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  • Neexistoval žádný rozdíl u pravděpodobnosti výskytu kostních zlomenin (5,1 % u placeba, 5,1 % u salmeterolu, 5,4 % u FP a 6,3 % u salmeterolu/flutikason-propionátu; stupeň rizika u salmeterolu/flutikason-propionátu vs. placebo: 1,22, 95% CI: 0,87 až 1,72; p = 0,248). (cs)
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