Product image of Mirtazapin Stada (Mirtazapine) supplied by GNH India

Mirtazapin Stada

Active Ingredient:
Mirtazapine
Origin:
EU

Mirtazapin Stada (Mirtazapine)

Mirtazapine, the active ingredient in Mirtazapin Stada, is a NaSSA (noradrenergic and specific serotonergic antidepressant) presented as an oral tablet for oral use. It is prescribed for the treatment of major depressive disorder in adult patients and helps improve mood, sleep, and appetite.

GNH India supplies Mirtazapin Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The product conforms to EU regulatory standards and is manufactured under GMP conditions. GNH India ensures reliable global distribution and regulatory compliance.

Manufacturer / TM Owner

Stadapharm Gmbh

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Indications & Clinical Uses

Mirtazapine is a NaSSA antidepressant used primarily in the treatment of mood disorders.

  • Major depressive disorder: reduces depressive symptoms and improves overall mood.
  • Depressive episodes with insomnia: promotes better sleep quality.
  • Depressive episodes with loss of appetite: stimulates appetite and weight gain.

How It Works

  • Mirtazapine antagonizes central presynaptic α2‑adrenergic receptors, leading to increased release of norepinephrine and serotonin. It also blocks 5‑HT2, 5‑HT3 and H1 receptors, which contributes to its antidepressant, anxiolytic, and sedative properties without directly stimulating serotonin reuptake.

Side Effects

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

Common Side Effects

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

Serious or Rare Side Effects

  • Agranulocytosis or severe neutropenia
  • Severe allergic reactions (e.g., angioedema, anaphylaxis)
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis
  • Suicidal thoughts or worsening depression
  • Hepatic dysfunction or jaundice
  • Seizures (rare).

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety aspects.

  • Hepatic function: assess liver enzymes in patients with hepatic impairment.
  • Mood monitoring: watch for worsening depression or emergence of suicidal ideation.
  • Cardiovascular status: use caution in patients with known heart disease.
  • Elderly patients: start at lower doses due to increased sensitivity to sedation.
  • Discontinuation: avoid abrupt cessation to reduce risk of rebound insomnia.
  • Store at below 25°C: keep in the original packaging, protect from moisture and light.

Avoid Interactions

Mirtazapine can interact with several drug classes, requiring careful management.

Major Interactions (Avoid)

  • Monoamine oxidase inhibitors (MAOIs): risk of hypertensive crisis.
  • CNS depressants (e.g., benzodiazepines, opioids): additive sedation.
  • Strong CYP2D6 inhibitors (e.g., fluoxetine, paroxetine): increase mirtazapine plasma levels.
  • Alcohol: may enhance sedative effects.
  • Other serotonergic agents: potential for serotonin syndrome.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., carbamazepine, phenytoin): may reduce efficacy.
  • Antihistamines: may increase anticholinergic burden.
  • Warfarin: monitor INR for possible anticoagulant effect alteration.
  • Lithium: observe lithium levels for potential toxicity.

Frequently Asked Questions

Mirtazapin Stada contains mirtazapine, which is prescribed to treat major depressive disorder in adult patients. It helps alleviate depressive symptoms, improve sleep, and increase appetite as part of a comprehensive treatment plan.

Mirtazapine blocks presynaptic α2‑adrenergic receptors, increasing norepinephrine and serotonin release. It also antagonizes 5‑HT2, 5‑HT3 and H1 receptors, providing antidepressant, anxiolytic, and sedative effects without directly inhibiting serotonin reuptake.

The appropriate dose of Mirtazapin Stada is determined by the prescribing clinician based on the individual’s clinical condition, response, and tolerability. Dosage adjustments are made according to professional medical guidance.

Safety data for mirtazapine in pregnancy and lactation are limited. Prescribers should weigh potential benefits against risks and consider alternative therapies when treating pregnant or nursing patients.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. 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 belongs to the NaSSA class, differing from SSRIs and SNRIs by its receptor‑blocking profile, which often results in pronounced sedative and appetite‑stimulating effects. This can be advantageous for patients with insomnia or weight loss, whereas other antidepressants may have a lower sedation risk.

Store the tablets at temperatures below 25 °C in their original container, protected from moisture and light. Do not expose the product to excessive heat or humidity to maintain its stability and potency.

Mirtazapin Stada is taken orally, usually once daily in the evening due to its sedative properties. The tablet should be swallowed whole with water and not chewed or crushed unless otherwise directed by a healthcare professional.

Serious risks include agranulocytosis, severe allergic reactions, Stevens‑Johnson syndrome, hepatic dysfunction, and the potential for worsening depression or emergence of suicidal thoughts, especially during treatment initiation or dose changes.

Mirtazapin Stada should be avoided in patients with known hypersensitivity to mirtazapine or any excipients, those currently on MAO inhibitors, and individuals with severe hepatic impairment unless specifically advised by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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