Sensations symptoms and conditions

I have been on Yaz for almost two years - I quit last week. I was put on it after being diagnosed with PMDD and, for the most part, it helped a lot and I thought it was the answer to all my problems. After the first year I was on it though, my symptoms started to return and worsen. I started having severe anxiety issues. It was as if my body couldn't process the stress in my life anymore (which was no more than any other college student with a medium-heavy workload) and its only reaction was to go into full-fledged panic mode. I experienced a steep drop in my self-esteem to the point where I'd sit and look out at everyone else wondering how it was that they could find so many things to be happy about. My life is pretty great - no severe illnesses, functional family, graduated with a degree, great friends, great church - and I couldn't think of any reason to be happy. No one should have to consciously and objectively list things to be happy about and then try to convince themselves that they just forgot about them. I found that I'd rather be alone than be with even my closest friends and family members. It was the sad version of my angry PMDD anti-socialness. Anyway, months of chronic stress and depression led to a panic attack last year that took me nearly two months to recover from (nausea; tingling sensations in my arms, legs and face; lack of appetite; tightness in my chest; trouble sleeping, etc...) and the sensation of detachment that comes with a panic attack has only recently begun to subside. This detached feeling lends itself well to having a cruddy memory. I'll look at pictures from a year ago and not remember what has happened between now and then - it feels as if those pictures are just from the other day or the other week. I don't really remember the semester of my panic attack. My memory feels second-hand, like someone told me about it but I never really lived it myself. I sometimes have moments where I just forget where I am when I'm driving to my sister's house, 15 minutes away. It only takes about a minute to regain my sense of direction and remember what street I'm on - but it's a scary minute! I don't think that all of my experiences were caused or made worse by the pill (I hope not, since when I actually need birth control for birth control purposes I'll have a hard time finding a low enough dosage that doesn't screw me up), but I'm going off of it to see how I feel on my own. I'd rather be mad for a week every month and combat it with more exercise, music and a fleet of vitamin B12 than be sad all the time.

I've been on Yasmin(Ocella) since July. At first I had no side affects and then just last week, I had shortness of breath, tingling all over, warm sensations in my body, headaches and blurry vision. I had to be rushed to the hospital by ambulance. It also seems like I'm having all sorts of thoughts that are keeping me paranoid and not sleeping. It also seems like my left breast is slightly larger than my right. I've never had any problems like this before so as of today I'm taking myself of this birth control pill.

I have been on Lisinopril 20 mg for the past 9 years. I can't believe I have taken it for such a long time. I noticed some strange chest sensations 2 years after taking it but pushed through it. Then I developed breast cancer and went through the chemo and radiation while continuing to take it. In the last 2 years and more recently in the last 3 months, I felt so many skipped beats that I had to check it out and I also have had significant hair thinning. I had a holter monitor, resting EKG, lots of bloodwork and was told that everything was normal. Normal???? Then why was I feeling so rotten and scared every time my chest decided to heave or get funny sensations in my throat. Doctors do not want to hear these types of complaints especially when you think it is related to a medication that they ordered.
So I decided to try an alternative approach. I have been taking fish oil, coenzyme 10, cholesterol nutritional supplement, Vit C, Vit E. I started these about a month ago while still taking Lisinopril. I finally stopped the Lisinopril yesterday so I'll see if I have any improvement of my symptoms.I also went to a website that showed 1% of people can have skipped heartbeats while on Lisinopril Here is the URL
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Hope this helps many of you who have similar episodes. MHS

