Levoxyl and endo

I have been taking Levoxyl for about 2 years. I have told my Endo doctor many that I have had headaches, nausea, stomach pains and have gained 40+ pounds in the 2 years. Every time I go in to review my blood tests and tell her I'm not feeling right I get the same respondents as a lot of you; they are you sure you are not pregnant? you need to change your diet and eat right? you exercising enough?...The Dr always seems to ignore my symptoms. The last 4 weeks have been Hell for me...I woke up one morning thinking my stomach was going to burst. I went to the Er. They did an ultrasound...found nothing..gave me stomach reflux meds and I went home. 2 days later the pain was a lot stronger right under the center below my rib cage. Went back to the er. They gave me more protonics and gave me a gi dr. I went to the GI doctor and got a contrast scan and then a scope. They of course found NOTHING. A week later I woke up again with the worst pain yet and the cold sweats...to the point where I was going to pass out...Went back to the Er where they gave me a cat scan. Everything was perfect the er doctor said. "They said they couldn't tell me what was wrong". I knew I wasn't going crazy and having all these symptoms but no one could explain why or what is was. I was getting fed up of being sick...So I took my Levoxyl like I do every morning and within 15 mins the pain was back. I went online to look up the side effects of Levoxyl and found this site. Its great to know that I am not the only one out there with these side effects from this medication and am not going crazy! I made an apt with my Endo Dr today called and told her this med was making me sick. She made me have an apt with her assistant. I printed off this page to show her I wasn't alone. As of today I am off of Levoxyl. Thanks to the new Dr who FINALLY listened to me. I do not have to take any other form of this med either. Since I just had a nodule not hypothyroidism. Please Can anyone tell me what they went through from withdrawal from this medication? and anything that helped it go away? and How long did the "detox" from Levoxyl last?

I have been on Levoxyl for about 2 1/2 years. Before I was on levothyroxine, but my new endo said the generics don't work, so he insists on the name brand. I've been taking it in the morning on an empty stomach, and have been battling extreme daytime fatigue ever since. At first I thought it was because I was unhealthy. I had LAP-band surgery, and I use a CPAP machine for my sleep apnea, and I lost 50 lbs, but I've hit a plateau that can't be explained by my food intake, and the fatigue is so debilitating. My GP is adjusting my anti-depressant to see if that makes a difference, but so far no. On my own I decided to start taking the Levoxyl at night before I go to bed. It's only been a couple of days, but I have noticed a marked improvement. I'll talk to my endo about it, and hopefully he'll be at least willing to consider the change.

On a side note, anti-depressants are the best medicine ever discovered. If you are feeling at all depressed, talk to your doctor. Whether the Levoxyl contributes to it or not, the anti-depressants help. I never want to go back in that black hole again.

I was diagnosed with Hashimoto's Thyroiditis (hypothyroidism) about 9 years ago. My teenager was diagnosed 2 years ago. I have done a good amount of research and have also learned a lot through experience.
*The most critical thing is to NOT accept a generic brand of thyroid replacement. My GYN, family doctor, and my endo (who specializes in thyroid) have told me that generic pharms are only required to match the original drug's ingredients/strength by 75%. As my GYN said, if you're in the business of making a profit, and you can get away with putting in 25% less of the expensive (and unfortunately, the essential) ingredient, that's what you're going to do!
*Measuring T4 alone may not reveal hypothyroidism in the early stages, and it will probably not show everything that is going with your thyroid. I knew something was not right, but my old GYN (got rid of her) tested T4 only and said I was fine. I went to an endo who measures 1/2 dozen indicators, including antibodies and thyroid uptake, and I was correctly diagnosed. He also diagnosed my son early on, albeit, my son was exhibiting numerous symptoms. Which brings up another point -
*Everyone exhibits a different degree of different symptoms. So don't be surprised if your thyroid levels are higher or lower than you thought they would be based on your symptoms.
*Find a doctor that will work with you. I had a doctor that insisted my dosage was correct, even though I was still feeling very tired, had dry skin, etc. I finally found a doctor that acknowledged that there is a range of "normal" thyroid function. He upped my med a little, and I've felt much better.
*Know the signs of too high of a dosage - restlessness, eye and muscle twitches, trouble sleeping, etc. Our endo has us come in 1 month after prescribing a new dosage to make sure it is enough or not too much. If I was exhibiting hyper symptoms, I would not wait 1 month to be rechecked.
*Hormonal changes of any kind can wreck havoc on your thyroid - whether you're a male teenager or a peri-menopausal woman. Your thyroid levels can change quickly. If my son or I experience any new symptoms - fatigue, rapid weight gain, unusually dry skin, muscle aches/pains, etc. - I make an appointment w/ the endo. My son's thyroid had plummeted the last time I took him in, and the endo adjusted his med. Illnesses (flu, pneumonia, etc.) can effect your thyroid levels, as well as stress, so have your levels checked after going through a serious bout.
*Once you have your dosage correctly set - watch your appetite! Hypothyroidism can reduce your appetite, and once you've got that corrected, your appetite comes back. Keep a food journal to track your calorie intake.
*Have an annual thyroid ultrasound to make sure your thyroid is not enlarged and to look for nodules (very common w/ hypothyroidism.)
*TAKE YOUR THYROID 1ST THING IN THE MORNING BY ITSELF 1 hour before you eat. I had a friend who was taking her calcium supplement along with her thyroid every day and later found out the calcium was basically canceling the thyroid. Her doctor should have warned her about this, but I think they assume we know these things. Vitamins, herbs, cold medicines, certain foods, and other medicines/supplements can greatly interfere with your thyroid replacement.
*Women with hypothyroidism should take a calcium supplement (take one with magnesium for better absorption) because we are at greater risk for osteoporosis. I take mine at night, so it does not interfere w/ my thyroid replacement.

