Back of my neck symptoms and conditions

I am 36 year old female and was prescribed Avelox for an ear infection and sinus infection. By day 5 I discontinued taking the drug. I've never had such a bad reaction to a medication. By day 5, I had major dizziness (the room was spinning), my heart was beating fast and I felt like I was going to pass out. I had a burning sensation along the back of my neck and a tightness in the left side of my chest. I had a headache and some nausea but felt completely out of it. My hands and feet jerked by themselves. I felt anxious and didn't know what else to do but go and lay down in bed. I tried to keep calm but then I started sobbing like a kid whose family pet died ( I can't remember the last time I cried). I was afraid to go to bed fearing that I would not wake up. What the heck... I will never take Avelox again.

After experiencing these effects, I looked on-line and found this site. Glad to know I'm not alone. I did go to sleep only to have mega weird dreams about motor vehicle accidents along the highway and eating a live crab/lobster creature only to have to bury it in the garden for a bunny??? Crazy and WTF ?!

I have been on lisinopril for almost 3 months started out with 20 mg a day and my doctor upped my dose to 40 mg a day after going back for a check bp was still high I guess. About a month ago was out in the sun for about 6 hours and ever since then my head has been flaking and itching and has some scabs on it I also have some red rash on the back of my neck. Has anyone else experience this? I can't get it to stop either I tried using Head and Shoulders for 2 weeks like the doctor told me but it doesn't help. Any suggestions?

Prescribed Bactrim for MRSA skin infection on my arm that I picked up at my local gym. Day 1 OK, Day 2 severe headache at the base of my skull. Day 3 continued headache, general nausea, gas. Day 4 I began to develop a low grade fever and dizziness. Almost passed out after walking just a half mile. Still a severe headache, weakness. Day 5 Headache, consistent fever of 103, chills and muscle aches, light hives visible, weakness, unable to sleep. Day 6 early am, couldn't sleep all night, went to the ER with the worst muscle aches and fever I have ever had. Hives now very clear and pronounced all over my torso. I was tested for the flu. Said it was not, but was a viral infection that was attacking my muscles. Muscle breakdown found in both blood and urine samples. ER physician changed medication to Clindamycin HCL. Told to stop Bactrim, but thought what I had was viral, not a reaction to the Bactrim. I continues to feel bad for a couple more days, but hives started to reduce, fever diminished and started to feel halfway human after being off Bactrim for a couple of days. Still not 100%. New med has it's issues too (have to take every 6 hours, can't lay down after taking it) and a nasty taste in mouth and stomach upset, loose stool. After 5 days of new med went back to my doctor. A secondary infection had set up in the Staph area. The fungal infection needed a different med. Now is 4 weeks later, after finishing all meds, still have an infection. Blood cultures taken to see if the infection is the staph or fungal. I have lost 8lb, have no taste buds, loose stool, severe stomach cramps/burning (now taking Activia to put back good bacteria in my stomach...no one told me to do this before!!). If Staph not gone, need IV antibiotic for a month. I am 50 year old female, but note I had taken this in my 30's without any problems. You can develop an allergic reaction to medicines previously OK for you. Beware of Bactrim. It kicked my behind!

I had the Mirena for 5yrs & had it replaced this past April. I had loved it (no menses) but little did I know of the adverse side effects that were plaguing me. I always had some depression, but wrote it off to cyclical hormones; cystic acne that seemed to be getting worse as the years went by; heart palpitations; NO libido; anxiousness. All this seemed to happen slowly over time for me. Once I had the new one inserted, I started noticing the part in my hair was becoming thinner, like balding; developed an eczema/rash on the back of my neck at the hairline; I felt like my hay fever was non-stop & got an ear infection/sinusitis for the first time ever; then the headaches which most recently turned into a migraine with visual changes coupled with insomnia. And I ached all over like I had the flu all the time. I had no clue that the Mirena could do this until I started researching & read the PHYSICIAN insert info! I discovered that out of 21 "adverse effects" I had at least 13 of them! I was mortified - being a Ob/Gyn RN, I felt I was really misled by the manufacturer & my doctors. I could not take the headaches & insomnia any longer. A week ago, desperate & could not wait until an appt., I went into the bathroom, pulled the strings myself & removed the sucker (being a RN, I have to tell you not to do that; I was willing to take the heat should something bad happen!). Over this last week, a HUGE difference for the better. NO headaches, insomnia, body aches, skin is clearing & my mood is getting better. I actually am feeling frisky for my hubby even (who by the way will be having a vasectomy in the next couple weeks & was fully supportive of me doing this). I am so disappointed as I LOVED the no period thing, but I am not willing to risk my well-being over that!

