Game symptoms and conditions

My allergies caused nearly constant painful sinus pressure, drippy nose (I should have bought stock in Kleenex to profit from my box-a-day use), asthma, getting gradually worse all the time--it was as though I'd had the flu for 10 years (I'm 54). I was taking Claritin in the morning and Zyrtec at night, which only toned down the most severe symptoms. I was on Prilosec as well, as one doctor though acid-reflux might exacerbate the asthma. My family and I are avid hikers, but I haven't been able to breathe well enough to join them for years, even with daily Ventolin and Flovent. I've only been taking Singulair for two weeks, but it has made all the difference. I feel "normal" instead of sick for the first time in a long time. So, for me, it does work. But my stomach's been killing me--like a bleeding ulcer (which I had 25 years ago). I'm hoping that will subside or going back on Prilosec (expensive!) will counteract it. I've also had the weirdest dreams--very vivid and disturbing. Because I did research online before taking Singulair (Doctor uttered not one syllable about side effects), I recognize the dreams are from the Singulair. Because I understand what is causing them, I can easily set them aside when I wake up. I think anyone who's had mental or emotion problems could be sent over the edge by the dreams unless they had a clear understanding and acceptance that the allergy drug caused them. I would be easy to think something was wrong with you to dream such bizarre, violent stuff. (I'd give examples, but I've truly trained myself to forget all about the dreams as soon as I wake us, so I don't remember the dream events now.) I'm quite concerned about children taking this drug. Maybe not everyone has this disturbing-dream side effect, but how could you explain them away to a four-year old? How would you even know if a younger child was having them? Even children old enough to comprehend shouldn't be subjected to horrific mental images, like the 16 year old above. A tip for people who Singulair helps, but they have the weird dreams--try Melatonin (over-the-counter supplement) at bedtime. I've used it to help me sleep in the past when life events kept my mind too active to sleep for several days at a time. Unlike sleeping pills, it doesn't make your tired the next day, you can wake up easily, and it's not habit-forming--it just lets you drift off on days you otherwise can't. Since I'm concerned about the long-term effects of anything taken frequently, I don't take Melatonin very often, but I did try it after the fourth day of Singulair dreams. I had no memory of weird dreams when I woke up, so it seemed to work, and I didn't remember dreaming the next night either. I only tried it that one day because, as I said, I've trained myself to not be bothered by the dreams.

Wow! So glad I am reading this. I had the Mirena inserted Feb 2006. I never put all these things together before today. I did a search to see if Mirena makes PMS worse, because for the first time I actually noted dates on my calendar for the last three months, of when I am a fight picking, agitated, quick to yell, mean, miserable, sooo easily pissed off psycho. ...I don't bleed at all anymore, and haven't in over a year now, so I just don't pay attention to "that time" anymore. So I'm reading the side effects I have attributed to turning 30 almost 3 years ago. (now 32) So the chin hair and fat tummy may NOT be my age...huh...who would think!? Not to mention sore breasts and wicked nipple soreness, and zits like a 15 year old at times. Oh, did I mention PMS like a crazed woman? I can't stand myself today! I was so mean to my kids and hubby today! And the scary thing, when I do it, I don NOT care at all! I actually want to be mean when I feel that rage, and it comes EASILY! I don't look for it, or pick fights...but cross me?....ohhh...NOT a good idea! And it's always within the first week of the month. I am calling my Doctor tomorrow morning...Game on baby! Get'er OUT! Good luck to you all!

I had a small stroke associated with weightlifting--my neurologist put me on lipitor 80 mg (despite the fact that my cholesterol was totally normal)--now about 3 months later my liver enzymes have doubled and I have developed a heart arrhythmia I never had before. I have had to go to the emergency department twice from palpitations and diaphoresis

