Doctors say symptoms and conditions

I just started Singulair 10 days ago and 3 days after I started I developed what I thought was a massive head cold. Pains at the base of my neck, followed by a stuffy head, sore throat, and a nasty cough. This dry, never-ending cough keeps me up at night. It takes over an hour to go to bed even after taking Nyquil and last night I even tried Rx cough syrup w/codeine, still over an hour to get to sleep. I cough to the point of gagging and sweating. This has been happening since last Monday and it's so embarrassing at work. I know people are afraid they are going to catch my "cold" If it were a cold, I would think I would be getting better by now, not worse. This morning I felt so bad that I decided to search the internet and found this post. I beginning to think it's the Singulair. I'm going to the doctor and then depending on what he says, I may try quitting the Singulair. I am miserable. I was reading the other posts and was amazed at the symptoms I've had but had not connected to Singulair yet. I had a vivid, scary dream last night and I don't usually dream much, but this was very real. I also had noticed lately that I keep thinking I see someone coming or passing by out of the corner of my eye, and I read someone's post that referred to shadows in your peripheral and I was shocked! This is exactly what I've been seeing. I would have never blamed it on the drug. I will see how things go once I quit taking it. This is unbelievable!

I am having bouts of very bad dizziness and faint feeling, my heart will begin racing and then I become very anxious and nervous and then my head begins to hurt. I feel like I am losing my mind because I have had so many tests run and doctors say I am normal. Anyone else have these problems????

After receiving my second vaccination I discovered pimples on my scalp, followed by hair loss. This condition is still reoccurring eight months later. Although doctors say this has nothing to do with Gardasil, it happened almost immediately after the second injection.

When a class action lawsuit is filed, let me know....this drug should be taken of off the market immediately. We started all of this with an OB/GYN that prescribed this “miracle pill” and now have had to go not only to our primary doctor, but also a psychiatrist, gastrenologist, college campus counselors, psychologists, psychiatrist, and the campus medical doctors; All the while, accumulating enormous doctor bills. All the doctors say, "No, Yasmin won't cause those problems" (except the college campus doctors..wonder why? Hmm.. could it be that they are not in private practice?)....well, I beg to differ. Everyone needs to give this website to their doctor so the doctors can hear from the patients that have taken this drug, and not listen to the pharmaceutical companies that are pushing this drug to be the "miracle pill". Maybe if enough people complain and go to the media, we can get rid of this drug!
My daughter who is 18 was put on Yasmin because of irregular periods, hormonal imbalance, etc. We were told it was the new “miracle pill”. It will make you loose weight, regulate your periods, clear up acne, you name it, it will fix it. Yeah, right.
She started taking this pill in March 2007. She was off at college but called to tell me she was experiencing horrible headaches, behind the eyes. She complained about her stomach hurting, but we just figured it was the stress of freshman year at college. Then she said she got where she couldn’t eat when she went to a restaurant. When she came home in May for the summer, I noticed a total personality change. For example, she was always a neat freak, and now she wouldn’t clean her room. The first day when she drove home, she started crying she was so mad about the traffic. Yes, she has always had a little road rage, but this was ridiculous.
By June, not only could she not be in crowds, like at a restaurant, but now she is having full blown panic attacks and IBS. We called the OBGYN and they said, “Yasmin won’t cause this, go see your primary doctor”. I knew that the only thing that had changed with her was taking the YASMINE. I knew it had something to do with all of this so I “Googled Yasmin” and this website (http://www.medications.com/se/yasmin) was the first one I looked at. All of her symptoms matched everyone else’s! I am so glad we found this website, it explained everything and I had her to stop Yasmin immediately.
So we went to the primary doctor, explained about the Yasmin and how we thought it was the culprit of everything. Of course this doctor also says, “Yasmin won’t cause that”. We told him to look it up on the internet and see how there are over 3000 complaints on this drug, more than any of the other drugs on the market.
Besides the emotional problems she starting having, her pulse and blood pressure was sky high, so he puts her on medicine for that, and puts her on an anxiety medicine and sends her to a psychiatrist. She is very thirsty all the time, and develops IBS. She can’t eat without having pains in her stomach. So, now we’ve have gone from having just irregular periods, to all of the above, plus a psychiatrist.
The psychiatrist doubles her medicine (and puts her Pamine for the IBS) because the panic attacks are gone, but she still is having a lot of nervousness, anxiety, can’t sleep at night, crazy thoughts, worrying all the time, etc. A month later he changes her medicine again, to Effexor. The first 2 weeks, she does okay, but the packet doubles the strength after 2 weeks. It takes 4 weeks for it to take full effect. Right after she doubles this medicine, it is like her senses are on hyper-mode. She can taste everything that is in her food (chili powder, seasonings, etc…), taste the metal in water, and she can hear someone’s phone vibrating, in another room.
Then she goes back to college at the end of August 2007, and it’s horrible. The Effexor is having bad, bad side effects. We called the psychiatrist that she was using at home and he doubled the dose. That was the worse thing they could’ve done. The side effects were worse than ever. I had her to immediately go to a psychiatrist on campus. She told him the whole story and he believed her! Needless to say we switched doctors. He then lowered her dose back down to ½ a dose and hopefully can slowly get her off of all this medicine.
The newest thing she has developed is being hypoglycemic. The campus psychiatrist sent her to a campus medical doctor and he told her that they would get to the bottom of this. He tested her for everything under the sun. Low blood sugar is the only thing they found. But, she hasn’t taken the Yasmin since May. No telling what the results would have came back like if it was done at the time she was taking Yasmin.
Thank goodness she has counselors and doctors there at the campus that believes that Yasmin can cause all of these problems, and are working with her. From what I have read from the people that have used this medicine, although most doctors do not agree, Yasmin takes like 6 months to get out of your system. I think I am going to believe the testimonials of the people who take this medicine, over a doctor who prescribes it.
If everyone goes to the media, their doctors, the FDA, congressmen, and make them aware of these horrible effects, surely we can get this drug off of the market! Does anyone know a class action lawyer that would pursue this? For my child to have to go through all of this is ridiculous, not to mention costly. What do we know of the long term effects this drug will have if it is doing all of this when you first start taking it?
If you have the same concerns as me about this drug, and would be interested in looking into a class action lawsuit, please email: ****** I would be interested to see how many would want to pursue this.