My husband was taking coumadin and then developed an infection. He was ordered Bactrim D.S twice a day and by the third day he was bleeding in his brain. He had to have bilateral subdural crainiotimies twice to flush out all the blood in his head. He almost died. He now has severe headaches and some short term memory loss.

I take a combo of Zoloft and Klonopin for anxiety. The medication helps control my anxiety problems, but now I suffer from severe headaches, upset stomach and weight gain. The biggest problem was my headaches. My Dr. suggested stretching exercises for my headaches and stiff neck. The stretching seemed to relieve my overall headaches, but would a trigger spot for an incredible flash of pain when I turned my head a certain way. I've found that resistant pressure seemed to help tremendously.

For example: If my headache was in a specific place just behind my left ear, I would place the heel of my left over the pain and push my head towards the heel of my hand and hold for ten seconds. If it was general tension in the back of my neck that is causing the pain, I would place the heel of my hand on my forehead and push my head toward my hand and hold for 10 seconds. Repeat as necessary. Hope this helps.

I see there are a lot people suffering from headaches so I thought I would share what kind of works for me. Does anyone else have any "works for me" stories?

I just turned 60 and thought all my aches and pains and cramps were due to age, but having read these posts, I believe it is the Januvia that is causing my problems.I am a type II diabetic. After taking Januvia for less than a month, I have been having trouble sleeping more than 4 hours per night. The back of my neck is stiff and hurting. Both my hands and in particular, my fingers are numb and tingling. I'm experiencing cramps in both legs and stiffness all over. I've had to force myself to stand up and walk. I have severe heartburn (something I've never suffered with). I, too, have absolutely no sexual desire.About two weeks ago, a lump about the size of a dime has formed on the cartilage on the front of my neck, just below my chin. My doctor says, "We'll just watch it." I just feel rotten! I am stopping this medicine today. I hope these side effects have not done any permanent damage to me. I'm sick of these doctor's using their patients as test subjects for new drugs! I'm definitely changing my internist because this is one of many instances where the drugs I have been prescribed have caused me extremely miserable side effects. Where in the world is a doctor that believes in improving his patient's health or curing the illness rather than "PRACTICING" Medicine and pushing drugs!

I found this page after searching for info about Helioplex and rashes.

I used Neutrogena Ultra Shear SPF 70 both last year and the year before without any problems. I have also used the moisturizer with Helioplex without any problems either.

However, this year the stuff has broken me out in the most terrible rash, both on my neck and on top of my wrists. Strangely enough I can smear the stuff on my face and no rash results, but this is really affecting my neck. It's itchy, scaly and looks a lot like hives.

I really think there is something up with this stuff - the fact that it didn't affect me until now suggests to me that perhaps it's changed my skin somehow over time. I wonder how many complaints they get?

I have been on generic Wellbutrin 150 mg for 3 weeks for PMS. The first week I had some strange side effects: heart racing with light-headedness, constant yawning, weird sensation at the back of my neck. They all went away and I felt fine.

However, I stopped taking it 3 days ago because of the severe cramping and diarrhea. My doctor warned me I would have stomach issues the first week - and I did - but now I have it the day after I have an alcoholic drink. So anytime I have a drink, which is several times a week, I have to expect spending an hour in the bathroom the next day. Not even Imodium can stop what's coming.

