Synthroid symptoms and conditions

i discovered that i had hyperthyroidism which was from grave's disease and grave's thyroid eye disease in jan. 2009. at the end of march i had my thyroid removed. never let anyone use the radiation treatment if it is in your eyes. my surgeon said if we had waited another week i would have been dead. they started me on 75 mcg of levoxyl. it made me mean, i prayed to God to let me die in my sleep every night. the dosage was changed to 88 mcg. my hair was falling out by the handfuls. i kept calling my dr. and being told it was normal. i lost 75% of my hair mass almost to non reversible. i have been on appearex and women's rogaine once a day and am using nioxin hair cleanser and conditioner for 2 months. i have new growth thank goodness. my toes almost froze off my feet, the headaches cannot even be described, i gained 40 lbs, this will be the 3rd time in 7 mos. they need to change my dosage to 100 mcg. my body cannot take it. today i am starting synthroid. until i found this site today i had no idea most of my agony was from levoxyl and it's side effects. thanks so much for all the information. good luck to everyone.

Started taking Lisinopril approx. 6 years. ago. Shortly afterwards I started a spiral downwards for no apparent reason. Did not connect this med. Shortly after starting it I was put on Synthroid for low thyroid. Started having loss of balance, dizziness, vision problems, muscle and nerve pain. B/P went up instead of going down. Have been to every type of Dr. (Neurologist, Dermatologist, Endocrinologist, Internist) and every nerve & muscle test and blood work came back negative. I have extreme cold in my hands and feet, increased back pain. headaches. This past week I have broken out in a rash on my torso and down both legs. The doctors answers are that I'm suffering from depression. The irony is that when the symptoms first started I questioned if I could be having a reaction to the medication and they flat out said no. After reading some of the comments as of today I am discontinuing the Lisinopril and will searce for something natural. I'm fed up with doctors and really short on cash from all the money spent trying to find an answer.

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 have been on Yasmin for 2 years now. It is the only BC I have ever been on and have LOVED it up until about 3 months ago. All of a sudden I started having heart palpitations, sever chest pains, extreme fatigue, very bloated in my stomach, low sex drive, pain and tingling in my arms and legs,dizziness, shortness of breath, trouble swallowing, weight gain and major mood swings! I went to the DR and they did an EKG (which was normal) Tested my blood (I now have a thyroid problem that I have never had before) and they did an ultrasound (Dr that I may have a murmur) on my heart and the results came back fine. So the DR prescribed me Synthroid for the thyroid problem and the DR said that should help me gain my energy back, loose some weight and would take care of the heart palpitations. The other symptoms he contributed to Stress (Panic Attacks) I have been on Synthroid for 5 weeks now and I don't feel any better in fact I feel worse!

This morning I seen a commercial for a lawsuit against Yaz or Yasmin. Well since I am non Yasmin I immediately did a search and came across this site. I have literally been sitting here all night reading all the comments from different women and now know what my problem is. My problem is YASMIN! I am not taking this anymore and have an appt with my Dr tomorrow to have them do whatever they need to do to see if I have any blockage or any other damage from using this pill. My chest pains and the tightness in my chest are so severe that it takes my breath away and I am only 24! I am not ready for children and don't want to deal with bad periods like I had before getting on the pill but I can not take this rise. PLEASE if you are on Yasmin please stop taking it immediately and call your doctor Your life could depend on it!! I am hoping like other people who have commented that after a few weeks of being off the pill that I will feel so much better. I hope I am getting off of it in time before I have done any further damage.

I feel bloated and hungry all the time since taking generic and switching to Synthroid for about a month now. I can hardly think as well. I am foggy brained and unenergetic physically and mentally. I am going to an herbalist who uses Nature's Sunshine products and said it is very simple to get back on track with sea kelp and black walnut. She is very experienced and has helped others.

also everyone on here are describing symptoms of hypothyroid if your having symptoms you might not be on enough.

