Living room symptoms and conditions

Extreme FEAR! I totally forgot to mention this side effect in my original post on Lipitor: EXTREME FEAR,paranoia, auditory hallucinations, Coincidentally, my friend (female) in Calif. also had the exact same paranoia: Man in closet wanting to kill us. We could not sleep in our own beds. We had to sleep in living room on couch. Extreme fear. Coincidentally, my neighbor had the same reaction AND the woman who sold me my new condo could not sleep in her bed and she was also taking Lipitor. She sat in a chair in her living room all night. Now this is a total of 4 women. I do not know if men experience these same fears. My Calif. friend and I used to take a mop handle and slam it into the walls of our Master closet looking for the guy who wanted to kill us. Even after we knew he wasn't there, we still couldn't sleep in that room. I quit Lipitor and my fear of this fictitious guy disappeared! Yayyy!

My wife who is 49 years old was prescribed Ambien to help her sleep she has Phybromyalgia so she is in a lot of pain and so sleep has been a fleeting thing. on Feb 12, 2009 she took it for the first time I work 11-7 and woke her at 8:30 am and didn't notice anything out of the ordinary until she came into the living room around 1:00 pm and appeared to stumble slightly this in it's self wasn't a big deal people trip all the time. It was the fact that she caught herself on the end table grabbing it and hesitated for a few seconds then turned around and carefully shuffled backed to the kitchen holding onto the hutch for balance. I asked her if she was ok she said yes but I could hear in her voice she was scared. I went to the kitchen and asked her again then she told me that her whole left side was numb and tingled. I asked her when it started she said it was that way when she got out of bed at 8:30 am. I told her she should have said something right away but she said "I thought it would just go away". I told her get your coat I'm taking her to the hospital. After spending a night in the hospital an MRI revealed that she had suffered a very mild STROKE. The taking of Ambien the night before for the first time to me was more than a coincidence. Her attending Neurologist said that there should be no lasting effects and the numbness and tingling would go away in time. Although even after telling them about taking Ambien for the first time the night before none of them thought much about Ambien being a possible cause for STROKE. I suppose I should consider her lucky as it could have been devastating. I would not recommend anyone taking this drug even with their doctor’s supervision.

I am SO sick at my stomach right now after reading all of these posts. My son is 2yrs old and was put on Singulair right after the new year. We have noticed a horrible change in his behavior....but we attributed it to his age and the fact that he is VERY strong-willed. However, thinking back, he has had some hallucinations. We had a babysitter tell us that when she tried to put him to bed that he cried and told her that there were monsters in the closet. When she picked him up and took him in the kitchen for a drink he kept reaching at the ceiling trying to grab something. Just last night he told me that he saw his Grammy dancing in the living room....my Mom wasn't even there. He has been throwing horrible fits to the point of gagging himself, hitting himself, kicking, hitting, screaming....you name it. At the end of them, I am usually in tears and we are both exhausted. I am not the only one who has experienced this with him....my Mom has too. He is also on Veramyst nose spray....both meds are for allergies. We have taken him off of both and decided to go a more natural route. We have bought local honey, an immune booster from teh health food store, and have him on a really good brand of liquid vitamins. It is hard as a parent to make decisions about your child. It is even worse when you realize that the decision you made has affected your child in a horrible way. I plan on giving him A LOT of attention tonight and giving him a big hug! I just want my fun, playful son back! Good luck to all of you and God Bless!

It's been almost 1 1/2 years since I have taken Levaquin for Bronchitis. I took it for only 3 days, after that I couldn't stand the pain and that was the only thing different so I knew it must have been the Levaquin. I suffered major, severe joint and muscle pain. I couldn't even walk down the stairs to the living room. As for lasting side effects, I am dealing with arthritis in my knees...which I never had before and I am only 40. I have severe tendinitis in my elbow which may require to correct. I know I am getting older but jeez....I am unsure if the arthritis and tendinitis is completely related to my reaction to the Levaquin, but what else could it be. I am not that old nor am I that out of shape. My only hope to spread the word about this evil toxic poison before someone else gets hurt.

