Lomotil Disease Interactions
There are 25 disease interactions with Lomotil (atropine / diphenoxylate).
- Autonomic neuropathy
- GI obstruction
- Glaucoma
- Obstructive uropathy
- Reactive airway diseases
- Myasthenia gravis
- Infectious diarrhea
- Liver/renal
- Cardiac disease
- Tachycardia
- Coronary artery disease
- Gastric ulcer
- Gastroesophageal reflux
- Ulcerative colitis
- Fluid/electrolytes
- Hepatic/renal dysfunction
- Toxic megacolon
- Liver disease
- Renal failure
- Dehydration
- Down's syndrome
- Hypertension
- Hyperthyroidism
- Diarrhea
- Fever
Anticholinergics (applies to Lomotil) autonomic neuropathy
Major Potential Hazard, High plausibility.
Agents with anticholinergic activity can exacerbate many of the manifestations of autonomic neuropathy, including tachycardia, anhidrosis, bladder atony, obstipation, dry mouth and eyes, cycloplegia and blurring of vision, and sexual impotence in males. Therapy with antimuscarinic agents and higher dosages of antispasmodic agents (e.g., dicyclomine or oxybutynin) should be administered cautiously in patients with autonomic neuropathy.
Anticholinergics (applies to Lomotil) GI obstruction
Major Potential Hazard, High plausibility. Applicable conditions: Esophageal Obstruction, Gastrointestinal Obstruction
Anticholinergics are contraindicated in patients with obstructive diseases such as achalasia, esophageal stricture or stenosis, pyloroduodenal stenosis, stenosing peptic ulcer, pyloric obstruction, and paralytic ileus. Anticholinergics may further suppress intestinal motility with resultant precipitation or aggravation of toxic megacolon.
Anticholinergics (applies to Lomotil) glaucoma
Major Potential Hazard, High plausibility. Applicable conditions: Glaucoma/Intraocular Hypertension
Anticholinergic agents are contraindicated in patients with primary glaucoma, a tendency toward glaucoma (narrow anterior chamber angle), or adhesions (synechiae) between the iris and lens, as well as for the elderly and others in whom undiagnosed glaucoma or excessive pressure in the eye may be present. Because anticholinergics cause mydriasis, they may exacerbate these conditions.
Anticholinergics (applies to Lomotil) obstructive uropathy
Major Potential Hazard, High plausibility. Applicable conditions: Urinary Retention
In general, the use of anticholinergic agents is contraindicated in patients with urinary retention and bladder neck obstruction caused by prostatic hypertrophy. Dysuria may occur and may require catheterization. Also, anticholinergic drugs may aggravate partial obstructive uropathy. Caution is advised even when using agents with mild to moderate anticholinergic activity, particularly in elderly patients.
Anticholinergics (applies to Lomotil) reactive airway diseases
Major Potential Hazard, Moderate plausibility. Applicable conditions: Asthma
The use of systemic anticholinergics is contraindicated in the treatment of lower respiratory tract symptoms including asthma. Muscarinic receptor antagonists reduce bronchial secretions, which can result in decreased fluidity and increased thickening of secretions. However, ipratropium does not produce these effects and can be used safely in treating asthma.
Antimuscarinics (applies to Lomotil) myasthenia gravis
Major Potential Hazard, Moderate plausibility.
Because antimuscarinic agents have anticholinergic effects, they are contraindicated in patients with myasthenia gravis. Their use may be appropriate to reduce adverse muscarinic effects caused by an anticholinesterase agent.