Since on 0.175mcg of synthyroid after thyroidectomy and neck dissection two years ago, I have started to feel great fatigue? I can go to sleep at anytime during the afternoon. I also have a lethargy and malaise of the mind! If you mention this to the G.P., nurse or consultant you get vague looks!! Can anyone help?

37 - Dx'd w/ Hyperthyroidism at 20 and have been on levoxyl since then. I started at .075 and was increased to .1 when I got pregnant w/ my 1st child at 29. I always thought I had anxiety so until I started reading the posts I didn't put it together. I was always shaky and nervous and super skinny before I was dx'd with hyper and after the treatment I was still anxious so I thought it was a different problem.

The anxiety has gotten much worse in the last few years w/ pressure, family, and career so I went to a psych last week and he gave me lexapro and klonopin. The klonopin had done nothing and I was treated 10 years ago with Zoloft which made things MUCH worse so I won't take the lexapro.

I recently switched to Synthroid .1 because I thought maybe the generic meds didn't work as well. I developed a small rash on my elbow a week or 2 later, then a week after that I got 2 big patches on my back over my kidneys. A bout 2 weeks later I developed a HORRIBLE itchy rash over my whole body. I thought the itching would drive me insane. I saw a dr who gave me prednisone (made me feel awful), after I took the dose pack it came back like crazy. I went to the ED and the dr gave me scabies medication (I was mortified) but nobody else in the house had anything. I went to the derm and they biopsied two areas and a week later have not given me the result. Meanwhile, I'm back on levoxyl and the rash is slowly getting better. It must have been the cause. Anybody else get that??

My doctor switched me from Levoxyl to Synthroid and lower the dosage too.From 150 mg to 125 and now I am on my 2nd day taking Synthroid. I started feeling so dizzy this morning about 2 hours after taking Synthroid. I had this problem in the past with Synthroid, Maybe my body will not take Synthroid very well.

I've had numerous side effects from Synthroid, but the ones that finally scared me off the drug were the thoughts of death, dying and suicide.

These thoughts came as casually as thoughts of what I'll wear tomorrow, which was more frightening. They also came unbidden. First, I was thinking about death generally. About a month later, I began thinking about dying, and the whole process of dying. Then, when I started thinking about just walking in front of a train, I got on the Internet and did some research.

Synthroid was the only medication I take daily, so I stopped taking it at once. And about a week later, the thoughts of death, dying and suicide stopped. My doctor refuses to prescribe natural thyroid, so I'm out of luck until I find a doctor who will help me.

I am 45 and had the device inserted in June. Since then I have had an annoying constant red-brown discharge and my period three times. My menstrual cramps are definitely greatly lessened but what is freaking me out (apart from the discharge) is the anxiety I am experiencing for no reason. I am also feeling depressed. I am greatly concerned as being on the pill many years ago I had a mild stroke and my doctor assured me that the hormones ion the Mirena stay in the uterus. Why then the sudden anxiety attacks? I have always been a really laid-back person - I can only relate this sudden appearance of anxiety to the Mirena - it started about two weeks after I had it inserted.

I am now debating whether to ride it out - has anyone had the anxiety subside?

I had to take Prednisone as pre-medication before a CT angiogram (had an allergic reaction to the dye in a previous exam). Dose was 50mg, 3x, 6 hrs apart. About an hour and a half after the first dose, I was feeling rather "out of it" and unwell. Took my BP out of curiosity: 145/104! It dropped later, but after the 2nd and 3rd dose (all this in a twelve hour period), both heart rate and BP stayed elevated (hit 128/minute pulse, beat my old record when I was hyperthyroid on Synthroid!)

It's hard to believe this doesn't have a deleterious effect on the body--for me, it was of course preferable to the risk of anaphylactic shock. But I really feel for all of you who have to take it for an extended period (and sure hope I never do). Maybe it helps at least to know your symptoms and actions are definitely a product of this drug and that you will feel better when you can stop taking it?

