Trauma symptoms and conditions

in 2006 i was attacked and bitten by a dog , the wounds became infected and was prescribed levaquin for the infection, about the 8th day of taking it i noticed bad joint pain, insomnia, anxiety, ringing of ears,and more symptoms, i was in good health before this, and have been in misery every day all day ever since!!!!
i have been told by my dr that i have fibromyalgia. if anyone has a doctor that will verify that the levaquin , and the trauma from the dog bite caused the fibromyalgia, please contact me , thanks

My son was on singulair for most of his infancy (11 mos- 22 mos old) we took him off of it when I started staying home with him. He was in daycare and was having breathing issues. We would give him the singulair and Zyrtec every morning. He became a very despondent baby. He would spend the ENTIRE day in the rocking chair at the daycare. After months and months of the teachers telling me this we decided it was best I stay home with him. He came off of the singulair and things got so much better for a while, he began to interact with us and others, not fearful anymore, and slept through the night. However other things have grown to be worse, as he has been developing...every day he seems more difficult to deal with. Now, 5, he is angry, fits of tantrums and rage, can't cope with his emotions, he actually kicked me today during one of these fits. He has been peeing in his room when he is sent there because he has been punished for one of these outbursts. What are the long term after effects of Singlair? Has anyone had this experience? Could the singulair have been given to him too early and now caused some sort of permanent nero or psychiatric condition? PLEASE ADVISE!!!! This Mom is really frightened.

My third day taking lowest dose of Lamictal. Have been taking Adderall and Cymbalta with no negative effects. I expressed to my doctor, that I am still sleeping a lot and sometimes don't even feel like getting up to taking my meds. When I do take them, I'm pretty great for about 6 hours, then right back to the couch.....
My doctor told me to stop the Cymbalta and start taking Lamictal. The first day I was my usual self, second day: dizzy, cloudy head with bad headache in temples. Weird throbbing in head. If I turn my head to fast, it feels like I need a extra second for the rest of me to catch up. I've been in bed, lifeless for the past two days. Don't feel that I can do much with my head like this. My hip bones and lower back ache.
My main concern is "Will these side effects subside?" I'm not Bipolar. I suffer from long term Depression/Anxiety triggered by abuse and trauma.
Please if anyone out there has felt similar effects from this drug, let me know. I want to give the drug a chance, but also would like to hear other's experiences.

I am a 48 year old woman, 5'1" (now 145 pounds). I had Mirena inserted almost exactly 5 years ago, and am scheduled to have it removed in 2 weeks. I gained 25 pounds over the course of the last three years; prior to that, my maximum weight for my whole (non pregnant) life was 123 (I was at 120 when Mirena was inserted, four years after the birth of my second child). I have always been very healthy, never abnormal blood tests except during my two pregnancies was tested as pre-gestational diabetic and had to watch my carbs.

I never put it together with Mirena until just recently, when I started doing research on hypothyroidism after a friend told me that my symptoms could be due to that problem. Depression, hair loss, acne on my back, and the terrible weight gain. I went to see my G.P. who referred me for blood work. I hoped to see evidence of low thyroid function (actual TSH value, 3.12 -- I was told this is normal on a range of .4 to 4.5). I also discovered that I now have high cholesterol (269 triglycerides, 251 total cholesterol, 46 HDL, and 151 LDL). My fasting (14 hours) glucose # is 99 (I was told this is normal on a range of 65-99 mg/dL), and my vitamin D, 25-OH is 21 (also was told this is still normal but low on a range of 20-100 ng/mL). I tried to give blood six months ago, and was turned down because of anemia, so I've been eating a lot of spinach, greens, and more red meat than I normally would, so I was interested to see if I am still anemic -- the red blood cell count is 3.8 (told it was normal on a range of 3.8-5.1 mill/uL). I mention these specific results because although I was told they were normal (except for cholesterol), when I physically went to the doctor's office and requested a copy of the results and did some research online I see that my thyroid IS actually low-functioning -- according to guidelines revised six years ago, anything over 3.0 is considered hypothyroid and should be treated. Plus, isn't a fasting glucose of 99 pretty high? Yet my doctor's only suggestion: diet and exercise. Good grief, I've been on a diet since I had my first child, 13 years ago. True, I don't exercise regularly (I'm a teacher and mom of 2; I never seem to have the me time.) I guess I have an excuse to get a gym membership now.

