Drug companies symptoms and conditions

I had back surgery in July and caught two infections from the hospital, Staph and pseudonymous. I had a picc-line put in and was put on Cipro oraly and Ancef. I got Steven Johnson syndrome from the Cipro and almost died. I looked like a burn victim and swelled from head to toe that was three weeks ago. They pulled me off the Ancef and Cipro. It took a week of me running 103 + temps and the dr. kept telling me its a virous until the rash showed up and my tongue swelled and private parts and throat started to swell shut before they decided to admit me. Then once all that was done and they figured it out they put me on impernem to kill both infections. They pulled my picc-last week and put me on Doxycycline. I have done my research and know that the two are related I asked my dr. what the chances were of a reaction again he told me less then 1%. Ha! I am seeing an infectious disease dr. by the way. Since I started the Doxycycline last Thursday I have developed hives I called the dr. and was told they are not worried about it because I am not running a 101 temp and I am not swelling, plus they don't even know if the Pseudonymous is cured. What do I do? If I go off the antibiotics I will die and if I stay on them I am probably going to die. My joints hurt all the time now and I am only 31. Do I look for a new dr.? Can someone please help me? This is the only website I have found so far where people have had the same reactions as me. These antibiotics are dangerous they need to be taken off the shelf. Thank you and good luck to everyone who is struggling with this.

After several attempts to lower my cholesterol, my doctor has settled on 40 mg of Lipitor, but, after reading these comments, I'm going to self-medicate and work my way off the drug completely. My main complaint is the fatigue and brain fog others have experienced. I do have a shoulder that has developed pain and weakness, and my legs don't seem to be as strong as they used to be, but it's the fatigue and memory/cognitive slowness that concern me the most. Also, like others, I assumed it was normal aging (I'm 58 and have been on statins for about eight years). I'll report my results after getting this stuff out of my system. Good luck to everyone going through this...we're not crazy after all, huh?

I took Cipro for 3 days back in March 2009. After 24 hrs, I was completely disoriented, had HUGE blisters appear on my feet (they are scars now) and lost my memory. Thank God my husband realized something was very wrong and took me to my Dr (the ER had prescribed the meds) He took me off of it, and my symptoms got better.

Since then, I have had pervasive short term memory loss, loss of vision (periods of blindness), and extreme exhaustion, joint pain, and body aches. My doctor is getting ready to send me for an MRI and EEG- this is after full body X-rays and huge amounts of bloodwork.

My life is not what it used to be. I have 3 small children, and I am terrified to be alone with them for fear of forgetting something crucial. My grades have suffered, and I can barely function.

I'm fed up. About 4 years ago I had a complete thyroidectomy and OMG my life has been a mess ever since, Yes, I needed the gland removed (it was a goiter pressing on my air way and esophagus), it needed to come out but OMG what a nightmare. Synthroid is a drug I can't figure out. I am convinced that this has ruined my life. I have developed chronic/non-stop head pain and pressure. My B.P. has gone up and now I'm on B.P. medicine. (still have severe head pain). It just never leaves me. E.R. visits/hospital stays and on and on. They treat me like I'm a complete lunatic because they can't seem to find anything organically wrong with me. Ummm-it hurts(my head). I am starting with a new Doctor who is a D.O. rather than an M.D. and I am praying that he finds what the **** is causing my pain. I feel like crap. The T.S.H. is in normal range but I have learned that the T.S.H. is not everything (even though my thyroid is gone). The isiots for lack od better description, are just too lazy to go the extra minute to find out what is wrong here. I just want to be able to function and this head pain will not let me do that. It is a nightmare and I have nothing but sympathy and empathy for anyone who suffers with pain on a daily basis.

The only constant is the Synthroid. Maybe I can't take this stuff. It has to be that my body just can't tolerate it and need something else or T3 added (I don't know). I just pray that this new doc can figure it out because I feel so helpless with this. My pain is always there squeezing and pressing. It is horrible. Maybe Synthroid is the culprit. Good luck to everyone.

Our government is allowing these big drug companies to kill us. I only took Cipro for two days for UTI and quit it. I am so much sicker now and it has been 3 days since I quit. I am bloated severely, my neck hurts so bad, I am nauseated. It won't go away.
I feel so bad for the elderly and the people that can look these poisons up.
The companies that make these should be sued. It is terrible. My UTIs always got better immediately on the old sulfa medicines I was given before and never had these side effects.
I can't sleep either.
Don't let anybody take this poison.

