Levothyroxin symptoms and conditions

Does anyone here ever had any tingling issues? I had total thyroidectomy in Feb. 2009. Felt good the first month or two and have gone down from there! Some days are good, some are bad. Never know from day to day how Im going to feel! I started out for about a month and a 1/2 on 125 levothyroxin.....then my doc lowered it to 100.......as of July 14th, Im now taking .88. The tingling Im getting is all over my body, different places, here and there. Ive had some heart rate issues for a couple of months now too and finally had my regular doc send to me see a heart doctor.
Thought maybe the tingling could be from low calcium.....it was normal, CBC was normal, ECHO was normal.....waiting on the holter test results right now. The heart doc gave me a prescription for Toprol. I told him I wasn't going to take it cuz sometimes my heart feels like its barely beating and Im afraid it will make it worse. Im glad I didn't get it! Ive read of too many side effects.
Palpitations, kinda fast heart beat with pounding.....sometimes it feels likes its barely beating! Most of this occurs when first laying down......every now and then while sitting, etc. I do not exercise.....and should but just don't find the time. I switched jobs around the time I found out I had several nodes on each side of my thyroid. I was getting tired a lot and just thought i worked too much. I went from a physical job to a sit down, 12 hour, graveyard shift. Since the surgery, Ive felt it more. Im tired of feeling like crap all the time......I was already going thru some perimenopause stuff before all of this! Before I ever found out about my thyroid, I did have real light pounding of heart when laying down and tingling every blue moon, but very mild as well.
Now with no thyroid.......and medicines with all the side effects......IM GOING NUTS!!! Right now the moodiness and tingling are whats bothering me the most. Some days Im really tired, others Im ok. My body gets hot off and on, no fever. The past 3 days my calves, feet, and ankles have started to swell........never before! Plus I get some throbs and pains in my legs and arms and under my arms here and there. I probably need a new doc and I change of medicine......but Im afraid.
For one, Ive decided to go back to a physical job........and hopefully it wont screw with my heart rate even more. Ive read up on tingling........Im guessing maybe its from all the damn stress since my calcium was normal. Does anyone here have any suggestions?????

After having my third child in Aug 08 I wanted to try the mirena since I always forgot to take the pill. I have 3 friends that have this piece if crap it and they are fine but me I feel like I'm going down hill. I had it inserted on thanksgiving eve 08 and about two weeks later I started with a rash on my neck, shoulder, and arm. My doctor told me it was the shingles. He also did blood work on me cause I haven't been in the doctors in awhile and my test came back that I had severe hypothyroidism in which I didn't feel any symptoms of it. My doctor started me on 100mcg of levothyroxin and every since than its been down hill. He decreased my amount to 50mcg due to heart palpitations, anxiety, depression, diarrhea, weakness, muscle aches (especially in the neck and shoulders) and fatigue. I really wonder if the Mirena cause my thyroid to be out of wack and currently even with only a week of being on 50mcg I am experiencing anxiety everyday that my doctor prescribed me Xanax in which I was scared to take because I do not do drugs. After reading all these forums I am having mine removed on Tuesday Feb 3rd and hopefully this is really the cause of my problems. Has anyone else experience the same as me. I hate not feeling myself and not being able to take full care of my children. This sucks and the Mirena should be off the market.

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).

HI,

As with many others I found singulair to be a miracle with asthma. No more rescue inhalers. I am not sure which of my current meds is causing the very vivid, often gruesome dreaming I have been having as THREE of them show this as a side effect. I am referring to Cymbalta, Xanax and Singulair. It may be that the combination of the three is just too much and is causing brain toxicity of some sort. I started cutting down the cymbalta, and also the Xanax days ago. I found myself still waking up remembering vivid dreams that I would rather forget. I remember them all like they just happened in living color and detail, days and weeks later. At first I thought it was interesting, but now I just want to FORGET THEM, anyone have ideas???? Help!!! ( I also developed depression and anxiety after being on singulair for several years which is how I ended up with the two additional meds.

5-12-08 Was put on 25mcg in Mar. 08. because of Hashimoto Disease &
Hypothyroidism. At first had more energy & no symptoms. After a month
severe pain in joints especially in hands & left wrist. Muscle spasms in
thighs, calves & shoulders. Neck & back pain. Also headaches. Am
bloated all the time and can't seem to lose weight. Force myself to stay
active, but difficult to do. Irritable because of pain. Oh yes, on l-7-08 my
TSH was 4.270 & 4-29-08 my TSH was 4.430 & Dr. doubled my Levothyroxine to 50mcg & after that above symptoms doubled to
excruciating. After reading this web site no one mentioned extreme dry
mouth, throat & nose with a metallic taste in their mouth as I have. Let
me know if anyone has had this problem. Thank God for this site & thank
all of you that confirmed my problems was not in my head like doctors
want you to think. Thanks M.