I started taking Levoxyl for Hashimoto's Thyroiditis several years ago and got a headache at the exact same time every day, exactly 9 hours after taking the pill. They switched me to Synthroid (which in the end didn't work so I went on Armour Thyroid and have been great since.)

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.

I was put on Yasmin several years ago to control symptoms caused by ovarian cysts. I was told this was pretty much the only solution. Against my better judgment, I went on it. Things were ok for a few months but I started having mild side effects. I didn't feel like myself and my sex drive was definitely gone. Two years ago I had my thyroid levels checked and found out my TSH level was very high. After doing some research, I found that birth control can affect thyroid levels. I contacted my general doctor and he confirmed my findings. I took Synthroid to control my thyroid for two weeks and had to get off of it. I was like a zombie. I called my general doctor back and asked about stopping everything. He said to contact my ob/gyn and if she ok'd it, then it was fine by him. They agreed but also said there is no connection with the pill and thyroid. Red flag #1. After being off of the pill, my sex drive has not returned. It has been two years now. I asked my ob/gyn to do a hormone profile and they said I was too young to be having any problems like that. Red flag #2. I was tired all the time and had no energy at all. My general doctor gave me pills for depression (which the main side effect is extreme drowsiness). I was so disgusted at this point, I went to a Homeopathic doctor. I was told I had adrenal fatigue (which can be caused by the pill). I have been on a course of natural supplements for a few months and have felt better than I have in a long time. However, the sex drive is still gone and due to the pill, may never return. This has been a horrible strain on my relationship. It's upsetting when you know you should be feeling a certain way and you just don't. I have given up on traditional medicine and the idea of pills being given out without knowing long-term side effects and causing even greater problems. Ladies, if you are experiencing problems on or off the pill, see your doctor. If they offer no help, find another doctor! Also, after looking up Yasmin in a pharmaceutical book, it is listed as one of the WORST pills and listed under definite do not take. Use this pill at your own risk.

I have been on this med for about 2 years. Until about 2 months ago, I had zero problems and it was great! About 2 months ago I started having SERIOUS issues. I had never had a palpitation or chest pain in my life and then I started having heart palpitations, chest pains, shortness of breath - sometimes it feels like I'm not going to be able to take the next breath. I was in the ER - they said it was my thyroid and gave me synthroid - that made everything worse so they gave me a beta blocker to cover up those symptoms. I quit taking ALL medication! I am not a pill taker and it doesn't make any sense to take a med and try to cover up those side effects/symptoms with the next med and so on. I can't find a good Dr. who will actually listen. I have been on the heart monitor and it found I was having PVC's all the time. I was then referred to a cardiologist - after a one thousand dollar visit with only an EKG he said my heart is fine - go home. I told every Dr. about Yaz - none of them could connect the dots! I thought I connected them....only by chance. I forgot to take my pill for a couple of days in the middle of all of this and stopped when I finally remembered to take one a couple of days later. I thought to myself.....hey - I've felt a little bit better the last couple of days. I was near the end of the pack so I QUIT taking them!! Best decision I ever made! Within 2 weeks my symptoms had pretty much disappeared! I thought I had it solved. I am 43 years old and in really good health. A few days ago my palpitations are back - but they are different this time. Before I had a "normal" heart rate but it felt like my heart was going to thump out of my chest. Now I have that PLUS a racing pulse! Chest pains are a part of daily life. Mornings and nights are the worst but I think it's going on all day - if I'm moving around I just don't notice it as much. These symptoms reappear a few days before I'm supposed to have my first period after quitting Yaz. I'm wondering if it's hormonal or menopause or if this stuff will just stick around for a while. I'm scared! I've read about people dieing and it's traced back to Yaz! I have a 6 year old precious daughter that I kiss good night and pray like heck that I get the next day with her! It's just not fair - I really wish I could find some answers. Anybody out there got any? Thanks.

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!!

Just want to survey everyone and ask for responses for the following 3 questions:

1. how long did you keep your Mirena and if you no longer have it, why did you have it removed?

