Terror symptoms and conditions

I started Wellbutrin XL about a month ago. I had a lot of trouble sleeping after about a week. I didn't feel tired at all. I just saw my doctor a few days ago and he switched me to Wellbutrin SR. He said that it doesn't stay in your system as long so I should be able to sleep. Has anyone tried this? Let me know. Thanks!

My son is 7 years old and was put on singulair for his asthma and allergies, my daughter who is 10, had been on it for over 2 years.
My son started experiencing, night terrors, out burst of crying, difficult to make decisions.
Anxiety attacks, panic attacks, did not want to go to school. After seeing his Doctor it was suggested that we pull him off the medicine. We started noticing changes within a few weeks. Please watch your child closely if on this drug. My daughter did not have side effects however we have taken her off this medicine also.
I would really be careful with this drug. Our family was in complete terror, watching your child struggling like this. USE CAUTION, IF YOU DECIDE TO TAKE THIS MEDICINE....

I was 50 and the doctor prescribed lipitor 10mg since my cholesterol had doubled in the past twelve months to 300. I took it for four months and began to have pain in one leg just below the knee. I had talked to a woman about 65 years old once who was walking on the sides of her feet and I had asked her what medical problem she had. She explained that her Lipitor had caused this terrible pain. You would think that I would have refused to take this drug. You see the doctor had already prescribed a very large dose of fish oil per day and the cholesterol had not fallen. However, I began taking it. About two weeks before my enzyme checkup I began to notice the pain in the leg just below my knee and I stopped taking the Lipitor. I expected the pain to subside, but it did not. My cholesterol level had risen and my doctor asked me if I was still taking the Lipitor. I explained that I had been of it for about two weeks. The doctor insisted that the pain probably wasn't associated with the Lipitor. The reason being my enzyme level was within the range of acceptable. I began taking it again. The doctor wanted to have another test within four weeks to check enzyme levels again. This time the enzyme levels were borderline high. So the doc recommended stopping the Lipitor for a while and then another enzyme level check. You see, my body was telling me something. The only new factor in my medications other than blood pressure was the Lipitor. It has been about three weeks since I stopped the Lipitor, yet I am continuing with even more pain in tops of feet and above one knee a know seems to have appeared. It is sore and feels like it is bruised. I am not a doctor, but I had done some investigating Lipitor on the internet and read that in some patients the Lipitor actually causes small to large fissures in the arteries of the heart. Also, the muscles begin to attack themselves, thus the pain and atrophy. I am going to start taking flax oil. One cardiologist reported that he two cases a week of heart attacks due to Lipitor. He was enraged that Lipitor is still being prescribed and manufactured. I just hope it doesn't take years to regain my original self without pain. I am an active person who likes to work outside, garden, snow-ski, and anything else I want to do. I am trying to search for a detox program for Lipitor overdose, not that I have overdosed. According to my body's signals, I have overdosed on a toxic drug. I pray that returning to normal won't take as long as I have heard some people say it has taken them. Please try some other alternative to Lipitor and the other debilitating statin drugs. I will have to start an exercise program, even though I have put it off for years. I hope my laziness about my physical fitness hasn't crippled me for life. I am 20 lbs overweight and never took it seriously. I hope others will discontinue to take this life-threatening and debilitating drug!!!!!!!!!!1

My brother passed away at 56 of a stroke. So after having my blood tests done, everything was high, cholesterol, CR Protein....doctor put me on 20mg of Lipitor....the very first day, I had severe muscle weakness in my upper thighs, back of my calves, pain in my knees, pain in my wrists, pain in my fingers. What a nightmare. I tried it for two more days, called the doctor told him, he said reduce the dose in half........not a chance, I told him I believe in quality of life, not quantity of life. I'd rather be dead, then live like that.......and yet the doctor didn't tell me to get off of Lipitor!!!

My son is 3 and has been on Singulair since around springtime (I think... I've lost count). Anyway, during this summer we noticed his behavior had just gone straight to hell. At first I was attributing it to the wonderful world of the three year old, but it was just getting ridiculous. He was having countless meltdowns, screaming bloody murder (I mean SCREAMING to the point of going hoarse), hitting, punching, slamming, banging, crying hysterically for ridiculous reasons, yelling out during the night, and showing OCD behaviors. I was fearing that he might have ADHD/OCD until my husband stumbled upon this website. I remember hearing stories about teenagers having horrible side effects from singulair, but didn't think it was affecting my son at 3. As I read the entries on this website I felt like they were talking about my son.