June 27/09
I am 65 yrs , very active. Play hockey, baseball, slopitch, and jog.
Started on Lipitor 10gm about 5 years ago. About 6 months later increased to 20gm. about 1 years later increased to 40 gm. Did not really notice any side effects. During that time cholesterol dropped from approx in Aug2005 to 8.01: ; Jan06 to 6.37:; Apr06 to 5.3 ; May09 @ 4.2. No problems noticed while on 40s for about 2 years.
June09 doctor increased to 80 gm !? Started to notice muscle cramps and pain . Also started to notice some stomach upsets.Thought I had strained a hamstring muscle from hard running acceleration but not sure now after reading some of the comments. Three days ago , although I always stretch for 1/2 to 3/4 an hour before every baseball which I play 4 times a week, I had very severe muscle cramps suddenly above my calf muscle just below the knee as I started to run to 1st base. I played the rest of the game but in pain and could not run hard . Could not sprint on my toes as I always did , so had to run about half speed but flat footed on the bases but painful,as we had only 9 players. Had hot shower Thursday night after game, massaged calf area with Wintercrest ointment. Got up this morning Friday , muscle sore but can walk on my toes. Tonight @ midnight slight soreness but most of the pain gone. I was thinking that I might have strained a calf muscle playing baseball but noway! I think it has to do with the doubling of the Lipitor from 40 to 80!!!! Will cut back back to 40 gm on my own till I see the doctor.
Will go to see my Doctor ASAP!!!

I am 16 years old and i have an orbital inflamatory psedotumor myositis, which causes me to see double. It is a condition the doctors are kind of just playing a gussing game in how long i will have to take the steroids. Everyone is different., i have been to many doctors and they have described it to me as an autoimmune disease within my eye and not my whole body. I was put on 60mg of prednisone. I have been taking it for over 3 weeks now. I was sapost to be symptom free within 2 days, but it took me 9 days before i noticed a difference in my vision. I am going on my fourth week now and still see double but not as bad. The prednisone has been absolutely awful. i handled it farley well the first 2 weeks and since then it has been pure hell. I do get bad mood swings,and i really don't mean to act the way i do. People i was once really close to don;t want to be around me anymore. Mostly i think i am frustrated with the acne it has given me. I am completely plastered now all over my face neck and chest. It is really embarrassing. I just wish other people realized how frustrating it is. Its like i wake up every morning and take an UGLY pill. I am really self conscious to begin with and was actually feeling pretty good about the way i looked until i had to start this medication. It really does suck. I can't even imagine what some of you are going through right now after reading everyones stories. My heart really does go out to everyone who has to deal with this, and i will pray for all of you. If any one has the same diagnosis as i do or knows anything about it and how long it takes to be treated please let me know. I am begging to worry because i don't think the prednisone is going to work for me. the doctors are thinking about putting me on methotrexate which i am also concerned about but it is not sapost to make you break out which is really all i am worried about right now. I have already back down from prom after working my but off to pay for my dress,and i really don't want my summer to be ruined. i wake up every day and want to hide in a whole were no one can see me. going to school is really hard to. The girls love to make fun of me and the guys are just kind of turned off from how i look.
How long does it take for the acne to go away after getting off the prednisone.and does it go away as you taper the drug down? also how long does it take before most people develop a moon face? i have a range of being on prednisone anywhere form 2 months to a year. There is a possibility that i will never be able to be off of it.

ok my brother was taking adderall for about 1 year I reali dont no what the milliagrams where but i do no they where orange pills not the capsuls.And about a month or so ago he actually said he thought he was having a heart attack so my g/ma took him to the hospital and the doc said it wasnt a heart attack but it was hypertentsion or something like that.Also if he started playin a game or anything it was like everything else disapeared.I swear when he was playin a game watching t.v or anything else it was like talking to a brick wall.He also was up for days and wouldnt eat anything he lost like 30pounds when he actually needed to gain 30 pounds to begin with.A couple of times he didnt take it and he would sleep and eat ALOT.But after he had his (what he thought heart attack) he quit taking it and it has been about 2 months now and i feel as if he is doing so much better now.The first month he was off it tho he as i mentioned earlier ate and sleep ALOT and had extrem mood swings.He was also very depressed. Was that from the adderall?

my aunt is 94 and was put on prednisone after having pneumonia. She is also diabetic, and has very poor kidney function. Her symptoms are restlessness confusion and constant playing with her hands or covers, this game may last into the night, just over and over placing one hand on top of the other. In looking for causes of this, I found it could be dementia or possible side effects of medication. We took her off prednisone and this behavior stopped

