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hi my name is T.im 17 and i have had severe asthma and allergies since i was 2. i was put on the singulair drug when i was 10 i started having nightmares about my percents dying and severe depression and anxiety.my parents thought it was just a phase kids go through.i realized all this didn't start happening until i started taking the drug, so i refused to take it anymore. well now im 7 years later my parents EMT,and pulmonologist.think its a wonderful idea to start taking it again so my parents give it to me and make sure i take it each night,bc my allergies are so bad. ive warned them once,but i guess they will all see what happens

My daughter who just turned 6 has been on Singulair for about 3 years now. Her behavior has not always been the best, but with her past medical history ( a preemie) and all the things we have gone through some times its just easier to give in than to fight over it!!! So last week she was suffering with her allergies and asthma and the doctor added a Claritin to be taken once daily. I didn't really think to much about it and thought well if it is going to help her the OKay. That was on Wednesday and by the week end she was literally coming "unglued". She was lying on the floor when she should have been in her seat at the dinner table. When she was in her seat she was doing "back bends" over the chair. We finally come to the conclusion that it had to be the Claritin, I looked up the active ingredient loratadine and knew I had to get her off it immediately. So now I started to investigate the Singulair as well, which I should have done long ago. Today will be the last day she takes Singulair as well. She has complained of her stomach hurting for a long time and I always blamed it on constipation, but it could be the Singulair. I can only pray that she will not have any lasting side affects.

I am a 48 year old female who had just recovered from pneumonia and was prescribed avelox for a lingering sinus infection. Within hours after taking just 1 400 mg pill, I began experiencing a severe reaction. First there was a rash all over my body, with swelling and flushing all over. Then I became nauseated to the point of dry heaves and my temp went to 104 digress. My body then had neurological shakes, I could not control them -- just like Parkinson. I had no energy to move. My husband rushed me to the ER where I was treated with steroids, liquid benadryl, nausea medicine and IV fluids. After a few hours, I was released. Two days later, after another trip to the ER because of tingling, rash and no blood flow to extremities the same treatment was given. It has now been two weeks and I am just now feeling like I am coming out of this and getting back to normal. I have just spent over 10 days in bed, untold amount of money at ER and lost two weeks of my life.. BTW, the ER Doc said he would never prescribe Avelox to anyone due to the numerous reactions he has seen. If there is a class action suit, count me in.. Never let anyone take this drug..

I'm posting again to let all of you know that you can remove mirena yourself!!!After calling several doctors to try to make an appointment ASAP i couldn't find one that would do it soon enough,so i started to research how to remove it...I found how to do it on the FDA website...it was not hard to do, if you can feel the string you can get it out,just pull very slowly,that is what the doctor will do anyway....it didn't hurt bad just a little pulling feeling... FOR ALL OF YOU THAT HAVE BEEN HAVING TERRIBLE SIDE AFFECTS LIKE I WAS PLEASE GO TO THE FDA WEBSITE WWW.FDA.COM..THERE IS A LINK YOU CAN CLICK ON TO TELL THEM ABOUT THE PROBLEMS YOU ARE HAVING FROM MIRENA...THAT'S THE ONLY WAY WE CAN HELP TO MAKE THEM AWARE OF THIS, AND HOPEFULLY STOP THEM FROM USING US AS LAB RATS!!!!

this is such old news, and such sad news, and I am so tired. Previous severe tendon pain, now after 6 mos. tendinitis on an mri in two ankle tendons, and a longitudinal tear in one tendon. sever pain after 10 weeks. do not know what to do anymore, I feel like the system has swallowed me up and no one wants to listen. Is someone out there for me???????????????//

My 20 yr old daughter was given Avelox 400mg to take one per day for 7 days for a sinus infection. Two hours after taking the first pill last night she became very drowsy and extremely nauseous and vomited several times. Her heart was racing and she felt unexplained anxiety as if she was having a panic attack, and couldn't sleep most of the night. Why don't doctors think before giving out medications!? Or at least warn the patient of these side effects which appear to be VERY common!

