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  • To znamená redukci četnosti středních až těžkých exacerbací o 25 % (95% CI: 19 % až 31 %; p < 0,001) ve srovnání s placebem, o 12 % ve srovnání se salmeterolem (95% CI: 5 % až 19 %, p = 0,002) a o 9 % ve srovnání s FP (95% CI: 1 % až 16 %, p = 0,024). (cs)
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