About 2 hours after taking my 18th day of generic Wellbutrin XL 150mg. (Sun)the palms of my hands started itching like crazy! No bumps or anything, just intense itching. I immediately applied 1% Hydrocortisone cream to them and after about 10 minutes that pretty much made all the itching go away. I didn't want a replay of that, so I kept applying the HC about every 4 hours all day long, or after washing my hands. That evening everything was okay. Then the next morning, my hands started itching again...so again I applied the HC cream again, and headed off for work...they itched SO bad, and this time it took about half an hour for the HC cream to even begin to work. Then about 20 minutes into the hand itching, the soles of my feet started itching..too wierd! I was driving, so I couldn't apply it to my right foot b/c it was on the gas pedal, but I applied the HC cream to my left foot, ahhhh! Then as soon as I could, I applied it to my right foot. It took about 10 minutes, but it was soon itch free. When it came time to retake my med, I decided not to risk it. I called my prescribing doctor and she was off, and some other doc just said to take Benadryl. Duh, I was at work and #1 didn't have any and #2 it makes me so sleepy, I can't function. Then later on in the day, my wrists got welts on them, then my left elbow got a huge set of welts on it, and itched like crazy...then a few hours later, my left ankle got a huge welt on it and it looked like my ankle was swollen and both my feet and ankles had pin pricking sensations....a few hours after that, my right leg started itching behind my knee...I could feel a welt through my slacks...so again, I went into the ladies room and applied HC cream and it helped. By now I've used 1/2 the new tube of HC cream! When I finally got home, I pulled off my clothes and I had huge welts (hives) all over the back of my right leg. Plus, a big long skinny (horizontal) welt where my bra and wrapped around me. Since I was home, I could take Benadryl...so I took 4 tsp. and jumped into a warm (not hot) bath (they say to use cool water but I couldn't do it) with a cup of baking soda. Felt SOOOO good! By the time I got out they felt much better. I kept taking the Benadryl every 3-4 hours all evening but by the time I went to bed, I had welts on the back of my left leg also and on my buttocks and hips. My head kind of itched here and there in weird places, more like pin pricks but I have really thick hair, so I can't tell if I have any welts there or not. I stayed home from work today to continue on the Benadryl and making sure it doesn't get any worse. It hurts to sit here typing as my panty line is in the middle of a big 3" welt. The Wellbutrin XL seemed to be helping my depression and anger issues, but I assume the MD will put me on something else. I really liked it. It did suppress my appetite during the day but not much at night. Oh well! I'm glad I'm not the only one with these symptoms.

I have had electrical feelings in my body since the first day of the first shot.
The first one was a shooting of electricity almost like I stuck my finger in an outlet. I was vacuuming the floor and I threw the vacuum out of my hand it was so intense. I thought that was weird since the handle is all plastic. Then I got another one brushing my teeth and they just kept happening. Now I have electric tingly sensations on the tops of my hands, in the bottoms of my feet, in the crease of my arms and down my forearms, and behind my knee and on the backs of my legs. It sometimes feels like a bug is crawling on me. I slapp it realizing nothing is there. Also have the sensation of an itch that I can't seem to find. I have these sensations all the time.. my face itches and my head itches.

I had the Mirena placed in 2004 after the birth of my second child. I had weight gain, mood swings, hungry all the time (i would sleep eat), depressed, joint pain and was tired all the time. I eventually got it removed 3 years later and my symptoms got even worse. I was severely depressed, my sleep pattern was abnormal, my mind was fuzzy, couldn't concentrate, joint pain worsened and had absolutely no energy. I started itching and having tingling sensations and "bug biting" pain/sensation especially in my extrementies. It was weird. It stimulated a hormonal response that affected my central nervous system. I know it did. I will never be convinced otherwise. It was a shock to my system. There needs to be studies done in this. I finally drug myself to the my general practitioner 3 months later and I thought that I would get admitted in a psych ward. I was hardly functioning. No kidding. I had no reason to be depressed. My life was better than ever. I was not admitted, but I was put through the ringer for tests and my healthcare bills became outrageous. I had tons of blood work, sleep studies, saw a neurologist, had a myelogram, mri, and put on several medications which added to the weight gain. It has been almost 2 years now and I am just now starting to feel like myself. All of the tests were inconclusive. The neurologist dx was something neuromuscular. I am not on any medication now, but am not 100%. But I know that damage was done and I am older. So I'm afraid that I will never feel great again. I wish I had never had the Mirena. Never. I know I miscarried once and suspect that it happened twice. I didn't have a period for those 3 years but it was not worth it. This product should be recalled.

I had a severe upper respiratory infection and regular well known antibiotics wouldn't kick it. I went back to the physician who prescribed Avelox. Within less than 2 minutes of taking the first pill out of the bottle I started getting sensations of bee's stinging my tongue everywhere and my lips were tight, purple and swollen. Within just minutes I started having a hard time breathing and the whites of my eyes were really bloody. Next thing I knew I could literally feel and hear my heart beat in my ears and everything sounded like I was in a tunnel. Within 5 minutes of taking the pill an ambulance was called and by the time they arrived my blood pressure was 70/16 with over 240 pulse.