I am taking him off of it to see what happens, but now I'm nervous that his asthma will flare. He's had quite a few asthma episodes since the fall allergy season has started. I suppose he'll need to go for awhile to get everything out of his system to see if the behavior changes, and then I hope to find a new preventative. We have Pulmicort and Xopenex and an inhaler ready!

*UPDATE* Well, it hasn't quite been two weeks since I've taken James off of Singulair and - I am not kidding you - his behavior improved the FIRST day. I want anyone who reads this to know that I am not an "alarmist", I DON'T freak out over everything I read, I do a lot of research (kind of obsessive myself :), so please understand that I am not one to usually write things like this...I mean, I pushed my allergist to give it to him in the first place! There are plenty of kids out there that are fine on Singulair, but some are not. I didn't make the connection to the Singulair since the average three year old is irrational and unpredictable anyway, but I KNEW something wasn't right. It wasn't just tantrums and whatever, his overall personality had done a 180. In the last two weeks my son has returned. He still, of course, has three year old moments, but he is back to the caring, loving, curious, excited, social, happy kid I had last year. One of the worst things we were seeing two weeks ago was bedtime behavior. BAD OCD behaviors - everything in his room had to be PERFECT. The curtains couldn't have a peek of light shining through, there could be nothing on the floor, everything had to be in order. He would obsess about things (creatures) coming into his room, when we would say goodnight and close the door he would scream and cry like someone was stabbing him and was petrified. The FIRST night that we stopped the Singulair he laid his head on his pillow, said goodnight and went to sleep. Please keep an eye out for personality changes in your kids.
*November update* it's been almost two months since we took James off Singulair and we haven't seen ONE BIT of the horrible behavior that we had w/ the Singulair! Normal "three-year-old moments", but no return of the "devil child", no OCD, nighttime freak-outs, violence, or any of it.

I commenced Lipitor 14 years ago at age 47. At that time I was a regular tennis player, walker and generally fit for my age. No problem with Lipitor for the first couple of years until I began to experience hip and low back pain. My GP diagnosed arthritis. Gradually became worse and I started to gather injuries (over stretched ligament in right knee which refused to heal, plantar fasciitis twice) My back pain became far worse, I persevered with tennis believing that exercise would help. I began to "trip" on the carpet and going up stairs (foot drop). I was sent for a CT scan in 2002 which showed spondylolisthesis and root canal stenosisss. On advice from doctor I stopped tennis. Referred to a neurosurgeon who after several months carried out a laminectomy in July 03. Cleared to recommence exercise in December 03 which is when my nightmare commenced. I developed bursitis in one hip, stopped walking until it settled, then excruciating pain in feet, and then bursitis in the other hip and continuing foot pain. I developed rib/back pain, again diagnosed as arthritis even though I felt the pain was muscular. I had one session of aqua aerobics and woke the next morning with plantar fasciitis which continued for 3 months even with doctor, physio and acupuncture treatment. I was then referred to a Spots Medicine Dr who ordered bone scans/x-rays which revealed a stress fracture in my foot. In 2006 I began to notice that my right arm had a tense feeling all the time, I had a loss of dexterity in my right hand which assumed a claw like appearance and my normally neat handwriting became practically illegible. My physio recommended I see a Rheumatologist who said I had "no more arthritis than I would see in any 62 yo", he sent me to a Neurologist who after 5 mins diagnosed Parkinson's Disease. Within 7 weeks of commencing the PD medication I was experiencing Restless Leg Syndrome every night. The neurologist said that my condition had "progressed" and increased the medication - twice. I was then getting RLS DAY AND NIGHT and getting no relief OR SLEEP!!! Finally after 12 months misery my GP suggested that I try coming off Lipitor to see if that was causing my body pain. Within 6 days I felt better, my muscles became less stiff and relax. I went back to my Neurologist who refused to accept my claims, he insists I still have atypical PD (because I do not have tremors). I told him the cure is worse than the complaint and against his advice I weaned myself off PD medication and Lipitor. It was hard going but I NO LONGER SUFFER FROM RLS AND MY DEXTERITY IS SLOWLY IMPROVING. I still have dexterity problems with my right fingers but the tense feeling in my right arm has gone and my "claw" hand is starting to relax My muscles feel bruised all the time. I am still taking my blood pressure tablets and 150mg of Co-Q10 a day. I have been off Lipitor 9 months. It has been a painful journed for the last 8 years and a nightmare for 12 months. My GP has marked my records as "allergy to statins" but says she just doesn't know if I have Parkinson's. I know that I will never take this awful drug again. My cholesterol has skyrocketed but I will have to try and lower it naturally and take the risk. I constantly feel like I have worked too long and hard in the garden, all my muscles are so sore. I really need to know if this damage is permanent and if this drug has caused Parkinson's Disease itself or just PD like symptoms. I guess I will just have to wait and see. I don't think doctor's believe us when we say Lipitor is doing damage to thousands of people. They love it!! When we are aging we are not surprised to get diagnosed with arthritis and this is why we take this medication unwittingly for so long.

