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About Sayana PressManaging ExpectationsSelf-administrationSupport & ResourcesVideosMaterials

Indicated for long term female contraception.  Click here for Sayana®-Press (medroxyprogesterone acetate) Prescribing Information.  Adverse event reporting information can be found at the bottom of the page.

Sayana®-Press: Injectable Female ContraceptiveAbout Sayana-Press

Prescribe women a LARC* injection convenient for their lifestyle and one which has been built on over 30 years of contraception heritage1. Sayana-Press is a smart device with a once-every-13-weeks administration schedule (+/-1 week) for eligible women.2

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Self-administration

Explore Sayana-Press and watch the self-administration film.

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Managing Expectations

What can women expect from Sayana-Press?

For a list of adverse events please refer to the SPC

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Useful Resources

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Sayana-Press Patient website

*Long acting reversible contraception
To read the full special warnings and precautions for use for Sayana-Press and see a full list of adverse events, refer to 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.

References

Depo-Provera® Summary of Product Characteristics. Available at: https://www.medicines.org.uk/emc/medicine/11121 Date accessed December 2020.Sayana-Press Summary of Product Characteristics. Available at: https://www.medicines.org.uk/emc/medicine/27798/SPC/SAYANA%2BPRESS%2B104%2Bmg%2B0.65%2Bml%2Bsuspension%2Bfor%2Binjection/ Date accessed December 2020.
PP-SAY-GBR-0187. February 2021

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Adverse events should also be reported to Pfizer Medical Information on 01304 616161

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