Funny thing symptoms and conditions

60 year old male on zocor for approximately 10 years. taking 80 mg daily.
only recently (within the last 18 months) i noticed some changes going on.
first i had joint pain in my feet, both feet, same areas. the foot pain went away but then the pain traveled up to the back of my legs, behind the knee,
when the muscle or tendons attach. every time i sat for awhile, then got up, the pain was brutal. that lasted about 3 months. later the pain shot up to the joints in my hands. both hands, same place on both hands. when i rotate my thumb or move it, the knuckle area of the thumbs, same place,
hurt bad. i will confront my health care provided at the va on these issues.
she disregarded my previous remarks and said arthritis, hands and feet and perhaps i overextended something at the gym on my behind the knee issue.
i think she is wrong. recently i had a severe cold and did not take the zocor for two days. the thumb pain subsided substantially. i resumed and the pain came back. now it feels as if the pain will travel back down to behind my knees again as i am beginning to feel a pull. any others out there with these issues???

Add me to the list. The funny thing is, I've taken Levaquin 4 or 5 times in the past without noticing any problems, but last week I was put on Biaxin for a sinus infection and had a terrible time with it, so the Dr. changed me to Levaquin, and now after 3 days I'm back in the same boat...heart racing, unable to sleep, elevated blood pressure, nauseous. It feels like my heart is on fire! I'm stopping this one today (only had 2 left.) This is awful, I know I was very sick and had to have some antibiotic, but after these two experiences I think I'd stick with the sinus infection!

I was diagnosed with adult allergic asthma one year ago at 38 years old. I started having problems breathing ONLY AT NIGHT on occasion and palpitations. Had a physical and ekg, totally normal. Went to allergist and they said I have alot of allergies and diagnosed me with the asthma. Funny thing, weeks before I biked 20 miles, hiked 12 miles, canoed 3 miles, played golf in a 3 day span and no problems. Since they told me this and started me on advair 250/50 I haven't been able to jog more than 2 miles or bike more than 8 to 10. Its very strange indeed, I have gotten more paranoid feelings when just get a little out of breath, and sometimes cant keep still in a car or sitting down. I cut back on sugar, sodium and started exercising a little every day, only 15 minutes and felt better. But came down with a cold recently and back to square one. I am trying to take the advair only ONCE a day instead of twice and almost feel withdrawal symptoms like shakiness, paranoia, irritability. I do have higher blood pressure than I should. Does anyone have any idea about this? I am really confused! Thanks... J

I was diagnosed with adult allergic asthma one year ago at 38 years old. I started having problems breathing ONLY AT NIGHT on occasion and palpitations. Had a physical and ekg, totally normal. Went to allergist and they said I have alot of allergies and diagnosed me with the asthma. Funny thing, weeks before I niked 20 miles, hiked 12 miles, canoed 3 miles, played golf in a 3 day span and no problems. Since they told me this and started me on advair I haven't been able to jog more than 2 miles or bike more than 8 to 10.

Its very strange indeed, I have gotten more paranoid feelings when just get a little out of breath, and sometimes cant keep still in a car or sitting down.

I cut back on sugar, sodium and started exercising a little every day, only 15 minutes. But came down with a cold recently and back to square one. I am trying to take the advair only ONCE a day instead of twice and almost feel withdrawal symptoms like shakiness, paranoia, irritability. Does anyone have any idea about this? I am really confused! Thanks... J

I was on SSRI's for a while (lexapro, zoloft) when I finally couldn't take the tiredness, weight consistency, and NO sex drive. So I tried Wellbutrin SR 150 2x a day. Started off at 150 for a few days and felt like I was given a new life! I had never felt so good. Then it was time to increase my does to the 300mg. I started getting headaches, dizziness, my ears are ringing so bad I can't hear very well anymore. So I went back down to 150mg per day. I don't feel as tired, but it's still there. The ringing won't go away and I am still dizzy. The funny thing is, is that I can almost guarantee it's the same time everyday. I get the dizziness and headaches around 3pm, they go away(most of the time I have to lay down) and by about 5pm they're gone, but by about 10pm they're back. And it happens every day like clockwork. I like the way I feel (minus the headaches and dizziness, and ringing) my brain doesn't feel "numb" like I did on the Zoloft or Lexapro, and I have lost a few pounds which doesn't hurt, but I don't think I should feel like this everyday. I want a medication that I can feel good on without headaches and dizziness. And PLEASE no ringing in the ears. It's good to know that other people are experiencing these side effects, I really thought I was the only one.

