Medical professionals symptoms and conditions

I had mine removed this week - thank the lord above!!! However, it has been rough and be forewarned that I experienced horrific cramping and HEAVY bleeding for nearly five days. I also had terrible back pains and some pain down my legs as well as some mental fogginess. I only had it in about one month and had gained 3 pounds and outgrown my bras! So now, two boxes of tampons later, I finally stopped bleeding altogether about 24 hours ago and the cramping has subsided. I feel mentally clearer and, believe it or not, have some semblance of libido - my husband is thrilled!

I am exploring other options for managing hormonal changes in perimenopause - including evening primrose oil and am still doing lots of yoga (even during the pain periods I did lots of yoga to help me manage)...Mainly, I feel so betrayed by the doctors (two women half my age) who insisted my symptoms were "all in my head" - to those of you planning for removal I encourage you to tell the medical professionals you work with that you are NOT crazy and NOT the only one experiencing these side effects. I personally believe that many women get too much progestin in the Mirena (which is not Progesterone, either) and this, in addition to overloading our estrogen, is enough to make us completely insane and miserable. I say let nature work its course as regards my own perimenopause and to those out there using Mirena for birth control I managed to avoid pregnancy with little concern using natural/rhythm methods and condoms as well as a diaphragm, conceiving my two beautiful (now teenage) sons without any intervention from hormones except my own. I am going to do peri and menopause the same way here on out. !!!!

Would love to hear how long it took for weight and stomach fat to go away after the removal from anyone who has been there - I eat very healthfully and exercise daily so I knew the pregnant look I got after that month with the Mirena was not due to one too many cookies )as my doctor seemed to infer !

I had the Mirena inserted 4.5 years ago. I had lost over 100 pounds and thought it would be a better option than taking the pill. I had few problems with spotting. I quickly gained back 80 pounds of the weight in the next six months with no variation in diet or exercise. I haven't been able to lose it. Five months ago my perfectly clear skin began to turn into an acne nightmare. I have lower abdominal pain and as of late a incredibly sensitive breasts. Have never experienced the amount of uncontrolled rage and anger that I have been going through. I have one child, I am 41 years old, and I plan to have it removed and do not plan to replace it. I too was very intimidated by my doctor. I hope she'll listen this time and help me. Some of us tend to be too submissive when we put our trust in medical professionals. Thank you for the voice of women who have had this experience. My friend has had no problems with it, inserted six months ago, and I hope she doesn't.

I am 40 years old and recently went to my medical facility as I have had a "viral" ear infection for almost a year now, and it is concerning me. I do not take medication typically. My new primary care provider recommended I try Singulair. So far I have taken three doses over three nights. The first night was horrifying, the dreams I had were so scary, and they were tied into reality which was even stranger as the drug also makes you wake up often, then when you fall back asleep your awake time ties into your dreams. I woke up in a numb state. Since then, I also have been extremely agitated, dizzy, mouth sores, acne, fuzzy thinking, light headed and severe fatigue and body aches. Thank goodness I checked out this webpage, as I too will stop taking this drug. I find it very disappointing, how are we suppose to be able to trust our medical professionals to help us with one of our most prized possessions, our bodies, when we are given something to clear up an ear infection only to have it affect numerous other aspects of our lives to such a serious degree with no mention from our medical professionals. This is ridiculous. I guess I'll live with the viral ear infection.......

i think all you people are just mental cases, this is all of your minds ways to try to rationalize being insane. Panic attacks on an antibiotic!! Come on, really do u all think its the dox?? Even the doctors don't believe u. Funny that its not on any of the common or less common side effects anywhere on the internet!!!

