Levothyroxine Side Effects (Page 12)
(Newest replies first)
Updated
I was recently diagnosed with an underactive thyroid. I have been taking levothyroxine for almost two weeks. For the last four or five days I have had a weird feeling. It is hard to explain. I don't really feel dizzy but I get a strange feeling in my head. I guess you would describe it as a head rush. Has anyone else had this feeling and will it go away as my body adjusts to the levothyroxine?
dtl.... you need to take it slowly. As you have tried different brands I assume you've told your doctor. Yes they made me so nauseus that eating was hard work and I felt dreadful as well. The nausea bit was sorted by taking stomach meds from the doctor (proton pump inhibitors) just for a month whilst my body adjusted. then the other bit I resolved by taking it slowly to give my body time to adjust. I worked on the principle that any was better than none (my TSH was 100+). I took 25mgs maybe once or twice a week until I could take it with no ill effect (remember that each change takes 6 weeks for it to build up to the maximum it can in the body). I then increased it 25mgs at a time increasing the number of days one at a time (if you see what I mean). It took me nearly 2 years to get to 100mgs daily with no ill effects but I can say it was worth it. In the last 6 months my hair has got thicker (than I ever remember it), my stamina has increased and my libido has returned. My doctor thought I was mad to start with but now he really sees the difference. I hope this helps. (Oh, It makes you feel weird because every cell in the body is affected by it and they go a bit haywire when they have been short for a while and then get some!)
I am hypothyroid w/a TSH of 45. ALL thyroid medications, even compounded, eventually make me nauseated and give me flu-like symptoms. I feel better when i stop, but I know i must take medication. Has anyone else had this problem?
Great to hear that people are getting some relief with Thyroxine. Ricky - what you are saying about how you are feeling is very concerning. I have to say that prior to taking medication i felt more like you are describing - particularly with the joint pain. I struggled to concentrate, and basically everything slowed down for me. Since being on the meds, i do feel better, but it has taken quite a few months to get there. Part of that i imagine would be from my dose being adjusted, and slowly increased. The type of medication is such that it takes time to settle into your system (? correct medical terminology for this:P). I wonder if there is something wrong with your dosage? Prior to being treated my hair was getting thinner and thinner (and it's already thin!!!), i had put on a small amount of weight, but was working out like a dog (running for 1 hour a day). Keep on trying to all of you that are suffering - you can get there eventually. My hair is now thickening, I've stabilised my weight, i look thinner in the face (prior i had jowls and i'm only 36) - i do suffer a horrid scaly rash on my arms and wonder if it's from med? Some things the doctors don't know, and sometimes they don't seem to care to find out. Good luck :)
Get exactly the same thing. Aftger exercising (running, biking) I have fainted briefly, with a pulse in the 150s.
I was diagnosed with hypothyroid approximately 4 months ago, my mother is also hypo and had been telling me for years to get checked. I do not like taking any type of medication and did not like the idea of taking a pill for the rest of my life. I have struggled with wieght gain for the past 10 years, I am 34 years old. I started taking levothyroxine about a month and a half ago and have seen many changes already, my "foggyness" has decreased as has my hair loss and in the last 4 weeks have started to loose some wieght. So far so good.
sometime after I started takin levothyroxin, I have had a terrible rash between my legs. it runs down both legs a little ways . I need some relief. Is it the medicine thats causing it?
After reading all of everyones storys. I know now the feeling of discomfort from its the meds the Dr gave me for my underactive thiroid. I have tingle sensation threw out my face and sharp joint pains . Also my hair is thinning out and the feeling of being drunk and dizzy . The Dr said my thiroid is 42.8 under being normal but I definitely felt like a million bucks before I started takeing this . It has slowed me down at work, I lift 100lb boss all night long so my joints are givein me sharp pains even when I'm just trying to drink a glass of water . I'm always cold when I shouldnt be. After seeing all of you people with this I know now its the meds . All done . Good luck
I've been taking a low dosage for over a year now. It's 25 mcg and at first I have to admit it gave me a feeling of being drunk. With time it got better. I take it at either 4:30 or 5:30 in the morning and then I sleep for another 3-4 hours afterwards and I wake up feeling fine.
It said u can take it at night also...u guys should try that. That way you don't feel the effects of it. Just a thought.
My understanding is that the thryroid is removed if it is not performing properly - if this happens you will certainly need thryroxine for the rest of your life :( - i have been on it for quite a few months now and it definately has its ups and downs in the way i feel; but having said that, i wonder how much of this is just what all human beings expect (can't always feel great!) and also females may suffer more with PMT on top etc... You really need to give the medication time to work in your system - i have also discovered to take it at the same time (pretty much exact) every day, and not to eat anything for around 2 hours after. Certain foods and multivitamins can also counteract the effectiveness of it. Much information is available on the web and can really be helpful. Good luck :)
I act the same way that I on top of it I am very moody and anything will set me off. I don't know what a thyroid does but I can not live with the moodness of the side effects. I almost lose a good friend not worth it. Can they take it out?
I have had the exact same problems for 21/2 years now and every doctor thinks I am crazy.
When you take thyroxine it is because your body is short of it...... Every cell in your body needs it so when you take it they all (the cells) sort of 'party' (hence palpitations) til your system readjusts back to having enough... hence all the weird side effects... It takes a long while for the body to adjust which is why side effects can be reduced by taking it slowly even very slowly.... slower than your doctor may want... but you have the symptoms, not them AND any thyroxine in your system is better than none so taking it slowly is far better than throwing the towel in and not taking it. Think of it as an 18 month adjustment programme. If you get there sooner great but if not be reassured you will get there. (there being a point where you feel better than you have for years!!) Talk to your doctors many will understand your problems and be happy to let you take it slower and if not and you go it alone keep them informed of the dose you really are taking. Don't just tell them what you think they want to hear as the more times they are told 'I need to go slower' by more people the better they will understand.
