My GPhad spoken to endocrinology who advised to keep trying more brands but I cannot get past 3-4 days without a severe reaction, constant retching and soul led over in pain, unable to sleep lying down and up in the night continually ill. Anyone else had this reaction? I am extremely worried if I cannot take anything.
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Da52
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I have tried Teva 50 mg mercury pharmacy 25mg. I have had problems with other meds in the past I react the same to anti depressants, HRT, snd cannot take antibiotics on an empty stomach. I have tried taking the mercury pharmacy after food but I was still as ill. I am not exaggerating when I say how poorly I was, my GP told me some people cannot take anti-depressants when I reacted to them, he said they were like poison to the body. Obviously I had a choice with that medication but this is different. I have tried anti nausea with meds in the past to no effect. I am feeling very vulnerable, I think myGP was happy to leave meds a bit as he said my thyroid progression had been very slow since 2007. It had dipped then bounced back a few times. What do you think of my recent results? I am seeing a homeopath to see if that can help.
I have had coeliac test which they say is unlikely. Result was 1.9 anything over 30 they say is coeliac but I have been gluten-free for 4 months/ I did include wheat in the week before the test. Why do you not recommend multivitamin if low vitamin an issue? What vitamins do I need?
Most contain iodine not recommended for anyone with autoimmune thyroid disease unless had iodine test even then iodine supplements have to managed extremely carefully by endocrinologist
Test vitamin D, folate, ferritin and B12 and see where you are
I am really concerned if I cannot tolerate the medication- humanbean has frightened me saying I will go mad and die in the next 12 years. I am not in a good place,
Currently no Glenmark in distribution network for distribution.McPammy takes Teva liquid levo, I think. I requested this brand. It is lactose, mannitol and maltitol free.
Don't touch Wockhardt liquid, as full of nasties!
Boots could only access Teva or Wockhardt liquid levo.
You can check each one by following through from my medicines document.
They are all fairly similar but there are differences.
helvella - Thyroid Hormone Medicines
I have created, and try to maintain, a document containing details of all thyroid hormone medicines in the UK and, in less detail, many others around the world.
It definitely appears easier to absorb. But at least some find large quantities of glycerol (or whatever other similar substance is used) intolerable - often causing gut issues.
It's not the fact that glycerol is a sugar. I could eat a teaspoon of sugar, honey, golden syrup etc., but I couldn't tolerate a teaspoon of glycerol when I had a trial of liquid levo prescribed.
'Side Effects
When taken by mouth: Glycerol is possibly safe when used short-term. Side effects might include headaches, dizziness, bloating, nausea, and diarrhea.'
Excipients in levothyroxine oral solution versus levothyroxine tablets – Wockhardt only. Other makes will vary.
The idea that levothyroxine oral solution products have less (or fewer!) excipients than tablets appears to be mis-placed.
Whether we consider the number of excipients. Or the quantities.
Weight
A typical 5ml dose of levothyroxine oral solution would weight around 5 grams.
A typical levothyroxine tablet would weigh around 100 milligrams. (I think many weigh less; a few might weigh more. This is just a typical dose. If you need multiple teaspoonfuls of levothyroxine oral solution, or take multiple tablets, that would have a significant effect.
But that 5 gram dose would inevitably be many times the weight of any conceivable tablet dose.
I see now McPammy has replied , and she is on Wockhardt liquid levothyroxine. For some reason I thought it was teva liquid. I was obviously wrong.I checked out the liquid levothyroxine last week as i needed one mannitol, lactose and maltitol free.
I knew Wockhardt didn't fit the bill for me and the Boots pharmacist said it had about everything in it I didn't want.
When I investigate it now I can only see maltitol as an ingredient I want to avoid. Like the Boots pharmacist, I seem to have seen an ingredient list for it that I now can't find.
Whatever we were looking at (and can't find now) also listed xanthan gum.
For those who find mannitol doesn't agree with them, xanthan gum should be avoided. It is derived from the sugar mannose, as is mannitol.
One of the foods where this is commonly used is commercial ice cream.
Thought it might be worth mentioning. It is a stabiliser in food.
I said that people with severe hypothyroidism could end up like that in Victorian times. Nobody in this century would be allowed to get anywhere near that bad.
People can sometimes end up in hospital being given thyroid hormones in a drip if things get very bad, but it is very rare.
