Product image of Irenor (Reboxetine) supplied by GNH India

Irenor

Active Ingredient:
Reboxetine
Origin:
EU

Irenor (Reboxetine)

Reboxetine, the active ingredient in Irenor, is a selective norepinephrine reuptake inhibitor presented as an oral tablet for oral administration. By increasing synaptic norepinephrine levels, it helps alleviate depressive symptoms. The medication is indicated for the management of major depressive disorder in adult patients who require pharmacologic therapy. It is typically prescribed when other first‑line agents are unsuitable or have been ineffective.

GNH India supplies Irenor as a licensed, GDP‑compliant international pharmaceutical supplier, providing the product to hospitals, pharmacies and clinics worldwide with quality assurance and reliable logistics.

Manufacturer / TM Owner

Pfizer S.L.

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Indications & Clinical Uses

Reboxetine is a selective norepinephrine reuptake inhibitor used in the treatment of depressive disorders.

  • Major depressive disorder: alleviates depressive symptoms and improves mood in adult patients.

How It Works

  • Reboxetine blocks the norepinephrine transporter (NET) on presynaptic neurons, preventing the reuptake of norepinephrine from the synaptic cleft. This inhibition raises extracellular norepinephrine concentrations, enhancing noradrenergic neurotransmission, which contributes to mood elevation and reduction of depressive symptoms.

Side Effects

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

Common Side Effects

  • Nausea: mild to moderate stomach upset that often resolves with continued use.
  • Dry mouth: reduced salivation leading to a feeling of thirst.
  • Insomnia: difficulty falling or staying asleep.
  • Dizziness: light‑headed sensation, especially when standing quickly.

Serious or Rare Side Effects

  • Elevated blood pressure: significant rise requiring medical monitoring.
  • Suicidal thoughts or behavior: emergence or worsening of depressive ideation.
  • Severe liver injury: rare hepatotoxicity presenting with jaundice or abnormal liver tests.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety measures.

  • Assess cardiovascular status: monitor blood pressure and heart rate regularly.
  • Review psychiatric history: watch for worsening depression or emergence of suicidal ideation.
  • Avoid abrupt discontinuation: taper the dose under medical supervision to reduce withdrawal effects.
  • Use caution in hepatic impairment: evaluate liver function and adjust therapy if necessary.
  • Pregnancy and lactation: discuss potential risks with the prescriber before use.
  • Store at ambient temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Reboxetine can interact with other medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Monoamine oxidase inhibitors (MAOIs): concurrent use may cause hypertensive crisis.
  • Tricyclic antidepressants: combined therapy can increase cardiovascular side effects.

Moderate Interactions (Monitor Closely):\n- Beta‑blockers: may mask tachycardia, requiring heart‑rate monitoring.

  • Antihypertensive agents: additive blood‑pressure‑lowering effect may occur.
  • CYP2D6 inhibitors (e.g., fluoxetine, quinidine): can raise reboxetine plasma concentrations, necessitating dose adjustment.

Frequently Asked Questions

Irenor contains reboxetine, which is prescribed for the treatment of major depressive disorder in adult patients. It helps improve mood and reduce depressive symptoms by enhancing norepinephrine activity in the brain.

Reboxetine inhibits the norepinephrine transporter, preventing the reuptake of norepinephrine into presynaptic neurons. This raises the level of norepinephrine in the synaptic cleft, strengthening noradrenergic signaling that is associated with mood regulation.

The dosage of Irenor is individualized by the prescribing clinician based on the patient’s condition, response, and tolerability. The prescriber determines the appropriate strength, frequency, and duration of therapy.

Safety data for reboxetine in pregnancy and lactation are limited. Healthcare providers should weigh potential benefits against possible risks and discuss these considerations with the patient before initiating therapy.

To place an order, submit an enquiry on the Irenor 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.

Irenor belongs to the selective norepinephrine reuptake inhibitor class, which differs from selective serotonin reuptake inhibitors (SSRIs) and tricyclic antidepressants. Its primary action is on norepinephrine rather than serotonin, offering an alternative mechanism for patients who do not respond adequately to SSRIs.

Irenor should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the tablets from moisture, excessive heat, and direct light to maintain stability.

Irenor is taken orally, usually with or without food, as directed by the prescribing clinician. The tablet should be swallowed whole with a glass of water and not crushed or chewed unless specifically instructed.

Serious risks include significant elevation of blood pressure, emergence or worsening of suicidal thoughts, and rare cases of severe liver injury. Patients should be monitored regularly for these events, especially during treatment initiation and dose changes.

Irenor is contraindicated in patients taking monoamine oxidase inhibitors, those with known hypersensitivity to reboxetine, and individuals with uncontrolled hypertension. It should also be used with caution in patients with severe hepatic impairment or a history of suicidal behavior.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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