Product image of Mirtazapine Teva Uk (Mirtazapine) supplied by GNH India

Mirtazapine Teva Uk

Active Ingredient:
Mirtazapine
Origin:
EU

Mirtazapine Teva Uk (Mirtazapine)

Mirtazapine, the active ingredient in Mirtazapine Teva Uk, 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.
GNH India supplies Mirtazapine Teva Uk as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Teva Uk Limited

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Indications & Clinical Uses

Mirtazapine is a noradrenergic and specific serotonergic antidepressant indicated for depressive disorders.

  • Major depressive disorder: alleviates depressive symptoms and improves mood in adults.
  • Depressive episodes associated with major depressive disorder: reduces severity and frequency of episodes.
  • Treatment‑resistant depression (as adjunct): may enhance response when other agents are insufficient.

How It Works

  • Mirtazapine antagonizes central presynaptic α2‑adrenergic receptors, increasing norepinephrine release, and blocks serotonin 5‑HT2 and 5‑HT3 receptors, enhancing serotonergic transmission while reducing associated side effects. This combined action raises synaptic concentrations of norepinephrine and serotonin, contributing to its antidepressant effect.

Side Effects

Mirtazapine may cause a range of adverse reactions that vary in frequency and severity.

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 difficult bowel movements.
  • Dizziness: sensation of light‑headedness.
  • Peripheral edema: mild swelling of the lower limbs.

Serious or Rare Side Effects

  • Agranulocytosis: severe reduction in white blood cells.
  • Seizures: occurrence of convulsive episodes.
  • Severe hypersensitivity: rash, swelling, or breathing difficulty.
  • Hepatic dysfunction: abnormal liver enzyme elevations.
  • Suicidal thoughts: emergence or worsening of suicidal ideation.
  • Hyponatremia: low blood sodium levels.

Precautions & Warnings

Before initiating therapy, consider patient‑specific factors and monitor for safety concerns.

  • Pregnancy: safety not established; weigh potential benefits against risks.
  • Breastfeeding: excreted in milk; assess infant risk before use.
  • Elderly patients: start at low dose and monitor for excessive sedation.
  • Hepatic impairment: dose adjustment may be required.
  • Concomitant CNS depressants: increased risk of sedation and respiratory depression.
  • Store at ambient temperature: keep below 25 °C, retain in 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 serotonin syndrome.
  • Central nervous system depressants (e.g., benzodiazepines, opioids): profound sedation.
  • Potent CYP2D6 inhibitors (e.g., fluoxetine, paroxetine): increased mirtazapine plasma levels.

Moderate Interactions (Monitor Closely)

  • Other serotonergic agents (e.g., SSRIs, SNRIs): potential additive serotonergic effects.
  • Anticholinergic drugs: heightened anticholinergic burden.
  • Alcohol: may exacerbate CNS depression.
  • Warfarin: possible alteration of INR, monitor coagulation parameters.

Frequently Asked Questions

Mirtazapine Teva Uk is an oral antidepressant belonging to the NaSSA class. It is prescribed primarily for the treatment of major depressive disorder in adult patients, helping to relieve depressive symptoms and improve overall mood.

Mirtazapine blocks presynaptic α2‑adrenergic receptors, which increases norepinephrine release, and antagonizes serotonin 5‑HT2 and 5‑HT3 receptors. This dual action raises the levels of norepinephrine and serotonin in the synapse, producing an antidepressant effect while reducing certain serotonergic side effects.

The appropriate dose of Mirtazapine Teva Uk 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 data for mirtazapine in pregnancy and lactation are limited. It should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision should be made in consultation with a healthcare professional.

To place an order, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India supplies 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 and SNRIs by its unique receptor profile, offering strong antihistaminic activity that can cause sedation and weight gain. It may be preferred when patients need a sedating effect or have poor response to other antidepressant classes.

Store the tablets at ambient temperature, preferably below 25 °C. Keep them in the original container, protect from moisture and direct light, and ensure the packaging remains tightly closed to maintain product stability.

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

Serious risks include agranulocytosis, severe hypersensitivity reactions, hepatic dysfunction, seizures, and the emergence or worsening of suicidal thoughts. Patients should be monitored closely for any signs of these conditions, especially during treatment initiation.

Mirtazapine is contraindicated in patients taking monoamine oxidase inhibitors (MAOIs) within 14 days, those with known hypersensitivity to the drug, and individuals with severe hepatic impairment without dose adjustment. It should also be used with caution in the elderly and in patients with a history of bipolar disorder.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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