I know a few people on here take it. I wish to bleeding heck we could get it in Australia but Sigma who make our T4 meds are unlikely to give up the monopoly! We have two T4 meds, Eutroxsig and Oroxine...Oroxine is the generic! Both are Sigma made!
Those I know on Tirosint rave about it. I suspect it is due to being able to be absorbed quickly and easier than stupid powdery sand filled tablets. ( Now don't jump on me, I joke when I say sand filled!)
Barb- What was your most recent T4 level? Mine is only at a 1.0 with a T3 of 3.8. I am on 125mg of tirosint and 20mcg of cytomel.
My doctor thinks that maybe the tirosint doesn't bind like the other meds, because it is utilized better. Kind of makes sense doesn't it?
Just got back my labs yesterday......... I'm on 100 mcg Tirosint; 5 mcg generic T3.
TSH 0.01 higher than last time, which was < 0.01 woohoo.........lol
FT3 3.7 pg/mL (range 2.3-4.2) vs 308 pg/dL (range 230-420) prior to Tirosint
FT4 1.5 ng/dL (range 0.8-1.8) vs 1.1 ng/dL (same range) prior to Tirosint
I must admit - I did a 'no no' by making 2 changes at the same time - switched to Tirosint and upped my dosage from 88 mcg levo to 100 mcg Tirosint - so not sure which one really made the difference....I'm thinking the tirosint had the most effect because I was once on 150 synthroid and neither of my FT's rose above about 1/4 range.........
I'm actually feeling better than I've felt in eons...........but do still have some minor symptoms, such as constipation and hair loss.
I might suggest that anyone who isn't doing so well on either synthroid or generic levo to give it a try............. nothing to lose...
Great feedback on Tirosint. I started Tirosint in July of 2010. I had sensitivity to fillers, dyes, and generics with levo. I have been on 150mcg of synthroid, 3-50mcg pills a day since the 50 mcgs are white with no fillers. My endo wanted to give Tirosint a try. We were excited since there's no dyes or fillers. After the first week I began to have severe headaches, nervousness, and hip pain. I continued with the Tirosint and the side effects got worse. My internal med Dr. insisted it was the Tirosint. The hip and joint pain became so severe I began Physical Therapy. 4 weeks after stopping Tirosint the headaches finally went away along with the nervousness. The joint/hip pain went away as quickly as it appeared. Not everyone is sensitive to levo, fillers, or dyes like I am. I have to think my body for some reason just can't tolerate it :(.
Did you start the Tirosint at the same 150 mcg dosage you had been on synthroid? Since there is apparently, better absorption with Tirosint, than with other thyroid meds, for some of us, and if you are really sensitive, you might have done better to start on a lower dosage.
I am curious if anyone has switched from desiccated thyroid to Tirosint? My endo is suggesting this to me because I am having a very difficult time acquiring the former in Florida. I have had remarkable improvement on the desiccated, and I'm afraid to go back to synthetic T4 only. I doubt he will give me T3 as well.
what dose were you on when taking synthroid and what was your starting dose of Tirosint. I would assume that if Tirosint is better absorbed one should probably start at a dose lower than their synthroid right?
My synthroid dosages ranged from 25 mcg to 150, then back down to 50 (this was done by my pcp, because he was watching TSH only - mine went to the basement right away, so he kept cutting my med back, even though my FT levels did not rise accordingly). When I started going to my endo, I was switched to generic levo, and we started slowly raising my meds, in order to adjust FT levels, rather than focusing on TSH.
When I started the Tirosint, I was at 88 mcg levo (not synthroid). I needed an increase, in levo, so we went up to 100 mcg with the Tirosint (I made 2 changes at once - changed dosage AND med - that's a "no no")....... While I felt good at that point, we were afraid I might tip the scale the other way (to hyper), so I'm now alternating 75 mcg with 100 mcg, for an average of 87.5/day.... I'm doing good on it, so most likely, when I see my endo again (depending on labs at the time), I'll go to 88 mcg Tirosint...... 88 -100 mcg seems to be my comfort level.
