Psychosis symptoms and conditions

I am on 75mg in the morning and 50mg in the evening (125mg/day total), for my seizure disorder. If I could get off of it I would because I know how bad psychiatric drugs are. I used to be on various antidepressants for about 4 or so years, until I learned that "mood disorders" are all a crock, and drug companies are making a killing off of all the psychiatric drugs. Did you know that it has never been proven that depression or bipolar or whatever is caused by chemical imbalances?? It has been proven, however, that psychiatric drugs mess up the brain. Do some research on this. Go to the sight ****** I am so thankful I am off antidepressants but my life will never be as good as it was before I ever put the first one in my mouth. I would encourage everybody who has been diagnosed with "bipolar" to slowly and gradually withdraw from your medication and don't give up until 6 months have past. It takes a very long time for the drugs to get out of your system and you will feel like you are going through hell as you withdraw but in the end it is all worth it. Back to the Lamictal, I have now been on it for about 4 years. It does not control my myoclonic jerks completely (I have Juvenile Myoclonic Epilepsy) but controls my grand mal seizures as long as I take care of myself. I have pretty much no side effects, except for possibly poor memory/forgetfullness/can't find the word I'm looking for/etc, and possibly some slight "ocd" tendencies. It is hard to distinguish from the leftover effects of being on antidepressants (which caused me a lot of anxiety, panic attacks, depression, etc), because I do have some mild anxiety left over from them, but has drastically improved. The man problem I am suffering now from the Lamictal is feeling the effects of it wearing off in the evenings. In the last few months I have been feeling that feeling on and off throughout the whole day!! And my myoclonic jerks are increasing. I really don't want to go up on my dosage due to the brain damage psychiatric drugs cause and all the bad side effects I could experience, but neither do I want to change medications because I am at a very stressful time in my life where I am already going through a lot of changes. No idea what to do. Just wish that God would heal me of my seizure disorder!!! (it is a kind I am told I will never grow out of) Even if I had to go through the withdrawal from the Lamictal it would be worth it! If only...

I want to post this because this site has given me good perspective on this Rx and side effects experienced by others; its good to know I am not alone. As far as an agenda, I have none, in fact I was all for the Singulair initially, because it seemed to be a good alternative to inhaled steriods which I had read could interfere with normal growth. My son, 4 yrs. old, with a diagnosis of Asthma, started Singulair about 2 weeks ago. Asthma seems to have been improved by Singulair. Within a couple days of starting it, though, he reported vivid (but not nightmare-ish) dreams, a week later he dropped his afternoon nap, which we were expecting to happen eventually, so didn't think much of it. He is a wild child generally, but we also noticed an uptick in bad and aggressive behavior within a day or two of starting the Singulair; we really clamped down on him though, so that effect has been somewhat muted. He has always occasionally complained of indigestion stomach aches, but these complaints have increased to several times a day in the last week, also complain of lower abdominal pain which he says is "different" than his earlier indigestion stomach aches. Last week or so he's been up late at night, had trouble going to sleep, looks a little pale with dark circles under his eyes ("he's becoming a Goth" I joked with my wife). Last night he got out of bed late, appeared disoriented and seemed to be half awake, half asleep. He was talking, but not making sense and seemed to be upset and/or confused, but when pressed he assurred me nothing was wrong and nothing hurt--put him back to bed and this morning he remembers getting up, but also keeps telling me he had a "weird" (not scarry) dream and that he keeps seeing it while he's awake. Luckily this weird dream was not scarry for him, but he was clearly a little freaked out by seeing it again this morning. He seemed o.k. heading off to preschool, but we are taking him off the Singulair as a precaution. My advice to anyone else out there seeing similar symptoms in their kids is to go with your gut -- I always tell people that a Doctor's job is to tell you the odds, like only 1 in 500 or 1 in 1000 kids will have a certain reaction, or condition, or illness, it is the parents' job to be sure that their kid is not that 1. So I'm taking my kid off the Singulair because I think he may be that 1 kid who experiences these unusual side-effects. How wide spread they are, I have no idea. I will get on my soapbox and say I think it's time for the FDA to require drug companies to conduct long and short term clinical studies on kids for any drug that will be prescribed to kids--entrusting our childrens' health and well being to a drug company's own short term study conducted on fully developed adults is foolish and insane.

