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Pooled analyses of short-term (4 to 16 weeks) placebo-controlled trials of 9 antidepressant drugs (SSRIs and others) in children and adolescents with major depressive disorder (MDD), obsessive compulsive disorder (OCD), or other psychiatric disorders (a total of 24 trials involving over 4400 patients) have revealed a greater risk of adverse events representing suicidal thinking or behavior (suicidality) during the first few months of treatment in those receiving antidepressants.

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Etoricoxib seems relatively safe, with the risk of thrombotic events similar to that of non-coxib NSAID diclofenac.

While any individual can develop delirium, adults with "bad brains" have a much lower threshold for delirium, be it from substance use, prescribed medications, metabolic disorders, or systemic infections.

Fluoxetine belongs to the family of antidepressants known as selective serotonin re-uptake inhibitors, or SSRIs.

Generic versions of both drug forms are available now in India and Australia.

Antipsychotic medications are most effective in treating the hallucinations and delusions associated with schizophrenia and other psychotic disorders, however they may not help with other symptoms such as motivation and emotional responsiveness.

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It is important to continue taking this medication even if you feel well, unless your doctor tells you to stop.

It may be possible to stop fluoxetine therapy without tapering.

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The risks associated with longer-term venlafaxine hydrochloride extended-release capsule use were assessed in an open-label study of children and adolescents who received venlafaxine hydrochloride extended-release capsules for up to six months.

Clinicians should consider using these types of pharmacokinetic-derived charts and tables when prescribing to patients whose genetic status is known.

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Prozac is so long lasting that one dose can be taken weekly.

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It is prescribed for the treatment of clinical depression and anxiety disorders.

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Results of this trial will guide policy-making with regard to pharmacogenetic screening prior to treatment with nortriptyline or venlafaxine among older patients with depression.

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Data from identical doses at different time points were collapsed into single bars for display purposes only.

Older adults may also be more likely to develop a type of salt imbalance (hyponatremia), especially if they are also taking "water pills" (diuretics).

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Adverse reactions, some of which were serious, have been reported in patients who have recently been discontinued from a monoamine oxidase inhibitor (MAOI) and started on venlafaxine, or who have recently had venlafaxine therapy discontinued prior to initiation of an MAOI.

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An overall tendency to mildly raised blood pressure may be apparent in 10% of individuals on venlafaxine, regardless of the daily dose ().

You must talk with your healthcare provider for complete information about the risks and benefits of using this medicine.

Headache, drowsiness, dizziness, nervousness, trouble sleeping, dry mouth, nausea, vomiting, blurred vision, altered taste, sweating, stomach upset, constipation, loss of appetite, anxiety, or yawning may occur.

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XR, other SNRIs (Serotonin and Norepinephrine Reuptake Inhibitors), or SSRIs (Selective Serotonin Reuptake Inhibitors), late in the third trimester have developed complications requiring prolonged hospitalization, respiratory support, and tube feeding.

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Patients should be advised to notify their physician if they become pregnant or intend to become pregnant during therapy.

As with most antidepressants, a small number of children and young adults taking this medication have experienced an occurrence or elevation of suicidal thinking.

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Venlafaxine extended release (XR) was effective and well tolerated in both the short-term and long-term treatment of panic disorder.

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Just as with other antidepressants, you've got to be sure to tell your doctor if you've ever had allergies to any antidepressants, foods, preservatives, or dyes, and if you have suffered from manic depression, convulsions, or seizures.

Serotonin syndrome has also been seen in patients taking venlafaxine alone, although rarely.

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Adverse effects of interest include but are not limited to nausea; diarrhea; headache; tremor; daytime sedation; decreased libido; failure to achieve orgasm; nervousness; insomnia; and more severe events, including suicide.

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In vivo, venlafaxine 75 mg by mouth every 12 hours did not alter the pharmacokinetics of a single 500 mg dose of tolbutamide or the CYP2C9 mediated formation of 4-hydroxy-tolbutamide.

It is possible that (Cymbalta, Xeristar, Yentreve), licensed by the FDA in autumn 2004, and (Ixel, Dalcipran, Toledomin), available in Europe, may be more effective than (Effexor) for a segment of the population that can benefit from dual serotonin-noradrenaline reuptake inhibition.

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All insurance policies and group benefit plans contain exclusions and limitations.

Acupuncture may provide temporary relief from chronic headache pain.

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This medication may also be used to treat attacks.

Duloxetine slightly increased the fasting serum glucose; however this effect was deemed to be of "minimal clinical significance".

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