You are right -- for most people, Tirosint is absorbed better, so if you need an increase, you could start at your current level of synthroid/levo, then retest after a few weeks and see what your levels are, then if you need a further increase, so it.......
If you are doing good on your current med, either stay there and don't rock the boat, or start Tirosint at the next lowest dose, retest in a few weeks and go from there.
I had my thyroid surgically removed about 6 years ago, due to cancer. I saw a new doctor last week and she prescribed tirosint-200mcg per day. I am very excited to see if this helps with being absolutely exhausted all the time and weight gain. She ran a lot of hormone tests, but not for T3. Should I have this checked? I asked her about T3, and she said she would put me on it, but not for any length of time. She wants to start with the tirosint and then try a diet pill of some kind. Do people stay on T3 permanently? Or will the tirosint be enough? I have been on Synthroid and the generic. She explained a lot to me and I like her much better than the last doctor I saw, but she talked a lot and did not listen to me or many of questions. I have always been tired, but not as bad as I am now and I have never had problems with my weight. Very Frustrating
You need to have FREE T3 tested every time you have TSH and Free T4 (she IS testing that isn't she or is she dosing strictly by TSH levels?)..
Yes, some people stay on T3 med indefinitely -- I've been on it for over 2 yrs, and have no intention of going off it any time soon. There are doctors who believe that giving T3 med causes osteoporosis and/or other conditions -- that's only a concern if your levels get too high and with regular testing (including Free T3 and Free T4 levels), that shouldn't happen.
Since Tirosint is basically hypoallergenic and absorbed more readily, it might be best if you try it alone for a while, but we'd need to see some lab results in order to be more specific about your individual situation.
If you have a copy of your latest labs, please post them, along with reference ranges, which vary from lab to lab, so must come from your own report. If you don't have a copy of the report, your doctor is obligated to provide you with one, upon, request.......
The doctor kept my test results. I know she wants my TSH levels around .03, and they are at 1.7. My labs for TSH have always been pretty stable until recently (last set of labs). I hadn't gone to the doctor for some time because of insurance. She also tested me for PCOS, which came out fine. She has no medical reason for the problems I'm having. I just started the Tirosint on Wednesday. I realize it must take a couple of weeks to notice if there is any change. I am so hopeful. I am only 43 and I should not feel this lousy. I'm so tired "all" the time. My job is stressful, and I work different shifts a lot, but even when I go to bed at 9pm, I don't feel much better than if I go to bed at 2am. As far as the cytomel--I was on that right after the surgery, but not since. I read all over on the internet about the benefits of T3, and my doctor sort of got mad. I don't want to do anything that is bad for me, but at what point is your quality of life more important?
I had thyroid cancer 3 years ago and now have hyposthyroidism, I recently starting taking trinosint, and it works wonderful. For two years I was off and on synthroid and levothyroxine, I felt tired and fatigued all the time. After as little as 2 weeks I started seeing a vast improvement; I am no longer tired, my weight is more managable, and I feel more energized to go about my normal activites. My endo told me the difference between the synthroid and trinosint is while synthroid is not a generic drug it still has fillers in it and dies, as compared to trinosint which is just pure thyroxine.
I had my thyroid removed also. I was miserable on both synthroid and levo. Then my endo prescribed Tirosint 88mcg. Like you, in 2 weeks, I noted a big difference. Much better. It's a little costly on my health insurance, but well worth the improvement in how I feel. I recommend it to anyone who is struggling on synthroid and levo.
KNOWING about tirosint is good to know..im learning so much from this website..i have nodules..and im getting the radiation pill to kill them..and to know there are diffrent wys to be treated is a blessing..when i go to my endo next week..i will ask her about the tirosint..any thing to feel normal again..is a blessing..or real close to it..
Has anyone had/have the diarrhea from taking Synthroid or Tirosint.I was taking the Synthroid first & had the diarrhea very bad I was afraid I was gonna dehydrate or get sicker it was so bad,recently I was switched to Tirosint.I still seem to have the runs but not as much as when I was on the Synthroid.The Dr. said he didnt think it was my med. causing my problem but he switched it just to make sure.I just found out I had a problem w/ my thyriod so I've only been on med. about 4 months.I dont normally have a sensitive stomach to any med. but my belly has been very jumpy & it seems like its since I started the med.'s.Can someone help me out here!!!