I just came from my Dr. and he prescribed Singular for my allergies. He really convinced me to take it. So it's day 2 and I haven't taken it yet. I told my Dr. that the commercial on T.V. said a list of side effects that out weighed the symptoms of my allergies. This website has totally convinced me that I just threw away $135.00, cause I refuse to take a medication that has so many awful side effects. thanks for everyones input on this medication. and I hope for the best of luck with the people that are having such a difficult time with their medical problems.

DON'T TAKE EFFEXOR unless you want be on a med forever. I did not have any problems getting on it but after two years I am wanting to get off of it because I think I am in a much better place. I have been tapering off and I am down to 37.5 and I just cant get off of it. I was all the way up to 150 so you would think all the down to where I am that I could get off this. NOPE!!!! I hate it i hate it I hate it. I don't mind being on it but I just don't think I need it...... but I am thinking my body is telling me differently. This just sucks getting off of it!!!!

GET AWAY FROM THIS DANGEROUS DRUG AS FAST AS YOU CAN . After 2 years of 40mg/day I could hardly walk due to severe joint pain. 3 different doctors all told me this drug was well tolerated and acted like I was stupid for complaining. All of them gave me the same speech and drew the same diagram on paper about why Lisinopril was the best drug out there. It amazed me that the drug companies had these guys so brainwashed.

When I told the doctor about some of these posts he said "Yeah, you can find any answer you want on the internet. People don't know what's going on" They wanted to give me more drugs to counteract the joint pain. They didn't know why my energy level was at an all-time low. It surely couldn't have been their wonder drug.

Needless to say, once I got away from this stuff I started feeling immediately better. I now take 5mg Norvasc and my blood pressure has dropped dramatically. I have lost weight, my joints are back to normal, I have energy. DON'T LET THE DOCTORS TALK YOU INTO LISINOPRIL .
IT'S YOUR LIFE.

I just wanted to openly share that I got some very encouraging responses from women on this site and it makes me feel SOOOOO good to just have support. So, I wanted to respond in an open forum and share a bit more of my experience:

To the women who wrote me:

Thank you for your response. You have no idea how good it makes me feel to know I'm NOT alone. My doctor truly IS ignorant and I am promptly switching. When I told her about what I'd found on line she was sure that it was all made up. She said she also googled the Mirena issues that I had talked about and found plenty of women claiming the same thing, but she said that doesn't make it true. CAN YOU BELIEVE THAT??? I mean really, I had no idea there were women on-line saying this about Mirena, so how would I even know to make up the SAME side effects as hundreds (probably thousands) of other women?!?!?! She should realize that they call it "practicing medicine" for a reason! And my Mirena cost my insurance company $1000.00...hmmmm...makes me wonder how much of a kick back the doctor's get for pushing it off on people. And I say "pusing" for a reason. I didn't even mention before that the doctor who put it in (the same OB who delivered my 3 month old) sat with me for 2 hours "convincing" me that my concerns about the device were uncalled for and that I should "go ahead and get it". I should have followed my own instincts, but went ahead and did it because my doctor (and her nurse) were making me feel stupid for worrying about the possible side effects, of which I had no idea that there were SO many. They only lead me to beleive there could be pregnancy symptoms and ectopic pregnancy (of which i was worried about that the most because I had already had a miscarriage where they thought it was ectopic). But against my better judgment I got it anyway....

So, when I went to take it out, I went to the OB that I had seen for all my prenatal visits because I didn't want to face the doctor that had pressured me. I figured the first doctor wouldn't want to take it out after only 10 or 12 days. I also thought the other OB (who knows me better and knows I don't have a history of any of the symptoms I've described) would understand and give me better advice as to why it might be happening. But SHE TOO didn't understand and had NEVER even heard of what I was telling her. I mean, really, you should have seen the way she looked at me during the visit. I think she would have had me committed right then and there if she could have. And even though I left there feeling better inside myself, I still wondered if some how I had made the whole thing up in my head. But after finding this site and reading your experience and the experiences of many other women, I truly feel so much better about my decision. I'm SO glad that i didn't wait!

There is another symptom that I didn't post before because it's a very morbid one. I would be watching TV or taking a shower or browsing the Internet and all of a sudden I would have a picture of myself lying dead on the bathroom floor from suicide. This truly freaked me out because my mind never goes to thoughts of suicide, but it was during the near two weeks of having the Mirena and it was happening more times than I care to admit. It was awful! I didn't even tell my doctor that part. She surely would have had me leaving her office in a straight jacket then. I mean my entire experience on Mirena was like an episode of the Twilght Zone. CREEPY!

