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Clotrimazol vs betametasona ) but not in the control group (Bethlehem Pharmaceutical) (OR, 0.78; 95% CI, 0.56–1.10; P =.03); and this significant reduction in incidence was also demonstrated patients with renal failure (OR, 0.61; 95% CI, 0.22–1.30; P =.02). No significant differences were observed in clinical outcomes between tadalafil and placebo. TidalVolume: Median tidal volume was significantly reduced at 24 and 48 months, in patients who received tadalafil (2.16 v 3.23 l; P =.002). The mean changes at end of the study were: 24 months: 0.24 l (0.01 at first 24 months); 48 months: 2.20 l (1.06 v 2.48 at first 24 months); and 52 months: 3.12 l (2.27 v 3.28 at first 24 months). ClinicalSafetyData The incidence of treatment-emergent adverse reactions during treatment with tadalafil was 4.4% at 24 months in placebo-treated patients (3.2% at Online pharmacy xanax australia 24 and 48 months, respectively); 9.5% at 52 months in tadalafil-treated patients (13.7% at first 48 months); and 23.8% at first 24 months of tadalafil and placebo (14.0% at 24 months and 16.6% 48 respectively) (Table 3). Adverse reactions were more frequent in those patients who received tadalafil but not placebo. In placebo patients, the incidence ratios of treatment-emergent adverse reactions were 1.10 (95% confidence interval, 1.01–1.18) for headache, 0.76 (95% confidence interval, 0.58–1.02) for dizziness, 0.58 (95% canada drug center free shipping confidence interval, 0.41–0.83) for nausea, 0.42 (95% confidence interval, 0.28–0.59) for urinary tract symptoms, 0.44 (95% confidence interval, 0.32–0.69) for asthenia, 0.33 (95% confidence interval, 0.25–0.40) for tinnitus, 0.24 (95% confidence interval, 0.23–0.29) for anemia, 0.23 (95% confidence interval, 0.18–0.25) for depression, 0.25 (95% confidence interval, 0.22–0.28) for anxiety, 0.19 (95% confidence interval, 0.15–0.24) for confusion, 0.16 (95% confidence interval, 0.14–0.18) for confusion about sex, 0.12 (95% confidence interval, 0.10–0.13) for sexual dysfunction, 0.12 (95% confidence interval, 0.08–0.15) for depression, 0.10 (95% confidence interval, 0.08–0.12) for somnolence, and 0.05 (95% confidence interval, 0.02–0.01) for headache. In tadalafil-treated patients, the incidence ratios of tadalafil-associated adverse reactions were slightly larger than for the placebo group: 1.04 (95% confidence interval, 1.01–1.07) for tinnitus at 24 months and 1.14 (1.04–1.21) at first 24 months and 1.03 (1.01–1.05) at first 52 months. The incidence ratios did not differ significantly. No significant association was observed of tadalafil treatment and death (OR, 0.94; confidence interval, 0.82–1.09) or hospitalization (OR, 0.96; confidence interval, 0.82–1.09) (Table 4). Table 4. Adverse Reaction Total No. Events P Value Tinnitus 14 12 1.00 dizziness 7 11 0.95 nausea 6 0.97 fatigue 10 0.83 somnolence 5 9 0.89 confusion about sex 4 9 0.90 anxiety 5 0.79 confusion about age 9 sex/age 4 0.86 tinnitus 3 9 0.77 insomnia 4 0.83 libido dysfunction 3 9 0.76 disorders 0.85 libido disturbances 3 9 0.72 abdominal pain 2 8 0.56 headache 0.53 dizziness 1 8 0.50 headache/nausea 0.49 abdominal discomfort 1 7 0.32 weight gain 4 0.16 headache 0 3 0.03 weight gain sexual dysfunction 1 3 0.