Wow! I can't believe what I'm reading. My son just turned 5 years old. He was put on Singular when he was 2 years old because he constantly had sinus infections. For the past year, I've just used it off and on when he starts to get stuffy. He is very well behaved, but has has trouble with nightmares. He just told me a few weeks ago that he knows that monsters aren't real, but he can't get them out of his head. I know people think I'm a softie because I let him fall asleep with me every night (his dad puts him in his own bed after he's fast asleep), but he is petrified to go to sleep by himself. I didn't understand it, but I could see the terror in his eyes. It all makes sense, now. Sometimes he plays so well by himself in his room, but other times he doesn't even want to go to the bathroom by himself because he's scared. I'm betting he was taking Singulair during the times he was scared to go into the bathroom himself. Unbelievable. We have to get the word out about this drug. I feel like such a horrible parent for not searching for these side effects sooner.

I came to the website to see if Singular suppressed the immune system because he's been getting horrible cold sores in the fall for the past 3 years. It seems to correspond with the time he started taking Singular. I know that Singulair can't cause cold sores, but if his immune system was suppressed, his body can't fight off the virus. 80% of us have the virus that causes cold sores, but most of our immune systems are able to keep the virus in check. During a cold or other illness which compromises the immune system, cold sores can pop out.

In any case, I've already flushed the remainder of his pills. He's also complained of stomach and leg aches. In fact, the docs made him give-up milk thinking he was lactose intolerant but it didn't help the stomach aches. Hopefully giving-up Singulair will help his tummy aches, too.

I've been on Levaquin for only 2 days, combined with Prednisone... Taking them due to a nasty sinus infection. One of these two meds is making every joint in my body hurts, as well as me having lost almost every bit of my sense of taste. I ate general tso's chicken today for lunch and could not taste anything, so as an experiment I ate one of those little red Chinese peppers that I normally throw out because they are WAY too hot - I couldn't taste a thing. Last night I had to drop the air condition down to 68 degrees as one of these two meds made me sweat very heavily and uncomfortably hot.

i was in the ER for what we thought was appendicitis. They hooked me up to the IV and within 2 minutes of the Reglan going into my body I started having a feeling of panic and terror I've never felt before in my life. I quick called my husband on the cell saying he need to come get me NOW! and I was so close to ripping the IV out of my arm, they had this blood pressure thing on my finger and the feeling of clautrophobia I had just from that and the IV being attached t ome was the most overwhelming paniced feeling I ever felt. Then, my whole body started uncontrollably convulsing. You can imagine how scary this was for both me and my husband, neither of us understood what was going on. The nurse gave me benadryl and the effects starting going away after about 10 minutes, at that point, my sanity started coming back and i literally could not stop smiling due to the relief I felt just coming back to normal. I still have panic feelings thinking back and remembering the experience. i can truly say it was horrific.

The nausea is tolerable, generally short-lived as long as I eat prior to taking the Chantix and drink plenty of water.

I have a sense of...fogginess....detachment, while at the same time, seem to sense clear hidden messages in the way people look at me, in what they're saying to each other, and to me. Yep, it's probably paranoia.