I will never put this drug in my body and I will never forget the levaquin night. Dad was already on an antibiotic. He’s been gone 8 years now so this is somewhat of a blur. His catheter sprung a leak so he had to go to the urologist. While there doc noticed a UTI and prescribed the levaquin. Even though dad was already on an antibiotic he was told to start the Levaquin once he was done with the other. Who knows if the infection was even there by the time he took the levaquin.
Dad was on drugs for seizures. (Unexplained seizures to this day)
I filled the prescription. I was the one down on him for being on so many drugs. I should have read and noticed it said not to take this drug if you’re taking seizure meds. I’d programmed myself by then that things are what they are and no one would listen to me about the drugs and side effects etc. They all see me as a witchdoctor as my husband would tell me. The doctor later told me he doesn’t have the staff to stand around checking drug interactions all day long…..
Dad took the levaquin. I said let’s get you out for a while and come down to my house. I drove the 2 miles to my house with him and by the time we arrived he could barely stand. It was all I could do to get him into the living room. He couldn’t get comfortable. He seemed out of sorts and agitated. I assumed it was his surroundings and he just wanted to be home in his chair. I struggled to get him to my car and back home. .
Once back to his house, we were talking, his eyes went off into a dead stair. He wasn’t aware of anything going on around him. They became fixated (seizure). This lasted a long minute or so and I watched his eyes come back and him come back to awareness. It was then I went to the printout info on taking this drug and saw to not take it with seizure drugs. I called the doctor and was told to immediately stop the drug. (if my memory serves me, he took one a day).
Later that evening, I went to check on him lying on the couch. He had this dopey smile on his face and when he spoke this really creepy gibberish came out. He wasn’t making any sense. I couldn’t understand a word he was saying. My sister and her boyfriend arrived. Dad was calling my husband by MY name and insisting he wanted to march. ( He used to march in the front of the parade every year in his sailor uniform) My sister and her boyfriend had to hold him up to march. His legs and muscles were too weak to hold himself up. He was like a noodle. He would not sit down or calm down. It was constant moving him from one place to another.
I offered to spend the night and sit with dad. It didn’t look like either of us was going to get much sleep that night. Dad laid awake most of the night. Occasionally he would speak to me and I could barely tell he was indeed in there ….. somewhere. He looked wired with a somewhat terrified look in his eyes. He could barely speak and just seemed to be on a bad trip. I moved him around the living room all night from couch to chair to chair. He finally fell asleep and I dozed. I woke to find he had slid out of the chair and was on the floor staring at me. Huge wide awake eyes looking at me when I woke. Mom woke up. We helped him to the kitchen for breakfast. He did really well walking. You could tell the drug was wearing off. I felt some relief. I went to work.
After work I went straight to dad’s to take him to the doctor. We all gathered in his office at the hospital to discuss trying to get dad off most or all of his drugs. We were grasping at anything to give him relief. Herbal remedies were finally being considered for some of his conditions. It was time for his next Levaquin dose. He went into what the dr. called a “life threatening” seizure.
He was rushed to ICU and pumped up on more drugs. It was said his seizure drug wasn’t working because…. He had a seizure. No one would even consider the Levaquin causing ANY of this. The “side effect” was simply treated with more heavy duty drugs. The new seizure drug was doing practically the same thing the Levaquin did! Or from what I’m reading and researching online now.. maybe it was the levaquin. Doctors would tell me it was long out of his system and wasn’t causing any adverse effects. You could watch them put the new seizure drug in him and watch him leave reality and his mind. I was later told he had a rare brain disease. They couldn’t explain why this was happening, nor would admit that dad was in there somewhere. I’d see him there when the drugs were wearing off, before the next dose would arrive. We’d hold normal conversations. My husband saw him too. All my other family members were FREEKING OUT at his condition and didn't have their minds about them... in my opinion. They couldn't and wouldn't believe a drug could cause any of this. I can’t recall the name of the seizure drug. I have this all written down somewhere around here!
I do believe though, they would have never changed the seizure drug if not for the levaquin causing a seizure by being prescribed because the doctor has no staff to check drug interactions. I will always believe it was the Levaquin that started him on his downhill climb to not being with us today. He was a strong man before Levaquin. He became weaker and weaker to the point of getting pneumonia and having a heart attack before leaving us 4 months later. Levaquin may not have been the end of him.. it was just the beginning of the end………….

I've been on topamax at 400mg 2x a day for about 8 years now. It is a great drug but it has HORRIBLE side effects! It ( along with lamictal) gives me WONDERFUL seizure control. And it is safe for pregnancy. BUT it has destroyed my memory. short term and long term I cant remember much of anything! The sexual side effects is just awful. It makes reaching an orgasm almost impossible! I am very scared that I may have full blown alzheimers by the time I am 30!

Has anyone gained they're memory back after stopping topamax?

