New blood test results after 2 months on Levo - Thyroid UK

Thyroid UK

141,182 members166,424 posts

New blood test results after 2 months on Levo

TheMudRunner profile image
14 Replies

Hi,

I posted a while back before I first saw a private GP and was put on 50mg of levothyroxine.

Weeks 1-3 or there abouts I felt that things were going well. I felt rested after a nights sleep for the first time in years, increased mental acuity, diminished itching of the skin, decreased thirst, and found that things like abrasions and spots were healing quickly. However, the last 5 weeks I’ve felt like these have all come back and it’s been a bit brutal. I also stopped eating gluten 8 weeks ago in the hope that too would reduce my TPO antibody levels.

I’ve just had my next lot of blood test results back (8am, levo taken 24hrs before, no biotin for previous 5 days etc), and the results are interesting. I’m not 100% sure what they mean save for the vitamin D and B12 supplementation has clearly worked as hoped. My TPO levels aren’t much different (70.4 vs 74), and I’m not sure what to make of my thyroid levels in general - any guidance before I see my GP again next Monday would be greatly appreciated 🙂

No ferritin or folate results this time around due to haemolysis issues with my blood sample I’m told, in case anyone wondered why they’re absent.

New results posted here. I’ll pop the previous ones in the comments 🙂

Thank you to anyone who is happy to help - it’s invaluable to have support from you!

Written by
TheMudRunner profile image
TheMudRunner
To view profiles and participate in discussions please or .
Read more about...
14 Replies
TheMudRunner profile image
TheMudRunner

And now for my original blood test results pre-levothyroxine.

Blood test results from Blue Horizon laboratory.
Jaydee1507 profile image
Jaydee1507Administrator in reply toTheMudRunner

I've removed the image from the main post as it showed your name. Do repost it in the comments once you've removed an identifying information. It might even be legible if posted in the comments. Images in the main post need to be very clear and show better as a comment.

TheMudRunner profile image
TheMudRunner in reply toJaydee1507

Oops - thought I’d removed details..! Thanks for flagging. I’ll resolve and repost 😀

TheMudRunner profile image
TheMudRunner

New set of test results here 😀

New test results
Jazzw profile image
Jazzw

Well, 50mcg levothyroxine is a starter dosage. I would say, given it’s been 2 months, it’s time to consider an increase to 75mcg. Your TSH is still above 2.0.

Re the antibodies, I wouldn’t stress about them too much. They’re going to do what they’re going to do—you can’t really gauge whether you’re slowing down the autoimmune attack on your thyroid by the level of antibodies. It doesn’t really work like that. Going gluten free is about reducing the autoimmune attack, not about reducing antibodies.

SlowDragon profile image
SlowDragonAdministrator

Free T4 (fT4) 16.6 pmol/L (12 - 22) 46.0%

Free T3 (fT3) 3.8 pmol/L (3.1 - 6.8) 18.9%

Most people when adequately treated will have Ft4 (levothyroxine) at approximately 70% or higher through range

And Ft3 ideally over 60% through range

Your results show you are ready for next 25mcg increase in levothyroxine to 75mcg daily

Retest again in another 2-3 months

TheMudRunner profile image
TheMudRunner in reply toSlowDragon

Thank you for this SlowDragon & Jazzw . I was a little concerned I might not have much luck getting the dose increased based on the TSH, and I really don’t feel great atm.

Is it usual to feel better, then worse when starting to take levothyroxin?

RuthieRuth profile image
RuthieRuth in reply toTheMudRunner

I understand that it is usual to go through some less than pleasant side effects when increasing dose - would be helpful to know in what way you don't feel great though? I am in the process of very slowly titrating up from 25mcg (after recovering from the horrors of starting on 100mcg which had me feeling totally hyper within 3 weeks, unable to sleep, crazy irritable, toilet all the time etc). Personally, I found I felt super hypo after 6 weeks on 50mcg (tired, brain fog, cold, no appetite). Now I'm on week 4 of 75mcg and feeling significantly better! Are you feeling not great hypo not great? Or not great hyper not great?

TheMudRunner profile image
TheMudRunner in reply toRuthieRuth

Hi RuthieRuth . I felt much better for weeks 1-3 (roughly). Energy was up, brain fog down, waking up feeling refreshed and rested, itchy skin stopped, even my dishydrotic eczema had cleared up..! Since then fatigue is back so not good Hypo not good, worse than before (though that might just be because I had 3 weeks of feeling a lot better than I have in years!), brain fog and motivation are down, skin dry and itchier again, and spots / eczema are back, It’s frustrating but I suspect due to having increased availability of thyroxine for the first few weeks and then lower levels as SlowDragon has suggested below.

I’ve glimpsed a world where I have good energy levels again and want it back 🫣😆

I hope you’re feeling better than you were? Being Hyper sounds no more fun than being hypo. It’s a delicate balance and I know it’s going to take time. Hard not to be a bit impatient though.