I was shocked last night on the news, when they reported that "there is no link between Singulair and suicide". I guess Merck is going to stick their heads in the sand, and let children continue to be harmed by a drug that I feel should never be prescribed to a child in the first place. I'm shocked at how young some of these children are! It makes me sad that Dr.'s, the FDA, and Merck will continue to put profit before the safety of the people being prescribed this drug and having terrible side effects from it...and most Dr.s are not fully aware of!!!!

My son is suffering from psychosis because of prednisone. He had severe poison ivy and was given 10 day course of pills that tapered and a shot. Since then he has been in the psych ward for a week , released given respirdal and lithium. After 3 weeks we tried to wean him from the respidal but the psychosis came right back. ;He is 17 and never had any symptoms of psychosis or mania before. He has every symptom now. BTW his psychosis did not appear until he was finished with the prednisone for several days. Will he ever recover?????

PREDNISONE.... a word that is unknown to the naive and despised by the the knowledgeable. Before i begin i want to tell you that prednisone for lack of better word F***ed me up. So heres my story with the pill. About a year ago i was officially diagnosed with Minimal Change Disease, now remember i am eighteen at the time, and was prescribed prednisone to cure the disease. Now being unaware of the severity of the drug and disease i casually continued life while taking 80mg per day of prednisone. Well this was good and all because it did in fact put me in remission, but the side effects were starting go surface. My face ballooned up "moon face", started experiencing random series of depression, became insomniatic, and unfortunately gained several pounds. Well this was not the end of side effects as for me. I continued with the medication and after 6 weeks of 80 mg i began my 5 week course of 60mg. Then after that i started 4 weeks on 40 mg and began tapering 5 mg every 2-3 weeks afterwards. Toward the middle of 60 mg the drug started taking its toll on my body as my skin lost its elasticity so i started getting gruesome strecht marks all over my body. I also became constipated for whatever reason most probably prednisone was at fault. I became very frightened actually terrified so i started to research about the drug in hopes of finding ways to avoid some side effects. In doing my research i found out very disturbing information regarding prednisone. Along with all the side effects that i mentioned above, prednisone also causes cateracts, glacoma, diabetes via insulin resistance, and osteoporosis. Now these i consider as the more severe permanent side effects as the list unfortunately is much longer. Finding out about the side effects i became extremely paranoid and started a very strict diet to hopefully avoid some permenat side effects. I admit reading about the information on prednisone created my paranoia and/or possible phycosis which ultimately led to my stress which led to my severe depression. Now this wasn't any old type of depression, i was sersiouly in need of some help. Everyone around me could tell something was wrong and really i dont blame then for in fact i felt as if my soul had died, the very essence of my being. Now magin if you can someone taking away your youth from you, sucking the very life out of you... thats exactly how i felt. To add along with the depression my grades became a wreck in college as i dropped several classes, lost a friend, developed problems with my parents as they tired to help me, and disrespected family relatives with my uncontrollable mood swings. A few weeks in of dieting and exercising i lost a lot of weight (15-20 pounds). As far as side effects non had changed i still had to deal with all that was mentioned above especially with the fragile skin that was a real burden as i had even a few stretch marks on my face from sleeping on my side. At this point of my long and what seemed to be a never ending journey i become exteremly weak. My body had no energy to run on as i refused to eat and when i did eat it was either foods that are considered free foods or protein nothing else. Everything at this time had been taken away from me including smoking marijuana (marijuana drops blood sugar as this would cause me to start feeling faint and lightheaded), alcohol (same as marijuana drops blood sugar), and the fact that i was not comfortable in my own skin (literally). I was driving myself insane. Everyday i was behind the computer searching for more and more. I was obsessed and became my worst nightmare. Oh by the way half in the medication therapy i showed 1+ grams of protein in my urine which my doctor possibly thought it could have been a relapse. This news i did not take lightly i had lost it and was prepared of comiting suicide. I cant lie, i really did not want to live anymore i just wanted to end this and suicide seemed like a very real and convienent possibility. If it had not been for my parents talking to me giving me a 3 hour speech and lecture i do not know what i would have done. Suicide at that point became out of the question because i could not do this to my family. So i went and purchased urine dip sticks to monitor the protein. The doctor had given me a 2 week window or chance to get back into remission or else he was going to prescribe me cytotoxic agents aka chemo therapy drugs. This was horrible news to me. So as i monitored my protein i found out of a very interesting trend. I noticed that my protein levels in the afternoon were in fact positive for protein and were usually up and down as far as how much but in the mornings i noticed i was always negative. Now this give me a huge bit of hope because when in researching about MCD months earlier i found out that there is a coniditon called orthostatic proteinuria which affects mostly young adolecent males and is a condition described as for some unknown reason there is protein loss in the afternoon when the person is upright and active then when they are supine or laying down the kidneys do not allow any portein loss. This condition is in fact harmless. I was very happy from then news and i told my doctor, he was somewhat doubting, but i don't blame him he is looking out for my best interest, but sure enough after the 2 weeks had past i went in again for my appointment after testing and i was negative for protein as i had expected. We began tapering after that point and i continusouly monitored my own tests at home and eventually i got off the steroid, actually today is that day after a 9 month period of heartache and distress. You know people say that they went to hell and back in a hard moment in life, well i went to hell stayed there for 9 months then came back. I feel so everyone who as ever needed to take steroids for long periods of time, i know its tough but believe it as it is indeed a potent drug and in most cases a miracle drug. It gave me a second chance at life and no matter how hard it was or how much pain it put me through i cannot complain for it did in fact cure me and thats why i can never hold any grudges. So thats my story i kno its not pretty but what can i say it is indeed mine whether i like it or not.

