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ALIMENTARY TRACT AND METABOLISM › DRUGS FOR FUNCTIONAL GASTROINTESTINAL DISORDERS › BELLADONNA AND DERIVATIVES, PLAIN › Belladonna alkaloids, semisynthetic, quaternary ammonium compounds
homatropine methylbromide
A03BB06
Forms & Strengths
- Tablet: 5 mg
- Combination products (e.g., with hydrocodone): various strengths
Adult Dosing
- Gastrointestinal disorders: 2.5 to 5 mg orally up to four times daily before meals
- Maximum daily dose: 30 mg
Pediatric Dosing
- Safety and efficacy not well established in pediatric patients
- Use generally not recommended or requires individualized expert dosing
Indications
- Adjunctive therapy in the treatment of peptic ulcer disease
- Management of irritable bowel syndrome and other functional gastrointestinal disorders characterized by hypermotility
Mechanism of Action
- Competitive antagonist at muscarinic acetylcholine receptors (anticholinergic/antispasmodic)
- Relaxes smooth muscle tone and decreases GI secretions by inhibiting parasympathetic nerve impulses
- Quaternary ammonium compound with limited penetration across the blood-brain barrier
Contraindications
- Glaucoma (narrow-angle)
- Obstructive uropathy (e.g., bladder neck obstruction due to prostatic hypertrophy)
- Obstructive disease of the gastrointestinal tract (e.g., achalasia, pyloroduodenal stenosis)
- Paralytic ileus, intestinal atony, or severe ulcerative colitis
- Myasthenia gravis
- Known hypersensitivity to homatropine or anticholinergics
Adverse Reactions
- Xerostomia (dry mouth)
- Blurred vision and cycloplegia
- Constipation and urinary retention
- Tachycardia and palpitations
- Drowsiness, dizziness, and headache
- Flushed, dry skin and reduced sweating (anhidrosis)
Drug Interactions
- Amantadine, antiparkinsonism drugs, and other anticholinergics: enhanced anticholinergic adverse effects
- Phenothiazines, tricyclic antidepressants: additive antimuscarinic toxicity
- Digoxin: increased serum concentrations due to decreased GI motility
- Metoclopramide: antagonism of GI prokinetic effects
Curated Content: Needs Vetting Before Put to Clinical Use