Product image of Mirtazapina Doc (Mirtazapine) supplied by GNH India

Mirtazapina Doc

Active Ingredient:
Mirtazapine
Origin:
EU

Mirtazapina Doc (Mirtazapine)

Mirtazapine, the active ingredient in Mirtazapina Doc, is a NaSSA (Noradrenergic and specific serotonergic antidepressant) presented as an oral tablet for oral use. It is prescribed for major depressive disorder in adult patients who require pharmacologic treatment.

GNH India supplies Mirtazapina Doc as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Doc Generici S.R.L.

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Indications & Clinical Uses

Mirtazapine is a noradrenergic and specific serotonergic antidepressant used primarily in depressive disorders.

  • Major depressive disorder: reduces depressive symptoms and improves overall mood.
  • Depressive episodes in bipolar disorder (adjunct): may lessen depressive phase severity when combined with a mood stabiliser.
  • Depression associated with chronic medical conditions: helps improve mood in patients with comorbid illnesses.

How It Works

  • Mirtazapine antagonises central presynaptic α2‑adrenergic receptors, enhancing noradrenaline release, and blocks serotonin 5‑HT2 and 5‑HT3 receptors while strongly inhibiting H1 histamine receptors. This combined activity increases serotonergic and noradrenergic neurotransmission, contributing to its antidepressant effect.

Side Effects

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

Common Side Effects

  • Sedation or drowsiness: feeling unusually sleepy.
  • Increased appetite and weight gain: heightened hunger leading to weight increase.
  • Dry mouth: reduced salivation.
  • Constipation: infrequent or hard stools.
  • Dizziness: sensation of light‑headedness.
  • Swelling of the limbs: peripheral oedema.

Serious or Rare Side Effects

  • Agranulocytosis: severe reduction in white blood cells.
  • Severe hypersensitivity: rash, itching, swelling, or difficulty breathing.
  • Suicidal thoughts: emergence or worsening of suicidal ideation.
  • Hepatic dysfunction: abnormal liver enzymes or jaundice.
  • Seizures: occurrence of convulsive episodes.
  • Unusual bleeding: spontaneous bruising or prolonged bleeding.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient history and monitor for specific risks.

  • Pregnancy: safety not established; avoid unless benefits outweigh risks.
  • Breastfeeding: excreted in milk; consider alternative therapy.
  • Elderly patients: start at low dose and monitor for sedation.
  • Hepatic impairment: dose adjustment may be required.
  • Concomitant CNS depressants: increased risk of excessive sedation.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture.

Avoid Interactions

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

Major Interactions (Avoid)

  • MAO inhibitors: risk of hypertensive crisis; discontinue MAOI at least 14 days prior.
  • CNS depressants (e.g., benzodiazepines, alcohol): profound sedation and respiratory depression.
  • CYP1A2 inhibitors (e.g., fluvoxamine): may increase mirtazapine plasma levels.

Moderate Interactions (Monitor Closely)

  • CYP2D6 substrates (e.g., codeine, tamoxifen): possible altered metabolism.
  • Anticholinergic agents: additive dry mouth and constipation.
  • Serotonergic agents (e.g., SSRIs, SNRIs): monitor for serotonin syndrome.

Frequently Asked Questions

Mirtazapina Doc contains mirtazapine, an antidepressant indicated for the treatment of major depressive disorder in adult patients. It helps alleviate depressive symptoms and improve overall mood when prescribed by a qualified healthcare professional.

Mirtazapine blocks central presynaptic α2‑adrenergic receptors, increasing noradrenaline release, and antagonises serotonin 5‑HT2 and 5‑HT3 receptors while strongly inhibiting H1 histamine receptors. This combined action enhances serotonergic and noradrenergic neurotransmission, producing an antidepressant effect.

The appropriate dose of Mirtazapina Doc is determined by the prescribing clinician based on the individual’s clinical condition, response, and tolerability. Dosage adjustments are made according to professional guidelines and patient needs.

Safety of mirtazapine in pregnancy has not been established, and it is excreted in breast milk. Use during pregnancy or lactation should only occur if the potential benefits outweigh the risks, and after consultation with a healthcare provider.

To 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 combined antagonism of α2‑adrenergic, 5‑HT2/5‑HT3 and H1 receptors. This profile often results in strong sedative effects and appetite stimulation, which can be advantageous for patients with insomnia or weight loss, but may be less suitable for those needing a non‑sedating option.

Mirtazapina Doc should be stored at ambient temperature, preferably below 25 °C. Keep the tablets in their original packaging, protect them from moisture and direct sunlight, and ensure they are out of reach of children.

Mirtazapina Doc is taken orally, usually once daily in the evening, with or without food, as directed by the prescriber. Swallow the tablet whole with a glass of water; do not crush or chew unless instructed otherwise.

Serious risks include agranulocytosis, severe hypersensitivity reactions, emergence or worsening of suicidal thoughts, hepatic dysfunction, seizures, and unusual bleeding. Patients should be monitored closely for these events, and any concerning symptoms should prompt immediate medical evaluation.

Mirtazapina Doc is contraindicated in patients with known hypersensitivity to mirtazapine or any of its excipients, and in those currently receiving monoamine oxidase inhibitors (MAOIs). Caution is advised for individuals with severe hepatic impairment, uncontrolled epilepsy, or a history of suicidal behaviour.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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