Inability symptoms and conditions

I started taking Toprol XL seven years ago to control palpitations. Side effects I have experienced include loss of hair, coldness in my hands and feet, probably due to the lower blood pressure, and, believe it or not, palpitations. I am somewhat, but not entirely, certain that the palpitations that I originally suffered from were from poor exercise, stress and a bad diet. The new palpitations I get are from squatting, reclining in certain positions, raising my legs up in a certain way which I attribute to side effects from this drug. I am trying to cut down on this drug, but it is hard. My heart has grown accustomed to it and it acts up whenever the dosage is reduced, no matter how slowly I do it. I want to get it down to 12.5 mg. I take about 18-19 mg now (I cut the 25mg in half and take one of the halves and cut it in half again). Some things about this drug: take it consistently, e.g., same time with same amount of food. It will give you some harmless, but scary, palps if you do not keep a regular pattern. Indeed, I can usually tell when a palp is Toprol-induced. Another thing is to be wary of doctors who have you double or quadruple a dosage at one time. Years ago my doctor told me to go from 12.5 to 50 mg after I complained of some palps that I now know were Toprol related. I thought he was nuts because my pulse was already way down due to this drug. I envisioned myself fainting. being a bad patient, I upped it to 25 instead. Later, after looking at a Holter monitor readout, the doctor calls me and says lower my dose to 25 because my overnight pulse was getting to a point that if I took anymore Toprol the pulse would be dangerously low. I never told him I did not listen to him. But I have to say I have not suffered all of the side effects listed on this site such as depression. The drug was and has been effective in controlling the palps that were driving me crazy. My palps were very bothersome and this drug gave me peace of mind. But, looking back, I think I could have brought about the same results with a healthier lifestyle. I am very cautious about taking myself completely off of it entirely and will do that with the guidance of a doctor, not the one mentioned above of course. But they are hard to find. Most of them will tell you beta blockers are the greatest and if you take dosages as low as mine there are no problems whatsoever.

I was on Topamax for 10 months at 100 mg twice a day. At first I experienced severe dizziness and actually passed out twice, so my doctor decreased the dose and had me increase it slowly, every two weeks instead of every week. The entire time I was taking Topamax, I was dizzy when standing, no matter how slowly I stood up, although I stopped passing out. I also experienced cognitive side effects such as memory loss, inability to 'find the right word' (I know everyone experiences this sometimes, but I was constantly having trouble speaking). I was in my first year of graduate school and had switched to Topamax, because I had been taking Depakote for over a year with little improvement in my migraines, and when I started my doctoral work I started having migraines daily. The Topamax did wonders for my migraines, reducing them to twice a month, but I had a severe decline in my academic performance due to its side effects. I had excellent grades as an undergraduate, but I had to take a leave of absence from grad school and switch to another medication and am now hoping that when I return to school I will be able to succeed. I actually considered changing my career choice and staying on the Topamax because it worked so well for my migraines, so if you aren't in school I would recommend you try it if nothing else has worked for you.

I began 15mg of Remeron per day about 1 month ago. At first, it was wonderful. I slept better than I had in years and my depression was reduced greatly. I felt hope for the first time in ages. However, about a week into it, I started to become aggitated VERY easily. I would get angry at anything. This has not subsided at all...in fact, it's worse. Now I wake in the middle of the night with my mind racing and either in a rage or STARVING. I eat a lot. It's nice to have my appetite back, but I crave sweets too much. I can accept that symptom if it wasn't for the rage and inability to stop my mind from switching between utter numbness to anger. I'm going to give it longer, in the hopes that it brings me back to where I was when I started taking it. If this keeps up though, I'll be in trouble.