my niece just got on singulair she thinks she is dying she gets so hot her temp was 102 she can't eat anything without vommiting she also has a discharge she now has to wear pantyliners and take monistat due to this medicine. she gets dizzy and is very depressed she has to go into counseling since the doctors say they cant find nothing wrong with her.she never had this many problems before this medication they call singulair. keep this in mind all you mothers out there reading this imagine buying monistat and pantyliners for your 7 year old daughter because of singulair.

My 12 year old son given Singulair yesterday by our pediatrician for a mild allergy problem (a sample package with a prescription to fill). There were no issueswith the first dose but he began vomiting after breakfast and again later that morning. After reading these posts I realize that as a parent we must be more cautious of the medications we give to our children and investigate possible side effects prior to treatment, no matter what the doctors say. I have not read any other signs of vomiting from these posts but a lot of other possible side effects that I am just not willing to take any chances with this medication. In the trash it goes.

I was prescribed 25 MCG tabs of levothyroxine (generic for Levoxyl) by my MD for my hypothyroid. (I was tested at a 4.5 reading -- just below a normal 5 reading). After 60 days of taking levothyroxine EXACTLY as prescribed (i.e.; on an empty stomach, 1st thing in the morning with a glass of water; no vitamins for at least 4 hrs afterward), I started to have symptoms that I've never experienced before: my hands began hurting so bad with joint pain; my lips felt numb; and I was sweating more than I ever had in my life. I decided to stop taking the medication due to these symptoms, and in about 7-10 days from stopping, ALL these symptoms had disappeared and have not returned to date. I relayed this information to my MD who told me that my symptoms had nothing to do with Levothyroxine and that I needed to continue taking the drug. It's more than strange to me how some MDs will not listen to his/her patient -- even more so now that I've read other info on the internet where many other people have had these same side effects taking levothyroxine!! On my own, I am now looking into taking an all natural alternative that I found on wellness resources called "Thyroid helper". I will not take Levothyroxine again if I can avoid it by taking an alternative. Has anyone else out there had success taking "Thyroid Helper"?

I have been on Toprol-XL 25mg for 3 months. Shortly after I started this medication I developed hip/upper thigh pain which feels better when I walk. It seems the muscles are very sore in my legs. Never had this prior to taking this medication. It just gives you a sick feeling. I am going to start weaning myself off of this med by cutting it down to 1/2 a tab. I will say one thing it has regulated the PAC's but perhaps the flutter in my chest that will not hurt me, is better than the side effects of this drug. Of course the doctors deny that this drug has these side effects.