I have been on prednisone on and off most of my life. I have sysyemic lupus and many other medical diagnosis--but I had a svere rash all over that didn't respond to PO steroids--even high doses--100 mg a day. I saw my dermatologist and she said the Kenalog wud clear it right up--not once did she mention ANY side effects. Now, I know me--and how I respond to medications. While on prednisone--I have to take sleeping pills, and anti-anxiety agents or I become truly psychotic. But I am telling you what--I have NEVER had such a psychotic--nervous reaction to anything. I was like a different person and taking 10 mg of valium, ambien and resperdal did NOTHING to combat theanxiety and psychosis caused by the kenalog---not sure if its metabolized differently than the PO steroids but I truly could not sit still for days after getting the injection. But I am telling ya--IT WORKED!!! In about 72 hours this horrific psoriasis looking rash was drying up and disappearing. I had no problem with it leaving a mark in my buttocks either--I just checked to make sure--but--this is a miracle medication--but the side effects are HORIYFYING!!!!!! iN FACT, i HAVE THE RASH BACK--MY pcp THINKS ITS FROM LUPUS AND ONCE AGAIN THE PO STEROIDA SRE DOING NOTHING--SO i AM GOING BACK TO THE DERMATOLOGIST TO GET ANOTHER SHOT--BUT WILL DEFIANTLY GET A PRESCRIPTION FOR xanax, valium AND ANYTHING TO MAKE ME SLEEP AND NOT GET THE PSYCHOSIS.Oh---it does causeyou to gain weight---I gained close to 25 pounds in 10 days and have yet to lose it. and I have been on steroids most of my life and not gained that much--EVER!!!!! And LASIX does nothing for the fluid retention and swelling. MY heart felt as tho it was gonna beat out of my chest--and my heart rate and blood pressure went sky high--and I am on caridzem 120, and toprol for HBP. If you can tolerate the side effects--than this medication will treat whatever ails ya!!!

This testimony should help strengthen our case for warnings for Singulair.

Neurologist Sought Warning for Pfizer Drug
By JEREMY SINGER-VINE
June 20, 2008; Page B10

A British neurologist who analyzed effects of the drug Neurontin told a court hearing Thursday that he advised its maker -- now a unit of Pfizer Inc. -- to include a warning on the drug's label for potential side effects of depression and aggression, but his advice wasn't followed.

The University of London neurologist, Michael R. Trimble, was testifying at a hearing to decide whether civil cases brought against Pfizer alleging suicides linked to Neurontin can proceed. The hearing was jointly held by judges for U.S. District Court in Boston and a New York state court who are hearing similar cases. In various lawsuits consolidated in the federal court, plaintiffs allege more than 100 suicides were connected to Neurontin usage.

