Hi Has anyone tried Teva levothyroxine solution, and had positive results compared to taking any levothyroxine tablets?
To cut a very long story short, the 75 mcg Wockhardt tablets I take are causing terrible pressure all over body and excruiciating burning through top of my head. So bad I collapse. I have tried many other brands that gave me horrible side effects, Wockhardt was the only brand I could tolerate but barely. Now this is happening.
I have been given 1 bottle of liquid to try, but Teva was the only one the pharmacist could get, ( well that's what he said). Out of all the brands to try I was really hoping it wouldn't be Teva.
I had RAI in 2010 and everything went down hill from there.
Thank you.
Written by
Razzydaz
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You haven't posted very often and theres nothing in your profile but what members have found is that they need all key vitamins at OPTIMAL levels for their thyroid hormone to work well.
Have you recently or could you ask your GP to test ferritin, folate, B12 & D3?
Private tests are available, see link for companies offering private blood tests & discount codes, some offer a blood draw service at an extra cost.thyroiduk.org/testing/priva...
There is also a new company offering walk in (includes free blood draw) & mail order blood tests in London, Kent, Sussex & Surrey areas. Check to see if there is a blood test company near you. onedaytests.com/products/ul...
Only do private tests on a Monday or Tuesday to avoid postal delays.
Our vitamin levels drop due to low stomach acid from being hypo. So then, in turn our thyroid hormone wont work well.
Most members here supplement their vitamin levels continuously.
I have not posted very often because I just gave up, after years trying everything including supplements etc to feel normal. I cannot get optimal with my FT3 level, even though I supplement with T3. Sadly it contributes to the burning so I can only take a little.
Last thing for me to try is the liquid but not getting my hopes up just yet, nothing else has worked.
I have just taken the thyroid advance test through Medichecks, I should get results tomorrow.
My thyroid tests always show me as high T4 and low T3. My cortisol is high at the moment too.
Even though I am now classed as hypo, my symptoms are more hyper than hypo.
I will 😊I am on 75 mcg levo (which doesnt last in my body very long) and 1.25 mcg liothyronine x 3 to prop up the slumps during the day. The 3rd I have to leave as close as I can going to sleep otherwise I am woken up as if I am being choked, with my heart pounding agressively.
Yes it is low, I feel like I do need more to last through the day, but I get such awful sensations and pain if I try to increase either. If I add any more levo my T4 would escalate far too high, its on 25.4 at the moment. And it feels like my body is going to explode most days from the pressure. 1.25 mcg T3 is a 5mcg tablet cut into 4 😊.
My last B12 was over the highest number in normal range. I do not even supplement that because it has been high for years.
No one From NHS ever questions why I can only take a low amount without a thyroid. Even when I try to ask. My results are always OK they say. My last visit the GP said oh we don't look at T4 or T3 just TSH, and 25.4 is fine because your TSH is good at 0.26.
Hopefully, my results for thyroid, vit d, B12, folate, etc will be back tomorrow. I will post them.
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I am now tablets.. works great, I take at 5:40am so I can enjoy coffee after 6:15am and then enjoy breakfast.. I wait over 4 hours after taking Levo, then I take meds and supplements.
I got this Hypothyroidism... it has effected my energy, weight gain of over 12 lbs, I feel Cold more, Constipation, hair loss, brittle hair and nails, muscle aches, and trigger finger right hand...also fatigue....
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