I've been on Tirosint for a year now and no problems with diarrhea.
You might be over medicated. Can you start a separate thread and post your current thyroid levels, along with reference ranges? That should be a minimum of TSH, Free T3 and Free T4. Don' t forget the reference ranges, as these vary from lab to lab, so must come from your own report.
I hope someone is still following this thread because I'm desperate for some advice! I recently switched to Tirosint from Armour and I'm having a rougher time than expected. I was on Synthroid for about 10 months and was doing "ok" but I really wanted to try Armour. So excited when my Dr agreed to try me on it so I switched about 7 months ago. I slowly declined and my hypo symptoms got worse. About 7 wks ago I got new labs and altho my TSH had almost tripled (0.68 to 1.88) its still "normal" so my dr refused to increase my dose. My free T4 was at the low end of the normal range. Plus I had gained back all 20 lbs I'd lost on Synthroid without any change to diet/exercise.
I was so frustrated I decided to switch back to a T4-only med and that's when my Dr told me about Tirosint. Seemed like a great option because I figured I'd get even better results than I did on Synthroid because of better absorption. So I took an old supply I had of Synthroid until I got my prescription for Tirosint (about 3wks) and I've been on Tirosint for about 4wks, for a total of 7wks on T4-only med.
I'm worried because I feel like I should be starting to improve by now but I feel worse than ever. My typical hypo symptoms are persisting and I continue to gain weight for no reason, plus I have awful anxiety and depression. I had some stomach issues for a few weeks like a previous poster mentioned but I have no idea if that was related to this med.
Should I be concerned that Tirosint just won't work for me? Which wouldn't make sense to me because Synthroid was decently effective and they're practically the same thing. Or is this just a result of switching from a combo med to T4-only med? I'm having trouble finding info on that kind of switch, everything I find refers to switching from T4-only to combo. Any advice? Thanks!
You need to give it a little more time in order to get a "true" reading of your labs. You should absolutely get your labs done after being on Tirosint for approximately 8 weeks. Then you will have a true reading. You need to make sure you have a Free T4 done with your TSH and a Free T3 to see how you are converting your T4 to T3. When you were on Armour, the T3 in it suppressed your TSH so it would make you look lower than you really are.
If your Free T4 continues to be in the low normal range, then you are hypo. You should be mid normal range.
Thank yeah I definitely plan to have her order free T3 next time, I'm not sure why but she never does. But my high TSH (when it almost tripled to 1.88) was while I was still taking Armour, right before I switched. I haven't had any labs done since switching. That's why I was so surprised because I've heard Armour really supresses TSH.
I guess I just thought 7 wks would b enough time to see some kind of improvement, but instead I've gotten worse...
I am new to hypothyroidism and I am not sure what my test results were to list right now but I started on Tirosint 75mg on Tuesday and I've been feeling so horrible! I am not sure if it's the meds or a coincidence that I started getting sick the same day I started the meds. I ended up in the ER a couple of hours after taking it with shortness of breath, chest tightness, tension headache, diarrhea, unquenchable thirst, dry mouth, my heart was fluttering and extreme fatigue. I've been this way the past few days and my Endo said to keep taking the medicine. I don't know what to do, as I stay home with my 2 yr old and just can't feel like this when I'm home alone with him. Is this normal or could something else be wrong with me? ER thought maybe allergies, went to Allergist today and it's not allergies, I do have an appt. with my PCP tomorrow and really hope it's something else that's curable ;) because I really really want Tirosint to work and I really want to start feeling better already!!
6 weeks ago I had a total thyroidectomy for multiple but localized pap carcinoma. I was on cytomel for 2 weeks and loved it. They took me off. Guess it is too hard on the pituitary with the up and down daily blood level swings.
Then they switched me to synthroid 137 micrograms. I weigh 140. I felt like hell. Depressed, crying, mood swings, wanted to jump out of my skin when I went to bed at night, not my normal althetic energetic self. 4 weeks later I had just started feeling a little better, but switched to tirosint in hopes that it was a better product. Had my labs checked same day. Results:
TSH was .06. ref range .4-4.