Dr. Trimble described what he said was a "plausible biological pathway" that could lead from the compound gabapentin -- the chemical name for Neurontin -- to suicidal behavior, hostility, and aggression. Dr. Trimble said that in 1995 and 1996, he was hired to write two confidential reports for Parke-Davis -- now a unit of Pfizer -- because the company "was concerned about psychosis in relation to their drug." Dr. Trimble said he was unable to find a link to psychosis, but noted effects of depression and aggression.

Lawyers for Pfizer argued at the hearing that the evidence linking the drug to suicidal side effects wasn't scientifically sound. Under cross-examination, they challenged his description of a pathway as a patchwork of studies that didn't prove a biological connection. Neurontin and generic forms of gabapentin are approved for treating epileptic convulsions, but have also been prescribed widely "off label" for other conditions.

In five of nine patient cases he analyzed in 1996, Dr. Trimble said he saw depression and aggression in patients who had no previous symptoms of the side effects, so he said he recommended to the company that the drug "should carry some kind of warning" for susceptible patients.

Thursday's proceedings were the initial phase of a hearing requested by Pfizer to challenge the opinions of the plaintiffs' experts. Under cross-examination and a subsequent examination by the plaintiffs' attorney, Dr. Trimble said the biological pathway between Pfizer's Neurontin and suicidal events were plausible and supported by a series of peer-reviewed neurology research.

You people are freaking me out. I just started today with my first dose of prednisone for my first bronchitis diagnosis. I've been sick for 3 months and thought this would be a good med for me to rid the coughing. I'm starting to reconsider taking any more if all I can expect is long term adverse effects. I took this once before years ago for a severe skin allergy. I got the psychosis initially but then adjusted the dose. Then, I would get euphoric and full of energy, like being on a stimulant. I had no idea the round face thing was due to this, I thought I just ate too much while I was home sick for 2 months. I think I'll try the herbal alternative route. If it works, I'll write again and let y'all know. Thanks for all the comments.

Following a deadly allergic reaction to Celebrex, I was given an injection of prednizone, and prescribed 60 mgs. of Prednizone per day for a week. By the third day, my anxiety and what they call "steroid psychosis" was so bad I thought I was going mad. I suffered horrible insomnia, crying attacks, paranoia, fear...you name it. On the fourth day, my knee swelled up horribly and walking was nearly impossible. I stopped taking Prednizone cold turkey on the fourth day (which you are NOT supposed to do, but my doctor didn't tell me that). It has been over 6 weeks since the episode and I am still suffering knee and joint pain, gained 26 pounds and have a red face and horrible acne. My knee has a horrific bulge still. I had an MRI on the knee, and they say that I have fluid buildup on the joint. I have no idea how long it will take to get this drug out of my system, but I would caution anyone to seriously reconsider taking it unless it is life threatening. I believe my allergic reaction could have been treated with just benadryl alone.

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.

Unfortunately my lawyer told me that they do not want to take our case because of the lack of evidence that Singulair has caused our daughters problems. :(

Does anyone out there have a pending class action lawsuit that We may be able to get in on? I have tons of proof that Singulair has caused our daughters problems and loss of almost 5 years of her elementary school career!

My phone number is *** and my email is ****** if You email me please put "Singulair" in Your subject line so I know it pertains to this posting.

Thank You in advance,
Chuck & Brenda
Jamestown New York

Effective after two weeks for some people - not effective for others. Side effects for some people - others do not report side effects. So why does Merck have to grow their market before they have any idea what's going on?

This isn't a big group of people in the study but it makes sense from what we are reading here. These researchers did examine the mast cells. We need to know about mast cells (while suppressed by montelukast) on a longer term basis.

J Asthma. 2008 Apr;45(3):243-50. Links
The efficacy of montelukast and airway mast cell profiles in patients with cough variant asthma.Kawai S, Baba K, Matsubara A, Shiono H, Okada T, Yamaguchi E.
Division of Respiratory Medicine and Allergology, Department of Internal Medicine, Aichi Medical University School of Medicine, Aichi, Japan.