The nightmares are horrible. I dream specifics about deaths of loved ones, in horrible detail. I also awaken at least once a night gasping in terror, unable to get a breath.

The thoughts of suicide are strangely comforting and don't seem wrong at all. I'm depressed, but comforted knowing that I can end it if I really want to. Bizarre and I know it on some level at least.

I'm bruising easily this time. I mean REALLY easily. A small bump results in a hard, raised, dark bruise.

I developed a rash on my stomach that's been there for 3 days but seems to be clearing today.

This is my 2nd time taking Chantix and I'm 3 weeks in. I had the same symptoms last time and expected them this time. I'm smoke free but plan to continue with the Chantix as long as possible. The urge to give in and have one cigarette is too strong post Chantix. I tell myself everyday that the thoughts are NOT me, and that I can let them come and not act on them because it's the drug, not me.

I took my son off Singular a month ago, some slight improvements with the sleep and behavior problems. I voiced my concerns with my doctor twice now he looks at me like Im crazy and then he goes on the PC and says he cant find any of these side affects im talking about. My son was an appointment to see an allergist specialist.

WOW Where to start. My 15 month old Daughter was put on it for "SUPPOSED" allergies which she don't have... But that's a totally different story. Anyways she was put on the granules. After taking if for about 5days I noticed VERY Significant side effects IMMEDIATELY. She would NOT eat for anything in the world which is odd because my 25lbs 15 months old (Mind you she was only 5lbs 4ox @ birth) was a Pigglet lol She also became VERY Winey & Clingy...She also began to have "Night Terrors' and when I say Night terrors I mean the full blown ones last about 20 minutes or so and the first one scared me to death I thought my little baby girl had went blind. The terrors started about Night 2. We took her off the Singulair before I found any of these Side Effect write ups and of course AGAINST Doctor's advise however I put her back on her Claritin. Her nose is drying up and Congestion is gone after rushing her to the ER with 104.2 fever and got her on Anti-Biotics & Albuterol. (Still another story lol) We noticed the next day a HUGE Difference is her personality and she was sooo HAPPY again. The first full day off the drug she slept through the night in her own bed WITHOUT a terror or even a bad dream. IT'S A MIRACLE I proclaimed that I had enough common sense after only 4days to get that mess out of my Daughter's Body. Needless to say she is a piglet again here only about 5 days after taking her off the med. and happy as a 15 month old should be lol

It's 2 am on my 7th day of taking Levaquin. I was prescribed the antibiotic after being diagnosed with a UTI. I still have a UTI even though I am finished with my dose. I am awake not because of insomnia, but because I've had my 5th nightmare this week. This one was so bad I woke up screaming and crying. I went outside for some air to try to cool off. I still felt terrible anger for the people in my nightmare and really felt like I was ready for the psych ward. Finally it hit me, the only thing I've done differently this week is taking Levaquin. These nightmares are intolerable! One was understandable I suppose but every night two bad nightmares a night! And these aren't just "someones chasing you" nightmares...these are terrors! After figuring this out I would stop taking this right away if I wasn't finished already. No one I know will ever take this medicine, I will tell everyone of this crazy medicine.

I wrote an earlier post but I am now reading alot of your posts where you say your child experienced FEAR on Singulair. That is so interesting. When my son was on it for around 3 years he would never sleep alone in his own bed and he would have episodes every night that would last up to 3 hours at bed time because I would try to get him to sleep in his own bed, even at 8 years old. I thought he was possessed!!!! He would scream and fight me and I would literally have to hold him down to get him to stay in bed. It was horrible. I'm not sure how a hullicination would be described but maybe that was part of it. All I know is that he turned into a totally different child. It was something out of a horror movie. I eventually gave up and let him sleep in our bed cause it was exhausting. He would just make blood curdling screams and the terror in his eyes was horrific. Then the next morning he would be fine like nothing had ever happened.
Now that he is off of Singulair he will sleep in his own bed with the light off all night. It was an amazing turn around. He also told me he's not scarred anymore.. Who knew????? Has anyone else experienced anything like that with their child????