Hi to all,
I have read all comments in complete shock. I am a 53 year old female.
I was prescribed Simvastatin just over 6 months ago (40mg). I am hypothyrod and also have very high blood pressure. About 6 weeks ago I started to have severe (and I mean severe), night sweats. The sheets are absolutely wringing wet as if someone has thrown a bowl of water over me,
The headaches that start within about 30 minutes of getting up every morning radiate from the middle of my forehead right across my right eye and it throbs all day. My throat is sore, my skin very dry, my vision seems very blurred (especially first thing in the morning), and I don't seem to be able to focus very well. My appetite is almost non existent and my shoulder, legs & feet hurt dreadfully and although I hate to admit this I am quite depressed at how I feel.
Three nights ago I decided to stop taking Simvastin and guess what...hay-ho, no night sweats, no cramp and the headache today was much less severe.
I am glad I found this site and for sure I will be visiting my doctor next week to advise my findings.
I think I would rather live on a diet of bread & water rather than go through this again.
Good Luck to all fellow sufferers.

It's been almost 1 1/2 years since I have taken Levaquin for Bronchitis. I took it for only 3 days, after that I couldn't stand the pain and that was the only thing different so I knew it must have been the Levaquin. I suffered major, severe joint and muscle pain. I couldn't even walk down the stairs to the living room. As for lasting side effects, I am dealing with arthritis in my knees...which I never had before and I am only 40. I have severe tendinitis in my elbow which may require to correct. I know I am getting older but jeez....I am unsure if the arthritis and tendinitis is completely related to my reaction to the Levaquin, but what else could it be. I am not that old nor am I that out of shape. My only hope to spread the word about this evil toxic poison before someone else gets hurt.

Hi everyone.
I was prescribed prednisone for a hand injury that the swelling would not go down. I took it for 4 weeks. In the end of the first week I started breaking out in a rash that itched like crazy. They were small bumps that had nothing in them and they itched so bad I scratched them raw in my sleep. I informed the doctor about the rash and he told me it was to late in the game to get any side effects. This medicine also caused me to become very irate from any little thing. It also made me to lose my job while under a workers comp doctors care. This was about 6 years ago and I still am battling the rashes. They come and go but when they are apparent they take a long time to go away. I used to heal very fast but now it takes forever for an injury to heal. I have had blood work done and even had my liver checked out. They say I am as healthy as a horse so to speak. The rashes have scarred me all over. The bumps would turn to sores that took about 6 months to heal and they hurt, burned and itched all the time. I tried everything to control the itch and pain. I finally mixed aspirin with alcohol and some lotion together and this helped enough to get a fairly good night sleep as I was becoming exhausted. I am learning to deal with it in time but I will never be the same. My thinking is far from my normal thinking.
I had a list of side effects from prednisone and it was four pages long and the very first one was, Instant Death! The only side effect I was told by the doctor was that I might become easily irritated. In my opinion I think all doctors should give you an option after he has presented you with ALL the side effects of a prescribed drug and let you be the judge if you should take it or not. I now have a different doctor and he has prednisone as a drug I can not take. This medicine might be good for some people but it can have life changing effects for those that can not take it.
I feel for anyone that has had bad effects from it and hope you get over it some day.

I have been on levothyroxine 75 for two months so far. I started off at 25 then up to 50 and now currently on 75. I have horrible lower back pain along with my knees aching too. It's all the time and Advil or aleve do nothing to relieve the pain. I am miserable and hate living like this. Doing some reading here and other sites I've read that this can be due to the med and some thing about the fillers in it. When I first started the the 75 that my doctor game me from samples at his office that were the name brand all was good. Now that I have been on the generic from my pharmacy I'm in pain. Am I off base here and does any one have similar issue's? I'm calling my endo when the office opens today to see him. Thanks for any info.

For all of the poor girls who are searching "mirena experiences" because you are looking for a sure thing contraceptive-
This site is only for people who have had BAD experiences. Read them all if you want, but take into consideration they are the 3%, or whatever number, that had problems. None of these women deserved it, asked for it, needed it, or wanted it, but unfortunately their bodies responded to it in such an ugly manor.