I am totally upset by reading the posts here. my son is just now 8 months old. he was put on singulair when he was just 6 months old. at first it seemed to be working...for maybe 2 weeks...then everything went crazy. he was started out on it when his pediatrician stated that he had asthma and apparently was on a very high dosage of it. they started him on 10 mg of the oral granules. before taking it he was a very happy baby, even with him being so young i never had any problems with him crying excessively or being massively irritated. since he started on the medication he has had massive irritability spells, constant fussing and crying and cant seem to fall asleep at night let alone stay asleep very long. i had taken him to the emergency room on christmas eve because a new problem showed up. he now was having a massive hard time breathing, he had a persistant cough, congestion in his chest and was almost always gasping for air. the staff at the hospital were in disbelief when they were informed that his pediatrician had put him on singulair at such a young age and at such a high dosage. i am now in the process of obtaining a lawyer and filing a lawsuit against the pediatrician for medical malpractice. this drug is very dangerous for anyone especially children. i would suggest anyone else having these problems with their child and this drug do the same. it can apparently cause long term lung damage, pulmonary disorders and even death. my son has been off of the medication since christmas eve and has already done a massive turn around. he sleeps well and through the night again, his breathing has improved and his cough is almost gone. they did say in the E.R that he has congestion in his chest due to the singulair but it should clear up over time with the help of zyrtec. please help make a stand and protect our children from the dangers our own pediatricians present to them.

I was prescribed 7 Levaquin (3- 750mg and 4- 500mg) on Friday December 12th 2008 for an ear infection. I was to take the 3- 750mg ones for the next 3 days and then start on the last 4- 500mg. The next evening Saturday, I started to get sharp pains in my left calf. I thought it was a charley horse and started limping around with pain. During the night I felt as if I was lying on golf balls and could not get comfortable.

The next morning the pain in the calf included soreness in the left hip area. I took an over-the-counter pain pill and went on my business. I also took the second 750mg Levaquin Saturday morning. Later that afternoon my right calf starting hurting with sharp pain as I walked around the house. This was really weird. The pain was exactly in the same area as the left side.

On Sunday morning (December 14th 2008) I took the 3rd 750mg Levaquin. That evening I started to put two and two together and had some thoughts the medication (Levaquin) was causing these side effects. I told my wife that I was going call my doctor on Monday (December 15th 2008) and let him know how much pain I was in. At this time I could hardly walk. I was walking with much pain and felt like I was walking like the Apes in the movie called “Planet of the Apes”.

I was now on the 500mg Levaquin. I took this pill Monday as scheduled. I called my doctors office Monday morning and talked to the lady that answered his phone. I explained my condition. She had me describe my symptoms twice. She told me she would give my message to my doctor. I did not receive a return that same day.

Tuesday morning I took the next 500mg Levaquin as scheduled required. Later that day I received a call from a lady at my doctor’s office. She told me that the doctor was going to phone in an additional prescription and where did I want it phoned to. I asked her what the doctor said about the additional 2- 500mg Levaquin pills I had left. Did he want me to stop taking them? She told me he didn’t say and he made no comment on my side effects.

My wife called the Pharmacist later Tuesday afternoon and the prescription was not there or not ready.

Wednesday morning I took the 2nd to last 500mg Levaquin dose as scheduled. Later that morning my wife called the Pharmacist and my new prescription was ready. We went and picked up the new medication that afternoon.

At this time I only had one more dose of the 500mg Levaquin and seeing-how the doctor didn’t tell me to stop taking the remaining last couple of pills I took it on Thursday morning to finish out the prescription.

I’ve been off Levaquin for about 3 days now. It’s now Sunday December 20, 2008 and many of my joints and muscles are in distress. I walk with much pain. I can hardly life my arm above my shoulders. Even my hands hurt when I try to make a fist. I hope this drug starts to wear off soon.

Along with my other medical problems, I have been starting to have thoughts of how unimportant I am. How I could become a burden to my family. My depression has gotten worse and thoughts of suicide have flashed into my mind. Those thoughts give me chills because I love my wife and know how much that would hurt her. I love life but I don’t want to get to the point that I can’t take care of myself. God must give me the courage to do what I have to do. I don’t know why I’m writing down the above information. This is so personal. This can’t be happing to me. It just doesn’t seem possible. I feel the pain in each of my joints in my hands as I type. It is as though I was not myself. I look at my hands and it seems as if I was in someone else’s body. I’m sure this is side effects of the Levaquin and should subside soon. Merry Christmas Everyone.

Hi, All

I normally do not post on websites, however, the issues that I read about in other toddler has me concerned for my grandson as well..