Antiperistaltic agents (applies to Lomotil) infectious diarrhea
Major Potential Hazard, High plausibility. Applicable conditions: Infectious Diarrhea/Enterocolitis/Gastroenteritis, Infectious Diarrhea/Enterocolitis/Gastroenteritis
The use of drugs with antiperistaltic activity (primarily antidiarrheal and antimuscarinic agents, but also antispasmodic agents such as dicyclomine or oxybutynin at high dosages) is contraindicated in patients with diarrhea due to pseudomembranous enterocolitis or enterotoxin-producing bacteria. These drugs may prolong and/or worsen diarrhea associated with organisms that invade the intestinal mucosa, such as toxigenic E. coli, Salmonella and Shigella, and pseudomembranous colitis due to broad-spectrum antibiotics. Other symptoms and complications such as fever, shedding of organisms and extraintestinal illness may also be increased or prolonged. In general, because antiperistaltic agents decrease gastrointestinal motility, they may delay the excretion of infective gastroenteric organisms or toxins and should be used cautiously in patients with any infectious diarrhea, particularly if accompanied by high fever or pus or blood in the stool. Some cough and cold and other combination products may occasionally include antimuscarinic agents for their drying effects and may, therefore, require careful selection when necessary.
Diphenoxylate (applies to Lomotil) liver/renal
Major Potential Hazard, Moderate plausibility. Applicable conditions: Renal Dysfunction, Hepatorenal Syndrome, Cholelithiasis with Obstruction, Liver Disease
Diphenoxylate should be used with extreme caution in patients with advanced hepatorenal disease and in all patients with abnormal liver function since hepatic coma may be precipitated. Diphenoxylate is contraindicated in patients with obstructive jaundice.
Anticholinergics (applies to Lomotil) cardiac disease
Moderate Potential Hazard, Moderate plausibility. Applicable conditions: Cardiovascular Disease
Anticholinergics block vagal inhibition of the SA nodal pacemaker. Therapy with anticholinergics should be administered cautiously to patients with tachycardia, congestive heart failure, or coronary artery disease. Premature ventricular depolarization, ventricular tachycardia, and fibrillation associated with anticholinergics are rare.
Anticholinergics (applies to Lomotil) tachycardia
Moderate Potential Hazard, Moderate plausibility. Applicable conditions: Arrhythmias
Anticholinergics block vagal inhibition of the SA nodal pacemaker. Therapy with anticholinergics should be administered cautiously in patients with tachycardia, congestive heart failure, or coronary artery disease. Premature ventricular depolarization or ventricular tachycardia or fibrillation associated with anticholinergics is rare.
Antimuscarinics (applies to Lomotil) coronary artery disease
Moderate Potential Hazard, Moderate plausibility. Applicable conditions: Ischemic Heart Disease, Arrhythmias
Antimuscarinic agents block vagal inhibition of the SA nodal pacemaker. These agents should be administered cautiously in patients with tachycardia, congestive heart failure, or coronary artery disease. Premature ventricular depolarization or ventricular tachycardia or fibrillation associated with antimuscarinic drugs is rare.
Antimuscarinics (applies to Lomotil) gastric ulcer
Moderate Potential Hazard, Low plausibility. Applicable conditions: Bleeding
Antimuscarinic agents may cause a delay in gastric emptying and possibly antral stasis in patients with gastric ulcer. Therapy with antimuscarinic agents should be administered cautiously to patients with gastric ulcer.
Antimuscarinics (applies to Lomotil) gastroesophageal reflux
Moderate Potential Hazard, Moderate plausibility. Applicable conditions: Gastroesophageal Reflux Disease
Antimuscarinic agents decrease gastric motility and relax the lower esophageal sphincter which promotes gastric retention and can aggravate reflux. These drugs should be administered cautiously in patients with gastroesophageal reflux or hiatal hernia associated with reflux esophagitis.
Antimuscarinics (applies to Lomotil) ulcerative colitis
Moderate Potential Hazard, Moderate plausibility.
Antimuscarinic agents may suppress intestinal motility and produce paralytic ileus with resultant precipitation of toxic megacolon. These drugs should be administered cautiously to patients with ulcerative colitis.
