MHRA
- Local brand name: Eliquis
- Status: approved
NICE has issued 4 UK HTA decisions
4 decisions from NICE for Eliquis in United Kingdom.
NICE recommended Eliquis for preventing stroke and systemic embolism in people with non-valvular atrial fibrillation. This decision was made without a Patient Access Scheme or commercial arrangement. No restrictions were placed on the use of Eliquis.
NICE recommended Eliquis for the treatment and secondary prevention of deep vein thrombosis and/or pulmonary embolism. This decision was made without a Patient Access Scheme or commercial arrangement. The cost-effectiveness of Eliquis was not reported in terms of ICER.
NICE recommended Eliquis for preventing venous thromboembolism after hip or knee replacement surgery. This decision was made without a Patient Access Scheme or commercial arrangement. The restriction text was not specified.
NICE recommended Eliquis for reversing anticoagulation from apixaban or rivaroxaban in the United Kingdom. This decision was made based on a commercial arrangement and a patient access scheme, which suggests that the cost of the drug was negotiated to be within the National Health Service's budget. There were no restrictions placed on the use of Eliquis for this indication.
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. MHRA has authorised it.
Bristol-Myers Squibb is the originator. The local marketing authorisation holder may differ — check the official source linked above.
Yes — 4 UK HTA decisions on record from NICE.