I have been on levothyroxine 75 for two months so far. I started off at 25 then up to 50 and now currently on 75. I have horrible lower back pain along with my knees aching too. It's all the time and Advil or aleve do nothing to relieve the pain. I am miserable and hate living like this. Doing some reading here and other sites I've read that this can be due to the med and some thing about the fillers in it. When I first started the the 75 that my doctor game me from samples at his office that were the name brand all was good. Now that I have been on the generic from my pharmacy I'm in pain. Am I off base here and does any one have similar issue's? I'm calling my endo when the office opens today to see him. Thanks for any info.

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'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).

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

I had always used the generic form of synthroid & then the generic form Levoxyl. The beginning of April 08' my endo prescribed me the brand name Levoxyl. I take 175mg. everyday. After several weeks I began to have terrible insomnia. It was weird because I initially fell asleep easily but began to wake up every hour of the night for no reason. This went on for weeks. I even tried taking Tylenol PM to help me sleep & I still would wake up every hour if not every other hour & I had very vivid dreams that I would remember. I began waking up in the mornings feeling exhausted from all the dreaming & all the waking up. I believe I became more depressed because I was so tired. Then I read on-line that someone else experienced this while taking Levoxyl. I switched back to the generic Levoxyl & now I can sleep through the night again. I still experience fatigue & have problems losing weight. None of that changed when I switched to the brand name anyway.

I have had a total thyroidectomy due to thyroid carcinoma about 2.5 -3 years ago. I have been on synthroid and levoxyl and both have caused tingling and numbness in my hands and feet, what I call a general fog (hard to concentrate or think, sometimes talk). I have been tested for neuropathy since endo said radiation may have caused issues. Only to be cleared by neurologist. Now endo switched does lower after rebout of cancer from 300mcg to 274mcg and have knee joints now going numb I want to sleep all the time, general weakness and now low testosterone levels.

I have been on Levoxyl for over 10 years with no problem. When I picked up my refill two weeks ago the pharmacist said that the pill may be a different color but it's just that the company that was making Levoxyl sold it to another company and is now making it. Within a week I was very itchy, then I started getting hives at night and waking up with them in the morning. I also developed severe heartburn. I feel very full and cannot lie down at night. I also can't eat very much at one time because of the heartburn/reflux. My family doctor advised I call my endo which I did. She advised me that she has had patients all week that are having problems with Levoxyl that never had them before. She took me off the Levoxyl and put me on Synthroid. I will start that tomorrow morning and hope I will get some relief soon. The pharmacist said I wasn't the only one going off the 'new' Levoxyl, others have been in all week exchanging their prescriptions as well. Has anyone else had this same situation?

I have been reading all the entries for this website and thought I would pass along some useful information. I have been on Levoxyl for 8 years now and have had lots of the symptoms that all these people have had. I then had an appointment with a great Endo doctor at the *** and discovered some interesting things. There is a number "range" they put all people into when checking your TSH levels, only problem is each person is different and even though the doctor may say your in the range, it may not by the right dosage for you. Unfortunately the only way to determine the correct range for you is to experiment with the dosages and it takes 3 months or more for your body to adjust. Also, thyroid hormones are accumulated in the body and depending how active you are is how you may feel. The hormone pill you take today will not be used by your body for up to 10 days, so if you feel good for a few days at rest, then exercise the next day you may feel drained. It will take a few days for your body to replenish the stockpile of hormones to feel "normal" again. A working thyroid makes hormones as needed, yours now does not so this is why so many people feel fatigued, or racing heart beat if they don't get enough exercise. I also had leg and muscle pain. The medication depletes your body of Calcium and B complex especially B12. My leg and muscle pain have disappeared. I still get headaches, but much less with the B12, and some days I still feel tired but I say again, your body cant regulate its needed thyroid hormone and a synthetic pill is only a substitute.. You will always have some side effects. Hope these tips help someone.