Here's my experience so far....Had it inserted 8/06/08. Insertion was fine. Felt that speculum more than I could feel the actual insertion of the mirena.
Slight cramping afterwards...not immediately-went home and for like 20 minutes had cramps lighter than my period cramps.
For the first week bled lightly, second week had an actual period, week three and week four just spotting. The doctor told me this can go on for up to six months...kinda worth it if you think about it.
No acne problems so far, my hair is fine (and trust me, if my hair was thinning, falling out, or anything like that I would take the mirena out!), muscles and joints feel like they did before pregnancy, still breastfeeding (I know that they say that the mirena will make you produce less breast milk-tell that to my breastfed 13 pound 24 inch long 2 month old. he would disagree)
My breasts are a little tender and at first I was slightly bloated (less than if I were on my period) but that has subsided. Abstained from sex for a month after insertion per my doctor's orders, so I will come back and post if there were any problems with that...NEXT WEEK! yay!
Know that I understand the side effects could show up later.

Now again, EVERYBODY will experience something different. We are interfering with nature. Birth control is one of the most unnatural things we could do to our body.

Again, since this site commonly comes up when searching the mirena, I want for women to know that it might work for them better than it did for others.

I was prescribed CIPROFLAXACIN 500 mg 28 tablets twice a day. I developed Achilles tendon on my right leg
while playing volleyball. I am using crutches and off from work with short term disability. This drug did not cure my existing problem
but created new problem. Even when such side effects were known to the Physicians and Pharmacists I was not made aware of this. As a United States of American citizen I am requesting FDA to please ban such drugs
that cause such side effects.

Well i went to the family memorial weekend get together,Everyone asked me how my son was doing,great i said since he is off of the singulair and we realized what had been happening to him.I was armed with jersey mommas blog,and passed it around.My cousins new girlfriend,who has 3 boys ,said my youngest has taken singulair for years he tolerates it well,has been a great drug for him,well great i said but just be informed,as the day went on,her youngest got in a game and through th ball as hard as he could at close range into the face of a younger child,Johnny johnny say sorry she said ,and looked at me and said Jihnny has ADD you know,well i said was he diagnosed before or after Singulair,she thought a moment,and said after.A seed was planted maybe shell start to put the clues of this drug together.

After 5 weeks of taking Yaz, I have developed hives, "lobster red" skin and itchiness from my ankles to my knees. The itching is was so bad, I was using a metal hair brush to scratch (I know, not good). It turns out, I'm allergic to Yasmine. Hives is one of the first side effects.

I stopped taking Yaz about 3-4 days ago and the hives went away completely last night (my doctor told me yaz stays in your system 7-10 days).

The doctor also told me, if you do develop hives on this medication, you need emergency help. Hives can spread very very quickly and they can obstruct your airway.

I personally did not go to the emergency room (I didn't know any better), I was able to control them with Benadryl.

I am sad I can no longer take this pill. It was awesome. It took away my appetite, no moodiness, no pms, no weight gain.

:-(

After visiting this web site everyday for the past four weeks, I feel the need to share my daughter's (and my families') experience with singulair. My 8 year old daughter was put on singulair aprx. 2 years ago in addition to zyrtec to treat her allergies. Shortly after starting the drug, she developed stomach pain. After a few weeks of chronic pain, I pursued help from our pediatrician. After visits to two different pediatric GI doctors, an allergist (to test for food allergies), and an orthopedic surgeon ( because of sudden leg pain), the results were inconclusive. During this time my daughter also became very sad, angry and fatigued. She also completely lost her appetite and refused to eat much of the time. I attributed all of these symptoms to her stomach pain . In addition, she developed difficult sleep patterns and would often wake-up exhausted in the morning. Over time she also began to have more and more "melt-downs", breaking into crying spells over the smallest provocation or challenge. I recently contacted my daughters pediatrician to discuss what other testing or direction we could take to help my daughter. In the interim of making that contact, a friend told me about this web site. As I read page after page of other parent's experiences, I was in tears. I felt as if I was reading about my own family for the past two years. I say "family" because when one child is living through this kind trauma, everyone in the family is negatively affected in some way. My husband and I felt completely frustrated and unable to help our daughter. Our older children began to resent the great amount of time and energy I spent on behalf of our daughter. My younger daughter who had always looked up to and loved her older sister was sad and confused by her sister's anger and impatience.On March 29th I took my daughter off singulair. Unbelievable. Within 2 days, my daughter's appetite returned. On the second day, she came home from school and requested a corn dog and then some ice cream. She suddenly wanted to eat breakfast again. She started smiling and laughing again. She has suddenly become capable and responsible for doing her homework and chores. She is going to sleep more quickly and waking up happy. The best part is having our daughter back...the sweet, wonderful, happy six year old who I feel like I lost for two years of her life! As a side note-the return call I got from my pediatrician was that he wanted my daughter to see a psychiatrist. That's how close we were to taking another (completely unnecessary) path to helping my daughter. I also recently spoke with my daughter's allergist about our experience. At first he was somewhat dismissive. I asked him to listen to me parent, to parent for just a moment. He seemed to soften and said he would take a second look at singulair and its side effects. I encourage every parent who's child has been so adversely affected by this drug to be proactive. First, please contact the FDA to report your experience. Second, talk to your children's physicians and share, with confidence your experience. Third, share this web site or a similar one with everyone you know. I have been astounded how many children are on singulair just within my own small circle (school, church and play group). I really believe one voice can make a difference. I have to believe that for the sake of all the children still suffering.

