Seven years symptoms and conditions

I have been taking Wellbutrin 300 xl ( i believe - here comes the "Brain Farts" i attribute to Wellbutrin ) for seven years. I can tell you that i have noticed a small very very small amount of hair loss compared to most people but as i read thru these posts it appeared to me that MOST of them stated generic Wellbutrin. I will say i have had more hair than i am comfortable with appearing in my shower and bathroom floor and sink from drying my hair BUT i have NOT had the scary experiences that i have read here. I came to this site because i had to quit taking my Wellbutrin cold turkey because of some changes in the law in my state i have to drive 50 miles away to see my N.P. and because the office i was going to and the one she works in act like they have to send fire signals to each other instead of email and i am out of meds! so i was searching for side effects i could expect until i can get my meds back. i will tell you it is nice to see that i am not alone but i think it sucks that any of us have to decide if taking the medication and side effects are worth it! i also have problems with memory, spelling,speech, following thru with my thoughts much less getting them out of my head and making sense to someone else. did that make sense? ! ? i personally didn't notice any weight loss. my husband says i have the patience of a flea and really dislike " hate" a lot of things. i don't notice this but go back a couple of sentences and you will understand :)
After being here and reading all that i have i am afraid to continue taking this medication so i think i will just let it go and see what happens. i am also taking lamictal and seroquel and xanax and i am pretty sure i would be just as afraid of them if i went and looked them up but i have the choice as i am sure most of you do ...... do you take the meds and deal or go off the meds and well ... die?

I have been taking 8 500 mg caps of pentasa a day for over seven years for what doctors told me was Crohn's Disease. I just found out that I don't have Crohn's Disease and I am in shock not to mention that I have lost over fifty pounds and in bad stomach and back pain. What is going on. I will add that the four day hospital stay has really hurt me emotionally, money wise and I am heart sick. Patricia

I have been reading all of your Simvastatin experiences with high interest and would like to share my adventures with all of you as well. My story began seven years ago when I was relatively healthy and enjoying life. My doctor prescribed Lipitor for my elevated cholesterol and two months later I found myself in the emergency room after having a severe bout with vertigo for the first time in my life. I have since spent the last seven years fighting this debilitating illness which continues to haunt me after having seen every top neurologist in my area and having taken every neurological test available. It would be as difficult to convince me that I was not somehow "poisoned" by Lipitor as it was for me to convince my doctor.

I was eventually prescribed Simvastatin 40MG and seemed to stabilize for a few years even though my dizziness problems persisted. Suddenly I began experiencing bouts of upset stomach and severe lower abdominal pain. I allowed my doctor to order basically every nasty test known to man in an effort to discover the cause of this new problem, but all have come up negative so far. Eventually I began to experience total exhaustion in the middle of my work day, not to mention the back, neck, and muscle pain that has been described so vividly in this forum. Basically, I have become a 53 year old man who feels much older, has absolutely no energy, and rarely has a day when I can honestly say I feel alive and well.

I am not a doctor and I can't honestly prove that Simvastatin is the cause of all of my problems. However, I do have common sense and after reading all of your thoughtful comments on the subject I would be foolish to at least not suspect that the drug may possibly be making me less healthy and not more healthy. Thank you all for opening my mind to this possibility and I certainly plan on discussing this with my doctor very soon, who may no longer by my doctor should he continue to insist that I take this nasty drug.

I had been on Yasmin for about seven years. I decided to get on the pill because I used to experience HORRIBLE menstrual cramps and pretty bad acne. For seven years, I thought that Yasmin was the BEST thing that ever happened to me. My cramps went away, my acne cleared up and my hair seemed healthier than ever.

In January, I decided to give my body a break and get off of the pill. I figured that seven years was a long time to be dependent on a drug. Since I have gotten off, I have had a RIDICULOUS amount of hair loss, terrible mood swings, hints of depression, wacky appetites, increased acne and my menstrual cramps are getting worse with each cycle. I have been off of the pill for 5 months now and I am wondering how long it takes before the drug is completely out of my system. Can anyone help?

