Smile symptoms and conditions

I was put on Singulair two weeks ago and since then I have have experienced everything from hyperactivity and insomnia to flu symptoms and loose bowel movements. I contacted my doctor after 3 days because I was having tingling in my hands and feet, flu symptoms, cramping etc but no fever and otherwise fine...He said the benefits outway the side effects so take half. I continued to take half. The cramping reduced and so did the other physical type side effects, but I started feeling like Superwoman. Instead of sleep I sterilized my house, wrote emails, tended to laundry, etc...and then continued my normal day with a smile and pep that I would not expect. I really had no desire to eat. The thought just made me cringe. After two days of no sleep and hyperactive state I decided I am done. I stopped taking it...and I took my son, 6, off it as well. He had been taking it for 4 years and was presenting with signs of hyperactivity. It has been one week...he turned yellow, became more hyperactive, talked about how the man in his room is gone now. He had struggled with sleep since he started Singulair but there were no side effects at the time that listed bad dreams, hallucinations, hyperactivity etc...It has been one week and we watched our son turn yellow as he withdrew ...he could have been spider man break dancing on the ceiling for the first few days. His teachers and even the bus driver had sent home warnings about his behavior "can't sit still" ...the last 3 days of school he has been on "green" which means great behavior. I do not think anyone should give this drug to kids...and it should not be given in sample forms either to any doctor trusting patient...without a full discussion of these side effects. I feel like I just went thru hell and put my son thru hell.

I was told by my doctor to go to the ER for my severe migraine. I was given Reglan, Toradol, and a third drug that I cannot remember. The drug was given through an IV. About four or five minutes after the drug was given (I was in the room alone) I began to feel strangely. I wasn't warned about any strange side effects so I began to worry what was going on.

The side effects started by feeling a GREAT and inexplicable sense of urgency...like I needed to get up and run somewhere important RIGHT AWAY. Shortly after, like thirty seconds later I was forced to jump up out of the bed, it was literally painful to be sitting in the bed. I needed to move...and NOW! I was trying to rationalize my behavior. I felt as if I was given some kind of psychological drug that screwed with my mind. I began to feel a terror unlike any terror I have ever known.

I was trying to reason myself back to calmness and sanity, but I began to feel the rest of my body go into convulsions. I was standing on the side of the bed in my hospital room and I clutched on to the bed rails and started rocking and twitching and crying hysterically. I wanted to rip my IV out and run like crazy. I became claustrophobic and my heart was pounding out of my chest. I was covered in a cold sweat and I felt like a knife was going into my heart. I was convinced I was having a true heart attack.

My doctor happened to walk by my room and the curtain was half open. He saw me crying and writhing on the side of the bed. He laughed at me and asked me what was wrong. I politely reminded him that he was the one with the medical degree and that he should tell me what was going on. He smiled a Mr. Rogers kind of smile and said, "dystonia....that's all. So, just relax." He made me sit on the bed and that is when the full body convulsions started. I was flopping like a fish out of water on the bed and the nurse started getting short with me telling me I needed to "calm down." I politely told her that it was not my disposition that was causing the freak out, but the chemical that she pumped me full of.

I kept asking what was going on and what "dystonia" was. I was treated like an irrational child and the doctor sat smiling at me like I was crazy. I was convinced I was literally dying. The nurse put the blood pressure cuff back on me and she started freaking out saying that if I didn't control my heart and bring it back down to normal that I was going to have a heart attack. I told her that was my complaint from the beginning of the allergic reaction. I thought I was having a heart attack.

Reluctantly, (and after ten minutes of suffering the most painful and slow torture) the doctor prescribed some benadryl. I was begging him at this point to sedate me because the pain, panic, and body convulsions were beyond my tolerance...that and I was terrified and not getting any answers. The doctor held me down in the bed after the benadryl was administered and he kept insisting I go to sleep. How can you sleep when you are suffering those kinds of symptoms and convinced you are dying (without so much as an explanation as to what is happening to your body)?