Sorry, but alcohol trumps WB. Too bad too, because it increased my sex drive and suppressed my appetite.

I have been taking Bupropion XL 150mg ("generic" Wellbutrin) once a day as a mood stabilizer everyday for exactly 2 weeks. I suddenly developed severe itching in random different areas on my body. My lower scalp, palms of my hands, and ankles were the first areas that itched but did not have any obvious marks on the skin as to what was causing it. About 3 hours later it became progressively worse and started showing tiny red raised areas in the previously stated places on my body and started to spread to my neck, wrists, mid-chest below my breasts, behind my knees, and upper thighs near the front panty lines, but even worse on my lower back.

I was becoming a bit scared and annoyed by the constant itching and the hives that were forming in those areas. I had never in my life had hives before. The bottoms of my feet were so itchy but they did not have any hives on them, they just itched! I took 2 benadryl and tried to sleep but woke up quite a bit during the night because of itching.

By morning, the hives were worse and especially on the back of my neck where it was swollen and red and I could not even bend my head back. My face was slightly swollen and my eyes were puffy as well. My right palm was so swollen and painful and I could not make a fist.

I called my doctor but he was on vacation, so I had to talk to a message service he had set up in his absence!
I went to the emergency walk-in care center near my home and was evaluated by a physician who concluded that all this was actually due to the Wellbutrin which I myself found hard to believe and wanted to deny it in my mind. He ordered me to stop taking it and prescribed all sorts of drugs to counteract the hives and itching.

I am writing this only about 9 hours after seeing the emergency physician and have had some rest and taken my prescribed medicines, Medrol ( a steroid-type drug) to treat the swelling, Hydroxyz hcl for the itching, Allegra for allergy, and Zantac for the side effects (stomach pain) of all these drugs I now have to take for a while!
The swelling has gone down a bit and itching has subsided somewhat. In conclusion I must note, that it was the pharmacy's decision to substitute the Wellbutrin my doctor had prescribed with a "generic" version (bupropion) that is still so new to the market and is still undergoing studies on human subjects. We are the guinea pigs and did not even know it.

I have taken Lamictal for 2 years now, I increased my dose a few months ago. It curbed my rage issues, and continued to stabilize my mood swings.I have had the side effects of some memory loss, problems recalling things in the past, minor things, like what happened in movies I may have seen in earlier months. I have hair loss, more than usual when not on the drug. I have definite speech issues, I can never relay what I am trying to say. I feel stupid. I am consulting another psychiatrist to discuss the side effects. I really don't like not being able to remember things as much as I did before I took this drug. I really, really don't like the lack of the ability to speak fluently or even to get the words out. It is embarrassing, it makes me look almost like I have a mental retardation. It sucks. I also am disappointed that my spouse seems to think all "our" issues are because of my mood disorder and if I somehow when I disagree with him and want to address these issues, then my medication is not working. I know if I am raging more or if I have an increase in anger, then I need to go on higher meds or change meds. But, as my psychiatrist said to me, not all my issues in life are all my fault.
Generally, lamictal is working, but I would like to have a greater memory recall and I would definitely like my speech problems to be resolved and it sure would be nice if my hair would become thick again.Also, I have some twitching problems occasionally, it is annoying too. I still have racing thoughts and panic attacks too, it has not changed those issues. Oh, and another side effect is headaches in the back of my neck at the top where my head meets the spine, they are annoying and if I take ibuprofen, I get even more stupid and spacey, almost like I am checked out. My older kids notice more than my spouse does. My older kids also let me know when I am raging more, in a better way than my spouse does. My advice, let those whom you can trust be the one's who give you feedback on how you are doing, rather than someone who doesn't want to take ownership for their own issues, that way you can truly trust if the med's are working or if they are at the right dose. This along with your psychiatrist's help and help from family and your own assessment will keep you on the right track.