Also, for the last year I've had increasing pain in my shoulder (I couldn't lay on my side, for example, and lately I can't reach behind me or over my head). An x-ray turned up mild bone degeneration, but not enough to cause the pain I've been having. I was referred to an orthopedist, who today diagnosed a shoulder rotator cuff injury (I've had no injury; he says it is a common degenerative complaint in the over-40 crowd). He gave me a cortisone injection and I'll be on PT for a while to see if the pain goes away. If not, I'll have to have an MRI and surgery to correct the tear.

I'm posting all of this in case it might be useful to someone out there who might be going through the same thing. I had a thyroid test done about six years ago at my OB/GYN, and it was normal then (though I don't have the number; I'll get it in 2 weeks at the OB/GYN). It will be interesting to learn whether my thyroid level has gone up since Mirena. Also, although my research suggests that the effects of these synthetic hormones do not wear off for some time, possibly even years, I will finally feel like there may be hope if my symptoms improve over the next few months when Mirena is gone. If so, I will share it with you.

If you are reading this, perhaps you have a similar story. I wish I had been more aggressive about checking out the possible causes of my many symptoms, but I let them go for years because, I guess, I just figured I'm a healthy woman who is no longer young. (Oh, one more thing: for the first year or even two years that I had Mirena, I had incredibly heavy periods. The blood flow was similar to that during the day or two after the vaginal births of my daughters. Don't know if that's significant, but it took a couple of years for my periods to get fairly normal on Mirena.)

On 3-25-09 I was started on Avelox for a sinus infection. I took my first pill that day and the second dose when I got up the next AM. I had the normal stomach upset that is normally associated with Avelox but by day 3, things drastically changed. My blood pressure was 168/105, sweating, feeling unattached to my surroundings, dizziness and PANIC. I ended up in the ER due to the panic, uncontrollable crying, feeling that I was dying, blurred vision, elevated heart rate. I felt psychotic! My doctor gave me a shot of Ativan and within 30 minutes, started to feel a little normal, but still had uncontrollable fear. Today is day 4 and am still dealing with the anxiety but have Ativan to take the edge off. I hope this goes away soon. No one should have to go through this trauma. I will never take Avelox again.

It is hard to tell what side effects come from which med but after reading other peoples experiences I think that its easier to put my finger on. I have been taking Lamictal and Lexapro since last spring/summer. I started to feel a lot better as soon as I started the Lamictal. I have a history of being severely depressed all the time. It has been a long road in search of the correct combo of meds. We added Lexapro and I got even better. I was on Wellbutrin and Topamax before this and it was too much drugs in my system causing loads of anxiety. I heard Topamax makes you Dopey so I was happy to get off that. I don't notice Lamictal doing the same thing. I think clearly now, but I do have trouble crying - which is fine with me. I am so sick of fucking crying everyday. Aren't you??? The whole point of treatment is to increase the quality of life and These drugs have definitely helped me to be happy which is all I care about. However, I do still wonder what I would feel like without them. It is tempting to stop once you feel this good. Why cant i just be able to feel this good naturally. WHY WHY WHY .

I am so happy to have found information concerning Zocor on the internet and this particular website. My husband and I started on Zocor about 3 months ago when our insurance company, Caremark would not pay for Lipitor which we were on for about 10 years prior with little side affects. I started to notice that my hair was falling out and I started to have insomnia, something I never suffered from. Also started to notice heart palpitations.
My husband, meanwhile had started to notice extreme joint pain in his thumbs and seemed to be spreading to his fingers. Since I'm fairly new to the internet and google, I goggled Zocor and I can only say that I was shocked to read about all the side affects that we were experiencing appear on the many websites. I feel sorry for all the men and women going thru the trauma of hair loss and pain and a lot of other side affects from this drug, who may not have access to this kind of information. I plan on emailing the FDA so at least Zocor should disclose these side affects.

My then 11 year old daughter received her first vaccine in June 2007, and third in December 2007. In January 2008, she began complaining of backaches and headaches. During the spring/summer 2008, she began having tremors, tingling and numbness in her legs and arms. She is always tired and never feels good. We have seen a neurologist and 2 neurosurgeons, had CT scans and MRIs. But no answers. She is on medication that has helped slightly, but she still suffers from a constant headache that she never ranks less that 4 on a scale of 1 to 10. Typically she rates it as a 7 or 8, and we have had a couple of 12s.