I have been taking Lamictal since October of 2007. I experienced some of the symptoms (muscle pain in the head and neck) before I started the medication. I have experienced panic attacks since July of 2005. I have had mild heart palpations since I was in my mid 20's (I'm 36 now). I have had what I would consider a below normal energy level since my mid 20's also. Ok so like everyone else I am thinking I'm a hypochondriac! However, I was diagnosed August 28th 2007 with having Lyme’s Disease and also Hyper-Thyroid (same time, same lab-work). Two weeks later I was diagnosed with Bi-Polar Disorder (this is one thing I knew I was battling but didn't know how to handle it). My physiatrist started me on Lamictal and I did the standard ramp up to 200mg. I also was started on a 90 day treatment of Dyoxicycline for the Lyme’s and Methimazole for the Hyper-Thyroid. I was very very weak and was only able to stay awake for short periods of time (4 to 5 hours max). Just an fyi, I am not overweight, lazy or unmotivated. I have the physical appearance of perfect health. This, I think works against me as the Dr's seem to think I'm just whining. Mater of fact; my Primary Care Physician never tested me for Lyme’s. I went to an Urgent Care Center which tested me for Lyme’s disease and I came back positive (they also tested my Thyroid levels and found the problem with my THS levels) I told my Dr the results and he insisted I have same test done again. Guess what, new tests, same results.
My symptoms today are very similar to what I have seen posted many times. Muscle pain (entire body, some areas worse than others), heart arrhythmia, racing heartbeat, intense palpitations, nausea, foggy “un-plugged” mind, fatigue, weak muscles, muscle cramping (especially after repetitive motion, such as strumming a guitar), panic attacks (much more severe) and the latest addition to the group, Insomnia. Muscles pain in my head, fore-head, jaw, temple, neck (front and back), shoulders, is terrible to say the least. The pressure in my fore-head (right under my brow) makes me feel like I need to close my eyes or rest (resting does not relieve anything). The front of my neck is so tight at times it feels like my jaw is being pried down. I could go on and on.
On my quest to find out what else is going on with my body I have had 2 Echocardiogram’s on my heart and abdomen, 2Nuclear Stress Tests, blood work out the wa-zoo, MRI of my brain, 2 CT’s of my Head and Neck, Chest X-rays, Endoscopy, Colonoscopy, and all revealing nothing.
Most doctor’s I have encountered seem to want to treat the symptoms, not the problem/disease. I believe I know why; we (the ones who are there for solutions) tell them what the symptoms are (how we feel). We of course are thinking “this will help with a diagnosis of the problem/disease”, when in fact (I feel); the doctor’s thought process stops there. They don't know what’s wrong with you but they do know what your symptoms are so....bingo, let's treat the symptoms. Don’t misunderstand what I am saying. I’m not saying, “Most doctor’s don’t know what they are doing” or “don’t take your meds”. I am saying you and I are one of the 20 to 30 patients most doctor’s see daily (100+ weekly). They may be caring and good people but they are just as human and fallible as you and I. My advice is this; (and I am taking my own advice) don’t always “pop” into your body what the doctor suggests/prescribes, without doing your own research. Heck most of us won’t buy a car or more importantly, send our kids off to a college with out doing your own research (we just don’t trust those shinny brochures). Your body and your health are worth you doing your own research. Just keep in mind, Pharmaceutical Reps are always at your Dr.’s office (sit in the waiting room for 10 minutes and I’m sure you will see one). Reps are paid to do one thing; encourage (push) the Dr.’s to promote use of the Pharmaceutical Companies drugs.
My wife and I have been doing our own research on Lamictal (after a year of taking this stuff) and the side effects associated with this drug. We have searched through many (many,many) web sites for information and we have talked with pharmacists and Dr’s for opinions. Although I’m am not thoroughly convinced that Lamictal is the cause of all of my symptoms, my wife and I have decided to lower my Lamictal slowly from 200mg to 100mg. I am now taking 150mg daily (three days now) and plan on staying at this level for a total of two weeks before lowering to 100mg. I do fear dropping the dosage to quickly (potential side effects) or lapsing into a mania. To help avoid a manic episode my wife and my immediate family are all “up-to-date” with my course of action. They are on “Red Alert” and have promised to keep a close eye on my behavior patterns and moods. (I don't want to put them through another hyper-mania episode, its much too devastating). I do want so badly to feel healthy and alive again and at this point I am rather frustrated with the Dr.'s ability to help me achieve this goal. Remember it is called “Practicing” Medicine. So now I’m going to practice a little, very carefully and cautiously.
As a foot note; I have recently (past two weeks) been re-tested for Lyme's with a negative response. I am keeping in mind Lyme's test are very inaccurate (still hoping this one is accurate). My thyroid is under control and normal, so.... let's see if dropping below 150mg of Lamictal will eliminate some of these other symptoms. I will keep you posted.
Erik

