Prescribing information and Adverse event reporting can be found at the bottom of the page

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Mirena (52mg Levonorgestrel) approved for 8 years contraception­

Mirena® was approved in the UK for extended duration of use in contraception for up to 8 years.

Contraception: Mirena is effective for 8 years for contraception and should be removed no later than 8 years after insertion.

Idiopathic menorrhagia: Mirena is effective for 5 years in the indication idiopathic menorrhagia. Clinical data (from clinical trials conducted in women of 18 years and over) beyond 5 years of use are limited, return of symptoms may indicate reduced efficacy. The system should be removed or replaced in case symptoms return. If symptoms have not returned after 5 years of use, continued use of the system may be considered. Remove or replace no later than 8 years after insertion. 

Protection from endometrial hyperplasia during oestrogenreplacement therapy: In the indication for protection from endometrial hyperplasia during oestrogen replacement therapy, clinical data (from clinical trials conducted in women of 18 years and over) beyond 4 years of use are limited. Mirena should therefore be removed no later than 4 years after insertion.

Kyleena (19.5mg levonorgestrel) patient support leaflets available in 10 languages

To eliminate waste where possible, we have decided to move towards digital-only patient support leaflets for Kyleena. By moving to digital-only leaflets we have been able to offer the patient support leaflet in a variety of languages on www.kyleena.co.uk/resources for patients to view, as well as below for your visibility. These languages include: Punjabi, Hindi, Greek, Welsh, Gujarati, Arabic, Turkish, Polish, Urdu and English.

You can view/download them from our patient materials section.

View them here

PP-PF-WHC-GB-1363 January 2024

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Reporting adverse events and quality complaints

 

Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard. Adverse events should also be reported to Bayer plc.

 

If you want to report an adverse event or quality complaint, reports can be directed to: Tel: 011820‍63500 or email: pvuk@bayer.com

 

Further information is available on the “contact” tab at www.bayer.co.uk.