I switched from a generic levothyroxine to Synthroid. After four days I awoke with extreme pain in one heel and the opposite knee. Both were caused by inflammations with no known cause in exercise or joint trauma. I switched back to the generic and both problems improved rapidly. Was Synthroid the cause? I don't know.

I have been on synthroid for about 6 months now. Some of the side effects I have been experiencing are numerous.I have hair loss, sometimes I get so ill that no one can stand to be around me, my weight has gone up about 30 pounds, my cholesterol levels went sky high so now I'm taking Crestor, I'm bloated most times, I have episodes where my face flushes and gets so red that it feels like its on fire, and now I've just started experiencing burning and aching of the legs, I'm tired a lot too! My doctor said I would lose the weight but every time I go for check ups and get on the scale it just keeps going up. I would like to know if anyone else out there is experiencing the burning and achy legs because I have been tested for everything and they can't find out what is going on. They of course say it's not the medication.It seems to never be. Does anyone feel me??

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 Levothyroxin (Synthroid generic) for about 5 months. I started on a low dosage and have been taking 75 mcg (which turned out to be the right dosage. I turned 59 years old in July and I had been gaining weight.Nothing startling--a few pounds a years that added up to about 50 pounds over time..I am losing weight now. The side effect I am most concerned about is a an inarticulateness I seem to have developed since I started taking the medication.I can't sepak civilly to my son who also turned 20 in July. I just want to scream at him all the time.

Is this a side effect of Synthroid? I don't think I have been losing my hair, fortunately, but it is dry and brittle...

I have been taking Synthroid for at least 10 years. I am on a very high dosage now175mcg. I have been on a lower dose but my counts were still low so my doctor put my dosage higher. I have been having a tremendous amount of body aches including finger joint aches and right flank problems. I have taken x-rays and various tests to determine what the pain is but I feel that after reading much of the side effects from this web site, much of what I am experiencing is from the Synthroid or Levothyroxin. I now feel that I need to take matters into my own hands and do more natural healing. Many doctors don't connect the dots to determine the real cause of your concerns.

I have been on 50mcg levothyroxin for 3 yrs. I recently have been having many side effects that occur on a daily basis such as: migraines, leg cramps, crazy menstraul periods, dizziness (which I believe is from low blood surgar levels), body temperature levels, unable to sleep at night, and an upset stomach. I am going to go to a doctor and get this all figured out because I am miserable. I am not someone you want to be around at night because I am extremely tired and not able to function even sometimes during the day I get that way. Thanks for this site cuz I was having all of these side effects and not sure from what but it all makes since now.

I have been taking Synthroid since Jan. 2006, am on 100mcg per day and all test results have been 'normal', I have been told to take this medication in the morning an hour before eating anything, if I do this...I have headache all day, I can't eat after an hour because I am so sick at my stomach there's no way. I feel hungry, but feel like if I eat it's coming right back up. Am having serious joint pain in hips, knees, elbows and wrists, my neck hurts really bad as well. I wake up to arms asleep anymore and just feel like I haven't slept in months...am very weak and very tired all of the time.

I have found that if I take my pill at night this gets a little better, but holy cow, don't tell your Dr. your taking it before bed...no, take it of a day. (don't know why this is a major thing?)

Anymore I feel like I am walking around with flu symptoms constantly, and the Synthroid hasn't done anything weight wise with me, because I was so HYPERthyroid before the RAI, I was very thin and looked like a bag of bones, have been waiting and excited about putting on weight...at one point I stopped taking the Synthroid and let myself go HYPO just so I could gain weight, it worked and I got up to about 130 pounds, was very HYPO so they told me critical that I get back on meds...I lost it again because it makes me so sick I can't eat.

NO-ONE can tell me the Synthroid is not the cause of this problem, if I stop taking it I feel WONDERFUL, but my test reults are bad. After a while of course my feet become numb and I end up having some bad hypo symptoms, have tried breaking pills in half....oh Lord no, need it all...

Have been told they are thinking about raising my dosage again anyway, I can't do this, I will break down in the office if they try to raise it. Right now my TSH is fine but my T4 is 'a tad bit' off. I am already an emotional wreck, if they raise my dosage I am going to try and go a different route with this, am on my 3rd Dr. at this point anyway...

I've been on levothyroxine for 3 months now. I have anxiety at night while trying to fall asleep. In the morning my hands feel so tight and are a bit swollen. My right knee and calf have started now too. My feet hurt when I get out of bed. After about 10 mins of walking they feel better. My face is also a bit puffy in the morning and I look tired all the time. I have pains on the right side of abdoman, just under my ribs....Is this normal? Could it be my liver from the meds?