I was on Yasmin for about 7 weeks. The first couple weeks seemed fine, just queezy stomach and some headaches. Then, when I was supposed to be PMSing, I became so lethargic and depressed I could barely function. I laid in bed for 2 days not eating, thinking my world was going to fall apart. I only had energy enough to do a small chore at home (like bathe or brush my teeth) then crawl back into bed. The worst is that, normally if I get down I know deep down it will pass and there's a light at the end of the tunnel. But with Yasmin, my brain is foggy and I feel like there's no hope, w the lack of energy is even more depressing because I can't motivate to do anything and get my mind off my worries. Now I can understand why people get suicidal on Yasmin. There's no reason for me to be so tired, I lift weights 3 times a week and w a trainer (luckily or I would never be motivated to get there), I'm lean and muscular and healthy. Well, after the PMS I never got my period either.
Then after freaking out for a few days (and at my poor boyfriend) I was more mellow for the next couple weeks but still nausea and headaches. Then 2nd month PMS started... same thing, just overwhelmingly depressed and unable to reason it away or snap out of it. I've lost my temper a few times. My energy level is so low I just want to lay in bed all day. Now I just figured out that it was because of Yasmin. I was beginning to worry that I was loosing my mind. I really wanted to stick it out another month to see if they would go away but at this rate I'm going to be in a mental ward by that time.

I admit that I may be prone to get depressed, however, I don't take anti-depressents (I tried Wellbutrin a few yrs. ago and it made me very high strung and irritable). I've figured out lifestyle changes to manage when i get down. I just do things that I enjoy when I get down. But Yasmin has made it so that I don't enjoy life, and I don't even have the energy to work out, go out with people so I can get my mind off of my gloom and doom. It's horrible what Yasmin has done, I have never experienced depression like this and I've been down some tough roads in my life. I always have an inner hope and light in me that keeps me going, and what I'm experiencing with Yasmin is that it kills any voice of hope or optimism leaving one disoriented and afraid. I have been off of it for the 2nd day now and hope things start to clear up soon. Good luck with your experience and I hope this helps... even now, I'm not sure if it really IS Yasmin or me, but I believe the posts people have written so I want to X Yasmin out of my life so I KNOW that no drug is making me this way.

My doctor put me on Neurontin for nerve damage to my foot related to heel spur surgery. I started taking it on the 17th of this month with it having no effect on the pain (I was only taking one dose a day at 300 mg). He has since upped me to 300 mgs twice a day. I am now having problems with bladder control, infrequent headaches, sleeplessness, inability to climax and horrible bloating and gas. If I hadn't been on other pain meds for the past 8 months, I would stop taking it. Any suggestions?

Severe side aches, inability to spell, severe fatiqued.See I cannot spell!!!!!!!!!!!! Headaches decreased but I cannot function with all these difficult side effects. I took topamax for four months. I worked up to 50 mg one in am one in pm. I had all kinds of test to see why i had the severe side Rightside ache. I have been off the topamax for 2.5 weeks. My side ache is very minimal. I will have to deal with the migraines another way.

hey me again. I forgot to mention why I am on topamax. I have a wierd face twitch, used to be a deliberate looking wink which now involves an entire head jerk to theleft and an inability to open my eyes, that my neuro thinks my be the result of focal seizures, also I have regular migraines and daily, literally daily headaches. Because of some other more personal issues and symptoms I feel like I might have Tourret's instead. Last week I had an EEG done. My face was moving so much it was unreadable. I had a second one done. I fell asleep and the twitch slowed down, then I had an MRI done. I find out the results of it all in two days. Will topamax help if it is Tourret's? Does any of this sound familiar? Thanks

I have been using this drug for about 8 months and have found some of the side effects can be horrible. However i am in the process of separation and im terrified to face this without them. I know i am rather numb and at times just unconnected because of the drug but without them i would be crying constantly and i hated that. I believe i have been depressed for some time and i know for me the benefits of this drug far out way the difficulties of depression! The crying, sleeplessness, inability to get anything accomplished depression sucks. For me i have not gained or lost i am about the same. My therapist tells me to go off them slowly once things settle down i am on 300 mg of them now of which i started on 75mg to start. So i will keep you updated to my progress with getting off them!

