Horrible nightmares symptoms and conditions

i posted on April 27th, on April 23rd, i stopped taking singulair, so i am here to UPDATE. after i stopped taking this death trap of a medicine, i already am seeing changes. i actually am breathing better then i have the whole time i was taking singulair, i can sleep through the night, and no HORRIBLE nightmares. jsut some normal ones, if any. but i feel like all the problems it has cause on my mental stability are still there, im guessing its going to get worse before it gets better with that. its really hard. now, me and my mom are starting to wonder if i ever had asthma in the first place, or if my dr. some how diagnosed me while i had a slight case of pneumonia. because the first time i was tested i was only breathing 60% of air, and even the nurses said i should be dead, or in an emergency room and she never not once, checked to see how my asthma was for 2 years. i honestly feel like i have been robbed of my life. its so hard to know something so little and simple, can have such a evil effect on you. because if i didn't have asthma i have been taking singulair for 2 years without needing it at all. imagine what that could have done. now im just so scared to sleep, because im scared i wont wake up. everything in my life is suffering and i don't feel like i have the strength to keep living the way ive been, im so scared every second, i am constantly checking my pulse, and now its even worse because i stopped the singulair. i already sent something to the FDA, and all that, but i doubt they'll listen. someone asked me a couple days ago "aren't you glad you at least found out your not alone" and i said "no, no one should ever have to go through what im going through, especially little kids". i feel like no one understands truly how hard this is, because its just an asthma medicine. this killed my mind, my spirit. and i don't know if ill ever be the same care-free person i once was. im constantly scared of everything, i always feel like no one wants to be around me, i just don't know. but not he positive side, im also not as weak, or tired during the day. i can actually bend down or reach up without feeling like a 98 year old women. my body is doing a lot better. its just my mind i really want back. i repost in a couple days, and hopefully everything will be a little better. PLEASE DO NOT TAKE SINGULAIR. i honestly think that, if it doesn't effect you at first it will in the long run. even if its 10 years later, you will start to slowly see something happening. just don't take it. i don't want anyone to feel, the way i do.

J.

I am an 80 year old male----quite good health except for having right hip replacement since 1988 industrial accident---several months ago, my orthopedic surgeon told me the severe pain; again in right hip, required surgery to correct. I had that surgery about 3 weeks ago and it went well--had usual pain, muscle cramps, but nothing alarming---I also had a left knee implant 4 years ago, so I know what to expect. I was discharged from hospital after 3 days and seemed OK-----however, I developed a mild infection the the drainage area of the surgery, my Orthopedic surgeon said not to take any chances and prescribed 500 milligrams of LEVAQUIN---one tablet each day fro 30 days!!!!~the very first day I took Levaquin, I was very stiff and sore in muscles, arms, legs and the worst insomnia I have ever experienced---I took a SECOND pill next day because I trust my doctor-----I immediately began having HORRIBLE NIGHTMARES, anxiety and absolutely unable to sleep longer than an hour at a time.----I feel like some of the descriptions that people said about LSD---I thank God I had sense to stop drug and am cleansing my system---I pray I am more successful in clearing this poison that some others I have read about-------BAN LEVAQUIUN it is a deadly, multifaceted poison that damages, muscles, eyes, joints ------THE WHOLE BODY!!!!! B.

When i STOPPED taking zoloft (i think i skipped a couple nights by accident) i had the most horrible nightmares i've ever had, and they were quite vivid, 4 nights in a row and i had a great deal of trouble sleeping (mainly due to the nightmares). when i awoke, or thought i was awake, i experienced sleep paralysis for the first time in my life. so, ragtopbaby, you are not alone it seems. my doctor wasn't concerned, but she said it generally happens as a side effect of taking it; she said nothing of withdrawal syndrome, but at that point i had not realized i wasn't taking it (i might have been so tired at night i just was forgetting). however, even before i missed a few doses, some noted that i was acting almost too happy, like i was manic. occasionally this also led to difficulty sleeping but for the most part it was just quite clear that the medicine was working very well.

Oh, I forgot...wicked horrible nightmares! (Maybe this is why I sleep anymore?) Still, I swear its a wonderful drug.