I took Ambien for 2 years. I had all of the common side effects: hallucinations, memory problems, loopiness, nightmares, etc. However, I eventually started smelling smoke all of the time. Since Ambien was the only drug I was on, I stopped taking it. After a couple of weeks, the smoke smell faded. Life went on as usual, and I became pregnant and gave birth to a beautiful boy. That night I couldn't fall asleep even though I was exhausted. I tossed and turned all night, and the nurse started showing concern for me. She asked if I wanted to try a sleeping pill, and contacted my doctor. They ended up giving me an Ambien that night, and that night, the smoke smell returned for a few days. Fast forward several months after giving up Ambien completely. I developed a nasty head cold that gave my sinuses a pounding. That was when the smell returned. I began to piece things together, and went to the doctor. I asked him if he thought the Ambien damaged my sense of smell and if sinus conditions like congestion, allergies, and sickness exacerbated the problem. He did first check me for a brain tumor, but agreed with my assessment. He has seen thing like this happen to people, although not specifically with Ambien since it was a newer drug. He thinks a combination of the drug and sinus problems permanently damaged my olfactory nerves. He told me to try Flonase, and within a week of smelling smoke, it goes away. seven years later, the smoke smell still comes and goes, but actually cues me to what is going on in my sinuses at the time. I know when my sinuses are congested or irritated, and I take Flonase for relief within a few days to a week. Not saying everyone will have this problem, but it is something to be aware of...

I have been on Toprol XL or the generic for over seven years. After the first two months on it I started to notice small, scaly patches appearing on my hands and arms. I was told this was just a coincidence. I had the areas biopsied and was told it was Granuloma Annular. Whatever?? Apparently there is no cure. I have never had any skin problems in my life and I,m sixty seven years old. I also noticed I,m constantly fatigued, cough constantly, still have heart palpitations and seldom get a good nights sleep. I,ve tried to get the doctor to discontinue it or put me on something else and they all act like they are afraid to try it. I,ve been tested and was told my PVC,s are benign, so why the concern? I just want to get off this stuff.

Hi, about seven years ago I complained to my doctor of noticing a little thinning at the top of my head. They referred me to a dermatologist who thought it was female hair pattern loss. It was minimal and he said that he rarely saw it get much worse in women. He suggested minoxidil. A year later, I relocated and the doctors at the health clinic noticed my blood pressure was slightly elevated. They put me on HCTZ. I am into healthy organic eating and was disturbed by the need to be on medication. They said HCTZ was a mild diuretic and never mentioned that hair loss is associated with it. After five years on HCTZ my hair loss is severe. I have lost half my hair and it is dry and brittle, no matter what styling products I use. I had long beautiful thick glossy natural hair, but the texture of my hair has totally changed. A few days ago, frustrated by the continual hair loss, I began searching for my own answers. In my first web search, I pulled up many connections to HCTZ and hair loss, including this site. As others have said, I am mad at myself for not taking my health care into my own hands sooner. I have stopped HCTZ and my blood pressure is being controlled by diet, exercise, and drinking plenty of water. What I would like to know-- is HCTZ hair loss reversible? Are there any reputable natural solutions to hair regrowth. (And minoxidil has been disappointing.) Thanks for your comments. They have helped immensely. GG.

I got my Mirena removed two weeks ago after seven years of carrying it around in my uterus. I had horribly painful periods before (like vomiting and fainting from the pain horrible), so I was glad to be rid of that.

What I'm not glad about, however, is the thick black BEARD HAIR that I've developed (which returned after expensive laser treatments), losing about a quarter of my previously thick hair (now I have to wear extensions to appear somewhat normal), and walking around for seven years with acne, a pooch that had me constantly pregnancy testing, hoohoo odor that sometime persisted despite bathing AT LEAST daily, and oh, the wonderful gas, bloating, and bowel irregularities that caused me constant anxiety in the tiny, quiet house I live in with my boyfriend.

Then there is the chronic pain for the past two years that they can't find the cause of - could this little miracle have anything to do with it?

I've brought these things up to doctors, all who knew I was on Mirena, and was always blown off. But it's obviously related, along with the my eyesight now being that of an 80-year-old, my very own snowstorm of dandruff no matter what I wash with, and, quite possible, the depression that no medication makes a dent in. None of which I had before Mirena came waltzing into my life.

Here's hoping for a return to normal now that it's out, and perhaps a lucrative class action lawsuit in the future that nets us each at least enough to get electrolysis and a hair transplant.

I THINK WE WERE DUPED!