I had a shot of Kenalog into my knee for a torn meniscus. About 2-3 hours after the shot, I started feeling very jittery and nauseous. Had to have someone drive me home from work. Called the doctor who administered the shot and he said it had nothing to do with the injection. Within 1 hour I barely had any strength to lift my arms. Called my primary doctor and she said to come right over. She said my heart murmur which is usually very soft and can barely be heard, was quite prominent now so she did an ekg, took blood and urine. The next day she called and said my sugar level was high. I had fasting blood tests taken 2 months earlier and never had a problem with my sugar level. Four days after the injection, I got my period so heavy (I'm 53 years old and before the injection my period was almost stopping). I have never in my life had a period this heavy. Neither doctor will admit that it had anything to do with Kenalog, but I'm certain it did. If this shot gave me diabetes, I will never forgive myself for getting it done... But, funny thing, the shot actually helped my knee and I can walk without pain. I'd rather have pain in my knee than diabetes and heavy periods.

Wow I'm glad I stumbled across this page.
I only started taking Yasmin 1 month ago after switching from LevlenEd which I was on for 4 months.On LevlenEd I found I was developing a redness in the face (not acne but almost like rosacea) which is something very uncommon for me as I have always had very clear and even toned skin. After visiting the doctor he switched me to Yasmin - something about the different combination of hormones in the tablet and that this should clear things up. Well it hasn't. In fact I've experienced so many horrible side effects of the pill that I decided tonight that I'm just going to stop taking it all together. Side effects include:
Extreme emotions
Massive increase in appetite resulting in excessive weight gain
Lack of motivation
Tiredness
Skin redness and swelling of the pores
Hot flushes at night resulting in sweat break outs (usually I'm actually cold at night and never sweat)
Decrease in libido and dryness during sex
Puffiness in the skin and a hot feeling
Sensitive muscles all over - around the ribs, tummy, arms - just touching and they feel lightly bruised
I'm usually a very active and fit person but have just felt so lethargic on the pill. Combine this with an increase in appetite and I now have a task ahead of my to loose this excess weight that I have put back on after working it off for so many years.
Before taking the pill I generally did not take any medications at all.
I am particularly interested to hear from anyone who may have experienced the same skin conditions that I found when on the pill.
The funny thing is that my sister is on Yasmin and has had no problems at all.
The only plus was that my breasts went up a whole size! A great thing for me!!
My boyfriend is just going to have to deal with the change in how we manage birth control because the side effects I've experienced over the last 5 months are just ridiculous!

Glad I took the time to read the noncommercial posts! During my thyroid check last year bloodwork showed high cholesterol. I was put on Crestor in addition to having my Synthroid dose adjusted. A few weeks later I was absolutely miserable. Couldn't get out of bed. Everything hurt. My doctor thought I was "depressed" and asked if I wanted anti-depressants. Not needing to add another pill to my daily repertoire - I declined. Six weeks later I am feeling worse and just want to lay down and cry. The doctor had no idea why I would be feeling that way and was convinced it was either depression or thyroid issue. I was getting ready to leave for a trip to Mexico that had been planned a year in advance and was non-refundable - and I didn't have the strength to even pack the stupid suitcase. The trip was a bust - I laid in a pool chair just feeling crappy. What a waste!

Funny thing - nobody stopped to consider I've had a thyroid problem for 20 years and this horrid nightmare just started after I started taking Crestor! A few weeks later I stopped the Crestor entirely and after a couple of months I felt back to normal. Now, three years later - I've been talked into taking Lipitor. In my naivety (because I explained to the doctor that Crestor made me ill) I trusted that it would be different. It's taken three weeks for me to put two and two together - but here I am again - muscle aches - can't get out of bed. Everything just hurts. My knees, arms, mostly shoulders and in between. With all that is an overall lethargic feeling. Lipitor stops today -and if the pattern continues and I feel better in a few weeks - it's no statins for me ever again. I'll just have to eat like I'm supposed to and hope for the best!

