Levoxyl symptoms and conditions

I have been on Levoxyl 0.112MG for about 18 years. I do have some of the symptoms described by others, hair loss, hot flashes, etc. , but I think the alternative to this is a lot worse. If I do not take it for long periods of time, it gets to the point where I am freezing cold and the bags that develop under my eyes are embarrassing. I think the problem with most of you that are having very bad side effects is the dosage. If the amount is off just a little bit you can feel like you were just run over by a truck. I went through this many years ago. I would suggest continuing to change the dosage until you get it right. I wish I did not have to take it but it is absolutely necessary in my case.

I've been taking phentermine for about 2 weeks now and I also take levoxyl .175. It seems like about 2 hours after I take the Phen, I feel overwhelming exhausted. It feels like I can't do anything during this period of time, it lasts for about 2 hours. Sometimes it I get 2 or 3 of these episodes in a day. What is going on? I can't find any info.

I have had no bad side effects whatsoever with Armour Thyroid. I was diagnosed 6 years ago with Hashimoto's Thyroiditis (before I became symptomatic, actually, it was dumb luck that my neurologist sent me to the endocrinologist for a slightly off T4 level.)

I was started on Levoxyl (sp?) which gave me a headache every single day at the exact same time, exactly 9 hours after taking the pill. Then I was given Synthroid at too high a level and had rare side effects which subsided when I went down.

However, a couple years later I became symptomatic for Hashimoto's and although my endocrinologist swore up and down that no one should take Armour Thyroid, I had read otherwise, and had asked about it an an online women's forum. 9 out of 10 women on the forum said they did much better on the Armour Thyroid, and my new wholistic physician said, "Interesting, those are the same statistics I have in my office."

All my Hashimoto's symptoms went away within 6 months after starting Armour Thyroid and I've had no problems in years.

Hello... I started taking Levothyroxine last July for slight hypothyroidism. I felt great for the first 6-7 months, but then in January the problems started for me. I was getting severe anxiety which the doctor said was stress and he also thought I was depressed. I knew I wasn't, but he put me on Ativan and Prozac. The week I took prozac was the worst week of my life. I thought the effects I had were from the prozac, but now I know now it was my thyroid spiking, which the doctor never checked my levels during this period. My heart rate doubled, I had insomnia, was gagging, sick, felt like my body was on speed and wanted to die. I was prescribed a beta blocker for my anxiety previously which I had never taken, but decided to take when my heart was racing, which helped me feel a bit better for the week, but I knew something was wrong. I had this happen again recently for about a week (and I was on nothing but levothyroxine). I know what anxiety is and I have never had anxiety or depression my whole life until these episodes that happen when taking this medication. By the time I went to the doctor to get labs done, I had been feeling a bit better and he said my levels were fine. I am now wondering if it's side effects from the meds or if it is spikes in my levels making me hyperthyroid instead. All I know is that I cannot live like this!! I have a 3 yr old and I need to be happy and healthy like I used to be before this medication... no more heart racing, racing thoughts, anxiety, and insomnia. Please help!!

I have been taking Levoxyl for approx. 5 years following having a total ablation of my thyroid due to follicular thyroid cancer. I am constantly tired, have joint pain, trouble sleeping and continue to experience weight gain. The doctor continues to tell me this is not from the medicine and to improve my diet. My vision has also gotten terrible over the past two years. Has anyone else experienced this and do you know of anything that helps?

I've been on levothyroxine 150mcg for about 3 months before that it was 100mcg and so on. I have gain lots of weight and tired all the time. depression also, headaches. I hate this gaining weight, sleepy all the time and depression is from gaining weight. I thought this med is to up boost my thryiode but it doesn't seem to be working. my dr. said I'm on the highest dose there is. I don't know what to do any more. I was thinking about taking myself off this but not sure what will happen if i do. I hope there is someone out there that might be able to let me know if they are going through the same things what they are doing and how they feel now.

Have been on Levoxyl for the past two years and have been having EXTREME hair loss. Would like to hear from anyone having this side effect who has had success with an alternative treatment....either a different drug or an alternate treatment such as Armour, etc. Is coming off Levoxyl cold turkey as dangerous as everyone says it is?