I've never written on a blog in my life, and now that I've just read this, my stomach is doing flip flops and my blood is runnung cold. I have an 11 year old son and a 9 year old daughter. They have both been on singulair for quite a few years. My son has been on ADHD meds now since about a year and a half after starting Singulair because we tried to avoid them. Every few weeks he tells me he has this empty feeling inside him that makes him really sad and he doesn't know what it is. It just feels empty. I'll usually read with him or play a game or walk our dog with him to help him feel better.
As for my daughter, she exhibits all of the symptoms I have read about. She talks about life being terrible( trust me, she has it pretty good), she has been diagnosed with an anxiety disorder, OCD and Tourette Syndrome. Every psychiatric medication we have tried has made her worse. She was always a confident, outgoing little girl, and then she just changed. She's had stomach aches, which the docs always thought were in her head. She gets headaches. She is extremely sensitive, won't let me even brush her hair or touch her. She has extreme mood swings and gets upset over the most miniscule things, then writes about them, even saying she realizes her anger was too much for what the situation was! I will stop Singulair immediately and see what happens. What a miracle it would be if all of their symptoms disappeared.

A two days off of singulair my son started with a sore throat and headache that didn't go away for 5 days., three days after that started he ran a low grade fever for two days. I've read about others who had the same thing happen, so if your just getting off the singulair you may feel like your getting sick.

I must let you know from experience with both drugs scientifically, Lipitor does lower your cholesterol levels, and when u want to talk cholesterol, talk, LDL's or HDL's donttalk general. Lipitor has been proven to reduce your LDL levels yes, but the standard dose regimen for Lipitor is 40 mg, NOT 10mg, further more once Lipitor does that at 40 mg, it ALSO STARTS LOWERING YOUR HDL's which are your good cholesterol. So dont be fooled that your cholesterol levels have dropped. Consider the patients out there who suffer from GENETIC/ FAMILIAL DYSLIPIDEMIA's . The game is totally different for GENETICALLY OBESE PAX as well.

I think all of you folks with side affects are are blaming your ills on Lipitor rather than putting the blame where it belongs: on your own mental health. I am a 65 YO male and I have been on Lipitor for more than six years now. I have no side affects, I work out four days per week with cardio and weights and feel that Lipitor should be added to the public water supply. My total cholesterol has gone from the high two hundreds to under one-forty on a single daily dose of 10mg. All of you hypochondriacs get a grip.

I am a 25 year old, who was perfectly healthy prior to recently when I was diagnosed with Nephritic Syndrome and Minimal Change Disease and possibly FSGS (kidney diseases) I was put on 60 mg of Prednisone for 1 month then I was lowered to 40 mg for one month and I am then dropping to 30 mg. I am also taking Fosamax for my bones and a Vitamin D pill because my last lab test showed low vitamin D levels.

