Product image of Mirtazapina Flas Alter (Mirtazapine) supplied by GNH India

Mirtazapina Flas Alter

Active Ingredient:
Mirtazapine
Origin:
EU

Mirtazapina Flas Alter (Mirtazapine)

Mirtazapine, the active ingredient in Mirtazapina Flas Alter, is a NaSSA (noradrenergic and specific serotonergic antidepressant) presented as an oral formulation for oral use. It is indicated for the treatment of major depressive disorder in adult patients.

GNH India supplies Mirtazapina Flas Alter as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable logistics for global distribution. Clients benefit from competitive pricing, regulatory support, and dedicated technical assistance throughout the procurement process.

Manufacturer / TM Owner

Laboratorios Alter, S.A.

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Indications & Clinical Uses

Mirtazapine is used primarily in the treatment of depressive disorders, acting on noradrenergic and serotonergic pathways.

  • Major depressive disorder: reduces depressive symptoms and improves mood in adult patients.
  • Depressive disorder with anxiety: alleviates both depressive and anxiety symptoms.
  • Treatment‑resistant depression: may be considered when other antidepressants have not provided adequate response.

How It Works

  • Mirtazapine exerts its antidepressant effect by antagonising central presynaptic α2‑adrenergic receptors, which increases the release of norepinephrine and serotonin. It also blocks postsynaptic 5‑HT2 and 5‑HT3 receptors and histamine H1 receptors, enhancing serotonergic transmission while producing sedative and appetite‑stimulating effects. These pharmacodynamic properties contribute to its efficacy in patients who have not responded to other agents.

Side Effects

Mirtazapine may cause a range of adverse reactions, varying from mild to serious.

Common Side Effects

  • Sedation or drowsiness: may cause daytime sleepiness, especially at treatment initiation.
  • Increased appetite and weight gain: patients often experience heightened hunger and gradual weight increase.
  • Dry mouth: reduced salivation leading to discomfort and potential dental issues.

Serious or Rare Side Effects

  • Agranulocytosis or severe neutropenia: marked reduction in white blood cells requiring immediate medical attention.
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis: severe skin reactions characterized by blistering and detachment.
  • Suicidal thoughts or behavior: emergence of suicidal ideation, particularly during early weeks of therapy.

Precautions & Warnings

When prescribing mirtazapine, several safety considerations should be observed.

  • Assess hepatic function: evaluate liver disease severity and adjust dosage if needed.
  • Monitor weight: regular checks are advised due to risk of significant weight gain.
  • Screen for suicidal ideation: closely observe patients, especially during the first few weeks.
  • Use caution in elderly: increased sensitivity to sedation and orthostatic hypotension.
  • Avoid abrupt discontinuation: tapering is recommended to prevent withdrawal symptoms.
  • Store at ambient temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Mirtazapine can interact with other medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • MAO inhibitors: concurrent use may precipitate hypertensive crisis.
  • Strong CYP2D6 inhibitors (e.g., fluoxetine, paroxetine): can raise mirtazapine plasma concentrations.
  • CNS depressants (e.g., benzodiazepines, alcohol): may enhance sedative effects.

Moderate Interactions (Monitor Closely)

  • Anticholinergic agents: additive dry‑mouth and constipation.
  • Other serotonergic drugs (e.g., SSRIs, SNRIs, tramadol): risk of serotonin syndrome.
  • Warfarin: possible alteration of INR, requiring coagulation monitoring.

Frequently Asked Questions

Mirtazapina Flas Alter contains mirtazapine, which is prescribed for the management of major depressive disorder in adult patients. It helps to alleviate depressive symptoms such as low mood, loss of interest, and associated anxiety, improving overall functional capacity.

Mirtazapine works by blocking presynaptic α2‑adrenergic receptors, leading to increased release of norepinephrine and serotonin. It also antagonises postsynaptic 5‑HT2, 5‑HT3 and histamine H1 receptors, which together enhance mood, promote sleep and stimulate appetite.

The appropriate dose of mirtazapine is individualized and determined by the prescribing clinician based on the patient’s clinical condition, response, and tolerability. Dosage adjustments are made according to therapeutic response and any observed side effects.

Safety data for mirtazapine in pregnancy and lactation are limited. Healthcare providers should weigh potential benefits against possible risks and discuss any concerns with the patient. Use only if clearly needed and under medical supervision.

To place an order, submit an enquiry on the product page at gnhindia.com specifying the required quantity of Mirtazapina Flas Alter. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Mirtazapine differs from SSRIs by its dual noradrenergic and serotonergic activity and strong antihistamine effect, which often leads to sedation and weight gain. While SSRIs primarily increase serotonin levels, mirtazapine may be preferred when patients need a sedating agent or have poor appetite, but individual response varies.

Store the product at ambient temperature, preferably below 25 °C. Keep it in the original packaging, protect it from moisture, heat and direct light to maintain stability throughout its shelf life.

Mirtazapina Flas Alter is taken orally. The tablet or capsule should be swallowed whole with a glass of water, with or without food, as directed by the prescribing clinician.

Serious adverse reactions include agranulocytosis or severe neutropenia, severe skin reactions such as Stevens‑Johnson syndrome, and emergence of suicidal thoughts or behaviors, especially during the early weeks of therapy. Immediate medical attention is required if any of these occur.

Mirtazapine should be avoided in individuals with known hypersensitivity to the drug, those who have taken an MAO inhibitor within the past 14 days, patients with severe hepatic impairment, and anyone for whom the risk‑benefit profile is unfavorable as assessed by their healthcare provider.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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