Sedative symptoms and conditions

Am I the only one this happened to??

I was taking Quasense back in 2007, I had only gone through one pack of it and in March of '07 I was having minor chest pain and getting slightly short of breath from simply walking up a flight of steps. The thing that pushed me to go to an immediate care was the fact that I jogged about 10 ft and got dizzy and short of breath. At the immediate care the doctor said I should go to the emergency room to take a test to check for blood clots. I wound up stuck in the intensive care unit for 5-6 days because I had blood clots in BOTH of my lungs that covered almost my entire lungs... I could have died if I didn't go into the ER when I did, a day or two later and I may not have made it. This is INSANE to me... they basically told me that if I wasn't so young (23 at the time) and healthy (I ran track for college) that I wouldn't have made it. I don't even smoke!

anyone have extreme fatigue w/ the wellbutrin, i mean like you have taken a sedative tired all day long no matter how much you sleep. If so do you know why this happens?? Please contact me anytime!!! I also have the dry itchy skin w/bumps and hair loss.

Hi!
I add Mirena inserted in arch. I had mine inserted, no for birth control, but to give me lighter periods. When I asked my doctor, they told me there were no side effects. I was fine for the first few months. I had a lot of spotting, but no more heavy periods. But I was getting headaches every day, lower back pain, and I was always tired. The realized something was wrong when I weighed myself and gained 7 pounds in two months. I am a very healthy eater with two small kids, I have no time to sit down, so I don't know how I could have gained the weight. I went to my regular md and got a complete physical. I went back two weeks later for the results and she told me all of my tests and the numbers were perfect. She sad I was in perfect health. She wanted to treat me for depression and give me a sedative to relax me. I told her I wasn't depressed and not going to take the meds. I forgot to mention to her about the mirena. When I got home I remembered that has been the only change in my life. I did the research, and so many of you had the same problems as me. Well I called my ob, and of course they said they never heard of such side effects, but I demanded it be taken out. I had it removed on Tuesday July 7th and I still have a lot of heavy bleeding, but at least I am feeling better. Good luck to you all.

I had the Mirena put in in March of last year. About a month ago I went to get it removed and they could not find the strings and had to refer me to a different doctor. I went to my referral appointment today and when trying to remove it with A LOT OF VERY PAINFUL EQUIPMENT the doctor told me the IUD may be misplaced in my urine wall. He then continued to tell me that I will have to get a sonogram and go to an out patient clinic, get a sedative and use scopes and cameras to remove it. I am very nervous. I have noticed weight gain and a lowered sex drive but besides that I have not had any problems. I have actually loved not having a period for the duration of it being in. But now that my husband want to have a child we can not remove it. The doctor also told me that I may have problems after I get it removed. As much as I have liked having the IUD I do not think it is worth the problems I am now facing

Have been on Welchol for IBS for many years. It stopped my IBS symptoms but does cause constipation. I try to eat healthier in order to help with that. About 3 months ago, I began having pain in my fingers. I thought it was probably due to carpal tunnel syndrome. In the last two weeks, the pain intensified and spread to all the knuckles on my hand; I also had swelling and redness. The pain then spread to my toes, the rest of the bones in my feet, wrists, elbows, shoulders, knees, and ankles. Next came stinging and burning and then sporadic numbness. By late afternoon, the fatigue was incredible, and I would become dizzy. I went to the doctor, and he ran every blood test available. Everything came back normal, which was great, but my doctor couldn't pinpoint what was causing my problems. He said none of my medicines would cause such symptoms.

My boss asked me if I was taking any cholesterol medication, and I told her I took Welchol for IBS. She said she had read article upon article connecting cholesterol medication to joint paint and encouraged me to check online to see if I could find any answers. This site was one of the many I found where other people mentioned symptoms very similar to my own. My boss suggested I mention this to my doctor. I was thrilled at the prospect of finding such an "easy" solution since my other medications are not easily replaced.

My doctor instantly said that there was "no way" that Welchol could cause these symptoms since -- as so many of your doctors have told you -- that it is not absorbed into the bloodstream. However, he approved my stopping Welchol as an "experiment". I noticed that many of you mentioned it took a few weeks or more for the symptoms to reduce. My doctor warned me again that this was not the solution and that in a couple days, he wants me to consider taking Neurontin or going on a sedative for stress. He thinks, since all the tests have come back negative, that stress is the real culprit.

I know that stress can cause many health problems, but it just seems too coincidental that so many of you have experienced the same symptoms I'm facing. Do you think I'm making the right decision? My symptoms are difficult to cope with at times, but they are not incapacitating. I would really like to try staying off of Welchol and see if it helps in the weeks to come instead of adding yet another medication to my list.