When I got to the ER they said I wasn't the only one with the same issue to this drug and 3 were within the week prior to my being there. When I said I had SVT Supra Ventricular Tachycardia the doctor said people with SA Node (Natural pace maker of the heart) issues which control the magnetic aspect of your heart biting it sends something in there to screw it up and make it a big mess. I wouldn't suggest this med to anyone as I did some other research on it through the web and their reports from the FDA and there were some pretty NASTY side and long term effects of it.

Needless to say; since this happened I've developed a panic disorder and my nervous system isn't working correctly. Again; be careful what you take.

Seriously this is ridiculous. I have been dealing with all of these same issues and have been debating on whether to see a counselor because I feel like I am losing my mind! My boyfriend tells me I have mood swings and my mom says she cant even talk to me anymore. I had an acquaintance at work tell me that she hopes that I am okay because I look so down. I am anxious and depressed - have to self talk just to get out of bed. During the month if I am not cramping - my breast are almost to sore to move. I read someone on hear define a side effect of vibrating sensations throughout their body I get that for at least a week and a half every month. I would describe it as how you feel when you first are coming down with the flu....kinda achey. I was actually off for a week a few months ago due to extreme vertigo. I wondered if there was a correlation...from what I read I guess so. I have severe lower back pain -sometimes to much to stand straight and walk. I am so frustrated because I was told no side effects. I had Norplant back in 1991 and gained 70 pounds in 5 months. Well I am up to 19 pounds with Mirena - it hasn't been quite a year. I told the doctors that I had significant weight gain with Norplant and developed a blood clot while using the pill. I was assured no such side effects with Mirena. Mirena was a great choice for women who cant take anything else! I feel so misled!

I am 18 years old. I started yaz three months ago. During my first month taking yaz, i had a really bad fever and started getting these electric shock sensations in my head. My heart was racing and I couldn't stop twitching. I was panicking and will skip the long er story but the doctor told me it was anxiety and an allergic reaction to my cough medicine and sent me home with vicodin and atavan. I got better and didn't have that sensation for the next week. However, I was growing increasingly anxious and panicky for no reason at all and would have long crying jags where I couldn't calm myself down. I am usually a very happy person, and I just feel so depressed. The shocks started coming again, along with the twitching and feelings of vertigo. I started thinking that maybe it could be the yaz causing it and went off it mid pack. I went to my doctor for the shocks and she had no clue. I had a mri of my brain and it came back normal. I have been off yaz for two weeks now, and have since seen a neurologist. She put me on an 80mg prednisone pack which she said would stop the shocks but only have me the worst migraine of my life and shaking so bad that I couldn't function or leave my bed for for four days. I went to a new neuro and am on an new migraine medication which seems to be working better as I am up and my headache is better. He seems to think the shocks are a result of yaz. Have any of you had this symptom, and the twitching? I feel like someone has turned an electricity switch in my body and I cant stop moving. I have no clue whats wrong with me and its really scary. The only way I can sleep at night is with ambien, and I cant stop twitching even during the day. If yaz can cause this why can they even sell this awful pill?

I’m 25 and I’m from the UK
I have been suffering from the Gynae condition Endometriosis for the past 14 years. I have tried virtually every contraceptive Pill / Injections/ Coil / Hormone tablets/ Patches / Implants going, I’ve had various surgeries and none of these have made the slightest improvement in my condition. I can experience anything from 2 – 6 periods in a 4week period and the pain is there on a daily basis, interfering in my everyday life
On recommendation from my Gynae consultant he suggested that I give the Mirena Coil another go, I had one first fitted when I was 17years old for the same condition and to be honest after the initial first few weeks of bleeding and slight pain I found it made a huge improvement, It completely stopped my periods and I was no longer in any pain and for once was seeing some normality in my life...that is until 2years into having it the Mirena decided to dislodge itself and imbed itself into the surrounding tissue and I had to have it surgically removed. So this time around when my consultant suggested that I give it another go I was a little skeptical after what happened last time but the fact that I have tried virtually everything going to try to help and nothing has worked I decided to give it another go, after all it did improve my condition last time, even though it did make me very ill at the end when it moved.
So I had the Mirena fitted just under a month ago now and I seriously wish I had not bothered, I am in more pain that I was with just the endometriosis pain, I’ve been bleeding really heavily ever since it was inserted, I am extremely moody and temperamental, My appetite has virtually disappeared yet I seem to be gaining weight around the mid drift area, I keep suffering from headaches which I rarely usually get and sickness and I’ve been experiencing these fluttering like sensations which remind me very much like the feelings I had when I was pregnant with my son but a pregnancy test showed negative so I don’t have a clue what that is. My skin and hair are also suffering as they seem to become increasingly greasy much quicker than usual and I’ve started to get patches of acne which I never even suffered from when I was growing up as a teenager.
Reading through all of your posts and the similarities in side effects I’m very much convinced that its the coil causing all of them and I am seriously considering getting it removed

