Disease Interactions

Serevent Diskus (salmeterol) Disease Interactions

There are 4 disease interactions with Serevent Diskus (salmeterol):

Beta-2 Adrenergic Bronchodilators (Includes Serevent Diskus) ⇔ Cardiovascular

Moderate Potential Hazard, Moderate 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 Serevent Diskus) ⇔ 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 Serevent Diskus) ⇔ 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 Serevent Diskus) ⇔ 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.


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Serevent Diskus (salmeterol) drug Interactions

There are 241 drug interactions with Serevent Diskus (salmeterol)

Serevent Diskus (salmeterol) food/lifestyle Interactions

There is 1 food/lifestyle interaction with Serevent Diskus (salmeterol)

See also...



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