Background. Cough variant asthma (CVA) is characterized by chronic cough without apparent wheezing; its pathophysiology is considered to be similar to that of classic asthma. Objective. The clinical effects of montelukast, a cysteinyl-leukotriene receptor antagonist, on cough variant asthma were assessed, and the activation profile of airway mast cells was examined. Methods. Montelukast (10 mg/day) was given orally to 36 CVA patients (25 women and 11 men; median age, 37.5 years). Before treatment, the patients' bronchial mucosa underwent a biopsy with a fiberoptic bronchoscope. The biopsy specimens were double stained with anti-CD63 antibody and anti-human tryptase antibody. Results. After 2 weeks of montelukast treatment, cough symptoms improved in 22 patients (the effective group) but did not improve in 14 patients (the ineffective group); in the ineffective group, the symptoms disappeared 2 weeks after they were switched to fluticasone propionate (400 mug/day) inhalation therapy. In the effective group, the time interval from the onset of symptoms to the initiation of treatment was significantly shorter than in the ineffective group. The bronchial mucosa biopsy specimens showed that the proportion of CD63-positive cells in tryptase-positive mast cells was significantly higher in the effective group than in the ineffective group; although the total numbers of mast cells were not different between the two groups. Conclusion. There is a subgroup of CVA patients in whom leukotrienes are closely involved in the pathogenesis of their chronic cough; activation of airway mast cells may be an essential feature in these patients.

PMID: 18415834

Hello, I was put on Prednisone for 12 days and made it through 11. It's been about 11 days since I've taken it and I'm still having symptoms. I have such bad anxiety and depression, mostly after dinner. My heart rate and blood pressure shoot up, and I have to pee every 15 mins. I had gone to the ER on the last day I was on it because I was having evil thoughts and crying uncontrollably. They told me it was probably steroidal psychosis and sent me to a shrink who now has me on Ativan until the Paxil she also prescribed me kicks in. Does ANYONE know how long this drug will be in my system? I took a tappered 12-day dose starting at 60mg. This drug may save lives, but it's really put hard times in mine. Any response is*****

Took mostly for seizures, but have been informally diagnosed with Bipolar II.

Had tremors at night, almost immediately, marked anxiety, weight loss, strange heat flashes, severe headaches (already have a migraine problem), complete w olfactory hallucinations (could have been breakthrough simple seizures, or headache auras).

Felt detached from myself and others. But the most disturbing symptom of all was auditory hallucinations. I have no history of psychosis and this only happened after starting Lamictal. Basically I could hear a constant chirping sound, subtle, but loud enough at night to keep me from sleeping unless my radio was playing to distract me from the sound. Could it have been a new form of seizure? Maybe, but regardless, the sounds started at the time I started this drug. Plus, according to a psychiatrist, I had no signs of psychosis, just the unexplained phantom sounds. One last possibility: Maybe an inner ear problem. Still would like to look into that.

People are right when they say this is still an experimental drug. If I had known what I was getting myself into, I never would have tried this drug to begin with. If any of you have had auditory hallucinations on this drug, without a history of any sort of hallucination or psychosis, PLEASE respond here and let me know about your experience. Thanks!

Took mostly for seizures, but have been informally diagnosed with Bipolar II.

Had tremors at night, almost immediately, marked anxiety, weight loss, strange heat flashes, severe headaches (already have a migraine problem), complete w olfactory hallucinations (could have been breakthrough simple seizures, or headache auras).

Felt detached from myself and others. But the most disturbing symptom of all was auditory hallucinations. I have no history of psychosis and this only happened after starting Lamictal. Basically I could hear a constant chirping sound, subtle, but loud enough at night to keep me from sleeping unless my radio was playing to distract me from the sound. Could it have been a new form of seizure? Maybe, but regardless, the sounds started at the time I started this drug. Plus, according to a psychiatrist, I had no signs of psychosis, just the unexplained phantom sounds. One last possibility: Maybe an inner ear problem. Still would like to look into that.

People are right when they say this is still an experimental drug. If I had known what I was getting myself into, I never would have tried this drug to begin with. If any of you have had auditory hallucinations on this drug, without a history of any sort of hallucination or psychosis, PLEASE respond here and let me know about your experience. Thanks!