I would appreciate your advice and thoughts. Thank you for your posts -- they have given me real hope for a solution.

I just started Toprol XL on Friday (four full days ago). I was put on it to decrease heart rate and palps, I have Inappropriate Sinus Tachycardia. I am 35 years old. I was prescribed to take 50mg twice a day, and I am on the generic. Almost immediately, stomach upset started with diarrhea. I still had some palps at 25 mg. twice a day, which the MD told me to start with for about two days. So, after doing the 25mg for two days twice daily, I went on to the 50mg twice daily. Last night I slept for twelve hours straight, and then felt like I had a sedative after I got up. After taking my next 50mg dose this morning, I got so sleepy again, and felt like sleeping and was in a fog after the twelve hours of sleep last night! I can't imagine mixing anything else with it that causes drowsiness, you would pass out. I feel like I can't think clearly,and feel more crabby and irritable. I called the MD this am. and was told to go back to 25mg twice a day, and that side effects would lessen over time. I have had this sinus tachycardia problem for years, and got diagnosed with it officially in 04. It is very annoying, with shortness of breath, pounding heart,and feeling like you are running a race which sitting still. I have also had an increase in feeling like it skips a beat. All this prompted the Toprol usage. It does help the heart rate and palps, but now I feel so tired I can hardly put one foot in front of the other. I try to walk for thirty min. at least five days a week, and today it was all I could do to make it. I have to watch my twenty month old daily, and I can't keep up with his energy now for sure. I plant to go back to the 25mg twice a day starting tomorrow, and maybe eventually get to the 25mg once daily. I never would recommend anyone stopped something like this cold turkey, you could find yourself in the ER, never play with any heart meds!! I pray that a slow decrease will be the answer to finding some symptom relief of my condition, yet still being able to function daily. Thank God also I am a stay at home mom for now, starting this and trying to work, I would be sleeping on the job!

Back in July I was experiencing rapid heart beats and shortness of breath. I'm a 43 white female with a high stress job. I went to the doctor expecting him to prescribe a sedative. He hooked me up to an EKG which showed I had a left bundle branch block. He then ordered blood work, chest x-rays, an ultra sound, and a nuclear stress test. All test came back fine, but my stress test showed a heart attack, which apparently is common with the left bundle block. I then wore a 24 hour Holter moniter which indicated tachycardia. That's when the doctor prescribed 50 mg Metoprolol. My BP and heart rate are now almost normal and the shortness of breath has gone away. I still experience a mild heaviness in my chest, but that is only when I allow my self to be stressed. I have gained over 5 pounds in less than 2 months and my dreams are more vivid than usual. One side effect that was listed on my drug info sheet that I haven't read about on this site described a cough, which I have had for over a month. I mentioned the cough to my doctor and he said it was prob post nasal drip so he prescribed 180 mg Fexofenadine and told me to cut the Metoprolol in half so I would be taking 25 mg. The Fexofenadine has helped with sneezing that I have always experienced, but the cough is still there. The cough is not always severe, but it has interrupted my sleep twice and my job once. The last bad coughing episode lasted 90 mins during the night. Has anyone else experienced the coughing side effect of Metoprolol?

I'm a 30 yr old healthy male. I went to the ER, and then the Dr., about 4 weeks ago after waking up with intense pain in the veins of my right arm and having pounding palps. I had just been told some extremely stressful news the night before, so I was pretty sure this was blood pressure & stress related. ... EKG showed Wolf-Parkinson-White syndrome, so that's what the Dr's assumed was the problem. I never knew what it was called, but I've had my heart race due to WPW many times since I was a young child .. this did not seem to be related. This was just pounding.

The cardiologist put me on 50mg of Toprol XL daily to control the WPW - even though that wasn't acting up. I left confused. Pharmacy issued generic Metoprolol Succinate mfg. by Sandoz.

I didn't want to be on meds, so I didn't take it for the first few days, hoping that I would return to normal. After all, I just woke up with this all of the sudden.. I had been fine the day before. Palps continued, though, so eventually I relented and started taking the meds.

The first two or three weeks were filled with ups and downs. Exhaustion, palpitations and anxiety would come and go.

This past weekend things got really bad. I began having anxiety attacks -- I think that's what it was, I'd never had one before -- and my vision was totally screwed up. I couldn't focus on anything and was sensitive to some lighting. Black text on a bright white screen (lcd monitor) was especially hard to read. I was completely in a dazed & confused state. Loud noises and crowds were bothering me... which was awful, considering it was my best friend's wedding. Also had headaches, lightheadedness & loss of appetite. These side effects came and went on Friday & Saturday and were pretty constant on Sunday & Monday.

