Class: Antimuscarinics/Antispasmodics
VA Class: AU350
CAS Number: 50-34-0
Introduction
Synthetic quaternary ammonium antimuscarinic.a b
Uses for Propantheline Bromide
Peptic Ulcer Disease
Adjunctive therapy in the treatment of peptic ulcer disease;a b however, no conclusive data that propantheline aids in the healing, decreases the rate of recurrence, or prevents complications of peptic ulcers.a c
With the advent of more effective therapies for the treatment of peptic ulcer disease, antimuscarinics have only limited usefulness in this condition. a c
Propantheline Bromide Dosage and Administration
Administration
Administer orally, preferably 30 minutes before meals and at bedtime.a b
Has also been administered IV or IM; however, a parenteral preparation is no longer commercially available in the US.a
Dosage
Available as propantheline bromide; dosage expressed in terms of the salt.a b
As with other antimuscarinics, higher than recommended dosage may be required for therapeutic effect.a c Titrate dosage until therapeutic effect is achieved or adverse effects become intolerable (using the lowest possible effective dosage).a c
Adults
Peptic Ulcer Disease
Oral
15 mg taken 30 minutes prior to each meal (3 times daily) and 30 mg at bedtime (total of 75 mg daily). b
In cases of mild manifestations or for patients of small stature: 7.5 mg 30 minutes before each meal (3 times daily) has been used, but this strength tablet is not currently commercially available.a One manufacturer (Roxane) states that it may be possible to break the 15-mg film-coated tablets in half without substantially damaging the tablets.a
Adjust dosage according to patient response and tolerance.b
Special Populations
Hepatic Impairment
No special population dosage recommendations at this time.b
Renal Impairment
No special population dosage recommendations at this time.b
Geriatric Patients
7.5 mg taken 30 minutes prior to each meal (3 times daily) has been used, but this strength tablet is not currently commercially available.a One manufacturer (Roxane) states that it may be possible to break the 15-mg film-coated tablets in half without substantially damaging the tablets.a
Cautions for Propantheline Bromide
Contraindications
Glaucoma (to avoid mydriasis).b c
Obstructive GI disease (e.g., pyloroduodenal stenosis, achalasia, paralytic ileus).b c
Obstructive uropathy (e.g., bladder neck obstruction caused by prostatic hypertrophy).b c
Intestinal atony (especially in geriatric or debilitated patients).b c
Severe ulcerative colitis or toxic megacolon complicating ulcerative colitis.b c
Acute hemorrhage when cardiovascular status is unstable.b c
Myasthenia gravis.b c
Warnings/Precautions
Warnings
Thermoregulatory Effects
Exposure to high environmental temperatures may result in heat prostration (e.g., fever, heat stroke) due to decreased sweating.b c Increased risk of hyperthermia in febrile patients.b c (See Advice to Patients.)
Diarrhea
May be an early sign of incomplete intestinal obstruction, especially in patients with ileostomy or colostomy.b c Do not use in such patients; use would be inappropriate and possibly harmful.b c
Overdosage
A curare-like action may occur (i.e., neuromuscular blockade leading to muscular weakness and possible paralysis).b
Large or toxic doses may produce marked CNS disturbances (e.g., restlessness, excitement, psychotic behavior), circulatory changes (e.g., flushing, hypotension, circulatory failure), respiratory failure, paralysis, and coma.b
Cardiovascular Effects
May increase heart rate.b Use with caution in patients with heart disease.b c
Sensitivity Reactions
Hypersensitivity Reactions
Risk of severe allergic or idiosyncratic reactions (e.g., anaphylaxis, urticaria, other dermatologic manifestations).b
General Precautions
CNS Effects
Risk of drowsiness or blurred vision.b Performance of activities requiring mental alertness and physical coordination (e.g., operating a vehicle or other machinery, performing hazardous work) may be impaired.b (See Advice to Patients.)b c
GI Effects
Caution in patients with gastric ulcer because of delayed gastric emptying and possible antral stasis.c
Caution in patients with hiatal hernia associated with reflux esophagitis; anticholinergics may aggravate this condition.b c