Like most of you all I am on Topamax 100mg. I am a 27 year old female that has suffered from severe migraines for over 20 years that would last up to 2-3 days and completely debilitated me. I would bleed from my tear ducts from the extreme pressure and I would need to be in a quiet, cold, closed off room to be left alone until the migraine was gone to continue on with my life. It was ruining my life and taking over my day to day routine. I could never really commit to anything without the constant worry in the back of my mind about a possible migraine until I found Topamax. Now on Topamax I went from 4-5 migraines weekly to 1-2 monthly, it is truly amazing, however there is a catch. Although the medication is wonderful and I will never get off of it at the rate of success that I am at, I do have side effects. I have extreme tingling in my extremities, (hands, feet) along with my face. It feels like they are constantly asleep. I also have noticed the poor tasting carbonating drinks along with my taste buds changing with certain foods that I use to be so fond of. I also have a very smokey haze where it almost feels euphoric if I wake up in the middle of the night. I have horrible nightmares of people that I have not seen in or thought of in years, memory loss and spelling issues-all goes away after 3-4 months of uses. I had shortness of breath, however that subsides as well with the use of the medications along with several other side effects. I have lost over 30lbs that is along with diet, so I can't say it is all Topamax. I have noticed little nodules that have been showing up on my hands since I stared taking the medication that I am in ? about I have a call in to my neurologist to see if he has heard of any such thing. Other than that I love the medication, because if not having migraines is one of the side effects-lol I can handle the side effects. I hope that this will help anyone that might have anything similar to what I am going through. If you can shed some light on my nodule situation please let me know. Thanks

Im sad to find out all the problems people are having from levaquin. But now Im able to put 2 and 2 together because Im realizing whats been compromising my health. This is my second year with bronchitis and my second prescription of levaquin. I now believe its what has caused me horrible nightmares, suicidal thoughts, irritation, mental anguish, stress tendon/muscle pain in my arms and shoulders. I bent over to pick up my dog to help him into the car and I got a terrible pain in my chest. I thought I was dying. And I still have a rattle in my lungs after 2 weeks of levaquin so it has not helped at all. If anything it has caused me more problems that has opened the door for additional medications of unknown origin. I wish I could find a real witch doctor.

I first had botox 3 weeks ago- I had one bruise from an injection site, but that didn't bother me. The worst was the anxiety- I felt constantly anxious and irritable, and I had horrible nightmares every night for about ten days. it got to the point where I dreaded going to sleep.
Ten days later the symptoms were gone and I had a smooth forehead but still a wrinkle between my eyes. After a consult with another doctor, I was talked into more botox - I wanted a filler instead. After the 8th injection I passed out. They put bed flat and gave me the rest. last night I felt really tired, and today I am extremely weak. Hope its very temporary-had to call in sick , and waiting for a call back from the doctor.

No, I am not a drug rep,I am simply just being honest.Not everyone has a terrible experience from this drug. I am sorry that so many of you have had so many bad reactions,just like any medication it may not be for everyone,but it does work for some.

I have been on metoprolol since 1995, and I would love to get off it. I does cause horrible nightmares, and high cholesterol, blood pressure increased,
tingling and numbness in my feet, difficulty concentrating, depression, You name it metoprolol does it

My 10 year old was prescribed levaquin for a sinus and ear infection, he has been "dizzy and lightheaded" and started having "horrible" nightmares. That was only after 1 dose. I don't think he'll be taking anymore. Thank You for this website! :) very informative.

I suddenly had high blood pressure. I was put on a heart monitor for 21 days because I was experiencing frequent palpitations. I was given 25 mg Metoprolol ER the genic for Toprol XL on June 6, 2008. I had the usual symptoms extreme fatigue, headache, constipation,swelling, weight gain for the first month. I am 59 yrs. old.
The second month I started to have horrible nightmares, and headaches that would not go away. On Aug.12 while driving home I started to hear voices, had blurred vision and hallucinations. I was driving fast and screaming to make the voices stop.. I ended up in a parking lot. I was crying and for a minute I had a bit of reality. I called the cardiologist office and told the nurse what was going on. She said to immediately stop the meds because I was having a rare serious side effect. I sat crying for awhile and was able to call a friend to pick me up. I stayed at home for 4 days. The entire time my hands shook and my headache was horrible. It was one week before I was able to function properly.
I called my pharmacist and she told me that this drug affects the central nervous system. 2 % of 100,000 people have this side effect. I told her that it was not written on my paper with the prescription. She said that because it is so rare they do not have put it on. She printed out the side effects for me from her web site. A site that is only accessible to pharmacists or Dr.'s. My Dr. wants me to try Cardizeim now and I do not want to because I am afraid. I told him that the BP was down to normal but he still wanted to because of the palpitations. I was given the option of the Cardiziem or seeing and Electrical Man at the Cardiology office. As of yet I have not taken the Cardiziem. This is the first time I have read this web site and I hope that this information may help someone. I finally feel good again except for the rapid heart beat and glad to be alive.

