Seeing things symptoms and conditions

My neurologist put me on Prednisone for cluster migraines. I started with 80 mg for 2 days, 60 mg/2, 40mg/2,20mg/2. It was so effective at keeping the cluster attacks from coming. I was so thankful to finally have something to stop the attacks. I have suffered with CH for 20 years and other than pain medication to abort an attack I never had anything that worked as a preventative. After taking the prescribed dosage I stopped taking the Prednisone. My neurologist warned me that this drug can be very effective short term but I would not want to have prolonged use because of the side effects. Unfortunately, when I stopped taking it my cluster migraines came back full force. So I went back on taking 20 mg daily. That was a BIG mistake. At first I was euphoric, on a constant high. I had so much energy even though I would only get about 4 hours sleep because my mind was racing from 2:00 am into the early morning hours. I would wake up with night sweats and needing to urinate 3 times per night. My face got puffy, I had terrible heartburn, increased thirst and a decreased appetite. My family was watching me wizz around like the Tazmanian Devil wondering why I was acting so bizarre. I thought I was seeing things so amazingly clear! The worse part of all is the itchy, red rash that started on my elbows, then knee caps. It has now spread up and down both arms and legs. I went to see my GP and I told him that I have never had any skin rash like this before. Could it be the Prednisone causing it? He of course said it was unlikely because Prednisone is used to clear up skin problems. Now having stumbled on to this site I realize that it must be the Prednisone doing this to me. I am unfortunately going to have to suck up the pain of the migraines and let them run their course until they leave me for a few years. I'm so disappointed that Prednisone isn't going to be the cure after all.

Man, I feel like a woman!! I got that terrible IUD out today! Not joking when I say as it left my body, it was almost like my old self re-entered!! I can't wait to see how much my body changes inside & out! If your having depression, low tolerance, no sex drive, seeing things, and all the other effects it puts you through, GET IT OUT!!
It is seriously hardly painful, as soon as you take a deep breath in, it's out just like that, go ahead take a quick deep breath in-that's how fast it is. No tears, not even eye watering!! Good luck to all of that still have it, but please get it out before it ruins you and everyone else around you!!

~God Bless

I had mirena put in 4 years ago. A lot has happened in those three years so I never paid attention I thought it was all because of stress. I have always had a good head on my shoulders but for the past year I feel like I am falling apart.weight gain,headaches,always tired always,lower back aches,moody,no sex drive at all,a thick white discharge,2 infections from the mirena,also it hurts during sex.I also bleed some times.and I think I am seeing things weird things or something is around me. I think my mind is going crazy. I keep thinking something bad is going to happen. Am I mentally going crazy. Even my husband thinks I'm going crazy. Could this all be because of the mirena?

I got mirena in January of 08, so I have had it about a year now. I have had constant depression, fatigue and chronic headaches. My eyes are are starting to ache now and I am having abdominal pain as well. I get this very odd tingling sensation through my whole body. I have been to so many doctors and like everyone else, all the sudden thought is it mirena? I called to make an appointment to get it taken out, still waiting for the call back. Please anyone write back and let me know if you experience this weird tingling and eye pain. I have also started to have anxiety and panic attacks as well. They put me on Valium and all sorts of stuff. I have anxiety because no one can explain all of these symptoms. I constantly just feel tired and angry. I hope when I get this out I can be NORMAL again.

THE FOLLOWING IS COPIED DIRECTLY FROM THE SINGULAIR WEBSITE.....

The side effects of SINGULAIR are usually mild, and generally did not cause patients to stop taking their medicine. The side effects in patients treated with SINGULAIR were similar in type and frequency to side effects in patients who were given a placebo (a pill containing no medicine).

The most common side effects with SINGULAIR include:

stomach pain
stomach or intestinal upset
heartburn
tiredness
fever
stuffy nose
cough
flu
upper respiratory infection
dizziness
headache
rash
Less common side effects that have happened with SINGULAIR include (listed alphabetically):

agitation including aggressive behavior, allergic reactions (including swelling of the face, lips, tongue, and/or throat, which may cause trouble breathing or swallowing), hives, and itching, bad/vivid dreams, increased bleeding tendency, bruising, diarrhea, drowsiness, hallucinations (seeing things that are not there), hepatitis, indigestion, inflammation of the pancreas, irritability, joint pain, muscle aches and muscle cramps, nausea, palpitations, pins and needles/numbness, restlessness, seizures (convulsions or fits), swelling, trouble sleeping, and vomiting.

