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

Mirabegron Teva

Active Ingredient:
Mirabegron
Origin:
EU

Mirabegron Teva (Mirabegron)

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

GNH India supplies Mirabegron Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory‑approved batches for global distribution. Clients benefit from reliable logistics, documentation support and consistent supply chain management.

Manufacturer / TM Owner

Teva Nederland B.V.

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Indications & Clinical Uses

Mirabegron is a β3‑adrenergic receptor agonist used to treat conditions within the overactive bladder disease family.

  • Overactive bladder: improves bladder capacity and reduces urgency episodes.
  • Urinary urgency: decreases frequency of sudden urges to void.
  • Urinary frequency: lowers daytime voiding episodes.
  • Urge urinary incontinence: reduces episodes of involuntary leakage.

How It Works

  • Mirabegron selectively stimulates β3‑adrenergic receptors located in the detrusor smooth muscle of the urinary bladder. Activation of these receptors leads to relaxation of the detrusor muscle, increasing bladder storage capacity and reducing involuntary contractions that cause urgency, frequency, and urge incontinence.

Side Effects

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

Common Side Effects

  • Hypertension: elevated blood pressure observed in some patients.
  • Nasopharyngitis: mild upper respiratory tract infection symptoms.
  • Headache: transient mild to moderate head pain.
  • Constipation: reduced bowel motility leading to hard stools.
  • Dry mouth: decreased salivary secretion.
  • Urinary retention: difficulty initiating or maintaining urine flow.

Serious or Rare Side Effects

  • Severe hypertension: marked increase in blood pressure requiring medical intervention.
  • Angioedema: swelling of face, lips, tongue or throat that may compromise airway.
  • Cardiac arrhythmias: irregular heart rhythms, including tachycardia.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety aspects.

  • Monitor blood pressure: check baseline and periodic readings during treatment.
  • Assess renal function: adjust use in patients with impaired kidney function.
  • Review cardiovascular history: use caution in patients with uncontrolled hypertension or heart disease.
  • Avoid use in uncontrolled hypertension: contraindicated when systolic BP exceeds 180 mmHg.
  • Use caution in the elderly: increased susceptibility to adverse effects.
  • Store at room temperature: keep in the original pack, protect from moisture and direct sunlight.

Avoid Interactions

Mirabegron can interact with other medicines, affecting its efficacy or safety.

Major Interactions (Avoid)

  • Strong CYP2D6 inhibitors (e.g., paroxetine, fluoxetine): may increase mirabegron plasma levels.
  • Antihypertensive agents (e.g., β‑blockers, ACE inhibitors): mirabegron may reduce their blood‑pressure‑lowering effect.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inhibitors (e.g., ketoconazole, erythromycin): may modestly raise mirabegron concentrations.
  • Diuretics: combined use can affect fluid balance and blood pressure.
  • Digoxin: mirabegron may increase digoxin levels, requiring monitoring.

Frequently Asked Questions

Mirabegron Teva is prescribed for adults with overactive bladder symptoms, including urinary urgency, increased frequency of urination, and urge urinary incontinence. It helps relax the bladder muscle, increasing storage capacity and reducing the need to void urgently.

Mirabegron selectively activates β3‑adrenergic receptors in the detrusor smooth muscle of the bladder. This activation causes muscle relaxation, which expands bladder capacity and diminishes involuntary contractions that trigger urgency and incontinence.

The appropriate dose of Mirabegron Teva is determined by the prescribing healthcare professional based on the patient’s medical condition, response to therapy, and any relevant safety considerations. Patients should follow the prescriber’s instructions exactly.

Safety data for mirabegron in pregnancy and lactation are limited, and the pregnancy category is listed as unknown. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made by a qualified clinician.

To request Mirabegron Teva, 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) than antimuscarinic agents. It does not carry the anticholinergic side‑effects such as dry mouth and constipation that are common with antimuscarinics, but it may raise blood pressure, which requires monitoring.

Mirabegron Teva tablets should be stored at room temperature, below 25 °C, in the original packaging to protect them from moisture and light. Do not store in areas with high humidity or extreme temperatures.

Mirabegron Teva is taken orally, usually once daily, with or without food. The tablet should be swallowed whole with a glass of water and not chewed or crushed, unless otherwise directed by a healthcare professional.

The most serious risks include significant hypertension, angioedema, and rare cardiac arrhythmias. Patients should be advised to seek immediate medical attention if they experience a sudden, severe increase in blood pressure, swelling of the face or throat, or irregular heartbeats.

Mirabegron Teva is contraindicated in patients with uncontrolled hypertension (systolic BP > 180 mmHg) and in those who have experienced severe hypersensitivity to mirabegron or any of its excipients. Caution is also advised for patients with severe renal or hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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