I was put on Effexor XR 75mg two years ago. After about a year on it, i decided i needed a stronger dose, so I was increased to 150mg. I felt happier than I ever have, but about six months in I started experiencing side effects. I have very vivid dreams. When they are good dreams, they are wonderful, but more often they are horrible nightmares, the most vivid nightmares you will ever experience in your life. This is the only real side effect, but it is bad enough i am thinking about discontinuing the medication. I know that the higher the dose of a medicine, the more side effects there are. There were no side effects at 75mg, but i felt more depressed than at 150mg. I also sometimes have other milder symptoms, but I also have hypoglycemia, so I don't know if the effects are from the medication or just a sugar drop.

My husband has been taking Omeprazole for about ten years now. About nine months ago he went in for a endoscopy and the doctor said she wanted to increase the omeprazole of 20mg 2xdaily because of the acid reflux. Several weeks after increasing this drug, my husband began getting very depressed. He losted all interest in our business and started having severe mood swings. He couldn't sleep at night, screaming with cramps in his legs, heart palpitations, blurred vision, ringing in ears, hot flashes, headaches behind the eyes. Some night I thought he was having a heart attack. It only got worse, hallucination began and horrible nightmares. He thought I was putting drugs and poison in his food. and felt like the world was against him. He became very violent toward me because of the hallucinations. We went for a follow up at his doctor and she suggested a psychiatry. Of course, my husband refused because he felt nothing was wrong, it was everyone else with the problem. His attacks got so bad, it was happen everyday, all day. We have two small children and we decided to split up for the children sake. My husband left for a week and when he left he refused to take the Omeprazole. He called me during that week and said he has felt great, he was able to sleep, no anxiety. He said to me if you are not putting drugs in my drink and food..it's got to be the omerprazole.
Of course the doctors said it's not possible...he has been off these pills for 8 days and it's unreal how this symptoms has disappeared. He is still having some side effects and withdraws. I don't know how long this will be in his system but I hope it goes away soon. THIS IS A DEVIL DRUG. He almost took his life and my too over OMEPRAZOLE. My doctor recently wrote this drug for me but I will not take it... We would never know about how serious this little pill for heartburn was if we didn't research it. When you get this drug from the pharmacy, they only list some side effects and not the serious one...How many more people out in the world is dealing with this same problem and not aware of these serious side effect. This almost destroyed our lives. WE NEED TO TAKE SOME KIND OF ACTION, SO THESE SERIOUS SIDE EFFECT HAVE TO BE LISTED..

My 13 yr old daughter was put on Singulair along with Asmanex and Clarinex for her asthma about 6 weeks ago. Everything seemed to be going very well at first and her symptoms were starting to get controlled. I started noticing after about 3 to 4 weeks that her temper and attitude were getting much worse. Anyone with children this age knows what I mean but this was like a 180 degree turn for her. Her actions were becoming totally out of character. Before I knew it she would cry and get highly upset over the least little thing. Week 5 came around and things totally bottomed out. She came home from school and WAS NOT HERSELF. Made comments about how she hated her life and it was not worth living. Later that evening we had a big argument because I was telling her nothing was worth saying that. She went totally out of control and I had to physically restrain her to calm her down. It appeared everything was better so she went to her room. I went down to check on her and she calmly told me that she had taken advil and tylenol pm and things would be better for her forever now. We went to the ER where they made us wait for at least an hour, then finally took her back. She had to drink two cups of charcoal and was poked and prodded repeatedly. They did a catheter to get a urine sample. She was very cooperative but also was in a complete daze so who knows. The poor child couldn't even lift her head up when she started the vomiting to get rid of the drugs. It was very upsetting and sad. Her heart rate and blood pressure went very low and I really thought in the back of my mind that this was it. Finally, after several hours she started coming out of it and they sent us home. The next evening when she was starting to really come around she proceeded to tell me how she had been seeing a man walking around in her bedroom at night and she was afraid to go down there. Breaking down and crying telling me about all of the horrible nightmares she had been having recently and didn't know why. I thought what am I dealing with here? This just isn't her. Three days ago I heard about singulair in the news and looked it up on the internet. OH MY GOD THIS SOUNDED LIKE US!!!!! I immediately had her stop taking it and the next day phoned her asthma specialist who agreed she should stop now. We are going to watch her for two weeks and see if any symptoms return and then decide if she needs something else or will be fine on just the Asmanex. As a side note, she also mentioned being unable to concentrate in school (unable to do even the simplest math problems) and that her brain felt confused or like something was missing. She said this had been bothering her for several weeks. I know it was this drug. They really need to take this off the market NOW and stop flirting with disaster. The only reason I posted this was to let others know they are not alone.

