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Sayana®-Press (medroxyprogesterone acetate) Prescribing Information. Adverse event reporting information can be found at the bottom of the page.
Depo-Provera® (medroxyprogesterone acetate) Prescribing Information.
Watch this guide on self-administrating Sayana-Press.
99% effective in preventing pregnancy if used according to the product recommendations of every 13 weeks (+/-7 days).3
Two open-label, multi-national, multi-centre, Phase III, 1-year trials were undertaken in order to assess the efficacy and safety of depot-medroxyprogesterone acetate subcutaneous (DMPA-SC injection).3
Conducted at 36 sites and involved 722 women in the ITT (Intent-To-Treat) population.
Conducted at 64 sites (including UK sites) and involved 1065 women in the ITT populations
Sayana-Press delivers an immediate† 13 weeks of contraception.2††
*Self-administration should be first performed under the supervision of an HCP following training of the woman in proper injection technique and schedule of administration.
†Providing the first injection is given during the first five days of a normal menstrual cycle and subsequent injections are given no later than thirteen weeks and seven days after the previous injection.
††Sayana-Press does not protect against sexually transmitted infections (STIs)
Read the full special warnings and precautions for use for Sayana-Press and see a full list of adverse events, in the Summary of Product Characteristics. The benefits of contraceptive options and their risks must be evaluated individually for each woman. If any of the conditions/risk factors mentioned is present, the benefits of Sayana-Press use should be weighed against the possible risks for each individual woman and discussed with the woman before she decides to start using it. In the event of aggravation, exacerbation or first appearance of any of these conditions or risk factors, the woman should contact her physician. The physician should then decide on whether Sayana-Press use should be discontinued.
What can women expect from Sayana-Press?
References:
Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search
for MHRA Yellow Card in Google Play or Apple App Store
Adverse events should also be reported to Pfizer Medical Information on 01304 616161
To access further materials, resources and receive communication about medicines and vaccines promoted by Pfizer.
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These pages are not intended for patients or for members of the general public. The healthcare professional web pages contain promotional content.
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PP-UNP-GBR-7812. January 2024