I eventually fell asleep five or ten minutes later and woke up being wheeled to CT scan for my migraine. The worst part was that I was begging for my husband the whole time (who was just outside the room fighting with the billing department). The doctor told me that he was going to get my husband and then just left. I went through that whole trauma alone.

And when I was released from the hospital two hours later no one ever bothered to explain to me that the muscle spasms, heart pain, palpitations, and panic attacks would continue for some time as the drug worked its way out of my system. The side effects lasted on a much more mild scale for two days following this episode. I wouldn't wish this terror on the worst person on earth. Why is this drug even offered to people?

Hi I'm 36, with high blood pressure. I have been on 25mg/day hydrochlorothiazide since July 08. I went in for normal 3month check up and Dr tells me that my bottom number is to high, so she gives me yet another pill to take(yep you guessed it) Lisinopril. I filled the RX in the morning, by lunch time, I felt sick to my stomach, dizzy, everything hurt. I thought I had gotten the flu. This was just 2 days before my daughter and my mothers birthday.(both the same day) We had big plans after all you only turn 18 once. I put a smile on and went to the party, but it was living hell. My Fiance' noticed that I didn't start feeling bad until after I had taken that new pill. I only took 1 a day for 3 days and it took me over a month to feel half way normal again.

I have to comment..... look at how many entries there are showing side effects.. so many people have the same symptoms. does this not open the eyes of others to accept that it can be a real problem to some people, admittedly not all, but it obviously doesn't agree with all of us. I could not believe my ears the other week when the local GP said that it's rare there are side effects, then 4 hours later a DR. in a hospital emergency department stated that statin drugs are very common for muscle problems, in particular one named brand (need I say more??) Couldn't wipe the smile off my face after hearing someone finally admitting it..
Come on professional people, start listening and accepting that people do know their own bodies and can see and feel so many vast changes in their day to day activities. Maybe guide people to a better understanding of diet and lifestyle before dishing out meds. so quickly. Give us some credit......some of us exercise regularly, we want to live healthy too and all this has done is put a stop to that luxury.
I have to add, I posted earlier this month, I AM getting much better each day, clearer thinking, vast improvement in mobility, so please stay positive and take care of yourselves, obviously we all need a little patience, hard to do after some long term suffering i know, we want overnight fixes just to feel normal again.. :-)

Hi, i have 26 yo, im a doctor and my boyfriend too, i started to take Yasmin 3 months ago and ive never been a depressed girl, who cries with every tv show or even a commercial, now I AM, ive been from a funny girl who always had a big smile on the face and make jokes of everything (and thats why my boyfriend love me) but during this last couple of months i just don't know why im crying for every stupid thing..and then i go...why the heck did i cry for that?...im just waiting for my menses and then im switching to evra and see how it works,
Oh...plus i think i have IBS, migraine like headaches, almost no sexual drive and poor lubrication during intercourse, but ive not gain weight and my skin face is without black spots. thats the only good thing about Yasmin, but definitely i think my mood swings are because Yasmin and thats the worst thing.