To ANYONE considering getting this SOB removed...DO IT! DO IT NOW!!!! It was well on it's way to ruining my life and I only had it in for nearly 2 weeks. If you just got it and you think that it's too soon for the device to be causing your symptoms...IT'S NOT! It started causing mine right away and it only got worse!!!! Get it out!!!

And thanks to the women who wrote me and encouraged me. I SO appreciate it!!! Like I said before, it's nice to know I'm in good company and I'm not alone. THANK GOD FOR THIS SITE!

As I have stated here before, I had a terrible time with side effects from Levaquin. Everything from extreme fatigue to a ruptured distal bicep tendon. The damage this stuff causes is not to be taken lightly. It is poison! For more info: ****** While a wiki might not represent a professional opinion, it sure does show that others are having similar problems. How long will the medical community continue to deny the reality of this stuff?

Today is Christmas day 2008. And a Merry Christmas to me ha!!!!!!!! I was given a prescription for the drug Levaquin on the 19th of December for a suspicion of pneumonia. The x rays done at the hospital found no evidence of pneumonia but my doctor wanted me to take it anyway because since I have asthma and my lungs sounded so bad I was told that I was at risk for developing any secondary infection that was out there. My husband filled the prescription on the 20th which was Saturday, took the first one of a seven day supply 500 mg tablets. About 4 hours after taking just one pill was awakened by severe and agonizing pain in both of my feet and my knees that I was writhing in pain. Since I have nerve damage in my feet anyhow I know what the pain that I normally experience feels like and instantly knew that this was not normal for me. When I thought that I finally might be able to walk I hobbled into the kitchen and dug the list of side affects out of the garbage (stupid me had not read them first.) I discovered that it was one of the side affects. Called the on call doctor in the morning since it was on the weekend and he stopped it immediately and put me on something else. I only took that one pill and since Saturday night every night I wake up in agonizing knee pain and I have never had pains in my knees before. The pain is so bad that I feel like I am ready to go on a morphine drip, or cut my legs off above the knees. Six days now from one pill, how much longer can this go on? I really feel bad for the people that contined to trust their doctors and continued with the full course of the medication and I realize that what I am experiencing is minor compared to what others are going through. This drug should come with a handout that says: Take this drug at a risk to your health!!!!!! Last night the pain lasted all night and I cried all night. Have to get through this day am entertaining for the holiday and have had no sleep. Actually getting afraid to go to sleep at this point.............D.

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

i had posted back a few weeks about my daughters situation on singulair well she has been off of the medication now for 3 and 1/2 weeks now and just starting last night she seemed to be a different child she has been on the med for about 14 months she is doing better in school not wanting to fight me on everything. now she is eating great which is scary when your child goes 3 weeks not eating due to being afraid.she was sent to mental health and the doctor said he had never heard of a reaction to singulair and she could go back on it we said it was not going to happen they said it was her being bull headed which we knew different.we were almost to the point where the doctor wanted to admit her to a physic unit . we had her off the med and within 1 week she started eating little by little we just about have her back to where she was.we video taped her having her fits and showed the dr. he just stated she is a handful. we let her see the tapes the other night she started to cry and asked what was wrong with her and we explained nothing baby it was the medicine that was making you do that and now everything is going to be ok .this is the 3rd time she has quit eating in 1 yr and we could not pin point it well now we think we know it was the medicine.they put her on zyrtec we only give it to her as needed not on a daily basis.

In people close to me I have seen the following side effects:

All statins have similar side effects. They can come at once or after many years.

Pain in neck, shoulders, elbows, hands, hips, legs, feet

Pains that keep moving to different parts of the body and could be unbearable -like nerve pains.

Head ache

Burning, tingling sensations in the different body parts mentiond above and numbness

Weakness in hands which caused the person to drop things

Hair loss, difficulties to swallow, ringing noise in the ears, loss of taste, memory problems - particularly with short term memory, difficulties to find words and to remember what just had been read, impotens, extreme sensitivity in the skin (abdomen).

Please "educate" yourself.

Read books and look for information in many different places. Remember to find out who is behind a certain webb-adress. Could it be a pharmaceutical company.

Unfortunately I am not allowed to write webb-adresses here - but Google the titles of the books/writers below and you will find some webb-adresses.