After 1 week on Lisnopril I developed tinnitus. I've recently been in touch with someone who beat me to it with Tinnitus developing after only two days. We've both have had Tinnitus for several months after never having had it before. Our doctors say ythat there can be many reasons for Tinnitus, That's baloney. Ours came from Lisinopril

My husband went on Lisinopril in Feb 07, his bp went down and was regulated his headaches almost left but then he had sinus surgery in mar or apr. He has now developed muscle twitching and now the "doctors" say he has Motor Neuron Disease.... I refuse to believe after reading everyone's side affects that this 41 year old with no family history of this other than 1/2 siblings with high bp that he has this disease. He has experienced neck stiffness like it is broken (had MRI) no broken bones or slipped disc, he has had the chills, hw has vision blurred issues, heaviness in his legs, left side of his body more prominent than the right, he has crazy dreams and thoughts, he feels like he is dying, he doesn't however have any coughs, he has anxiety which they put him on anti depressant. After reading others comment I researched this med, it was developed by venom in a poisonous Brazilian snake. My husband as a child would get bitten by wasps, fire ants etc.. they would rush him to ER for meds and he used to take shots if stung, swells up like a balloon. So in my theory this med has the snake bite affects and I believe this has caused him to have this neuron disease but I can't prove it. His muscles twitch all the time. I believe this drug has been slowly poisoning him to a eventually paralysis to death. I have begged the doctor to take him off. He has but now he is on Atenolol, which is not much better but has no snake venom or ACE inhibitors. Please people email me. I am desperate we need to band together.
Thanks you Joann

My mother is ninety-one and is on Toprol-XL and has been for almost two years now. She started having some vivid dreams about one of her boys running away (her children have been out of the house for 25 years now) and not coming home. We thought it was the beginning of Alzheimer's and are starting her on Aricept. Could any body help me with this. She has always been very healthy until her heart attack two years ago and has never liked to take medication. She keeps asking if it could be the medicine, but the doctors say," No, these medicines are good for you!"

I am so glad to read all of this information. I am a 40 year old female. I have suffered 2 PEs. I have varied from being on 10 mg of warfarin to 25 mg a day. This is the first time I got to go 1 month between INR checks. I'm on 11 mg/day with INR of 2.1. I am having SEVERE recurrent headaches, sleepless nights, feeling tired all the time, and problems with my memory. Drs tell me they don't know what this is from and there are no side effects to warfarin. I have a vena cava filter in and I'm on the medicine for the rest of my life. Glad to hear I'm not losing my mind (just having horrible side effects regardless of what the doctors say!)

Been on warfarin about 3 weeks due to an a-fib condition.. Dose is 2.5mg a day. Since starting I cannot sleep, feel very tired and fatigued and slight sour stomach. Doctors say this is due to the a-fib but I don't think so. All I hear from my doctors is no side effects. Hs anyone else experienced these symptoms, and/or is there a website where I can find some answers.

Love it, love it, love it!!! None of the funky problems described here and I agree with the post about the fact that most doctors say no medication would have such an instaneous effect the way many have described it here. Sure, I suppose some things don't work for everyone and that maybe what's going on with many of the ladies who wrote here but I wasn't convinced. By reading the full postings here, lots of these folks had depression and reactions to other BC anyway. They may simply be unable to tolerate hormones but I can say I LOVE the ring as do all my friends who are on it.
Just one girl's opinion...

My second run in with a blood clot resulted in passing out on my way to pick up my 8 yr old daughter and being rushed to the ER because of a PE (near death), I'm thankful to be alive however (no reason for PE and being on coumadin for the rest of my life) I feel so tired now, I don't want to go to work, I can't concentrate, I suffer from dizzy spells, I'm always hungry (weight gain), nausea sometimes. before passing out I was working out, doing Taebo, the balance ball thing, walking. Now I feel like I'm and old woman. I'm 32 yrs old and taking #5 coumadin and I feel so bad the majority of the time and yes the doctors say "it's shouldn't be the coumadin" but I think it is my whole world has changed and I'm just trying to get back to being the fun, outgoing, active me. I miss myself so much, its like I'm depressed. I MISS MYSELF.

Symptoms which were not in existence prior to staring on warfarin although my doctors say they don't think it's warfarin I'm sure it is. I usually need to take around 9.5 to 10mg but my INR is never stable.
Side effects are extreme fatigue, fuzzy thinking, forgetfulness, hot rosy cheeks.