Is anyone thinking that the drug company knew all of this, and therefore has been marketing specifically to women who have just given birth... this way, the postpartum symptoms are the scapegoat:

bleeding
cramping
hair loss (very common 3 months after.. I believe I lost more than most)
insomnia (very common after delivery due to motherly hormones have
you on high-alert))
No sex drive (because we're either breastfeeding, hormonal, or just feel
fat)
Mood swings (because of our ever-changing post-partum hormones)
depression, crying (must be Post-Partum Depression!)
Joint pain, back pain (we're carrying our new baby around too much)
Bingeing and Food cravings (we're home alone and bored or
breastfeeding)
No sex drive (we are bitchy, unsociable, depressed, feel overweight and have no energy.. I'm surprised they still want to have sex with us?!!)

The first two months I was on NuvaRing, I thought it was the best thing on earth. Unlike previous attempts with various HBC, my breasts didn't hurt and I didn't seem to gain weight. It also steadied my out-of-control PMS symptoms and made my period lighter and my cramps disappear. Those are definitely on the PRO side of things. Shortly after starting NR, I met a new boyfriend and after both being tested for STDs, we decided to ditch condoms. Woo-hoo! At first, we had great sex and I had no problem having orgasms. But as time progressed, I became extremely dry down there and developed constant yeast infections. Plus frequent low-grade headaches (sometimes escalating to migraine-like headaches), night sweats, itchiness, insomnia, and exhaustion. Now I find it extremely difficult to get physically aroused (before, a 30-second sex scene in a movie could get me off) and nearly impossible to orgasm. I have very little interest in sex, either, which sucks because I am finally in love with the most amazing man. I have told him time and again that its the NuvaRing, and he says he believe me, but I can tell he thinks it's him. So, we've decided to give condoms another try. I took out the NuvaRing. I guess I'd rather have nasty PMS and a painful period than lose intimacy and sexual pleasure. Just curious: Has anyone used the copper IUD (non-hormonal) or a diaphragm with any success? Thanks and good luck.

I was 50 and the doctor prescribed lipitor 10mg since my cholesterol had doubled in the past twelve months to 300. I took it for four months and began to have pain in one leg just below the knee. I had talked to a woman about 65 years old once who was walking on the sides of her feet and I had asked her what medical problem she had. She explained that her Lipitor had caused this terrible pain. You would think that I would have refused to take this drug. You see the doctor had already prescribed a very large dose of fish oil per day and the cholesterol had not fallen. However, I began taking it. About two weeks before my enzyme checkup I began to notice the pain in the leg just below my knee and I stopped taking the Lipitor. I expected the pain to subside, but it did not. My cholesterol level had risen and my doctor asked me if I was still taking the Lipitor. I explained that I had been of it for about two weeks. The doctor insisted that the pain probably wasn't associated with the Lipitor. The reason being my enzyme level was within the range of acceptable. I began taking it again. The doctor wanted to have another test within four weeks to check enzyme levels again. This time the enzyme levels were borderline high. So the doc recommended stopping the Lipitor for a while and then another enzyme level check. You see, my body was telling me something. The only new factor in my medications other than blood pressure was the Lipitor. It has been about three weeks since I stopped the Lipitor, yet I am continuing with even more pain in tops of feet and above one knee a know seems to have appeared. It is sore and feels like it is bruised. I am not a doctor, but I had done some investigating Lipitor on the internet and read that in some patients the Lipitor actually causes small to large fissures in the arteries of the heart. Also, the muscles begin to attack themselves, thus the pain and atrophy. I am going to start taking flax oil. One cardiologist reported that he two cases a week of heart attacks due to Lipitor. He was enraged that Lipitor is still being prescribed and manufactured. I just hope it doesn't take years to regain my original self without pain. I am an active person who likes to work outside, garden, snow-ski, and anything else I want to do. I am trying to search for a detox program for Lipitor overdose, not that I have overdosed. According to my body's signals, I have overdosed on a toxic drug. I pray that returning to normal won't take as long as I have heard some people say it has taken them. Please try some other alternative to Lipitor and the other debilitating statin drugs. I will have to start an exercise program, even though I have put it off for years. I hope my laziness about my physical fitness hasn't crippled me for life. I am 20 lbs overweight and never took it seriously. I hope others will discontinue to take this life-threatening and debilitating drug!!!!!!!!!!1