All I was trying to impress upon you is that your doctor's suggestion that you don't treat your hypothyroidism was not a good one. Since your TSH is between 5 and 7 and you have positive thyroid antibodies, and your doctor has said there has been little change in your results since 2007 it suggests that you have mild autoimmune hypothyroidism.
Ask your doctor to refer you to someone who tests for allergies. If you've had similar reactions to multiple pills for multiple health problems you need to find out what the problem is, because you might get away with not taking thyroid hormones for a few years but what happens if something much more immediately serious happens e.g. a car accident or a heart attack?
You need to fix this problem if you want to have a good quality of life.
Thank you for your reply, I have always known I have medication problems snd tried to follow a healthy lifestyle to avoid statins, diabetes medication etc. This has really floored me and given me such anxiety I just want a resolution.
My GP was going to monitor me and test at 3 months if no real change then st 6 months eventually going to 12 months if he was happy with me and I was not unwell. He wasn’t abandoning me.
I have tried a few brands and I much prefer Wockhardt brand. I was told by Wockhardt customer services that a bottle of 50mcg oral liquid Levothyroxine is £97. A bottle lasts my 2 weeks. So, it’s more like £200 a month. Expensive indeed. It was suggested in writing to my GP from my private only Endocrinologist. My GP prescribed it straight away without any issue. The reason behind it was to reduce excipients and also so I can take 68mcg easily a day. I also split my daily 68mcg dose leaving a few hours apart. This also helps me. I’m also on T3 twice a day. I feel very well (except I recently tested positive for covid 🙄). Took 13 days to test negative! I’m much better now and back to my old energised self thankfully.
I note your having problems with your thyroid medication, l'm in the same situation in that I'm lactose intolorent and have colitis, as slowdragon said the fillers can affect us, my first lot of T4 contained lactose it took months of me having bad stomach /bowle/ vomiting and awful thyroid blood results for the gp to get me on lactose free T4 but unfortunately I still had the same side affects, the lactose free T4 contained mannitol which still affected me, I finally got on T3 lactose free and felt much better, but T3 is very hard to obtain, I was put bk on T4 lactose free in March 2022 and all my side affects and symptoms have returned, I'm seeing an endo in Aug and I'm going to have a good talk about how this medication is affecting me and my thyroid levels, I'm also going to ask for liquid Thyroxine, as I to can't take certain medication like asprin, antibiotics, anti inflammatory drug, I couldn't even stomach the anti thyroid drugs.. It will be interesting to see what this endo recommends. 🤔🤔🤔
It's flipping teva... 🤦♀️ I was also on teva T3 that was OK on my stomach/bowles but gave me a very bad metallic taste in my mouth, as you may know I came of the T3 teva as my gp said my symptoms were due to it
Symptoms:
Frequency urinating
Server thirst
Bad joint pains / bad bone vibration
Irregular heart beat
Bad headaches
Muscle cramps
Throat pain /throbbing.. ( no thyroid)
Croaky voice
Sweating
She decrease my T3 on theses results.. (TSH.. 0.05...T3..6.6)
Decreased from 40mg to 30mg I then went hypo🤦♀️ it was then I'd had enough and came off T3 ( teva) went on T4 (teva) 50mg to show her it is not the t3 causing the symptoms ( I still have them) makes no difference, so now she as said because of my side effects to the T4 which I had when on it in 2019, I need to see the endocrinologist, but she will not put me bk on the t3.. As you know 2 endocrinologist diagnosed me with primary hyperparathyroidism in 2020..unsurprisingly they are still dragging their heels on this diagnosis 🤦♀️.. I see the endo on the 3rd Aug.. Its a flipping mess slowdragon 😔😔 so she has left me under medicated and by now very hypo.. 😤
I've been trying to get my gp to see me face to face to discuss this but I've only been given phone appointments, the last was May the one the gp told me to decrease my T4 from 50mg to 25mg until I see the endo, I had a very bad appointment before that with another gp who refused to acknowledge the Parathyroid levels being the cause of my symptoms ( another gp who as no idea what their talking about) PTH... 8.1..PTH 9.5...ranges.. 1.60...6.90.) the only thing I found with the teva T3 was the metallic taste its the same with the T4 to.. But never had any bowle/stomach problems with teva T3... So the gp should really have put me bk on it like I asked, instead of keeping me hypo until I see the endo.. I'm contacting the surgery on Monday because I know that endos like having your up to date bloods when you see them, last one was May 16 with TSH of 6.04 range.. 0.30..4.50..on 50mg can't imagine what it will be now only being on 25mg since May?.. 😔
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