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  • Odhadovaná tříletá pravděpodobnost výskytu pneumonie hlášená jako nežádoucí příhoda byla 12,3% u placeba, 13,3 % u salmeterolu, 18,3 % u flutikason-propionátu, 19,6 % u salmeterolu-FP (poměrné riziko pro salmeterol-FP versus placebo: 1,64; 95 % Cl: 1,33 až 2,01, p<0,001). (cs)
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