Rarely, asthmatic patients taking SINGULAIR have experienced a condition that includes certain symptoms that do not go away or that get worse. These occur usually, but not always, in patients who were taking steroid pills by mouth for asthma and those steroids were being slowly lowered or stopped. Although SINGULAIR has not been shown to cause this condition, you must tell your doctor right away if you get one or more of these symptoms:

a feeling of pins and needles or numbness of arms or legs
a flu-like illness
rash
severe inflammation (pain and swelling) of the sinuses (sinusitis)
These are not all the possible side effects of SINGULAIR. For more information ask your doctor or pharmacist.
Talk to your doctor if you think you have side effects from taking SINGULAIR.

I have been taking Yaz for one month to give it a shot... Yaz isn't making me as horrible as far as moody like depo was, but definitely feeling a little crazy. I started having hallucinations! I checked out other posts and I am not alone...weird how it effects everyone differently...These weren't scary hallucinations, but seeing things that aren't there is scary enough. Also feeling extremely weepy and tired, back pain but thought my body was just adjusting. Always hungry, bloated but then a couple weeks and it seems I am 5lbs thinner. I am just not doing well with the Yaz and will have to think of something else. I never had acne, always regular periods but was starting to have longer PMS symptoms so wanted to get on a low hormone BC to help that. If anyone knows of something that worked for them, please let me know!!

I have recently started the first pack of Femcon, I am on my 2nd week and just started spotting today, I have experienced EXTREME weight LOSS. I have lost seven lbs in 2 weeks. I exercise regularly but have never had results like this. I have zero appetite and horrid cramping in my lower back and abdomen. The weight loss worries me as do the bad cramps. We aren't talking "ouch thats uncomfortable", its more like I think I might die if these cramps don't subside NOW! I have no change in libido or vivid dreams. But I read on one of the other post a lady said feeling like she is seeing things out of the corner of her eyes...when I read that I thought Thank god I'm not going crazy, someone else has the same side effect. I am going to stick it out but in my opinion this is MUCH better than that awful NuvaRing where I was severely depressed and exhausted!

I've been on 300 mg's of Lamcital since last December. Great drug, really helps my mania get under control. Lithium wasn't cutting it for me with my depression, in fact the side effects were making me even more depressed. My pdoc decided to try out Geodon (at 100 mg's). In the most part, it has been great. I feel alive and like myself again for the first time in years. But...
I wonder if making me so stable has also given my mind way to much time to over- analyze what I see and do. I see things out of the corner of my eye all of the time. I had something appear right in front of me the other day. I can no longer sleep past seven in the morning. And I have three facial twitches: my lower lip, the arc in my left eyebrow and the very top of my forehead where the first of my hair follicles start on my widow's peak. Those drive me nuts.
I am also on 40 mg's of Propranolol (Anderall) and Cytomel for my thyroid. For having such a severe case of BP, it's nice to be on so few medications. Geodon has been a lifesaver and has given me back my creativity and my marriage. I'll take seeing things and facial twitches any day for those.

I started Femcon FE for the first time 3 1/2 weeks ago, and have noticed weight gain (5-7lbs), severe bloating, pains in my abdomen, not depressed, but definitely not as upbeat & positive as usual. I also have been much more jumpy, thinking I'm seeing things out of the corner of my eye... I have been on birth control for many years, and have never had such noticeable changes as with this one!! YUCK! I'm thinking about going back to my old pill!!! I'm so glad I found this site, I could not figure out why I felt so different all of a sudden!

I honestly do not like taking Geodon. It can have negative effects on your heart. However I have been taking Geodon for at least six months now.

If I miss just one dose I start to feel extreme withdrawal. My withdrawal side effects are blurred vision, nausea, headache, and weakness.

And I've never had withdrawal from a medicine before. But for some reason it's really bad with Geodon.