My mother was put on Prednisone to hopefully shrink a benign tumor on her colon. When she went into a psychosis, they weaned her off. That was two months ago. The psychosis has resolved but she is now in a state of dementia. I feel like I've lost my mother. I wish there was some help. I don't know if she'll ever recover.

My son took 60mg of prednisone for 5 days for his asthma. On the 5th day he had a complete psychotic break. He had a smaller break the next day and then seemed to be doing better. 5 days later he had another episode. When will this end? I wonder if we will need to medicate him for the psychosis. He is only 9 and he doesn't understand what is happening to him and neither do we.

I have only been on Yasmin for 2 weeks and it has been the worst 2 weeks of my life. Very shortly after commencing the pill I noticed a range of horrible symptoms including: no sex drive (I used to require sex 1-2 times a day), severe depression, irritability, nastiness and rage bordering on psychosis (I went from a calm gentle person to almost losing my job after abusing my boss for no reason and also seriously damaged several other working relationships), bad acne, agonizingly painful breasts - went from DD to F cup!, nausea, headaches, dizziness, confusion.

I made the link to the pill and stopped taking it today. Thank goodness that my very sweet understanding boyfriend has put up with me through all this. I am still patching things up with my boss but may never undue the damage to my career caused as a result of my near psychotic reaction to this pill. I will never ever try this pill again. In fact, the experience has made me scared to try ANY pill. My doctor really pushed this pill on me when I approached him for birth control - he said it was the best one ever with few side effects and gave me several packets for free. As far as I'm concerned they can't even give it away. I have thrown the rest in the bin.

I'm not sure what to think about Advair. My 16 yr old son has asthma & has been on Advair for a few years & did well for the most part. While on vacation last summer he came down w/2 ear infections & quickly went downhill. He had an attack & was nearly closed up completely; went to the ER & received several breathing treatments, a steroid shot & was released w/oral steroid prescription/antibiotics. The next afternoon he had another attck & went back to the ER. He was given breathing treatments & then an IV steroid treatment. He immediately got a raging headache & got morphine for the pain, started severely hallucinating & violently flipped for hours. He eventually was well enough to leave & woke up the next morn as a vegetable. Didn't know where he was...was hallucinating, couldn't walk etc. We went back home to his family doctor. It turned out the steroids was the culprit. I didn't know Advair was a form of steroid, & the IV steroids caused his psychosis, & he just had too much steroids in his system overall. A few days later he came out of it. My mother had said she heard Advair can cause severe infections & actually worsen asthma. I asked his DR & he said there were other reasons for those problems which didn't pertain to my son, so he's still taking Advair.

Ever since that episode, he is much more susceptible to EVERYTHING. First semester of school he missed a total of 10 days. He'd also been having horrible mood swings, could not sleep at night & then went into a depression. So he was precribed a low dosage of Elavil. This was about 10 weeks ago. 12 days ago he started wheezing & coughing, so we did his at home nebulizer treatments. He went to the DR & was diagnosed w/bronchitus & was given a Z-pak. Last weekend he worsened, took him back to the DR Monday & was diagnosed w/walking pnemonia. He was given another Z-pak & oral steroids. He's slowly getting better, but has missed 9 days of school & I don't know when he'll be well enough to return.

My mom researched Advair again & found that you shouldn't take it w/Elavil, which he is still taking. She also found that side effects from Advair are eveything my son is dealing with. My husband thinks she's nuts, but I have to wonder can Advair actually be making my son worse?

I had a really bad time on this medication. Side effects included -

swelling of the feet and ankles, loss of memory including names of close friends, sleeplessness, psychosis, paranoia, loss of appetite. I lost my mind, in fact. Far from "taking the edge" off my highs, it magnified the high to a previously unreached level.

I have been taking Geodon for about 4-5 years. I was diagnosed with schizophrena in 97. I had tried Seroquel and Zyprexa prior but quit because I still heard things. I saw things. I had disillusions. On top of this, I have extreme anxiety as a symptom. I saw my doctor as a drug dealer trying to take my money. At $240 an hour, he probably was.