The first few times taking this drug I had extreme nausea even though I had tolerated most previous antibiotics and pills pretty well up to this point.
I thought it was a little odd, but that it would pass.

The nausea finally did pass, but for the past two weeks I have been taking it I've been doing almost nothing but sleeping, and having extreme spells of tiredness.

Gradually every day has just gotten worse and worse than the next while on these pills. I don't want to get out of bed and lately have looked at the clock to see that I've been in bed for twelve hours at a time.

Now, I'm also in very advanced college courses. I initially attributed my sudden inaccuracy and inability to focus on the fact that I was just nervous about the courses, the material, but each day my concentration got worse, and worse and worse. It feels like I have ADD or something, which I've never had.
I felt like I was going insane when I could not even get through a page of material without wanting to jump up and shake myself around (also because of the numbness I got in my legs and arms). Not like me at all.

I have been dizzy, weak, incredibly tired and cold all the time, and entirely unable to focus all since I've started taken these pills. Unlike many of the other people's symtoms posted here, I've experienced severe chills and cold/ numbness in my whole body rather than heat? Except when I go in the sun, which then feels like I'm burning up.

Today was the last straw when I couldn't even get up out of bed, drive normally I was so dizzy, could not normally read one page of material, and the sun felt like it was burning my eyes out.

And reading some of the even worse symptoms others have had, this drug is not worth all the pain and possible permanent damage just to kill a few of these pimples.

I take topamax for migraines. I'm still feeling this out. When I first started about 2 months ago I went through all kinds of crazy symptoms. My husband thought I was loosing it. For some reason my doctor wanted to start me out right away with about 50 in am and 50 at night. The first month was rough.
I read the pamplets and took myself down to a lower dose and worked up slower as the company suggest. I not only had tingly hands and extremties.
But outburst of weeping and anger like never before. Like triple the pms symptoms. There were just all kinds of weird things. In this 2nd month I am taking 100 in the am and 25-50 in the evening. I am now experiencing the acne, itchy skin, inability to concentrate, apathy. Insomnia. In general I don't get chronic headaches. But have yet to see menstrual migraines subside. Sill feeling my way through this. You cannot stop this med abruptly. As many meds. Do not tell you how dangerous they are to stop abruptly. I think every one is individual. Soda's are not flat for me, but enhanced. More carbonated. Which I like. Strange I know.

I am a 27 y/o male in good physical condition (i did a triathlon 2 months ago) I was prescribed levaquin 750mg a week ago for an throat infection and fever. After the first dose I had sever abdominal pain (like someone was stabbing me). After the 3rd dose my back started to hurting and my calf's cramped up. I stopped the medication immediately. It has been 5 days since I stopped the medication and I have a burning sensation on my back. It is on both sides and stretches around toward my stomach. It feels like I have bad sunburn but there is no redness, swelling or discoloration. I also still have fever and muscle spasms all over my body (mostly in my legs). I went to my doctor yesterday and he is running a bunch of blood testes and I hope he can find a way to treat the symptoms. Does anyone know how long this should last? I just want it to go away so I can get on with my life. Any help or suggestions are appreciated.

I'm a 36 yo. female weighing in at 119 lbs. About four (4) weeks ago, I found out that my cholesterol is 221/154 so my doctor started me on Vytorin (10/20 mg). I started to - noticeably - not feel like myself about 2-3 weeks ago, but I thought it was just 'female' sickness. Once that factor played itself out I got concerned because I was progressively feeling worse. In general my physical symptoms were feeling extremely tired, nauseous, weakness, constipation, gas, diarrhea, dizzy & lightheaded and inability to concentrate and/or focus. On the 'mental' side, I have a history of panic attacks, depression and social anxiety disorder but they have all been kept under control with medication - that is, until I started taking Vytorin. I'm literally known for my friendliness and sweetness, etc. but for the past couple of weeks I've been in a constant bad mood, cranky, very easily annoyed about things and at people, depressed, anxious and generally uninterested in things that normally excite me. This past Friday night I was, once again, very upset and depressed about how bad I felt and wondering what was wrong with me, etc., and it hit me. The only thing I've done different in/for the past month was the introduction of the Vytorin into my system. I found myself almost crying I was so relieved to have figured out what the problem was. It's been 2 days since I stopped taking the Vytorin and today has been the best I've felt - physically and mentally - in 3 weeks. Hopefully, I'll continue to get back to my 'old self'! (Thanks to everyone else for sharing their side effect(s) symptoms on this site. It helped me verify mine.)

