Experiences with

Wockhardt levothyroxine

Hi I just read on another site anyone over the age of 50 shouldn't take Wockhardt brand of levothyroxine. Surely this can't be true. I've been taking 50/75 mcgs of this brand for 9 months as I've reacted badly to other brands

I am taking 50mcg levothyroxine Wockhardt I was given five doses of 2,0000 Vitamin D and have side effects e er since TSH was 0.06 FT3 was 5.0 FT4 was 17.0 Folate Ferritin and B12 not taken Thyroid Peroxoxidase antibodies 31.8 abnormal taken on 8th April

Is anyone aware of a supply issue in UK of Wockhardt Levothyroxine? I was unable to fulfil my usual prescription in England last week, and have faced the same problem attempting to get it instead in Wales this week, with only Teva or Accord offered.

Hello, I have only ever taken wockhardt levothyroxine, for 5 years, since diagnosed, but the pharmacy have just given me the crescent brand, saying they don't know what brand they are getting until it arrives, and that's what's arrived.

I have not posted for sometime.I usually have my levothyroxine in wockhardt brand as I have found I tolerate this.. My endo and GP agree and it is on my notes and also on pharmacy notes. However when I have collected my prescription tonight teva has been dispensed and 1 box of Mercurypharma.

Hi all, I've experienced a lot of hair loss over the past 6 weeks since being issued with crescent pharma 25mcg levothyroxine tablets (previously either teva or wockhardt which I've been OK on). I take 87.5mcg levo daily, so a 50mcg accord tablet, plus 1 and a half 25mcg tablets.

16 weeks after going up to 50 levothyroxine (2 × 25 wockhardt) these are my levels Serum TSH level 2.23 mIU/L [0.27 - 4.2] Serum free T4 level 17.1 pmol/L [12.0 - 22.0] 8 weeks ago I took my levothyroxine before my test - I remembered not to this time GP is very resistant to me having more

(Diagnosed with possible subclinical hypothyroidism in Nov 23 and put on 25 levothyroxine wockhardt (also struggling with meno and have exciting CFS/ME, FM, hypermobility, IBS) After 12 weeks (Feb 24), raised it 50 levothyroxine Mercury & I had a big reaction to it so now I'm on 2x25 wockhardt after

I have recently had my 25mcg Levothyroxine brand changed from Wockhardt to Teva and I have been getting a lot of headaches, more than usual and lightheaded and nauseous.

Just been informed that Wockhardt costs the pharmacy an extra £1 a box, so if I want them to order it in for me I will have to pay the extra cost. The alternative is Teva which quite clearly has the thyroxine market all sewn up 😡.I am willing to pay the extra to get the brand I need however it is the

I have Hashimotos and am therefore on Levothyroxine. I am having trouble getting the prescribed brand, Wockhardt, from any of my local chemists and the pharmacists seem reluctant to order it in for me. Always take this particular brand as it does not contain Acacia to which I am allergic.

anyone else find they get constipation on Accord? Might be total coincidence but I’m now on accord and constipated - after being fine on Wockhardt.

As I glumly predicted, following allergic reactions to several brands of levothyroxine, my GP has flat out refused to reissue a prescription for Brillpharma liquid levothyroxine. Cost. To get it installed as a regular prescription will require me going back to the hospital allergy department and making

I would welcome any observations on the below. For several years I have been taking 175mcg of Thyroxine. I have Hashi disease. For several months I have had pulsatile tinnitus in my left ear. I saw the GP who referred me to a ENT Consultant. Various tests completed including a blood test for my Thyroid

Wasn’t sure whether to start new post as this is a follow on from my post about chronic pain & using finger prick tests? I have been diagnosed with Hashimoto’s & UA. I only have left side of thyroid which is very inflamed (thyroid inferno) & been referred from ENT to Endocrinology. My first 2 months

I persauded my endo to get my levo increased by 25mcg and I agreed to reduce my T3 by 12.5mcg. I have already previously reduced my 3 by 12.5mcg. I was on 50mcg and 75 mcg levo until my last blood when I was advised here to reduce T3. I have been fasting for Ramadan which I was told reduces conversion

Hi,My last thyroid panels have seen a significant drop in FT4 over two tests compared to the two tests I took last year; 9th October '24: 9.5 pmol/L Range 12 - 22 5th October '24: 9.9 pmol/L Range 12 - 22 24th Jan '25: 7.3 pmol/L Range 7.7 22 27th March '25: 7.2 pmol/L Range 7.7 22 All testing

I hope you can advise me as I am feeling let down and worried after my second appointment with an endocrinologist. I started on 50 mcg Levothyroxine in January (weight = 70kg) when my TSH was 10.5 (0.27 - 4.20); T4 was 12.1 (12 - 22); and T3 was 4.6 (3.1-6.8). TPA antibodies were 95 and TG antibodies

Hello I got my 6 week results following an increase of Levo from 50mcgs to 100mcgs. The tests are as follows: TSH - 0.02 range (0.35-4.94) T3 - 4.30 range (2.63-5.7) T4 - 19.20 range (9.01-19.05) I feel the best in a long time but GP wants to decrease meds!

Hello, After two tests showing extremely high T4/T3 levels my GP has decided to start treatment with carbimazole while I wait for my referral to the endocrinologist. I am assuming this is a hashis hyper swing since I was put on levothyroxine last year for having a slightly under-active thyroid and