Oh my gosh!!! I can't even begin to tell you how grateful I am that my husband found this website. I had my Mirena placed a little less than 6 months ago at my six-week follow up visit after having my 8th and last child. My husband and I (and OB/GYN) decided this was the best option because I can't tolerate birth control pills (the estrogen gives me major migraines). Anyway, I was told that I would have some spotting but it would go away and after about a year I may not have a period at all. I had just finished the bleeding that comes after having a baby and I breastfeed so I don't normally have a period anyway until a couple months after I'm done breastfeeding...well let me tell you I bled off an on for the first 3 months with cramping. More on than off and it was just downright annoying cause I didn't know when to expect it so I always had to be prepared. But I stuck it out cause I knew that was a possible side effect. What I didn't know was all the other possible side effects. I think I've experienced just about all the ones listed in all the posts I've read. I thought I was going crazy!!! I have had severe mood swings and I guess depression. I've never been a depressed person so I wasn't even sure what the symptoms were, but now I do. I don't feel like doing much of anything. I don't want to go anywhere...I just want to be a hermit at home. I love my husband and all my children, especially my little 6 month old boy and his never ending smile (which is what keeps me going) but there have been days where the littlest thing sets me off and pushes me over the edge and then I just want to rip somebody's head off! Completely irrational thoughts too. None of this is me at all!!! It wasn't until about a week ago when my husband and I were talking about it and I was crying and telling him that I didn't know what was wrong with me and that I thought I was going crazy and that I just wanted to be myself again and be happy...that he pointed out that the only other time he has seen me moody at all is when I'm pregnant (and then not even close to this degree). It was then that the light bulb went off! If Mirena makes your body think you're pregnant by releasing hormones then it only stands to reason that you may have some of the same side effects as pregnancy. I already had an appt. with my OB/GYN to get the strings cut shorter (my husband could feel them during intercourse and it was painful) so we decided that I should address my concerns at my appt. Well I did and my dr. told me that the mood swings and depression could very well be a symptom of the Mirena and it's hormones. He said that there was no way of knowing just how much hormones is too much for me and everyone is affected differently but that if it were his wife with the same complaints he would tell her to yank it. He said if I wasn't convinced about Mirena being the culprit that maybe I could seek counseling to talk about my "craziness" (my word...not his) but asked me to make a follow-up appt. with him in a week anyway and in the meantime come home and discuss it with my husband. My husband actually found this site and immediately sent me the link after reading some of the stories posted here. I'm eternally grateful to him...Now I know I'm not going crazy and I also know that I'm not alone! Needless to say...I'm keeping my appointment for this Wednesday and can't wait to have the Mirena removed and I'm not seeking counseling, lol!
Symptoms I've experienced:
Major mood swings
depression
exhaustion
back ache
weight gain
chest pain
anxiety
jitters
loss of concentration/focus
NO libido
joint pain
bloating
throat obstruction feeling

There's probably even more that I've just not connected to this stupid Mirena. Oh well...I just can't wait to be normal again! Anyone considering this type of Birth Control should really think twice and know what you might possibly be in for. Could work great for you, but then again, maybe not!!

Wow! I'm on day 4 of my new nuvaring. Last night I curled up in bed and contemplated 15 different ways to kill myself. That was after I kicked my cat across the room so I wouldn't go belt my sassy daughter across the face. And this was suppose to EVEN OUT my mood swings. I'm 40 and going through a lot of internal changes emotionally, some of which can be blamed on changing hormone levels. I was hoping to alleviate the mood swings (which compared to this aren't that severe!) I'm removing the ring today after reading many of the posts on this site. I can't wait to just be my regular moody self-lol! Oh, and I have to apologize to my cat who hasn't come near me since yesterday. :(

I started the NuvaRing three weeks ago and I took it out on Thursday so I can start my period. For the last few days I have been depressed, moody and ready to punch anyone that looks at me the wrong way. I am very active and usually always smiling I feel like it's painful to even try and crack a smile now. I am having a very hard time concentrating even if it's just a phone conversation. I didn't think it was from the NuvaRing until I found this site. I will probably discontinue use.

Well ladies, after reading about all of your experiences with mirena, I'm a little concerned to say the least. I have had mirena inserted for about 4 months now and really haven't had any problems with me personally. I did check out the website to see if any of your husbands/boyfriends had any complaints. My husband said that he could feel the strings during intercourse and they were painful. I went back to my ob/gyn to have her trim them but they are still "pricking" him. My libido is great but what good is that if my husband is afraid to have sex with me?? Anyone else having this probelm or am I the lucky one?? By the way, insertion was absolutely painless for me but I am 32 with 2 children

