Concomitant use may potentiate sympathetic effects. While long-term treatment effects of fluticasone inhalation on BMD in the chronic obstructive pulmonary disease (COPD) population have not been studied, a 2 year study of fluticasone (inhalation aerosol 88 or 440 mcg twice daily) in asthma patients found no statistically significant changes in BMD via dual-energy X-ray absorptiometry (DEXA) at the lumbar spine. Mitoxantrone: (Minor) Because systemically administered corticosteroids exhibit immunosuppressive effects when given in high doses and/or for extended periods, additive effects may be seen with other immunosuppressives or antineoplastic agents. Bismuth Subsalicylate: (Moderate) Monitor for gastrointestinal toxicity during concurrent corticosteroid and salicylate use. In drug interaction studies, coadministration with strong inhibitors increased plasma fluticasone propionate exposure resulting in 45% to 86% decreases in serum cortisol AUC. Patient & Family Education Dapagliflozin; Metformin: (Moderate) Monitor blood glucose during concomitant corticosteroid and metformin use; a metformin dose adjustment may be necessary. Both corticosteroids and thiazide diuretics cause increased renal potassium loss. Introduction. Corticosteroids may increase blood glucose concentrations. Phenobarbital: (Moderate) Coadministration may result in decreased exposure to fluticasone. Epinephrine: (Moderate) Monitor blood pressure and heart rate during concomitant epinephrine and salmeterol use. Use of a beta-1-selective (cardioselective) beta blocker is recommended whenever possible when this combination of drugs must be used together. Methenamine; Sodium Salicylate: (Moderate) Monitor for gastrointestinal toxicity during concurrent corticosteroid and salicylate use. Coadministration with another strong CYP3A inhibitor increased salmeterol overall exposure 16-fold mainly due to increased bioavailability of the swallowed portion of the dose. In patients receiving concomitant corticosteroids and chronic use of salicylates, withdrawal of corticosteroids may result in salicylism because corticosteroids enhance renal clearance of salicylates and their withdrawal is followed by return to normal rates of renal clearance. Oxymetholone: (Moderate) Concomitant use of oxymetholone with corticosteroids or corticotropin, ACTH may cause increased edema. Use of a beta-1-selective (cardioselective) beta blocker is recommended whenever possible when this combination of drugs must be used together. (Major) Coadministration of inhaled fluticasone propionate and clarithromycin is not recommended; use caution with inhaled fluticasone furoate. Decreased insulin production may occur in the pancreas due to a direct effect on pancreatic beta cells. SABAs should not be used on a regular basis (e.g., 4 times a day) while taking formoterol. Both corticosteroids and thiazide diuretics cause increased renal potassium loss. Fatalities have been reported in association with excessive use of inhaled sympathomimetic drugs. (Major) Coadministration of inhaled fluticasone propionate and ketoconazole is not recommended; use caution with inhaled fluticasone furoate. Dosage adjustments may be necessary, and closer monitoring of clinical and/or adverse effects is warranted when carbamazepine is used with fluticasone. Aspirin, ASA; Carisoprodol; Codeine: (Moderate) Monitor for gastrointestinal toxicity during concurrent corticosteroid and salicylate use. Sodium Phenylbutyrate; Taurursodiol: (Moderate) The concurrent use of corticosteroids with sodium phenylbutyrate may increase plasma ammonia levels (hyperammonemia) by causing the breakdown of body protein. Signs and symptoms of excessive beta-adrenergic stimulation commonly include tachyarrhythmias, hypertension, and tremor. Fluticasone is a CYP3A4 substrate; cobicistat is a strong CYP3A4 inhibitor. Concomitant use may potentiate sympathetic effects. Corticosteroids stimulate hepatic glucose production and inhibit peripheral glucose uptake into muscle and fatty tissues, producing insulin resistance. Clarithromycin: (Major) Avoid concomitant use of salmeterol with clarithromycin. Use of a beta-1-selective (cardioselective) beta blocker is recommended whenever possible when this combination of drugs must be used together. In drug interaction studies, coadministration with strong inhibitors increased plasma fluticasone exposure resulting in 45% to 86% decreases in serum cortisol AUC. Dexamethasone administration on long bone tissue in vitro resulted in a decrease of local synthesis of IGF-1. Use of a beta-1-selective (cardioselective) beta blocker is recommended whenever possible when this combination of