After reading all of the comments, I am embarrassed to say that I have taken omeprazole for the past 2 years. Originally, I began taking it for nausea from GERD. I began taking it soon after the death of my cousin (as I figured the anxiety from her death caused my stomach issues). I began to become depressed shortly after, which I also attributed to her death, financial issues, etc. However, when life got better I was still depressed and anxious. Two years passed and I still couldn't figure out why I felt so bad mentally. Not to mention I was mildly nauseous most of the time and NEVER had a normal appetite. I would only know it was time to eat when I felt faint. Light-headedness, stomach cramps and lethargy were also side-effects that I experienced almost daily. The worst part was that I didn't know if the nausea was caused by my stomach issues or by the omeprazole. It was obviously the omeprazole. About 2 months ago I switched to Prevacid which caused much less nausea but many of the other side effects were still there although a little less. I weened myself off completely (which I would recommend to anyone) and I actually feel like my old self again mentally and physically. I didn't realize how low my energy was until this last week that I've been off those meds. I'm actually HAPPY again, I WANT TO EAT something, I have ENERGY, and no light-headedness or stomach pain at all. It saddens me to think that I spent over the last 2 years feeling this way needlessly and thinking that I was crazy. There ARE other alternatives to acid reflux, GERD, etc out there that are much safer and more tolerable. If any of you are experiencing some of the symptoms that I or others have described, explore other options before you just "get used to" feeling like crap.

I recently had Novocaine injected for a lower molar crown insertion. After one week I have been experiencing jaw pain, tooth sensitivity (the molar), sore gum's around to the front (top and bottom), some inner ear sensations, headache and neck pain on that side and muscle actions causing my teeth to chatter rapidly. These effects seem to worsen when I lay down or even worse when I drink alcohol.

I'm 28 years old woman...
I was prescribed Ulcerative Colitis 5 years ago. I have been on prednisone 4 or 5 times since then for periods of three to four months experiencing the typical symptoms and side effects. I had a new flare up and 2 weeks ago my doctor prescribe prednisone again, but this time he told me to take 40 mg a day for 7 days and then stop it, TOTALLY.
He said that it was safe and even better than the old strategy of reducing the dosage slowly over a 2-3 months period, so I accepted.
I've never felt so bad in my life, not even when I was a moody teenager.
These days I have felt so miserable, so depressed...I am an optimistic person, really positive and easygoing but these last three days I have changed completely: anguish, anxiety, panic, alienation, it's like living in someonelse's body,...
Yesterday morning I couldn't go to work, I just sat for breakfast and start crying in front of my boyfriend in a desperate way...I spent two hours crying because I couldn't establish a connection between my body and me, I felt that I was trapped in a strange body...
The funny thing is that my doctor doesn't really acknowledge these sensations, he thinks that the emotional distress is due to sth else and not prednisone!
Apart from that, my bones, muscles and joints hurt terribly...

If you feel depressed, prepare herbal tea. It cleans your body and your sprit. Good options are mint and lemon zest, orange zest and chamomile