My son (14 years old) was given levaquin for a sinus and ear infection
2 weeks ago. Around the same time he began practices for his high school baseball team. He complained about his legs being stiff and aching. We assumed it was the intense practices causing his muscles to ache. After a week on the drug, he could barely walk and his knees were swollen. We were very concerned and looked up the side effects of levaquin on the internet. We were shocked and angry when we found out that levaquin should not be given to children under the age of 18 because on the possibility of joint and tendon problems. Today we went to the orthopedist and he drained a lot of fluid off of both knees (it looked like about a 1/2 cup from each).The doctor thinks it has to be a side effect of the drug, because the symptoms began at the same time. He doesn't
think after examining the knee and having him perform certain tasks that he has damaged any tendons. He has all the symptoms of rheumatiod arthritis. He is very athletic and plays competitive sports and we are praying that his knees are not permanently damaged by this drug. Parents please research all drugs and there side effects before giving them to your children! Doctor's DO make mistakes!! The pharmacist failed us too.

Hi . I am a 69yr old male. My doctor has recently increased my Lipitor from 20 to 40mg. My cholesterol reading was 3.6 which he considered to high after a quad bypass. I am suffering painful cramps down the front of both lower legs as well as cramps down the back of my lower right leg. I plan to revert to 20mg to see if the cramps stop. I am not sure if I should stop completely.

Yaz was not what I'd hoped for...Instead, of relieving pre-menstrual symptoms, it only extended and exaggerated them. I had feelings of extreme apathy, exhaustion (i could sleep at any time), severe mood swings, headaches, weight gain, bloating, increased appetite, blood pressure increase from 90/60 to 120/75, cramping(both intestinal and uterine w/spotting), and dyspenea. I felt like my whole life and body were sliding down a hill. .. BAD feeling ....depression! This was only after taking it10 days. Immediately, I knew it was the Yaz. The first pill I took for almost 2 years 20 years ago...I was miserable. Since then, I've tried different pills all with the same results. Ironically, I had to take pergonal to ovulate and get pregnant. (My quadruplets are 12yrs.old and wonderful!) After a year of convincing, my long-time Dr., a female close to my age, thought Yaz would be great for me. I was supposed to take it for 3 mts. The symptoms were like a train. I'd be insane, dead or both in three months. I stopped and it was like stopping a train...severe headache, and more of the same symptoms, but each day is better. I can and you can read your body and listen to it. Do not let self -doubt slide in...Medical professionals want to help you and they should listen; if they don't, they are missing half of the picture, your picture. This time, quite honestly and even b/f I read this board, it made me wonder how many lives are affected
by such...I mean depression, clots, blood pressure, headaches, weight issues and many others...even the divorce rate. We have to have birth control. For me I'll just stick to a little bit of acne, and predictable PMSuntil I go into menopause. I know that others need something very different, and I encourage you to keep searching and communicating.

My 3 year old son was just prescribed Singulair today. After reading the pamphlet that came with the trial pack, I decided to do more research. All of the side effects that most people have mentioned on this post are listed in the pamphlet. I don't know if I will put my son on this medicine but thought I should mention the importance of actually reading the pamphlets that come with your medicine.

I was only on Seroquel for 5 days at 50mg, and have been off it for about a week, but my blood pressure has jumped from about 118/85 to 140/89. The medical professionals that I have encountered seem indifferent, but I have cold and clammy pulsating in my throat, I feel my pulse everywhere (which is at 98 bpm), I keep sweating, and I have this overall tinging sensation like things are "falling asleep". Is it possible that it is associated with the Seroquel?