I had a Mirena coil fitted about 3 years ago. It was brilliant. I had it fitted because I suffered terribly with painful periods. Not heavy though. I had it for about a year, then had it removed to try for a baby with my partner. I already have a 19 year old son. I didn't get pregnant, now, I believe a good thing, and I had a second Mirena fitted. Let's put it this way, it's not acting like the first one did. I get headaches, hot flushes, bloating, depression, crying, muscle ache, especially arms and hands. I have dizzy spells, and can't stand around for a while as I feel faint. I am overweight, and always intend to do some exercise, and control eating habits a bit, but when your mind isn't right, how can you? It's a vicious circle. Obviously I appreciate that some of how I feel is my weight issue, but as I said, it's hard to do anything about it when you can't get the incentive because your mind is working overtime! The bleeding though, is basically the same as the first coil. It stopped near enough straight away, but at this moment I am having what isn't really a period, but is stranger and little heavier than spotting! I also get sharp pains now and again at the moment, and am very bloated. Doctor said about a month ago, that the coil could still be settling! We will see! Any replies would be great, I hope I haven't rambled on!!! Ha.. Pauline, Gloucestershire

After having taken various statins for over 8 yrs., my Doc decided my bad cholesterol wasn't coming down fast enough to suit him. A yr. ago, he put me on Vytorin, not the advised dosage, 10/40, but 10/80. I have been suffering from severe panic attacks for over 30 yrs., but they had been bought under control with meds..With the Vytorin, the panic attacks have started again, I am horribly depressed, afraid to go anywhere and panic at the thought of anyone coming to visit. I also have night sweats and muscle pain in my arms so badly it is agony to stretch. Muddled thinking, outbursts against those I love, inability to concentrate, etc. finally caused me to seek my own remedy. After reading of others' experiences with Vytorin, I put 2 and 2 together and stopped taking it on my own, My doc's gonna have a fit when he finds out. But 2 wks. after stopping, my energy levewl has returned the depression is not as bad and the panic attacks are easing. The bad pain is still there; don't know if that will ever go away.....

I have just come across this site, while looking to find out why I have been experiencing heart palpitations for the past two months - out of the blue!!! and usually "exercise" induced. I had some tests and have been told they are Premature Atrial Contractions "PACs". I started taking Yasmin in April, after having tried others over the past year (tri-cyclen lo and alesse) which did not work for me as the progestin was not strong enough. I am in my 40s and never took the pill before. Yasmin was great, it significantly reduced my "physical" pms (severe inflamation, severe bloating, severe sore breasts) which I experience for 2-3 weeks a month. However, sometime in mid to late June, I started getting palpitations/tremors out of the blue. The first episode freaked me out and lasted for about two weeks. At first I thought it was allergy medication mixed with my thyroid med, which can happen - but I cut out the allergy meds and still got them. They seem to come about 6hrs to a day after I fexercise/figure skate and they last from 2 to 5 five days. It's very irritating and nerve wracking, and I feel very agitated. I am also out of breath more than usual when walking up stairs, a little light headed and have some tightness in the chest. My legs also are weak, which makes no sense given my exercise regimen. I then lowered my thyroid replacement from .125 synthroid to .100 - too much thyroid med can cause some palpitations. Anyone who has mistakenly taken a second thyroid pill having forgotten that they already took one will understand. Even with the lower dose I am still getting the palpilations. I am totally at a loss as to why all of a sudden this is happening to me (perhaps perimenopause??). I have had the odd flutter here and there in my live, but nothing like this. It just doesn't make any sense ag ll. Can one's health just change like this overnight?. I am otherwise healthy, slim, have "lower" blood pressure (apprx 100-90/70-60)I skate 3 to 5 times a week, I have a full time job and yes I do push myself, but this is getting ridiculous. The only thing I can attribute it to is the Yasmin, ... but my symptoms only started after a few months not instantly, whereas it would seem that most of the the women here noticed the side effects faster. I hate to stop the Yasmin because I will have to return to pms "hell", but I suppose I will give it a try to see if the palpitations subside. At this point, I have been offered a low dose "beta blocker" and have refused. I am stunned to think that all of a sudden I have heart issues, especially since my Dr has always kidded me my that I will never have heart problems with my blood pressure. I will stop the Yasmin tonight and post another message in a few weeks one it is out my system. Here's hoping it is the Yasmin.
KarenSkaterGirl

