Product image of Mirabegron supplied by GNH India

Mirabegron

Active Ingredient:
Mirabegron
Origin:
EU

Mirabegron

Mirabegron, the active ingredient in Mirabegron, is a β3‑adrenergic receptor agonist presented as an oral tablet for systemic use. It is indicated for the management of overactive bladder, reducing urinary urgency, frequency and incontinence episodes in adult patients.

GNH India supplies Mirabegron as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, providing reliable sourcing for regulated markets. The product complies with EU pharmacopeial specifications and undergoes rigorous quality control. It is packaged in moisture‑protected blisters to preserve tablet integrity during transport.

Manufacturer / TM Owner

Adalvo Limited

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Indications & Clinical Uses

Mirabegron is used to treat conditions related to overactive bladder by targeting β3‑adrenergic receptors in the bladder detrusor muscle.

  • Overactive bladder: increases functional bladder capacity and reduces urgency episodes.
  • Urinary urgency: lessens the sudden, compelling need to void.
  • Urinary frequency: decreases the number of daily voids, improving quality of life.

How It Works

  • Mirabegron selectively activates β3‑adrenergic receptors located on detrusor smooth muscle. Receptor activation raises intracellular cyclic AMP, leading to relaxation of the detrusor muscle during the storage phase of the micturition cycle. This relaxation expands bladder capacity and diminishes involuntary contractions, thereby reducing urgency, frequency, and urge incontinence in patients with overactive bladder.

Side Effects

Adverse reactions may occur with Mirabegron use. Patients should be aware of both common and serious possibilities.

Common Side Effects

  • Hypertension: elevated blood pressure readings.
  • Headache: mild to moderate intensity.
  • Nasopharyngitis: inflammation of the nasal passages and throat.
  • Urinary tract infection: signs of infection such as dysuria.
  • Constipation: reduced bowel movements.
  • Dry mouth: decreased salivation.

Serious or Rare Side Effects

  • Angioedema: swelling of face, lips, or tongue.
  • Severe hypertension: rapid and significant blood pressure rise.
  • Urinary retention: difficulty initiating or maintaining urine flow.
  • Tachycardia: increased heart rate.
  • Allergic reactions: rash, pruritus, or anaphylaxis.
  • Myocardial infarction: rare cardiac events.

Precautions & Warnings

Before initiating Mirabegron, clinicians should consider several safety measures.

  • Blood pressure monitoring: check baseline and periodic readings.
  • Renal function assessment: evaluate creatinine clearance in patients with kidney disease.
  • Urinary retention evaluation: ensure no pre‑existing obstruction.
  • Uncontrolled hypertension: avoid use in patients with severe hypertension.
  • Concomitant β‑agonists: use caution when combined with other β‑adrenergic agents.
  • Store at ambient temperature: keep in the original pack, protect from moisture.

Avoid Interactions

Mirabegron may interact with other medicines; some combinations require avoidance while others need close monitoring.

Major Interactions (Avoid)

  • Strong CYP2D6 inhibitors (e.g., paroxetine, fluoxetine): increase Mirabegron exposure.
  • Norepinephrine reuptake inhibitors (e.g., duloxetine): may raise blood pressure.
  • Other β‑agonists: additive cardiovascular effects.

Moderate Interactions (Monitor Closely)

  • Diuretics: potential alterations in fluid balance.
  • Anticholinergics: heightened risk of urinary retention.
  • NSAIDs: may affect renal function, especially in susceptible patients.

Frequently Asked Questions

Mirabegron is prescribed to manage overactive bladder symptoms, including urinary urgency, frequency, and urge incontinence, by increasing bladder capacity in adult patients.

Mirabegron selectively stimulates β3‑adrenergic receptors on detrusor smooth muscle, raising cyclic AMP levels, which relaxes the muscle during bladder filling and reduces involuntary contractions.

The dose of Mirabegron is determined by the prescribing clinician based on the patient’s condition, renal function, and response; patients should follow the prescriber’s instructions.

The safety of Mirabegron in pregnancy and lactation has not been established. It should be used only if the potential benefit justifies any potential risk to the fetus or infant.

Submit an enquiry on the Mirabegron 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 antimuscarinics, Mirabegron works via β3‑adrenergic activation rather than cholinergic blockade, offering an alternative for patients who experience anticholinergic side effects such as dry mouth or constipation.

Store Mirabegron tablets at ambient temperature, below 25 °C, in the original packaging. Protect the tablets from moisture and direct sunlight to maintain stability.

Mirabegron is taken orally as a tablet, usually with or without food, according to the prescriber’s directions. Swallow the tablet whole with water; do not crush or split unless instructed.

Serious risks include significant hypertension, angioedema, urinary retention, tachycardia, and rare cardiac events such as myocardial infarction. Patients should seek immediate medical attention if these symptoms develop.

Mirabegron should be avoided in patients with uncontrolled hypertension, severe urinary retention, or known hypersensitivity to the drug. Caution is also advised for individuals taking strong CYP2D6 inhibitors.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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