2009
DOI: 10.1007/s00228-009-0653-4
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Drug interactions between inhaled corticosteroids and enzymatic inhibitors

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Cited by 43 publications
(25 citation statements)
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“…By searching PubMed and the references of pertinent articles, and by contacting relevant drug companies, we identified 51 case reports published in English regarding adverse effects with the use of inhaled ( n = 45), intranasal ( n = 2), and combination inhaled and intranasal ( n = 4) corticosteroids and PIs (Table ) . Papers were published between the years 1999 and 2012.…”
Section: Case Reports On Corticosteroid−protease Inhibitor Drug−drug mentioning
confidence: 99%
“…By searching PubMed and the references of pertinent articles, and by contacting relevant drug companies, we identified 51 case reports published in English regarding adverse effects with the use of inhaled ( n = 45), intranasal ( n = 2), and combination inhaled and intranasal ( n = 4) corticosteroids and PIs (Table ) . Papers were published between the years 1999 and 2012.…”
Section: Case Reports On Corticosteroid−protease Inhibitor Drug−drug mentioning
confidence: 99%
“…This is well demonstrated in a case series of 46 patients on inhaled steroids who developed adrenal insufficiency. Fifteen of the cases were possibly due to a drug interaction with known cytochrome p450 inhibitors, including itraconazole, ritonavir, verapamil, and diltiazem [15]. Other known inhibitors include etomidate, diltiazem, and grapefruit juice.…”
Section: Discussionmentioning
confidence: 99%
“…For evaluation of at-risk patients, the low-dose (0.5–1  μ g) ACTH stimulation test is thought to be more sensitive for diagnosing secondary adrenal suppression, as the usual 250  μ g dose is supraphysiologic and might lead to false negative results. However, some studies do not support the superiority of one test over the other, particularly as both may lead to false negative results [15]. …”
Section: Discussionmentioning
confidence: 99%
“…In this real-life scenario it becomes clinically important to prevent (or recognize) the side effects which are relative to the pharmacodynamic and pharmacokinetic properties of specific ICSs, and to a variable extent influenced by the interaction with other concomitant pharmacological classes [63]. In their clinical practice, clinicians should therefore be aware of the main determinants of drug interactions, such as first pass metabolism and bioavailability.…”
Section: Pneumoniamentioning
confidence: 99%