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

Magrilan

Active Ingredient:
Fluoxetine Hydrochloride
Origin:
EU

Magrilan (Fluoxetine Hydrochloride)

Fluoxetine Hydrochloride, the active ingredient in Magrilan, is a selective serotonin reuptake inhibitor (SSRI) presented as an oral tablet for oral use. It is prescribed for major depressive disorder and several related psychiatric conditions in adult patients and is commonly utilized in clinical practice.

GNH India supplies Magrilan as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. Our distribution network adheres to stringent quality standards, ensuring product integrity from manufacturing sites in the EU to end‑users across multiple continents.

Manufacturer / TM Owner

Medochemie Ltd.

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Indications & Clinical Uses

Fluoxetine Hydrochloride is an SSRI that modulates serotonergic pathways to treat several psychiatric disorders.

  • Major depressive disorder: reduces depressive symptoms and improves overall mood.
  • Obsessive‑compulsive disorder: lessens compulsive thoughts and repetitive behaviors.
  • Panic disorder: decreases frequency and intensity of panic attacks.
  • Bulimia nervosa: helps control binge‑eating episodes and associated urges.
  • Premenstrual dysphoric disorder: alleviates mood swings and physical symptoms linked to the menstrual cycle.

How It Works

  • Fluoxetine selectively inhibits the serotonin transporter (SERT) on presynaptic neurons, blocking reuptake of serotonin (5‑HT) from the synaptic cleft. This increases extracellular serotonin concentrations, enhancing serotonergic neurotransmission throughout central nervous system pathways that regulate mood, anxiety, and appetite. The drug’s high affinity for SERT and minimal activity at other receptors underlies its therapeutic profile as an antidepressant.

Side Effects

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

Common Side Effects

  • Nausea
  • Headache
  • Insomnia
  • Dry mouth

Serious or Rare Side Effects

  • Serotonin syndrome
  • Suicidal thoughts or behavior
  • Severe allergic reaction (anaphylaxis)
  • Hyponatremia

Precautions & Warnings

When prescribing or dispensing Magrilan, consider the following precautions.

  • Assess psychiatric history: evaluate for depression severity and suicidal risk before initiating therapy.
  • Monitor for suicidal ideation: especially during the first few weeks of treatment or dosage changes.
  • Avoid abrupt discontinuation: taper the dose under medical supervision to reduce withdrawal symptoms.
  • Use caution in hepatic impairment: dose adjustment may be required in patients with liver dysfunction.
  • Contraindicated with MAO inhibitors: ensure a minimum 14‑day washout period when switching.
  • Store at ambient temperature: keep below 25 °C in the original container, protect from moisture and light.

Avoid Interactions

Fluoxetine can interact with several medicines; awareness of the interaction level is essential.

Major Interactions (Avoid)

  • Monoamine oxidase inhibitors (MAOIs): risk of serotonin syndrome; maintain at least a 14‑day washout period.
  • Pimozide or thioridazine: may cause cardiac arrhythmias when combined.
  • Linezolid or other serotonergic antibiotics: increase serotonin levels, raising syndrome risk.

Moderate Interactions (Monitor Closely)

  • NSAIDs and anticoagulants: may increase bleeding tendency.
  • CYP2D6 inhibitors (e.g., quinidine): can raise fluoxetine plasma levels.
  • Alcohol: may exacerbate CNS side effects such as dizziness or sedation.

Frequently Asked Questions

Magrilan contains fluoxetine hydrochloride, an SSRI indicated for the treatment of major depressive disorder, obsessive‑compulsive disorder, panic disorder, bulimia nervosa, and premenstrual dysphoric disorder in adult patients.

Fluoxetine blocks the serotonin transporter (SERT), preventing reuptake of serotonin into presynaptic neurons. This raises serotonin levels in the synaptic cleft, enhancing serotonergic signaling that influences mood, anxiety, and appetite regulation.

The appropriate dose of Magrilan is determined by the prescribing clinician based on the patient’s condition, response, and tolerability. Dosage regimens may vary, and any adjustments should be made under medical supervision.

Safety data for fluoxetine during pregnancy and lactation are limited, and the pregnancy category is listed as unknown. Clinicians should weigh potential benefits against risks and consider alternative therapies when appropriate.

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 (fluoxetine) is a long‑acting SSRI with a relatively long half‑life, which can simplify dosing and reduce withdrawal risk compared with shorter‑acting SSRIs. It shares the class‑wide efficacy for depression but may differ in side‑effect profiles and drug‑interaction potential.

Store Magrilan tablets at ambient temperature, preferably below 25 °C, in the original packaging. Protect from moisture, heat, and direct sunlight to maintain product stability throughout its shelf life.

Magrilan is taken orally, usually once daily with or without food, as directed by a healthcare professional. The tablet should be swallowed whole with water and not crushed or chewed unless specifically instructed.

Serious risks include serotonin syndrome, emergence of suicidal thoughts or behaviors, severe allergic reactions, hyponatremia, and cardiac arrhythmias in patients with pre‑existing conditions. Immediate medical attention is required if any of these symptoms appear.

Magrilan is contraindicated in individuals taking monoamine oxidase inhibitors (MAOIs) within the past 14 days, those with known hypersensitivity to fluoxetine, and patients with a history of severe serotonin syndrome. Caution is also advised for patients with uncontrolled narrow‑angle glaucoma or severe hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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