I am on 150 mg of Toprol XL daily for about 2 years. AFter I started on the Toprol within 3 months I noticed my hair was much thinner. I did not associate the two until the next time I saw my beautician, and the first thing she asked me about was if I was taking blood pressure meds. Her experience with many heads of hair had given her this knowledge. I have found others who say the same. My doctors say they have never seen hair thinning as a side effect. Does everyone have to go bald before this is acknowledged?

I have had hives on and off since taking Levaquin. The doctors say it is not from the medicine but an allergy. I just went to the dermatologist today and she said it couldn't be the medicine because I took it too long ago.

Had cortisone shot two days later had severe pain in Heart (not chest) lasted no longer then 60 seconds. Pain grew intensity started at 1 and went to about an 8. Thought I was going to dye. Pain was horrible. Went away as fast as it came. About 5 minutes later got in car to go to work 3pm. 5 miles down the rd, arches of both feet started itching and tingling really bad, had to take shore off to itch, fingers then started tingling and itching too. Anus also started itching, thank goodness not bad, had hemmoriods removed two years ago. Made it to work, Caregiver, could not work still itching and tired, head dizzy, weakness, waited two hours before I could drive home. Was ill all weekend, heart started beating irregular, now it is worse. Told Doctor, she said I had anxiety attack and gave me another shot. Heart got worse, swelling of feet and fingers, depression, dizzy, really sad. Christmas time and could not shop because I was too tired and fatiqued. Went into hospital, potassium level low was ok before, irregular heart beat worse, heart hurts all the time, fatiqued all the time, short of breath, dizzy a lot. Cannot do the things I used to do. Cannot sleep on my back, have to sleep in recliner or wedge pillow, cannot stand having weight on my chest especially on my heart. Have to go slow, been 1year 2 months now and doc said it would go away after 7 months, another one of her patients had this happen to him and she said he was better in 7 months. Doctors say I will have to live with it now. I say no.

I had the shot in my right glute in April of 2006 and I have a hole the size of a lime in my hip now. For all those that have had this happen how long does it take to stop it from eating tissue away. It is still getting bigger every month and has yet to stop. The doctors say that this is the first time they have seen this and others at the office had the same drug injected and having the same problem but not as severe as mine. I never was told that this could be a side effect and I would never have had this shot given to me. I am a 21 year old and have a huge hole in my hip, not right. Please if anyone has any info, let me know when I could expect it to stop eating my hip away.

My son, who is 3 years old and 8 months old has been taking singulair for more than a month now and we noticed that he started having some kind of tic disorder. it started with eye widening and blinking then lately he had several unusual jerky movements of the neck and upper extremities. We do not know if this is a type of Hyperkinesia (exaggerated muscular movements) which is one of the side effects written in the manufacturer's drug information sheet. We are very concerned if we should start discontinuing the medication.

how many of you read all the lists of side effect on every medication you have been prescribed i know one thing i bet u we all will now i took birth control pills for 15 years on and off never had any problems except for pimples or sore boobs minor things so when people or doctors say yasmin could not possibly cause these debilitating symptoms they dont have a clue this birth control pill yasmin is different from all of them dont ask me why becuase i am not sure all i know is that it screws up our bodies and it is an ugly mess to try to fix. doctors even, i think they are unaware of yasmins unique ingredient its different its ugly and symptoms after taking it prove that something is very uniquely wrong women have been off 6 mos 8 mos 1 year and still not feeling 100 percent we are all screaming out do not take this pill its to high risk that you might develop symptoms i did not notice them untill 2 years on this poison i loved it at first and had recommended it to people now look at me a mess 4 mos off if you decide to take yasmin please know that if you devlop bad side effects even if you stop taking this med your symptoms will not go away any time soon read onnnnnnnn dont be a fool take something else do your body a favor and stay away from this devil pill yasmin

My mother took Yutopar when she was 5 months pregnant with me and continued to take it until she delivered. At first I appeared to be a healthy baby but within hours of my birth I became increasingly sick. Now at 19 years old I have an unknown condition that causes my muscles to be very weak and force me to rely on my wheelchair for ALL mobility needs. I have used my wheelchair all my life and have had numerous tests, including 3 muscle biopsies, to try to find a diagnosis but the doctors do not know what it is. My parents both think it is Yutopar, but the doctors say no however they are unable to say what caused this.

Hi, not sure if these are all an effect of Yasmin but have been on it about 7 months now and have experienced things I haven't before...Migraines and headaches as soon as I wake up, sluggish and nearly always tired, change in appetite, anxiety and palpitations, breathlessness occassionally. Loss of energy to go to the gym etc. Dizziness. Slight depression and emotional. Sounds great eh?! Before this I had Logynon which I came off because of various other reasons...it just seems to get worse yet the doctors say I am 100% healthy!

