Valproate (Belvo, Convulex, Depakote, Dyzantil, Epilim, Epilim Chrono or Chronosphere, Episenta, Epival, and Syonell▼): review by two specialists is required for initiating valproate but not for male patients already taking valproate
Review by two specialists remains in place for patients initiating valproate under 55 years of age but the Commission on Human Medicines (CHM) has advised that it will not be required for men (or males) currently taking valproate.
Three infographics have been developed to provide clarity regarding valproate prescribing.
Advice for Healthcare Professionals:
- the CHM has advised that a review by two specialists is required for initiating valproate under 55 years but not for men who are already taking valproate
- three infographics have been produced to clarify in which situations review by two specialists may be required:
- a list of who might qualify as a specialist can be found at Valproate safety measures
- report suspected adverse reactions associated with valproate on Yellow Card
Reminder of previous advice for healthcare professionals:
Patients under 55 years of age starting valproate
- valproate must not be started in new patients (male or female) younger than 55 years unless two specialists independently consider and document that there is no other effective or tolerated treatment, or there are compelling reasons that the reproductive risks do not apply. For many patients, other effective treatment options are available to treat their bipolar disorder or epilepsy
- information on permanent reasons or compelling reasons as to why the reproductive risks may not apply to a patient may be sought from clinical guidance
Women and girls of childbearing potential currently taking valproate
- at their next annual specialist review, women and girls of childbearing potential receiving valproate should have their treatment reviewed using the revised Annual Risk Acknowledgement Form. At this review, if the patient has never been reviewed by two specialists either at initiation or annual review, a second specialist signature will be needed if the patient is to continue on valproate. Women do not need to be recalled for an additional review. Once a patient has received a treatment review by two specialists, subsequent annual reviews only require one specialist
Men currently taking valproate
- as a precaution, recommend that male patients and their female sexual partner use effective contraception (condoms, plus effective contraception used by female sexual partner) throughout the valproate treatment period and for 3 months after stopping valproate, to allow for one completed sperm cycle not exposed to valproate
- at their next regular treatment review, discuss with men on oral valproate treatment whether they are planning to father a child in the next year and if they are, refer to a specialist to discuss most appropriate treatment options
- advise men not to donate sperm during valproate treatment and for 3 months after stopping valproate
- if a female reports they are pregnant or planning a pregnancy with a man on valproate, refer them for prenatal counselling
Advice for Healthcare Professionals to Provide to Patients:
- do not stop taking valproate without advice from a specialist. This is because epilepsy or bipolar disorder may worsen without treatment
- if you are on valproate, please attend any offered appointments to discuss your treatment and talk to a healthcare professional if you are concerned
- if you wish to discuss family planning, please contact a healthcare professional
Background
Valproate treatment and reproductive risks
Valproate (as sodium valproate, valproic acid or valproate semisodium) is authorised for the treatment of epilepsy and bipolar disorder. Valproate is known to have potential risks of major congenital malformations or neurodevelopmental disorders in children when mothers take valproate during pregnancy. More recently, the risk of a range of neurodevelopmental disorders in children born to fathers taking valproate compared to other antiseizures medicines has been described.
Studies have shown that the use of valproate during pregnancy is associated with risks of physical defects, in around 1 in 9 babies exposed, and neurodevelopmental disorders, in around 3-4 in 10 babies when mothers use valproate in pregnancy. There is a much lower potential risk of neurodevelopmental disorders, in around 5 in 100 babies when fathers take valproate in the 3 months before conception. Additional reproductive risks of valproate in male patients include infertility in humans and evidence of testicular toxicity in animals.
In 2022, the Commission on Human Medicines (CHM) reviewed the latest data on the reproductive risks with valproate. Their advice was communicated in Drug Safety Update December 2022. The CHM formed an implementation group to advise on the safe introduction of the new measures into clinical practice.
The measures were applied first to all new patients under 55 years old and women of childbearing potential already under specialist review. The National Patient Safety Alert on 28 November 2023 and Drug Safety Update January 2024 provided further advice on the implementation of these requirements.
No requirement for specialist review of men currently taking valproate was introduced at this time unless the male patient was planning to father a child. The CHM recommended that any further measures should consider advice from healthcare professionals and patients developed in light of experience with the initial phase.
Recent review and updated advice
Review by two specialists remains in place for all patients initiating valproate under 55 years of age but the CHM has advised that it will not be required for men (or males) currently taking valproate. Given the recent recommendations in Drug Safety Update September 2024, the CHM advised that there is already sufficient risk minimisation in place for this patient group but that this position should be kept under review. In addition to the Drug Safety Update September 2024, further information on the reproductive risks for males can be found in a Public Assessment Report published in November 2023. Any patient wishing to change their medication should be referred to a specialist.
The information considered by CHM and the advice issued is presented in a Public Assessment Report.
Three infographics have been produced to clarify in which instances two specialist review may be required:
Reporting advice
Healthcare professionals, patients, and caregivers are asked to submit reports using the Yellow Card scheme electronically using:
- the Yellow Card website.
- the Yellow Card app; download from the Apple App Store or Google Play Store
- some clinical IT systems for healthcare professionals (EMIS, SystmOne, Vision, MiDatabank, and Ulysses)
When reporting suspected adverse drug reactions, please provide as much information as possible, including information about medical history, any concomitant medication, onset timing, and treatment dates.
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Article citation: MHRA Safety Update volume 18, issue 7: February 2025: 1