I wrote about a year ago. My 17 year old daughter was suicidal and horribly depressed during the year she was on Singular. Her asthma doctor had seen this is girls her age and took her off it immediately. Turns out it was not even helping the asthma as she improved on only Asthmanex.
She got better after being off Singluar 2 weeks but was never the happy, outgoing girl she had been before she started. She is now suffering again form an episode of major depression.

Are the effects of this drug permanent? She got so much better after she stopped it, it was like I had her back, almost. She never made ti back the whole way.
I filed a post-marketing MedWatch adverse drug report form one year ago. It is the only way we can prove what is going on. I used to be a certified clinical research co-oridinator. The FDA can't know unless we tell them. Please let them know what a dangerous drug this can be.

My son has been on Singulair for about a year and a half...it really seemed to help his allergies...at least at first. This winter has been very dry and I have been having to give him other over the counter allergy medication as the Singulair isn't helping much. He also started losing weight..just not hungry. At first that was ok as he needed to lose a little but then he was getting too thin. He wasn't eating much at school but refused to take a lunch from home. I took him to the doctor just recently to see if he was physical ok since I didn't know what was causing the weight loss. The blood testing showed everything was normal and I just told him he had to start eating better...he has somewhat...but also he finally told me he has been feeling very depressed...seriously depressed and having suicidal thoughts too due to some kids picking on him at school.

I knew there were problems as he complained alot but I had no idea it was this serious. I have taken him out of that school. Right now I don't know if the Singulair could be adding to this depression or if its all just due to the bullies. While he complained a lot he never acted as if it was bothering him that badly or I would have gone to the school about it. Anyway I stopped the Singulair and am going to see if his mood improves or not. After reading some of the scary posts on here regarding the side effects I am wondering if this is a good idea stopping it or not. I am waiting for a call back from his doctor on it. Since its once a day..its kind of hard to wean them off of it...but I could cut it in half ..do that for a few days, then cut it smaller and so forth. His is chewable so I could do that with no problems. He is 13.

I used to receive a Kenalog injection once a year to treat my skin. It worked great. Best drug, nothing compares to it. After a few years it worked so great that I didn't have to receive the shot anymore.

This drug is far too helpful in the medical field for it to be removed because of its side effects. Never had a problem with getting a hole "in my butt" either... Not that I let A LOT of people look at my butt anyway. There's a reason why you're told what the side effects could be, if you don't like them then tell the doctor you don't want to take the medicine.

If you're a model, then have it photoshopped out... We know now that's what they do anyway. You give young girls bad impressions thinking they have to be perfect, when you're not.

I have been taking Crestor since early September 08. Prior to that I was on Vytorin for quite awhile. I now have right sided parthesia and my face tingles constantly on the right side. I have had MRIs MRAs not to mention blood tests that say my kidneys are spilling calcium. No one seems to have a clue what is going on. My feet and legs hurt so bad if I sit for too long I can't hardly walk. My uncle passed away from ALS and now I'm really scared that all of these statins are killing me slowly. I wonder if I quite taking this drug will I have a heart attack. I really just don't know what to do.

I have had trouble standing from a sitting position. My internal medicine Dr. ran some blood tests and discovered I have elevated muscle enzymes. My psychiatrist convinced my internist that I needed to have physical therapy instead of coming off the Abilify. If my muscle enzymes are elevated it indicates that I have had muscle trauma due to the Abilify.

My mom was put on Levaquin for 3 days to follow up on a Colitis diagnosis. She began hallucinating, hearing voices, can't sleep, loss of balance, among other things. We suspect it's Levaquin and took her off yesterday.....how long until she gets back to normal? She seems to be getting worse even though she is off it now.

I started Wellbutrin in the beginning of December. Someone very close to me passed away and I developed severe anxiety with some depression. I took some control of it with simply taking Ativan, but the doctor insisted I get on something for depression as well. I didn't really understand why I need to take a pill when I was just fine before this event.... but ok, I agreed.

I was prescribed Wellbutrin XL 150 mg. I was optimistic about it. She said it might improve my focus, give me some energy back, had no sexual side effects.