I have been trying to self diagnose myself for months now and Mirena was the last think I thought of!! I can't believe how bad my life has gotten since I had Mirena inserted 10/07.

I had surgery 08/07 relating to thyroid cancer and thought that my side effects were a result of the surgery, but I have not improved and it's been 10 months. I had my thyroid medicine increased and no improvement in my fatigue. I was evaluated for sleep apnea and got a CPAP machine and no improvement in my energy level. I've gained about 30 pounds and haven't had my period since the Mirena was put in. My depression is getting progressively worse. I've been feeling like I'm at the end of my rope and I FINALLY googled Mirena and found this website. I pray to God that this is the answer to my prayers!

I spoke with my boss today and asked her for her opinion if she could remember how I was before the Mirena and now. She said that she had noticed a considerable difference in my sales, attitude and attention to detail. I can't tell you how many times I've been late for work because I couldn't get out of bed in the morning. She said that I come in with a glazed look on my face every day and she can tell that my fatigue is getting worse. (I dozed off last week during a teleconference and she was NOT happy with me.)

The funny thing is that when I called my gyno's office today and asked to make an appointment to have my IUD removed and that I thought I was having problems with it, the receptionist immediately asked if it was the Mirena. I tried to ask her if I was the only calling with problems and felt like she was dancing around the subject when I kept questioning her and then she referred me to a nurse. The nurse didn't want to make the appointment, but for once I was persistent and told her I wanted it out or else!

I had a copper IUD for 6 years and don't remember ever having any of these issues. I'm switching back to that!

I hope that my life gets back to normal! My appointment isn't until 7/9/08 so I'm kind of excited (wish I had the energy to be more excited) to see if this is the answer to my problems.

I have been taking Doxy since 5/22/08 for mild acne had a couple spots on my shoulders and being the summer season just wanted my clear skin back , just yesterday I've notice my lips very dry and swollen but more so today than before, my hands tingle from lotions or just water kind of like when your foot falls asleep. it's weird, but my skin feels very dry and tight all over not very comfortable I don't think I will continue with the medication I mean I only had a couple bumps now I've got a all kinds of things going on but as I read below I'm not alone. funny thing is the shoulder bumps went away fast but a couple new ones popped up elsewhere go figure right? oh well nothings perfect I guess. I wonder how long before my lips go back to normal.

I started taking Yaz 3 weeks ago and I am feeling very sick, this headache wont go away ,stomach pain that's constant and dizziness and diarrhea I did not have this pain before, it just started when I started taking Yaz I should have research this Birth Control before I started taking it .Does anyone know how long it takes for this Birth control to be out of your system.

My son is off singulair for two weeks now and is showing improvements. He was on it for 7 years and at the beginning we blamed it on steriods, even though his dose was low. When he went off the steroids, the behavior didn't stop. I questioned the allerist if the singulair could be doing it, but was told no, it doesn't have those side effects. I don't blame the doctors because they weren't given the info. He was extremely emotional, cried for no reason, had no confidence, didn't like himself. We on more than one occasion have told his older sister that when he hits his teenage years we would have to watch him for suicide, as his reaction to problems was sooo out of whack! He was on motrin for headaches 4-5 days a week(blamed it on sinusses). Unexplained stomachaches. These symptoms came on over years, not right away. I have always thought that the steroids had done damage because he took them when he was so young. Until the news reports hit, and I started reading other people's stories and doing the "OMG, that's my kid!", I never put the problems on singulair. I was still skeptical, but took him off. His symptoms immediately got 100x's worse for a week. But funny thing is, his headaches are gone, his stomachaches are gone and he seems much less emotional. The strangest thing is, EVERY night, he comes in to kiss us good night 7 or 8 times, and sometimes by the 7th time he is crying and can't explain why. This has been going on for YEARS, EVERYNIGHT, never a break. It stopped! Just stopped cold 7 days ago. Comes in once, says goodnight, leaves and falls asleep. I know this isn't a coincidence. After years of wondering what's wrong with my kid, now I feel like I've been poisoning my him for 7 years. I'm not skeptical anymore.