I have had great experiences with Levothyroxine. I am no longer tired, achey, grumpy, constipated. I feel great. I am only 27 years old and got my hypothyroidism from having my first child. I am excited that my levels are now normal after 3 months (TSH was 25.89). I was on .50 mcg now I am on .75. Feel great!
I am a medical technician and have found that a lot of people who start on a certain medication for hypothyriodism, such as Synthroid - do not fair well if they have to switch. My doctor always says NOT to switch...not EVER. She repeats over and over again to check my prescription every time I receive it. That means checking the pills against each other, because hypothyroidism medication is one of the highest missed - filled prescription. If I were anyone who has had to switch, I would demand to be put back on your original meds. Have your physician write up your symptoms with the new meds and make a recommendation to the insurance company that you NEED synthriod.

ive been on levothyroxine for about 6 years...... for an underactive thyroid gland and i am stunned reading all these side effects as for about 4 years ive suffered from severe joint paint, fatigue ,very low moods , foggy brain, mood swings hair loss, all i want to do is sleep and even then im still tired.
I am 35 and feel about 80 as my back hips legs calfs and feet all hurt so bad.
I have been to the doctors so many times and got no where.
ive been told your in pain because your depressed( who would not be depressed ) but i said i am depressed cause im in such pain.
i remember asking once if it was due to the thyroid or the drug and the doctor said your levels are fine and the drug gives no side effects.
I feel like stopping it right now to be honest.
I only got it after my third pregnancy and i remember reading once it can correct itself as it could be caused by pregnancy ????? any ideas.
ive copied and pasted a lot of these comments and i will be making a trip to doctors to be fobbed off again im sure ....but its worth a try

Hello, told my doctor today of leg cramps, facial rashes and numbness in feet....and specifically asked if they were related to Synthroid? He said no, I have been on it for 2months...and just upped script to .50mcg....and cramps are worse....I am going off the meds. I am in excellent health @ 64 and only went to this Doctor because of back pain.....was tested for a myriad of things...I had none of the symptoms for hypothyroidism.....what natural remedies are there for this . E.

I had my thyroid out due to cancer on 1/22/08. then because of having to take a high amt of levoxyl (synthetic thyroid hormone) I was put on metoprolol for the palpitations. I recently had more surgery to take out cancerous lymph nodes in neck and my dose of metoprolol was increased from 25 to 50 mgs. I was only on 50 mgs for about 4 weeks when I developed depression, insomnia, swollen belly, acid reflux, swollen legs and anxiety. My mind started to go off on me and I had convinced myself that the cancer was in my brain and that's why I felt like I was dying. I was told by my doc that this med does not usually cause depression. I went over the facts and realized I felt pretty good until I started taking this drug. Even on the 25 mgs my legs which are really skinny, started to look like lumpy cottage cheese but I figured it was due to the thyroid removal. I didn't take it at all today because I just want to be rid of it. I know I need to wean off but how long do I have to?

I'm on 50mg of Levoxyl I'm 42. I have experienced major gas and heartburn. I have no sex drive anymore and just feel like I'm in a box and can't get out. I thought by seeing a specialist it would help. I just don't know anymore. I told my doctor about my side effects and he said this medication has no side effects. Hmmm after reading all this I am printing and giving it to him. Anyone feel the same. Especially the gas and heartburn?

Boy, this could take a while. Have been on generic Levoxyl for more than 7 yrs(can't say exactly how long since I stay "fuzzy headed" all the time). Anyway, about a yr ago I became so depressed I went off all my meds -- I'm a diabetic on insulin and also have high blood pressure. I felt good!To try and make this story a little shorter, I went on a diet and lost 70 lbs -- went from 310 down to 240. Then I went back on meds. In less than a yr, have regained all the weight I lost. Also, my legs swell and ache so badly it makes walking painful. Hands, wrists and knees throb constantly. Intermittent headaches so bad I have to wear sunglasses just to tolerate indoor lighting. Hair loss is so severe I'm considering a wig. Skin is dry and itchy and lotions help not at all. Any work I have to do I must accomplish before noon because by early afternoon the fatigue is debilitating. I'm currently on 300mcg of Levothyroxine (up from 250mcg 2 months ago) and doctor wants to increase dosage even more. Had no idea there were other people suffering the same problems until I stumbled upon this site. I take the medication as prescribed (with perhaps less than the recommended full glass of water) but plenty of coffee. Discovered on another site that the coffee may be inhibiting the drug's absorption. I feel so helpless/hopeless. Am considering going back off the Levothyroxine but am seriously worried about high T3/T4 levels. Thanks for listening; guess I just needed to vent.