Wait a minute!!!!! Let me say that I have really been spooked by everyone testimonials regarding Yasmin. Although I AM sympathetic and very sorry to hear of all you r health problems, I think that before we all get into a panic over this, we need to take other things into serious consideration. We have no clue what one anothers lifestyle is. Their diet, weight, allergies, stress issues , medical issues, other medications, exercise, genes, and sometimes age. I myself have suffered from hair loss, digestive issues, constipation, eyesight changes, fibroid/fatty lump in my breast, migraines, moodiness & poor circulation. And that was BEFORE I went on the pill. Sorry to say….but I’ve learned that these issues all come with age. I’m 39. And at age 35 I started seeing all these changes in my body. I was on NO medication and in pretty good health and would see a doctor regularly just to make sure. Some of these symptoms that were experiencing just might be due to the fact that were getting OLDER!! I even became somewhat lactose intolerant literally overnight. And one lady said in here that there is lactose in the pills. So maybe some of you are more susceptible to it.
And remember, the chemicals and hormones they’re putting in the pill…isn’t All Natural. They’re chemicals!!! Which can be hard on the body. (God did not design us for them). And a lot different from what I remember 20 years ago. When I used to take the pill you had to wait at LEAST a month before you can be safe from pregnancy. Now it’s only a WEEK! Hmmm…..that’s an obvious difference/change/warning….whatever you want to call it. Maybe the pill isn’t such a necessity for some of us. Maybe just a change in diet and vitamins might help us. For just pregnancy protection…maybe try another method like condoms, shots, diaphragm, etc….. I admit that I was having headaches ever since I started the pill 4 days ago. But then I realized that I only got them when I would sneek a cigarette 4 times a day. Shame on me!! That’s the ONE THING they tell you NOT to do. But now I know it’s not worth the pain and risk to my health. I didn’t smoke yet today and….no headache!! But I have not had any other side effects……YET. But when I do, I will look at other issues in my life that are going on….Diet, water intake, stress, genetics, normal woman changes, etc. I’m not saying that all your symptoms are nothing or not related toYasmin, but maybe look at the big picture before you overreact.

I had septocaine for 2 minor fillings in feb 2008. It took me until nov after seeing a number of dental and medical professionals to be diagnosed with trigeminal neuropathic pain in the V2 region. I'm still in a lot of pain with no relief in site. I can't sleep, I can barely eat because all my teeth shifted from the poor dental work and I can't concentrate on anything. This drug ruined my life.

I am 52 and took levaquin (the doctor described as a very high dose needed for what he felt was a generalized infection he couldn't pinpoint). Within 2 days I began feeling very weak. I also had moved to a new town and couldn't return to the prescribing doctor. I felt so very weak and felt actual pain in my heart I became very scared and went to a friends because I was afraid to be alone. I called the local pharmacist and was instructed to stop taking the levaquin. The following day I went to a new doctor in my new town and my nightmare began.
The new doctor stated "you have a very large heart murmur". I told him no doctor ever told me this before and he insisted they must have, I just don't remember. He decided to do an echo and diagnosed aortic stenosis. He stated it didn't require surgery, yet but would in a few years.
Fast forward to now, 2 moves for my work and changing doctors. Also, to be frank I think a firm denial on my part that I could not have heart trouble diagnosed under the age of 50.
I have received a variety of "borderline" diagnosis'. From COPD, Hepatitis and an inability for my heart to pump proper blood flow to my lungs. While I have had "many" diagnosis there isn't anything concrete and no caused determined or resulting changes to be made to improve my general health.
The one symptom I have, that seems to have worsen as time passes is that what I do seems to build up over time. Energy used and strength used (to carry something while walking) seems to build up to the point of exhaustion and inability to even get out of bed. I have been hospitalized for chest pain 4 times in the last year. The last one being after a business trip, where I took a train and needed to roll and/or carry a very large suitcase. the first night I began to feel weak. The second night my face swelled to a cartoonish state overnight and I began to feel very congested, coughing continually. I didn't go to the hospital because I didn't want to be in the hospital away from home. I Stayed at the conference and returned at the end of the week. A friend took me to the hospital and I was in Congestive Heart Failure. Once released from the hospital, I began to arrange to move back to my home state, to be closer to my family. Now I am here and if I do much of anything (even heavy housework) within days I am too weak to do anything. I am barely managing because I am not working, but I must return to work because I am fast becoming broke. But, how can I take a new job if I know that I can't work long-term. I haven't found a new doctor yet, because most here are not taking new patients and I am just not sure the type of doctor to go to. I am also afraid that they are just stabbing in the dark. Diagnosing borderline "everything" and the treatments for not knowing what is going on could make things worse.
If you have read this far..thank you. If you could reply with suggestions, please do. I feel like my health has been ruined and I don't know what to do to get it back. I only took levaquin for 3 days and all this time later, I still feel pain in my heart. Which is the strangest thing because "before" levaquin I "never" actually felt my heart at all.
Any suggestions , I would be the most grateful.