2. how many of you had your thyroid checked? who's came back abnormal? what were the levels?

(I'm a medical student doing research on this one since I believe the levonorgestrel affects our thyroid hormone. My TSH was elevated to 5.2 which is considered "subclinical HYPOthyroidism". This was mid cycle when my natural progesterone AND synthetic progestin were cumulatively high. When I had it rechecked 6 weeks later (around my period when any natural progesterone level is gone) it was normalized at 1.5. So I think that the P+P screws up our thyroid and can throw us into a high TSH and "hypothyroid state". The opposite effect may be true during menstruation and we can become HYPERthyroid for a few days... hence the really bad anxiety?!)

3. where is everyone from? perhaps we can have support group meetings?

I'm fed up. About 4 years ago I had a complete thyroidectomy and OMG my life has been a mess ever since, Yes, I needed the gland removed (it was a goiter pressing on my air way and esophagus), it needed to come out but OMG what a nightmare. Synthroid is a drug I can't figure out. I am convinced that this has ruined my life. I have developed chronic/non-stop head pain and pressure. My B.P. has gone up and now I'm on B.P. medicine. (still have severe head pain). It just never leaves me. E.R. visits/hospital stays and on and on. They treat me like I'm a complete lunatic because they can't seem to find anything organically wrong with me. Ummm-it hurts(my head). I am starting with a new Doctor who is a D.O. rather than an M.D. and I am praying that he finds what the **** is causing my pain. I feel like crap. The T.S.H. is in normal range but I have learned that the T.S.H. is not everything (even though my thyroid is gone). The isiots for lack od better description, are just too lazy to go the extra minute to find out what is wrong here. I just want to be able to function and this head pain will not let me do that. It is a nightmare and I have nothing but sympathy and empathy for anyone who suffers with pain on a daily basis.

The only constant is the Synthroid. Maybe I can't take this stuff. It has to be that my body just can't tolerate it and need something else or T3 added (I don't know). I just pray that this new doc can figure it out because I feel so helpless with this. My pain is always there squeezing and pressing. It is horrible. Maybe Synthroid is the culprit. Good luck to everyone.

I am 34 years old. Back in 1985 I had most of my thyroid removed, due to a tumor attached to it. Since I was 10 until my late 20s, I was on Synthroid. By age 19 I had 3 knee surgeries to remove arthritis. I have suffered most of my life with joint pains, dry skin, weight that is like a roller coaster, and being tired most of the time. In my 20s I was put on Levoxyl. I has been on Levoxyl for several years now. Since being on Levoxyl I have been fighting anxiety, racing heart, joint pain in fingers and ankles, sudden dizziness to the point where i have to sit or pass-out. I feel like I'm 80 and not 34. After reading this site I am printing all this out and taking it to my doctor. No telling how much damage has been done after all these years.

Has anyone had problems with their eyes on this medication, my have been going blurry and then I get a terrible headache.

weight-gain/ alternatives have been availalable.."Amour-thyroid" about.com any alternative medicine sites! Thy-Aid..etc,Synthroid does nothing for thy,roid issue Everything starts there! Bio-denticals deals w/ harmonal...read and learn..FDA lies! Alternatives have "Cured" ask "Breakthrough" Susann Sommers book w/ doctors! Larry King! Truth re: real cures for thyroid,not HRT's..yet another that has killed and/or close to from...Side-effects..alt's do not have side-effects.soon,if enough people stop being lazy and so afraid to take what will keep them alive and happy only then will ALT'S push the bad FDA approved poisons away! Both MUST be explored,but the FDA make billions w/ doctors who get kick backs from each script they write for the infamous SIN-Throid,made my life a horror..hypothyroid issue does not need syn! There are better natural things! Headaches,never get the right dose! Right thyroid tests? Endocrinologists will use those bio-denticals bec- hormone & Thy go together,for all of the idiots out there who think their doctors are sooo good,slowly they are killing them in many ways!