Free T4 was 1.6 ref range .8-1.8
T3 98 ref range 76-181
Thyroglobulin 3.3 ref range 2.0-35
TG antibodies <20 ref range <20
I think they want my TSH between .2 and .5
5 days later i feel terrible! Not sure what it is from. I am in bed for the last two days. Hot all the time, when I am normally not so. GI distress. Malaise, queezy, like I have a flu without the muscle and joint pain. I might have guessed it is from too much salt intake over the weekend and that affecting my inner ears, but I am sweating and the windows are open. Yes it is Texas, but it it not that warm here.
I read that Tirosint should not be taken with SSRIs, yet I take cymbalta. I am wondering if synthroid also should not be taken with SSRIs.
Synthroid & Triosint are both pure T4 meds. So from a hormone and chemical standpoint they are identical. So drug interactions would likely also be identical unless the drug interaction is caused from the fillers in the Synthroid and Triosint has no fillers or dyes.
You're symptoms of hot & sweaty indicate that you may have switched over to being Hyper. Due to the fact that Triosint is a liquid type cap and not a dry pill. The absorption of Triosint is higher than synthroid. I understand the premanufactured doses of Triosint are different and smaller doses than synthroid for this reason.
Your lab results show you to be near the very top of the range for FT4. So with the addition of a higher absorption or efficiency of the Triosint it I suppose is possible that the FT4 level is even higher now.
What was the dosage of synthorid (137 mcg I think) and what is the dose of Triosint you are taking now?
T4 meds are usually slow acting so it is a bit odd for you to suddenly go Hyper in a few days. May be some other allergic reaction or something to the medicine itself.
Do you have your lab results of where you felt good on the T3 Cytomel only regiment?
It also appears that you have only a TOTAL T3 lab result and not a FREE T3 test done.
It sounds like you might be over medicated, and possibly need to drop your dosage of Tirosint.
flyingfool - your understanding of Tirosint is incorrect. The pre-manufactured dosages of Tirosint are equivalent to either Synthroid or generic Levo. They are NOT different or smaller. No matter what the brand, the amount of medication is the same (i.e - 100 mcg is 100 mcg - it's just a difference of pill, with fillers/binders vs gelcap w/o fillers/binders.)
"Tirosint is available in 13 mcg, 25 mcg, 50 mcg, 75 mcg, 88 mcg, 100 mcg, 112 mcg, 125 mcg, 137 mcg, and 150 mcg dosage sizes."
These are the same dosages available in Synthroid or other brands.
Thank you for the clarification. I thought I had read that the Triosint capsules were 88 mcg for example instead of 100 mcg Synthroid because of the better absorption of Triosint so they would have the anticipated identical final result.
Good. Learned something new today.
But the thought that if she was on 137 mcg or Synthorid and if she is taking the same 137 mcg of Triosint, with the better absorption the already high T4 may have gone up even higher, resulting in hyper symptoms for her I think still seems sound.
Reaction seems fairly fast but she may have been on the edge of hyper to start with and this just pushed her over the edge.
Because of the better absorption of Tirosint over pill type meds, some people who have been on pill type med, may need to drop down a notch when they take Tirosint; however, that's not always the case and the same dosages are available for both types of med.
I agree that scary is most likely over medicated and should probably cut back her dosage.
Seems like a good medication for those with allergy to Synthroid fillers, but there is nothing revolutionary about this drug. Yes it may 'absorb' a little bit better / quicker, but if you take your Synthroid like you should, on an empty stomach with a full glass of water, it's not worth switching over unless your just doing TERRIBLE on Synthroid, even then I might recommend Armour. IMHO, nothing to see here, liquid Synthroid..
Yes, the T3 med is a pill; you can take it at the same time as the Tirosint, or not, whichever works best for you. It would also depend on the dosage of T3 med.
