Buy Escitalopram (Lexapro) pills online

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Indications and usage:

Lexapro (Escitalopram Oxalate) is a selective serotonin reuptake inhibitor (SSRI) indicated for:

  • acute and maintenance treatment of major depressive disorder (MDD) in adults and adolescents aged 12-17 years
  • acute treatment of generalized anxiety disorder (GAD) in adults
  • obsessive-compulsive disorder (OCD)
  • social anxiety disorder (SAD)
  • panic disorder with or without agoraphobia
  • bipolar disorder
  • borderline personality disorder
  • somatoform pain disorder
  • body dysmorphic disorder
  • fibromyalgia
  • impulse disorders
  • trichotillomania
  • irritable bowel syndrome
  • reducing the symptoms of premenstrual syndrome
  • premenstrual dysphoric disorder
  • vulvodynia

    Dosage and administration:

  • Lexapro should generally be administered once daily, morning or evening with or without food.
  • No additional benefits seen at 20 mg/day dose.
  • 10 mg/day is the recommended dose for most elderly patients and patients with hepatic impairment.
  • No dosage adjustment for patients with mild or moderate renal impairment. Use caution in patients with severe renal impairment.
  • Discontinuing Escitalopram: a gradual dose reduction is recommended.

    Dosage forms and strengths:

  • Lexapro (Escitalopram Oxalate) scored tablets: 5 mg, 10 mg, 20 mg.
  • Lexapro (Escitalopram Oxalate) oral solution: 1 mg per mL.


  • Serotonin syndrome and MAOIs: do not use MAOIs intended to treat psychiatric disorders with Lexapro or within 14 days of stopping treatment with Lexapro. Do not use Lexapro within 14 days of stopping an MAOI intended to treat psychiatric disorders. In addition, do not start Lexapro in a patient who is being treated with linezolid or intravenous methylene blue.
  • Pimozide: do not use concomitantly.
  • Known hypersensitivity to escitalopram or citalopram or any of the inactive ingredients.

    Warnings and precautions:

  • Clinical worsening/suicide risk: monitor for clinical worsening, suicidality and unusual change in behavior, especially, during the initial few months of therapy or at times of dose changes.
  • Serotonin syndrome: serotonin syndrome has been reported with SSRIs and SNRIs, including Lexapro, both when taken alone, but especially when co-administered with other serotonergic agents (including triptans, tricyclic antidepressants, fentanyl, lithium, tramadol, tryptophan, buspirone, amphetamines, and St. John's Wort). If such symptoms occur, discontinue Lexapro and initiate supportive treatment. If concomitant use of Lexapro with other serotonergic drugs is clinically warranted, patients should be made aware of a potential increased risk for serotonin syndrome, particularly during treatment initiation and dose increases.
  • Discontinuation of treatment with escitalopram oxalate: a gradual reduction in dose rather than abrupt cessation is recommended whenever possible.
  • Seizures: prescribe with care in patients with a history of seizure.
  • Activation of mania/hypomania: use cautiously in patients with a history of mania.
  • Hyponatremia: can occur in association with SIADH.
  • Abnormal bleeding: use caution in concomitant use with NSAIDs, aspirin, warfarin or other drugs that affect coagulation.
  • Interference with cognitive and motor performance: use caution when operating machinery.
  • Angle closure glaucoma: angle closure glaucoma has occurred in patients with untreated anatomically narrow angles treated with antidepressants.
  • Use in patients with concomitant illness: use caution in patients with diseases or conditions that produce altered metabolism or hemodynamic responses.


    Human experience

    In clinical trials of escitalopram, there were reports of escitalopram overdose, including overdoses of up to 600 mg, with no associated fatalities. During the postmarketing evaluation of escitalopram, Lexapro overdoses involving overdoses of over 1000 mg have been reported. As with other SSRIs, a fatal outcome in a patient who has taken an overdose of escitalopram has been rarely reported.

    Symptoms most often accompanying escitalopram overdose, alone or in combination with other drugs and/or alcohol, included convulsions, coma, dizziness, hypotension, insomnia, nausea, vomiting, sinus tachycardia, somnolence, and ECG changes (including QT prolongation and very rare cases of torsade de pointes). Acute renal failure has been very rarely reported accompanying overdose.

    Management of overdose

    Establish and maintain an airway to ensure adequate ventilation and oxygenation. Gastric evacuation by lavage and use of activated charcoal should be considered. Careful observation and cardiac and vital sign monitoring are recommended, along with general symptomatic and supportive care. Due to the large volume of distribution of escitalopram, forced diuresis, dialysis, hemoperfusion, and exchange transfusion are unlikely to be of benefit. There are no specific antidotes for Lexapro.

    In managing overdosage, consider the possibility of multiple-drug involvement. The physician should consider contacting a poison control center for additional information on the treatment of any overdose.

    Adverse reactions, side effects:

    Most commonly observed side effects (incidence >= 5% and at least twice the incidence of placebo patients) of escitalopram are: insomnia, ejaculation disorder (primarily ejaculatory delay), nausea, sweating increased, fatigue and somnolence, decreased libido, and anorgasmia.

    To report suspected adverse reactions of Lexapro (Escitalopram Oxalate) tablets, contact Allergan pharmaceutical company or your local FDA.

    Drug interactions:

    Concomitant use with SSRIs, SNRIs or tryptophan is not recommended.

    Use caution when concomitant use with drugs that affect hemostasis (NSAIDs, aspirin, warfarin).

    Use in specific populations:

  • Pregnancy: use only if the potential benefit justifies the potential risk to the fetus.
  • Nursing mothers: caution should be exercised when administered to a nursing woman.
  • Pediatric use: safety and effectiveness of Lexapro has not been established in pediatric MDD patients less than 12 years of age.

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