drugs must be used together. Concomitant use may potentiate sympathetic effects. (Minor) Hypokalemia associated with thiazide diuretics can be acutely worsened by beta-agonists, especially when the recommended dose of the beta-agonist is exceeded. Concomitant use increases the risk of GI bleeding. Monitor patients for increased pressor effect if these agents are administered concomitantly. Vincristine Liposomal: (Moderate) Use sodium phosphate cautiously with corticosteroids, especially mineralocorticoids or corticotropin, ACTH, as concurrent use can cause hypernatremia. The first look at the 'middle aged Love Island' set has been released, which has already been nicknamed the 'Viagra House' by locals after single parents searched for love Signs and symptoms of excessive beta-adrenergic stimulation commonly include tachyarrhythmias, hypertension, and tremor. Salmeterol is a CYP3A substrate and grapefruit juice is a strong CYP3A inhibitor. Decreased insulin production may occur in the pancreas due to a direct effect on pancreatic beta cells. Brompheniramine; Pseudoephedrine: (Moderate) Monitor blood pressure and heart rate during concomitant salmeterol and pseudoephedrine use. Carbinoxamine; Pseudoephedrine: (Moderate) Monitor blood pressure and heart rate during concomitant salmeterol and pseudoephedrine use. Coadminister with caution and careful monitoring. Safety and efficacy of Advair HFA, Airduo Digihaler, and Airduo Respiclick have not been established.Less than 4 years: Safety and efficacy have not been established. More serious effects are rare, but may result in additive cardiovascular effects such as increased blood pressure and heart rate. HFA aerosol for oral inhalation (Advair HFA):[44026]Administer via oral inhalation.Prime the inhaler before first use with 4 test sprays away from the face. Fluticasone; salmeterol is contraindicated in the treatment of status asthmaticus or acute bronchospasm (acute asthma attack). Pseudoephedrine; Triprolidine: (Moderate) Monitor blood pressure and heart rate during concomitant salmeterol and pseudoephedrine use. Coadministration with ketoconazole increased salmeterol overall exposure 16-fold mainly due to increased bioavailability of the swallowed portion of the dose. Lidocaine; Epinephrine: (Moderate) Monitor blood pressure and heart rate during concomitant epinephrine and salmeterol use. Signs and symptoms of excessive beta-adrenergic stimulation commonly include tachyarrhythmias, hypertension, and tremor. Thrush. Torsemide: (Moderate) Use beta-agonists and loop diuretics with caution due to risk for ECG changes and/or hypokalemia. Chlorothiazide: (Moderate) Monitor potassium concentrations during concomitant corticosteroid and thiazide diuretic use due to risk for additive hypokalemia; potassium supplementation may be necessary. Acute symptoms should be treated with inhaled short-acting beta-2 agonists (SABA) such as albuterol. Tranylcypromine: (Moderate) Use beta-agonists with caution in patients receiving concomitant monoamine oxidase inhibitors (MAOIs) or within 14 days of stopping treatment with MAOIs because the action of beta-agonists on the cardiovascular system may be potentiated. It is not intended to be a substitute for the exercise of professional judgment. Nursing Considerations Across the Lifespan Signs and symptoms of excessive beta-adrenergic stimulation commonly include tachyarrhythmias, hypertension, and tremor. Although documentation is lacking, coadministration of echinacea with immunosuppressants is not recommended by some resources. Corticosteroids may increase blood glucose concentrations. Fluticasone is a CYP3A4 substrate; clarithromycin is a strong CYP3A4 inhibitor. The federal Omnibus Budget Reconciliation Act (OBRA) regulates medication use in residents of long-term care facilities (LTCFs). Concomitant use may potentiate sympathetic effects. In patients receiving concomitant corticosteroids and chronic use of salicylates, withdrawal of corticosteroids may result in salicylism because corticosteroids enhance renal clearance of salicylates and their withdrawal is followed by return to normal rates of renal clearance. Concomitant use increases the risk of GI bleeding. Remove the Inhub from the mouth, hold the breath for at least 10 seconds, and then exhale slowly.Instruct patient to close the Inhub, which will also reset the dose lever for the next scheduled dose.Following administration, instruct patient to rinse the mouth with water to minimize dry mouth. Advair HFA should be used for patients not adequately controlled on a long-term asthma control medication such as an inhaled corticosteroid (ICS) or whose disease warrants