I was given Levaquin for a kidney infection. It seemed to help break my fever but after only one dose, I broke out in rash and later that night had tingling in my legs. My hand felt numb. When I called the oncall doctor she told attributed to anxiety. I told her I was anxious because all of a sudden my hand had gone numb and knowing that was a danger sign I refused to take anymore. Later that night, I could not walk or stand or bear weight on my legs. My shins and Achilles tendons were burning and only because of the internet did I know what was happening to me. Only 1 out of three doctors would agree I was having a drug reaction. For some odd reason, the doctors REFUSE to believe or acknowledge this was caused by Levaquin. No wonder the side effects are "rare" if no doctor will acknowledge the pain their patients are going through....how can the drug companies get any real feedback. Funny thing is only after I sent an email out to my team essentially warning them about this drug did I find out my coworker who had been on medical leave had suffered the same fate of torn achilles tendon and only after 3 months of PT is finally walking without pain. WHAT IS WRONG WITH our world when no one will listen to us. Thank God for the internet. I can walk now and have no pain standing (lasted only 2 and half days) but I am scared about the future as I know the results are lingering. I have been exhausted this whole weekend and wonder if its just me recovering as my PCP had me quit all antibiotics even at the risk of getting my kidney infection back. Well nice to know our stories are the same...and its not in our heads. BTW, my ER doctor told me it was a good drug and very unlikely the cause of my leg pains. They rather believed I had pneumonia or lyme's disease before they would believe it was caused by their beloved drug. All I can think now is I hope one day they are given this drug and it cripples them like it has so many others. Sometimes that is the only way they will acknowledge the truth. It has to happen to them or someone they love.

It seems that everyone is having similar symptoms. I have been on Doxy for about 14 days now and I'm feeling worse every day. I am on it because i had been bitten by a tick and contracted Lyme disease. I don't know much about the disease but it has me freaked out. I started taking the antibiotic 2 weeks after being bitten; losing my balance and almost falling to the ground. I also had a couple of dizzy spells after eating. I seemed to feel a little bit better the first week of taking it but started feeling the side effects. It started out with the occasional dizzy spell then came the exhaustion, anxiety, depression, lower back aches, soreness in the back of my eyes, stiff neck, headache in the back of my head, flu like shivers, racing heart, and complete body aches. I also found out the hard way not to go out into the sun while on Doxy. Felt like the tops of my hands were being pricked with a million needles and burning. I wish I could stop taking the drug and be done, but I am already scared about the outcome of the Lyme disease. I hope I can feel normal again soon.

Ok.. I've been Neurontin for three or four years up to 800 mg 5 times a day for glossopharyngeal neuralgia (extreme Pain in one of the cranial nerves in the throat) any way when the symptoms go into remission i back off from tacking the drug... Since this is my third time coming off I have really tried to pay attention to the feelings and sensations surrounding sided effects.. The biggest thing that I have noticed is more of an emotional problem. the drug seems to make everything OK.. or mountains seem like mole hills. my first time I came off, I had a hard time sleeping and would find myself crying over nothing... I just couldn't cope with my own mind. I feel like the drug subdued everything, The fog or haze it puts you in sorta makes the whole world a wonderful place. I have lost my sex drive and have a hard time working now.. I'm going off it again slowly and am having a hard time completely letting go because it has kept me from being depressed.. I feel more depressed when coming off neuronton than I did on it. I believe long time use of the drug is some what emotionally addictive.. Just be prepared to feel your emotions again once you are off.

When I started my little emotional rollercoaster @ age 35, they classified me as being bi-polar with generalized anxiety disorder. I put myself into a treatment center after feeling like I was going to go crazy. I used to work in the medical field and I should have known better. They doped me up on 1000mg of Lithium, and 9oomg of Depakote. Lithium can be hard to regulate and dangerous; coming from a person who can sneeze and lose two pounds Depakote just turned out to be a fat pill (180 to 210 in three months). I went through the guinea pig stage Every SSR they put me on had a very bad side effect, Paxil being the worst. After two days of taking it the racing thoughts and feeling out being out of control made me want to jump out the window. I could not even call 911 as I felt I would go even more insane. I really almost did not make it through it. I discussed it with my new Dr. and he suggested Lamictal. I have been on Lamictal for over 4 years at 300mg a day. It has stabilized my moods but I still argue with the doctor about my diagnosis as I feel I am more Cyclothymic , my mood swings are not as pronounced and can last from a few hours to a few days. Since first taking the med I noticed the memory loss, my train of thought going out the window, bloated, the feeling of having a fever, but not. One of the most important affects, if I am an hour or so late from my regular scheduled dose I get dizzy and my shoulders and neck start to tingle and get numb. Just two weeks I requested an increase in the dosage to 400mg to see if it would help with my underlying depression that every other combo has not addressed. Since then I have been a bit more of a whack job. (Emotionally)Two days after the increase I had a very hyper mania day, I had to leave work early for fear I would lose control of my mouth, do or say something very ADHD. I took two days off and seemed to be fine after that. This Sunday I went downhill as soon as I woke up. I wanted to cry, but couldn’t and I did not know why; I felt void of emotions except for sadness, lacked the energy to want to deal with people, even my other half, wondering why I was even here. (Physically) I have noticed heart palpitations and muscle spasms in my face and arms. I looked up side effects and found this site and wanted to add to it. I have tried just about everything out there that I can and nothing will really work as good as this one. Combos with it do nothing for me either. It really freaks me out that the thing I am taking so I do not feel the way I do is making me feel that way to the extreme. I am letting my Dr. know that I will be taking myself off this dosage.