Caution in patients with ulcerative colitis.b c Large doses may suppress intestinal motility resulting in paralytic ileus and causing or precipitating toxic megacolon.b c
Concomitant Illnesses
Use with caution in patients with hyperthyroidism, autonomic neuropathy, CHD, CHF, cardiac tachyarrhythmia, or hypertension. b
Specific Populations
Pregnancy
Category C.b
Lactation
Not known if propantheline is distributed into human milk.b Caution if used in nursing women.b
May suppress lactation.b c
Pediatric Use
Safety and efficacy not established.b c
Geriatric Use
Use with caution.b c
Hepatic Impairment
Use with caution in patients with hepatic disease. b
Renal Impairment
Use with caution in patients with renal disease.b
Common Adverse Effects
Xerostomia,b decreased sweating,b adverse ophthalmic effects (e.g., blurred vision, mydriasis, cycloplegia, increased ocular tension).b
Interactions for Propantheline Bromide
Drugs with Anticholinergic Effects
Additive adverse effects resulting from cholinergic blockade (e.g., xerostomia, blurred vision, constipation).c Advise of possibility of increased anticholinergic effects.c
Orally Administered Drugs
Potential pharmacokinetic interaction (altered GI absorption of various drugs).b c Antimuscarinics may inhibit GI motility, delay gastric emptying, and prolong GI transit time.b c
Specific Drugs
Drug | Interaction | Comments |
---|---|---|
Acetaminophen | Decrease rate but not extent of acetaminophen absorption; may delay onset of acetaminophen therapeutic effectsc | |
Antacids | Possible decreased absorption of antimuscarinicc | Administer at least 1 hour before antacidsc |
Antiarrhythmic agents, type I (e.g., disopyramide, procainamide, quinidine) | Possible additive adverse anticholinergic effectsb c | Inform patient of possibilityc |
Antidepressants, tricyclic | Possible additive adverse anticholinergic effectsb c | Inform patient of possibilityc |
Antihistamines | Possible additive adverse anticholinergic effectsb c | Inform patient of possibilityc |
Antiparkinsonian agents | Possible additive adverse anticholinergic effectsc | Inform patient of possibilityc |
Belladonna alkaloids | Possible additive adverse anticholinergic effectsb | |
Corticosteroids | Possible increased IOPb c | |
Digoxin | Increased serum digoxin concentration with slowly dissolving digoxin tabletsb c | Use digoxin oral solution or rapidly dissolving tablets; observe for signs of digoxin toxicityb c |
Ketoconazole | Possible decreased ketoconazole absorptionc | Administer antimuscarinic ≥2 hours after ketoconazolec |
Levodopa | Possible increased gastric levodopa metabolism, resulting in decreased levodopa absorptionc | Possible levodopa toxicity if antimuscarinic is discontinued without a concomitant reduction in levodopa dosagec |
Meperidine | Possible additive adverse anticholinergic effectsb c | Inform patient of possibilityc |
Phenothiazines | Possible additive adverse anticholinergic effects; possible potentiation of sedative effectsb c | Inform patient of possibilityc |
Potassium chloride | Antimuscarinics may slow GI transit, increasing risk of potassium chloride GI mucosal toxicityc | Administer concomitantly with caution (especially with wax matrix potassium chloride preparations)c |
Riboflavin | Delayed rate but increased extent of riboflavin absorption reportedc |
Propantheline Bromide Pharmacokinetics
Absorption
Bioavailability
Incompletely absorbed from the GI tract because completely ionized.a
Peak plasma concentrations occur about one hour after a single oral dose.b
Food
Extent of absorption is substantially decreased by food.a
Distribution
Possesses poor lipid solubility.a Limited ability to distribute into CNS or eye.a
Not known whether propantheline is distributed into milk.b
Elimination
Metabolism
Extensively metabolized, primarily by hydrolysis, to the inactive compounds xanthene-9-carboxylic acid and (2-hydroxyethyl) diisopropylmethylammonium bromide.a b c
Elimination Route
70% of the dose is excreted in the urine, mostly as metabolites.b
Half-life
Elimination half-life: 1.6 hours.b
Stability
Storage
Oral
Tablets
20–25°C.b
ActionsActions
Competitively inhibits acetylcholine or other cholinergic stimuli at autonomic effectors innervated by postganglionic cholinergic nerves and, to a lesser extent, on smooth muscles that lack cholinergic innervation.c