I have being taking thyroid medicine since 1994. I was diagnosed with Hyperthyroidism and prescribed Synthroid. It didn't work. Instruct to take radioactive pill. Now, diagnoses change to Hypothyroidism. Prescribe Levoxyl. Endocrinologist said I would lose weight, but instead I have gone from a size 8 to 16. I feel really bad when I miss my doses. Really anxious when I take it every day. I am noticing that I have moles growing out and spreading all over my body. Switch back to Synthroid three months ago. That when start experiencing a great deal of hair loss. Decide to switch back to Levoxyl but a lower dose. The hair loss has slowed down a little. But, hair is growing slowly. I am having problems focusing and some memory loss. I really don't know what to do. I have change endocrinologist twice. I really think that Levoxyl and Synthroid have bad side effects on human after long term usage. I am miserable because I can't control my weight. I know that it has something to do with this medicine. If anyone know of some other medicine that would Hypothyroidism in check without all of the side effects that I mention. Please share it with me.

I HAVE BEEN TAKING LEVOXYL FOR 22YRS AND I FEEL LIKE I CAN NEVER GET SLEEP,I TAKE MY PILL IN THE MORNING AND CAN'T SLEEP ALL NITE AND AM TIRED OF IT,I WISH THEY HAD AN ALTERNATIVE.THAT WAY I CAN SLEEP AND NOT BE DEPRESSED ALL THE TIME

I am extremely hot and sweaty, memory loss, fatigue, aching hands, dizzy at times and most recently had a fainting spell (black out) while I was attending a movie -- it started with dizziness and then I became totally burning up hot and wet with sweat so much so that my hair was wet -- this lasted about 1/2 hour and ended with the dry heaves. Please let me know if anyone has experienced this. I had my thyroid blasted with radioactive iodine about 3 years ago (Graves Disease) and I have been hotter than blazes since that time. I am on 112mcg of levoxyl

Has anyone noticed that when taking Levoxyl you have some irritation after urination. I seem to have a nervous feeling in the urinary tract and after urinating it seems like I have a sensation of irritation. I have had tests for infections but nothing showed up, I am considered Hyperthyroid because of my dose of 150 mcg which is where Endo. wants me to be. I would appreciate anyone who has any input. I do not know if levoxyl makes your urine more acidic or not.

I have been taking levoxyl for 2 yrs now. I am getting migraines/headaches an average of 3-4 times a week. I have had a ct scan and everthing came back ok. I am
suspecting that it is the levoxyl and I am going to stop taking
the medication. I take levoxyl for hypothyroidism. Does
anyone else experience headaches as a side affect. I have
also notices memory loss and trouble concrentrating

After surgery for a goiter with numerous nodules, I was started on 100 levothyroxine and felt fine. Due to too high TSH level (10+), dosage was increased to 150 and I went to the other end of the scale (.45). and the dosage was lowered to 137. Now my GP has reduced to 125 due to fatigue and depression. Have been at that level for 2 weeks and still have some depression and insomnia. Should I seek advice from my endo?? or keep waiting to see if these symptoms subside. It obviously is not easy to wait but don't want to compound the issue.

I was diagnosed with Hypothyroidism 2 years ago and originally I was prescribed synthroid. I was tired and cold all the time. I was switched by my doctor to Levoxyl 50 mcg about a year ago. I am only 10 lbs overweight I still have not been able to lose. Over the last 4 months I trained and and completed a 26.2 mile marathon and 3 different 13.1 miles half marathons (running) I have not lost any weight.
My enodocrinologist has recommended that I get checked again to see if the dosage needs adjustment. I have a feeling it is too high.I have recently had some symptoms such as hot and cold flashes, headaches, heart palpitations. I have more energy now than ever in my life. Other than the hypothyroidism I am healthy and should not have heart palpitations. and my endo says that the amount of running may have shocked my body into working more efficiently. I am to be tested in a few weeks. I don't know if this is true but I also heard that if you buy medications that are on the shelf too long that they lose some of
their potency.