The Great Cholesterol Con (Anthony Colpo)

--------------------"--------------- (Malcolm McKendrick) - this is another book

The Cholesterol Myths (Uffe Ravnskov)

Malignant Medical Myths (Joel F. Kauffman)

Overdosed America (John Abramson)

Lipitor - thief of memory (Duane Graveline)
Duane G. has an interesting site

The Truth About The Drug Companies (Marcia Angell)

Google "Stopped our statins" and you will find this webb-site.

Under print articles to the left you will find an interesting article from Weston Price Foundation.

It takes time to look for information and then read it, but often it`s quite essential to do that and to make up your own mind.

It`s your body and you know best how you feel.

Remember it`s a lot of money involved and that`s why news about serious side effects quite often are delayed.

The cholesterol issue - that high cholesterol should cause heart attacks etc - is very controversial. But it`s only the pharmaceutical companies who have the money to "brainwash" by advertisements, ghostwriters etc.

I hope my suggestions can make you more interested in the medications that you are taking.

Finally - a very interesting book about a certain kind of antibiotics - Bitter Pills by Stephen Fried.

English is not my native language but I was forced to read a lot of English books because of the suffering of my relatives, but without the Internet I would not have found them.

Remember new drugs are not necessarily better than old, but always more unsafe. They are also more expensive and that`s why they are so highly promoted.

This is my third posting. At this URL thousands of people have recounted how they were were poisoned by medicine that was supposed to make them well. Reading these accounts is like watching a science fiction horror film. One after another over the course of five years since medicines.com began posting their respective experiences, another hapless victim falls headlong into the levaquin trap. It's like watching cars crash on a fog-filled highway. Suggestible doctors rely upon marketing representations by pharmaceutical reps. Doe-eyed patients fill with confidence their doctors' prescriptions. A small percentage of these presciptees --- what % we likely will never know --- suffers severe adverse reactions that change their lives forever. There are several thousand accounts of adverse drug reactions (ADRs) re: levaquin on this website alone. There must be ten times that number of computer illiterates or incurious who experienced ADRs but who never posted their stories on medicines.com. Insofar as Levequin poisoning can appear many months after the prescription-taker discontinued taking his/her prescription, one wonders separately how many people became blind-sided by symptoms which the ADR sufferer never remotely traced back to quinolones. Suddenly out-of-the-blue a hapless victim is felled by symptoms that require exhaustive medical testing. No-one intended this DNA-changing drug to create full employment for medical personnel. Ironically Levaquin poisoning has created a pharmaceutical aftermarket for medical professionals who occupy a no-lose proposition: Either Levaquin will cure what ails you now, or consequent Levaquin poisoning will put you at the head of the line for additional testing. The right hand unwittingly prescribes a poison while the left hand tests you and treats you for a possible antidote! It's really a half-wit's delight with possibly deadly consequences. The FDA bows to the invisible hand of deregulation and social Darwinism: What doesn't kill you makes you better. If enough people complain about their ADRs, the FDA might or might not post a black box warning about the prescription drug's adverse effect. But unaddressed is the crucial link between commission-incented pharmaceutical marketing reps and their prey ---- harried doctors who are too busy to read the contraindications' fine print. Big pharmacy knows well the drill, and has earmarked a percentage of company profits and set them aside to cover the inevitable lawsuits from crippled Levqauin consumers and/or their heirs. Big pharma's profits exceed big pharma's court-mandated awards. The hubaballo dies-down about the time the FDA has weighed-in with warnings and after big pharma has retired its belatedly discredited antibiotic in favor of marketing a **miracle** new generation replacement. It's Sisyphus (look it up) all over! It's hard not to be cynical and bitter. This is the equivalent of taking incoming "friendly fire" in the medical profession. With ADRs like these who needs illness? Just take the medicine and proceed right to sick.

email me at ****** i would love to get in on a class action lawsuit cause these people need to be stopped they messed my body up and ladies don't need to have this as an option

Wow what it is with all these doctors not knowing these side effects, don't they know that there butts are hanging in the wind,the law protects the drug companies ,but doctors you are not immune

A 5.4 billion dollar annual profit for the drug companies and our government makes it impossible for victims to file malpractice charges? What is going on here???

Hmmm.

My advice to all is to go see your doctor and discuss this with your doctor.
A doctor can help you much more than a bunch of postings over the internet.

I took Yasmin for 4 years and had no issues. I gained a little more weight, but considering everything else it did to help me with the PCOS, that is okay.