topamax = no more bubbles in your soda

that was the first thing i noticed, and i had trouble believing THAT could be a side effect from a medication. soda and beer and seltzer all tasted the same, but felt completely flat. it didn't feel like a mistake on my brain's part, it just felt like someone had sabotaged EVERY bubbly beverage i happened to try.

little did i know it was only the begining. i have tried many drugs, treating mood disorders, and after topamax i swore to only "treat" my "mood disorders" with time-tested mother approved drugs that make sense. ok thats a bit harsh, but topamax made me miserable.

after the carbonation episode, which never improved (until i stopped the drug), i noticed substantial mental dulling, inability to follow conversation, inability to form intelligent sentences, make connections, etc. sometimes my body would just burst into sensations of being on some psychedelic drug. was i floating? was i tingling? was i swirling? did i even care? nah... i began sleeping all day, or most of the day, or something in between. slowly my muscles and joints began to hurt. then they basically stopped working. i couldn't bend or stretch or do anything without feeling like i was 95 years old. i became an insane bitch (meaner than usual, but without the wit or speed to be an impressive bitch). i lost ANYTHING close to an appetite. my sense of humor turned into an uncarbonated mush.

i dont even remember stopping. i was 18 at the time, and im assuming one of parents noticed that i had aged 80 years in one month's time, and stepped in... offered me a soda pop... and gently guided me back to the doctors office.

definitely my favorite and most bizarre tale of side effects. too bad i can't remember all the hell that took place. i wish it had been videotaped or something.

ok so be careful with that stuff. it you NEED to try it, try it, but start slow... and take note of the side effects... and good luck : )

I have been taking it at 2mg per day now for 2 days. Fatigue, lightheadedness, inability to think clearly, mild tremors in fingers and forearms. Am coming off of Klonopin (clonazepam) which I was at 3mg per day after starting out at .5mg on April 20th, 2007. I am using both concurrently with the new EMSAM patch at 9mg/24hr. Think I am going to discontinue the Gabitril and take the next step (pdoc said that it would likely be Lamictal).

I recently was given 200mg over the recommended pharmaceutical dose of Lamictal. My dr.'s partner prescribed this after a trip to the ER for a seizure to get me by until I could see my regular neurologist at the beg. of the week. The extra dose caused major blurred vision side effects, inability to walk, extreme sensitivity to light, and nausea. I am now at 400mg of Lamictal and starting Topomax with it so I hope this works. Any thoughts from anyone else taking this med combo?

I have been on topamax for almost a year now. I had been having a nearly constant migraine cycle for three months which had to be broken with migranol nasal spray. I then started on escalating dosages of topamax. By 100mg I realized that life was wonderful but that I couldn't retain much information which was a problem as I had just gone back to school for an advanced degree. Upon consultation with my doctor, we reduced my dosage to 50mg and things improved dramatically.

I have experienced some fingertip and toe tingling which have been completely tolerable. I take the medication right before bed so that I don't have problems with fatigue during the day. I do get out of breath easily when I exert myself and carbonated beverages taste horrible. But my migraines are under control.