My experience with Ambien CR is from a family member point of view. My father-in-law has only been taking it for 2 weeks and I was unaware of any side effects, until last night. My husband & I live directly across the street from my father-in-law - so at about 9:30 pm we received a call from his dad saying he had fell (he is not an elderly man either - 44 yrs. old) walking to his door & needed help up. He told my husband he had taken 2 - 5mg of Ambien about 40 minutes ago so he was tired & going to bed- so my husband walked him into the house. Everything seemed okay so he came home. An hour later I went out on our porch and noticed his dad was lying at the end of the drive way face up not moving. I yelled for my husband and he went over and woke his dad up - my husband & brother-in-law helped him in the house. He got undressed and got into bed.
About 20 minutes later (I was still on the porch at this point) I saw him walk out of the house AGAIN and get a beer out of the cooler and start walking down the street in his underwear. I again yelled for my husband and when he caught up to him he was talking to the shrubs and telling my husband our neighbors cat was out (which it wasn't) and he was trying to catch it. Again we put him in his room and told him to lay down - which he did. We went home and were watching a movie in the living room and all of sudden we hear his dad's truck start up! My husband ran out the door - thankfully in time to catch him. His dad proceeded to tell him he needed to go get ice for the cooler (which BTW - was full of ice) and he is still just in his underwear. We convince him to come inside and lay down (at this point very argumentative). This time my husband stays there for a long time. An hour later he came out again ate half a gallon of ice cream and went to bed. This morning he got up went to work and has no memory of anything that I just described.
This medication seems horrible. My husband caught him the other night eating a pack of 20 cupcakes and didn't realize he was sleepwalking/eating. The more I read about this medication it seems like our trouble is just beginning. I just fear that one night we won't be home and something will happen to him or someone else. Please consider all the risks before taking it - it not only effects you, it puts your family at risk also.

I had Mirena put in in April 08, I did not have the bad cramping when inserted or any cramping after, how ever I did start bleeding 2 1/2 weeks later and it continued for almost 15 days, and then every 8 days after that I would start "spotting". Just recently the spotting has slowed, but I am bloated ALL the time I have had Looser stools I get nauseated easily IM VERY stressed and tired, and I had a great sex drive before, now I don't even thing about it and pretty well shun my husband who now sleeps in the living room. I have a blood clotting disorder where I cannot take certain forms of birth control and I was told that this was the best option now I wonder if the mini pill is better?!

I was given 20 mg of Prednisone for 10 days for a rash and joint pain.
The pain went away and I felt great the rash got a little better. Two days ago I took my last pill. I woke up that night and my knees gave out. By morning I was great! Next night I woke with knee problem again had to slide down the stairs to the living room. I got to wondering if the knee thing could be associated with the Prednisone. I got on line and read all this terrible stuff. I am so Horrified! Today I am in pain like my body is bruised and my face is swollen a little. I have acid reflux as well. Non of this is typical for me. My knee thing is ok again, but I am just appalled! I have no MED insurance. I hope this isn't the beginning of worse things I am not taking that drug now. The Dr. didn't say I needed to taper...

I hope I have not damaged myself by taking this drug! My heart goes out to all of you! My question is - Why are the Dr.'s prescribing this terrible drug?

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

I have MS and have been taking Ambien for a few months now to help me sleep. My husband and daughter told me this morning that last night I got up from bed and was completely naked and walked out into the living room. They said I looked very wasted and was looking all around the house for some soda and them went back to bed. I can't remember any of this. It scares me. what if they were not home, would I of drove to the store naked looking for soda? This is a very dangerous side effect. It only happened one othere time when I got up and was surfing the TV channels looking for a TV program. Again, I don't remeber it happening. I also It is making my MS symptoms worse, I am having more stiffness and spasms along with blurred vision.

This medication causes more ailments than it cures!! I am so thankful that I found this website! I searched Lisinopril on Google in hopes of finding how long the side effects lasted. Every day, from day 1 and for 6 days after starting this med, I suffered from severe stomach pains, constant nausea, headache, pain in my left shoulder, dry cough, depression, interrupted sleep, severe fatigue and one of the most distressing side effects for me personally was the "fuzziness" that enveloped my mental abilities. I kept hoping the side effects would abate. I was used to getting on the treadmill 6 days per week. After starting this med, I barely had the energy to walk from the bedroom to a chair in the living room where I sat for most of the day. I didn't feel capable of driving my car...didn't want to put anyone's life in jeopardy.

When I found this website, read the posts and saw that the side effects do not seem to lessen but in fact seem to worsen with time, I immediately had my RX for Univasc refilled and went back on it. That was 4 days ago and I am happy to say I feel I'm 95% better. The only lasting side effect is some fatigue and drowsiness...even that is improving, daily. I will start back on the treadmill tomorrow!

I had been on Univasc for 6 years. The only side effects I had were a runny nose and dry cough which lasted 3 days then completely disappeared. The only reason I went off the Univasc is my insurance no longer covers it! The Lisinopril is covered and only costs $10 per month...I would pay them $10 a month to NOT take the horrible stuff!!!!

I'm 58 years old and retired last year. The saying, "You are never to old to learn", is very true! In the future, if I have to start any new medications, I will research it BEFORE I start taking it!!!!!

Thanks to all of you who posted your symptoms...it was very helpful and I'm very grateful!!