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ALIMENTARY TRACT AND METABOLISM › DRUGS FOR FUNCTIONAL GASTROINTESTINAL DISORDERS › DRUGS FOR FUNCTIONAL GASTROINTESTINAL DISORDERS › Synthetic anticholinergics, quaternary ammonium compounds
pipenzolate
A03AB14
Forms & Strengths
- Pipenzolate bromide: Oral tablet (5 mg)
- Pipenzolate bromide: Oral drops or elixir formulations (availability varies by region)
Adult Dosing
- Peptic ulcer disease and gastrointestinal hypermotility: 5 mg orally 3 times daily, adjusted according to patient response and tolerance
- Maximum recommended daily dose: Typically 15 mg to 30 mg divided into 3 to 4 doses
Pediatric Dosing
- Safety and efficacy in pediatric patients have not been established; use is generally not recommended
Indications
- Adjunctive therapy in the treatment of peptic ulcer disease
- Management of gastrointestinal hypermotility and hypersecretion disorders
Mechanism of Action
- Synthetic quaternary ammonium anticholinergic agent
- Competitively blocks acetylcholine at muscarinic receptors on gastrointestinal smooth muscle, secretory cells, and the enteric nervous system
- Reduces gastric acid secretion and gastrointestinal motility
Contraindications
- Hypersensitivity to pipenzolate or other anticholinergic agents
- Narrow-angle glaucoma
- Gastrointestinal obstruction, paralytic ileus, or toxic megacolon
- Severe ulcerative colitis or myasthenia gravis
- Obstructive uropathy (e.g., prostatic hypertrophy with urinary retention)
Adverse Reactions
- Xerostomia (dry mouth)
- Blurred vision, mydriasis, and cycloplegia
- Constipation and urinary retention
- Tachycardia and palpitations
- Dizziness, drowsiness, and headache
- Reduced sweating leading to potential heat intolerance
Drug Interactions
- Amantadine, anti-parkinsonism drugs, and tricyclic antidepressants may potentiate anticholinergic side effects
- Antacids may decrease absorption of anticholinergic agents; administer separately
- May antagonize the gastrointestinal motility effects of prokinetic agents such as metoclopramide or cisapride
Curated Content: Needs Vetting Before Put to Clinical Use