimer's disease: randomised double blind placebo controlled trial.
Ballard C, Margallo-Lana M, Juszczak E, Douglas S, Swann A, Thomas A, O'brien J, Everratt A, Sadler S, Maddison C, Lee L, Bannister C, Elvish R, Jacoby R.
Institute of Psychiatry, King's College, London SE5 8AF.

OBJECTIVES: To determine the respective efficacy of quetiapine and rivastigmine for agitation in people with dementia in institutional care and to evaluate these treatments with respect to change in cognitive performance. DESIGN: Randomised double blind (clinician, patient, outcomes assessor) placebo controlled trial. SETTING: Care facilities in the north east of England. PARTICIPANTS: 93 patients with Alzheimer's disease, dementia, and clinically significant agitation. INTERVENTION: Atypical antipsychotic (quetiapine), cholinesterase inhibitor (rivastigmine), or placebo (double dummy). MAIN OUTCOME MEASURES: Agitation (Cohen-Mansfield agitation inventory) and cognition (severe impairment battery) at baseline and at six weeks and 26 weeks. The primary outcome was agitation inventory at six weeks. RESULTS: 31 patients were randomised to each group, and 80 (86%) started treatment (25 rivastigmine, 26 quetiapine, 29 placebo), of whom 71 (89%) tolerated the maximum protocol dose (22 rivastigmine, 23 quetiapine, 26 placebo). Compared with placebo, neither group showed significant differences in improvement on the agitation inventory either at six weeks or 26 weeks. Fifty six patients scored >10 on the severe impairment battery at baseline, 46 (82%) of whom were included in the analysis at six week follow up (14 rivastigmine, 14 quetiapine, 18 placebo). For quetiapine the change in severe impairment battery score from baseline was estimated as an average of -14.6 points (95% confidence interval -25.3 to -4.0) lower (that is, worse) than in the placebo group at six weeks (P=0.009) and -15.4 points (-27.0 to -3.8) lower at 26 weeks (P=0.01). The corresponding changes with rivastigmine were -3.5 points (-13.1 to 6.2) lower at six weeks (P=0.5) and -7.5 points (-21.0 to 6.0) lower at 26 weeks (P=0.3). CONCLUSIONS: Neither quetiapine nor rivastigmine are effective in the treatment of agitation in people with dementia in institutional care. Compared with placebo, quetiapine is associated with significantly greater cognitive decline.
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Int J Neuropsychopharmacol. 2005 Mar 01;:1-8.
Effects of quetiapine and haloperidol on body mass index and glycaemic control: a long-term, randomized, controlled trial.
Emsley R, Turner HJ, Schronen J, Botha K, Smit R, Oosthuizen PP.
Department of Psychiatry, University of Stellenbosch, Cape Town, South Africa.

The topic of antipsychotic-induced weight-gain and its relationship to glucose metabolism is under-studied. We evaluated the long-term effects of a new-generation antipsychotic, quetiapine and a conventional antipsychotic, haloperidol on body mass index (BMI) and glycaemic control in patients with schizophrenia previously treated with conventional antipsychotics. Forty-five clinically stable patients with schizophrenia participated in this randomized, investigator-blinded, parallel-group comparison of flexible doses of quetiapine and haloperidol treatment over 52 wk. Primary outcome measures were change from baseline in BMI and glycosylated haemoglobin (HBA1c) levels. There were no between-group differences at any of the time-points for BMI (F=1.90, p=0.1) and HBA1c (F=1.17, p=0.3) values, and there were no significant changes in BMI from baseline for either group. HBA1c levels decreased significantly at end-point for the haloperidol group (-1.5%, p=0.04), but not for the quetiapine group (-0.3%, p=0.5). Although the sample was not generally obese (mean baseline BMI 25.5+/-6.3 kg/m2), a large proportion exhibited evidence of abnormal glycaemic control prior to randomization (mean HBA1c 6.7+/-1.9%), with 48% having values that were at least mildly elevated (HBA1c >6.1%) and 19% markedly elevated (HBA1c >7%). The number of subjects with elevated HBA1c values decreased from baseline in both the haloperidol and quetiapine treatment groups. These findings suggest that switching treatment from a conventional antipsychotic to quetiapine is not associated with weight gain or worsening of glycaemic control, even in the long term. The study also highlights the high incidence of unrecognized glucose dysregulation in patients with schizophrenia receiving conventional antipsychotic treatment.

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Drug information

GENERIC NAME: quetiapine
BRAND NAME: Seroquel


DRUG CLASS AND MECHANISM: Quetiapine is an oral drug that is used for treating psychoses, for example, schizophrenia. Although the mechanism of action of quetiapine is unknown, like other anti-psychotics, it inhibits communication between nerves of the brain. It does this by blocking receptors on the nerves for several neurotransmitters, the chemicals that nerves use to communicate with each other. It is thought that its beneficial effect is due to blocking of the dopamine type 2 (D2) and serotonin type 2 (5-HT2) receptors.

