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medroxyprogesterone acetate (Sayana® Press)

 

Status: Medicine does not meet criteria for AWMSG assessment

Excluded from appraisal by AWMSG as meets exclusion criteria 6. See AWMSG criteria for appraising a medicine (PDF, 430Kb) for information.

Medicine details

Medicine name medroxyprogesterone acetate (Sayana® Press)
Formulation 104 mg/0.65 ml suspension for injection
Reference number 2222
Indication

Long-term female contraception. Each subcutaneous injection prevents ovulation and provides contraception for at least 13 weeks (+/- 1 week). However, it should be taken into consideration that the return to fertility (ovulation) may be delayed for up to one year. Since loss of bone mineral density (BMD) may occur in females of all ages who use Sayana® Press long-term, a risk/benefit assessment, which also takes into consideration the decrease in BMD that occurs during pregnancy and/or lactation, should be considered. In adolescents, use of Sayana® Press is only indicated when other contraceptive methods are considered unsuitable or unacceptable, due to unknown long-term effects of bone loss associated with Sayana® Press during the critical period of bone accretion. Sayana® Press has not been studied in women under the age of 18 years but data is available for intramuscular medroxyprogesterone acetate in this population

Company Pfizer Ltd
BNF chapter Obstetrics, gynaecology & urinary tract disorders
Assessment type N/A
Status Medicine does not meet criteria for AWMSG assessment
Date of issue 05/06/2013
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