Antiperistaltic agents (applies to Lomotil) fluid/electrolytes
Moderate Potential Hazard, High plausibility. Applicable conditions: Dehydration
Diarrhea can cause severe dehydration and electrolyte imbalance. Fluid accumulation within the GI track due to antiperistaltic-associated decrease in peristalsis can further aggravate dehydration and electrolyte imbalance. Antiperistaltic agents should be administered cautiously in patients with electrolyte imbalance and rehydration and electrolyte replacement should be initiated prior to initiation of therapy.
Antiperistaltic agents (applies to Lomotil) hepatic/renal dysfunction
Moderate Potential Hazard, High plausibility. Applicable conditions: Liver Disease
Therapy with antiperistaltic agents should be administered with extreme caution in patients with hepatorenal disease or abnormal liver enzymes. Antiperistaltic agents are metabolized by the liver (diphenoxylate to an active form) and primarily excreted in the feces. Hepatic coma can be precipitated.
Antiperistaltic agents (applies to Lomotil) toxic megacolon
Moderate Potential Hazard, Moderate plausibility. Applicable conditions: Inflammatory Bowel Disease
Decreased intestinal motility and prolonged transit time have resulted in toxic megacolon in patients with acute ulcerative colitis. Paralytic ileus has also occurred. Antiperistaltic agent GI motility and prolongs transit time and therapy should be administered cautiously in these patients.
Atropine-like agents (applies to Lomotil) liver disease
Moderate Potential Hazard, Moderate plausibility.
Atropine-like agents undergo significant hepatic metabolism. Therapy with atropine-like agents should be administered cautiously to patients with liver disease.
Atropine-like agents (applies to Lomotil) renal failure
Moderate Potential Hazard, Moderate plausibility. Applicable conditions: Renal Dysfunction
Atropine-like agents are primarily eliminated by the kidney. Therapy with atropine-like agents should be administered cautiously to patients with renal disease.
Diphenoxylate (applies to Lomotil) dehydration
Moderate Potential Hazard, Moderate plausibility. Applicable conditions: Electrolyte Abnormalities
Diphenoxylate should be withheld in patients with severe dehydration or electrolyte imbalance until appropriate corrective therapy has been initiated.
Diphenoxylate (applies to Lomotil) Down's syndrome
Moderate Potential Hazard, Moderate plausibility.
Since a subtherapeutic dose of atropine has been added to the diphenoxylate hydrochloride, consideration should be given to the precautions relating to the use of atropine. Diphenoxylate should be used with caution in patients with Down's syndrome since signs of atropinism may occur even with recommended doses.
Anticholinergics (applies to Lomotil) hypertension
Minor Potential Hazard, Low plausibility.
Cardiovascular effects of anticholinergics may exacerbate hypertension. Therapy with anticholinergic agents should be administered cautiously in patients with hypertension.
Anticholinergics (applies to Lomotil) hyperthyroidism
Minor Potential Hazard, Low plausibility.
In general, agents with anticholinergic activity may exacerbate hyperthyroidism. Therapy with anticholinergics should be administered cautiously in patients with hyperthyroidism. Thyroid levels should be monitored if usage is prolonged.
Antimuscarinics (applies to Lomotil) diarrhea
Minor Potential Hazard, Moderate plausibility.
Diarrhea may be a symptom of incomplete intestinal obstruction, especially in patients with ileostomy or colostomy. Antimuscarinic agents may further aggravate the diarrhea. Therefore, these drugs should be administered cautiously in patients with diarrhea.
Atropine-like agents (applies to Lomotil) fever
Minor Potential Hazard, Low plausibility.
Atropine-like agents may increase the risk of hyperthermia in patients with fever by producing anhidrosis. Therapy with atropine-like agents should be administered cautiously in febrile patients.
Lomotil drug interactions
There are 301 drug interactions with Lomotil (atropine / diphenoxylate).
Lomotil alcohol/food interactions
There are 2 alcohol/food interactions with Lomotil (atropine / diphenoxylate).
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Drug Interaction Classification
Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit. | |
Moderately clinically significant. Usually avoid combinations; use it only under special circumstances. | |
Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan. | |
No interaction information available. |
Further information
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