i've been on bactrim dm for about a week now (2 doses/day for 14 days) for a possible MRSA infection (should know the results tomorrow...hopefully). about 2 or 3 days into it, i felt extremely lethargic and achy (all my joints were sore and almost 'warm'). woke up in the middle of the night a few days ago with my entire tongue feeling numb and the base of my skull hurting like hell and my lymph nodes on the back of my neck swelling and sore to the touch. since then, i've had chronic pain in this area. after reading some of the posts here, i decided to stop my dose until i could speak to my doctor since i wasn't able to speak to him yet today, i decided to resume bactrim until i can get on something else. it's a terrible feeling being trapped between treatment for a potential MRSA infection and stopping treatment because of the possibility of serious side effects. i just took another dose moments ago and am honestly worried i've made a mistake. but what choice do i have when faced with the possibility of an infection that is also very serious? i can't do nothing...

i honestly don't have a lot of options with a MRSA infection...i see people on here mentioning cipro or levaquin, but these also have tons of posts on here about crazy side effects.

this past week has been a living nightmare...

i hope those of you who have experienced such terrible problems with bactrim will find something that helps you...

This site may have saved my life! My blood pressure & cholesterol meds were changed last Sept., and like Virge, 3 months later I had a severe vertigo attack (while driving). Long story short, I have been a wreck ever since...feeling dizzy & faint, anxiety attacks, spiking BP, acute insomnia, soreness in the back of my neck, overly sensitive to bright lights and loud sounds, and several reactions to anti-anxiety meds & vitamin B pills (some of which placed me in ER!).

I've seen over 20 different doctors & specialists, and NOT ONE has ever questioned the Simvastatin. A couple weeks ago, I Googled Simvastatin & vertigo and saw that vertigo was listed as a side-effect...then I saw the notes on this site. This prompted another visit to my doctor.

I've been off it ever since, and have noticed a substantial change for the better (I can sleep well again!) - although I'm still always dizzy and my BP has risen. I'm hoping that by taking it for so long, I haven't incurred any substantial long-term side-effects! I'm also wondering why some of us react so negatively to the drug - if there is another underlying medical condition that would cause such an adverse reaction?

I am a 72 yrs old female. Put on Lisinopril-HCTZ 10-12.5mg 2 yrs. ago. Took Cozaar until drug provider (AARP) wouldn't pay for and told my doc to use Lisinopril. For a while I was ok...then the trouble started. Nausea, dizziness, headaches and swelling of legs and feet. All slow to happen. Then shortness of breath, cough and itching. Leg cramps got me up pacing and in agony several time nightly. Had a creepy feeling in the back of my neck, joint aches, tiredness, stomach PAIN, hot tingles in feet and toes late in the day. Slight weight gain, a runny nose and sneezing in the AM.. Hot one minute, cold the next. At some point I realized I had a feeling of ill-health, a def. loss of my usual feeling of well-being. I was edge, nervous and finally got depressed enough to call a psychologist. That's when I found this web site. Therapist told me to tell my doc and maybe get another BP med. instead of L. Ten days ago I stopped taking it and went back on the Cozaar...I will pay for it myself. I just want to feel good again. The mental anguish this drug has produced shouldn't happen to anyone. Also, I shouldn't have to find a web site that tells me I'm taking poison either. Last night I slept straight thru the night w/o awaking. First time in God knows when. Still some nausea but I can tell the effects of Lisinopril and lessening. Take hope all u people who have posted here...I think it will get better for you now that u don't take that snake juice anymore. I think it's good that we all stopped it before we started slithering through the grass of our front lawns. This too shall pass. Thanks for posting here for me so that I could finally feel good again. I owe you a huge debt for my sanity.

