- Active Ingredients
Product Documentation
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View RMM (Lenalidomide Information for the Patients)
Last updated on this site: 30 Oct 2024
Updated to v2.0
View RMM (Lenalidomide Patient Information Card)Last updated on this site: 30 Oct 2024
Updated
If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in the package leaflet. You can also report side effects directly via the Yellow Card Scheme at yellowcard.mhra.gov.uk. By reporting side effects, you can help provide more information on the safety of this medicine.
Report a side effect or a product complaintLenalidomide Accord 15mg Hard Capsules
- PL Number:
- PLGB 20075/1295
- MA Holder:
- Accord Healthcare Limited
- Product Classification:
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POM
- Product Status:
- Active
Product Documentation
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View Summary of Product Characteristics (SmPC- Lenalidomide Accord 15 mg Hard Capsules)
Last updated on this site: 07 Aug 2024
1) To update section 4.4, 4.8 and 5.1 of SmPC in line with the reference product (Revlimid; 2.5 mg, 5 mg, 7.5 mg, 10 mg, 15 mg, 20 mg, 25 mg Capsule, hard; EU procedure reference number: EMEA/H/C/000717/II/0126; MAH: Bristol Myers Squibb Pharma EEIG).
2) To update sections 4.4 of SmPC and updating RMP in line with the reference product (Revlimid; 2.5 mg, 5 mg, 7.5 mg, 10 mg, 15 mg, 20 mg, 25 mg Capsule, hard; EU procedure reference number: EMEA/H/C/000717/II/0123; MAH: Bristol Myers Squibb Pharma EEIG).
View Patient Information Leaflet (PIL- Lenalidomide Accord 2.5 mg, 5 mg, 7.5 mg, 10 mg, 15 mg, 20 mg, 25 mg Hard Capsules)Last updated on this site: 27 Jun 2023
Description of update:
1) To update sections 4.2 and 4.4 of SmPC and section 2 of leaflet in-line with the reference product (Revlimid; 2.5 mg, 5 mg, 7.5 mg, 10 mg, 15 mg, 20 mg, 25 mg Capsule, hard; EU procedure reference number: EMEA/H/C/000717/II/0122; MAH: Bristol Myers Squibb Pharma EEIG).
2) To update section 5.1 of the SmPC in-line with the reference product (Revlimid; 2.5 mg, 5 mg, 7.5 mg, 10 mg, 15 mg, 20 mg, 25 mg Capsule, hard; EU procedure reference number: EMEA/H/C/000717/II/0124; MAH: Bristol Myers Squibb Pharma EEIG). Additionally, editorial updates have been made to sections 4.2, 4.4, 4.5, 4.8, 5.1 of SmPC and section 2, 3 and 4 of PIL in line with reference products.
PIL sections updated: 2, 3, 6.
If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in the package leaflet. You can also report side effects directly via the Yellow Card Scheme at yellowcard.mhra.gov.uk. By reporting side effects, you can help provide more information on the safety of this medicine.
Report a side effect or a product complaint
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