48 year old patient diagnosed with heavy menstrual bleeding 2 years ago. She had an IUS Mirena® (levonorgestrel) fitted and had no issues until 6 weeks ago. The patient started developing episodic period pain lasting 2-3 hours. These patient case studies are all fictitious.
RP-PF-WHC-GB-1033 May 2022
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: email@example.com
Further information is available on the “contact” tab at www.bayer.co.uk.