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The hazard ratio for survival in the Femara arm compared to the tamoxifen arm was 0, mod grf (1-29) (cjc-1295 no dac) 2 mg peptides.
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Note: ‘During treatment’ includes 30 days after last dose. Differences were based on risk ratios and 95% confidence intervals. Table 3 Sequential treatment versus Femara monotherapy ‘ adverse events with significant differences. Note : Reporting period is during treatment or within 30 days of stopping treatment. Description of selected adverse reactions. In the adjuvant setting, in addition to the data presented in Table 2, the following adverse events were reported for Femara and tamoxifen, respectively (at median treatment duration of 60 months plus 30 days): angina requiring surgery (1. In the extended adjuvant setting for Femara (median duration of treatment 5 years) and placebo (median duration of treatment 3 years), respectively: angina requiring surgery (0. Events marked * were statistically significantly different in the two treatment arms. For skeletal safety data from the adjuvant setting, please refer to Table 2. In the extended adjuvant setting, significantly more patients treated with Femara experienced bone fractures or osteoporosis (bone fractures, 10. Median duration of treatment was 5 years for Femara, compared with 3 years for placebo. Reporting of suspected adverse reactions. Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme at: www. Isolated cases of overdose with Femara have been reported. No specific treatment for overdose is known; treatment should be symptomatic and supportive. Pharmacotherapeutic group: Endocrine therapy. undefined Selected baseline characteristics for the study population are shown in Table 8, mod grf (1-29) (cjc-1295 no dac) 2 mg peptides. 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