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Musculoskeletal: Myalgia; arthralgia; pathological fracture Nervous: Somnolence; confusion; insomnia; anxiety; nervousness Respiratory: Sinusitis; bronchitis; rhinitis Skin and Appendages: Hair thinning; pruritus Urogenital: Urinary tract infection; breast pain The incidences of the following adverse event groups arimidex potentially causally related to one or both of the therapies because of their pharmacology, were statistically analyzed: weight gain, edema, thromboembolic disease, gastrointestinal disturbance, hot flushes, and vaginal dryness .
These six groups, and the arimidex adverse events captured in the groups, were prospectively defined .
The results are shown in the arimidex table below .
NDA 20-541/S-016 Table 13 – arimidex Number (n) and Percentage of Patients Megestrol Acetate Adverse Event Group Gastrointestinal Disturbance Thromboembolic Disease More patients treated with megestrol acetate reported weight gain as an adverse event compared to patients treated with ARIMIDEX 1 mg (p<0 .
Other differences were arimidex not statistically significant .
An examination of the magnitude arimidex of change in weight in all patients was also conducted .
Thirty-four percent (87/253) of the patients treated with megestrol acetate experienced weight gain of 5% or more and 11% (27/253) of the patients treated with megestrol acetate anastrozole india anastrozol y fiebre anastrozole noael anastrozole recommended dosage arimidex hot experienced weight gain of 10% or more .
Among patients treated with ARIMIDEX 1 mg, 13% [33/262] experienced weight gain of 5% or more arimidex and 3% [6/262] experienced weight gain of 10% or more .
On average, this 5 to 10% weight gain represented between 6 arimidex and 12 pounds .

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