I already had experienced some bad side effects due to singulair with my daughter. She had become moody, emotional, having nightmares and those are just a few to mention. However, my son had no side effects. When I went to my children's pediatrician, she agreed some children do experience some side effects like my daughter was having. But somehow she didn't see it as quite a concern. I vowed then and there to take both my children off it. Then my son continued having his allergies and over the counter zyrtec didn't seem to help him. I went back to the dr. and because I trust her and have known her for many years....she convinced my to put him back on singulair since he had never had any previous side effects. Well, its been maybe 2 months and now I see my son acting strange. He is not himself. The normal activities he used to enjoy don't interest him anymore. For the last few days, he has been wanting to lay down and he says he's sleepy. To me, he is acting like someone who is depressed and he's only 5!!!!!! I am taking him back to the dr. and taking him off this horrible drug! For all you parents out there...I think we should all go with our "motherly" instincts and do what we think is best for our children. We are the ones that know our children on a day to day basis..not the doctor's. So I am kicking myself for not sticking to my original instincts. My daughter improved drastically! Even her teacher noticed a difference. Please if you notice something, take action before the drug does more damage.

First I want to say, after reading several posts, that it seems a lot of you are taking Topamax without food, which may be causing your "spaciness." My doctor suggested always taking it with food, even though it says with or without food, and I only experienced spaciness the few times I took it at bedtime without food. Once I started taking it with breakfast and dinner, that never happened again.

I am a 48 year old woman, prescribed Topamax in September of 08 for migraine associated vertigo without headaches, with facial numbness. The first thing I noticed was I immediately had headaches, which to me indicated it was dehydrating me as that is the only time I get a "normal" headache. So I knew I had to drink a lot of water. Soon after starting Topamax I developed a dry cough that lasted the entire time I was on the med. I did not relate it to the drug at the time, however. It never even occurred to me. After about two months on the drug I started having trouble breathing with extreme dryness in my airways. I was prescribed an albuterol inhaler which did not help. I was then prescribed a corticosteroid inhaler which also did not help. I thought the trouble breathing was from taking Nadolol which I was prescribed for occasional heart fluttering - the neurologist said this was a normal side effect of Topamax. I stopped taking the Nadolol but the trouble breathing continued. I also had more migraines with vertigo and facial numbness than before I started taking the drug. I hoped it would eventually stop and the drug would kick in to help the vertigo, so I stayed on the drug. I had very minor tingling in my feet, but it was tolerable. I became very stressed out, had trouble sleeping, depression, my face started breaking out in November (and still is), I lost interest in everything that I normally enjoy - reading, photography, following politics in the news (sort of an obsession of mine). In December I was so depressed that for the first time in my 11 year career I started canceling appointments and eventually took three weeks off from work to "re-group." In January the neurologist decided that we would increase the dose from 100 mg to 150 mg for one more month, and if it did not get rid of my migraines with vertigo, we would discontinue the drug. The first day on the increased dose I had a killer headache, and I drank 150 ounces of water before it went away. That night I did not have to go to the bathroom during the night, unheard of for me. That's a lot of water to drink and not have to pee. Within two days of increasing the dose, my cough became much worse, and within three days, the breathing became more difficult. Within five days, I was having trouble speaking because my airways felt so dry. I called the doctor the next morning and he said it was not the drug, but if I wanted to, stop taking it. So I went off it cold turkey, per his instructions. I had rebound migraines every day for a week or two and my heart was pounding, sometimes for three or four hours at a time. Eventually the cough and trouble breathing went away, however, I had to continue drinking lots of water or I would notice that I didn't have to urinate, sometimes not at all. Again, unheard of for me. I saw a cardiologist at the neurologist's urging and they said the heart pounding was just anxiety. I disagree, as did another doctor of mine. We both believe it was withdrawal. I have now found out (by getting copies of my medical records) that the neurologist is now attributing all of my side effects from the Topamax to "somatization." In other words, psychosomatic - not a side effect, but just a way of getting medical attention. I am seeing a few people on this board who have also experienced a dry cough and trouble breathing. Can I have the same side effects as other people and have them still be psychosomatic, even though I had no idea those side effects could occur? I don't think so.

