I don't like to complain here or anywhere really, and try to keep my head down, as I am one of few who have managed to keep my T3 monotherapy going for around 11 years now, and fought off attempts to stop it, and even managed to hold on to it moving house. Just a few weeks ago my new GP summoned me for an appointment due to 'abnormal results' from my TFT (for this read low TSH no doubt). I sent her a 2 page A4 letter complete with reasons and evidence of why she should not worry on my account, and all has gone quiet again for now.......
Well this question is really about the fact that since I moved here, over a year ago, I have been prescribed 4 different brands of T3 (20mcg per tab as I am on 50 mcg per day), and some seem to work well and some seem to make me ill and how I can deal with this. In my previous place, Cornwall, I had Mercury Pharma specified on prescription, because Teva came instead one day, and made me ill. I managed to then get it marked on current prescription as NOT Teva and had no problem getting it regularly from Boots in Cornwall.
They managed to get me Mercury Pharma for a while here, but then couldn't (I wonder if they were looking for Mercury Pharma on the formulary, when it's actually on there under Advanz now). Then they got me Morningside for a while, and I believe that I was better on this than MP, but now they cannot get Morningside. So they have now sent me Viatris and since starting it just over a week ago my health has crashed badly, but I am doubting that it is the Viatris as I feel I should not jump to conclusions. Since being on it my symptoms have changed - fatigue and brain fog for 2 days, followed by fatigue, muscle pain, headaches, knee pain, Plantar Fasciitis flare up, now that's all gone, and I have a familiar symptom of a sinus soreness and fatigue. I have felt so unwell on Viatris, that I have also been trying adding in an extra 5 mcg.
I decided to try and be scientific as I have a small stash of each of these brands in my drawer!! I am trying each one for 2 weeks and taking BP and pulse and temp to see if any difference there - nothing significant so far on 2 brands tried. Then I will change and see if I get worse or better for the next 2 weeks (I would expect the difficult symptoms to calm down on the MP and especially the Morningside if this is an objective problem). I had Covid in Sept and was unwell for weeks afterwards, but I don't think it is that as I had improved a lot, though not as well as I was. It could be that I am going down with a cold, or it could be the change of seasons.
I just dread having to go through this all with the pharmaceutical team at the GP (they were actually OK when I got No Teva put on the prescription), but especially the pharmacists at Boots, who are behind the scenes, and hard to access. I am doing this method above so I can give myself more confidence that my health really does change on this Sigma Viatris, for the worse. I have just managed to find on a local map, an independent pharmacy, so that may be a possible route to get better treatment if Boots fail me here.
I did see that one other person on here a while back had tried Sigma Viatris and they too were putting it on a par with Teva T3. Is there anyone else who has tried the Viatris and had any problems please?