He started to live with us in Georgia three months ago. He was 20 months old. Over Labor Day weekend he developed a severe sinus infection and virus with a fever. Against our better judgment then, we allowed his doctor to prescribe an antibiotic which seem to help him for about two weeks, but her began having excessive mucus and coughing constantly. He had no fever. When we returned to the doctor, they suggested that he use Claritin because he had no infections, but a lot of mucus and drainage. Claritin worked, however, the side effects were he was a little sluggish. The doctor recommended trying Singular. We tried it for three weeks. Over that three weeks, we noticed that his appetite decreased and his aggression level increased where he started a fight with another toddler. He is normally an easy going little boy. He has been very aggressive lately, plus he has had dry coughing and gagging worse than when he was on Claritin. When I read the literature that says this medication causes sinusitis, I immediately decided to discontinue it. He will not be using this medicine again. It may be great for some children, but they really ought to make parents aware of the side effects. They are awful.

Went off simvastatin in March, all pain went away within a couple of months, but muscle weakness in legs remained. In October, found out my cholesterol is sky high, over 325. So Dr. wanted to try Crestor 5 mg. Within 1 week, I had overwhelming fatigue, could hardly stay awake during the day and the weakness in my legs was getting worse. So I just went off Crestor. Frustrating!!

My son is almost 5 now and has severe food and inhalant allergies, along with sever asthma. When he was 3 he was hospitalized for 4 days because of his asthma. I have been warned that only 1% of asthmatics will ever be hospitalized, so I've made sure he stays on all his meds. He has been on Singular ever since he was 15 months old. At first it was a God send. Everyday was a constant challenged, fussy, icthy red eyes, constant flow of mucous and wheezing. I would have to pin him down 6 times a day with the inhaler, but when Singular came "poof" it was like magic. He was on Singular when he was hospitalized and is now on 3 meds; Zrytec, Singular and Q-var all given to him everyday. Lately we have had some major issues come up for him. I think I have the next J. D. living with me. NO FOR REAL. My next step is a shrink. You might think I'm mean for saying it, but I don't know how else to describe it. When I was driving he asked for some gum, because I wouldn't let him pick out his own piece, he got out of his car seat and started hitting me over and over again, pulled my hair and tried to "break my arm" as he put it. I had to pull over and I couldn't get him to calm down he kept slapping me in the face and kicking me not only was I embarrassed, but it hurt, I was crying. I have finally come here trying to see if other children, who are on Singular, have had similar episodes. He is a very good boy most of the time and aggression is a hit and miss. I don't know what to do.

Just wanted to offer a follow-up on our daughters behavior since getting off Singulair and Advair. AMAZING difference. She is a pretty normal 12 year old now. The most noticable thing to me is her voice. On the drugs she always sounded so gruff and angry. Now she sounds sweet. She smiles so much more and is not eager to become angry. I can reason with her more now when there is a disagreement. It will be a long process to break habits of behavior that have developed over the past ten years, (yes, ten years, she started these poisons when she was two years old) We are very hopeful for her future. I am so very thankful that I was led to this site.

My 7 yr old daughter has been off of Singulair for 12 days now. The change in her personality is amazing. She experienced two nights of strange dreams and waking in the middle of the night. We put her back on Flovent once a day as a substitute. Her aggression and frustration went away within days. She is so happy and content with herself. I can see that she is no longer frustrated by emotions that she could not explain. She's silly, funny, happy. She no longer hates us, pulls her hair, or tries to slap herself because she's thinks she deserves it. She has been on the drug since she was 3-1/2. We were doing family therapy to try to help her. This is no longer needed. She's back to her old self. What a shame no one warned us of this potential side effect. I also wondered how I missed the news story since I just found this site in September 2008. The news story about Singulair came out in March - just around Spring Break. Since we were out of the country, I missed the news. Isn't that a convenient time of the year to break a story? I'm sure many other families missed the news.