SlowDragon profile image
SlowDragonAdministrator in reply toTheMudRunner

Yes very common

Initially body welcomes extra hormone and your metabolism starts to pick up…..then your body realises after few weeks that you’re not taking enough replacement thyroid hormone so hypothyroid symptoms start to return

As dose increases over coming months this see-saw will diminish and it will often take longer between dose increases

TheMudRunner profile image
TheMudRunner in reply toSlowDragon

That was my thought process, but I’d half convinced myself I was just having a psychosomatic uplift for the first while..! Phew. I’m definitely looking forward to getting the next step started on Monday. Would it be reckless to go up to 75mg by splitting a 50mg tablet (so taking 1.5 tablets) before then..?

TheMudRunner profile image
TheMudRunner in reply toSlowDragon

Thank you so much for replying too - you’re a fount of valuable knowledge 😀

SlowDragon profile image
SlowDragonAdministrator in reply toTheMudRunner

Which brand of levothyroxine are you currently taking

Ideally stick with same brand as you increase

Only change one thing at a time or you won’t know what is causing what

Have you got appointment with GP organised

You might start increasing by 1/4 of 50mcg tablet now

Cut into 1/4’s using sharp craft scalpel or pill cutter

Then when you get increase on prescription you can go up to 75mcg daily

Many people find Levothyroxine brands are not interchangeable.

Most easily available (and often most easily tolerated) are Mercury Pharma or Accord

Mercury Pharma make 25mcg, 50mcg and 100mcg tablets 

Mercury Pharma also boxed as Eltroxin. Both often listed by company name on pharmacy database - Advanz

Accord only make 50mcg and 100mcg tablets. Accord is also boxed as Almus via Boots, 

Wockhardt is very well tolerated, but only available in 25mcg tablets. Some people remain on Wockhardt, taking their daily dose as a number of tablets 

July 2024

Crescent levothyroxine. Dosages: 12.5, 25, 50, 75, 100

(Not yet known if all approved dosages are or will be available).

Excipients: lactose monohydrate, maize starch, croscarmellose sodium, gelatin and magnesium stearate.

Lactose free brands - currently Teva or Vencamil only

Teva makes 25mcg, 50mcg, 75mcg and 100mcg

Many patients do NOT get on well with Teva brand of Levothyroxine.

Teva is lactose free.But Teva contains mannitol as a filler instead of lactose, which seems to be possible cause of problems. Mannitol seems to upset many people, it changes gut biome 

Teva is (currently) 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)

Vencamil (currently 100mcg only) is lactose free and mannitol free. 25mcg and 50mcg tablets hopefully available from summer 2024

March 2023 - Aristo now called Vencamil

healthunlocked.com/thyroidu...

healthunlocked.com/thyroidu...

Helpful post about different brands

healthunlocked.com/thyroidu...

List of different brands available in U.K.

thyroiduk.org/if-you-are-hy...

Posts that mention Teva

healthunlocked.com/search/p...

Teva poll

healthunlocked.com/thyroidu...

Once you find a brand that suits you, best to make sure to only get that one at each prescription.

Watch out for brand change when dose is increased or at repeat prescription.

Government guidelines for GP in support of patients if you find it difficult/impossible to change brands

gov.uk/drug-safety-update/l...

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.

academic.oup.com/jcem/artic...

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).

And here

pharmacymagazine.co.uk/clin...

Discussed here too

healthunlocked.com/thyroidu...

TheMudRunner profile image
TheMudRunner in reply toSlowDragon

Hi,

I’m on Almus, though from a local pharmacy rather than Boots. Useful to know that Boots may also stock it, and I will make a point of asking my GP to state the same brand again (though sounds like Accord is the same which is useful to know).

I’ve ordered a pill splitter as sounds like that may well be necessary if I stick with the Almus brand - one that does 1/4 tablets if necessary. Sounds as though good fortune has meant I have started on a generally well tolerated brand at least. Perhaps one less thing to think about for now which is a bonus.

Thanks again, and I will post an update after I see my GP on the 22nd July. Not far off at all now 😀

Not what you're looking for?

You may also like...

Test results help

Hi all I am a Hashimoto’s sufferer but have never been put on medication because, although my TPO...
Paolatello profile image

Blood test results

Hi everyone. I’ve had some test results back. I had RAI in 2011 for hyperthyroidism and I’m...
HypoFrog profile image

Thyroid Blood Test Results

Hi all, I finally managed to get a copy of my thyroid blood test results but there is so little...
NiaJayne profile image

Test results

Posted a couple of weeks back but have now got my results. Was diagnosed 20 years ago with an under...
WhitmoreSJ profile image

Stopped levo as not helping - blood results

Hi all, I’m new to the Forum! Can someone help me make sense of my blood results please.? I was...

Moderation team

See all
Jaydee1507 profile image
Jaydee1507Administrator
PurpleNails profile image
PurpleNailsAdministrator
SlowDragon profile image
SlowDragonAdministrator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.