After 2 years of being off the medicine, I was quite a mess. In retrospect, my psychosis was influencing my thoughts. In an attempt to be normal by not being on medication, I had reached a whole new definition of abnormal thinking. I justified it by thinking I was a psychic and not psychotic. Hey, if spirits spoke to John Edwards, why not to me. They do make sense sometimes. They are just intrusive.

I came to a point of depression. I had never thought of killing myself before but it became an obsession. I just wanted it all to end. So back with the doctor and he prescribes me Zoloft and Geodon. The Zoloft had to go after 2 weeks because it made me extremely anxious. Anxiety causes increased thoughts and more anxiety.

I stayed on the Geodon. My doctor said that 120mg was the theraputic dose but I take 80 at night. Does it help. I guess. I have forgotten how I was before it. I still hear voices but my anxiety is under control. I can sleep at night when I take it without feeling like I am privy to some celestrial conversation. I haven't layed in bed worrying for years. I forgot a pill last week and had a restless sleep and that isn't fun.

I get hateful thoughts when I am getting close to the night. Anxiety starts to build and I am uncomfortable for a few hours. It takes about 3 hours for me to have an effect. I don't have the side effects other than insomnia when I skip. Sleep is impossible.

The major problem I have been having lately is with my memory. I feel like I am living life with a chemical labotomy. I can study for tests and pass but then forget the material shortly after. I can't remember if today was yesterday or a week before. This could be because I'm getting old though.

After reading the post by guest 12715, I did a search on symptoms of low potassium and this is what I found

Weakness, tiredness, or cramping in arm or leg muscles, sometimes severe enough to cause inability to move arms or legs due to weakness (much like a paralysis)
Tingling or numbness
Nausea or vomiting
Abdominal cramping, bloating
Constipation
Palpitations (feeling your heart beat irregularly)
Passing large amounts of urine or feeling very thirsty most of the time
Fainting due to low blood pressure
Abnormal psychological behavior (depression, psychosis, delirium), confusion, or seeing or hearing things (hallucinations)

Sounds like the list of symptoms some of us are experiencing.
Since Yasmin contains a diuretic and diuretics are a cause of low potassium this kind of makes sense. Might be worth getting it checked out. I have been off Yasmin for 6 weeks now and I'm still experiencing nausea, tiredness, abdominal bloating and thirst.

I have just started taking ultracet today. I was prescribed 2 tabs 4x's a day. I have taken 4 tabs so far. The pain is better but the pharmicist told me and my partner to watch out for psychotic episodes since I am taking 20 mg of Paxil a day. SCARY!!! So far just stomach upset. But not intolerable. NO PAIN!! I have suffered from chronic pain for 3 years after I tore my scapula away from the muscle and ligaments. I do feel a little wired. I was also told it was non habit forming. I have taken morphine and loritab but cannot handle the withdrawl. I think 8 tabs a day is a lot. Let you know as the days progress. Especially about the psychosis. My Dr. was informed about the Paxil and said it should not become a problem. We will see.

I have used ambien appropriately 10 mg and abused (up to 90 mg) for 5 years staight. Most all side effects said here are true and worsen over the years and with dose increase. It does give you a "high" but totally destroys your brain and mind. It worsens depression for sure and has produced some psychosis with me. I have gone in and out of treatment for this drug and have made horrid decisions while taking it that have ruined my life. I beleive it is worse and more insidious than alcohol or any other drug. I believe i have permanent brain damage from it don't recognize myself or others anymore, chronic derealization, etc. Please stop taking or dont start. Once you get hooked you are hooked.
ps. anyone know some good places to detox off ambien in orange county, ca area. It is still pretty unheard of in treatment centers

Daughter 17 years of age 6 months pregnant
broke out in hives last Thursday. Was put on prednisone. 20 mgs per pill. Took 3 pills Friday, 3 pills on Saturday, 2 on Sunday and went into a psychosis she's been confused, hallucinating, paranoid, you name she is. They put her on Haldol now, she took her 3rd dose today. She suppose to take the Haldol for 7 days. I had to take the week off from work to be with her. I'm not upset with that but I do think the ER dr is an ass and should not of given her such a high dose of prednisone

Please keep her & her baby in our prayers