I have a theory that Topamax interferes with hormones which causes a lot of the side effects like lack of concentration, memory loss, anxiety, depression, insomnia, acne, and hair loss - all symptoms of peri-menopause and menopause. Ask any woman in her 40's or 50's if she has these symptoms and most of them will say yes. My face has not been this broken out since high school! My hair is falling out at a rapid rate. I won't even bother mentioning these to the neurologist. He'll just say it's not the drug.

I'm very frustrated and not sure what to do at this point. The neurologist has me taking a supplement called Migrelief now, but I think it takes three months to kick in, so I have no relief at this point.

Has anyone else experienced the trouble breathing with dry cough? I don't believe for a moment that it was psychosomatic.

Wow! I must be the latest in a long line of Lipitor users and apparently pain sufferers. I have been on Lipitor for over a year. I am 56 years old, active and healthy (thank God). Around November 2008, I noticed a "twinge" in my left hip while sleeping. This has gotten progressively worse over the months and I thought it was due to arthritis (which runs in my family). But after reading these blogs, I am not so sure. If anyone has anything definitive regarding this, ie: tests, studies, etc., I would really appreciate a point in the right direction for more information. I was thinking (until today) that I was headed for hip surgery or something equally drastic. Now that I have a clue that it may be the Lipitor, I want to investigate further and then, if necessary, change to another medication that won't break me down like this. My heart goes out to anyone that has suffered through hip pain. It is a miserable, painful condition that saps your energy and your desire to even move sometimes. I appreciate any help you can offer. God bless all of you. - L. B. ******

hey everyone...reading every post makes me even more scared now. I was diagnosed with Bells Palsy on Jan. 13th. My doctor prescribed me prednisone and valtrex. 5 days, twice a day, 20 mgs. On the 18th i was finished with the pills. Very happy because the bells palsy went away. On my birthday, January 23rd. I washed my faced with Biore skin cleanser (which ive used for years) and it felt like as if my face was peeling off as i was washing it! I got so scared when i rinsed my face i actually felt my skin turning to leather. I got out of the shower and my face was round and beet red and my eyes were puffy and face was very very dry...The next day i woke up and my face was worse. I called my doctor and he told me go straight to the emergency room that i was having an allergic reaction to a skin chemical and get treated for an allergic reaction. I did just that. The hospital gave me another dose of prednisone. 60mgs the first day then again the same dosage that my other doctor prescribed me. Im scared to death now to take this pill. Yeah, my face went down and is not beet red anymore but what's going to happen next week once i come off??? i don't want to go against what the hospital gave me, but as im reading these posts, im up at 2:55 am and not sleeping..! help!

Hello! My name is Angelita and I am so happy that I found this website. I had the Mirena put in about 4 months ago. Thank "GOD" I had it taken out today. I've been dealing with headaches, fatigue, hair loss, acne, mood swings, upper and lower back pains, insomnia, cramps that felt like contractions, weight gain, hot flashes and joint pain as well. I seriously feel as though the "DEVIL" lives with in me, because I have been so mean towards my family. Taking all the strength with in me that at times I don't even want to get out of bed. I don't even want to leave my house to spend time with my family, because I am to tired to get up and get ready, and I feel ugly due to my weight gain and acne out breaks. For 4 months Mirena has stolen my life! I demanded yesterday that my doctor take it out! I told him that if he did not have the time to send me to another doctor who did because I wanted it out! He called me in the morning and asked if I could be there at 2:00, with a big smile I showed up. It didn't hurt when he took it out, but I did feel like a rush around my pelvic area. I felt like a drain sort of speak. Pressure like a period was about to start, although I have not started to bleed. Does anyone know when I should expect to bleed and when will all the other symptoms go away?

