I wonder if anybody has the same problem as I have. I have been taking Liothyronine made by Mercury Pharma for many years along with Levothyroxine and my symptoms have stabilised. However the Pharmacy recently swapped me to Morningside and I began to feel extremely tired with unexplained weigh gain with a few days of taking the new table. My following prescription again gave me yet another brand by Tevn and again I don't feel as well as I did on the Mercury tablets.
Has anybody else experienced anything like this and any ideas how I can get back to my original make of liothyronine?
Any advise / help appreciated. Many thanks.
Kerry
Written by
kerrylouisa1966
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It is quite common for people to do well on one brand and not so well on another. Now that you know which brand works best for you, tell the pharmacy that they must fill your prescription only with that brand.
When you collect your tablets, check before you leave the shop that they have given you the ones you want. If they are the wrong ones, don't accept them. If they say they haven't got the brand you want, ask for your prescription back so that you can take it to another pharmacy who can supply the ones you want.
Thank you I have read your blog as well, I think given I now have 2 different tablets I'll swap to the Teva ones as they don't seem to give me the afternoon tiredness that Morningside do. Also interesting to see symptoms of nausea which I didn't associate with the change of tablet but maybe it is? Thanks again for your replies very helpful.
I had the same problem, and my local pharmacy refused to order Mercury as they said it cost them too much. (Some deal they had with the manufacturers?) Went to Boots and they order Mercury in for me.
When I asked my pharmacist to make sure I was only given MP, she starchily told me it was very expensive and I should think myself lucky I was getting it.
I got a list of all the different types of Lio prescribed in Britain (from this site!) and took it to my pharmacist. There were pennies difference between each brand.
Then I went to my doc who contacted them and told them I must only be given MP.
I’ve learned that you have to kick up a fuss in this game!
I get Mercury Pharma written on my prescription as I was allergic to Morningside, I refused to have Teva afte4 the Levo made me so unwell, the BNF say you should have a blood test after brand change after 2 months, so what the pharmacy are saving pennies as will cost nhs more to keep having blood tests so don’t let them Get away with a cheaper brand as it’s not saving NHS money and risks your health !
That is very interesting about the blood test as nobody has said anything and I've now had 3 different tablets in the space of six months :-(. No blood test has been recommended though. Hope you got yours sorted.
To be fair I haven't as yet been back to the chemist to ask them to change so that is the first thing I will do. I was put off as I mailed the doctor about the issues and they just simply replied that all tablets were the same so though it was just me. I am glad in a way (although it i sad that we are all suffering) that it is not just me so they will be my next point of call if I can't get them swapped at Boots. Thanks again for responding.
I was told by My pharmacy that Mercury Pharma no longer available as they had merged with another company now called Adco. Ordered this- packaging same as mercury pharma and tablets seem to be the same. Expire 2/19 so may be old MP stock, but worth discussing with your pharmacist.
I was on mercury and they gave me teva liothyronine. I have noticed the difference in symptoms. I went to the pharmacy to ask for mercury again and the said to me I can't have it as every time they order it they have to pay an extra £5 on the prescription. I haven't been well on it so now have gone back to my tiremol that I purchased from Turkey. Its so frustrating when you start to get better then they move the goal posts. Think I will try and go to another chemist with the prescription. Just so annoyingly. 😡
Oh no that is awful that you have had to source yourself. I will try at Boots and see what happens. I hope you get yourself sorted out. It is very frustrating.
I am currently going through exactly the same thing been extremely stable on mercury pharma for 5 years then pharmacy said out of stock uk so put me on morningside months later same thing out of stock so was given Teva all hell broke lose as it turned my body upside down & inside out found out I’m allergic so pharmacy said that’s all they have go & find it yourself with the help from this site I changed pharmacy & now on another brand thyrobon Germany one I have just had bloods & my results say it all I’m out of range & back to the consultant I go on Tuesday how much money is that all going to waste I feel your pain hang in there xx
i was given morningside a few months ago and felt ill on it. asked boots to change back to mercury pharma and they did with no problem. i am thinking of moving soon away and am very worried i wont be allowed it somewhere else
I wasn't doing well at all on MP and was about to request a different brand when out of the blue my next prescription contained Teva Lio. (I'm one of the odd folk who do get on with it lol!) I felt a huge improvement in less than a couple of days and decided I'd like to stick with it but next trip to the pharmacy it was back to MP - previous change had been a supply issue. I said I'd like Teva from now on and was told I could only have it if the GP stated 'Must be Teva' on my prescription due to the cost (but as someone else mentioned,there's actually little difference between cost of brands and if it works... what's the problem?!). If you find a brand that suits you, stick to your guns! It may be useful if you can get your GP add your specific brand to your prescription ... I wrote a note to mine explaining how much better I felt after changing to the new brand. So much easier than trying to find a pharmacy with the right one in stock and my pharmacy now have a note on their system too. Good luck!
Hi Everyone. Just to give you an update. Boots have been brilliant and they have managed to source the Mercury Pharma tablets for me and I have them in my hand now .
However not sure if any of you have been told, but when I asked my doctor for a prescription to actually get the tablets he told me that the Government had written to doctors to advise them that the liothyronine in general is very likely to be withdrawn completely from the UK market so we won't be able to get it any more, regardless of make.
Has anybody else heard this and also does anybody buy their own medication and if so how much does it cost? I am quite worried about this to be honest.
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