Product image of Mirabegron Teva Uk (Mirabegron) supplied by GNH India

Mirabegron Teva Uk

Active Ingredient:
Mirabegron
Origin:
EU

Mirabegron Teva Uk (Mirabegron)

Mirabegron, the active ingredient in Mirabegron Teva Uk, is a β3‑adrenergic receptor agonist presented as an oral tablet for systemic use. It is indicated for the treatment of overactive bladder symptoms such as urinary urgency, frequency, and urge incontinence in adults.

GNH India supplies Mirabegron Teva Uk as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring quality‑controlled manufacturing, regulatory compliance, and reliable distribution across multiple markets.

Manufacturer / TM Owner

Teva Uk Limited

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Indications & Clinical Uses

Mirabegron acts on the β3‑adrenergic pathway to improve bladder storage function in patients with overactive bladder.

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

How It Works

  • Mirabegron activates β3‑adrenergic receptors located in the detrusor smooth muscle of the bladder. Receptor activation stimulates cyclic AMP production, leading to relaxation of the detrusor muscle during the storage phase, thereby increasing functional bladder capacity and reducing involuntary contractions that cause urgency and frequency.

Side Effects

Common Side Effects

  • Hypertension: elevated blood pressure may be observed.
  • Nasopharyngitis: mild upper respiratory tract infection symptoms.
  • Headache: occasional mild to moderate headache.
  • Constipation: reduced bowel motility.
  • Dry mouth: decreased salivation.
  • Urinary retention: difficulty initiating urination.

Serious or Rare Side Effects

  • Severe hypertension: marked increase in blood pressure requiring medical attention.
  • Angioedema: swelling of face, lips, tongue, or throat.
  • Tachycardia: rapid heart rate.
  • Acute urinary retention: inability to void, may need catheterization.
  • Allergic reactions: rash, pruritus, or anaphylaxis.
  • Renal impairment: worsening kidney function in susceptible individuals.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient-specific factors and monitor for adverse events.

  • Assess blood pressure: ensure baseline control before starting.
  • Monitor urinary retention: watch for signs of incomplete bladder emptying.
  • Review renal function: adjust use in patients with impaired kidneys.
  • Evaluate hepatic status: consider dose modification if liver disease is present.
  • Avoid use in uncontrolled hypertension: risk of exacerbation.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Mirabegron may alter the pharmacokinetics of co‑administered medicines and vice versa.

Major Interactions (Avoid)

  • Strong CYP2D6 inhibitors (e.g., fluoxetine, paroxetine): increase mirabegron exposure.
  • Potent CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): raise plasma levels.
  • Anticholinergic agents: may exacerbate urinary retention.

Moderate Interactions (Monitor Closely)

  • Moderate CYP2D6 inhibitors (e.g., duloxetine): require dose adjustment.
  • CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce efficacy.
  • Antihypertensives: monitor blood pressure for additive effects.
  • Diuretics: watch for fluid‑electrolyte shifts.
  • NSAIDs: may increase risk of hypertension.

Frequently Asked Questions

Mirabegron Teva Uk is prescribed to manage symptoms of overactive bladder, including urinary urgency, increased frequency, and urge incontinence. It works by relaxing the bladder muscle, allowing it to hold more urine and reducing involuntary contractions.

Mirabegron activates β3‑adrenergic receptors in the detrusor muscle of the bladder. This activation raises cyclic AMP levels, leading to smooth‑muscle relaxation during the storage phase, which increases bladder capacity and lessens urgency and frequency.

The appropriate dose of mirabegron is determined by the prescribing healthcare professional based on the patient’s condition, renal and hepatic function, and response to therapy. Dosage adjustments are individualized and should follow the prescriber’s instructions.

Safety data for mirabegron in pregnancy and lactation are limited. It should only be used if the potential benefit justifies any potential risk to the fetus or infant, and the decision must be made by a qualified healthcare provider.

To place an order, 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.

Mirabegron belongs to a different class (β3‑adrenergic agonist) and does not have the anticholinergic side‑effects such as dry mouth or constipation that are common with antimuscarinics. It may be preferred in patients who cannot tolerate antimuscarinic therapy, though individual response varies.

Mirabegron tablets should be stored at room temperature, below 25 °C, in the original packaging. Keep the product away from moisture, heat, and direct sunlight to maintain stability.

The medication is taken orally, usually once daily, with or without food. Patients should swallow the tablet whole with a glass of water and follow the dosing schedule prescribed by their clinician.

Serious risks include significant hypertension, severe urinary retention, angioedema, and rare allergic reactions such as anaphylaxis. Patients should seek immediate medical attention if they experience rapid heartbeat, swelling of the face or throat, or inability to urinate.

Mirabegron is contraindicated in patients with uncontrolled hypertension, severe urinary retention, or known hypersensitivity to the drug. Caution is also advised for individuals with significant renal or hepatic impairment, and it should be avoided in those taking strong CYP2D6 or CYP3A4 inhibitors.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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