2010
DOI: 10.4103/1817-1737.62468
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New FDA safety warnings for LABAs: A call for asthma guidelines revisit for solo beta agonist

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Cited by 5 publications
(9 citation statements)
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“…[ 137 ] Based on this evidence, the Saudi Food and Drug Administration withdrew all LABA monotherapy medications from the Saudi market by the end of 2010. [ 138 ] Therefore, the SINA panel has limited the use of relievers to SABA or formoterol containing combination when SMART approach is used Alternative and generally less-effective strategies include the continuation of ICS as a monotherapy by increasing the dose to the medium-high dose range (Evidence A),[ 137 139 ] and the addition of LTRA to a low-medium dose ICS (Evidence A),[ 140 141 ] especially in patients with concomitant rhinitis. [ 142 ] The addition of sustained release theophylline to a low-medium dose ICS is a possible but not favorable choice (Evidence B)[ 143 ] Tiotropium is a long-acting anticholinergic agent approved for the treatment of chronic obstructive pulmonary disease (COPD).…”
Section: Methodsmentioning
confidence: 99%
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“…[ 137 ] Based on this evidence, the Saudi Food and Drug Administration withdrew all LABA monotherapy medications from the Saudi market by the end of 2010. [ 138 ] Therefore, the SINA panel has limited the use of relievers to SABA or formoterol containing combination when SMART approach is used Alternative and generally less-effective strategies include the continuation of ICS as a monotherapy by increasing the dose to the medium-high dose range (Evidence A),[ 137 139 ] and the addition of LTRA to a low-medium dose ICS (Evidence A),[ 140 141 ] especially in patients with concomitant rhinitis. [ 142 ] The addition of sustained release theophylline to a low-medium dose ICS is a possible but not favorable choice (Evidence B)[ 143 ] Tiotropium is a long-acting anticholinergic agent approved for the treatment of chronic obstructive pulmonary disease (COPD).…”
Section: Methodsmentioning
confidence: 99%
“…[ 137 ] Based on this evidence, the Saudi Food and Drug Administration withdrew all LABA monotherapy medications from the Saudi market by the end of 2010. [ 138 ] Therefore, the SINA panel has limited the use of relievers to SABA or formoterol containing combination when SMART approach is used…”
Section: Methodsmentioning
confidence: 99%
“…[129] Based on this evidence, the Saudi Food and Drug Administration withdrew all LABA monotherapy medications from the Saudi market by the end of 2010. [130] Therefore, the SINA panel has limited the use of relievers to SABA or to formoterol when combined with ICSAlternative and generally less effective strategies include the continuation of ICS as a monotherapy by increasing the dose to the medium-high-dose range (Evidence A),[129131] or the addition of LTRA to a low-medium-dose ICS (Evidence A),[132133] especially in patients with concomitant rhinitis. [134] The addition of sustained release theophylline to a low-medium dose ICS is a possible but less favorable choice (Evidence B)[135]Tiotropium is a long-acting anticholinergic agent approved for the treatment of chronic obstructive pulmonary disease (COPD).…”
Section: Pharmacological Management In Adults and Adolescentmentioning
confidence: 99%
“…[60] Based on this evidence, the Saudi FDA withdrew all LABA monotherapy medications from the Saudi market by the end of 2010. [142] Therefore, the SINA panel has limited the use of relievers to SABA.Alternative, but in general less-effective strategies include: the continuation of ICS as a monotherapy by increasing the dose to the medium- to high-dose range (Evidence A),[60143] and the addition of LTRA to a low-medium dose ICS (Evidence A),[144145] especially in patients with concomitant rhinitis. [146] The addition of sustained release theophylline to a low-medium dose ICS is a third alternative choice (Evidence B).…”
Section: Treatment (Pharmacologic) Stepsmentioning
confidence: 99%
“…[60] Based on this evidence, the Saudi FDA withdrew all LABA monotherapy medications from the Saudi market by the end of 2010. [142] Therefore, the SINA panel has limited the use of relievers to SABA.…”
Section: Treatment (Pharmacologic) Stepsmentioning
confidence: 99%