I just had Mirena implanted and it was not a pleasant experience. I have a high threshold for pain and delivered my children naturally and without medication. I wish I had been given a valium and prescription strength Motrain for this procedure. I passed out and was weak and dizzy the remainder of the morning.
I have read all the posted comments from everyone and am scared to death to wait and see which bizzare side effects will overcome me. I am a true believer that the medical professionals (doctors) are not keenly aware of the general public's documentation on side effects and in this case Mirena. I took the Chantrix (stop smoking drug) this summer and the worst side effects possible presented themselves to me. I quit the drug after 3 weeks of progressively worse symptoms such as nightmarish dreams, auditory hallucinations, depression and stomach aches.
I am going to have Mirena removed immediately -- Monday next week if possible -- because I do not want to experience anywhere near the degree of suffering the poor ladies have in these examples

I just came across an article on the online "Huffington Post" by Dr. Doug Bremner, who researched the connection between accutane and depression, called "If Prescription Meds Don't Kill You They Might Drive You Crazy" He explains the link between Singulair, Leukotrienes in the brain and depression. There are numerous articles by him as well that are definitely worth reading.

Jenna M.
Parents United for Pharmaceutical Safety and Accountability

Hi everyone,
I cannot live without xanax and its terrible, I have been on them for 5 months and have tried to stop them and its a nightmare. I suffer memory loss, have blackouts that I do not remember what I have said after a few drinks. It does help ease the social anxiety. But I have become moody, sleepy. . Does anyone else have these problems?

I've been taking Fosamax once a week for about 4 months. During that time what began-before taking Fosamax-as mild pain in my lower back-has gotten progressively worse. This is the only negative possible symptom I’ve experienced, but of late it has increased and spread to my hips. I decided to stop taking it today, and see if it makes any difference. If it does, I will post another reply here with details.

I think all reading these personal accounts should consider this: obviously many medical professionals see far more benefit than loss in the majority of users. My osteoporosis was only diagnosed via a bone scan 6 months ago. -2.5 The increased pain and worsening conditions in my back might in fact be much worse if I hadn’t started taking the Fosamax. One must beware of apophenia setting in with self diagnosis.

Most posting here already had serious medical needs to have Fosamax prescribed in the first place, given a small percentage of diagnostic errors. Most of the conditions I’ve seen described vary greatly, and without a serious study are purely antidotal. I suspect there are legitimate adverse reactions, but for now the percentage and severity remains a big unknown. There seem to be some activists here, so get a campaign going for publicly funded analysis of the now considerable amount of data on file.

If my back gets better, I’ll still be unsure as it might have been a delayed benefit from the drug. Likely I will take Fosamax again either way. If it doesn’t improve in several months I’ll assume F-max wasn’t the cause and begin taking it again. If it gets better, I will take F-max again to see if the problems return when I do. If they don’t I’ll keep taking it. If they do, that will red-line my ‘coincidence meter’ and I’ll never touch the stuff again.

I hope some will find my approach to our common dilemma helpful. We all have to be our own advocates within the modern health care cabal. I worry about the old adage that when we do so, we have a fool for a client. Feel free to criticize my reasoning, and thanks to all the others that took the time to share your experience. It helped me make my decision, and I’ll share the results in about 6 months.