I'm on 88 mcg Tirosint, with an additional 5 mcg generic T3. I take my Tirosint when I first get up in the morning, then, since I'm on such a low dose of T3, I wait and take that later in the morning. Most people find it beneficial to split their T3 med into more than one dose, but again, because my dose is so small, it's not worth the hassle. If you ask the doctor to prescribe the medication in 5 mcg pills, it's easy to split the dose, without having to actually cut the pills, thereby being able to keep your levels more steady. For instance, if you were on 10 mcg/day, you could take 1 5 mcg pill in the morning, and the other around noon, or so, but it's best not to take T3 after about 3:00, or it could interfere with sleep.
Check with your insurance company about the Tirosint. My insurance pays for it, but not as much as they pay for a generic levo.
I am on both: 150 mcg Tirosint and 25 mcg Cytomel. I take my Tirosint in the morning and half of my 25 mcg pill at same time. I then take the other 1/2 approximately 5-6 hours later.
My insurance reimburses me for the cost of synthroid, so i only have a small amount to cover on that one. It is well worth the cost to me!
Tirosint has been absolutely wonderful for me! I would never want to go back on any of the other T4 meds.
Thanks for your input. I am going to look into it.
Right now I am waiting ( hanging in there) for my 6 week test date and to level out on what I am on. I know I will most likely need to go up in at least the T4. The increase may be 115mcg from 110 mcgs.
I am wondering, I read from their web site that it is absorbed 103% over the pill form that is only 88% ....makes me think that I would do okay at 112 mcgs. But first I want to see how the blood tests for my Frees are
I have been on 88mcg Tirosint now for 14 days, and I too have had chest tightness with heart palps. All my labs came back below the normal range. My dr now wants to switch me to Levoxyl. My symptoms are subsiding & I'd like to give Tirosint a little longer to work. Are you still taking Tirosint & how are you feeling?
I switched to Tirosint from Synthroid over a year ago. Switched to the same dosage and it was too much. I now take half of the amount of Tirosint that I was taking with Synthroid and doing much better. My body absorbed Tirosint much better than Synthroid.
I really like Tirosint as my allergy problems with Synthroid have all gone away.
I just started tirosint, have had headaches, panic attacks, pain in my lower abdomen, face numbness and muscle weakness. I'm on 100 mcg, feel better at night than during the day with an appetite at night but not during the day. Will be talking to my doctor tomorrow about this along with gastro problems and quick rise in BP's too. I'm allergic to all kinds of stuff, so additive free isn't always the best either I guess. So you aren;t the only one.
If you are already pregnant, I'm not sure it's a good idea to switch. While some people have reactions to dyes and fillers in regular levo pills, they are not "harmful", unless you have a reaction and if you haven't yet, you probably won't.
The only difference between Tirosint and other brands of levothyroxine is that Tirosint is a gel cap, which dissolves more quickly and is supposed to have a higher absorption rate. Some people find that they have to start Tirosint at a lower dosage because of the better dissolution and absorption.
No reason you shouldn't be able to take Tirosint during pregnancy. As always, with pregnancy, make sure your thyroid hormone levels are tested monthly, throughout your pregnancy, because dosage may have to be increased, in order to insure adequate hormones for both you and the growing fetus.
I am using Tirosint. It is awesome! The doc said he only trusts this med because this has the least fluctuation in the hormon strength. Its made in Switzerland by a company called Akrimax. My doctor said the absorbtion is also a lot better also since its a gel capsule, Looks like a small vitamin D. I will never go back to other pills. I was feeling awful on generic levothyroxine my hair was falling out I gained weight I was tired and bloced up.
I am using tirosint. It is awesome! The doc said he only trusts this med because this has the least fluctuation in the hormon strength. Its made in Switzerland by a company called Akrimax. It is also absorbed a lot better into your system since it is a gel cap. It looks like a small vitamin D. I will never go back to the generic levothyroxine. My hair was falling out I gained weight and felt awful until my doc put me on this medication. I felt the difference within 10 days.
Kitchen_cook24 hasn't been active on the forum since her post on this thread, back in Jan 2011, so it's unlikely that you get a response from her.
If you would like to start your own thread, since this is a very old and long thread, maybe we can help you figure out why you're having difficulties.
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