hello - so I have been fortunate in having a forward thinking endocrinologist (as per listing). He has enrolled me in a 3mth trial of liothyronine on the basis that >15 yrs on a very high dose of thyroxine (300mcg) may have desensitised my conversion to t3 after my t4 was halved after menopause 10 yrs ago. It’s now one third of that high dose.
It’s two doses of the lowest dose possible and I wasn’t sure whether I needed to have the second one an hr before/ two hours after food.
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hi slow dragon -many thanks re advice on timings etc. It’s two doses and i will defer second one for a few days as suggested. I was advised to discontinue if I get regular palpitations which is a possibility given my cardiac history. I don’t know what my blood results were from that NHS Trust. It’s two doses. I’m just about to do my bloods again but I was really quite bad with debilitating muscle & joint pain when taking vit D gels, vit k2, magnesium, and the b complex advised in this site. So I’ve stopped them all and restarted vit d spray which I got in special offer. Aches etc now almost back to baseline.
I don’t know what my blood results were from that NHS Trust.
You are legally entitled to printed copies of your blood test results and ranges.
The best way to get access to current and historic blood test results is to register for online access to your medical record and blood test results
UK GP practices are supposed to offer everyone online access for blood test results. Ring and ask if this is available and apply to do so if possible, if it is you may need "enhanced access" to see blood results.
T4 varies according to what pharmacist can access - Mercury, Accord, Aristo, northstar and teva.
I can easily access my GP blood results and my Christie data but haven’t yet got that access for the acute trust. They use a third party (nonNHS) data provider who have limited options re data storage.
The D3 spray has K2 in it which means it’s the B complex recommended on here that aggravated something.
would I need thyroid antibodies testing? I dont have Hashis - it’s a congenital chromosome disorder that causes my hypothyroidism and deafness.
Many people find Levothyroxine brands are not interchangeable.
Many patients do NOT get on well with Teva brand of Levothyroxine.
Teva contains mannitol as a filler, which seems to be possible cause of problems. Teva is the only brand that makes 75mcg tablet. So if avoiding Teva for 75mcg dose ask for 25mcg to add to 50mcg or just extra 50mcg tablets to cut in half
But for some people (usually if lactose intolerant, Teva is by far the best option)
Aristo (100mcg only) are lactose free and mannitol free.
Most easily available (and often most easily tolerated) are Mercury Pharma or Accord
Mercury Pharma make 25mcg, 50mcg and 100mcg tablets
Accord only make 50mcg and 100mcg tablets
Accord is also boxed as Almus via Boots, and Northstar 50mcg and 100mcg via Lloyds ....but Accord doesn’t make 25mcg tablets
If a patient reports persistent symptoms when switching between different levothyroxine tablet formulations, consider consistently prescribing a specific product known to be well tolerated by the patient.
If symptoms or poor control of thyroid function persist (despite adhering to a specific product), consider prescribing levothyroxine in an oral solution formulation.
Physicians should: 1) alert patients that preparations may be switched at the pharmacy; 2) encourage patients to ask to remain on the same preparation at every pharmacy refill; and 3) make sure patients understand the need to have their TSH retested and the potential for dosing readjusted every time their LT4 preparation is switched (18).
if you want GP to specify specific brand it must be written in certain way on prescription
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