I started taking Lipitor 12 years ( 1997 ) ago as my Cholesterol was at 315. I was always athletic but had a crappy diet. My Cholesterol dropped to 200 within a year. However, in 2001 I ruptured my left Achilles playing tennis. Thought nothing much and that I hadn't stretched enough. Recovered from that and started playing tennis again in 2002. Within three weeks of playing again, I ruptured my RIGHT achilles! At that point I started to question the effect of Lipitor on muscles/tendons with various medical "professionals". ALL said it was nothing to do with medication. I quickly developed a tingling/numbness in both feet that doctors said could not be happening but it WAS!

I've had MRI's, nerve conduction tests, wondered if it was diabetic, alcohol, etc. Finally found sites such as this where real life experiences validated my concerns over this statin. I told my Dr. I was quitting Lipitor last Monday, she had no problem with that. This is Saturday night and I'm sitting here with a NOTICEABLE decrease in my numbness/tingling in both feet that I've had for the past TWELVE YEARS!!

I hope that the statin did cause my "mild sensory polyneuropathy" as was diagnosed in 2002. As of right now, it seems to be getting better in less than one week! I can flex my toes with NO pain and my feet don't feel like dead weights.

I WILL NEVER USE A STATIN AGAIN!

HEY PSYCHMEDMAN TURN OFF YOUR CAPS LOCK and get off your high-horse. If you listened to patients instead of trying to tell them whats wrong with them and you know better, you will help them. It sounds to me like your more interested in showing everyone how smart you are than making people well. Just because your body doesn't have adverse effects, and even if the majority of the population doesn't, does not mean that people are making this up. I have no other medications, never been treated for any mental illness, and I don't believe I have one, but I have had a physically debilitating condition that no doctor has been able to diagnose for over a year. I have resisted taking anything for a "mental condition" because I know that is not what started my trouble, but I allowed them to treat me for it now because after being in this situation for a while, I am feeling a little depressed.

I did not even think to go anywhere to see about any side-effects or suspect the Bupropion that have have been taking for just a few days until a nurse (yes there are other medical professionals that disagree with you, I know this must be a shock) told me his opinion was that the drug's side-effects out-weigh the benefits, and how surprising, the recent headaches, lucid dreams/nightmares & joint pain I HAD ALREADY EXPERIENCED, NOT SOMETHING I READ ABOUT FIRST were being experienced by others on the same drug. I am not you, everyone's chemestry is different, and different drugs affect us all differently. I hope that you change your attitude and open your mind a little more so you can be more helpful than arrogant.

I will not be taking this drug again at any dose, for any reason. I was only taking 75 mg for 2-3 days and I had these side effects.

I do want to say to anyone thinking of going off this or any other mind altering drug DO NOT GO OFF COLD TURKEY especially if you have been taking it long term and or high dosages as this can be more harmful and dangerous than the current effects, it may cause a psychotic episode. If you want information to back this up, you can see for yourself where several medical journals have been sounding the alarm on several of these drugs at:
http://www.drugawareness.org/ .. don't be put-off by the intro video if you like me are not a Michael Moor fan, I'm not and I still think he is off on a lot of what he says and does, but on some of what he is saying on this point I cannot ignore the statements by medical professionals relaying the findings of academic research, but much of it is unpopular because I believe, the people who have had good results are much like our friend PSYCHMEDMAN who thinks his experience is going to be everyone else's too.

