Atropine Sulfate / Scopolamine Hydrobromide / Hyoscyamine Sulfate / Phenobarbital
Pronouncation: (AT-troe-peen SULL-fate/skoe-POLE-uh-meen HIGH-droe-BROE-mide/high-oh-SIGH-uh-meen SULL-fate/fee-no-BAR-bih-tahl)Class: GI anticholinergic combination
Trade Names:
Donnatal
- Tablets 0.0194 mg atropine sulfate/0.0065 mg scopolamine hydrobromide/0.1037 mg hyoscyamine sulfate/16.2 mg phenobarbital
- Elixir 0.0194 mg atropine sulfate/0.0065 mg scopolamine hydrobromide/0.1037 mg hyoscyamine sulfate/16.2 mg phenobarbital
Trade Names:
Donnatal Extentabs
- Tablets, extended-release 0.0582 mg atropine sulfate/0.0195 mg scopolamine hydrobromide/0.3111 mg hyoscyamine sulfate/48.6 mg phenobarbital
Pharmacology
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Promotes peripheral anticholinergic/antispasmodic action (decreases GI motility); provides mild sedation.
Indications and Usage
Possibly effective for treatment of irritable bowel syndrome and acute enterocolitis. Also may be useful as adjunctive therapy for duodenal ulcer.
Contraindications
Glaucoma; obstructive uropathy; obstructive disease of the GI tract; paralytic ileus; intestinal atony in elderly or debilitated patient; severe ulcerative colitis; toxic megacolon complicating ulcerative colitis; hepatic or renal disease; tachycardia; myocardial ischemia; unstable CV status in acute hemorrhage; myasthenia gravis; acute intermittent porphyrinuria.
Dosage and Administration
AdultsPO 1 to 2 tablets 3 to 4 times daily; 1 extended-release tablet every 12 h; 5 to 10 mL elixir 3 to 4 times daily according to condition and severity of symptoms.
ChildrenPO 0.5 to 5 mL elixir every 4 to 6 h, according to body weight.
Storage/Stability
Store in a cool, dry place.
Drug Interactions
AnticoagulantsAnticoagulant effects may be decreased.
Anticholinergic agentsAdditive anticholinergic effects.
HaloperidolWorsened schizophrenic symptoms; decreased haloperidol concentrations.
PhenothiazinesDecreased antipsychotic effects and increased anticholinergic effects may occur.
Laboratory Test Interactions
None well documented.
Adverse Reactions
Cardiovascular
Bradycardia; flushing; palpitations; tachycardia.
CNS
CNS stimulation (restlessness, tremor); confusion; dizziness; drowsiness; fever (especially in children); headache; insomnia; mental confusion or excitement (especially in the elderly, even with small doses); nervousness; psychosis; weakness.
Dermatologic
Urticaria and other dermal manifestations of allergic reaction.
EENT
Altered taste perception; blurred vision; cycloplegia; dilated pupils; increased IOP; mydriasis; nasal congestion; photophobia.
GI
bloated feeling; constipation; dysphagia; heartburn; nausea; paralytic ileus; vomiting; xerostomia.
Genitourinary
Impotence; urinary hesitancy and retention.
Miscellaneous
Decreased sweating; severe allergic reactions, including anaphylaxis; suppression of lactation.
Precautions
Pregnancy
Category C .
Lactation
If possible, do not use.
Elderly
May react with agitation, drowsiness, and other untoward manifestations even with small doses.
Special Risk Patients
Used with caution in patients with neuropathy, hepatic or renal disease, hyperthyroidism, coronary artery disease, CHF, arrhythmias, hypertension, or tachycardia. May complicate gastric ulcer treatment.
Addiction potential
May be habit forming; when possible, not given to addiction-prone individual.
Diarrhea
May be symptom of incomplete intestinal obstruction, especially in patients with ileostomy or colostomy and, therefore, may serve as contraindication.
Heat prostration
Can occur in presence of high ambient temperature because of interference with normal sweating.
Potentially hazardous tasks
May produce drowsiness, dizziness, or blurred vision.
Overdosage
Symptoms
Dry mouth, thirst, vomiting, nausea, abdominal distention, CNS stimulation, delirium, drowsiness, restlessness, stupor, fever, seizures, hallucinations, convulsions, coma, “flat” EEG, circulatory failure, tachycardia, weak pulse, hypertension, hypotension, respiratory depression, palpitations, arrhythmias, urinary urgency, blurred vision, dilated pupils, photophobia, rash, dry and hot skin.
Patient Information
- Caution patient to have adequate oral intake.
- Advise patient to include fiber in diet to prevent constipation.
- Caution patient to limit exposure to high ambient temperatures.
- Advise patient that dilated pupils may be experienced.
- Warn patient that product may cause excitability or sedation. Remind patient not to drive or operate heavy machinery if sedation occurs.
- Advise patient to notify health care provider if confusion, disorientation, ataxia, nausea, vomiting, diarrhea, abdominal distention, or elevated body temperature occurs.
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Irritable Bowel Syndrome, Enterocolitis
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