I'm going to ask me Doctor about this.

I have a 15 yr old son, that has been on Singulair for 4 years. He used to complain to me about not being able to sleep through the night, he couldn't concentrate at school. He was an honor roll student. Then he became short tempered. He also isolated himself, and no motivation. He would not want to do anything. He was depressed. Does not want to shower or anything. He has absolutely no self worth. He would talk about having these problems and I would just say to him that maybe it was just the changes going on. New school, changes to his body, it's just those times where changes and expectations are harder. Some handle it better than others. Than everything just continued to go down hill. My son is very intelligent, so when mom did not listen, he decided to self medicate. Went online to try find out what was going on. Tried to find what would help him. He learned quite alot about pharmacology(spelling???) at any rate he then started experimenting with other drugs. Prescriptions drugs. He just wanted desperately to be happy. I found out about this. He was getting into trouble at school, grades fell. So we then sought counceling and then a psychiatrist. They put him on all kinds of meds. Prozac, Ridilin anti pshychotic drugs. You name it my son has probably done it. Now my son is an addict. I now hear all these things about Singulair don't know what to think.??????? I have had him a drug treatment program of which he was kicked out for overdosing. Then, the hospital of which just put him on more drugs. I don't know what to do. He has asthma, when he does not take his Singulair the asthma really kicks in. I know this we are going to look for something else to treat his asthma. I need input. My thoughts are simple. I believe that it is possible that the problems my have started with Singulair but then my son took a step further. I think to try to survive. But in the mean time he is now an addict and I'm scared of whatever permanent damage that may have occured over the years. Are there any other parents out there, that think their teenager might be going through the same problems? If so PLEASE reply to this message.

I kind of think CNN and the FDA are intellegent enough to figure out that they should NOT get information off this website. What makes everyone think all these posts are real? First you have to weed out the pranksters who post here for fun, then you have to weed out the competitors to Merck who post here to bust chops, and then you have to weed out the ones who really have a psychiatric condition and get their jollies by posting made up stories.....shall I go on? This is the INTERNET people!!! Anyone with one, two or ten verifyable emails can sign up (I have 11 email addresses myself). I have been intrigued to see the same people posting under multiple user names. Then you go to the other boards and see them there. If you really study these messages you can figure them out. So my point is, NOT ALL THESES STORIES ARE REAL. I think I would be generous in saying 25% of these posts are legit. I would hope that no government agency or news agency is going to risk their reputation on a public forum message board.

I just contacted CNN to give them a tip/heads up to our message board so that they can consider doing a news story about this situation to raise awareness. Please send them your concerns and personal story to:
http://www.cnn.com/feedback/forms/form11b.html?2
If enough of us email them, they will start to listen.

Lourdes
Mother of Julian
(severely affected by Singulair use)
Suffered severe head drops seizures, obsessive compulsive and agressive behavior and night terror and hallucinations.

Repeating Our Story:

Repeating my post from way down below - IN CASE someone's child with these head drops is looking for someone with similar symptoms. WELL - Thank God! It is so about time! My son, age 6 now was given a very grim outcome/future by two top pediatric neurologists 2 years ago when he started having not the typical seizures we associate with epilepsy (no epilepsy in our family) - his head would drop forward - like his muscle tone in his neck would collapse for a few seconds and he would literally bang his head on tables (this was when he was 3.5 yrs old) - my husband and I always knew in our heart of hearts it WAS THE SINGULAIR he had been taking for 1 year after he had a bad coughing spell the year before - not formally diagnosed with asthma - but the pediatricians insisted it would only benefit him to continue to take it. When we noticed these head drops and his eyes would at times roll back in a matter of just a second or two and he was the most loving, caring and affectionate child and turned into an aggressive and obsessive compulsive child, who also began to have HALLUCINATIONS at night - he would sit up in bed and be seeing things and scream and cry, WE JUST KNEW IT WAS THE SINGULAIR and we stopped it COLD TURKEY on Oct. 31st 2005 - against the advice of the pediatrician. We took him to a neurologist and we told him about our suspicions about the Singulair he, just like the pediatrician brushed it off, but he had an MRI and an EEG - the MRI came back normal, but the EEG was devastating!!! We were told to get ready and pray alot - that our little boy would become a vegetable and would require assisted living for the rest of his life. That he had a rare form of seizure disorder for which there was no cure. We took him then to Duke University Hospital and had him checked by the top pediatric neurologist for a second opinion - he gave him another EEG and the diagnosis from this dr. was even worst - he would probably die an early age due to the severity of his condition and that he would lose all his motor skills and regress to a vegetable. Those were the worst days of our lives. We went back home and put him on anti-seizure medication and prayed ALOT - even strangers added him to their prayer list. Well, the seizures stopped in late January 2006 and just last March of 2007 he had another EEG and it was NORMAL - he was weaned off the anti-seizure medication and is thriving and his a great kindergarten student. Doctors cannot explain how he was cured - there is just no explanation. Aside from the faith we have in God's hand in this cure, we just KNOW THAT STOPPING THE SINGULAIR saved him from further damage and probably loss of life. He is the most affectionate and caring little boy you can imagine and I do want to point out that his speech was affected in our hearts, we know it was the Singulair but in the last year his speech has improved dramatically and he is doing just fine. My husband and I have been struggling to get awareness about the dangers of Singulair and children but the doctors do not believe us. At our last appointment with the pediatric neurologist, I told him, "one day, you will see that we were right about our suspicion regarding Singulair". I do want to add that it was just too much coincidence that when he went for his first EEG in Dec. of 2005, there was another little boy in the room next door that his parents suspected Singulair as the culprit too. If anyone wants to email me and if there is anything I can do to help with my own personal testimony - please email me starwedd2@aol.com - I will be glad to share any other information. LET'S RAISE AWARENESS TOGETHER and stop more damage from occuring. Remember, my son (post is far down) almost became a vegetable and was given a grim prognosis by 2 pediatric neurologists including the top one at Duke. No cure we were told. But we always knew it was Singulair. He was cured and there is no medical explanation. Had he continued to take it he would be the vegetable they had predicted he'd become. Okay, I just emailed DATELINE NBC - please be sure to submit your children's adverse reactions story to them - here is the email address: Dateline@NBCUNI.com I also tried emailing ABC for PrimeTime and 20/20 but they use regular snail mail for story suggestions - please do your part and mail out your story to them at: To submit a story idea to one of the ABC News shows listed below, write a single page letter including your name, phone number, and address. Include photocopies of backup information. On the outside of the envelope, write "Story Idea." If a producer is interested in your story, he/she will contact you. Here are the show addresses: 20/20 147 Columbus Avenue New York, NY 10023 Primetime 147 Columbus Avenue New York, NY 10023 Together we will do something to help avoid more tragedies I went ahead and reported our experience online to the FDA: https://www.accessdata.fda.gov/scripts/medwatch/medwatch_online.cfm

Repeating my post from way down below - IN CASE someone's child with these head drops is looking for someone with similar symptoms.

WELL - Thank God! It is so about time! My son, age 6 now was given a very grim outcome/future by two top pediatric neurologists 2 years ago when he started having not the typical seizures we associate with epilepsy (no epilepsy in our family) - his head would drop forward - like his muscle tone in his neck would collapse for a few seconds and he would literally bang his head on tables (this was when he was 3.5 yrs old) - my husband and I always knew in our heart of hearts it WAS THE SINGULAIR he had been taking for 1 year after he had a bad coughing spell the year before - not formally diagnosed with asthma - but the pediatricians insisted it would only benefit him to continue to take it. When we noticed these head drops and his eyes would at times roll back in a matter of just a second or two and he was the most loving, caring and affectionate child and turned into an aggressive and obsessive compulsive child, who also began to have HALLUCINATIONS at night - he would sit up in bed and be seeing things and scream and cry, WE JUST KNEW IT WAS THE SINGULAIR and we stopped it COLD TURKEY on Oct. 31st 2005 - against the advice of the pediatrician. We took him to a neurologist and we told him about our suspicions about the Singulair he, just like the pediatrician brushed it off, but he had an MRI and an EEG - the MRI came back normal, but the EEG was devastating!!! We were told to get ready and pray a lot - that our little boy would become a vegetable and would require assisted living for the rest of his life. That he had a rare form of seizure disorder for which there was no cure.
We took him then to Duke University Hospital and had him checked by the top pediatric neurologist for a second opinion - he gave him another EEG and the diagnosis from this dr. was even worst - he would probably die an early age due to the severity of his condition and that he would lose all his motor skills and regress to a vegetable. Those were the worst days of our lives. We went back home and put him on anti-seizure medication and prayed A LOT - even strangers added him to their prayer list. Well, the seizures stopped in late January 2006 and just last March of 2007 he had another EEG and it was NORMAL - he was weaned off the anti-seizure medication and is thriving and his a great kindergarten student.
Doctors cannot explain how he was cured - there is just no explanation.
Aside from the faith we have in God's hand in this cure, we just KNOW THAT STOPPING THE SINGULAIR saved him from further damage and probably loss of life.