My 9 1/2 yr old son started Singulair in July 2004 when he was 5 yrs old.Looking back now we realize that he started showing signs immediately. We only gave him Singulair in the fall when he had the most trouble with his asthma. His asthma was under control immediately but was not worth the damage that was done. He complained of pains in his legs that I just thought was growing pains. He would sometimes run a fever with no other symptoms of being sick and then the fever would go away. He would also feel like he always had to go to the bathroom, especially after he went to bed. I gave him Singulair at 7pm before he went to bed. The biggest change we noticed in him was the signs of attention deficit. We first noticed that he kept getting out of his seat at dinner time. No matter how many times we told him to sit down he would sit down and then a little while later he would get right back up. We realized after a while that he wasn't doing it to be defient he just couldn't help himself. I asked his Kindergarten teacher if he had trouble sitting in his seat or with attention but she didn't think he was any worse than any of the other Kindergarten kids. In 1st grade, at the beginning of the year, his teacher said he had trouble keeping his attention but then by January she said he was a different kid. We usually stopped giving him Singulair in December. The same thing happened with his 2nd grade teacher. I question his allergist in the fall of 2nd grade but his allergist said Singulair wasn't the cause for his ADHD symptoms. When his 3rd grade teacher contacted us in Oct 07 with the same complaints I realized that it must be the Singulair. I looked online for Singulair side effects and came across this website. I couldn't believe it. I was so disappointed in myself for not doing it sooner but we took him off Singulair immediately. I called his allergist the next morning and questioned him for a second time and he told me that sometimes parents of kids with ADHD just look for something to blame for their childs behavior. I couldn't believe he said it to me. We made an appointment at Children's Hospital Boston to have him evaluated for ADHD just in case but couldn't get an appointment until Feb 08. When we had him evaluated he had been off Singulair for over 3 months. The neurologist said he did not have ADHD. When I asked him if he thought Singulair could have been to blame for the symptoms he was showing and he said there was "compelling evidence" that showed Singulair does cause ADHD symptoms in some children. We were happy that he did not have ADHD but were so sad that we gave him this medicine for 3 years without realizing what damage it was doing. My biggest fear now is that there may be long term damage. All his symptoms have gone away but sometimes he still seems a little out of it and I don't know if it is just his age or his personality or if it might still be some long term effect from the Singulair. He is such a sweet, loving, caring boy and I hope that I didn't do any long term damage by giving his this horrible medicine. I hope that something will be done soon to get this medicine off the market. My prayers go out to all the families who lost children on this medicine. I can't even imagine the pain you are feeling but I thank you for getting your story out and saving other children! I am thankful that I was able to get informed by this website because God knows my allergist wasn't looking out for my son! His asthma has been under control since being off Singulair and just seems like a happier child over all!
Thank you!

This is just amazing to me. My son was prescribed singulair for asthma when he was 8, he is 19 now. I only kept my son on this medication for about 4 weeks. I noticed a HUGE change in his personality, defiant and very fired up. I took him off, because there was just no talking to him. It made a difference, he was back to normal. I said something to his doctor, and he didn't know what to think, he said that the drug shouldn't alter his personality, it's an asthma medicine. I'm glad i listened to my gut instinct and took him off. My doctor just prescribed singulair to me for severe allergies and i wanted to see what the side effects where. I had NO idea i would see the side effect, that i knew my son was having 10 years ago, when this medicine first came out. I am speechless...

I am just slightly hypothyroid and could go without meds, but decided to try meds, and endocrinologist suggested Levoxyl 50 mcg per day. First day on the drug, felt exhausted by night time, next morning, usually jump out of bed for workout and was extremely tired at the gym, no energy, was starving during the day even after breakfast which is unusual for me, and exhausted by evening, and third day woke up with swollen glands and exhaustion, knew something was up. Decided to research the side effects and found others with similar symptoms and didn't like long term effects so I am going off the drug and hoping I caused no damage to my system. My doctor's reaction was "impossible" that the drug could cause this. My reaction was, "no thank you, I think for myself, know my body, and know this drug caused this reaction." I was feeling fine before 3 days ago, and how could so many have similar symptoms if it isn't the drug.

I was diagnosed as having Hypothyroidism in 1-07. My TSH was 83 and I was sleepy all the time, moody and anxious, hair falling out, gaining weight, heavy clotting peiods, etc. I was 51 and it was all blamed for a while in perimenopause. I have been on Synthroid .50 since then and some things are better like hair loss and sleepiness. My last check a few months ago was 1.3. What I hate most of all is waking up after a few hours of sleep and I feeing like I am on some kind of speed. My mind is wide awake and jumping from one thought to another, sometimes sweating heavily with my heart racing. I was diagnosed 10 years ago with Inappropriate Sinus Tachycardia and was on Beta blockers for a while. I have a new doctor now and never discussed this with her. The anxiety is awful sometimes too . I start to get fears of not being able to swallow or breathe but can keep it under control. An average night of sleep is five broken up hours of sleep and every now and then from exhaustion I will get close to seven hours. I am foggy headed a lot but I never hardly yawn or feel sleepy in the daytime.

My daughter has had a very difficult year, with many of the symptoms described in postings related to Yasmin. Please will everyone who has experienced the negative effects of this drug go to the website: www.FDA.gov and file a report. They do not ask for personal identification, but you can describe your symptoms, tests, hospitalizations, etc in great detail. You can also file a report with the drug manufacturer, but this will carry greater weight if your doctor files it on your behalf. Under certain circumstances, related to the severity of your adverse reaction, I believe the manufacturer is required to follow up with the FDA, and respond to your complaint.