I took it in the morning, and usually with at least something in my stomach. The first 3 days of taking it, I was severely unstable. I think if I didn't have my boyfriend, I would be dead right now. I would cry uncontrollably, for no reason, pace, have terrible anxiety... I remember going through my closet, throwing things around, looking for a belt, throwing a few on the bed and taking one and tightening it around my neck.. I then walked around and was looking for a place to hang myself.. Luckily my boyfriend got home because he had a bad feeling about what was happening with me... otherwise I, to this day, do not know what I would have done.

After the first 3 days... things sort of calmed down... sometimes I would feel "better" in little spurts the first week.

I also had my sex drive for the first 2 weeks and it was good. I still wasn't "happy" but the medication wasn't doing any significant harm.

In the 3rd week, I lost interest in nearly everything. I didn't want to step foot outside. I stopped talking to my family, stopped answering my phone, I would lay in bed for hours, thinking of depressive things. I began eating, a lot. Constantly. Which shocked me since it is supposedly supposed to suppress appetite. I stopped going to school.

In the 4th week, and last, things gradually, and then quite suddenly just went downhill. It started with me becoming very agitated, snapping at everyone. My mental clarity was out the window. When someone said something, it took me a long time to register it, if I ever did. Sometimes my boyfriend would look at me after saying something and I would realize, oh my god, he said something... I really didn't hear/listen anymore. I was brain dead to everything except these horrible thoughts of just wanting to die. As the days progressed in the 4th week, I became more and more depressed. If I had to describe it, I would say it was a mental breakdown. I would cry hysterically over nothing. Absolutely nothing. I couldn't think of a single reason. I would start to cry while brushing my hair, while eating, sitting, watching a movie... I would cry 20 or more times a day. I really wanted to die because I could not bear it anymore. I felt like this was the end and it was going to end.. I wanted to inflict injury on myself, but focused my thoughts on more "permanent" damage -- suicide. I became obsessed with buying a gun. I swear if I had one, I would not be here. I would hit myself, all over my legs, while sobbing uncontrollably on the floor. Days later my boyfriend would ask where the bruises came from because it would be in such a weird area that there was no way i walked into something... and I would tell him I had no idea, and I didn't..... until later I realized it was me, hitting myself.... I felt very depersonalized. I felt unpredictable and I felt that I was not sure what I was going to do next, I was afraid of myself and very paranoid. I lost my appetite and never wanted to eat, thinking of food made me nauseous. I felt sick to my stomach. My anxiety was through the roof. My mind wouldn't stop spinning with thoughts, repetitive... until eventually it lead to another breakdown.

With my luck, it reached it's worst around the new year when everything was closed and I couldn't get a hold of anybody. I desperately called mental emergency facilities but all they said they could do was commit me for at least 72 hours and I didn't want that. I just wanted this to end, NOW, not be trapped in another hell hole. My mental doctor was closed so I tried to see my primary care and he was too afraid to mess with anything and told me to double my ativan dosage (WHAT! Because of Wellbutrin, I went from taking .5 or less mg of ativan a day to taking 2mg or more and still, it barely did anything!), so I went to the ER, and they did nothing, except tell me that the only way to help me would be if I went to a hospital for 72 hours. I said NO. It is ridiculous to allow someone to get this bad, and to not help them immediately, instead leave it up to them, to either be placed in some state run down mental facility or kill themselves that day.

I got a hold of my doctor the next day and she switched it immediately.

My husband entered the hospital in Nov of 2005 for a surgery. He almost died in the recovery room and from there things went from bad to worse. They put him on a massive dosage of Prednisone. 95 days later we were able to come home. About 2 weeks later he started vomiting and lost all energy. We returned to the hospital and the diagnosis came down as acute adrenal insufficiency. He was pumped full of Prednisone again. From there he went to a very slow wean and he got completely off the drug. No problems. This year he suffered a fall resulting in extreme trauma and blood loss. Back to the hospital where it was determined that his adrenals were again in crisis. Got him all mended and on the way out the door when a nurse decided that he should have a pneumovax. Within 24 hours we were back in the hospital with my husband in critical condition with three life threatening situations. His kidneys were shutting down, his blood pressure was beyond the danger zone (low) and he had cellulitis. Back home again to another slow wean. We are down to 5mg now and are hopeful at the next appointment to be able to start weaning further and back to zero. We were given Dexamethasone Sodium Phosphate for injection in case of any trauma in the future. In addition, my husband now wears a MediAlert bracelet which notes his condition and that in case of accident/trauma Dexamethasone Sodium Phosphate is to be given. Anyone on steroids should register with MediAlert at ******