I am so glad I'm not the only one that has the crazy symptoms. I am being treated for an inflammation in my optic nerve. I woke up over a month ago now with double-vision. I was on 100mg a day for seven days then went down to 60mg. I feel like I'm high all the time though. I have to take my pills at 7 in the morning and they are still effecting me until about 2 or 3 in the afternoon. I can't drive or do anything that would take a lot of concentration cause I just feel out of it around my eyes. Also I have tingling in my face and arm. Not sure if this is a side effect or if its the possibility that I may have Multiple Sclerosis. (getting an M.R.I. done for further testing) Does anyone else have those tingling sensations?
My vision has almost come back to normal now. The Prednisone has done wonders for that, but I really hate taking it.

I have to admit I am dumbfounded. I "stumbled" upon this information tonight.
I am a very healthy and active 40 year old female with no health issues other than seasonal allergies and asthma. I went to the dr. 4 weeks ago for a sinus infection. I was prescribed 5 days of Levaquin (called a “Lev-pak”??). The sinus infection seemed better but the symptoms of that came back after 10 days and I went back to the dr. only to be prescribed a 2nd round of the same medication. Again the sinus infection seemed to get better and now a month later I went to the same dr. again today because the sinus problem came back but worse. Today I was prescribed a different antibiotic called Avalox. Since I had not heard of this drug I decided to look it up before taking it.
I now look back over the last month and am horrified that I have had these bizarre symptoms and here they are experienced by 100's of other people. And this is just one website, with people that took time to speak up. Just one. All of sudden I already feel better because I can explain so much. Not once was I warned about this drug either by the doctor or my pharmacist.
Everything I am about to describe I have either blamed on still being sick (and getting sicker from the presumed infection) or have blamed on other meds taken in addition for congestion, headache, stomach problems, wheezing, etc.

I have had ridiculous sleep patterns. I was either SO awake some nights that I felt like I could run 10 miles or SO exhausted by bedtime that I could barely walk up the stairs to get to bed. I have had extreme nightmares and dreams. In addition I have had at times practically NO peripheral vision combined with a blinding headache. I also had ringing in one or both ears that was very random. I seriously thought several times that I might have a brain tumor. I have had all these weird stomach issues. I have felt bloated and my abdomen area has been painful at times. I also have gone from either having bad diarrhea to being very constipated. My heart has raced at times both while doing physical activity OR sitting still. For about 3 days after the first round I had sharp pains in my left side (abdomen and arm). I have experienced bizarre hot flashes combined with being freezing cold minutes later with no fever at all. And last my right leg, particularly my knee and foot have just hurt at odd times (just waking up, walking up and down stairs, after sitting for a few minutes). All of these things separated seem so random so I never suspected Levaquin. Having read page after page…they are ALL explained.

I can’t tell you how much better I feel right this moment. I feel sane again. I will never, ever take Levaquin again and am so thankful I was smart enough to get information before taking Avalox, which would have been round three of this poisonous family of antibiotics. I don't know how long it will take for the Levaquin symptoms to go away but at least I'll know why these things are happening. Thank you.

My 13 year old son started taking singulair Nov 13, 2008 for seasonal allergies. Three weeks later teachers at school recognized a change in behavior that was not typical or noticed prior to the medication. The end of Dec. 2008 loss of appetite and increased mood changes and noticeable aggression toward others and unable to change his feeling even knowing his thoughts & feelings were awful and not typical or right. Jan 13, 2009 we realized it was the med and he stopped taking singulair. Not only is my son still trying to recover from physical effects, he currently is trying to recover emotionally. No longer able to attend school and in a home-bound education program. Would not recommend this drug to anyone. Was taken to the emergency room 3 times within the last month and a half for physical issues and choking sensations & loss of weight. Was admitted to the hospital twice and the hospital admitted him to a psychiatric treatment facility once and currently he is going to a psychologist weekly all within the last month and a half. Prior to taking singulair no major issues.