I am a twenty-nine-year-old man who was recently diagnosed with Type 2 diabetes. I also have had a diagnosis of hypertension for nearly seven years, but have not been on any medications for the condition in as long. I was prescribed Metformin for the diabetes; Pravastatin to raise my HDL; and Lisinopril for the hypertension. I took myself off the statin after I read all the nasty things it can do to your body long-term a month ago. Since then I have been feeling crappy nearly every day; finding it hard to sleep, and when I do, get restful sleep; and I am overcome with attacks of weakness and fatigue while I am out and about each day. At first, I attributed these symptoms to weakness from the diabetes or withdrawal from the statin, but after reading the posts here I am beginning to wonder if its the Lisinopril instead. I take five mgs a day, and it has helped level out the blood pressure, but I experience palpitations and a higher systolic pressure sometimes. Especially when I don't take the drug at the same time. Any thoughts?

I started taking Lipitor in 2004 and by 2008 was taking 40mg daily. I'm not sure exactly when certain symptoms manifested themselves, as looking back they now seem insidious, but I do know they became bad enough in 2008 I went off the drug myself, especially after reading postings like those at this website. After being off the drug for a month, it was clear to me the most of the symptoms dissipated, but it did have a residual affect. I realized I had suffered a loss of range of motion (ROM) in my left arm (frozen shoulder) and have been in physical therapy for over a month to restored 80% of it. I could not have done this while staying on Lipitor as I was experiencing “deep” muscle pain and weakness. I still have some weakness and pain in my left arm and shoulder and don’t know if it is permanent.

I am Hypothyroid and take Synthroid and am currently going through menopause and am on partial HRT. I took no other meds other than the Lipitor. At one point, I thought my symptoms were stress related, but realized my symptoms were causing the stress. Aside from the muscle pain, spasms, tingling and numbness experienced in my left extremities, I experienced gastro intestinal disturbances, occasional vertigo, some lower back problems and other aching in other extremities (like that of flu symptoms). I also suffered recurrent mental fogs, which I initially attributed to some lack of regular exercise (although I lead a relatively an active life), but that was not the case, as even after aerobic activity the tingling and pain would resume.

When I told my physician I had stopped taking the Lipitor (at that time for nearly a month), he didn't blink an eye. I agree with previous blog; the idea of statins are to lengthen your life, but what kind of life is it when you are in misery and nothing short of ceasing the medication brings relief?

I'm not advocating everyone "doctor themselves. Listen to your physician, but most importantly listen to your body and trust your instincts when it comes to these types of medications. Symptoms listed about scripts described as "rare" are usually not that rare at all. You are not crazy.

I was put on Lipitor 10 mg. last Spring about 8 mos. ago. I have never taken medications/drugs other than aspirin or Motrin or antihistamines. Since that time I have had a strange combination of unexplained symptoms arise throughout the months. These sx's included: Headaches, stiff neck and severe neck pain, acute shoulder pain, hip pains, joint pains, severe knee pain (tendon or Ligament problems?) and loss of movement, hair loss, jaw pain and some memory confusion. Initially, I had severe HA's for several months, but attributed them to stress, however, I had never experienced HA's as a common occurrence. Then we went away to our Maui house to get away from stress, HA's continued, along with leg and shoulder pains. At the same time, I started noticing several strands of hair falling out if lightly touched my hair to move it out of my face. The pains seemed to move around my body at different times, for no apparent reason. I am used to daily exercise, living in CO in the mountains @ high altitude, not usually having muscle soreness. Now, given my leg and knee pains have gotten so bad, I cannot hike and have difficulty climbing my stairs. Skiing is out. Snorkeling caused leg cramps. No explained reason for having muscle tenderness or soreness without my usual exercise at present time. When the pain leaves one area it tends to arise in a different part of my body. At the present time, my hair loss has subsided, as also my jaw pain and headaches. However, my leg pains and knee pains are so acute (for no apparent reason) it is impossible to exercise and difficult to walk that I looked up adverse reactions to Lipitor, finding all my sx's most probably might be attributed to this drug. Partially my fault for not looking up RX information prior, especially being a medical professional for many years. My husband kept throwing away the info when purchasing the RX. Too many unexplained symptoms, I decided to obtain the drug info. myself. I tended to make excuses for months, such as: I am getting older, under stress, must be an old injury, not exercising properly, need PT therapy etc.... I am dc/ing the drug immediately and have an appt. with my MD on 1/5/09 to discuss.