I took myself off of the pill for nearly 3 years because I was mad at my OBGYN for never being in the office so I stopped going.

I recently started the Yasmin again and I am glad.

Yasmin is mostly designed for women with PCOS or who need estrogen supplements. Yasmin is not for everybody. You should discuss this with your doctor to determine if Yasmin is right for you.

I am looking into filing a class action against Merck.
Please contact me if you are interested
jmc-lampwork at charter dot net.

Together we can make a difference to make sure no one else suffers silently without knowing the reason...

My son started on 5mg Singulair in 1999. Later that year and the next at the age of 10, my husband and I realized he seemed really depressed. I took him to his pediatrician, who talked to my son at length about anything that might be bothering him, if someone had try to touch him, etc.,etc. Nothing. He had been a really happy outgoing child. Now he was not. The next year in 4th grade he seemed to be worse. We kept an eye on him. There were no warnings whatsoever about Singulair causing emotional problems, depression etc. at that time. Shortly after he started 5th grade, we moved to another city with almost no air pollution in the area we picked to live, and he was still "down". But a few months after we moved, even though we left long time friends, etc., I took him off the Singulair, as he was not really having asthma. The kid got happy again--he was was my happy cheerful boy! I don't believe this is coincidence. Then when he started Middle School in 6th Grade, his school was old and dusty with no doubt mold problems and he started having breathing problems pretty bad again. We started him on Singulair again, for the next three years that he was at this school. He tanked emotionally. Hated himself. Was so depressed it was scary. I kept telling him it was adolescence and it would get better. Then he started a new high school, and was off the Singulair for 6 months, and he was happy again. Then he got flu and bronchitis and was back on it and emotionally tanked again, and never really came out of it. Though out these episodes a few times he told me he thought the medicine was making him feel weird. He last took the 10mg Singulair in 2006, the beginning of his sophomore year when he was sick. His depression exploded and he became suicidal. He was diagnosed with depression in April of 2007 and went on Zoloft. He was not on Singulair then. Then he became suicidal again in August of 2007. His depression medication was changed. He got worse. We found a psychiatrist who was able to help some, but could find no background reason for depression. There is some depression in the family, but none of these relatives became depressed until adulthood. He became suicidal again in November of 2007 and went through outpatient care at the local children's and psychiatric hospital. He came out somewhat better, with skills to help monitor himself. He had more med side effects and has changed meds again. Now he is on 40mg Prozac daily now and doing a lot better, and since we saw the news about Singulair a few days ago, he is extremely better. He is almost back. I would rather go the emergency room 5 times a year then go through this again. We were not given a choice. What are the long term effects of this drug for someone who has been on it through adolescence? No one knows. How can a drug with this sort of side effect for children be allowed on the market? I feel blindsided by the FDA and Merck. If his Dr. in 1999 knew about this side effect she would have never put him on this drug, nor would I have allowed it. I say sue the bastards.

when my son (now five) first started treatment for allergies at almost 3, he went on zyrtec and singulair. he was moody, grumy, and needy. i just assumed he was 3. after about 10 months the allergist switched him to pcm chewables with his singulair and he turned evil. for example, he wasn't quite 4 and attacked me one night because he didn't want a bath. it took several minutes to pry his hands of of my neck. it scared me to death. since he was already on singulair i assumed it was the pcm and finally found a pharmacist who said that it "might" can have those side effects. the allergist wouldn't accept that it could do that and wouldn't change his prescription. finally went to new allergist who changed him back to zyrtec but wanted to stay on singulair due to new asthma diagnosis. his behavior got better, but still very moody - many ppl said "spoil" because of huge meltdowns over nothing. he is now 5 and has been on allergy shots for a year. about 6 months ago the doctor said could take him off zyrtec but keep on singulair. i thought yay! mood will get better. it didn't. he was still getting notes from kindergarten teacher for talking too much, fighting, moodiness, meltdowns, etc. we took him off singulair to see how asthma would do since allergies doing better. he started getting greenlights! we still have some meltdowns and moodiness. but, it is slowly getting better. i wonder how long it takes to clear out of their system?
in the last six months we have periodilly put him back on zyrtec and singulair when allergies acting up. his teacher tends to send home notes that week asking if he is on medicine. it never occurred to me that it could be the singulair! what scares me is that 3 weeks ago he said he wanted to get a knife and cut his head off so he could "go to Jesus". i talked to him and finally decided he was just talking, don't think he truly meant it. but now, i look back and realize he was on singulair at the time!
the scary thing is that my one-year old is also on it for asthma. i got put on it recently for chronic sinus problems and my husband has been on it for years! i think I will not be giving it to any one until we talk to the doctor!

as a side note i have a friend with a 22 mo old that drs have tried to put on singulair off and on since she was 12 mo or so. every time it makes her unable to sleep. mother agreed to try it again recently because child's asthma was so bad and they ended up at the ER because the baby couldn't quit crying!