My 9 year old son was on Singulair for about 4 weeks. His whole personality changed. He cried all the time, he would not sleep alone, he had headaches, dizziness, tummy aches and horrible nightmares. His whole bodyy broke out in a rash and even now after 2 months of taking him off he is still covered in a rash. He was so sad all the time and so irritated. He would yell at us and was so angry all the time. He still is not back to himself. I see where people say their kids are back to their old selfs. I know my son is better but he still is having a hard time focusing in school and crys easily. He seems as though he is not the same child. I wonder if these side effects can cause permanent damage in some way. This is all so scarey. Drs. need to talk and help these children, NOW

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????

As I stated in an earlier post, my 3 year daughter takes Singulair and my 7 year old son took it until December 2007. I've been concerned about my daughter but after reading some of these posts I now wonder if this drug was impacting my son negatively. For the past year and a half/two years, he was waking up several times a week due to horrible nightmares or night terrors. He would cry out and when I would get to him his hair would be ringing wet. Although he would talk to me, he never made any sense but he was scared to death. He would never remember the episode the next morning. It's been months since he had an episode and I mentioned to a friend a few weeks ago that he seemed to have finally gotten through that phase. After reading these posts, it makes more sense. He stopped taking Singulair in December!

Okay so I'm reading all of your postings and I about to totally flip out. My 6 yr old was diagnosed with a very mild case of asthma (an occasional cough that got worse with colds) when he was around 3. The doctor prescribed him Singular and I'm almost positive they started him at 5mg and now I'm reading that it's not recommend at that dose until 6yrs. He is very prone to severe mood swings....one minute screaming "I hate you!" and making commits like "I'll get a knife and kill myself!" to acting like there is nothing wrong and the previous outburst had never occurred. As a rule he is an extremely lovable kid but has these sudden outbursts. Having said this he has been off the medication since October with out any noticeable change. My concern is that if this medication has these types of side effects could it have long term or permanent effects on such young and still developing children. Has anyone else out there had their child off the meds for more than 6 months and not seen improvement in their behavior?

my son 7 year old son started having horrible nightmares that resulted in sharing a room with me. I thought he might be going through some kind of phase, but I will now discuss it with his DR. since the nightmares started about a week of being on Singulair

I took 150 mg a day for a little more than five years. I was afraid to stop taking it due to the horrible way you feel just missing one dose! Yes, I gained approximately 30 lbs (and I go to the gym!), my cholesterol went way up, I had horrible nightmares, and right before I stopped taking it I started having bouts of double vision. I stopped taking it almost a year ago. I have lost some of the weight. I still, after all this time, am having brain zaps in the middle of the night, still don't sleep well, still have bad dreams and still have regular bouts of double vision. I have been to a neurologist who sent me for a brain mri (normal) and blood work (normal). He has recommended I get another doctor to look at me. In other words, there is no obvious reason for the bouts of double vision. I blame five years of Effexor XR for all of this! My doctor should have never allowed me to continue on this drug for so long!