My daughter was on singulair for about 2 years, off and on. Being a teenager, we thought some of the behavior problems were just a "teen" thing. She became dispondent, wanting to sleep all the time. She was hateful and resentful towards her family. She became depressed and talked of suicide. I didn't know what to do. We sought depression counciling.
My mother called me to tell me of the news report she saw. It described what we were going thru exactly!!!
I would NEVER have dreamed an allergy drug could have taken away my loving child and left a terror in its wake!
She has been off the drug for a few weeks now, and I can see a HUGE difference in her behavior. She is getting back to her old self. She told me she didn't realize just how bad it was until she stopped the drug and now feels so very good (read normal!). How terrible!
Even as I am typing this a singulair comercial is playing on TV. How DARE they!
Money and lawsuits will not bring back the years our children have lost, but big companies only respond when "profits" are involved. If there is a lawsuit, I too want no money from it. I do, however, want the drug company to have to pay and pay dearly for what they have done. The money could go to a children's charity.
Maybe the drug company didn't know before, but they know now and the drug is still being sold!

I am a 32 year old sane woman with a degree in Psychology. I was prescribed levaquin for walking pneumonia. This is day 7, and I am in tears because I truly thought I was having a psychotic break for the past 5 days. My roller-coaster of symptoms include emotional instability, paranoia, violent thoughts, thoughts of hopelessness and suicide, overwhelming gloom, facial numbness, insomnia, and the feeling of tingling in my mouth and throat. I am going to stop taking this medicine right now, and I've already called my doctor. I just wish I would have linked this to the only medicine I'm taking much sooner.

I am going on day 4 of stopping my Effexor cold turkey. I was on 300 mg and taking 20 mg of Pexeva. I am stopping cold turkey after being on this medication for three years. The withdrawals are terrible, I don't know why any doctor in their right mind would ever prescribe this medication for anyone. I have those wonderful brain zaps every ten seconds, the only thing that momentarily makes me sane is food, as if the 30 pounds this medication has gained me aren't enough, stopping it is going to pack on another 30. I am a bundle of anger and rage directed at anyone within distance. I am at the toilet every night waiting and praying that I can just throw up. When I finally can fall asleep I am jolted awake in a puddle of sweat having just had yet another nightmare. And when I say nightmare, I mean the kind that have me screaming out loud in terror waking my husband. Minor daily tasks are ignored due to the fact that putting one foot in front of the other is too much to handle. I can't stand this feeling and only pray for the day that it will stop.

My daughter is a chronic asthmatic and has been on Prednisone for over one year. Since then she has experienced headaches, nausea, sleeplessness, depression, extreme anxiety, mood swings, blurred vision, aching... just about all of the side effects listed. Of particular concern to me are the mood swings, which at this time we are considering having her evaluated. I didn't realize that this drug could do soo much in terms of her behavior. Please help me to understand what is going on with her. She is 12 years old.

I was given levaquin 500 mg 6 days ago for phlebitis. Since I started I have had terrible anxiety, panic attacks, fear of dying, nightmares, crying jags, and very sore neck and shoulders. I called my doctor today and asked about the side effects of this medicine. I am NOT going to finish my 10 day dosage. I'm done. I've never been so miserable. This is strange because all this past summer I took low-dose levaquin, 250 mg 4 days a week because I have bartonellosis, a co-infection of Lyme disease. It didn't bother me beyond some leg pain then, but now it's a whole new story. I am TERRIFIED of this antibiotic and modern Western medicine in general.

I don't think my last post went through...my 22 mo old was given omnicef for pneumonia 2 days ago - the very first night he woke up screaming like crazy, lasted off an on for an hour or so, maybe more. He is NOT a sleep terror toddler and never has had sleep problems. The next day he did the same thing when waking up from his nap, the screaming and crankiness lasted about 30-45 min. It is now 2am and he's been doing it off and on for an hour again. My husband is with him and I am reading every one else's posts with the same effects on their kids. I just went over the omnicef website with a fine tooth comb - NOTHING on this side effect - it's rediculous. This is found on the internet by too many people making these middle of the night posts - i'd probably recomend they put a little more money into research and figure out what in the world is going on and why so many people are having the same experience. I'll be calling my doctor in the morning! He has also been really crabby since starting it - he'll just scream and 'freak out' at the drop of a hat - kind of like terrible 2's X 10 - and he was not previously like that either.

