Serious adverse events with regular formoterol and inhaled corticosteroids

Cates CJ, Lasserson TJ, Jaeschke R

Published Online:

April 15, 2009

There has been some concern raised at the possibility of increased serious adverse events following administration of formoterol, a long-acting beta-agonist, to people with asthma. We analysed data from 14 studies in adults and seven in children. Too few deaths occurred in the trials to gain any conclusive reassurance that regular formoterol taken with inhaled corticosteroids either reduces the risk of mortality, or in fact does not increase it (all four deaths that did occur, including one related to asthma, were among 6,594 patients taking formoterol with inhaled corticosteroids). Serious adverse events were very similar in adults with and without formoterol. Although there were more events on formoterol in children, the difference was not big enough to rule out this as being a chance finding. Similarly, decreased risk of asthma-related serious adverse events in adults and increased risk among children taking formoterol could be also be chance findings.

Abstract (click to read)

Background:

Epidemiological evidence has suggested a link between beta2-agonists and increases in asthma mortality. There has been much debate about possible causal links for this association, and whether regular (daily) long-acting beta2-agonists are safe when used alone or in conjunction with inhaled corticosteroids.

Objectives:

The aim of this review is to assess the risk of fatal and non-fatal serious adverse events in trials that randomised patients with chronic asthma to regular formoterol with inhaled corticosteroids versus the same dose of inhaled corticosteroids alone.

Search strategy:

Trials were identified using the Cochrane Airways Group Specialised Register of trials. Web sites of clinical trial registers were checked for unpublished trial data and Food and Drug Administration (FDA) submissions in relation to formoterol were also checked. The date of the most recent search was October 2008.

Selection criteria:

Controlled parallel design clinical trials on patients of any age and severity of asthma were included if they randomised patients to treatment with regular formoterol and inhaled corticosteroids, and were of at least 12 weeks duration.

Data collection and analysis:

Two authors independently selected trials for inclusion in the review. Outcome data were independently extracted by two authors. Unpublished data on mortality and serious adverse events were obtained from the sponsors.

Main results:

The review included 14 studies on adults and adolescents (8,028 participants) and seven studies on children and adolescents (2,788 participants). Data on all cause fatal and non-fatal serious adverse events were found for all studies, and the overall risk of bias was low.

Four deaths occurred on regular formoterol with inhaled corticosteroids, and none on regular inhaled corticosteroids alone. All the deaths were in adults, and one was reported to be asthma-related. The difference was not statistically significant.

Non-fatal serious adverse events of any cause were very similar in adults [Peto Odds Ratio 0.99 (95% CI 0.74 to 1.33)], and an increase in events in children on regular formoterol was not statistically significant [Peto Odds Ratio 1.62 (95% CI 0.80 to 3.28)].

Asthma related serious adverse events on formoterol were lower in adults [Peto Odds Ratio 0.53 (95% CI 0.28 to 1.00)] and although they were higher in children [Peto Odds Ratio 1.49 (95% CI 0.48 to 4.61)], this was not statistically significant.

Authors' conclusions:

It is not possible, from the data in this review, to reassure people with asthma that inhaled corticosteroids with regular formoterol carries no risk of increasing mortality in comparison to inhaled corticosteroids alone as all four deaths occurred among 6,594 people using inhaled corticosteroids with formoterol. On the other hand, we have found no conclusive evidence of harm and there was only one asthma related death registered during over 3,000 patient year observation on formoterol. In adults, the decrease in asthma-related serious adverse events on regular formoterol with inhaled corticosteroids was not accompanied by a decrease in all cause serious adverse events. In children the number of events was too small, and consequently the results too imprecise, to determine whether the increase in all cause non-fatal serious adverse events found in the previous meta-analysis on regular formoterol alone is abolished by the additional use of inhaled corticosteroids. Clinical decisions and information for patients regarding regular use of formoterol have to take into account the balance between known symptomatic benefits of formoterol and the degree of uncertainty and concern associated with its potential harmful effects.

This record should be cited as:

Cates CJ, Lasserson TJ, Jaeschke R. Regular treatment with formoterol and inhaled steroids for chronic asthma: serious adverse events. Cochrane Database of Systematic Reviews 2009, Issue 2. Art. No.: CD006924. DOI: 10.1002/14651858.CD006924.pub2

Assessed as up to date:

November 21, 2008

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Primary Review Group:

Airways Group

Asthma topics:

Treating with Medications > Combination Inhalers

Treating with Medications > Chronic Asthma > Combination and additive therapies

Health topics:

Lungs & airways > Asthma (chronic) > Combination/additive drug treatment

Cochrane Summaries^beta

Independent high-quality evidence for health care decision making

Serious adverse events with regular formoterol and inhaled corticosteroids

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