Drug Guide
Glycopyrrolate
Classification
Therapeutic: Anticholinergic agent
Pharmacological: Muscarinic receptor antagonist
FDA Approved Indications
- Preoperative control of secretions in airway management
- Peptic ulcer disease (off-label in some cases)
- Management of excessive salivation (sialorrhea)
Mechanism of Action
Glycopyrrolate competitively inhibits muscarinic acetylcholine receptors, reducing secretions and gastrointestinal motility.
Dosage and Administration
Adult: For preoperative secretions: 0.2 mg IV or IM; may repeat every 30-60 min as needed. For sialorrhea: 1-2 mg orally 2-3 times daily.
Pediatric: Doses vary by age and indication; for sialorrhea, typically 0.02-0.04 mg/kg orally, divided doses.
Geriatric: Start at lower end of dosing range due to increased sensitivity.
Renal Impairment: Use with caution; adjust dose based on severity.
Hepatic Impairment: No specific adjustments recommended; monitor closely.
Pharmacokinetics
Absorption: Absorbed rapidly after IM or IV administration; oral absorption variable.
Distribution: Widely distributed, crosses the blood-brain barrier to a limited extent.
Metabolism: Metabolized partially in the liver.
Excretion: Primarily excreted unchanged in urine.
Half Life: Approximately 2-3 hours.
Contraindications
- Glaucoma (narrow-angle)
- Obstructive uropathy
- Myasthenia gravis
- Known hypersensitivity to glycopyrrolate
Precautions
- Use with caution in patients with tachycardia, GI obstruction, or hepatic impairment.
- Pregnancy Category C; use only if clearly needed.
- Lactation: caution advised; consider risks and benefits.
Adverse Reactions - Common
- Dry mouth (Common)
- Blurred vision (Common)
- Urinary retention (Common)
- Constipation (Common)
Adverse Reactions - Serious
- Tachycardia or arrhythmias (Uncommon)
- Anaphylaxis (Rare)
- Acute narrow-angle glaucoma (Rare)
Drug-Drug Interactions
- Other anticholinergic agents (additive effects)
- AChE inhibitors (antagonistic interaction)
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor respiratory status, secretions, heart rate, urinary output, and bowel function.
Diagnoses:
- Risk for impaired comfort due to dry mouth or vision changes
- Risk for urinary retention
Implementation: Administer as directed, monitor for adverse effects, educate patient about dry mouth management.
Evaluation: Assess reduction in secretions and relief of symptoms, monitor for adverse reactions.
Patient/Family Teaching
- Take medication exactly as prescribed.
- Report new or worsening symptoms, especially urinary retention, vision changes, or severe dry mouth.
- Maintain hydration and good oral hygiene.
- Avoid activities requiring alertness until response is known.
Special Considerations
Black Box Warnings:
- No black box warnings issued.
Genetic Factors: None specified.
Lab Test Interference: May affect certain diagnostic tests involving urine or secretions.
Overdose Management
Signs/Symptoms: Severe dry mouth, blurred vision, hot dry skin, hallucinations, tachycardia, urinary retention.
Treatment: Supportive care, activated charcoal if ingestion is recent, and measures to reduce body temperature. Physostigmine may be considered in severe cases under medical supervision.
Storage and Handling
Storage: Store at room temperature, away from moisture and light.
Stability: Stable under recommended conditions for shelf life specified by manufacturer.