Feeling normal after TEVA levothyroxine - Thyroid UK

Thyroid UK

141,182 membersβ€’166,423 posts

Feeling normal after TEVA levothyroxine

β€’32 Replies

Hi,

I wonder, has anyone experienced a similar situation as me on the new formulation TEVA levothyroxine and if so, how long does it take for the symptoms to subside?

Was given upped dosage of 25 mcg new formulation TEVa by my pharmacist along with my usual 100 mcg of usual brand Activis. Took them for 5 weeks but felt increasingly unwell, unimaginable anxiety and panic, insomnia, aching at the back of legs, down my arms, chest pains, difficulty processing information and word retrieval.

Light bulb moment! Realised although bloods revealed I was low and I needed a little more levo, my symptoms were typical and mild compared to the symptoms I have experienced since adding the 25 mcg of TEVA.

I've changed back now to both doses of Activis brand levo. I just want to feel like me again. Anyone been there, done that? 😊

Read more about...

The ability to reply to this post has been turned off.

32 Replies
β€’
Kitti1 profile image
Kitti1

Hi woodelf67

Yep been there done that. I was on 125mg for just over 3 weeks and ended up bed ridden last week, so poorly 😠. And yep anxiety through the roof, still is.

Another member said she'd been through this over Christmas and it has taken 6 weeks back on actavis to feel fully back to normal.

I am extra frustrated as I have my first order of t3 here & ready to go ( chomping at the bit ). My bloods test kit arriving any day now and my stupid chemist has just put the spanner in the works as I really need to leave it 6 weeks till I do my bloods now ( as recommended by greygoose - makes sense ) 😀 Fuming ! Going to have to have serious words there.

Have I mentioned yellow card to you before ?

β€’ in reply toKitti1

Thanks Kitti1,

You may have mentioned yellow card, yes. I will fill it out for sure.

Thankyou for your reply. Hoping we both feel better soon. 6 weeks can't come quick enough. πŸ™

Milpol profile image
Milpolβ€’ in reply toKitti1

Hi woodelf67,

I am new to all this , just starting my journey. I am on 25 mcg of new Teva formulation. I am fine on it, but please would you explain what 'yellow card' is ? Many thanks,

Milpol x

β€’ in reply toMilpol

Hi Milpol!

I'm not too sure myself.

Kitty1 suggested there is a yellow card system you can fill in online to report bad reactions or side effects from switching meds or specific meds. I may have that wrong...

It's great to hear you have no side effects from TEVA levothyroxine.

Woodelf

Milpol profile image
Milpolβ€’ in reply to

Many thanks wood elf, I will check it out, just in case. I'm only on a very small dose at moment, but it's good to know if I increase my dose and don't feel great.

Good luck on your journey to better health x

β€’ in reply toMilpol

You too Milpol. Good luck! 😊

β€’ in reply toMilpol

Milpol, I've tried to find the link, but cannot locate it. I wonder if you ask Kitty1, she may be more successful than me.

The people on this forum are very kind and helpful 😊

Milpol profile image
Milpolβ€’ in reply to

Thanks. Yes, they are great, I agree. I am learning so much from the kind folks on here. I knew nothing about being hypo until I joined the group!😊

Kitti1 profile image
Kitti1β€’ in reply to

Pretty new to all this too and don't know how to do links.

This is the address yellow card.mhra.gov.uk never know that may come up as a link πŸ‘

Locky1971 profile image
Locky1971

I had new formulation teva 50mcg. Used it for 3 days,ached like mad and felt dreadful. Stopped and switched back to mercury pharma and symptoms eased off the first day I'd stopped taking teva brand. Left it a week and tried the teva again and the same problem. What the hell are they adding to their new formula? I will be returning the unused tablets to my pharmacy. I have filled in a yellow card online for the teva brand levothyroxine. I suggest everyone does and then they'll look into it. Am I right in thinking that teva were stopped from making levothyroxine a few years ago as their levels weren't consistent.

β€’ in reply toLocky1971

do you know Locky, I started feeling unwell on day 3 or 4, but read somewhere that you can feel worse before getting better when raising your thyroxine intake. Didn't imagine for a minute it was new meds. Still thinking is it or isn't it, but surely too coincidental if so many have had similar experiences upon taking it? Thank you 😊

Kitti1 profile image
Kitti1β€’ in reply toLocky1971

Hi Locky1971

Yep I read that too. When my pharmacist randomly gave me Teva instead of usual brand I googled them & read that.

I would think Woodelf that the symptoms should be pretty minimal for the last 2-3 weeks, certainly hope so I need some sleep. But will probably affect a bloods.

Hope we are all feeling better soon πŸ‘

Never wanted anything quite so badly Locky.

Hope we all feel well again soon.

Take care. 😊

I meant Hi Kitty1,

I think I've just made my point πŸ˜‚πŸ˜‚

SlowDragon profile image
SlowDragonAdministrator

Read the last three paragraphs on this article below - it clearly states patients should be advised never to accept change of brand of thyroxine & that GP's should be made aware of this too

Personally I keep a copy of this article in my bag to show Pharmacist when they try give me different brands.

I can only tolerate Mercury Pharma

endocrine.org/-/media/endos...

β€’ in reply toSlowDragon

Thankyou slow dragon, that's very helpful. Will do the same.