PREPARATIONS: Quetiapine is available as 25 mg (peach), 100 mg (yellow) and 200 mg (white) tablets.

STORAGE:Tablets should be stored at room temperature, 15-30°C (59-86°F).

PRESCRIBED FOR: Quetiapine is used to treat severe mental disorders like schizophrenia, which are characterized by distorted thoughts, perceptions, and emotions,.

DOSING: Quetiapine usually is taken twice or three times per day. The dose usually is increased slowly over several days to weeks to achieve the desired effect. Quetiapine can be taken with or without food.

DRUG INTERACTIONS: Phenytoin (Dilantin) markedly decreases the amount of quetiapine that is absorbed from the intestine and thereby reduces its effectiveness. Thus, patients taking phenytoin require higher doses of quetiapine.

Quetiapine can cause orthostatic hypotension, a drop in blood pressure that occurs upon rising that may cause dizziness or light-headedness. Diazepam (Valium) or related benzodiazepines and alcohol can promote the orthostatic hypotension caused by quetiapine, and they should not be taken together with quetiapine.

Quetiapine can add to the sedating effects of other drugs that cause sedation. Such drugs include narcotic pain relievers (e.g. Percocet), barbiturates, sedatives such as alprazolam (Xanax) and clonazepam (Klonopin), ethanol, and blood pressure drugs that can cause orthostatic hypotension, such as prazosin (Minipress) and terazosin (Hytrin).

Quetiapine is eliminated from the body by an enzyme in the liver called cytochrome P450 3A. There is a concern that drugs that strongly interfere with the enzyme, e.g., ketoconazole (Nizoral), itraconazole (Sporanox), fluconazole (Diflucan), and erythromycin, clarithromycin (Biaxin), nefazodone (Serzone), Verapamil (Calan, Isoptin, Verelan), or diltiazem (Cardizem, Tiazac, Dilacor) may cause elevated and toxic levels of quetiapine.

PREGNANCY: There are no adequate studies of quetiapine in pregnant women. Studies in animals are inconsistent. Some studies suggest effects on the fetus and others show no effects. Quetiapine can be used in pregnancy if the physician feels that it is necessary.

NURSING MOTHERS: Quetiapine is excreted in the milk of animals during lactation. It is not known if it is excreted in human milk, but it is recommended that women taking quetiapine not breast feed.

SIDE EFFECTS: Quetiapine can cause orthostatic hypotension especially during the first 3-5 day period of treatment, when it is restarted after temporary discontinuation, and after an increase in the dose. The risk of orthostatic hypotension is about 1 in 100 (one of every hundred patients who takes quetiapine). Quetiapine frequently causes tiredness (1 in 5 patients), especially during the first 3-5 days of treatment. Because of this tiredness, care should be exercised in any activity requiring mental alertness, such as operating a motor vehicle (including automobiles) or hazardous machinery. Less common side effects include seizures (1 in 125 patients) and hypothyroidism (1 in 250 patients).

As with other antipsychotics, long-term use of quetiapine may lead to a potentially irreversible condition called tardive dyskinesia which consists of involuntary movements of the jaw, lips, and tongue.

A potentially fatal complex referred to as neuroleptic malignant syndrome (NMS) has been reported with antipsychotic drugs, and two possible cases of NMS have been reported with quetiapine. Patients who develop NMS may have high fevers, muscle rigidity, altered mental status, irregular pulse or blood pressure, rapid heart rate, excessive sweating, and heart arrhythmias.

In animals, quetiapine has been associated with the development of cataracts, and cataracts have been reported in patients using quetiapine for prolonged periods. Although it is not clear if quetiapine is responsible for the cataracts seen in humans, eye examinations by slit-lamp (to identify cataracts before they impair vision) are recommended at the beginning of treatment and every six months during treatment. If cataracts form, treatment should be discontinued.

Quetiapine may increase blood concentrations of cholesterol and triglycerides by 11% and 17%, respectively.

Although there is no clear link between quetiapine and diabetes, patients should be tested during treatment for elevated blood-sugars. Additionally, persons with risk factors for diabetes, including obesity or a family history of diabetes, should have their fasting levels of blood sugar tested before starting treatment and periodically throughout treatment to detect the onset of diabetes. Any patient developing symptoms that suggest diabetes during treatment should be tested for diabetes.

Caution! Before starting to take this medicine, it is vital that you should consult your doctor! Do not use it on your own initiative, without medical advice.

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SEROQUEL - GENERIC (antipsychotic) (generic - what is it?)
Substance: Quetiapine
Dosage
Packing
Price
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25 mg
100 tab
USD 49.00
100 mg
100 tab
USD 62.00
200 mg
100 tab
USD 124.00
 

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