I think we need to change the name of this drug to
"Lipi-terror". It would certainly be appropriate.

My 13 year old daughter was diagonosed with asthma about 5-6 months ago. She was then prescribed singulair along with 250/50 Advair. Not even thinking about the meds being a problem my daughter has turned into a terror. The school has called a few times about behavior problems in school. Her grades are also dropping drastically. She has never had any kind of problems like this before. She is very angry, depressed,with many mood swings. I know that she is 13 but this is not normal. Her teacher reccommends she seek counseling as I agreed. Then I thought of this medication and wondered could this be the root of the problem? I called the doctor and he told me to take her off of singulair and see if I notice any difference in a week. It has only been 2 days so I guess we will see. This is really beginning to worry me. I want my daughter back.. If anyone has anything to share please email me at ****** Thanks, Cindi

Horrible Evil Nightmares!!!

The second night I took zoloft I had the most terrifying nightmare in my life. I woke up in the middle of the night in my bedroom with severe terror and then I felt as if I was possessed by Satan. I heard Satan's voice telling me to murder and eat my wife who was sleeping next to me. Then I began to attack my wife and tear away at her flesh, eating her alive and screaming and laughing hysterically. This seemed like it was going on forever. Then my wife woke me up. She told me I had been screaming in my sleep. I told her I had a nightmare where she was killed by someone. I love my wife very very much and I've never ever had a homicidal thought towards anyone, let alone my wife. This dream felt so real and frightened me so badly that I didn't take another zoloft again.

My son has been on Singulair since he was one. He will be four in September. No noticeable side effects and it has helped decrease the amount of asthma flare-ups. He continues to be a happy, intelligent child. I have a co-worker who's son, five years old I think, who experienced the same type of behaviorial issues in most of the posts involving children. Her son took Singulair for one week and became an instant terror. Thankfully, the medicine has been a positive remedy for my son but I am concerned with the long term consequences of using this medicine. I plan on printing this page and taking it with me to my son's next pediactric visit.

I started Lamicatal May 19th, 2005. I was warned by my doctor of dangerous rash and itching. If so, stop taking medication, call him if not too bad that I need to call 911 to go to the hospital. On my print out from the CVS pharmacy is clearly stated: Serious (sometimes fatal) skin rashes have occured while using this medicine. Immediately notify your doctor if you develop any type of rash. If this medicine is the cause of the rash, the medicine must be stopped. Even after stopping this medicine. It is still possible for the rash to cause permanent or life-threatening scarring along with other problems.

Possible Side Effects:
drowsiness, trouble sleeping, dizziness, nausea, vomiting, loss of appetite, muscle aches, double vision, blurred vision, fatigue, weakness, headache, shakiness, or clumsiness.

Symptoms of an Allergic Reaction include:
rash, itching, hives, fever, swollen glands, swelling of the lips or tongue, painful sores in the mouth or around the eyes, severe dizziness, or trouble breathing.

Symptoms of Overdose:
may include unusual dizziness, serve headache, unusual sleepiness, involuntary eye movements, and loss of consciousness.

I starting itching really bad the second day on the medication. To the point I had huge bruises allover me. I got a spurt of energy that I have not had in several years the second night but not since then. I can't go to sleep at night. Even taking 6 Tylenol PM and a Klonapin I don't get sleepy until around 9 to 100am in the morning and then I sleep all day long. I have started to have frequent headaches, suspious bumps around my mouth area. My muscles ache, too. It is Memorial day weekend so I can't call my doctor but I am going to on Tuesday. I have (MDD) Major Depression Disorder, Manic Depression, (TRD) Treatment Resistent Disorder. Nothing I have taken thus far has helped me with my depression.

Does anyone have first hand knowledge on ECT treatment? I am seriouly considering this procedure. I am desperate but I have no insurance or money because I haven't be able to work for 9 years now. This is the only thing that has kept me from getting the ECT treatments, is money! I have contacted every Talk show, hospital, clinical trials and no luck in finding free help with ECT.

Any ideas, guidance or suggestions would be most appreciated, I am dire to get help soon or I won't make it.
Sincerely,
Lost Hope