My local pharmacist's reply to my request for my usual brand was, 'Ok, I'll humour you.'

It's so frustrating.

Thankyou

SlowDragon profile image
SlowDragonAdministratorβ€’ in reply to

Yep - over 20 years ago I had similar experience with GP - who thought I was "barking" for even suggesting this

Was at that time, getting different brand almost every time I got prescription. Ended up extremely ill (wheelchair/bedridden)

Long slow improvement when, at my own insistence, I always had Eltroxin until that was discontinued & had to move to MP. (Which is not as good)

β€’ in reply toSlowDragon

It's good to know there are others out there who have gone through the same Slowdragon, although not good for you obviously. Thankyou for sharing.

Kitti1 profile image
Kitti1β€’ in reply to

That's shocking ! 😀 Woodelf that your pharmacist said ' I'll humour you ' !

β€’ in reply toKitti1

I know, unbelievable! Thyroid symptoms and problems seem to be misunderstood. 😳

teenarocks profile image
teenarocksβ€’ in reply toSlowDragon

Thanks for posting this article. Such good information to keep on hand for the pharmacist and the doctor too!!

blondpalomino profile image
blondpalominoβ€’ in reply toSlowDragon

Mercury pharma used to be Goldshield,when I took these a few years ago they didn't seem to be working for me at all. I tried Teva previously before they went off the market,they seemed to be stronger and give me a boost.I didn't notice any side effects at that time.I take Wockhart now and have for a long time, I was thinking about trying Teva again now they are back, but maybe I won't after everyone's comments!

Gary19610 profile image
Gary19610

Stay away from TEVA most Thyroid groups on Facebook have done nothing but complaints how poly there was and stop taking it and went back to what there was taking before

β€’ in reply toGary19610

Thankyou Gary. 😊

Gary19610 profile image
Gary19610β€’ in reply to

Your well come.I tried different brands of Levo and stick to one has the other's made me poly it's something to do with the fillers in the tablets

β€’ in reply toGary19610

😊

Kitti1 profile image
Kitti1β€’ in reply to

May I ask if you've seen a post that went up roughly 24hrs ago. Grassroots Campaign Anyone ? If you haven't seen it please have a read πŸ‘

DavyB profile image
DavyB

Hi

I also had a bad reaction to Teva a month ago when switched over to it. I had a reaction to something in it: Itchy skin all over within a few days. (probably some filler?) Switched back to Wockhart brand and was fine within a few days. Tried the Teva again (to confirm) and had same problems. So back onto Wockhart and fine again.

Spoke to pharmacy and they were happy to make a note on my file that Teva no good for me.

This is the yellow card system you can fill out:

Yellow Card Report: yellowcard.mhra.gov.uk/

nightingale-56 profile image
nightingale-56

Hidden I have not taken the Teva but did try the Mercury Pharma Eltroxin. I could only stand it for 3 days as in this time I could barely walk and the left side of my head felt numb. I only tried this as the local CCG had asked me because I was previously on Goldshield Eltroxin. The MP Eltroxin was supposed to be exactly the same. It definitely was not. Would not take the Teva because it has Acacia Powder in it. Am now on 75 mcg of Wockhardt and feel as though I need a higher dose, but no go from the GP at the moment. Seeing Endo soon so will have a go at trying to geet a raise from him. Am also taking 6.25 mcg of T3 (self-funded) but cannot raise this or my FT3 goes down.

β€’ in reply tonightingale-56

Hi J-bee,

Sounds like it been quite a journey for you. It just goes to show, what suits one doesn't necessarily suit another.

I'm feeling as though I still need my doseage raised but wonder if bad reaction to TEVA may have hampered the levothyroxine conversion and thus its effectiveness in making me feel better. Blood test on Tuesday and still hoping to improve in the meantime after only stopping TEVA on Thursday.

Thankyou for sharing. 😊

debbies147 profile image
debbies147

ive been taking the teva for a few weeks and feeling the same symptoms you described , did doctor change yours for you and are you feeling better?

Clutter profile image
Clutterβ€’ in reply todebbies147

Debbies147,

Woodelf67 has left the forum so won't be replying and I am therefore closing this thread to replies.

If you are feeling unwell since switching to Teva you should advise your pharmacist and request the Levothyroxine you previously felt well on when your next prescription is dispensed. If the pharmacist won't oblige ask for the prescription back and take it elsewhere. Some, but not all, pharmacists will exchange the left over Teva you are taking for an alternative make.

Please report your adverse symptoms via yellowcard.mhra.gov.uk/

The ability to reply to this post has been turned off.

Not what you're looking for?

You may also like...

Teva

I'm another thyroid sufferer who has gone downhill since taking the new Teva formulation. I have...
ElsaElsa55 profile image
β€’

Teva? General consensus on reformulation?

I take 150 mcg of Activis levo and have done so without any problems for last few years after I was...
janiebell profile image
β€’

So what do people think of teva (new formulation) levothyroxine?

This basically carries on from my first post if u would like to read your more than welcome.. So...
ThyroidObsessed profile image
β€’

Teva!!!

Hi All, So after being on a 'new' formulation of levothyroxine made by Teva UK Ltd for two weeks,...
JillOliver profile image
β€’

Teva Levothyroxine: Allergy Alert

Hi all Following a recent post of mine, I have final results on this issue :) Having been on...
DavyB profile image
β€’

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.