I am dizzy constantly and can not live a normal life, I can not drive or do any activities that I had previously done. My chest is so tight and constricted all of the time, my heart rate is so fast and pounds at my chest. I have no energy to do anything, I can barely open a door at times. I am beginning to grow unwanted hair on my face. My abdomen is always bloated. I have pain in my rib cage, and shoulders. I feel very sore throughout my entire body. I do not really sleep at night, so I look very tired all the time.

I have actually lost weight, I have no appetite at all. I am down 10-15lbs.

Now for the Pro- my Kidney Diseases are currently in remission and this has happened much faster than the Nephrologist had thought.

I am very anxious to getting my life back to normal and getting off the Prednisone.

Has any one else experienced increased heart rate, chest tightness, or rib pain?

I wish everyone the best in their roads to recovery!!

I have asthma as well as my son and daughter. We all take Singulair and I thank God for this medication that allows us to live a normal life. I grew up with asthma and since this kind of medicine was not available, know how it feels to be a kid and not able to keep up. I felt like I was out of shape and blamed myself. Not until I started taking Singulair did I realize what it was like to take a full breath and it literally gave me back part of my life. My children are athletic and love to compete. Before Singulair, my daughter was taken to the emergency room by ambulance because of asthma, even with her inhaler. Since she started Singulair, she can play an entire game and now even playing at college level. We have not experienced one side effect, only blessings!!!

About eight to ten years ago i had a violent reaction to lactaid. I had taken it numerous time before with no problems and then I woke up one morning - had a bowl of cereal and a lactaid pill - within the hour I was experiencing severe stomach pain along with vomiting and diarrhea. I thought it might have been due to the fact that i had had very little to eat the day before and only a bowl of cereal that morning with the extra strength pill.

the following weekend i was brave enough to try it again with some ice cream at night (this time i had a full stomach from dinner). BIG mistake - this time it was worse - the stomach pain was out of this world (i have a high pain threshold but this had me in the fetal position) and i couldnt leave the toilet and trash can for a few hours. My girlfriend was scared and called one of those nurse hot lines. they told her to coat my stomach with some kaopectate - which seemed to help. I checked the bottle of lactaid - and the expiration date had passed - so i threw it away and swore off of lactaid pills. fortunately they came out with the lactaid milk!

Fast forward to now - never touched the stuff again. well the other day I was out of lactaid milk and my wife (yes the same girlfriend) had picked up some samples of lactaid pills at a trade show - so I guess with the passage of time - I forgot how painful and miserable the other experiences had been - so i took the pill. Nothing happened!

Last night i decide to take another one because i had a craving for ice cream (had been awhile!). I figured it was ok since i had no reaction a week ago. Well sure enough - within the hour I was on the floor in severe stomach pain - followed by vomiting and diarrhea. This time we had kaopectate in the house - so i started taking it - well i just threw it right back up.

This episode lasted about an hour and a half this time. There was a metallic taste in my mouth about the third time i vomited, and the fifth and final time, there was puddle of yellow liquid that came out at the end.

I have taken Levaquin 500 mg daily for the last 7 days. I am quitting it today! I am so tired. Cannot sleep! Have severe pain in both of my hips! I do not have a history of sleep disorder or hip pain!!! I even have severe pain in both of my shoulders now as well. My doctors insist this isn't from the med. My pharmacist differs in that opinion!! This stuff is POISON!!!
I am a registered nurse and will preach this to any and everyone who will listen!!!
I only pray I will not suffer a tendon rupture even after I have stopped this med! If that happens I will contact an attorney! Can we get a class-action lawsuit for all of us and to prevent others from this terrible experience???

I'm a 50 year old male, very active but plagued with hereditary induced cholesterol. My first experience with Lipitor was that it was a miracle drug for me. Unfortunately after taking continually for 6 months, I keep on developing muscle strains on my legs which forces me to stop playing tennis for a month. I also believe I ruptured my Achilles tendon about two years ago because of taking Lipitor.

Anyway, after stopping taking Lipitor, in just 3 weeks, my legs felt stronger and I'm pretty quick in my game again.

Another side effect is the aging effect it makes on my face. It sags, making me a lot older. Stopping my medication also quickly tightened my facial skin, making me look younger again. In fact , on the street I will know if somebody is on Lipitor even if nobody told me. The skin will be like very soft, double chin will be really sagging.

The problem is doctors don't believe this. When I tell them they dismiss it.