He is the most affectionate and caring little boy you can imagine and I do want to point out that his speech was affected in our hearts, we know it was the Singulair but in the last year his speech has improved dramatically and he is doing just fine.

My husband and I have been struggling to get awareness about the dangers of Singulair and children but the doctors do not believe us. At our last appointment with the pediatric neurologist, I told him, "one day, you will see that we were right about our suspicion regarding Singulair".

I do want to add that it was just too much coincidence that when he went for his first EEG in Dec. of 2005, there was another little boy in the room next door that his parents suspected Singulair as the culprit too.

If anyone wants to email me and if there is anything I can do to help with my own personal testimony - please email me ****** - I will be glad to share any other information.

LET'S RAISE AWARENESS TOGETHER and stop more damage from occurring. Remember, my son (post is far down) almost became a vegetable and was given a grim prognosis by 2 pediatric neurologists including the top one at Duke. No cure we were told. But we always knew it was Singulair. He was cured and there is no medical explanation. Had he continued to take it he would be the vegetable they had predicted he'd become.

Okay, I just emailed DATELINE NBC - please be sure to submit your children's adverse reactions story to them - here is the email address:
*******

I also tried emailing ABC for PrimeTime and 20/20 but they use regular snail mail for story suggestions - please do your part and mail out your story to them at:

To submit a story idea to one of the ABC News shows listed below, write a single page letter including your name, phone number, and address. Include photocopies of backup information. On the outside of the envelope, write "Story Idea." If a producer is interested in your story, he/she will contact you. Here are the show addresses:

20/20
147 Columbus Avenue
New York, NY 10023

Primetime
147 Columbus Avenue
New York, NY 10023

Together we will do something to help avoid more tragedies

I went ahead and reported our experience online to the FDA:
https://www.accessdata.fda.gov/scripts/medwatch/medwatch_online.cfm

FILE YOUR REPORT - TOO.

WELL - Thank God! It is so about time! My son, age 6 now was given a very grim outcome/future by two top pediatric neurologists 2 years ago when he started having not the typical seizures we associate with epilepsy (no epilepsy in our family) - his head would drop forward - like his muscle tone in his neck would collapse for a few seconds and he would literally bang his head on tables (this was when he was 3.5 yrs old) - my husband and I always knew in our heart of hearts it WAS THE SINGULAIR he had been taking for 1 year after he had a bad coughing spell the year before - not formally diagnosed with asthma - but the pediatricians insisted it would only benefit him to continue to take it. When we noticed these head drops and his eyes would at times roll back in a matter of just a second or two and he was the most loving, caring and affectionate child and turned into an aggressive and obsessive compulsive child, who also began to have HALLUCINATIONS at night - he would sit up in bed and be seeing things and scream and cry, WE JUST KNEW IT WAS THE SINGULAIR and we stopped it COLD TURKEY on Oct. 31st 2005 - against the advice of the pediatrician. We took him to a neurologist and we told him about our suspicions about the Singulair he, just like the pediatrician brushed it off, but he had an MRI and an EEG - the MRI came back normal, but the EEG was devastating!!! We were told to get ready and pray a lot - that our little boy would become a vegetable and would require assisted living for the rest of his life. That he had a rare form of seizure disorder for which there was no cure.
We took him then to Duke University Hospital and had him checked by the top pediatric neurologist for a second opinion - he gave him another EEG and the diagnosis from this dr. was even worst - he would probably die an early age due to the severity of his condition and that he would lose all his motor skills and regress to a vegetable. Those were the worst days of our lives. We went back home and put him on anti-seizure medication and prayed A LOT - even strangers added him to their prayer list. Well, the seizures stopped in late January 2006 and just last March of 2007 he had another EEG and it was NORMAL - he was weaned off the anti-seizure medication and is thriving and his a great kindergarten student.
Doctors cannot explain how he was cured - there is just no explanation.
Aside from the faith we have in God's hand in this cure, we just KNOW THAT STOPPING THE SINGULAIR saved him from further damage and probably loss of life.