The company that manufactures Levaquin is called ORTHO-McNEIL. They have a main website.

I have entered here before also.

I can't believe that so many of us are telling the world here what happened to us taking Levaquin...and NOBODY...is doing anything about this !

These stories are not made up or exaggerated. These stories are telling us that we are being given a poison!

If someone just printed out all of the stories on this board and put them in a book form and mailed it to "all" the newspapers in the country...maybe then this insane denial and non-concern would end! Maybe then the nation would see and acknowledge the massive damage this drug is doing to thousands!

Just read these stories...what more does our FDA have to see before they shut down the administering of this toxic substance?

It's been a year since I took 7 days worth of Levaquin.

I did "not" have the swollen throat and hives and red skin "immediate" reaction to Levaquin. Therefore, my doctors say it didn't damage me. They get angry if I bring up this possibility.

But within 24 hours of taking this drug I awoke at home in the night with burning pain in my shoulders, arms and hands so bad I was calling out. I was so confused. I had never felt anything like this before. My hands would also get cold and go numb.

My insides went haywire this first time too. My bladder would feel the urge and then not. I was feeling wincing sharp pains all over. I could not sleep except for a short nightmare type thing. I was anxiety ridden. Shaking inside and out. My legs felt weird. My sensitivity to cold became unbelievablely extreme. I was freezing.

Next morning my stomach went into literal shock with pain and I had to call an ambulance to go back to the ER as I was seconds away from passing out. The weakness? So bad....let me repeat that...SO BAD that I could not lift my hands while laying down! My entire body felt like it was going to die.

I could not walk, legs so weak and body shakey, and feeling so unbalanced. Crying with pain and anxiety and just unbelievable crashing of everything. Lost 35 pounds in 2+ months! Couldn't eat. Metallic taste in throat. Still have most of these symptoms after 1 year! Sorry to tell you all this last point.

Since all my tests "supposedly" haven't shown anything that would explain these most extreme conditions...I have been relegated to the psychiatric area almost totally.

Yes, my nervous system has been effected...damaged.
Yes, I get so anxious and depressed and scared and frantic at times with my suffering and non-treatment and adversarial treatment. Have lost my self-confidence of my body.

My regular doctors have found ways to dump me or schedule me so infrequently they are really out of this situation.

It is like living in cold war Russia. I have made too much protests against my regular doctors refusal to consider levaquin...and now my record is full of psych visits. Once you have these on your record. Let me tell you...most new doctors eyes get real big when they first see these. They label you immediately and silently to themselves as a "problem" case. Your care is different because of this. It's an incredible injustice and almost Kafka'n in it's implications.

But that's just one of the "levaquin" poisoning problems. A medical community refusing to acknowledging it...and if you protest to much to their view...you will be sent off to the psych ward.

54 years and I never saw a psychiatrist in my life. 54 years and I never ever had a problem with drugs, alcohol, the law or even in my first and still on-going 25 year long marriage. I have raised two responsible kids...both working and in college. I had a wonderfully social job as a hotel concierge that I loved for 5 years previous to this "levaquin" poisoning.

But with this case, my normal past means nothing. I am just all of a sudden a nut case for complaining too much about my belief that Levaquin did this to me. That Levaquin destroyed me. Especially since the doctors say they can't explain why I got so sick and I am still so sick. I still feel like I am going to die almost every other day! And it's been a year.

Also, my statute-of-limitations one year period to sue the hospital that gave me this drug ( and never ever told me to quit taking it even after I came rushing back to them with these incredible, unprecedented symptoms just 1 or 2 days after they prescribed it to me and were told it was the only medicine I was taking ) and the drug company that manufactures Levaquin ( Ortho-McNeil ) are almost up.

Not one lawyer I have contacted out of maybe 50 will even consider taking this case. They say it's too hard to prove, drug companes can ruin them they are so rich and powerful and that Bush has limited suit awards to 250,000 dollars and they would need a lot of this to prove you have been damaged!

They say if my liver failed and I died and I had never had liver problems before I took Levaquin...that they would then "consider" taking on a case like mine. But as long as I am alive I haven't got a chance.

I wrote to Ortho-McNeil and told them their product Levaquin has destroyed me and I asked for their financial help with my tens of thousands of dollars I owe in medical bills as financially I am also ruined. I also asked them to help me finanically get more specific, technical tests done beyond my small ton area. Never a word back.