initiation of treatment with both an ICS and long-acting beta 2-adrenergic agonist . In . In drug interaction studies, coadministration with strong inhibitors increased plasma fluticasone propionate exposure resulting in 45% to 86% decreases in serum cortisol AUC. Concomitant use increases the risk of GI bleeding. With salmeterol, however, the bronchodilator effects persist at greater than half of the maximum effect for 12 hours, whereas with albuterol, PEFR and FEV-1 return to baseline within 6 hours. INTRODUCTION salmeterol (sal- met -er-ole) Serevent Classification Therapeutic: bronchodilators Pharmacologic: adrenergics Indications Long-term control of reversible airway obstruction due to asthma and for maintenance treatment of asthma and prevention of bronchospasm. 1 actuation of 250/50 (250 mcg fluticasone and 50 mcg salmeterol per actuation) inhaled orally twice daily, morning and night, approximately 12 hours apart. Concomitant use increases the risk of GI bleeding. Spironolactone; Hydrochlorothiazide, HCTZ: (Moderate) Monitor potassium concentrations during concomitant corticosteroid and thiazide diuretic use due to risk for additive hypokalemia; potassium supplementation may be necessary. A strong inhibitor increased fluticasone furoate exposure by 1.33-fold with a 27% reduction in weighted mean serum cortisol; this change does not necessitate dose adjustment of fluticasone furoate. Do not swallow the water.Clean inhaler mouthpiece at least once weekly.Do not place the canister in water to assess the remaining amount.Discard inhaler when the counter reads 000, or after the expiration date on the package, whichever comes first. Concurrent use may increase risk of hypoglycemia because of loss of the counter-regulatory cortisol response. Concomitant use may potentiate sympathetic effects. Salmeterol is a CYP3A substrate and ceritinib is a strong CYP3A inhibitor. Salmeterol: Protein binding of salmeterol is approximately 94% to 98% of the serum concentration. Monitor the patient's lung and cardiovascular status closely. Both corticosteroids and thiazide diuretics cause increased renal potassium loss. Cocaine: (Moderate) Additive effects and increased toxicity might be observed when using cocaine with beta-agonists, which are sympathomimetic agents. Less than 5% of a dose is excreted in the urine as metabolites. Risk factors for impaired glucose tolerance due to corticosteroids include the corticosteroid dose and duration of treatment. Concomitant use may potentiate sympathetic effects. Promethazine; Phenylephrine: (Moderate) Caution and close observation should also be used when salmeterol is used concurrently with other adrenergic sympathomimetics, administered by any route, to avoid potential for increased cardiovascular effects. Chlorthalidone: (Moderate) Monitor potassium concentrations during concomitant corticosteroid and thiazide diuretic use due to risk for additive hypokalemia; potassium supplementation may be necessary. The oral systemic bioavailability of fluticasone propionate was less than 1%, primarily due to incomplete absorption and presystemic metabolism in the gut and liver. (Moderate) Monitor potassium concentrations during concomitant corticosteroid and epinephrine use due to risk for additive hypokalemia; potassium supplementation may be necessary. Use of a beta-1-selective (cardioselective) beta blocker is recommended whenever possible when this combination of drugs must be used together. Triamterene; Hydrochlorothiazide, HCTZ: (Moderate) Monitor potassium concentrations during concomitant corticosteroid and thiazide diuretic use due to risk for additive hypokalemia; potassium supplementation may be necessary. Salsalate: (Moderate) Monitor for gastrointestinal toxicity during concurrent corticosteroid and salicylate use. Both corticosteroids and thiazide diuretics cause increased renal potassium loss. In a pharmacokinetic trial, micafungin had no effect on the pharmacokinetics of prednisolone. Beta-agonists and beta-blockers are pharmacologic opposites and will counteract each other to some extent when given concomitantly, especially when non-cardioselective beta blockers are used. Not indicated for the relief of acute bronchospasm. Affected cytochrome P450 (CYP450) isoenzymes and drug transporters: CYP3A4Fluticasone: The potential for fluticasone to inhibit or induce metabolic enzymes and transporter systems is negligible at low respiratory inhalation doses. The 2004 guidelines of the National Asthma Education and Prevention Program (NAEPP) Asthma and Pregnancy Working Group consider a combination of inhaled corticosteroids (ICS) with long-acting inhaled beta-2 agonists (LABAs) to be one preferred treatment option for moderate asthma in pregnancy and lactation; however, use of medium dose inhaled corticosteroids is also a preferred option. Increasing SABA use is a sign of deteriorating disease for which prompt medical attention is required. Corticosteroids stimulate hepatic glucose production and inhibit peripheral glucose uptake into muscle and fatty tissues, producing insulin resistance. Phenobarbital; Hyoscyamine; Atropine; Scopolamine: (Moderate) Coadministration may result in decreased exposure to fluticasone. (Moderate) The therapeutic effect of phenylephrine may be increased in patient receiving corticosteroids, such as hydrocortisone. Carbinoxamine; Dextromethorphan; Pseudoephedrine: (Moderate) Monitor blood pressure and heart rate during concomitant salmeterol and pseudoephedrine use. For other situations where corticosteroids are used for treating non-life threatening conditions, mifepristone may lead to reduced corticosteroid efficacy and exacerbation or deterioration of such conditions. (Moderate) Monitor potassium concentrations during concomitant corticosteroid and epinephrine use due to risk for additive hypokalemia; potassium supplementation may be necessary. If the patient has exacerbations, consider triple therapy with a long-acting muscarinic antagonist (LAMA), a LABA, and an ICS. Monitor diabetics closely for loss of glycemic control. Signs and symptoms of excessive beta-adrenergic stimulation commonly include tachyarrhythmias, hypertension, and tremor. Fluticasone is a steroid that prevents the release of substances in the body that cause inflammation. Use of a beta-1-selective (cardioselective) beta blocker is recommended whenever possible when this combination of drugs must be used together. It works by relaxing muscles in the airways to improve breathing. Consider checking potassium levels if clinically indicated. A strong inhibitor increased fluticasone furoate exposure by 1.33-fold with a 27% reduction in weighted mean serum cortisol; this change does not necessitate dose adjustment of fluticasone furoate. Beta-agonists can sometimes increase heart rate or have other cardiovascular effects, particularly when used in high doses or if hypokalemia is present. Photo: Andreas Neumann. Monoamine oxidase inhibitors: (Moderate) Use beta-agonists with caution in patients receiving concomitant monoamine oxidase inhibitors (MAOIs) or within 14 days of stopping treatment with MAOIs because the action of beta-agonists on the cardiovascular system may be potentiated. Butabarbital: (Moderate) Coadministration may result in decreased exposure to fluticasone. Infants born to mothers taking substantial corticosteroid doses during pregnancy should be monitored for signs of hypoadrenalism. Corticosteroids may increase blood glucose concentrations. (Moderate) The therapeutic effect of phenylephrine may be increased in patient receiving corticosteroids, such as hydrocortisone. Risk factors for impaired glucose tolerance due to corticosteroids include the corticosteroid dose and duration of treatment. Vonoprazan; Amoxicillin; Clarithromycin: (Major) Avoid concomitant use of salmeterol with clarithromycin. Concomitant use increases salmeterol exposure and may increase the incidence and severity of salmeterol-related adverse effects. In drug interaction studies, coadministration with strong inhibitors increased plasma fluticasone exposure resulting in 45% to 86% decreases in serum cortisol AUC. Penicillamine: (Major) Agents such as immunosuppressives have adverse reactions similar to those of penicillamine. Coadministration can result in overdosage. Beta-agonists can sometimes increase heart rate or have other cardiovascular effects, particularly when used in high doses or if hypokalemia is present. Use of a beta-1-selective (cardioselective) beta blocker is recommended whenever possible when this combination of drugs must be used together. Acetaminophen; Chlorpheniramine; Dextromethorphan; Phenylephrine: (Moderate) Caution and close observation should also be used when salmeterol is used concurrently with other adrenergic sympathomimetics, administered by any route, to avoid potential for increased cardiovascular effects. 