Product image of Mirabegron Avansor (Mirabegron) supplied by GNH India

Mirabegron Avansor

Active Ingredient:
Mirabegron
Origin:
EU

Mirabegron Avansor (Mirabegron)

Mirabegron, the active ingredient in Mirabegron Avansor, is a β3‑adrenergic receptor agonist presented as an oral tablet for oral use. It is indicated for the management of overactive bladder symptoms, including urinary urgency and frequency, in adult patients and can improve quality of life.

GNH India supplies Mirabegron Avansor as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory documentation to support import and distribution. Customers benefit from reliable lead times and comprehensive technical support.

Manufacturer / TM Owner

Avansor Pharma Oy

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Indications & Clinical Uses

Mirabegron acts on the β3‑adrenergic receptors of the bladder detrusor muscle, addressing overactive bladder and related symptoms.

  • Overactive bladder: increases bladder capacity and reduces urgency and frequency.
  • Urinary urgency: lessens sudden urge to void, improving control.
  • Urinary frequency: decreases the number of daily voids, enhancing daily activities.

How It Works

  • Mirabegron selectively stimulates β3‑adrenergic receptors located on the detrusor smooth muscle of the urinary bladder. Activation of these receptors raises intracellular cyclic adenosine monophosphate (cAMP) levels, leading to relaxation of the detrusor during the storage phase. This relaxation expands functional bladder capacity, thereby diminishing involuntary contractions that cause urgency and frequency. The effect is dose‑dependent and persists throughout the dosing interval, providing continuous symptom control without directly affecting the sphincter or causing anticholinergic activity.

Side Effects

Mirabegron may be associated with a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Hypertension
  • Nasopharyngitis
  • Headache

Serious or Rare Side Effects

  • Severe hypertension
  • Urinary retention requiring catheterisation
  • Angioedema

Precautions & Warnings

When prescribing Mirabegron, consider the following precautions:

  • Renal impairment: assess renal function and consider dose adjustment.
  • Hepatic impairment: use with caution in patients with moderate hepatic dysfunction.
  • Hypertension: monitor blood pressure regularly during therapy.
  • Concomitant use with strong CYP2D6 inhibitors: may increase mirabegron exposure.
  • Pregnancy: safety not established; avoid unless benefits outweigh risks.
  • Store at ambient temperature: keep in original container, protect from moisture and light.

Avoid Interactions

Mirabegron can interact with several drug classes; awareness of these interactions helps optimise therapy.

Major Interactions (Avoid)

  • Strong CYP2D6 inhibitors (e.g., paroxetine, fluoxetine): may markedly increase mirabegron plasma concentrations.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): can raise exposure and risk of adverse events.
  • Co‑administration with anticholinergic agents for bladder: may reduce therapeutic benefit.

Moderate Interactions (Monitor Closely)

  • Diuretics: may enhance hypotensive effect, monitor blood pressure.
  • Nitrates: additive vasodilatory effect, observe for dizziness.
  • Other β3‑adrenergic agonists: potential additive pharmacodynamic effect.

Frequently Asked Questions

Mirabegron Avansor is prescribed for the treatment of overactive bladder symptoms, including urinary urgency, frequency, and urge incontinence. It helps increase bladder capacity and reduce the frequency of involuntary bladder contractions in adult patients.

Mirabegron selectively activates β3‑adrenergic receptors on the detrusor smooth muscle of the bladder. This activation raises intracellular cAMP, causing muscle relaxation during the storage phase, which expands bladder capacity and lessens urgency and frequency.

The prescribed dose of mirabegron is determined by the treating physician based on the individual’s clinical condition, renal and hepatic function, and response to therapy. Dose adjustments may be made according to professional guidelines.

Safety data for mirabegron during pregnancy and lactation are limited. It is generally advised to avoid use unless the potential benefit justifies the potential risk to the fetus or infant, and the decision should be made by a qualified 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 required import documentation.

The primary alternative for overactive bladder is the antimuscarinic class (e.g., oxybutynin). Mirabegron, as a β3‑adrenergic agonist, does not have anticholinergic side effects such as dry mouth or constipation, and may be better tolerated in patients who experience those adverse effects with antimuscarinics.

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

Mirabegron Avansor is taken orally as a tablet. The tablet should be swallowed whole with a glass of water and can be taken with or without food, as directed by the prescribing clinician.

Serious risks include severe hypertension, urinary retention that may require catheterisation, and angioedema. Patients should be monitored for rapid increases in blood pressure, difficulty emptying the bladder, and signs of allergic reactions such as swelling of the face or throat.

Mirabegron is contraindicated in patients with uncontrolled severe hypertension, known hypersensitivity to mirabegron or any excipients, and those who are unable to tolerate the drug’s effects on bladder function. Caution is also advised in patients with significant renal or hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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