Holly,
I'm in my sixties and although I have a good head of hair, I notice, particularly when I wash my hair, I'm losing a fair amount. I've been on levothyroxine for 5 weeks. My dosage is 0.075. That and a couple of sore teeth are my main problems. I haven't seen any reference to headaches but I'm getting mild headaches from somewhere which I didn't have 6 weeks ago.
I, too, have a couple of teeth hurting since I started levothyroxine five weeks ago. I'm in my 60's so thought I might need a root canal. Visited my dentist - following X-rays and dental exam everything is ticket-boo!
Thanks PJ. As each day goes by I learn something new about taking this medication. My doctor is still trying to get my TSH levels back into the reference ranges - this is why she has increased it as I found I was starting to feel very tired again, and achy arms and legs. Thanks for the advice of increasing it gradually - def worth a try. I am feeling better today, but have to say the last 3 days were terrible - and it's a worry for me that there is no warning this was going to happen. I had a blood test yesterday so will be interesting to see the results - will keep you posted. Great news for you that you are feeling so much better - I can completely understand that you are reluctant to have bloods taken
Hi Mumsy...if you felt OK on the lower dose.. go back to it until you feel right again then increase your dose slowly..... if you feel uncomfortable about this ask your doctor if you can take it more slowly 50mcgs is a big jump... You may even need to increase it by 25mcgs on one day a week until you feel ok then 2 days etc etc..... This is what I did (and kept going back a bit each time I felt weird and only updating it monthly cos it takes about 6 weeks to balance out each adjustment)... It's taken me 20 months to get it right (and I need a blood test to check but I'm avoiding it)... I feel good, have lost some weight and got my libido back so as far as I'm concerned I'm sorted..... hence blood test avoidance.... Anyway if your doctor is reluctant either go it alone or push the point with him.... he shouldn't mind as you're more likely to comply and take them if you feel ok. Hope this helps... NFWE
I have finally found a site with info from people going through what i am! Yay! I had my thyroxine increased from 100mcg to 150mcg around 4 weeks ago as my thyroid gland does not produce anything anymore. For the last 2 days i have felt terrible, racing pulse at times, hot then cold, extremely tired and fuzzy feeling. Had similar feelings around 8 weeks after first being put on the medication (have now been on it for around 4 months). I am hating it - I have a little girl who I feel I have wasted yet another day being too tired to do anything with her - I just don't know what to do
I've been taking synthoid .025 last years for 2 month. Had no side effect at all
Now, I'm in africa and i have to take the pills that comes from france and it,s called Levothyrox. same dosage. I've been having nausea and now, I can't sleep.
Wonder what the problem is. really weird. I just red on a site that in the first few weeks, we can have side effect as if we would be on surdosage because the body is re-getting started. So, I hope my side effects will go away
i have had a terrible reaction to levothyroxine pills, as a rash that as swollen and is very sore can anybody give me any advise yours thankfully john
I developed a goiter years ago and was having fluctuations from hypothyroid to hyperhyroid. My thryoid was treated with radioactive iodine to stop all thyroid function and then I was started on Armour thyroid hormone. It was the only thyroid medication that didn't cause side effects, because it is made from a hog's thyroid and is more natural for the body to accept. It helped for a few years, but after awhile it no longer gave me enough energy and I was tired all the time, although my blood tests showed a normal thyroid level. Eventually I found a doctor who prescribed compounded T3. It gave me energy, and it stopped the neuropathic pains I was having in my leg. Then Levothyroxin was added, so I was taking compounded T3 and also Levothyroxin that would supply T4. Eventually the doctor had me take kelp which supplies the iodine a thyroid needs. The kelp iodine cleared my head from the fogginess I was feeling. My leg continued to get weaker and caused falls. MRIs showed the leg weakness was due to spinal cord damage in my neck caused by a whiplash accident years ago. Recently my thyroid must have begun working some because now I don't need the Levothyroxin. I am taking only T3. Removing the Levothyroxin has caused me to have a calmness, energy, and my leg is stronger. I need to continue taking the compounded T3. Only the compounded type is helpful for me, because it is more natural. God is a great healer and I have found he gave me/us a body that responds best to natural remedies. I just wanted to share this because perhaps someone else can benefit from it.
More Discussions:
just started taken levothyroxine 50mcg, what are the side effects ? my pills are white in color, small, oval . ## Levoth...
I had a total thyroid removal in June 2014. Was 1st put on 124mg of Levothyroxine, later 112 mg and swelling in both fee...
Hi, I've taken Nitrofur-Macr 100mg and did ok with it. I recently had to start taking Levothyroxine 50mg for a thyro...
Bought levothyroxine 75mcg at pharmacy in Costa Rica. Packaging says made by Merck in Mexico. White pill with 75 on one ...
I don't feel so confused anymore. Now I know all of you are going through the same thing. My doctor put me on 50mcg ...
I had a total throdectomy 2 years ago due to thyroid cancer. I have been on 150 - 200mg Levothyroxine daily. Side effect...
I recieved a letter from my health care provider saying that i cannot continue getting Levothyroxine 50mcg tablet that t...
I was recently diagnosed with Hypothyroidism after having my thyroid tested and my TSH was 5.9. I have been taking Levot...
I've been taking Levothyroxine 25mg for almost four months, first three months was fine, now seem to be having dizzy...
I was a perfectly healthy 14 year old until I grew very tired and went to see a doctor. We got blood work done & my ...