I am 49 yr old male and was diagnosed with a severe upper respiratory infection. Was put on Prednisone for 20 days. I never did experience depression, but I did experience the hyper state and was full of energy big time. It was actually nice ...had felt better than I had in a long time. Two of the side effects that I have been experiencing is sweating a lot more than normal ... I mean just the littlest of exercise and my shirt is soaked. Also my back and the back of my neck has broken out with acne ... that really hurts. I am using Desoximetasone which is a prescription cream and it has almost cleared all my acne up. I was about 250lbs and lost to 235lbs in the twenty days I was on it. I never changed my eating habits ...weight just fell off ...... man I wish they could put that it another pill without all the side effects. Now that I have been off for a couple of weeks ...I have gained some of the weight back ... but I'm really trying to change my eating habits and get back to 235 and go lower.
I wonder if everyone posting would also put their blood type on their comments. There are so many different opinions of Prednisone ...there has to be a reason why you have so many effects for some and very little for others. I did research this drug while I ws taking it and read that if you take it for longer than 30 days that your body will stop making the natural prednisone that it makes. Thats why you hear when people take it for long periods of time ...you are destined to take for the rest of your life.
As far as lung condition, I can breathe again and I think I'm totally cured ... I have a follow up with my lung doctor next week.
My prayers are with you guys .... I agree .. I don't think I want to take Prednisone ever again. My blood type is AB+

Hi, I just got the Mirena back in April and I have had nothing but problems from the get go. First they had trouble inserting the Mirena so instead of 5 minutes it took more like 20 minutes....by the time they got finished I started sweating really bad. I went to stand up and almost passed out. They laid me on a bed, put an ice pack behind my neck and gave me water. They checked my blood pressure and it was VERY low. 15 minutes later my blood pressure still wasn't coming back up so I was not allowed to leave. They started telling me that some people's bodies go into a form of shock and that was probably what happened and they were worried about my blood pressure not coming back up and possibly having to take me over to the emergency in order to get my blood pressure back up. Well about ten minutes later they finally get my blood pressure back up to normal so they finally let me leave their office. I get out to my vehicle and all of a sudden I feel like I am fixing to pass out again. I laid down and called a friend to come and pick me up. I kept an ice pack on the back of my neck for another 30 minutes while resting before I finally felt better again. A couple hours later came the pain. Very bad pain that lasted for the next two weeks and I am usually a person that can take pain. Finally the pain eased up after that and now I only get pain once in a while but here I am 3 months later and I am still bleeding. I feel tired all the time, I've had a lot of migraines, it is painful during sex sometimes, my sex drive has almost totally vanished and my energy level is almost at 0. I have also been experiencing stomach problems and a bloated feeling. I am EXTREMELY tired all the time. I never feel like I get a good nights sleep. I have also been experiencing hair loss but I didn't know if that was from the Mirena or not until I started reading posts on here. Now my bleeding is slowly getting worse the past few weeks. Not only am I bleeding still but now it is coming out in little clots too. Now I am getting worried so I have made an appointment to go back in. I came on here hoping I can find someone that has had the same problem so I wouldn't have to worry until the appointment. Its really disgusting and I am so sick of having this mirena in already.

Good luck to those of you that haven't already experienced these same side effects already......

I was prescribes Levaquin 500mg for 10 days for sinusitis. On the second day, I woke up with a migraine and took Aleve. The headache accompanied by dizziness lasted 10 days or so. As time has passed, I have pain in my right shoulder and bicep and stiff/swollen joints in the back of my neck. It has been 4 months since I took Levaquin and my symptoms have only gotten worse. I have been on bed rest for a week just after a simple 5 minutes on an elliptical machine. Additional problems along the way have been anemia, my vision got extremely worse with retinal degeneration, anxiety, diarrhea, fatigue, irritability, and numbness in my hands and feet. My doctor says he believes me but mentioned fibromyalgia. My symptoms don't even fit that disease. Friends don't believe me either. I am a pharmaceutical rep. The FDA needs to pull this drug off the market. Why won't they do it? Someone has a connection someone. I am almost 31 years old and I don't know how much more my body can take. I miss my friends, tennis, and even normal daily tasks like opening a car door and sitting for an extended period of time. DO NOT TAKE LEZAQUIN EVER.

