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Adverse event reporting can be found at the bottom of the page

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About Sayana PressManaging ExpectationsSelf-administrationSupport & ResourcesVideosMaterials

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. 

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
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.

References

Depo-Provera® Summary of Product Characteristics.Sayana-Press Summary of Product Characteristics.
PP-SAY-GBR-0216. January 2023

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

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