I've been on it for about 2 months, the first month nothing really happened...but the last month its just been getting worse and worse. Light headed, sweaty hands, cold feet, tinglinging in the fingers, heart palpitations, etc...the worst are the heart palps, and light headedness (I feel like I might pass out right now!). I stopped taking it today, my last pill was yesterday morning, so hopefully the side effects will subside today or tomorrow.

for those who went off the drug, how long did it take for the side affects to disappear?

I was on the Depo Provera birth control shot for roughly 6 years. It did stop my periods but that was the only good thing about this shot! I am now 30 years old and it has been about 2 years since I stopped receiving the injection. My teeth are decaying so rapidly that they chip and break as if they are made of layers (like a flaky biscuit). When I first started the injections my smile was pretty perfect. My diet and daily regimens have not changed so I can only attribute the dental issues to this birth control shot.
I also suffered from lowered sexual drive, depression, mood swings/anxiety and insomnia while on the treatment. After several years of my issues getting worse I linked them to the shot and no longer received the injections. Since then my other symptoms have gone away but the tooth decay still lingers.
Is there anyone else out there with these same issues? I desperately would love to find help or others like myself.

Has anybody had a problem with their gums thickening. It's actually the area behind my upper teeth not the gums around my teeth. As a result, my teeth are being pushed forward making me self conscious of my smile. I'd like to get off this medicine but the other medications seem just as bad. Has anybody had any luck finding alternatives to medication?

I took reglan in 1990 for the treatment of escophagitis (sorry if spelling is wrong). Had severe life threatening reaction (acute dystonic) and was rushed to hospital. Basically, it started the day after taking it. My face was stuck in a permanent Joker-like smile and it was painful. Thought I was going nuts, I was only 18 at the time, and then took another pill as prescribed. Later, my face stuck in an open mouth gaze position, I could not shut my mouth, it would spring right back open. Then, I lost my speech and spoke like a baby. At that point, my parents realized there was something seriously wrong (they had previously thought it was just me being nervous or something) and called the doctor. I was rushed to the hospital, and on the way I couldn't breathe. My bottom jaw shifted to the right, and my top jaw shifted to the left, and the pain was excruciating. I chipped my front tooth right off. My face was all twisted.

This went away after I was given Benadryl in the ER but I then developed the facial tic associated with Reglan, on the left side of my face. I am 36 years old now and a trial lawyer and singer who is always in the public eye. Luckily, the twitch is slight and only affects my left side, and mostly when I speak because it involves muscle movement. I was prescribed this drug 14 years before it was approved by the FDA. I would tell everyone I know never to take this drug, not even once. Its so dangerous and if I knew of the side effects I would have ever agreed to take it. Its very, very embarrassing to have this twitch. No one ever told me how dangerous this drug was. Hope this post may help someone. Thanks for reading.

IS THIS SITE AN ANSWER TO OUR PRAYERS?

A little while ago less than two hours, after a very emotional, difficult battle with my daughter, we had yet another heart to heart to try to do better. At the end of our talk WE PRAYED for guidance to know how to help the situation. So I'm here looking for a link to her behavior fron the ADHD medication and I see someone had posted about Singulair side effects. I was floored! I have never thought that Singulair was not a safe drug. No doctor has ever mentioned any negative side effects to me regarding it. The more I'm reading about it the more in shock I am. Have I and her doctors been doing this to my daughter? My 12 1/2 yo daughter has been on Singulair for probably 10 years. She was a 28 week preemie and had severe lung issues so it was a needed medication. Her behavior has worsened the older she has gotten. Because of mostly anger issues and problems in school about a year ago she was started on ADHD medications. We are currently trying to find "the right one" . I feel so awful. Could all her misery have been caused by this little pill that was suppose to help her? Why has her pulmonoligist continued to give it to her although she has not had any serious asthma problems in years? I think I will stop all medications and see what happens. My daughter has also been on amytriptylin for about six months also for severe migraines. What do you think? Should I stop all of them cold turkey or gradually decrease one at a time? I would GREATLY appreciate any advise.
Thank you

