Product image of Glykopyrroniumbromid Accord (Glycopyrronium Bromide) supplied by GNH India

Glykopyrroniumbromid Accord

Active Ingredient:
Glycopyrronium Bromide
Origin:
EU

Glykopyrroniumbromid Accord (Glycopyrronium Bromide)

Glykopyrroniumbromid Accord is an injectable solution containing the anticholinergic agent glycopyrronium bromide. It is supplied in a sterile formulation for intramuscular or intravenous administration and is marketed in the European Union as a prescription‑only medication. Glycopyrronium bromide acts as a competitive muscarinic receptor antagonist, reducing secretions and producing bronchodilation. The product is used in peri‑operative settings and for certain respiratory conditions and chronic obstructive pulmonary disease (COPD) management.

Manufacturer / TM Owner

Accord Healthcare B.V.

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Indications & Clinical Uses

Glykopyrroniumbromid Accord is indicated for several clinical situations where reduction of secretions or bronchodilation is desired.

  • Pre‑operative reduction of salivary, respiratory and gastric secretions to facilitate anesthesia.
  • Adjunct therapy for chronic obstructive pulmonary disease (COPD) to improve airflow.
  • Management of acute bronchospasm in asthma when other bronchodilators are insufficient.
  • Control of excessive airway secretions during mechanical ventilation.
  • Use as an antisecretory agent in patients with excessive oral or bronchial secretions.

Side Effects

The safety profile of glycopyrronium bromide reflects its anticholinergic activity and includes both frequent and rare adverse events.

Common

  • Dry mouth (xerostomia) or reduced salivation.
  • Throat irritation, hoarseness or dysphagia.
  • Mild constipation or decreased gastrointestinal motility.
  • Transient increase in heart rate (tachycardia) without other cardiac symptoms.
  • Blurred vision or difficulty focusing due to pupil dilation.
  • Nausea or mild abdominal discomfort.

Serious

  • Severe bronchospasm or paradoxical airway narrowing requiring emergency intervention.
  • Acute urinary retention leading to painful bladder distension.
  • Allergic reactions including rash, angioedema, bronchial edema or anaphylaxis.
  • Cardiac arrhythmias such as atrial fibrillation or ventricular ectopy.
  • Marked hypotension or shock secondary to excessive anticholinergic effect.

Precautions & Warnings

When prescribing Glykopyrroniumbromid Accord, clinicians should evaluate patient‑specific factors and monitor for conditions that may be worsened by anticholinergic activity.

  • Use caution in patients with glaucoma, especially narrow‑angle type.
  • Avoid in individuals with known urinary outflow obstruction or severe prostatic hypertrophy.
  • Assess cardiac history; tachyarrhythmias may be exacerbated.
  • Consider dose adjustment or close monitoring in the elderly or those with renal impairment.
  • Do not administer to patients with known hypersensitivity to glycopyrronium bromide or formulation excipients.
  • Evaluate pregnancy status; safety data are limited.

Avoid Interactions

Glycopyrronium bromide can modify the pharmacodynamic or pharmacokinetic profile of several medicines; awareness of these interactions helps prevent adverse outcomes.

Avoid

  • Concurrent use with other anticholinergic agents (e.g., atropine, ipratropium) may increase anticholinergic burden.
  • Co‑administration with potent cholinesterase inhibitors (e.g., neostigmine) may reduce therapeutic effect.

Use with caution

  • Beta‑adrenergic bronchodilators (e.g., albuterol) – monitor for additive cardiovascular effects.
  • Cardiac glycosides (e.g., digoxin) – anticholinergic activity may alter heart rate control.
  • Anesthetic agents that depress respiration – observe for enhanced bronchial secretions control.
  • Diuretics – monitor electrolytes if significant fluid shifts occur.

Frequently Asked Questions

Glykopyrroniumbromid Accord is supplied as a sterile injectable solution that can be given by intramuscular or intravenous injection.

The product is marketed in the European Union and is not listed as an approved medication in the United States.

Yes, it is indicated as an adjunct bronchodilator for patients with COPD to help improve airflow and reduce airway secretions.

Common adverse effects include dry mouth, throat irritation, mild constipation, transient tachycardia, blurred vision, and mild nausea.

Patients with narrow‑angle glaucoma should use the drug with caution because anticholinergic activity can increase intra‑ocular pressure.

Concurrent use with other anticholinergics should be avoided, as it may amplify anticholinergic side effects such as dry mouth and tachycardia.

It competitively blocks muscarinic acetylcholine receptors, which decreases glandular secretion in the salivary, respiratory, and gastric tracts.

Elderly patients should be monitored for urinary retention, cardiovascular effects, and heightened anticholinergic sensitivity.

Pregnancy safety data are limited; the drug should be prescribed only if the potential benefit justifies the potential risk to the fetus.

Discontinue the medication immediately and provide appropriate medical treatment for the allergic reaction, which may include antihistamines or epinephrine.

Renal impairment may increase drug exposure; dose adjustment or close clinical monitoring is recommended in patients with reduced kidney function.

Baseline assessment of cardiac function, renal function, and evaluation for glaucoma or urinary obstruction is advisable before initiating treatment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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