Hi,
I have been on Warfarin since 2002. I suffered multiple pulmonary embolism's in both lungs. My first was in May 2002 and even though I had excruciating pain in my left shoulder area & could not lay down as this worsened the pain, the NHS x-rayed my torso!!!! & sent me home with medication for a kidney infection. I gave it a few weeks but the pain did not go completely & was moving to my right side, I was coughing up 'tablespoon' size clots of blood. My GP was not happy & spoke to a colleague at the hospital. I was sent straight in,(July) thorough tests done & I was found to have suffered multiple PE's.
I tried to sue them for medical negligence but it was turned away by the court as there was not enough evidence on my notes ie; some info was not written down & most was unreadable to even other medical professionals.
Since Aug 2002 I have been on Warfarin & am on this for life.
A blood test showed that I had a genetic blood disorder called 'Factor V (5) Leiden heterozygote'. This causes my blood to form clots much easier & quicker than the average person. If you have this disorder, as a woman it is important that each time you have a child you are treated with Heperin after each birth. I had 5 children & was not treated therefore I suffered with my PE's.My children have been tested for this & 3 of them have it. My daughter was glad she found out before having children as she hasn't had to suffer what I went through.
I ask one thing.... Please TELL your GP that you want a test for the above disorder. As I suffered my PE's & that I have this blood disorder I have to stay on Warfarin for life.
If you need any more info I will tell you as much as I know. Feel free to ask questions. my email is; ******

I had a huge allergic reaction from a bee sting so the urgent care Dr. prescribed a Kenalog shot. I thought that if it would reduce my huge arm it sounded good. Well, not so good as others who have had the shot have described. I am so happy to read the side affects of others because I was starting to think that there was something serious was going on with me. I started mt period after a week after my previous one and have had this period for seven days. I usually only have five day periods and have been very regular. I called my obgyn and they said that the pharmacist stated that this is not a side affect of Kenalog. This is obviously not true and the medical professionals should be aware of this awful side affect. I have also had a dull headache for a week which has also worried me. I guess I will try to wait it out. How long does this crazy shot stay in your system?

i posted late last week regarding my 4 year old son who had been on singulair for about a month, two weeks steadily. he had turned into an aggressive, whining child who was getting upset over every little thing. he was back to throwing tantrums like a 2 year old and not listening at all. he had his last dose of singulair four nights ago. i am happy to report that he seems to be back to his normal self both at home and at daycare! i am so glad i found this site or he may still be on it today with me just assuming he was going through some sort of phase. it's unfortunate that the medical professionals in the U.S. don't seem to be taking this situation seriously, so we need to stand up for ourselves and our children. keep the information coming, they can't ignore this forever!

I can hardly believe what I have read on this board. It is my son's story repeated over and over again and the sad fact is that I never put 2 and 2 together until I saw the news stories last week. My son has been on Singulair for years (he is now 7 years old) along with other drugs for asthma. We recently started taking him to a therapist because of his extreme unhappiness, violent temper tantrums, bad nightmares, many tics, and overall negative attitude. I took him off the singulair 5 days ago and cannot believe the results so far. My son is not affectionate in any way, does not even like a simple pat on the back, no hugs or kisses for sure. Two days ago he came over and gave me a kiss and a hug out of the clear blue. I cannot express enough what this meant to me. I have 3 other children that can't get enough of hugs and kisses, but coming from my 7 year old it just brought me to tears. The hugs have continued and he even told me that he loved me. The therapist had me convinced that he had a sensory deprivation disorder... until now. I cannot believe that until now I have not heard anything metioned in the news and that the medical professionals are so quick to dismiss claims against Singulair.
I am so thankful that I have found this website and for all of the people that have taken the time to include their experiences as it is evidence that there are serious problems when it comes to prescribing Singulair to children. I cannot help but to be saddened when I think of all the years I have lost to this with my son. All the time spent in frustration and tears over what I thought were serious behavior issues on his part. Not to say that I never expect any negative behavior out of a child, but certainly not like I have had to endure in the last years. The last few days have been amazing...I pray it continues. Shame on Merck for not being forthcoming and only keeping their bottom line in mind.

