Product image of Ipratropium Enfants Unidose Teva (Ipratropium Bromide Monohydrate) supplied by GNH India

Ipratropium Enfants Unidose Teva

Active Ingredient:
Ipratropium Bromide Monohydrate
Origin:
EU

Ipratropium Enfants Unidose Teva (Ipratropium Bromide Monohydrate)

Ipratropium Bromide, the active ingredient in Ipratropium Enfants Unidose Teva, is an anticholinergic (muscarinic antagonist) presented as a unit‑dose inhalation preparation for inhalation use. It provides bronchodilation by blocking muscarinic receptors in the airway smooth muscle, and is indicated for the treatment of bronchospasm associated with asthma in children and chronic obstructive pulmonary disease.

GNH India supplies Ipratropium Enfants Unidose Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with a focus on meeting the needs of pediatric respiratory care in the European market.

Manufacturer / TM Owner

Teva Santé

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Indications & Clinical Uses

Ipratropium bromide is a bronchodilator that acts on muscarinic receptors to relieve airway narrowing in several respiratory conditions.

  • Asthma (children): reduces bronchoconstriction and improves breathing in pediatric patients.
  • Chronic obstructive pulmonary disease (COPD): provides maintenance bronchodilation to ease airflow limitation.
  • Bronchospasm: rapidly relaxes airway smooth muscle during acute episodes.

How It Works

  • Ipratropium bromide competitively antagonizes muscarinic (M3) receptors on airway smooth muscle, inhibiting acetylcholine‑mediated bronchoconstriction. This blockade prevents calcium influx, leading to relaxation of the bronchial smooth muscle and increased airway diameter, thereby improving airflow and reducing respiratory resistance.

Side Effects

Adverse reactions may occur with inhaled ipratropium bromide. Most are mild and reversible, but rare serious events have been reported.

Common Side Effects

  • Dry mouth: reduced salivation after inhalation.
  • Cough: transient irritation of the airway.
  • Throat irritation: mild soreness or discomfort.
  • Hoarseness: temporary voice changes.
  • Nasal congestion: mild blockage of nasal passages.
  • Headache: occasional mild headache.

Serious or Rare Side Effects

  • Paradoxical bronchospasm: worsening of airway obstruction.
  • Allergic reactions: rash, itching, or swelling.
  • Angioedema: swelling of lips, tongue, or face.
  • Severe respiratory distress: difficulty breathing requiring medical attention.
  • Cardiac arrhythmias: rare irregular heartbeats.
  • Vision changes: blurred vision or eye irritation.

Precautions & Warnings

Use ipratropium bromide with caution in specific clinical situations and follow recommended handling procedures.

  • Pregnancy: discuss potential risks with a healthcare professional before use.
  • Breastfeeding: consider possible drug transfer to infant; consult a physician.
  • Pediatric use: ensure proper technique with the unidose device for children.
  • Pre‑existing glaucoma: monitor intra‑ocular pressure as anticholinergic effects may exacerbate.
  • Cardiovascular disease: observe for any changes in heart rate or rhythm.
  • Store below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Ipratropium bromide may interact with other medications that affect cholinergic pathways or respiratory function.

Major Interactions (Avoid)

  • Beta‑agonists combined with high‑dose anticholinergics: may increase risk of cardiovascular side effects.
  • Tricyclic antidepressants: additive anticholinergic burden.

Moderate Interactions (Monitor Closely):\n- Other inhaled bronchodilators (e.g., albuterol): monitor for synergistic bronchodilation.

  • Antihistamines with anticholinergic properties: watch for excessive dryness.
  • Muscarinic antagonists (e.g., tiotropium): assess cumulative anticholinergic effect.
  • MAO inhibitors: potential for increased cholinergic side effects.
  • Theophylline: monitor for altered respiratory response.

Frequently Asked Questions

Ipratropium Enfants Unidose Teva contains ipratropium bromide, an anticholinergic bronchodilator indicated for the relief of bronchospasm in children with asthma, for maintenance therapy in chronic obstructive pulmonary disease (COPD), and for acute bronchospastic episodes.

Ipratropium bromide blocks muscarinic M3 receptors on airway smooth muscle, preventing acetylcholine‑induced contraction. This inhibition reduces calcium entry into the cells, leading to relaxation of the bronchial muscles, widening the airways and improving airflow.

The prescribed dose of Ipratropium Enfants Unidose Teva is determined by the treating physician based on the patient’s age, weight, severity of disease, and response to therapy. Dosing instructions are provided on the prescription label and should be followed exactly.

Safety data for ipratropium bromide in pregnancy are limited. It should only be used if the potential benefit justifies any potential risk to the fetus. Breastfeeding mothers should consult their healthcare provider, as the drug may be excreted in breast milk.

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 required import documentation.

Ipratropium is an anticholinergic bronchodilator that works by blocking muscarinic receptors, whereas beta‑agonists (e.g., albuterol) stimulate beta‑2 receptors to cause bronchodilation. Ipratropium is often used in combination with beta‑agonists for additive effect, especially in COPD, and has a lower risk of tachycardia compared with beta‑agonists.

The inhaler should be stored below 25 °C (77 °F), protected from moisture, heat and direct sunlight. Keep the device in its original packaging until use, and discard any unit‑dose cartridges that appear damaged or expired.

The medication is delivered via a unit‑dose inhaler. The patient or caregiver should prime the device according to the manufacturer’s instructions, then inhale the dose slowly and deeply, holding the breath for a few seconds before exhaling. Proper technique ensures optimal drug delivery to the lungs.

Serious adverse events, although rare, include paradoxical bronchospasm, severe allergic reactions such as angioedema, and significant cardiac arrhythmias. Patients should seek immediate medical attention if they experience worsening breathing, swelling of the face or throat, or irregular heartbeats.

Ipratropium should be avoided in patients with a known hypersensitivity to ipratropium bromide or any component of the inhaler. Caution is also advised for individuals with narrow‑angle glaucoma, urinary retention, or severe cardiovascular disease, and it should only be used under medical supervision in these cases.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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