I have a Ph.D. in molecular biology and a few years of neuroscience research under my belt. I would like to say that it is EXTREMELY important for people to understand that no medication is going to work identically for any two people. What works for one person, may not work for everyone. I know people who swear by imitrex but this medication does absolutely nothing for me. You have to be your own advocate when it comes to medications and treatments. Your genetics will also determine how well, if at all, you respond to any medication. For some topamax is a life saver, for others it will be the bane of their existence. This will always be the case for any medication. Be tolerant of others' experiences and understanding of each others' pain and progress will be made.

Daily episodes of pulmonary arrest, congestive heart failure leading to heart surgery, loss of motor control, curling of the right foot into a club foot that could not be uncurled, nerve damage, numbness in toes, loss of memory, depression, anxiety, dry eyes, elbow pain, intense neck pain and stiffness, backaches, leg spasms, loss of balance, hair loss, permanent "hissing" in the ears, inability to concentrate, inability to walk, nausea, elbow pain, jaw pain, debilitating exhaustion, impotence, flaking skin.

Has anyone on Lisinopril experienced upper GI problems such as Achalasia, trouble eating, reflux, or getting food 'stuck' in the esophagus?
My wife has lost 50 lbs in a year due to inability to eat from what was initially diagnosed as Achalasia (rare disease that affects the operation of the muscles in the esophagus and/or lower esophageal sphincter at the top of the stomach). However, Botox injections in the LES provided little relief which is not typical for Achalasia patients. She tests negative for Barrett's Syndrome and any form of Connective Tissue Disease (or arthritis).
My MD recently put me on Lisinopril (another horror story); while I was researching the drug, I noticed that it could cause muscle weakness. My wife backtracked the date that she was put on Lisinopril and it coincided with the onset of her GI problems. While monitoring her BP several times a day, she has cut back to 1/2 dose and has shown a marked improvement in the last 10 days. (It is too early to say with certainty that Lisinopril is causing the GI problems.)
Has anyone experienced similar problems?

I started taking Lisinopril for my bp about 2 1/2 months ago and even though it did lower my bp, I started having strange side-effects. It started out with drowsiness throughout the day, no matter how much sleep I got. And, waking up feeling drowsy even after 8-10 hours of sleep. Then, I started getting strange aches and pains throughout my body, like I was getting over a stomach flu. My asthma also flared up and I started having to use my inhaler for the first time in almost 15 years (usually I just need it after exercise.) The side-effects continued to get worse over the next months with increased fatigue, drowsiness, coughing, anxiety, muscle aches, poor concentration, feeling like my nerves were "shot," headache, weakness, tightness in my lungs, numbness in my hands and feet, and just plain feeling bad.
I made an appointment to see my doctor because I thought there was something seriously wrong with me. It crossed my mind that I might be feeling this way because of the Lisinopril. I stumbled across this website and after reading everyone's testimonials, I decided to stop the Lisinopril. I haven't taken it in 3 1/2 days, and I am already feeling much better. I would rather try a more holistic approach to lowering my bp then taking Lisinopril.
I hope this helps someone else out there who might be going through the same thing.

Uncharacteristic loss of libido, inability to lose postpartum weight, unexplained weight gain.

Acute onset of double vision , inability to judge distances, inability to maintain lane while driving on highway; speech aphasia occurence immediately after vision decrement. Resulted in near accident on highway.

Had been on medication for 4 years without a similar event occuring.

Titrated off medication.

Hi

Who put the listing of things that can occur from Yaz Yasmine

I read the Asthenia
I have alot of these symptoms

Now have severe short term memory loss major brain fog still have shaking and tingling in arms

Iam so confused off Yaz 4 months on it for 3 weeks
Still not back to work I cant work due to brain fog and my lack of concentration and inability to focus

Do alot of you have that???
How do we get better??

I was almost miticulous prior to this the brain fog seems to have gotten worse other things a little better

Iam acting so out of character for myself

What is this Asthenia thing????