Albuterol/ipratropium Disease Interactions

There are 6 disease interactions with albuterol/ipratropium:

Albuterol Er (Includes Albuterol/ipratropium) ↔ Gi Narrowing

Moderate Potential Hazard, Moderate plausibility

Applies to: Gastrointestinal Obstruction

The extended-release formulation of albuterol (Proventil Repetabs, Volmax) contains a non-deformable material. There have been rare reports of obstructive symptoms in patients with known strictures following the ingestion of similar sustained-release products. Therapy with the extended-release formulation of albuterol should be administered cautiously in patients with preexisting severe gastrointestinal narrowing or obstruction, whether pathologic or iatrogenic.


Beta-2 Adrenergic Bronchodilators (Includes Albuterol/ipratropium) ↔ Cardiovascular

Moderate Potential Hazard, High plausibility

Applies to: Heart Disease, Hypertension, Hyperthyroidism

Adrenergic bronchodilators can stimulate cardiovascular beta-1 and beta-2 receptors, occasionally producing adverse effects such as tachycardia, palpitation, ECG changes, peripheral vasodilation, and blood pressure changes. Direct stimulation of cardiac tissues is mediated by beta-1 receptors and thus less likely to occur with beta-2-selective agents such as albuterol. However, beta-2-selectivity is not absolute and can be lost with larger doses. High dosages of these agents have been associated with precipitation or aggravation of angina, myocardial ischemia, and cardiac arrhythmias. Therapy with adrenergic bronchodilators should be administered cautiously in patients with sensitivity to sympathomimetic amines, hyperthyroidism or underlying cardiovascular disorders, especially coronary insufficiency, cardiac arrhythmias, or hypertension. The recommended dosages should not be exceeded. Systemic adverse effects are minimized but not abolished by administration of these agents via oral inhalation.


Beta-2 Adrenergic Bronchodilators (Includes Albuterol/ipratropium) ↔ Diabetes

Moderate Potential Hazard, Low plausibility

Applies to: Diabetes Mellitus

Adrenergic bronchodilators may cause increases in blood glucose concentrations. These effects are usually transient and slight but may be significant with dosages higher than those normally recommended. Large doses of IV albuterol (not commercially available in the U.S.) and terbutaline sulfate have been reported to exacerbate preexisting diabetes mellitus and ketoacidosis. Therapy with adrenergic bronchodilators should be administered cautiously in patients with diabetes mellitus. Closer monitoring of blood glucose concentrations may be appropriate.


Beta-2 Adrenergic Bronchodilators (Includes Albuterol/ipratropium) ↔ Hypokalemia

Moderate Potential Hazard, Moderate plausibility

Applies to: Hypokalemia

Adrenergic bronchodilators may cause decreases in serum potassium concentrations, primarily when given by nebulization or intravenous administration. Although this effect is usually transient and does not require supplementation, clinically significant hypokalemia may occur in some patients, with the potential to induce cardiovascular adverse effects. The relevance of these observations to oral or oral aerosol/powder for inhalation therapy is unknown. Therapy with adrenergic bronchodilators should be administered cautiously in patients with or predisposed to hypokalemia.


Beta-2 Adrenergic Bronchodilators (Includes Albuterol/ipratropium) ↔ Seizures

Moderate Potential Hazard, Low plausibility

Applies to: Seizures

Adrenergic bronchodilators may cause CNS stimulation. Seizures have been reported rarely in patients treated with terbutaline. Therapy with adrenergic bronchodilators should be administered cautiously in patients with seizure disorders. Systemic adverse effects are minimized but not abolished by administration of these agents via oral inhalation.


Ipratropium/Tiotropium (Includes Albuterol/ipratropium) ↔ Anticholinergic Effects

Moderate Potential Hazard, Low plausibility

Applies to: Urinary Retention, Glaucoma (Narrow Angle)

Ipratropium and tiotropium are anticholinergic agents. Although systemic effects are rarely seen due to the poor absorption of quaternary ammonium compounds from gastrointestinal and nasal mucosa, there have been reports of increased intraocular pressure and precipitation or exacerbation of angle-closure glaucoma following inadvertent contact of the eye with aerosolized or nebulized drug. Accordingly, therapy with ipratropium and tiotropium should be administered cautiously in patients with urinary retention/obstruction or angle-closure glaucoma. Measures should be taken to minimize ocular exposure to these drugs (e.g., keeping eyes closed during administration by oral inhalation; use of a mouthpiece rather than face mask during nebulization). Urinary retention has been reported occasionally in patients receiving larger doses of ipratropium by nebulizer.


You should also know about...

albuterol/ipratropium drug Interactions

There are 614 drug interactions with albuterol/ipratropium

albuterol/ipratropium alcohol/food Interactions

There is 1 alcohol/food interaction with albuterol/ipratropium

See also...

Drug Interaction Classification

The classifications below are a general guideline only. It is difficult to determine the relevance of a particular drug interaction to any individual given the large number of variables.

Major Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit.
Moderate Moderately clinically significant. Usually avoid combinations; use it only under special circumstances.
Minor 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.

Do not stop taking any medications without consulting your healthcare provider.


Disclaimer: Every effort has been made to ensure that the information provided by Multum is accurate, up-to-date, and complete, but no guarantee is made to that effect. In addition, the drug information contained herein may be time sensitive and should not be utilized as a reference resource beyond the date hereof. Multum's drug information does not endorse drugs, diagnose patients, or recommend therapy. Multum's drug information is a reference resource designed as supplement to, and not a substitute for, the expertise, skill , knowledge, and judgement of healthcare practitioners in patient care. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug of drug combination is safe, effective, or appropriate for any given patient. Multum Information Services, Inc. does not assume any responsibility for any aspect of healthcare administered with the aid of information Multum provides. Copyright 2000-2012 Multum Information Services, Inc. The information in contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse, or pharmacist.

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