I was put on Levoxyl for 20 years. Hair kept falling out, muscles aches, acid reflux, plantar fasciitis, carpel tunel, tired, cranky, brain fog. I could barely walk and had developed a stutter. I was to be tested for Alzheimers at 45. I was told there was no other drug for hypothyroidism and it wasn't the Levoxyl doing these things to me.

Well I found another drug thanks to the internet and Yahoo Natural Thyroid Group. It was Armour. I have been on Armour for about 2 years now. All those problems I had on Levoxyl are gone. Completely GONE! Wasn't the Levoxyl huh?

extremely depressed after a week of taking levoxyl. Also face is swollen, eye swollen and red and face and eyes burn. These were the same symptoms after taking synthroid after a week. What's next? I am close to being suicidal after having survived lung cancer, surgery, chemo and radiation. To get another primary cancer and have things slide downhill after such a remarkable recovery, I can do nothing but cry after making the decision to have a cancerous thyroid removed that could have served me for years and years since it was such a slow growing cancer. I should have followed my instincts and just left it alone. Now all I want to do is lie on the couch and cry.

I too was a picture of health even with my TSH being off. My old doctor retired and a new one prescribed the levothyroxine.
I never have felt so rotten in my life. Extreme fatigue to the point I am given up many activities I've been involved in for years. Headaches and joint and body pain. I feel like I was hit by a truck!
I stopped the meds and felt fine..cept my cholesterol went up to 262 and my tsh 7 something.
The doctor scared me back on to the levothyroxine.
I am desperate. I wish I knew what to do.

I have been on Levoxyl for years. Have experienced all the side affects this medication has and then some more! My hair loss and thinning, depression, bone aches, headaches, fatigue, and much more...finally I asked the doctor is there was anything else out there in the market which had less side effects....there is a natural product which has been in the market for many years called Armour Thyroid (*******). All I know is that if I continued to take Levoxyl, I will most likely end up in bed for life...I am only 43 yrs old and would like to have at least "normal" energy for my age. There is NO reason I should feel a lot older and I know for a fact it is the medication. I have only been taking Armour Thyroid for just a few days but will report my well being in about the next 30 days. Since I was on 100mg of Levoxyl a day, am taking two grains of 30 mg a day for a total of 60 mg of Armour a day. In about 25 days I go for blood work to check levels, so far I experience a bit of nausea right after I take the "new" medication but it does not last all day. Hopefully, this new med will give me my LIFE back! Thanks for reading.

Hi l have it all too and more!! I am so fed up :( lm cracking up! Does any one get sternum area pain cramps? They scare me the most l cant move :( Sick of docs passing me off grrrrrr

I am a female and was diagnosed with Hashimoto's three years ago (looking at old childhood photos I've probably had this all my life) and have taken Levoxyl and Synthroid in escalating doses over time. Initially 25mcg for about a year and that was the endo plan until bloodwork indicated a need for more. I quit taking it after a year as it seemed I was gaining weight. After a few months went to a different endo and he started the treatment again with 25 (I weighed 160 at the time) and now has worked it to 100mcg (I now weigh 178!!!). I thought that with the higher dose I would have more of a weight loss effect (definitely not weight gain) and thought I'd have more energy, better brain function and happier outlook. I am experiencing the complete opposite. The last time I visited the endo and he looked at my weight gain he just said to "stop it". I work out almost every day for 45 minutes to 2 hours, have a job that at times requires arduous work, I eat a very healthy diet full of fiber, low in fat, low in carbs. I'm always hungry and feel like eating to make up for a lack of energy. I come home from work exhausted. This isn't living. I've had it with the Synthroid and any form of T-4 alone. I'm going to see a natural healthcare professional to try Armour because none of the medical doctors I've seen will prescribe it or synthetic T-3.

I've been taking levoxyl for 8 years now with mostly good success. My endo doctor recently upped my dose due to lab results (I think the test results were bad). Now I feel horrible. Headache, dizzy/lightheaded, blood pressure increased, tightness in throat, and muscle cramping. I've been to many specialists concerning the dizziness - everyone says I'm OK; cardiologist, ENT, and neurologist. The symptoms started a few weeks after the dose increase, and have worsened in the last week or two (about 2.5 months out).

