MHRA
- Local brand name: Neofordex
- Status: approved
NICE has issued 22 UK HTA decisions
22 decisions from NICE for Decadron in United Kingdom.
NICE has made a decision about Decadron for the treatment of previously treated multiple myeloma. Unfortunately, the details of the decision are not publicly available. The decision date and the cost-effectiveness assessment (ICER) are also not reported.
NICE recommended Decadron for the treatment of previously treated multiple myeloma. This decision was made with the support of a Patient Access Scheme and a commercial arrangement. No restrictions were placed on the use of Decadron.
NICE recommended Decadron for the treatment of previously treated multiple myeloma. This decision was made based on a patient access scheme and commercial arrangement. No restrictions were placed on the use of Decadron.
NICE recommended Decadron for treating relapsed and refractory multiple myeloma after 4 or more treatments. This decision was made without a reported ICER. A commercial arrangement was in place for this recommendation.
NICE made a decision to terminate the appraisal of Decadron for treating relapsed or refractory multiple myeloma. This decision means that NICE will not make a recommendation on the use of Decadron for this indication. The cost-effectiveness of Decadron was not reported as part of this decision.
NICE recommended Decadron for the treatment of untreated multiple myeloma when a stem cell transplant is unsuitable. This decision was made based on a commercial arrangement. No restriction or condition was placed on the use of Decadron for this indication.
NICE recommended Decadron for the treatment of previously treated multiple myeloma. This decision was made based on a patient access scheme and commercial arrangement. No restrictions were placed on the use of Decadron.
NICE recommended Decadron for treating relapsed or refractory multiple myeloma. This decision was made based on a patient access scheme and commercial arrangement. No restrictions were placed on the use of Decadron for this indication.
NICE made a decision to terminate the appraisal of Decadron for treating relapsed or refractory multiple myeloma. This decision means that NICE will not make a recommendation on the use of Decadron for this indication. The cost-effectiveness of Decadron was not reported as part of this decision.
NICE recommended Decadron for treating diabetic macular oedema. This decision was made without a reported cost-effectiveness analysis. There are no restrictions or conditions associated with this recommendation.
NICE made a decision to terminate the appraisal of Decadron for treating relapsed or refractory multiple myeloma. This decision means that NICE will not be making a recommendation on the use of Decadron for this indication. The decision to terminate was made without a recommendation on cost-effectiveness or a patient access scheme.
NICE made a decision to terminate the appraisal of Decadron for treating relapsed or refractory multiple myeloma. This decision means that NICE will not make a recommendation on the use of Decadron for this indication. The cost-effectiveness of Decadron was not reported as part of this decision.
NICE recommended Decadron for the treatment of previously treated multiple myeloma. This decision was made based on a Patient Access Scheme and a commercial arrangement. No restrictions were placed on the use of Decadron.
NICE recommended Decadron for treating relapsed and refractory multiple myeloma. This decision was made based on a commercial arrangement, which suggests that the drug's price was negotiated with the manufacturer. No restrictions were placed on the use of Decadron for this indication.
NICE made a decision to terminate the appraisal of Decadron for the treatment of untreated multiple myeloma. This decision means that NICE will not be making a recommendation on the use of Decadron for this indication. The cost-effectiveness of Decadron was not reported as part of this decision.
NICE made a decision to terminate the appraisal of Decadron for treating relapsed or refractory multiple myeloma. This decision means that NICE will not make a recommendation on the use of Decadron for this indication. The cost-effectiveness of Decadron was not reported as part of this decision.
NICE recommended Decadron for the treatment of macular oedema secondary to retinal vein occlusion. This decision was made without any restrictions or conditions. The cost basis of this decision is not reported.
NICE made a decision to terminate the appraisal of Decadron for the treatment of untreated multiple myeloma. This decision means that NICE will not make a recommendation on the use of Decadron for this indication. The decision to terminate was made without a recommendation on the cost-effectiveness of Decadron, as the ICER was not reported.
NICE recommended Decadron for the treatment of multiple myeloma in adults who have had one treatment with bortezomib. This decision was made based on a commercial arrangement. No restriction or condition was placed on the use of Decadron.
NICE recommended Decadron for the treatment of previously untreated multiple myeloma. This decision was made based on a commercial arrangement, indicating a negotiated price with the manufacturer. No restrictions or conditions were placed on the use of Decadron for this indication.
NICE recommended Decadron for treating non-infectious uveitis. This decision was made without a Patient Access Scheme or commercial arrangement. No restrictions were placed on the use of Decadron for this indication.
NICE made a decision to terminate the appraisal of Decadron for treating relapsed or refractory multiple myeloma. This decision means that NICE will not make a recommendation on the use of Decadron for this indication. The cost-effectiveness of Decadron was not reported as part of this decision.
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. MHRA has authorised it.
Generic (originally Merck) is the originator. The local marketing authorisation holder may differ — check the official source linked above.
Yes — 22 UK HTA decisions on record from NICE.