Have stopped taking Zocor today after finally accepting that my life has changed since taking this medication....am too weak to open a soda bottle, keep twisting words, memory is shot, Hips, knees and ankles scream whenever I have been sitting for more than 15 minutes....light headed, dizzy and constant headache...want to just curl up in a ball and cover my head for loss of ambition. I am exhausted all of the time.

I have been on Lisinopril for approx 5 years, during a routine year end blood work-up, I have developed a problems with my creatine levels 1.48 and Glom Filt Rate, Est 37. My physician had me do a 24 hr urine for further testing but insisted that I no longer take the Lisinopril. Several of the tests have come in and he advised me that I have only 50% blood flow to my kidneys. It appears to me that the Lisinopril has caused some kidney damage. I also have a great deal of muscle pain, but do to my age (55 years) I thought it was jus a part of the aging process. What do you think?

4 months ago started on preastatin 20mg increased within 1 month to 40mg; could not stand up without help; stopped statins at that time. CPK done 157, this was done to show me I wasn't in danger of rhabdomylysis, I continue to suffer with swelling R leg and severe pain. Leg is still swollen 4 months later.....I am professional RN in ICU ,,can't really do my job as necessary...Should I file for disability; or does someone have an answer to provide relief for this malady???

I think some of the severe symptoms reported here are just that.. severe, and as advised on the drug information insert they can happen, and should be reported to your doctor. We are led to believe our doctors will stop the meds and try something else. If they are not willing to do that, or try to convince us it's all in our heads then... we should stop the meds ourselves and find another dr. These side effects are real, and scary. I've stopped cholesterol meds for that reason. I don't need a dr. to tell me to stop... I know my body, and how I feel and know when something isn't right.

I've been on Lisinopril for two weeks now. I was initially on the diuretic Hydrochlorothiazide, but had so much arrhythmia that I thought my heart would jump out of my throat. The dr. discontinued that after less than a week, and put me on Lisinopril. I am a bit dizzy sometimes, and do have a mild cough, but I had the cough before the meds so I can't really blame it on that. However, for all those with the problem of coughing and headaches... I read at drugs.com that you should take this medication with a full glass of water, and drink lots of water throughout the day. This tip was not in the drug handout and I thought that odd. Something so easy, and yet left out. Luckily, I drink water at my desk all day at work. This weekend while home I didn't drink water and had a horrible headache the entire time. I never connected it until I read that you should drink lots of water. Back to work today and drinking water and my headache is gone. It's worth a try, it might help. My husband is on Lisinopril/HCTZ combo, has been for at least 3-4 years with no adverse side effects.

We are all different, medication effects all of us in different ways. I hope I never experience the kinds of side effects I'm reading about here. If so, I'll be off the drug in short order. My dr. told me there are loads of other medications we can try. While there are side effects to everything we take, mild is ok but no one should put up with life altering and/or life threatening side effects like what I am reading here.

I am a 54 year old male who started taking Lipitor about 4 years ago. It seemed OK at first, but over the next several years I began to have increasing amounts of joint pain after exercise. Nor muscle pain, joint pain. And it seemed to be a result of exercise. By the time I stopped it, I was hurting after everything, not just exercise. I felt better within the first two weeks, but it took about 4 months for me to be able to exercise vigorously again. Over the years I seemed to have forgotten how much vitality I used to have. I am a physician, and because of the long lag time until I felt better, I wondered whether improvement might have related to other factors, so after about 5 months I decided to restart Lipitor. It surprised me that after just one dose, I got back all of the joint pain and fatigue when I was at my worst on Lipitor. I was really hurting. Needless to say, I didn't take any more.

Coincidentally, a physician friend of mine who had statin induced polyneuropathy had a similar experience. After his symptoms went away he found that after only one dose the entire polyneuropathy came back.

Stopping and restarting the drug is a way to test the correlation between the drug and the side effect. For such a large spectrum of side effects to recur after only a single dose, it argues that the problems that my friend and I had was due to some sort of immune memory response. I have not seen this in the medical literature.

I am off it now for about 8 months and am able to comfortably play singles tennis and jog - much more energy (and I took 200 mg of CoQ10 a day with the Lipitor).

Due to the large amount of people who suffer devastating side effects from Lipitor and other statins, I would like to encourage each and everyone of you to tell your story on home video and post that video on****** This will be one of the best ways to alert the world to the dangers of this drug.