I have been on Levoxyl for about 9 years and have felt awful. I have had weight loss, dry hair, thinning hair,dry skin, muscle aches, migraines and the list goes on. I just got out of the hospital Monday after 4 days of testing of my heart and lungs. I was admitted for racing heart. The doctor's conclusion was anxiety! They said that Levoxyl has nothing to do with my rapid heart rate. The endocrinologist prescribed taking levoxyl .050 on day and .075 the next also a beta blocker, Xanax and Zoloft. I can not take any of these meds b/c they make it almost worse. I KNOW it is not Anxiety and it from the Levoxyl but what do I do?? I am a mess right now can not be in this condition with four young kids and a husband. None of the doctors would say it was the Levoxyl and instead prescribed more and told me to check up with blood work in 6 weeks. I took the .050 yesterday around noon and by 7:30pm my heart rate picked up again and continued until 4:30 this morning. I can not sleep more then 2 hours at a time and wakeup feeling like I am crawling out of my skin. PLEASE let me know of any solutions.

My mother and I have both been diagnosed with Hashimoto's Thyroiditis and we both take levothyroxine. We both experience extreme pain and she has been diagnosed with fibromyalgia. I have not been diagnosed with fibromyalgia but I experience the pain body also. Another thing. I have been losing my hair. No reason, it's falling out from the root and I have some serious thinning. Memory...what memory. I can't remember anything. Has anyone received advise from a MD? Thanks

55 year old female
I have been on Toprol 5 years. 50mg. it works for me but since it went generic,I wonder...I am on 10mg lexapro and December started the vivelle-dot for my hotflashes. It is now June and the last 4 weeks my hair is falling out big time.
It is so thin I have to wear a scarf as not to scare small children at work.!! :)
I have talked to a couple of hairdressers and they have told me many of they're clients with thinning hair were on Toprol.
Anyone heard of this? Please help me figure this out.

I am a 34 y/o male who started taking 10mg/day of lisinopril on May 15th. My blood pressure at the time was 140/118, pretty high I guess! I was feeling it too in the form of headaches. The doc wrote the script for me and I filled it that night. I should also mention that this is not the first time I have taken Lisinopril. I stopped taking it back in March because the script ran out. I don't seem to recall any kind of side-effects the first time, but I could be wrong. Anyway, I also take Levoxyl for my hypothyroidism, and it is a pretty hefty dose, 225mcg a day.

So, for the first week, I was doing pretty good on it. No coughing, or any of the listed side effects listed for the med. Then, about a week into it, I started having numbness in the right three toes on my right foot. When I say numb, I don't mean I could not feel anything, it was like touching your skin with a t-shirt over it. I could feel it, just kind of topically numb. I had a 'patch' of this numb skin right behind those same three toes and several other areas up the front and back of my right calve. I delt with this for a few days, thinking it was my shoes I was wearing at work. They were pretty worn out on the outer edges. I got new shoes on Monday, June 2nd. I wore them to work on the next day. At the end of the day, my calves felt kind of tired. The next day, they felt kind of tired still. I found this sort of weird. From that point on, my high anxiety really kicked in. I don't want to mention the thoughts I am having about what it could be that is causing this. I forgot to mention that I have not been sleeping well lately either since I started taking the Lisinppril again. I guess overall, I feel exhausted and weak. More so in my legs. To add to it, my lower back hurts like mad. I have two herniated discs and mild arthritis in it from damage from years ago. Also, for the past week, a pain has been developing in my left shoulder blade in my back. It is worse in the morning, and had gradually been getting worse for about a week. Today, it was awful.

I have ready a lot of the messages about the side effects different people are having. My question is, has anyone ever been on the lisinopril, gone off of it for whatever reason, having had no bad side effects, then gone back on it only to start having these bad side effects that you did not have before?

I have stopped taking the lisinopril on the 5th and have a doctor's appointment on the 9th to find out what is going on. I don't feel good at all. Can anyone relate?

I am just slightly hypothyroid and could go without meds, but decided to try meds, and endocrinologist suggested Levoxyl 50 mcg per day. First day on the drug, felt exhausted by night time, next morning, usually jump out of bed for workout and was extremely tired at the gym, no energy, was starving during the day even after breakfast which is unusual for me, and exhausted by evening, and third day woke up with swollen glands and exhaustion, knew something was up. Decided to research the side effects and found others with similar symptoms and didn't like long term effects so I am going off the drug and hoping I caused no damage to my system. My doctor's reaction was "impossible" that the drug could cause this. My reaction was, "no thank you, I think for myself, know my body, and know this drug caused this reaction." I was feeling fine before 3 days ago, and how could so many have similar symptoms if it isn't the drug.