I thought my fatigue and mild depression symptoms were something separate but after reading these posts, it sounds like they could be linked to taking Synthroid? I've been on it for 2 years now. At first, I felt great. I started feeling tired again & my dr. upped the dosage. I just saw him today & complained of feeling tired, depressed, and getting light-headed and off balance at times. He wrote me a Rx for anti-depressants and changed my blood pressure Rx. I'm thinking about trying a Naturopathic Dr. to see if I can get the results I need without all the side affects. It couldn't hurt to get another opinion.

My symptoms started with aches in my ankles and I thought I should stop wearing heals for a while. But then the tingling pain moved up into my lower legs and then my arms/wrists over a period of a few days. I felt like I was having constant shin-splints. I was heavy joint/muscle pains. Then the back of my head hurt really bad on the left side, just at the top of my neck/bottom of my head, and was also really sore to the touch. Then massive headaches. Probably migraines, although I have never had them before. My MD immediately put me on celebrex, which did nothing. I was eating Advil and Tylenol like candy and couldn’t sleep. So the doc put me on steroids (prednisone). That took the pain away. After a few days, while at work, the vision in my left eye went in and out (perfect vision to completely gone). I have never had any issue with my eyesight before - perfect vision. Then at one point (actually while I was in for my first MRI) my vision never came back. No one thought it was serious enough until I demanded to go to the hospital. I spent three days in the hospital, where they ran tests after tests (including MRI, Lumbar Puncture, blood work, neurological tests, echogardiogram, dobblers, etc). Upon leaving the hospital actually diagnosed me with Optic Neurosis, and gave me a 15% chance of getting MS later in life. We were all relieved it was not MS, like they originally suspected. After going to the Eye Dr, they told me that was not the case. This kind of eye stuff only happens to people in their 80’s! I will never regain my vision. If my diagnosis had been optic neurosis, it would not explain the joint pain. I have seen specialist after specialist over the last two months, and they still have no idea. Every test I have undergone has come back clear and I am perfectly healthy. My doc said we might have to go with the retinal specialists theory - which was a piece of cholesterol that clogged the artery in my eye. I just don’t get why a piece of cholesterol would have caused me so much pain over the rest of my body. After viewing this site and the Mirena pamphlet that I found online they give to the doctors, I really think it was the cause. The packet even notes, if you have symptoms like visual loss and headaches/migraines for the first time, to remove it immediately! I did not get mine removed until a month after my vision loss. Every doc I have seen I have asked if it was Mirena and not one of them thinks that could be the cause. But it is ironic, that when you see someone for the first time, the first question they ask is if you are on birth control or any other medications! I think I need to show them this site, so they can read other women’s symptoms. I did also have all the other symptoms as well - weight gain, irritable, oily skin, cramps, moodiness, vaginal odor, gross discharge, headaches, nausea, low sex drive, hot flashes, anxiety, restlessness at times, fatigue, and the list could really go on and on.

Hello,
I posted earlier and here is an update "POST MIRENA"
It hurt for only about 20 seconds and it was over. EASY You can do it!
I had the mirena put in Oct. 2007 and nursed my daughter for a year until Sept. 2008. Just the last 6 weeks started having these symptoms and went to my MD/Osteopath because when I called my OB-GYN she said it has nothing to do with the mirena and to see my regular MD. He has been fabulous and I have had several tests that I have listed as well as taken the mirena out!
My symptoms:
Lower back pain
tingling in my arms, feet and lips
cramps
low energy
I had my mirena taken out on April 30, 2009 and am just starting to feel better post mirena. I had these tests:
* MRI on back/spine
* MS test(Vision Evoked Potential)
*blood work
*Thyroid (it's been low since Oct. so I'm taking Synthroid)
*Vitamin D
ALL NEGATIVE ...Thankfully!:)
You never know....I just pray I continue to improve and get my life back and feel healthy!:)) From other posts it sounds like it takes a little while. Does this sound familiar? Please respond....