He is the most affectionate and caring little boy you can imagine and I do want to point out that his speech was affected in our hearts, we know it was the Singulair but in the last year his speech has improved dramatically and he is doing just fine.

My husband and I have been struggling to get awareness about the dangers of Singulair and children but the doctors do not believe us. At our last appointment with the pediatric neurologist, I told him, "one day, you will see that we were right about our suspicion regarding Singulair".

I do want to add that it was just too much coincidence that when he went for his first EEG in Dec. of 2005, there was another little boy in the room next door that his parents suspected Singulair as the culprit too.

If anyone wants to email me and if there is anything I can do to help with my own personal testimony - please email me ****** - I will be glad to share any other information.

My fifteen year old son—all star athlete, good student, always following the rules has been through hell and back with this too, and is still feeling the stigma. After being on Singulair about 6 months, he started hearing and seeing things. He woke the whole house up one night with a blood-curdling scream. We immediately sought help and i started investigating the side-effects of Singulair. Every doctor we spoke too, Primary care, Allergy specialist, and 2 psychiatrists, discounted my theory that the Singulair might be causing all this. He did express having depressed emotions and thoughts of suicide. This kid had no previous pre-existing conditions that would account for these symptoms. Thank god the Psychs ruled out schizophrenia, which was what we were all afraid of, including my very intuitive son. I NOW FEEL LIKE I HAVE TO DO SOMETHING. This is so wrong. I tried to speak up about it and was swept under the rug many times. Please tell me if there are lucrative organizations i can report this too. My kids has been emotionally injured from this drug and it seems there are many more that have actually years from their childhood.

I was really relieved to have found this information. I thought I was loosing it! I am 38 and was having bursts of rage, crying for nothing... could it be menopause? NO! Unfortunately these are not listed for physicians as side effects so my doctor friend then just thought I was nuts.
The vivid dreams were a more positive side effect for me, but seeing things while awake wasn't quiet as fun. So, I'm off the Zyrtec.
I know people are saying we sound crazy, but bottom line is not all medications are for everyone. And we should know about these potential issues so if they do arise we know its the medication and not something else.

My mother actually already posted about my experience with Levaquin, but I thought I would add my own story.
After being perscribed Levaquin and taking only one...I couldn't sleep, my heart rate (normally below 60) was at atleast 110, I thought people were outside my house and envisioned them talking about killing me. I have never felt this way in my life. It was very scary and I called the ER to ask if I should continue taking the meds. They told me to take another and see what happens... Thank goodness I threw it up, because after reading these horror stories, I'm afraid I may have had permanent damage. This drug is absolutely awful for those with side effects. Stop taking them at the first sign of symptoms like these. Most doctors it looks like are oblivious to the fact that this is happening.

I was on Singulair for about 5-6 years and I rarely had an asthma attack. I had the vivid dreams that are common with Singulair, but that didn't bother me. I also had the occasional earache, but it was tolerable. My last 3 months of taking this drug, I started "seeing things." I would see shadows darting out of the corner of my eye. At the time I was waitressing and I went out to wait on a table that I thought was there. When I looked up to take their order, there was no one there. One night I almost got into an accident because I thought a car was behind me that was tailing me when there wasn't one. It was at that point that I really started to freak out. I thought I was going insane, possibly schizophrenia. One day I was flipping through a magazine and happened to see an ad for Singulair. I read through all the fine print and saw that a rare side effect was hallucinations! It all made sense at that point and I knew I wasn't going crazy!