I have a 16 year old daughter that has always been extremely healthy, very out going, very happy and energetic...until YAZ! My daughter was put on Yaz for irregular periods, it was nice that it helped her (very) mild acne. The first couple of months were fine, but then she started having a lot of symptoms...hair falling out, heart palpitations, bloating, depression, anger, crying, down mood all the time, I have rarely seen her smile in months, leg/joint pain, anxiety/nervousness, I can see her shake a lot, wanting to be by herself (which is totally not like her at all.) This medicine has helped her acne and period cramps, but totally destroyed her personality and her happiness! Is it worth the price...absolute NOT! I AM TAKING MY DAUGHTER OFF YAZ TODAY!!! Honestly, I do fear what this medicine could do to her life if she is not taken off of it ASAP. How sad this medication is even available, much less being prescribed to 16 year old! I only wish I would have known about this before my daughter took this evil pill! I am so sorry for those of you that have gone through all of this as well.

I started using lipitor from my doctor, it lowered my cholesterol all around but I started to have lower back pains. At first I thought it might be prostate cancer, but after having to MRI's done they found no cancer, thank god. But I went to an orthopedic surgeon to see what the problem was. He looked at the mri's and saw lower dics hitting my nerve endings. He also thought that it might be muscle problems so he gave me 3 epidurals and that helped for a while took away about 50% of my pain, but I still have the pain, It is hard for me to get comfortable when I sit or even when I am sleeping. I don't want to think that it is the lipitor that is doing it to me but after talking with others I feel it is time to talk to my doctor about it. My doctor said that lipitor is the safest one that will do very little harm to my liver. I am not a doctor so I would not know.. My cholesterol level was 246 at one time now it is 175. I am now facing possible spine fusion to help correct my disc problem. But will also ask doctor to prescribe something else.

Alan

I was put on Loestrin24 Fe to control bleeding until such a time as I could have surgery. I took the first pill and started experiencing a sever mood swing right away. I became angry and depressed. My breast were tender. after a month the Anger and Depression were out of control. I was as hateful as I have ever been. My relationships were effected by my extremely negative attitude (which is completely out of character for me) and my sex drive well there was none. I suppose that is one method for birth control.... I started to notice fatigue, couldn't get out of bed had no energy, tightness in the chest and shortness of breath. Blood Clots...NOT FUN... NOT SAFE...

I noticed my old self returning almost immediately after stopping the pill. I don't think I cracked one smile the whole time I was on them. I am glad to be off and I will never take birth control again.

Please please if you are having sever symptoms. Shortness of breath and chest pains. DON'T WAIT to be TOLD to get off of them.... GET OFF OF THEM and GO to the ER immediately. YOU are talking about your LIFE...

My daughter was on Singulair for about 4 weeks this spring. She went from an outgoing talkative 15 yr old to being withdrawn and sad. Her symptoms were feeling hopeless, headaches, stomach pain, constantly tired. She was sleeping 9-10 hours at night without feeling like she had slept at all. She would fall asleep in class (not her normal at all). Her teachers noticed that she had stopped participating in class and seemed "sad". I took her to her pediatrician and she ordered blood work and an ultrasound of the abdomen-all of which came back normal. I toyed with the idea that maybe she was becoming clinically depressed. I researched her symptoms and came across others who had similar symptoms while on Singulair. I took her off Singulair and have noticed an improvement in her mood. Her teacher commented yesterday that it was nice to see her smile again and being happy. She told her that she noticed that she had seemed "sad" these last few weeks. I hope that they take seriously these potential problems with this drug. I will never allow my daughter to take this or any other related drug.

An element of the side effects of Singulair that are listed here are musculo-skeletal symptoms. Quinolones such as levaquin are known to cause those issues. Singulair is a quinoline, while not the exact same category, their roots are similar. It makes the possibility that the symptoms have a common cause worth pursuing.

Here is an example of some poor rats in Tokyo that were selected to prove that the symptoms in humans were real. Maybe we should tell the levaquin board that at least some of their problems have been known since 1997.