I have been on Synthroid since about 1995. I had a thyroidectomy and do not have a thyroid anymore. I have been on 0.175 mcg for about 10 years and did not have any side effects except for fatigue and a little depression.Everything else was pretty good. My TSH is registering low so my doctor moved me to 0.1 mcg of Synthroid and 5 micrograms of Cytomel. I took this for about three weeks and for the last 1.5 weeks have had awful headaches and the dryest eyes ever. Something, I have not experienced before. My doctor keeps saying he wants to help me but does not listen to
any of my symptoms. I actually pulled off the symptoms from the list online of hypothyroidism and have 15 out of about 20. I am wondering why I felt so much better on the higher dose than this low dose. Can anyone releate. I am starting to think maybe my body is not processing this right. The funny thing is is that my lab work came back with normal results today, which means my doc is probably going to keep me where I am and I feel the worst I have felt in ten years.

It would have been about 4 years ago My Doctor prescribed Singulair for my 16 year old son. He became very hateful and always in a bad mood and at times major fits of anger. At one point he got so angry ridding in the car together that I pulled over and made him get out and walk home in the rain because he was punching the interior of the car windows, and I was worried he would break them and hurt himself and others. He ran away from home....and so on...you get the drift. He quit the Singulair and is scared to take anything new now. He says he take Benadryl and uses Albuterol but won't take anything else. Now I started taking Singualar a year ago and I have done okay on it however I know that sometimes I snap at things that in the past I didn't. The funny thing is when the doctor gave it to me I mentioned to him the effects it had on my son and he looked at me like I was crazy!

WOW! I cant believe this, I happened to see the news this morning about the correlation between Singulair and suicide. After reading all the posts, I am amazed, how many stories describe my 13 year old son. He has been on Singulair since he was 5! We have gone thought he ADHD, BI Polar diagnoses, taking medications and therapy. Funny thing, once we stopped the meds for ADHD and Bi Polar, we did not see a difference in his behavior. We have just chalked it up to an emotional child. He has said since he was 5 that he wished he would die (hence starting therapy for depression) quick temper, loss of attention in school, leg pains (growing pains as I was told by the doctor) and the list goes on..... We just this week stopped the Singulair, hoping he has outgrown his childhood asthma and also due to loss of insurance, we could not afford it, and then this morning I see the news! It pains me that all these years I have spent trying to help my child with his emotional issues and it may be linked to a medication that helped him breathe. It is nice to know that so many others have the same problems and he is not the only one. I hope also that the effects are not permanent and the meds come out of his system quickly!

I am just one more: moody, ansy, and of course weight gain. My OB told me that the wight gain was because it makes me hungrier and to watch what I eat. BS. I don't like fast food, I don't eat after 6 PM, I don't snack between meals. I am calling him tomorrow. Mirena is coming out.
The funny thing is I am having all this simtoms and never thought of been coming from my IUD. I have to say I have it for almost 3 years and only had two periods, I love that. But its no worthy, my hubby is happier than me that I came to my senses.
I really appreciate all you ladies and husbands comments. Thank you God for putting me in this site.

I'm 17 years old.
I started taking birth control to help lighten my periods and reduce cramps. I also thought it would be nice to know exactly when they were coming.

Back in November (07), I started taking Yaz. I bled through the whole first pack. I bled halfway through the second pack until the end. I bled halfway through the third pack until the end. By the end of the third pack i already had a new prescription lined up for ALESSE.

I started taking Aviane, which is the generic version of Alesse. I started bleeding on the 13th day of my first pack until the end. I'm on my second pack and started bleeding on the 10th day.

I called my doctor and she said I needed more proestregin. So, she prescribed Loestrin. However, what she prescribed me is the the 21 pills with the 7 day period.. But I have free samples of Loestin with 24 pills and a four day period. My question is, does it matter which one, like, will the length affect anything?

After reading some of these posts it freaked me out, but everyone responds differently. I'm going to give it a shot when this Aviane runs out. Just thought I'd share my experience with other pills. Funny thing is, I have two friends who take Yaz with NO problems, and two friends who take Aviane with NO problems. All these girls are different sizes, weights, taking it for different reasons.. so once again, it affects everyone differently. Good luck, ladies.