I was on the low dose, 100/50, for 2 years. I had blurry vision in my right eye and lethargy. Last week I woke up and could not breathe AT ALL. I was choking for about 45 seconds with no air coming in. I have read that Advair can bring on sleep apnea. After a couple of days of doing research, I stopped cold turkey. My vision cleared up in a day and my lethargy is gone. I am now using apple cider vinegar for my asthma (brought on by my 2 dogs and cat) and so far, all is well. How that stuff is legal, I don't know.

I am 31 and I have been on YAZ for a month now. My two friends have been on it for two months and suffered nausea and that was it. They love this BC!! I have not taken BC for two years but with my history of ovarian cancer (diagnosed at 24, been cancer-free for seven years!!) and my horrible periods I decided to get back on something. My oncologist put me on YAZ once I told him how the first day of my period keeps me home from work or I miss out on social activities due to the awful cramps. The only side effects I have experienced are being on my period for a month and bloating. The period is light but I still have to wear a tampon non-stop and that is not so good for the old sex life with my husband. I have never been pregnant, but I feel like I am with the stupid bloating I am having. I am going to give it another two weeks if nothing has changed I am quitting. Good Luck to everyone!!!

I have taken toprol for seven years. I never had any bad side effects and it controlled my blood pressure most of the time. However, I suffer from anxiety and depression and was recently put on Lexapro. My heart rate dropped into the 40's and I was exhausted all the time. Turns out Lexapro interacts with Toprol in that the drug (Toprol) does not break down in your system and keeps building up! Because the Lexapro was helping my anxiety I decided to lower the Toprol dosage. Down to 12.5 mg and still extremely low heart rate and fatigue. Decided to go off the Toprol and monitor my blood pressure, which has been amazingly good so far. Went off completely six days ago and it has been rough. Anxiety, insomnia, pounding heart, heart palpitations. This stuff is a real B*tch to get off from. Have talked to both the pharmacist and my doctor and both said to NOT start taking it again. There are plenty of newer medications out there. I also experienced weight gain when I first started taking it...I think because it slows your metabolism down. So now I am on xanax to counteract the Toprol until the Lexapro kicks in more. It it isn't one thing, it's another.

Have any of you seen this site: http://www.askapatient.com/viewrating.asp?drug=20829&name=SINGULAIR - the side effects we all recently began discussing is documented from users and parents of users as far back as seven years ago!
Why is it that the FDA just became concerned and Merck had no clue of these reports?? Interesting and distressing wouldn't you say?

My daughter is seven years old. She was diagnosed with asthma when she was around two years old and, for years, suffered with the night cough associated with childhood asthma.

When Singulair came along, my initial reaction was that of joy. My husband and I could not believe that we no longer heard coughing throughout the night. However, while on this drug, we also noticed that she underwent a change. Sometimes, she seemed terribly sad and withdrawn. Other times, she became angry and even aggressive. We rarely saw her smile. It also seemed like she was in some sort of fog much of the time. About a week ago, I found her on the floor of our office. She had just gotten out of the shower, and I was getting her pajamas for her. The towel was not around her and she was shaking violently and crying. She explained that she had the chills, but it was clear that she didn't even comprehend that her towel was not around her. We all know our kids, and, I'm telling you that this scene was frightening. This was not at all my daughter.

In addition to the mental/emotional changes, she also had physical symptoms including sudden and frequent headaches, fatique, stomach pain, and bed wetting. A day after her "breakdown" in our home office, my husband called me from work and told me that he had just been reading MSNBC and that there was an article about the negative side effects of Singulair. When he listed things that matched what our daughter had been going through since on this drug, it was both comforting and horrifying. I am relieved to know that there is nothing wrong with my daughter psychologically, but I am furious that she and so many others have been treated like guinea pigs. We took out daughter off Singulair the very same night that my husband came across the article on Singulair, and she hasn't had any of the mental or physical symptoms that she had been experiencing...the change was that drastic. Currently, we are only using her inhaler and Benadryl at night. She has a doctor's appointment next month, and I will tell the doctor about our experience.

I have my little girl back, but I can't help but wonder how many families are going through this and do not have a clue that Singulair could be the problem. Other than reporting this to our pediatrician, is their another agency I should contact?