100 mcg fluticasone/50 mcg salmeterol (1 actuation of 100 mcg fluticasone/50 mcg salmeterol) or 250 mcg fluticasone/50 mcg salmeterol (1 actuation of 250 mcg fluticasone/50 mcg salmeterol) or 500 mcg fluticasone/50 mcg salmeterol (1 actuation of 500 mcg fluticasone/50 mcg salmeterol) inhaled by mouth twice daily, approximately every 12 hours. Neostigmine: (Moderate) Concomitant use of anticholinesterase agents, such as neostigmine, and systemic corticosteroids may produce severe weakness in patients with myasthenia gravis. Irbesartan; Hydrochlorothiazide, HCTZ: (Moderate) Monitor potassium concentrations during concomitant corticosteroid and thiazide diuretic use due to risk for additive hypokalemia; potassium supplementation may be necessary. Beta-agonists and beta-blockers are pharmacologic opposites and will counteract each other to some extent when given concomitantly, especially when non-cardioselective beta blockers are used. In drug interaction studies, coadministration with strong inhibitors increased plasma fluticasone exposure resulting in 45% to 86% decreases in serum cortisol AUC. In drug interaction studies, coadministration with strong inhibitors increased plasma fluticasone propionate exposure resulting in 45% to 86% decreases in serum cortisol AUC. Concomitant use may potentiate sympathetic effects. Metyrapone: (Major) Medications which affect pituitary or adrenocortical function, including all corticosteroid therapy, should be discontinued prior to and during testing with metyrapone. The elimination half-life of orally administered salmeterol was determined to be about 3 to 5 hours. Choline Salicylate; Magnesium Salicylate: (Moderate) Monitor for gastrointestinal toxicity during concurrent corticosteroid and salicylate use. Increasing SABA use is a sign of deteriorating disease for which prompt medical attention is required. The choice of using a mouthpiece versus a face mask with a spacer/VHC device must be made based on the skills and understanding of each individual patient. Insulin Glargine; Lixisenatide: (Moderate) Monitor blood glucose during concomitant corticosteroid and incretin mimetic use; an incretin mimetic dose adjustment may be necessary. This monograph discusses the use of fluticasone; salmeterol combination product for treating asthma. For breathing in only. Darunavir; Cobicistat; Emtricitabine; Tenofovir alafenamide: (Major) Avoid concomitant use of salmeterol with cobicistat. Nadolol: (Moderate) Beta-blockers will block the pulmonary effects of inhaled beta-agonists, and in some cases may exacerbate bronchospasm in patients with reactive airways. Holding the Inhub mouthpiece level to, but away from, the mouth, exhale. Testosterone: (Moderate) Monitor for fluid retention during concurrent corticosteroid and testosterone use. Beta-agonists and beta-blockers are pharmacologic opposites and will counteract each other to some extent when given concomitantly, especially when non-cardioselective beta blockers are used. To minimize the effects of orally inhaled corticosteroids, each patient should be titrated to the lowest effective dose. Monitor cardiovascular status with periodic ECG, BP, and HR determinations. Salmeterol is a CYP3A substrate and chloramphenicol is a strong CYP3A inhibitor. Corticosteroids stimulate hepatic glucose production and inhibit peripheral glucose uptake into muscle and fatty tissues, producing insulin resistance. Concomitant use may potentiate sympathetic effects. (Major) Coadministration of inhaled fluticasone propionate and clarithromycin is not recommended; use caution with inhaled fluticasone furoate. Estrogens may decrease the hepatic clearance of corticosteroids thereby increasing their effect. Close monitoring is recommended in patients with a change in vision or with a history of increased intraocular pressure, glaucoma, and/or cataracts. Corticosteroids may increase blood glucose concentrations. Glimepiride: (Moderate) Monitor blood glucose during concomitant corticosteroid and sulfonylurea use; a sulfonylurea dose adjustment may be necessary. Both corticosteroids and thiazide diuretics cause increased renal potassium loss. Administration of L-asparaginase after rather than before corticosteroids reportedly has produced fewer hypersensitivity reactions. There are reports of enhanced as well as diminished effects of anticoagulants when given concurrently with corticosteroids; however, limited published data exist, and the mechanism of the interaction is not well described. Concomitant use increases salmeterol exposure and may increase the incidence and severity of salmeterol-related adverse effects. 5 Salmeterol was first described in . Beta-agonists can sometimes increase heart rate or have other cardiovascular effects, particularly when used in high doses or if hypokalemia is present. Base starting dose on prior asthma therapy and disease severity. 