What everyone needs to know is that the adrenals are responsible for a person's feeling of well being. When you are on a steroid, you need to wean very, very slowly to let your adrenals start doing the job on their own. The reason Prednisone is often prescribed is that it comes in as low of a dosage as 1mg and can be split 4 ways for 1/4th mg per dosage. For those that cannot tolerate Prednisone, Hydrocortisone is available. 10 mg of Hydrocortisone is the same as 2.5 mg of Prednisone. Hydrocortisone can also be split.

I have had numerous side effects with tramadol (nausea, heart skipping beats, restless legs at night) but I was too desperate and needed something so I just started taking 2 half pills a day (total of 50 mg). Well, now I've quit after about 2 years because I have sudden onset swelling and tendinitis in both of my achilles tendons. There was absolutely no trauma involved and tramadol was my only medication. After doing research online, I found that this is a rare side effect to some other medications but it hasn't been mentioned for tramadol. I truly believe this is a side effect that just hasn't been reported yet. Also, it can lead to both tendons rupturing. I just hope I stopped the medication in time so that it doesn't lead to that. It's only been a few days and I have a lot of pain and difficulty with stairs. I think this will take a while to get over -- like all orthopedic related problems.

I am a healthy 58 yr old woman. On May 20 2008, I went to the dentist to have two small fillings done. At the time of the shot I experienced what felt as though I had received an electrical jolt because the shot hit my nerve. This jolt radiated down to my ovaries. I complained to the dentist instantly. Right after the visit I started noticing that my hair was thinning. On June 17, 2008 at my normal hair appointment I commented to the beautician that my hair was thinning. On June 27, 2008 at the second visit to the dentist I experience the same problem from the shot and again told the dentist of problem. By July 18th I noticed some extreme hair loss in two locations on my scalp. I pointed out my hair loss condition to the Dermatologist at the Cleveland Clinic on July 18, 2008 he referred me to a hair loss specialist. On September 2, 2008 I meet the specialist she stated that the hair loss was caused by some extreme stress to my system. I told her about the dental work and my reaction to the injection. She said that could have been the catalyst that started this problem. The doctor said if there is some "shock to the system", as many as 70% of the scalp hairs are then shed in large numbers about 1 to 2 months after the "shock". This sudden increase in hair loss, usually described as the hair coming out in handfuls is called acute telogen effluvium. Has anyone else had a similar experience?

My experience with Yasmin was very similar to the one posted by "vpompon19" on October 26th 2007.

I took Yasmin for only a month. The day after I started, I had those symptoms:

- Nausea that last day and night
- Complete loss of appetite.
- Extreme fatigue
- Sleeping over 8 hours and still feeling tired
- Brain fog - inability to concentrate on anything
- Irritability
- Hypersensibility - I would cry for nothing...
- Feeling extremely nervous and nauseous when I had only half a green tea!
- Heartburn (I suffer from acid reflux but it was almost gone until I started Yasmin)
- Depression

When i stopped, I had the most painful period I've had for at least 8 years.
Plus I immediately started an urinary tract infection (which I never had before).

Two weeks later I experienced unbearable back pain. The doctor told me I had a herniated disk but I didn't force or had any trauma so I was sceptical. It turned out to be mononucleosis!

So thank you not Yasmin for having wasting at least 2 months of my life (so far), not mentioning the fear I had a more serious disease... No more birth control pill for me ever. I took another brand (Marvelon) for 7 years, then I stopped one year and my Irritable Bowel Syndrome disappeared. But my acne came back (even though I took Accutane when I was 15 - which I'm sure is the cause of my uncontrollable acid reflux).

I found out there are natural, safer and cheaper contraceptive methods. Don't wait until your doctor or the education system tell you about them because you'll be dead already.

M.

