T3 why is it so expensive in the UK as I believe it costs GPs £53 to prescribe it?
I buy Tiromel for my daughter when I'm in Turkey & it is less than a £1 for 28 tablets. Daughter is doing just as well on the Tiromel as the UK T3.
T3 why is it so expensive in the UK as I believe it costs GPs £53 to prescribe it?
I buy Tiromel for my daughter when I'm in Turkey & it is less than a £1 for 28 tablets. Daughter is doing just as well on the Tiromel as the UK T3.
It's a puzzle to me as well. I don't know why it is so expensive in the UK.
There is only the one version, made by mercury pharma ( formerly Goldshiled) which is licensed for uk use. So as there is no competition, they can charge what they like!
OK that figures; guess the answer is Bad Pharma & stupid NHS for not sourcing elsewhere!
Obviously any other product would need to be licensed in order to be supplier (though unlicensed products will be allowed short term).
So far as I know, it is up to individual pharmaceutical companies (whether importers, manufacturers, or whatever) to apply for licences. If none do, I cannot see how any other product can come to market?
Quite why the people who agree charges with pharmaceutical companies accept such high costs, I do not understand.
(I think it is these people: Pharmaceutical Services Negotiating Committee
)
Rod
I'm not sure if you've noticed but were ripped off in this country, good and proper....!
Rip off Britain ...... at it's best
psnc.org.uk/data/files/Brok...
The above link takes you to a page on psnc.org.uk which shows the cost of a pack of 28 Liothyronine (T3) to be £52.46! With a pack of Tiromel from Turkey at only £3.50 for one hundred tablets and a pack of 30 tablets from Uni-Pharma in Greece costing only 2 euro.
I will be writing to psnc to ask why they are agreeing to pay such inflated amounts of money out of public funds! It is disgraceful!!!
I will provide a copy of my letter on a blog, so that other members can copy and paste it into an emal to send to them as well.
Please see the letter I have just posted as a blog. I've said people are free to copy and paste it into their own email. The more people that lobby the more chance there will be of getting things changed.