I've started taking this medication for a week now for a bad case of sinus infection. Its so bad the doctors say it is backed up in my head and isn't draining.My eyes get really red, migraines and headaches causes really bad pressure in head and I also have fluid in my ears. I guess this is why it was prescribed to me. I woke up one morning and my face was all swollen on the left side of my face and my lymph nodes in the back of my neck are all swollen for about 3 days now(looks like lumps in the neck). Anyway, I decided to leave the house for one day since I started taking this SMZ-TMP DS, I ended up catching hives throughout my body and got tingling every day after that. I read the bottle and it says Do Not be EXPOSED to excessive exposure to direct and/or artificial sunlight and it was quite sunny that day. I don't know if my meds are working but I think I will be seeing another Dr. to change to another medication.

Hi
I started taking 10 mg. daily ofLipitor 8 yrs. ago and about a year later I was diagnosed with Fibromyalgia. There's no test for Fibro, just blood tests to elimate everything else ex: Lupus, RA etc. I've been suffering so much from muscle pain, all the tender points as in Fibro and also diagnosed with chronic fatigue syndrome. Three doctors diagnosed me with Fibro. and chronic fatigue. I had most of the symptoms everyone else is complaining about also. The pain in my stomach muscles are just about gone too.

It reached a point three weeks ago when I was having sharp pains all over my body and muscle cramps and charlie horses at night and I could just about walk up the stairs my hips hurt so much that decided to stop Lipitor. I was so tired all the time and in constant pain.

My doctors said it couldn't be the Lipitor. The pain in most of the tender points are just about gone but I know it will take a while to get out of my system. I lost muscle strength over the years and hope to get that back. I'm 64 years old and know it will take awhile .

I went to my doctor Tuesday and told him I took myself off the Lipitor and that I now remember being diagnosed with Fibro shortly after going on Lipitor. He got so mad at me and said that Lipitor doesn't cause a disease. As I said there's no test for Fibro and it's not a disease it's a syndrome or condition where the brain sends pain signals to the tender point muscles but there's nothing actually wrong with the muscles. I told him that 6 years ago when I tried going off Lipitor for 3 months and joined a gym, Curves, I felt fine and thought I was in remission. Then when I started taking Lipitor again I couldn't do the exercise in Curves and had to stop going. It never dawned on me it was the Lipitor.

I now have a problem with my heart, one condition I might have been born with but the Arrthymia I don't know about. My heart beats too many beats and it beats 4 beats and the 5th beat is backwards. Now I'm on 25mg of Topricin (the generic) beta blocker to slow down the heart beats. I don't know if this is caused by the Lipitor or not. My cardiologist said that Lipitor can affect every muscle in your body and she suggested that I get a RX for a blood test to tell whether I have muscle damage. I went for the test Tuesday but haven't received the results yet.

I'm going to change doctors, I don't like my doctor's attitude with me over the Lipitor. These doctors think they're God. When I told him on Tuesday about the 3 months that I felt fine 6 years ago he said that there are other drugs besides statins to lower cholesterol. I don't want to go on any drugs and the non statin drugs can cause intestinal blockage, he got upset when I told him that too. I'm going to try to lower it with flaxseed and fiber and see if that works. I go to Weight Watchers and kept 17 lbs. off for 6 years now, I do try and eat healthy.

I can't believe it cost me almost 8 years of my life in pain. It's even hard for me to get down on the floor with my granchildren, I have to crawl to the couch or chair to lift myself up and I get tired so easily. I just hope I get back to normal.

I'm so glad I found this website and figured out what was wrong with me. I hope my writing helps someone else dignosed with Fibromyalgia and taking a statin.

Thanks for listening.
Marie

I have been on Levaquin for 5 days and have had an ache and tightness in the back of my neck since the first day. I have slept very poorly for the last three nights and over the last two days have developed significant chest pain..feels like the muscles in my chest and upper abdomen are in a constant contraction. I went to my internist yesterday thinking it may be an unfamiliar type of asthma attack. I used my inhaler on the way and blood oxygen was fine when I got there but the chest pain continued. I was given a chest Xray and an EKG, both of which were fine. My doctor did not feel that it could be the Levaquin and advised me to continue it. The contractions in my chest have continued, almost crushing at times. The neck pain has been continuous. I am stopping the Levaquin and willing to risk having the infection return.

