Product image of Magrilan (Fluoxetine Hydrochloride) supplied by GNH India

Magrilan

Active Ingredient:
Fluoxetine Hydrochloride
Origin:
EU

Magrilan (Fluoxetine Hydrochloride)

Fluoxetine, the active ingredient in Magrilan, is a selective serotonin reuptake inhibitor (SSRI) presented as an oral tablet for oral use. It is prescribed to treat depressive and anxiety‑related disorders in adult patients, helping to restore normal mood balance and reduce compulsive symptoms.

GNH India supplies Magrilan as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, adhering to stringent quality standards and providing reliable global distribution. The company ensures compliance with EU pharmacopeial specifications and offers comprehensive support for regulatory documentation.

Manufacturer / TM Owner

Medochemie Ltd.

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Indications & Clinical Uses

  • Fluoxetine acts on the serotonergic pathway and is indicated for several psychiatric conditions.
  • Major depressive disorder: alleviates depressive symptoms and improves functional outcomes.
  • Obsessive‑compulsive disorder: reduces obsessions and compulsive behaviors.
  • Panic disorder: decreases frequency and severity of panic attacks.
  • Bulimia nervosa: helps reduce binge‑eating and purging cycles.
  • Premenstrual dysphoric disorder: eases mood swings and physical symptoms associated with the luteal phase.

How It Works

  • Fluoxetine selectively inhibits the serotonin transporter (SERT) on presynaptic neurons, blocking reuptake of serotonin from the synaptic cleft. This increases extracellular serotonin concentrations, enhancing serotonergic neurotransmission and leading to downstream neuroadaptive changes that improve mood and anxiety regulation.

Side Effects

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

Common Side Effects

  • Nausea
  • Headache
  • Insomnia
  • Dry mouth
  • Diarrhea

Serious or Rare Side Effects

  • Suicidal thoughts or behavior
  • Serotonin syndrome
  • Severe allergic reaction (anaphylaxis)
  • Abnormal bleeding or bruising

Precautions & Warnings

  • Before initiating therapy, clinicians should consider several safety measures.
  • Assess psychiatric history: monitor for worsening depression or emergence of suicidal ideation, especially during early treatment.
  • Avoid abrupt discontinuation: taper under medical supervision to reduce discontinuation syndrome.
  • Use caution in patients with hepatic impairment: dose adjustment may be required.
  • Consider drug interactions: review concomitant serotonergic agents.
  • Store at ambient temperature: keep in original container, protect from moisture and light.

Avoid Interactions

Fluoxetine interacts with several drug classes; careful assessment is required.

Major Interactions (Avoid)

  • Monoamine oxidase inhibitors (MAOIs): risk of serotonin syndrome.
  • Tricyclic antidepressants: increased risk of cardiac toxicity.
  • Pimozide: can cause serious cardiac effects.

Moderate Interactions (Monitor Closely)

  • NSAIDs or anticoagulants: may increase bleeding risk.
  • CYP2D6 inhibitors (e.g., quinidine): may raise fluoxetine plasma levels.

Frequently Asked Questions

Magrilan (fluoxetine) is approved for major depressive disorder, obsessive‑compulsive disorder, panic disorder, bulimia nervosa, and premenstrual dysphoric disorder. In each condition it helps to alleviate core symptoms such as low mood, intrusive thoughts, panic attacks, binge‑purge cycles, or severe menstrual‑related mood changes.

Fluoxetine blocks the serotonin transporter on presynaptic nerve terminals, preventing reuptake of serotonin. This raises serotonin levels in the synaptic cleft, enhancing serotonergic signaling and promoting neurochemical adaptations that improve mood, reduce anxiety, and lessen compulsive behaviors.

The exact dose of Magrilan is individualized by the prescribing clinician based on the patient’s diagnosis, severity of symptoms, treatment response, and any relevant medical conditions. Dosage adjustments are made during follow‑up visits to achieve optimal therapeutic effect while minimizing side effects.

The safety of fluoxetine during pregnancy and lactation has not been definitively established. Healthcare providers weigh potential benefits against possible risks to the fetus or infant. Women who are pregnant, planning pregnancy, or breastfeeding should discuss treatment options with their physician.

To request Magrilan, 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.

Magrilan belongs to the SSRI class, which generally offers a favorable side‑effect profile compared with older tricyclic antidepressants and monoamine oxidase inhibitors. Compared with other SSRIs, fluoxetine has a long half‑life, which may simplify dosing but also requires careful tapering to avoid discontinuation symptoms.

Magrilan tablets should be stored at ambient temperature, below 25 °C (77 °F). Keep them in the original packaging, protect from moisture and direct light, and store out of reach of children.

Magrilan is taken orally as a tablet. It should be swallowed whole with a glass of water, with or without food, as directed by the prescriber. Patients should follow the dosing schedule provided and not alter the regimen without medical advice.

The most serious risks include the emergence of suicidal thoughts or behaviors, especially in young adults during early treatment, and serotonin syndrome, a potentially life‑threatening condition that can occur when fluoxetine is combined with other serotonergic agents. Severe allergic reactions and abnormal bleeding are also rare but critical concerns.

Magrilan should be avoided in individuals who are currently taking monoamine oxidase inhibitors, have a known hypersensitivity to fluoxetine or any tablet excipients, or have uncontrolled narrow‑angle glaucoma. Caution is also advised for patients with severe hepatic impairment or a history of bipolar disorder, where mood switching may occur.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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