Product image of Mirtastad (Mirtazapine) supplied by GNH India

Mirtastad

Active Ingredient:
Mirtazapine
Origin:
EU

Mirtastad (Mirtazapine)

Mirtazapine, the active ingredient in Mirtastad, is a NaSSA (noradrenergic and specific serotonergic antidepressant) presented as an oral dosage form for oral use. It is prescribed for the treatment of major depressive disorder in adult patients.

GNH India supplies Mirtastad as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company follows stringent quality standards and provides regulatory documentation to support import and distribution across multiple regions. Our reliable logistics network ensures timely delivery and product integrity for healthcare providers.

Manufacturer / TM Owner

Stada Arzneimittel Ag

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Indications & Clinical Uses

  • Mirtazapine is indicated for depressive disorders and is used primarily in the management of major depressive episodes.
  • Major depressive disorder: reduces core depressive symptoms such as low mood, loss of interest, and impaired concentration, thereby improving overall functioning in adult patients.
  • Treatment‑resistant depression: may be introduced as an adjunct when standard antidepressants (e.g., SSRIs or SNRIs) have not achieved adequate clinical response, offering an alternative mechanism of action.
  • Depressive episodes with prominent insomnia or anxiety: helps alleviate sleep disturbances and anxiety symptoms that frequently accompany depression, contributing to better sleep quality and reduced agitation.

How It Works

  • Mirtazapine acts as an antagonist at central presynaptic α2‑adrenergic receptors, which disinhibits norepinephrine release. It also blocks postsynaptic 5‑HT2 and 5‑HT3 receptors and histamine H1 receptors, enhancing serotonergic transmission while reducing serotonergic side‑effects. This pharmacologic profile also contributes to its sedative properties and appetite stimulation, which are clinically relevant.

Side Effects

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

Common Side Effects

  • Sedation or drowsiness
  • Increased appetite leading to weight gain
  • Dry mouth
  • Constipation

Serious or Rare Side Effects

  • Agranulocytosis or severe neutropenia
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis
  • Suicidal thoughts or behavior, especially early in treatment
  • Hyponatremia due to syndrome of inappropriate antidiuretic hormone secretion (SIADH)

Precautions & Warnings

When prescribing mirtazapine, clinicians should consider several safety precautions to minimize risk.

  • Monitor weight: patients may experience significant weight gain and should have regular weight checks.
  • Assess for suicidal ideation: especially during the initial weeks of therapy or dose changes.
  • Evaluate hepatic function: dose adjustment may be needed in severe liver impairment.
  • Caution with CNS depressants: concurrent use can enhance sedation and impair psychomotor performance.
  • Avoid abrupt discontinuation: tapering is recommended to reduce risk of withdrawal symptoms.
  • Store at room temperature (below 25°C): keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Mirtazapine can interact with other medicines; awareness of major and moderate interactions helps ensure safe use.

Major Interactions (Avoid)

  • Monoamine oxidase inhibitors (MAOIs): concurrent use may cause hypertensive crisis or serotonin syndrome.
  • Linezolid or other reversible MAO inhibitors: risk of severe serotonin toxicity.
  • Other serotonergic agents (e.g., SSRIs, SNRIs, triptans): increased risk of serotonin syndrome.

Moderate Interactions (Monitor Closely)

  • Central nervous system depressants (e.g., benzodiazepines, alcohol): may enhance sedation and respiratory depression.
  • CYP2D6 inhibitors (e.g., fluoxetine, paroxetine): can raise mirtazapine plasma levels.
  • Antihypertensive drugs: additive hypotensive effect may occur.
  • Anticholinergic medications: may worsen dry mouth and constipation.

Frequently Asked Questions

Mirtastad contains the active ingredient mirtazapine and is prescribed for the treatment of major depressive disorder in adult patients. It helps alleviate depressive symptoms such as low mood, loss of interest, and impaired concentration, improving overall functional status.

Mirtazapine works by blocking presynaptic α2‑adrenergic receptors, which increases norepinephrine release, and by antagonising postsynaptic 5‑HT2, 5‑HT3 and histamine H1 receptors. This combined action enhances noradrenergic and serotonergic neurotransmission while reducing certain serotonergic side‑effects, producing antidepressant and anxiolytic effects.

The appropriate dose of Mirtastad is determined by the prescribing physician based on the individual’s clinical condition, response to therapy, and tolerability. Dosage may be adjusted over time, and patients should follow the specific instructions provided by their healthcare professional.

Safety data for mirtazapine in pregnancy and lactation are limited. The drug should only be used if the potential benefit justifies any potential risk to the fetus or infant. Healthcare providers will evaluate the risk‑benefit profile for each patient before prescribing.

To request Mirtastad, submit an enquiry on the product page at gnhindia.com indicating the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including any cold‑chain requirements) and necessary import documentation.

Mirtastad belongs to the NaSSA class, offering a distinct mechanism compared with SSRIs or SNRIs that primarily inhibit serotonin reuptake. Its receptor profile provides strong sedative and appetite‑stimulating effects, which can be advantageous for patients with insomnia or weight loss, but may be less suitable for those who wish to avoid these effects.

Mirtastad should be stored at room temperature, below 25 °C, in its original packaging. Keep the product away from moisture, direct sunlight, and excessive heat. Ensure the container is tightly closed to maintain stability throughout its shelf life.

Mirtastad is taken orally, usually once daily, with or without food, as directed by the prescribing clinician. Patients should swallow the tablet whole with a glass of water and avoid crushing or chewing unless specifically instructed otherwise.

Serious risks include agranulocytosis or severe neutropenia, Stevens‑Johnson syndrome or toxic epidermal necrolysis, hyponatremia due to SIADH, and the emergence or worsening of suicidal thoughts, particularly during the early phase of treatment or after dose changes.

Mirtastad is contraindicated in patients with known hypersensitivity to mirtazapine or any of its excipients. Caution is advised for individuals taking monoamine oxidase inhibitors, those with severe hepatic impairment, or patients with a history of severe allergic reactions to similar agents.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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