I usually have allergy headaches in the morning which would go away after taking 1 Benadryl w/ Tylenol. About a week ago my doctor started me on Singulair because she was concerned about me taking Tylenol daily. The last few days I've had terrible headaches that linger most of the day. (I've continued to take the Benadryl w/ Tylenol to try to help the headaches, but it's just not working.) Today is day 7 with the Singulair, and the headaches seem to be getting worse. Are headaches common with Singulair?

I have been on synthroid for about 6 months now. Some of the side effects I have been experiencing are numerous.I have hair loss, sometimes I get so ill that no one can stand to be around me, my weight has gone up about 30 pounds, my cholesterol levels went sky high so now I'm taking Crestor, I'm bloated most times, I have episodes where my face flushes and gets so red that it feels like its on fire, and now I've just started experiencing burning and aching of the legs, I'm tired a lot too! My doctor said I would lose the weight but every time I go for check ups and get on the scale it just keeps going up. I would like to know if anyone else out there is experiencing the burning and achy legs because I have been tested for everything and they can't find out what is going on. They of course say it's not the medication.It seems to never be. Does anyone feel me??

hello everyone
i am a full time college student and I believe that i have some side effects from synthroid. As i was reading everyones blog i notice that some people feel the same way that i do. At times i feel that i'm normal but if something upsetting happens i get really tired, depress, and I have a never time concentrating at school and home. My body hurts all the time. especially my joints and i feel that i don't want to do anything. I have about a year left until i graduate and its the going to be hard. I cry sometimes for no reason. help! i'm going to talk to my doctor but if any body else feels the same way please reply.

I was prescribed Citro for a ear infection so after 10 days of taking Cipro 500mg 2 times a day, less than 2 days after that I broke out with a fever ranging from 104. - 102.4 for about 3 days at the same time I had joint pain all over my body and pain in my upper legs. On the 4th day after that I broke out in a rash all over my legs and buttocks area, I called the doc that prescribed me Cipro and she said my symptoms had nothing to with the Cipro. I see my dermatologist 5 days after and I find I have a allergic reaction to Cipro. So beware and always get a second, third opinion.

Fever after 1 day of usage, rash and hives

This website may not have saved my life, but it has certainly saved my sanity. Beginning in May 2007 I was prescribed Toprol XL for a supposed heart condition. I was instructed to begin with 50 mg per day and go to 100 mg per day after 10 days. Since I already had the 50 mg tablets, I simply started taking 2 of them together when I raised the dosage. On July 25 I ran out of the 50 mg tabs and filled a prescription for 100 mg tabs. Immediately upon starting the 100 mg tabs I began experiencing side effects which increased in severity daily. By Monday July 30 I was convinced I was losing my mind. Then I discovered this website, and read that many other people had suffered in the same way. What I have trouble grasping is why the same dosage had different effects. I tolerated the 100 mg/day dose just fine when taking 2 50 mg tabs, but the 100 mg was dreadful. I've checked the pills, and both the 50 mg and 100 mg are Astra-Zeneca products, not generic. The markings, shape and size are consistent with 100 mg tabs, so I haven't been inadvertently given an overdose. I immediately backed off the dosage, and am gradually going to reduce and stop the medication. I urge anyone who is having these problems not to stop at reporting them here, but also to contact Astra-Zeneca at www.astrazeneca.com, and to report them to the FDA's Medwatch website, www.fda.gov/medwatch. It may seem fruitless to contact Astra Zeneca, but they need to be made aware of these problems.

I have had thyroid disease for 6 years. I just had my medicine increase less than one week ago from 125 mcg to 150 mcg. The endocrinologist did this with a lab result from over 6 months ago and I was never retested before he upped my dose. 2 days after my new dose I broke out in a rash head to toe. The next day I started itching and went to my doctor and she said I have no idea what is going on with you. Then I went to the Pharmasist and he said you are having an allergic reaction to the dye in the 150 mcg blue tablets (125 mcg are white). The following day I got new medication I now am taking 3 50 mcg tablets. But I now am swollen ankles to feet and elbows to hands. My hands are like balloons. When I go to bed at night my hands are completely numb. Has anyone else had any symptoms like this?? Help I cannot figure this out. I am thinking that I may be over medicated. Thank you Heidi