I had the MIRENA IUD inserted on January 11th, 2008. 10 weeks after my sons’ birth. It is now February 18th I have went over a full month of consistent bleeding. After 13 days of non-stop bleeding, no breaks in between, called the doctor just to get advised to take ibuprofen for menstrual cramps. That was not of my concern, how long was I to be bleeding for, however was. Never got an answer, and now the cramping too are of big concern. Just yesterday, while I was at Wal-Mart, I had cramps so bad they stopped me dead in my tracks. I have never, never ever had a menstrual cycle longer than 3 days and cramps so bad I couldn't go to work. Just over these past two weeks my skin has become so horrible, I do not get acne ladies, and I now have acne all over my back, chest, arms and patches on my face. Also, in odd places, who gets acne behind their neck and ears? I don't know, do you? I had breast tenderness for about 1 to 2 weeks; still have dizziness every other day. I have 2 kids, had an epidural with both and had no issues with lower back pain. Think I do now? Well, of course I do! Funny thing too, I didn't know that mood swings were a side effect, and my boyfriend says to me the other day, "you have been real mean for like the past month!" The only thing I can say that has not been a problem is my sex drive. Even though I have been bleeding for over a month I have had some very, very light days. This IUD has not interfered with my interest in sex. I actually want it more now than ever... but that’s probably because I am so in love with the man that gave me the two loves of my life!!!! And not the MIRENA IUD... lol!!!

I have been on Topamax since October of 2007. I currently take 150 mg (split in AM and PM) for migraines. The drug is working wonderfully for the migraines but I am finding that I cannot do my job anymore due to the side effects and am not considering filing for disability. I am so fatigued all the time I literally cannot keep up with my work load. I have the tingling in my feet and hands, the funny taste of soda, the forgetfulness, and the "cannot find the word" thing. But the biggest problem is just that I cannot get everything done that I used to be able to get done due to plain old fatigue. I am so tired all the time. I find myself crying all the time due to constant stress of not being able to do what I used to. It took me a while to admit to myself that I couldn't to it anymore ( that nasty ego was in the way) but I finally had to admit that I couldn't keep up like I did before I was on the Topamax. I don't want to give up the Topamax and go back to the daily migraines and if I find a different job I lose all my retirement. I'm a teacher so I don't get any social security so my only alternative is to go for disability due to my having to take Topamax. I may have to hire an attorney to help me but after fighting migraines and trying to work my entire life, I surrender.

Dr. put me on Loestrin 24 on Dec 9, 2007. Immediately my period stopped (after a non-stop episode for 14 days) but then I started gaining weight (15 lbs), rapid heart rate after climbing 5 steps, extreme irritability to almost psycho stage and the kicker, my blood pressure kept shooting up. Today, it was at 154/99.

At the time I saw my OB/GYN a week ago, my BP was at 150/99 and she said she wasn't concerned. She doesn't feel that the pills have anything to do with my BP, weight gain or increased irritability. All my life, I've never had high BP until I got on these pills. I know my body.

Funny thing, my general practitioner was very concerned about my BP and told me to bring it down in 2 weeks or he's putting me on pills.

I've spotted for 5 days and am now on full-blown period (day 3) and it's heavy and my cramps are very painful. I have decided I will not to take the Loestrin starting tomorrow even though I risk the chance of having on-going periods.

I don't feel comfortable putting my heart at risk because of some pill supposedly regulating my period. Doesn't seem regulated with 5 days of minor spotting/clotting then full-on period. I have no clue how long it will last but at my age (45) guess that's just part of the cycle of being a woman.

I have been taking Levoxyl for 1 1/2 yrs, I had my thyroid removed due to severe hyperthyroid. In the past year, I have been getting pains and weakness in my hands. It is so bad now, I can't open a jar or lift a frying pan. It hurts sooo bad. My legs hurt and my knees have real bad joint pain.
The funny thing is, it's not every day and not always both knees. It is however all the time in my hands. Last week I went to an Arthritis specialist in San Antonio. He ran every blood test avail. Tested for Rhum. arthritis, Lyme disease, AA, and all kinds of stuff. He x-rayed my knees and injected cortisone in my knees and hands. - that hurt -
He found nothing wrong!
I searched on line tonight for "Levoxyl and joint pain" and this site came up. Boy am I glad I am not the only one who is questioning this horribly possible side effect. Oh, I also have memory loss. I feel like I am 80 yrs old. Just to make sure you know what type of person I am, here goes: I am fit, active, 37 yrs old and 115 lbs, I eat well and take vitamins, non smoker, non drinker.
On Monday, I am calling my doctor. I am printing this web site and all of the postings like mine. There must be something I can be put on that will fix this. Can anyone tell me if they have no Thyroid and have gotten off this stuff; does the hand pain stop? Does it get better or is this permanent damage?