I have been taking Lisinopril 40mg.for about 4 months now for high BP. It works very well for the BP issue. Since I have started taking it I have had the dry cough, but its not so bad that I would have change anything because of the fact that it IS helping my BP. I have also noticed that I have been getting the numbness in my arms mostly my left. My Nephrologist mentioned that its Steal Syndrom caused from my Fistula Creation (dialysis access). After reading these posted side affects I think its from Lisinopril. ALSO, in the past 2 months I have been getting acne. First thought it was from my diet, but I have not changed anything in my diet. Its almost like my body is trying to get rid of something in my system. This is not the ordinary acne problem, this is on my face, back of my neck(hairline), on my shoulders and back. The "acne" gets very bad and when I get something out of the sores it has a very strong metallic type smell. Also, I am experiencing the itching, which has been getting worse the past few days. As of today I will NOT be taking any more Lisinopril. I am certain Lisinopril is the cause of all of my problems. Has anyone experienced acne from this product??

Thanks,
Shawn
36yo, Minnesota

I took Yaz for 1.5 weeks. The day after I started it I broke out into a rash that I thought was poison ivy. It wasn't...it was the YAZ. I immediately stopped taking it. That was a month ago, and I still have my rash. I've been on 3 different steroids and 2 different anti-histamines. Still have the rash. Is anyone else having this problem?

I've been on Lamictal for the past 2 years. I had suffered from depression from the age of 15, which was subsequently diagnosed as bi-polar at age 37 and treated with Lamictal at 39. I started on 25 mg increasing to 100.

It literally changed my life. I felt completely normal, without having lost my personality and didn't have these huge ups and downs. My short term memory, which was never very good, has become worse.

I have now got a rash. This maybe because I was feeling so great, that I didn't take my tabs for a few days, then resumed at my normal dose.

I have moved and so am no longer in contact with the doctor who prescribed this to me. I just can't bear to go back to the space I was in before I took Lamictal and am going to try starting at a low dose and building up again.

Good luck to anyone trying this. For my bi-polar condition it literally changed my life. I was never really happy before, and I can say that i am often content these days, and positive.

about three months after taking simvastatin I had a bad attack of vertigo and have been suffering with dizziness & feeling off balance, also panic attacks have ocurred, I did not experience this before taking this drug. This has now been going on for 4 months. has anybody else experienced this.

I just found this site and I decided to respond. I have been taking Singulair on and off for about 5 or 6 years. When I first started taking it, it seemed to help my asthma quite a bit. I didn't notice any side effects, but then again I was taking a few other meds that I thought might be a culprit. I hadn't taken the Singulair for about 6 or 8 months because everything was going good. About 2 months ago I began having a few flare ups, so I thought I would go back on the Singulair. Now I am 57 y/o and been on most of my meds for about 10 years or so. When I added in the 10 mg dose of Singulair before bedtime, I began to notice dramatic side effects. Along with the more vivid dreams, in the first few days I noticed when I awoke I was real tired. Now that is unusual because I have always been an early riser and ready to go. Some days I felt like I didn't want to get out of bed. As the days went by, I noticed that I was waking up a lot at night and had a constant "hissing" noise in my ears. The noise would last thru the first few hours of the day and subside. In the last week or so, I began to awake with horrible headaches. The headaches started in the back of my neck and migrated to the top front of my head. I am not a headache person, so these are very unusual.

I have also noticed small painful bumps on my scalp. There has been a noticable thinning of my hair as well. I'm not sure if it can be attributed to the Singulair or just being old!

I will be going off the Singulair as of today to see if all these symptoms disappear. I will post a response in a week or so.