I started taking Levaquin in December for a respiratory infection (500mg for 10 days). The only side effects I noticed while taking it was a terrible headache, insomnia and anxiety. I experienced that after the first dose. The next day I called my Dr. to tell him and he said he would prescribe Ativan and I should continue with my prescription. I wish I had listened to my common sense, but I listened to the doctor. I finished the prescription and felt somewhat better from the infection but after 10 days of being off the Levaquin, I started to get a burning pain in my left arm. At first I thought it was a blood clot or something. Two days later, the pain had spread to both arms. The pain was so intense I thought I was going to pass out. I had severe joint and muscle pain. I suspected it was the Levaquin when I found this and other websites where people have been describing their experiences. I made copies of a lot of information to take to the doctor. When I went the doctor I described my pain and tried to show him the information, but he didn't believe me. He said it was not caused by the Levaquin. Since then, the pain has spread to my knees. I have decided to find a new doctor since I refuse to waste my time on a doctor who doesn't even believe me. I called the FDA to file a med watch and they said they were going to send me paperwork..guess what..that was last week and I still haven't gotten paperwork. I believe that everyone is trying to keep this undercover! I am going to go to their website and download my own forms and file.
Two weeks ago I started taking a regimen of vitamins: Daily 3000 mg vitamin C, one B Complex, Milk Thistle, 1000 mg Calcium, 500 mg Magnesium, Potassium, and a Probiotic supplement. I don't know if these have helped me, but I do want to say that I feel better than I felt two weeks ago. I still have a lot of pain, but it's not as severe as it was. I'm hoping that it goes away soon. I am spreading the word among family and friends to NEVER take anything in the quinolinone family of antibiotics. I really don't believe that these side effects are as rare as they say. I just believe many people don't report because most don't connect the dots that their symptoms were caused by the antibiotic. My symptoms didn't start until almost two weeks after I completed the antibiotics. I was just lucky enough to have figured it out. The other symptoms I am having are muscle twitching, trouble focusing, insomnia, and cold hands/feet. I also just once had a ringing in my left ear that made me feel like I lost some of my hearing after it finished. I hope that's not the case. I will continue to pray for all of you.

Geodon was not worth it for me. I took 60 mg in the evenings and noticed I had a clenched jaw, anxiety, blurred vision, late menstrual periods, and HORRIBLE insomnia. I took myself off it with no problems.

Daughter 19 was treated for depression with 10mg of Lexapro for 4 months and developed every horrible side effect- seritonin toxic reactiom- stomach, headaches, insomnia, lethargy, nightmares, appetite, etc.. Weaning off slowly with increased side effects. Finally clear after two weeks of hell and Mono. Slept 10 hours a day, could not swallow, depressed by recent events but managed to go abroad for 6 weeks a month later and seemed much better. Just before she left she began taking Loestrin24 FE and has been on it for 4 months. She has been having a variety of abdominal symptoms, headaches, insomnia, cramps, lethargy, weight gain, nausea.mood swings. Of course she is having stess about her furure and her horrific recent experiences and is very sensitive to medication. A half of a 5mg. Lunesta knocks her out. The only medication she is taking is Loestrin24 FE. Tonight I decided to look up the side effects of this pill that she seemed to tolerate well (no breakthrough bleeding, shorter periods) and could this be the cause of her problems? She is going to a doctor very soon but now is off our health care plan (magic-19 and she left college) so we cannot run from one specialist to another. Anyone have any advice or similar experience?

I have been on 150 mg of Wellbutrin XL for a little more than 3 weeks. I am also taking 100 mg of Lamictal a day just upped that dose yesterday from 50 mg both to treat bipolar disorder (which I am not thoroughly convinced I have!) I can't tell which drug is causing which side effect, they both cause a lot of the same things. I have experienced strange dreams and horrible nightmares, itchy skin, hair loss (which I believe is from the Lamictal), acne on my face, back and shoulders, extreme mood swings and irritability, extreme fatigue, difficulty with hand-eye coordination, difficulty with words (speaking and writing), generally fuzzy headed, dizziness, waking at night with a pounding heart, joint and muscle soreness, heavy period that has lasted a lot longer than normal, stuffy nose, hacking cough and that about does it.

Basically, it sucks and I want to go off at least the Lamictal and see if the Wellbutrin is kinder on it's own. I just don't think this is going to work for me. It's been pretty rough the last few weeks, I hope I can come up with something I can tolerate.

good luck all!
~A

I've been on Topamax since just Tuesday, 10/9/07. I find that I get very tired a couple hours after taking it and I have horrible nightmares and very dark thoughts, too. Diet coke tastes so HORRBILE which is bad because I loved my diet cokes, but then again I guess that's good b/c I need to stop drinking them anyway. My worst side effect is that I have horrible mood swings. Is this normal? Is this going to go away over time? Because if not, I'm going to stop taking it now. This is not like me and I am not going to subject my family to this - losing weight is not THAT important to me. Thanks for any help. :(

P. S. I'm taking 25 mg in the morning, afternoon and evening.