Here is some perspective for you all. I take Singulair and do well on it and in ACTUAL studies it has one of the safest safety records. Understand that post marketing reporting does not mean there is a correlation between the event and the product. Throughout the life of a drug the companies must disclose any report of side effects reported to them REGARDLESS of causality. A popular antihistamine that is OVER THE COUNTER also has suicidal thinking/behavior listed in its post marketing section. However, just because patients who had reported having these thoughts while taking the product doesn't mean it was a result of the product! Maybe they had a depressive personality and were also on multiple other medicines to treat that. You must look at the "Adverse Reactions, Warnings and Precautions" sections of package inserts to see the side effects that were actually seen in studies. You can die from ulcers derived from over use of aspirin or ibuprofen. Decongestants can throw off your blood pressure and these events are documented in actual studies! Listen to your bodies when taking any med. If you feel differently report it to your doctor.

These are all drugs people, there are potential side effects. There are also side effects to those "natural" over the counter remedies that are not nearly as regulated by the FDA or studies by the drug companies.

To anyone out there who has experienced side effects to singulair timed to when you started it, talk to your doctor, stop taking it and see if it goes away. Same advice for any product prescription or over the counter medicine. Side effects can be a combination of many factors (what other meds are you taking?) But understand for many people this product is the safest and most effective treatment for them. The FDA and Merck are reviewing all information to see if there is any correlation to the reporting. But singulair been around for about 10 years and prescibed to billions of people and is known to be one of the safer medicines out there overall.

In between the legitimate posts on this site I get the sense there is a lot of ambulance chasing going on. People looking to cash in on this big drug companies. We want drugs, we want them cheap and with no side effects which is not a reality. Keep stepping up the regulation and make the companies hire more lawers to protect themselves and jump through even more hoops and see what happens to the price and access to new meds. Even better, see how regulation has impacted the development of new medicines around the world (here's a tip, it will dramatically decrease). Drug companies certainly aren't perfect but which industry is?

Please, when taking any medicine over the counter, prescription or herbal supplement listen to your bodies to see if the potential benefits of the product outway the risks or side effects. Report any changes to your doctor.

I am upset because neither the Pharmacist or my Doctor were any help. I thought I was going crazy. I have been on this med. for 6 or 7 weeks of which have been absolute misery. I have experienced numbness and tingling in my finger tips, headaches, yellowing of my skin, severe nausea but never throwing up, unable to eat and yet gaining weight, severe dizziness and nearly passing out, fatigue, pain in my legs when I exert myself (climbing stairs to my bedroom), unable to stay asleep at night, leg cramps, stomach pains, anxiety!!, depression, grouchy, extreme bleeding with my monthly cycle (my normal cycle is 3 to 5 days this cycle lasted 3 weeks and counting), coldness, heart palpitations, chest pains, wheezing and deep dry hacking cough. I just felt like I was going to die also thought it could possibly be menopause, low blood pressure (90/60). Because BP was low I took 1/2 the dosage day before yesterday (5mg). Yesterday I stopped taking it altogether and I was able to eat (yeah!!!!) with only minor nausea. Today my legs are not hurting as bad going up and down the stairs and my bleeding has really slowed down. I don't have a headache but I am still coughing and am having the problem with the numbness and tingling in my fingertips. I see dramatic improvement. I believe if my husband had not researched the side effects of this drug online, it would have killed me. Also he thinks that women should not take this drug because of the emotional impact on the husband! Also I am so angry that his happened to me in full sight of the medical professionals !@!@!@ I will be posting this message on as many medical sites that will take it.

As a pediatrician I write for singulair every day.
The medication is for allergies.
Allergies cause adenoidal swelling, which cause sleep disturbances which makes the child tired the next day with makes him over weight, less attentive, hyper and eventually act out.
This in turn makes the child experience parental, peers and teachers criticism/ abuse, with leads to the child feel inadequate, embarrassed, frustrated and eventually depressed and suicidal.

Yes, singulair does cause behavioral change but they appear within the first couple of peels, the rest is due to allergies, lack of medical care, i.e. sleep, singulair, and zyrtec deficiency.
Allergy shots cause 4 times the incidence of suicidally than singulair, and Ritalin 10 times more.
They say in hebrew "once a stone is thrown into a well, thousands of smart people won't find it".
Check it, it's true.