I stopped taking Singulair and then started to have breathing problems (I wasn't taking anything for my asthma at that point). I went to the doctor and he laughed when I told him about the hallucinations being from Singulair. He told me to go back on it and see if it happened again. The second or third day I started to see shadows again. I lasted about a week and then just stopped and went to Advair. It doesn't help much.

It makes me really sad that Singulair did this to me. It was the only time in my life where I didn't have to worry about breathing. Now I have to take prednisone about twice a year, which I never had to do on Singulair. I just wanted to write this in case anyone else was experiencing anything similar.

My father has always been level-headed and NOT ever prone to hallucinations. He is a rational and
He is in the hospital and for 4 days they have had him on this drug. . After a few days on it, he started seeing things that don't exist. He can be lucid one moment and then anxious and paranoid the next. He slips in and out of this irrational behavior. He becomes filled with fear that he is being abandoned by us and in an unknown place. He sees people and things that don't exist. He sweats and
trembles. We are very worried. Aren't there other antibiotics available? We are complaining, but hospital tries to pretend they have no clue as to these side effects.
NOW, After reading more about this dangerous and mind-altering drug, we believe that it needs to be withdrawn from the market and further tested. We are going through hell and my poor father is extremely confused and getting worse. We fear what will happen next. What can we do to get the hospital to withdraw this drug from him while at the ssame time continue to meet his needs? before this drug was administered, he was mentally stable. To clear an infection (pneumonia, which started in the hospital) do we need to sit by and watch an intelligent man become extremely disoriented, shakey, panicked and progressively becoming delusional???

My daughter is 7 years old. She has severe skin problems due to allergies. She has been complaining of stomach aches after a week or so of singulair which seem to have gotten worse. When she first started using it she also started having a lot of fear, nervousness, and anxiety- seeing things that aren't there etc. I was hoping that these side effects would go away since it seems to have helped her allergies and skin. However, after reading the remarks of others, I am very concerned. I think I will try skipping her dose tonight and see what happens tomorrow- maybe taper it off slowly. We switched to singulair because claritain makes her tired, and benedryl makes her extremely tired as well as see things that aren't there. Anyone had any good experience with any other allergy meds which may help with allergies and atopic dermatitis?

I have been on geodon for 6 weeks and i could say i have experience some horrible things such as seeing things at the corners of my eyes and hearing voices. I can't stay put for one second, feeling rejected by my doctor, unable to accomplish things that I know that I can very easy, having problems with my blood pressure dropping to 90/60. This usually happens in the mornings and gets so bad that I have to left work and come home. I feel confused and light-headed, can't sleep. For four weeks I went with two hours of sleep a day. I feel that its causing problems with my marriage. For the moment, my doctor has me on 60 mg of geodon and on 2 mg of klonopin. I don't know which two of them are the worst, I have been to the hospital twice for maniac attacks. The only thing good about the geodon was that I lost 30 pounds. The way I feel I rather be fat than feel like shit.
OG

I do not by any means recommend this drug. I went into the hospital with an eptopic pregnancy. Went unresponsive after surgery and was put into ICU. Immediatly was put on reglan I went into a catatonic state. Biting my tongue grinding my jaw clinching my teeth together so tight. Could not speak or see. My fiance thought I was going to become a vegtable. I could hear but not able to respond. I was seeing things. Not able to eat or look at anyone straight in the eye. My fiance noticed that when I was given the medicine is when I went into this state. He demanded that I be taken off this drug. I came back to reality about 4 days after being taken off. I WOULD NOT EVER TAKE THIS DRUG.

My son who is age 3 starting taking Singulair 4 days ago and yes it help his problem but the difference in him, attitude, not sleeping, not being able to stay in one place at a time, thinking that he was seeing things when they were not even there has been the bad point. No longer will he be on this drug!

I took this medication on 9/02/04 for my strep throat. Within 2 1/2 hrs I started to feel very sick, my whole body started to get tight and i started seeing things, It was very scarey, becareful when taking it...I should of been stronger and have demanded for the prescirption i usually take which is ZITHROMAX, for streap throat or any troat infection.