24 yr female diagnosed with PE and DVT. I have been on Warfarin since may of 08 and it has turned my world upside down. Weight gain (20lbs in 3 months), major hair loss, very bad acne, and memory loss. Not to mention i can't shave my legs or anything else for that matter with out getting major in grown hairs. I NEVER had any of these problems before. I am loosing muscle mass and feel as if I am a 70 year old woman. I don't know what to do but cry. The doctors keep telling me its not the medicine but I feel it is, my body is telling me it is. things are not easy, and it is affecting me I feel for the rest of my life.

I am so sorry to read about the bad experiences with Mirena. For myself I was put on it to keep hyperplasia and the beginnings of an oestrogen dependent cancer at bay. I was very hesitant at the thought of having something in me but oral progesterone had left me bloated, with awful migraines and terrible mood swings.

Once the Mirena had been inserted, It took a few months for all the bleeding I had been having to calm down and eventually stop altogether, but the most wonderful thing to me about Mirena were the side effects it had on me. My monthly migraines completely disappeared, so did my terrible depressive PMT, and best of all, the severe almost disabling pain from endometriosis was completely gone! I began to be one of those blessed women who hardly know they are having a period.

Five years later and a repeat one was put in last week. I have an extremely gentle and skilled gynae and a lot of the problems I am reading about seem to be related to incorrect insertion that is leading to terrible pain afterwards, because the darn thing is to low in the uterus and is sticking into the poor woman.

I quite understand those for whom is just seems not to be suitable, but for me I wish I had known about it's wonderful effect on endometriosis, migraines and PMT years ago. I would have taken it for that alone 20 years ago. And it is keeping me cancer free. My sex drive has also not diminished on it at all.

So I post this just to balance the negative experiences. Above all get a skilled and gentle Gynae.......that is the secret of skilled, speedy, and gentle insertion of an IUD.

I am a loving mother of a 5 1/2 year old boy. He has been on Singulair for over 3 years. In this past 3 years my son has suffered in an unspeakable amount. He came down with Rota Virus and was hospitalized at 2. He then came in contact with Pneumonia in the hospital while he was there. They automatically put him on Singulair, Zyrtec, Prednisone, and antibiotics to treat the pneumonia. Since that day, my son has gone though more tests than I have in my entire life. He has had asthma, sinusitis, leg cramping ( to the point he cannot walk for 2 years), IBS, Acid reflux,(they gave him laxatives for a year that made things worse and addicted to them also), stomach pain, constipation and diarrhea back and forth. He also got Erythema Mulitforme TWICE, while on this drug. All of which the doctors said could NOT be caused by Singulair. He has had several Upper GI's and CT scans. Along with Barium enemas, several hundreds of blood tests, and many many pokes and prodded that were not necessary. All since he has been on Singulair. He now has frequent bathroom trips, depression, confusion, and anger outbursts. He also has to go to the restroom every 5 minutes. He has had genital swelling, and many other aches and pains. None of which his "doctor" ever said could be a result of Singulair. I am 100% sure it was!!!! He currently has anxiety and emotional sporadic issues causing problems in school The teachers and counselors say that it is so strange because there is no TRIGGER and the outbursts are completely inconsistent. His preschool teacher and director are sure he has ADHD. Well, we had him tested and he does not have any part of it. He has no learning disability what-so-ever. So that brought me back to square one. He is in a positive loving enviroment. How could he be depressed and want to hurt everyone around him? He cannot sit still. He cries and says he is 'stupid" and "can't think" like the other boys. He has nightmares and cannot sleep alone. He is scared of everyone and everything. So, as I sit here crying, I realized that this has all been a reaction of his "medicine" Singulair. He never should have gone through all of those painful tests, only to prove they couldn't find anything. So many treatments and sound full advice speeches from his doctors. How could they be so naive and selfish in the life of my son?