I decided to quit Toprol cold-turkey on Sunday. I have been 2 days without. I have used L-Theamine to reduce stress and keep my blood pressure steady. It seems to be working. I also began taking CoQ10 today after reading some good things about it here.

My vision & mental focus is beginning to improve after 3 days of disabilitating problems. Anxiety has also improved. I even attempted to "get back to normal" at work today, but had to leave after only an hour of strenuous exercise in the heat. Vision problems returned, anxiety set in. It's like riding a really freaking scary roller coaster, except with a legitimate fear that this thing might kill you.

I will update this as time goes by, to let you all know how things worked out for me. I'm really hoping to be mostly back to normal in another day or two, since I haven't been on for very long. Hopefully this will be of help to someone in the future. Damn, I Wish I had never gotten on this stuff.

Hello! I've been taking Lamictal for about 6 years now. I'm diagnosed as BP II and have the most difficulty with depression. I currently take 500 mg-- 400 mg at night and 100 mg in the morning. I have to say that Lamictal has been very good to me for the most part. As long as I don't put myself into extremely stressful positions-- such as my last job-- I do quite well. I also take a combination of supplements with Lamictal which seem to give the extra push that I needed to completely get out of my last depression. I take 1000 mg EPA (fish oil), B-100 Complex, Folic Acid, Cal-Mag, multivitamin (high quality, organic), Vitamin D (at least 1000 mg) and a few others.

I notice that when I take it at night if I don't go to sleep right away, my mouth and tongue will tingle. Sometimes when I take it in the morning, I feel foggy and dizzy and sometimes get vertigo. Every now and then the side effects seem to get worse, which I am not sure about. I started searching on the internet because I've been noticing that the "tip of the tongue" problem has been occurring more and more often. I often cannot think of the word I want, simple things even. As others have mentioned, I also have difficulty with memory. I am still very successful, currently pursuing a 2nd Master's Degree, but have noticed that achieving the same level of quality of work takes a lot more effort than during my previous degrees.

I do have some periods of anger/irritability and have recently been sleeping a lot, though it probably has a lot more to do with the time of year-- winter with less light-- than anything else.

I am particularly worried about my memory loss and inability to sound "well-spoken" in a setting which demands that of me. It is frustrating! I don't want to do any lasting harm on my brain. After increasing to 500 mg from 400 mg, I have noticed more of these brain issues, but I'm also doing so much better mood wise!

I just began taking taking 25 mg of Topamax 3 times a day for about 1 week. I have the general side effects: loss of taste, tingling in feet and hands etc... however, my doctor insisted I would be much calmer (I am fairly hyper) and would be able to sleep better. I feel as though I am much more irritable with my young children ( less patience) and I am not sleeping all that great. Has anyone else had these side effects? As far as the headaches, at first, I actually was getting MORE migraines, butthey and the daily headaches seem to have subsided. However, I have not yet experienced the typical menstrual headache/migraines which are the worst for me.

My husband's side effect is an inability to sleep well and feeling very restless, having to get up out of bed and keep moving his body, legs and arms, in order to try to get relief from the restlessness. Must take sedative to sleep.

I have recently (one and half weeks ago now) had an epidural spinal injection to help alleviate severe lower disc and leg pain. I was not told what steroid was used but have recently learnt that it was probably Kenalog.

The pain has almost totally alleviated which is great and long may it continue but I have had some very strange side effects. I seem to have a permanently salty taste in my mouth and I cannot easily tolerate caffeine or alcohol in any small quantity (one glass of wine). I have also been feeling very tired due a constantly heavy menstrual period that has now lasted eleven days which is very unusual for me as I am pre-menopausal and they usually last around 3 to five days max. I have also had a couple of dizzy spells and feel quite nauseous sometimes during the day. I have not been able to sleep very well at night (insommnia) - my sleep patterns seem to be all out. I get tired during the day and am wide awake until four or five a.m. in the morning. I also had several hot flushes just after the injection (far more than usual and of longer duration) but these do seem to have alleviated now. I have lost some weight and have little appetite although I do try and eat as I am not overweight at all and need to keep to a normal weight.

All in all, even though the pain has gone, I seem to have acquired different problems which I was unprepared for and not informed about from my consultant or hospital staff. They just said I would feel tired from the sedative for a few days I had at the time when the injection was administered.

Does anyone have any idea how long the menstrual problom will last???

increased heart rate -from 83 to 91 beats per minute. My heart pounds so hard & fast that I can feel it in my chest & feel a throb in my neck and ears. This causes great difficulty sleeping -wake up over and over! Have to take a sedative & even this, which used to do the trick, now only partially works.