1: Toxicol Pathol. 1997 Nov-Dec;25(6):635-43.Links
Toxic effects of quinolone antibacterial agents on the musculoskeletal system in juvenile rats.Kashida Y, Kato M.
Drug Safety Research Laboratory, Daiichi Pharmaceutical Co., Ltd., Tokyo, Japan. JDN07402@niftyserve.or.jp

Quinolone antibacterial agents have adverse effects on the musculoskeletal system in humans, consisting mainly of myalgia and arthralgia, and additionally of tendon disorders and rhabdomyolysis. The present study was conducted to examine the toxic effects of quinolones on the musculoskeletal system in juvenile rats using light microscopy, 5-bromo-2'-deoxyuridine (BrdU) immunohistochemistry and electron microscopy. Single oral administration of 900 mg/kg pefloxacin (PFLX) or levofloxacin (LVFX) was found to induce lesions in the muscle + fascia, tendon + sheath, and synovial membrane, in addition to articular cartilage in the fore- and hindlimbs. Articular cartilage lesions were not necessarily associated with changes in the muscle, tendon, and synovial membrane, or the reverse. Among all lesions, the ankle and elbow showed the highest incidence and severity. Changes were more severe in the PFLX than in the LVFX group. Lesions in the muscle + fascia, tendon + sheath, and synovial membrane were similar and characterized by edema and increased number of mononuclear cells, many of which were positively stained with BrdU, as well as vascular endothelial cells in the Achilles tendon sheath and synovial membrane in the ankle. Electron microscopic examination revealed an increased number of fibroblasts and macrophages and collagen deposition in the matrix of the synovial membrane and tendon sheath. Capillary endothelial cells were hypertrophied, increased in number, and stratified. These results suggest that quinolones have toxic potentials in the muscle, tendon, and synovial membrane in addition to articular cartilage, and that local vascular hyperpermeability may contribute to the development of these lesions.

PMID: 9437810

My name is Bobby and I've been dating a girl who has been through some tough times. She took my advice and started taking an antidepressant, Celexa, 5 weeks ago. 3 Weeks after starting the Celexa, we began to have the relationship I always knew we could. I love her so much and for one week I was the Happiest man in the world.
Unfortunately, against my advice she started taking Yaz a week after beginning the Celexa. I told her that beginning two new drugs at once will eliminate the ability to identify which drug is causing which affects whether they be positive or negative.
After 3 weeks of Celexa and 2 weeks of Yaz, my girlfriend started acting alive and excited about life again!! She even started losing weight because of her beautiful new-found energy and zest for everything. She was playful, she was laughing, she was sexual, she was the girl of my dreams and we fell more in love than ever.
One week later (After 4 weeks of Celexa, and after 3 weeks of Yaz) a monster emerged who no longer can stand the sight of me. She doesn't want me to touch her, hug her, or even kiss her. She doesn't sleep at night. She screams and yells at me for being annoying when I'm doing things that once made her smile with love in her eyes.
I found an apartment today and decided to move out... I have never been treated so poorly by anyone in my life before. She's aggressive and verbally abusive. She's been complaining that people are talking about her and she seems paranoid. I made the mistakes of taking steroids a while back and I can tell you she is the monster now that I was then and both Yaz and steroids affect hormone levels and I'm telling you I just can't believe how many relationships this drug must be ruining.
Tonight I took the Yaz and threw all of it out. She got mad at me because she's afraid that she'll stop losing weight... I mean she's just completely lost perspective. I showed her pictures of us happy together and she still chose losing 3 more pounds over our relationship. I'm losing my mind... Just a few weeks ago she reminded me again that she wants to marry me and give me babies. Where has my future wife and future mother of my children gone??

I'M LIVING IN FEAR THAT SHE WILL FIND A WAY TO GET MORE YAZ B4 SHE'S BEEN OFF LONG ENOUGH TO SEE WHAT IT'S TURNED HER INTO.

SOMEBODY PLEASE HELP!!!
******