FAQ's
Starting Ryeqo
One tablet of Ryeqo must be taken once daily, at around the same time each day, with or without food. Ryeqo can be taken without interruption.1
When starting treatment, the first tablet must be taken within 5 days of the onset of menstrual bleeding. If treatment is initiated on another day of the menstrual cycle, irregular and/or heavy bleeding may initially occur. Pregnancy must be ruled out prior to initiating treatment with Ryeqo.1
Treatment recommended to be limited to 24 months, with extension of therapy conditional on stability of DXA and reassessment of risk/benefit in the individual patient by the treating physician.1
If a dose is missed, treatment must be taken as soon as possible and then continue the next day at the usual time. If doses are missed for 2 or more consecutive days, a non-hormonal method of contraception is to be used for the next 7 days of treatment.1
Store at room temperature (below 30ºC).1
Contraception and Fertility
Ryeqo usually leads to a reduction in menstrual blood loss or amenorrhoea within the first 2 months of treatment.1 After 24 weeks of Ryeqo treatment in clinical studies, amenorrhoea was achieved in 65.2% of patients with endometriosis and 51.6% of patients with uterine fibroids.1 At 52 weeks this number increased to 79.6% and 70.6%, respectively.1–3
Women of childbearing potential should be advised that ovulation will return rapidly after discontinuing treatment. A discussion with the patient, regarding appropriate contraceptive methods, must therefore take place prior to discontinuing treatment and alternative contraception needs to be started immediately after discontinuation of treatment.1
Safety Considerations
Ryeqo was generally well tolerated in clinical trials.2,4 The most common adverse drug reactions for patients being treated for endometriosis were headache (17.0%) and hot flush (11.7%).1
Assessment of bone mineral density via a DXA scan is recommended at baseline and then annually after starting treatment. Use of Ryeqo is recommended to be limited to 24 months, with extension of therapy conditional on stability of DXA and reassessment of risk/benefit in the individual patient by the treating physician.1
Ryeqo is contraindicated in patients with: concomitant use of hormonal contraceptives; headaches with focal neurological symptoms or migraine headaches with aura; osteoporosis; pregnancy or breastfeeding; VTE/ATE (past or present); thrombophilic disorders; sex steroid influenced malignancies; liver tumours; severe hepatic disease; genital bleeding of unknown aetiology and hypersensitivity to active substances/excipients.1
Symptom Improvements
Many women see a significant effect on their symptoms as soon as four weeks. If it takes a little longer for your patient to see improvements, this is completely normal.3,4
References
1. Ryeqo Approved Product Information. January 2024.
2. Becker CM et al. Human Reproduction. 2024;39(3):526–537.
3. Al-Hendy A et al. Obstet Gynecol. 2022;140:920–30.
4. Giudice LC et al. Lancet. 2022;399:2267–2279.