At usual doses, antimuscarinics principally antagonize cholinergic stimuli at muscarinic receptors and have little or no effect on cholinergic stimuli at nicotinic receptors. c
Antimuscarinics also have been referred to as anticholinergics (cholinergic blocking agents), but this term is appropriate only when it describes the antagonism of cholinergic stimuli at any cholinergic receptor, whether muscarinic or nicotinic.c
Antimuscarinics also have been referred to as parasympatholytics since the antagonized functions principally are under the parasympathetic division of the nervous system.c
Inhibits GI motility and diminishes gastric acid secretion.b c
Inhibits the action of acetylcholine at the postganglionic nerve endings of the parasympathetic nervous system. b
Advice to Patients
Potential for hyperthermia and heat prostration; avoid exposure to high environmental temperature and use with caution when febrile.b c
Risk of drowsiness or blurred vision; exercise caution when performing activities requiring mental alertness (e.g., driving a motor vehicle, operating machinery) or when performing other hazardous work.b
Importance of informing clinicians of existing or contemplated concomitant therapy, including prescription and OTC drugs, as well as any concomitant illnesses.b
Importance of women informing clinicians if they are or plan to become pregnant or plan to breast-feed.b c
Importance of informing patients of other important precautionary information.a b c (See Cautions.)
Preparations
Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details.
* available from one or more manufacturer, distributor, and/or repackager by generic (nonproprietary) name
Routes | Dosage Forms | Strengths | Brand Names | Manufacturer |
---|---|---|---|---|
Oral | Tablets | 15 mg* | Propantheline Bromide Tablets | Roxane |
Comparative Pricing
This pricing information is subject to change at the sole discretion of DS Pharmacy. This pricing information was updated 03/2011. Actual costs to patients will vary depending on the use of specific retail or mail-order locations and health insurance copays.
Propantheline Bromide 15MG Tablets (ROXANE): 30/$22.65 or 90/$47.35
Disclaimer
This report on medications is for your information only, and is not considered individual patient advice. Because of the changing nature of drug information, please consult your physician or pharmacist about specific clinical use.
The American Society of Health-System Pharmacists, Inc. and Drugs.com represent that the information provided hereunder was formulated with a reasonable standard of care, and in conformity with professional standards in the field. The American Society of Health-System Pharmacists, Inc. and Drugs.com make no representations or warranties, express or implied, including, but not limited to, any implied warranty of merchantability and/or fitness for a particular purpose, with respect to such information and specifically disclaims all such warranties. Users are advised that decisions regarding drug therapy are complex medical decisions requiring the independent, informed decision of an appropriate health care professional, and the information is provided for informational purposes only. The entire monograph for a drug should be reviewed for a thorough understanding of the drug's actions, uses and side effects. The American Society of Health-System Pharmacists, Inc. and Drugs.com do not endorse or recommend the use of any drug. The information is not a substitute for medical care.
AHFS Drug Information. © Copyright, 1959-2011, Selected Revisions June 2008. American Society of Health-System Pharmacists, Inc., 7272 Wisconsin Avenue, Bethesda, Maryland 20814.
References
a. AHFS drug information 2007. McEvoy GK, ed. Propantheline. Bethesda, MD: American Society of Health-System Pharmacists; 2007:page [1286].
b. Roxane Laboratories. Propantheline bromide tablets prescribing information. Columbus, OH; 2005 Nov.
c. AHFS drug information 2007. McEvoy GK, ed. Antimuscarinics/Antispasmodics General Statement. Bethesda, MD: American Society of Health-System Pharmacists; 2007:pages [1259-1267].
More Propantheline Bromide resources
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