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

Mirtazapin Krka

Active Ingredient:
Mirtazapine
Origin:
EU

Mirtazapin Krka (Mirtazapine)

Mirtazapine, the active ingredient in Mirtazapin Krka, is a NaSSA presented as an oral dosage form for oral use. It is indicated for the treatment of major depressive disorder in adult patients.
GNH India supplies Mirtazapin Krka as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Krka, D.D., Novo Mesto

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Indications & Clinical Uses

Mirtazapine acts as an antidepressant within the NaSSA class, targeting depressive disorders.

  • Major depressive disorder: alleviates depressive symptoms and improves mood in adults.
  • Depressive episodes associated with bipolar disorder: may be used as an adjunct to stabilize mood under specialist supervision.
  • Treatment‑resistant depression: considered when first‑line agents are ineffective, under careful clinical evaluation.

How It Works

  • Mirtazapine antagonizes central presynaptic α2‑adrenergic receptors, enhancing noradrenergic release, and blocks 5‑HT2, 5‑HT3 and H1 receptors, which together increase serotonergic and noradrenergic neurotransmission while providing antihistaminic effects that contribute to its therapeutic profile.

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
  • Orthostatic hypotension

Serious or Rare Side Effects

  • Agranulocytosis or severe neutropenia
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis
  • Suicidal thoughts or behavior, especially early in treatment
  • Seizures
  • Hepatic dysfunction
  • Severe allergic reactions (anaphylaxis)

Precautions & Warnings

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

  • Monitor weight: watch for significant gain and metabolic changes.
  • Assess mood: watch for emergence of suicidal ideation, especially in early treatment.
  • Evaluate liver function: consider baseline tests in patients with hepatic disease.
  • Caution with CNS depressants: avoid excessive sedation when combined with alcohol or benzodiazepines.
  • Store below 25°C: keep in the original pack, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Monoamine oxidase inhibitors (MAOIs): risk of hypertensive crisis.
  • Other serotonergic agents (e.g., SSRIs, SNRIs, tramadol): potential serotonin syndrome.
  • CNS depressants (e.g., alcohol, benzodiazepines): enhanced sedation.
  • CYP2D6 inhibitors (e.g., fluoxetine, paroxetine): increased mirtazapine plasma levels.
  • Anticholinergic drugs: additive anticholinergic burden.

Moderate Interactions (Monitor Closely)

  • Antihypertensives: possible additive hypotensive effect.
  • Carbamazepine: may reduce mirtazapine concentrations.
  • Warfarin: monitor INR for possible alteration.
  • Anticonvulsants: may affect seizure threshold.
  • Herbal supplements (e.g., St. John’s wort): could modify serotonergic activity.

Frequently Asked Questions

Mirtazapin Krka contains the active ingredient mirtazapine, which is prescribed primarily for the treatment of major depressive disorder in adults. It helps alleviate depressive symptoms by enhancing noradrenergic and serotonergic neurotransmission.

Mirtazapine blocks presynaptic α2‑adrenergic receptors, leading to increased release of norepinephrine and serotonin. It also antagonizes 5‑HT2, 5‑HT3 and H1 receptors, which together improve mood, reduce anxiety and produce a sedative effect.

The appropriate dose of Mirtazapin Krka is determined by the prescribing clinician based on the patient’s condition, response to therapy and tolerability. Dosage adjustments are made according to individual clinical judgment.

Safety data for mirtazapine in pregnancy and lactation are limited. The prescriber should weigh potential benefits against possible risks and consider alternative treatments when appropriate.

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.

Mirtazapin Krka (mirtazapine) belongs to the NaSSA class, differing from SSRIs and SNRIs by its receptor profile. It often provides stronger sedative and appetite‑stimulating effects, which can be advantageous in patients with insomnia or weight loss, but may be less suitable for those who need to avoid sedation.

Mirtazapin Krka should be stored at temperatures below 25 °C in its original packaging, protected from moisture and direct sunlight. Keep the product out of reach of children and do not use if the packaging is damaged.

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

Serious risks include the potential for agranulocytosis, severe allergic reactions such as Stevens‑Johnson syndrome, and the emergence of suicidal thoughts, particularly during the initial weeks of therapy. Prompt medical attention is required if any of these occur.

Mirtazapin Krka is contraindicated in patients taking monoamine oxidase inhibitors (MAOIs) within the past 14 days, those with known hypersensitivity to mirtazapine, and individuals with severe hepatic impairment without specialist supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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