ACTIVELLA® 0.5mg/0.1 mg bleeding profile

In a clinical trial, ACTIVELLA® 0.5 mg/0.1 mg demonstrated a similar bleeding profile when compared with placebo.1,8

88% of women treated with ACTIVELLA® 0.5 mg/0.1 mg were amenorrheic after 6 months.1 Only 1% of women treated with ACTIVELLA® 0.5 mg/0.1 mg discontinued because of bleeding.9

ACTIVELLA® 0.5 mg/0.1 mg – Similar bleeding profile when compared with placebo

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Important Safety Information

REFERENCES:

  • 1. ACTIVELLA® [package insert]. Princeton, NJ: Novo Nordisk Inc; 2007.
  • 8. Panay N, Ylikorkala O, Archer DF, Gut R, Lang E. Ultra-low-dose estradiol and norethisterone acetate: effective menopausal symptom relief. Climacteric. 2007;10:120-131.
  • 9. Data on file. CTR. Novo Nordisk Inc, Princeton, NJ. Trial ID: ALD-1537.