55 mcg fluticasone/14 mcg salmeterol (1 actuation of 55 mcg fluticasone/14 mcg salmeterol) or 113 mcg fluticasone/14 mcg salmeterol (1 actuation of 113 mcg fluticasone/14 mcg salmeterol) or 232 mcg fluticasone/14 mcg salmeterol (1 actuation of 232 mcg fluticasone/14 mcg salmeterol) inhaled by mouth twice daily, approximately every 12 hours. Risk factors for impaired glucose tolerance due to corticosteroids include the corticosteroid dose and duration of treatment. In multiple sclerosis (MS) clinical trials, an increase in infections was seen in patients concurrently receiving short courses of corticosteroids. Increasing SABA use is a sign of deteriorating disease for which prompt medical attention is required. L-Asparaginase transiently inhibits insulin production contributing to hyperglycemia seen during concurrent corticosteroid therapy. Remove the Diskus from the mouth, hold the breath for at least 10 seconds, and then exhale slowly.Instruct patient to close the Diskus, which will also reset the dose lever for the next scheduled dose.Following administration, instruct patient to rinse the mouth with water to minimize dry mouth. Corticosteroids may increase blood glucose concentrations. Use of a beta-1-selective (cardioselective) beta blocker is recommended whenever possible when this combination of drugs must be used together. Concomitant use increases salmeterol exposure and may increase the incidence and severity of salmeterol-related adverse effects. Sublingual Viagra is powerful medicine in the therapy of erectile dysfunction/infertility in men. Corticosteroids stimulate hepatic glucose production and inhibit peripheral glucose uptake into muscle and fatty tissues, producing insulin resistance. Monitor patients for any signs or symptoms of unexplained muscle pain, tenderness, or weakness, particularly during periods of upward dosage titration. Decreased insulin production may occur in the pancreas due to a direct effect on pancreatic beta cells. 50 ADVAIR HFA contains salmeterol (the same medicine found in SEREVENT). Phenytoin: (Moderate) Monitor for decreased corticosteroid efficacy if fluticasone is used with phenytoin; a dosage increase may be necessary. In drug interaction studies, coadministration with strong inhibitors increased plasma fluticasone propionate exposure resulting in 45% to 86% decreases in serum cortisol AUC. An acute myopathy has been observed with the use of high doses of corticosteroids in patients receiving concomitant long-term therapy with neuromuscular blockers. Coadministration with another strong CYP3A inhibitor increased salmeterol overall exposure 16-fold mainly due to increased bioavailability of the swallowed portion of the dose. Bisoprolol; Hydrochlorothiazide, HCTZ: (Moderate) Beta-blockers will block the pulmonary effects of inhaled beta-agonists, and in some cases may exacerbate bronchospasm in patients with reactive airways. Risk factors for impaired glucose tolerance due to corticosteroids include the corticosteroid dose and duration of treatment. Salmeterol is a CYP3A substrate and darunavir is a strong CYP3A inhibitor. Close monitoring of electrolytes should occur in patients receiving these drugs concomitantly. In drug interaction studies, coadministration with strong inhibitors increased plasma fluticasone exposure resulting in 45% to 86% decreases in serum cortisol AUC. Hydrochlorothiazide, HCTZ: (Moderate) Monitor potassium concentrations during concomitant corticosteroid and thiazide diuretic use due to risk for additive hypokalemia; potassium supplementation may be necessary. Corticosteroids stimulate hepatic glucose production and inhibit peripheral glucose uptake into muscle and fatty tissues, producing insulin resistance. Corticosteroids stimulate hepatic glucose production and inhibit peripheral glucose uptake into muscle and fatty tissues, producing insulin resistance. Alpha-glucosidase Inhibitors: (Moderate) Monitor patients receiving antidiabetic agents closely for worsening glycemic control when corticosteroids are instituted and for signs of hypoglycemia when corticosteroids are discontinued. Ribociclib; Letrozole: (Major) Avoid concomitant use of salmeterol with ribociclib. Beta-agonists and beta-blockers are pharmacologic opposites and will counteract each other to some extent when given concomitantly, especially when non-cardioselective beta blockers are used. Growth inhibition has been observed in some children (all ages) following therapy with high-dose fluticasone propionate inhalations. Fluoxymesterone: (Moderate) Coadministration of corticosteroids and fluoxymesterone may increase the risk of edema, especially in patients with underlying cardiac or hepatic disease. Increased systemic corticosteroid effects, including Cushing's syndrome and adrenal suppression, may occur. Nursing Implications . 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