Kerrville TX

IA huge thanks to you guys for putting this info out there, because I'm sure the Singulair website wouldn't go into detail about this, and tell about side effects it has: FYI -->

This was what I found on the Singulair website, no more, no less (see post below this one please)

'm really sad to hear that these things happened to you guys and your children.

My 8yr old (55 lbs) son got a cough that ended up lasting about 4 weeks, so i finally took him to his pediatrician. He gave him a breathing treatment and hinted at him having asthma- but he wasn't sure. We have no family history of asthma and in my mind i thought it was pretty far fetched, but we continued the breathing treatment for about 2 weeks and my son cleared right up.

We came back in the Friday after Thanksgiving for a check up and his doctor said that my son sounded much better. The doctor said that looking over my son's medical history (not much of anything) he said he could have asthma-but he wanted to put him on Singulair for the next 3 months until the winter is over.

He said it would be a preventative measure to keep my son's symptoms from "flaring" up. The doctors said " This is not a steroid, and there are NO side effects. Its a once daily chew able for children." I thought-hmmm that's a first, a drug with no side effects. Then I was thinking" "What symptoms was the doctor referring to?" He had a really bad cough he got while visiting his dad's family (bug going around). But I held my tongue and just nodded. He wrote out the prescription, and I left. I heisted as I pulled out in front of the pharmacy and then kept driving.

I felt uneasy about the whole thing. Giving him a daily medication for a condition (asthma) I doubted my son had. Glad I did my homework, I decided to not fill the prescription. I don't feel the least bit guilty for not giving him the meds.

I took Yaz for 7 days. In that amount of time, I began experience the most horrific symptoms I have experienced in my life. They included: chest pains, nausea, vomiting, arm pain, and the feeling of imminent death (these caused me to go to the emergency room since they are classic heart attack symptoms for a woman); leg and arm weakness; lethargy; migrane; panic attacks; severe insomnia, diarrhea, and vision problems that caused my contact lens perscription to change and night time vision had profound halos when driving, etc. I was literally unable to stomach any normal food portions I was so nauseous. I normally run 3 miles and could not even make it to the gym for weeks. I was afraid to stay home alone with my 4 year-old and 17 month-old for fear something would happen to me while they were in my care. At the ER they found low potassium levels (which makes no sense given Yaz has a potassium sparring diuretic component). In another blood test, I had elevated iron, which I have never had previously.

I am 35 and have been on bcp's periodically for 12-15 years. I have never had any of these symptoms prior to this experience. I have never had anxiety, depression, or any other underlying health condition. I immediately stopped taking the pills once I made the connection. So far, my recovery has been slow, but at least it is improving. I resent that my ob/gyn and internist both said that the pill would be out of my system in 24 hours. The effects are clearly long lasting (I am approximately 7 weeks off of Yaz).

Finally, my eye doctor, of all people, said that he has seen and heard of people having problems similar to mine and that it was understandable that I would have anxiety when I felt like I was dying from a heart attack. No one perscribing this medication bothered to tell me of the diuretic component or any component that was going to affect depression. I am attorney and have always thrived under pressure, not turned into a panic attack ridden mess like this medication caused.

As for the previous post who stated these are common symptoms described by women, at 35, I know the difference between my normal body function and the hell that began when I started taking Yaz. Unless you have experienced this, then you clearly would not understand. I appreciate that Yaz and Yasmin have worked well for some, but that clearly has not been my personal experience. So, I write this not to discourage someone who has had a positive experience, but to provide support for anyone else who has suffered like I have.

i had to take Deoxycycline 100mg once a day for a month to treat a skin infection which improved but OMG for the first time in my life I started to feel really WORTHLESS and DEPRESSED I was SAD most of the time and i lost my intrest in the things that i ENJOYED the most , I couldn't concentrate or study and the funny thing is that i did not SUSPECT the medication at all I thouught it was just me you know but when i read what happned to you guys i knew that there must be something because Depression was not listed on Deoxycycline side effects on the FDA site