When I called my pediatrician of 5 years, she told me that " parents that have children with behavioral problems will LOOK for something to blame their problems on." She also said "drug companies only put side effects on their labels to PROTECT the drug companies. (as she laughed at me) They are not always valid". Then she said "if you take you child off of Singulair you will be playing Russian Roulette in his life." Then she said that all children around 5 or 6 go though this emotional time in their lives." She told me that if I take my child off of Singulair that she would no longer be a part of his health regimen for his asthma. She told me to see a Pulmonologist for further treatment.
Who is paying who? This is my son's life???????? I decided to go with my mother-gut instinct and get him off of this medicine. No matter what. He has been a different person since. He is currently going though a lot of side effects and withdrawals (leg pain, insomnia, hic-ups, emotional distress) but every day is getting better. How can the drug companies say that this is a "wonder drug?" There are more reported side effected patients then clinical studied patients! How can a "medication" that stimulates the brain not be connected to other problems? This "medication" interferes with the bio synthesis and action of LTs and has been marketed as NOVEL medication against asthma and allergic rhinitis. Who the hell is playing God here??? The pocket books of Merck or our over PAID "doctors?" Who pays the price? Our children? Or us. Thank god I found this before it was too late. I would not be able to withstand the pain of losing my son due to their lack of scientific evidence. They are lucky I am one of the smart ones. I will not settle for less than Justice for the drug companies and their paid "doctors?" You all end up in the same place. HELL

There are 18 million people on this drug. Most of them are children. Please save a life if not your own child's life. Thank You

I am replying to my first post here yesterday....So today I didn't give my 3 yr old son the singulair and do not plan on it ever again! I have to say though...I am very very concerned. I think tonight I truly saw one of the bad behavioral side effects :( He got upset over something so small. Said he didn't love any of us, he didn't want Chinese which is his favorite! He didn't want to do any of the things that we gave him options on that he normally would jump right up to do! This devastated me! I right away thought to myself is this going to get worse before it gets better? He is still complaining of back pain which I know that will take some time. He punched a little boy just before dinner in the neck. He walked out of the neighbors house to go home and usually I have to carry him out. This is seriously scaring me! I'm not sure what to do ? My fiance, his father, doesn't understand and started to yell at him for his behavior. (We don't get much time to talk and when I try to his dad just says he is ok but I know, deep down he isn't) I am the one with him everyday at home taking care of him. I am now being more patient with this behavior when normally I would lose patience and punish him with time outs. Do I continue to do time outs?
Why should I punish him when its not all him ? This is so unfair :( I mean, he is a boy and yes he acts like one. Doesn't share at times, hits sometimes, he is a or was a normal 3 year old boy. His dad will follow my footsteps on this as he see's how I handle things but I'm a little witty on how to handle it now. At this point I am babying my baby! I will tell him when things he does is not right but I'm at the point now that I don't want to send him to preschool! Do I inform the teachers? Can someone give me some words? Its just hard because he is my oldest and is only 3 so not only am I learning to deal with regular behaviors, I now have to understand how to cope and deal with this until its over. Thank you in advance very much for any help and advice!!!!

I am currently taking levaquin for a sinus and double inner ear infection, i have also taken this antibiotic before,i am 35 years old. I think this drug works wonderfully and tell the doctor this drug works the best for me.i have noticed a harder time falling asleep if i take it too late in the evening and some mild stomach cramping if i do not eat at least 2 hours prior to taking it.i also take it with a full glass of water.some of the side affects listed in this blog that people are describing are normal if you read your insert that comes with the medication.And if you follow the directions and eat and drink with a full glass of water the side effects are not as severe.Unless you are allergic to the drug,i do not find it bothersome knowing i will not be taking it forever and it is just temporary that i will be having a hard time falling asleep.i do eventually fall asleep.My suggestion while taking this medication if you are in reasonably good health,is to read the directions about eating and drinking plenty of water and don't panic,that just makes things worse.

I have to say I'm really, really bad with taking pills, so nuvaring is pretty much my only option as far as birth control goes. (plus I'm getting married soon, so I'm hoping that it's not the ring)
I've had Nuvaring in for 9 days now (my first time using it) and I've begun noticing some odd things. I can't say I'm super-attuned to my body, so I'm not sure if it's the ring or not.
My gynecologist says I have Poly-Cystic-Ovarian-Syndrome, which means I probably have cysts on my ovaries. I'm also overweight. Recently I've noticed cramping and pain on my right ovary. I've also noticed slight depression, but I'm also going through finals, so not sure there either. I'm experiencing little pinches of pain in different spots all over my body, especially in my arms, legs, and back. I also had an unexplained nosebleed out of the blue this week, and I've never had one before. (no nose trauma or anything) I'm also noticing I'm bruising very easily, but I'm not sure at all if that is recent. Are these side effects of the nuvaring, or something more serious and unrelated? (or else just stress maybe?)