Product image of Opipramol 1 A Pharma (Opipramol Hydrochloride) supplied by GNH India

Opipramol 1 A Pharma

Active Ingredient:
Opipramol Hydrochloride
Origin:
EU

Opipramol 1 A Pharma (Opipramol Hydrochloride)

Opipramol Hydrochloride, the active ingredient in Opipramol 1 A Pharma, is an anxiolytic presented as an oral tablet for oral use. It is employed to alleviate anxiety symptoms and related mood disturbances in adult patients.
GNH India supplies Opipramol 1 A Pharma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

1 A Pharma Gmbh

1
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Indications & Clinical Uses

Opipramol is an anxiolytic that acts on central nervous system pathways involved in anxiety and mood regulation.

  • Generalized Anxiety Disorder: reduces excessive worry and tension.
  • Somatoform Disorder: alleviates medically unexplained physical symptoms linked to anxiety.
  • Depressive Disorder (adjunct): improves mood and sleep when used alongside other antidepressants.

How It Works

  • Opipramol exerts its therapeutic effect primarily through agonism at sigma‑1 receptors, which modulates neurotransmitter release and neuronal excitability. It also inhibits the reuptake of serotonin and norepinephrine and displays antihistaminic and anticholinergic activity, contributing to its anxiolytic and sedative properties.

Side Effects

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

Common Side Effects

  • Drowsiness: feeling unusually sleepy or fatigued.
  • Dry mouth: reduced salivation leading to discomfort.
  • Constipation: infrequent or difficult bowel movements.
  • Dizziness: light‑headed sensation, especially on standing.
  • Weight gain: gradual increase in body weight.
  • Blurred vision: temporary visual disturbances.

Serious or Rare Side Effects

  • Cardiac arrhythmia: irregular heart rhythm requiring medical attention.
  • Severe hypotension: marked drop in blood pressure causing faintness.
  • Seizures: convulsive episodes in susceptible individuals.
  • Hepatic dysfunction: abnormal liver enzymes or hepatitis.
  • Agranulocytosis: dangerously low white‑blood‑cell count.
  • Suicidal ideation: emergence of thoughts of self‑harm.

Precautions & Warnings

Before initiating Opipramol therapy, consider the following safety measures.

  • Cardiac assessment: evaluate history of heart disease or arrhythmias.
  • Liver monitoring: perform baseline and periodic liver function tests.
  • Gradual discontinuation: taper the dose to avoid withdrawal symptoms.
  • Elderly caution: start at lower doses due to increased sensitivity.
  • Alcohol avoidance: refrain from consuming alcohol as it may enhance sedation.
  • Store at room temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Opipramol can interact with several medication classes; awareness of these interactions helps prevent adverse outcomes.

Major Interactions (Avoid)

  • Monoamine oxidase inhibitors (MAOIs): risk of hypertensive crisis.
  • Central nervous system depressants (e.g., benzodiazepines, opioids): additive sedation and respiratory depression.
  • Alcohol: potentiates sedative effects and impairs coordination.

Moderate Interactions (Monitor Closely)

  • Antihistamines: may increase drowsiness.
  • Anticholinergic agents: enhance dry‑mouth and constipation.
  • CYP450 inhibitors (e.g., fluoxetine): can raise Opipramol plasma levels.
  • CYP450 inducers (e.g., carbamazepine): may reduce therapeutic effect.
  • Antihypertensives: monitor blood pressure for additive hypotensive effect.

Frequently Asked Questions

Opipramol 1 A Pharma is prescribed primarily for anxiety‑related conditions such as generalized anxiety disorder, somatoform disorders, and as an adjunct in depressive disorders to improve mood and sleep quality.

The drug acts as a sigma‑1 receptor agonist, modulating neurotransmitter release, while also inhibiting serotonin and norepinephrine reuptake and displaying antihistaminic and anticholinergic properties, which together produce anxiolytic and sedative effects.

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

Safety data are limited; therefore Opipramol should only be used during pregnancy or lactation if the potential benefit justifies the possible risk to the fetus or infant. Consultation with a healthcare professional is essential.

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.

Unlike benzodiazepines, Opipramol has a lower risk of dependence and primarily exerts its effect through sigma‑1 receptor agonism and serotonin‑norepinephrine reuptake inhibition, offering a different side‑effect profile that may be preferable for some patients.

Store the tablets at room temperature, below 25 °C, in the original container, protected from moisture and direct sunlight. Do not refrigerate or freeze the product.

Opipramol 1 A Pharma is taken orally, usually with or without food, as directed by the prescribing physician. Swallow the tablet whole with a glass of water.

Serious adverse events can include cardiac arrhythmias, severe hypotension, seizures, hepatic dysfunction, agranulocytosis, and emergence of suicidal thoughts. Patients should seek immediate medical attention if any of these occur.

Individuals with known hypersensitivity to Opipramol or any excipients, those currently on MAO inhibitors, patients with severe cardiac conduction disorders, and persons with uncontrolled glaucoma should avoid using this medication.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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