Are there people that have not experienced any side effects of Singulair I saw a question, and the answer is that they are the ones that are not going to post here. Millions of people and especially kids are fine with this medication and have no reason to look for this site. Will some people get side effects from Singulair, yes, but unfortunately there is not a drug out there that will cause no side effects.

People saying this could cause all kids to suicide is a bit disturbing. If you want to take a look the most popular allergy medication, Zyrtec has had suicide listed in their information for awhile. The reason these allergy medications have to have them listed is because they are heavily prescribed because of the great amount of allergy sufferers and any time some one passes in a car crash, accidental death, or unfortunately even suicide they have to list all medicines they are on. Obviously with popular medications more people from these cases will exist than the less popular ones. Drug companies are protecting themselves because of the litigious society we live in and have to place all kinds of occurrences there and not to say in this case, but a lot of people are always looking to blame others for something instead of taking responsibility for themselves.

I don't think doctors are prescribing these medicines because they do not want what is best for each of their patients. There is no conspiracy, and I would trust their view and years of studying and practice to someone's inexperienced diagnosis on this forum when I have no idea what their background and job is on here. I do not look to consult my son's teacher to fix a leak in my roof, so I go to my doctor for advice on medicine and not consult someone not in the field.

Sorry about this harshness, but someone showed me this board and as a parent who has their son on Singulair with great results and even trusted my doctor when they suggested to try it in my one year old son I will continue to listen to their advice. I have heard numerous people in the medical community tell me Singulair is one of the cleanest drugs out there, but again there isn't a drug with no side effects. I am sorry that not all parents have achieved the great effects my kids have had with this drug, but I think most have and thus not had the need to find this board.

I was prescribed 750 mg of Levaquin for a skin infection after a minor burn. On the third day I noticed flashing lights in my right eye and the next day I felt as though I was looking through a black lace curtain. It has now settled into a large thread like floater that is in my central vision. My eye doctor said it is a large vitreous tear which is permanent. I also had tinnitus and burning on my lips and tongue which stopped after I stopped the medication. Two weeks after stopping the meds, I was biking and lost my balance. I turned my ankle, not violently, but it resulted in ruptured tendons all around the ankle. Three days after that, my right shoulder began popping in and out of its socket. Each evening, I had a low grade fever and chills. I'd wake up in the middle of the night drenched in sweat. I also had a rough eczema-like rash on my elbow and neck, however that has gone away. I'm sleeping better now and last night I did not have a fever or night sweats. My ankle is improving and I can now get through the day without having to take Advil. The shoulder is still popping when I extend my arm, but I'm hoping that will improve with time. So far, the only permanent damage seems to be the eye floater. It's annoying, but I'm adjusting. I'm planning to go back to the gym today, but honestly, I'm feeling like a ticking time bomb and I worry that new symptoms will continue to pop up. Has anyone out there been completely symptom free for any period of time? Has anyone discussed their case with an attorney?

I am so so FURIOUS with Merck and Singulair! No child especially the innocence of a 4year should be ripped from them from the damn drug companies. Do you know Singulair is one of the biggest money makers for them. Not fair!! I wonder how they would like to pay for my sons mental health bills now!! at $175 a pop because I am not sending him to any old psychiatrist. His pediatrician said it can take up to 6months for Singulair to clear your system. However the Serotonin imbalance that it may create may not. You may need to be put on depression meds, as I am afraid my 4 year old, yes my 4 year old may be put on. And for those of you who wonder. He comes from a very happily married loving home, and no problems at his catholic school. He had no reason for his ugly symptoms of wanting to die at 4 years old. He has been medically evaluated for everything, including a CT and MRI and was cleared!!! It was the Singulair!!!!! Thank god we have all found this website. I wish you all luck and please inform as many as you can. I do not want to see anyone suffer anymore from this. Innocence has been lost. God be with the poor family who lost their 17year from suicide due to this med!!!