I am a 24 Female that was prescribed 50 mg twice a day for my mood swings, migraines, and being overweight. I have been on topamax for two days now. My family physician prescribed this to me knowing that I am sensitive on medications at first. Well I had no idea that these particular side effects were from this drug until I found this website. I have had 24/7 nausea for 2 days straight, throwing up, BAD tingling in my legs (needle sensations), irritability, inability to concentrate or spell. It's terrible because my job AND FUTURE require me to concentrate, SPELL, and REMEMBER which are three things that I have completely lost while being on topamax. I cannot even type. The greatest impairment I have is what I call ZONING OUT which is - I will being doing something such as watching a tv show or reading an article and I must have dozed off in my brain for a few minutes and then came back. It literally feels as if I left my body for several minutes and then came back! It's a very strange feeling! I would only recommend this medication for someone that has tried EVERY OTHER HEADACHE medication!

Ok so im 18 years old and I pass out frequently, I have been unsuccessfully diagnosed with several different theories over the past two years, Recently some doctors though that my passing out may be an aura to the headaches and migraines i receive after, my doctor just prescribed Topamax to me and Im really nervous about taking it after reading about these side effects, has anyone else been prescribed topamax who has similar symptoms?

To make a long story short (I think). Taking Celexa (20 mg) for more than 4 years definitely caused decreased sexual sensations (numbed nerves), though it did change my life. In October Switched to Wellbutrin XL. Withdrawal from Celexa was not easy but Libido is definitely back. Problem is I am angry ALL the time at my husband. In fact, I've been angry almost from the get go from switching to Wellbutrin. I have also been puzzled by slight hair loss in the back of my head at the hairline. I have of late experienced abrupt halts in thought processes and my periods, though I am 45, have suddenly become irregularly. Frankly I didn't realize that Wellbutrin could likely be the cause of these symptoms until I read some of these posts. I really would like to wean off of this drug (was prescribed 300 mg but have taken 150 mg due to feelings of being 'wigged' out on higher dosage - did up the ante for just over a week to see if that would help but didn't seem to matter)...Nevertheless, I really think Wellbutrin is causing me to feel deep resentment toward my husband. This is not a usual emotion for me and it pretty well started immediately after I began taking Wellbutrin. I really could use your opinions(s). IS THE WELLBUTRIN causing the anger??? Did the Celexa simply MASK existing problems??? Is it a combination of both. Is this depression again or am I in the process of slipping back in??? (anger was not a previous symptom of my depression though black clouds, low esteem, doom and gloom and sadness were) Also, aside from anger and sheer resentment, I feel as if I'm spinning my wheels, that I'm in rut and that no matter how I try to move forward, I can't - I really feel lost and am so angry at my husband and see him in such a different way that it is almost to the point of being ridiculous). THANK-YOU so much for your replies.

I started Levaquin 500mg on Jan 27th for a sinus infection. Two days later I woke up and almost passed out upon standing. My heart was racing and my blood pressure dropped. I had to call my husband home from work to take me to the ER. I also started to get nauseated,chills and weakness in my legs. After being hydrated at the ER I was sent home to finish my meds which was a 10 day course. My symptoms became increasingly worse over the past week. Dizzyness,weakness,fatigue,rapid heart rate with some PVC"s, no appetite,nausea,pain in my back,shoulders and left hip. I also have a red rash on my chest and face. I experienced a heavy sensation in the back of my head, compounded by a crawling sensation. My body will flush upon standing , I get night sweats and difficulty breathing. I have also suffered with some kind of wierd sensations in my eyes that has my sight screwed up in some weird way. I have also been on this side of confusion or forgetfullness and nearly having panic attacks. This is some kind of freaky horrible drug. The day I went to the ER my left leg went numb. I have one pill left and didnt take it today. The doctor I saw today says it could be the Levaquin. HA!!!! I am praying for all on here..

No horror stories to report. Was on Lexapro 20mg for several years. Am switching to the generic Celexa soon because that is what insurance will pay. I have had weight gain problems with Lexapro, hope that subsides with the Celexa.

At times I did notice "weird sensations" while taking Lexapro. Seemed to come on if I missed taking the med or took it late. Almost like some type of withdrawal symptom. I just work hard at taking it as prescribed. Lexapro worked well for the Panic/Anxiety though. Will let you know how things go with the Celexa in a few weeks.