Allergic reactions symptoms and conditions

I am an intensive care physician , one day we got a 75 year old male patient for acute allergic skin manifestation and general body swelling , the patient has been taking Lamictal tablets for seizures control after brain surgery few months before his presentation the patient was put on i.v steroid therapy along with antihistamine, on the second day we noticed that his skin is peeling off and his breathing got embarrassed , the case was diagnosed as( TOXIC EPIDERMAL NECROLYSIS) which is the most severe form of drug allergic reactions as a side effect of Lamictal administration , one week later the patient died due to acute respiratory failure (ARDS) however he was on mechanical ventilation support.

I've been on and off singulair for several years. I had a horrible bout of bronchitis that then triggered bronchial reactive disease and I now have allergic reactions to certain chemicals (some spray deodorants, etc.) Singulair worked so much better for me than advair, I was thrilled to be able to talk and breathe. As a teacher I would sometimes have to stop the lecture to get my breath again and drink some water if I inhaled the slightest amount of chalk dust or something.

After reading the comments on this website I am going to discontinue taking singulair. I used to be this skinny person and never, ever worried about my weight. At the age of 37 I had a rip-snortin' major depressive episode with insomnia that had me miss 3 days of sleep (this is on no medication of any kind) and panic attacks and suicidal thoughts and impulses that I'd never had before. Imipramine was my first prescribed med (in 1991) and worked like magic. It cheered me up, calmed me down and made me sleep. I went from 135 pounds to 155 pounds in just several months. I finally got switched to effexor and trazodone, but there's really not been much weight loss. I'd hover around 150-160, but then with singulair added in the last several years I am 170 lbs. I can't believe I am a fat person now and do not over eat. I can't go off my psychiatric medication because it runs in our family and if I taper off I am...uh...crazy. My insomnia is tenacious when I am without medication and then that makes depression and anxiety worse. I never want to have a panic attack again.

I just ran out of my singulair prescription about a week or two ago. I am breathing and speaking fairly normally and my husband and I now have to pay for our own health insurance which is exorbitant and I just didn't feel like renewing the prescription in order to save money. I was pondering my weight gain today and just decided to google singulair and weight gain and I just can't believe it.

I have also experienced hair loss, but my hair is so thick it still looks basically the same. My husband and I have noticed over the last several years that I lose lots of hair after I wash it and there is a mass of hair in the shower stall.

My memory may have been adversely affected by taking singulair. I thought it's just getting older. I am 55. It's been the last several years that I have started to have problems remembering things. I have always had to work with my husband in helping him remember things (it's been life long with him: he is an absent minded professor. He has a genius IQ, is an M.I.T. grad, is an excellent engineer and can't remember his mother's birthday, what plans we have for the week-end, no matter how major, etc. to save his life.) I feel like I am becoming more like my husband in being hopeless and helpless about remembering what's happening from one day to the next. It could very possibly be the singulair. There has been a marked difference in my memory over the last several years. It is embarrassing. I sub for the school district and once showed up on the wrong day at a school and another time didn't show up and they had to call me up and get me out of bed to go to work. I also teach piano and never used to forget who was coming when. Again, I don't know if I can blame this on singulair causing memory loss, but there would be times when someone would knock on the door and I'd be surprised to find a piano student standing there. I feel like I am getting Alzheimer's. My grandmother had it for 17 years. My mom has always been afraid of getting it but she is 80 and is just now starting to show signs of real forgetfulness. I explained to her what my lapses in memory are like and she is shocked to hear that they are similar to hers. My mind just will completely go blank. I will have this thought, get distracted, and just a moment later will struggle to remember the previous thought and there is just a void, peace, blankness, white screen in my mind. Maybe it is getting older, but maybe it's the singulair. Since I'm just recently off it I'm going to pay attention and see if my memory improves or if it is just old age.

Also, my joint problems have been nearly ruining my life the last several years. I don't know if this is exacerbated by my singulair use or not. Bursitis in the hips runs in my family like crazy. We re-sided and painted our house several years ago and my bursitis started to flare up and has been bad since then, but it's also about the time I started taking singulair. I had to quit a sales job this summer because my bursitis has become so bad. Sometimes I can hardly walk. It is nearly unbearable. I get cortisone injections every 6 months, but need it every 2 months. I wonder if my discontinuation of singulair will ease my joint pain? I'm going to track that as well.

For me: weight gain, hair loss, joint pain, some dizziness are possible side effects from singulair.

Thank you to everyone who has contributed to this site. I am never taking singulair again.

I was prescribed this as an inexpensive option to treat a long-term sinus infection in March 2008. I had no prior history of allergic reactions or prior health problems. After 3 days (6 doses) my whole body was in throbbing pain, I felt like my skin was on fire, and I was seeing spots, and had difficulty breathing. I initially had NO RASH or visible/external signs while taking the medication. I immediately stopped taking the medication and saw my doctor, but symptoms persisted for a week. My doctor prescribed prednisone, and had to up the dosage two weeks later when a rash formed over my torso and legs and persisted for 2 months.

I am so glad that I am not the only one who has experienced this - not that I want others to experience it, but you know what I mean, it is nice to have some answers!!! I went in to get an allergy shot for my horrible allergies about eight months ago - I have had one done previously a couple years ago, with no problems, and this second one seemed fine too. My allergies are so much better, i can breathe and am not sneezing constantly, etc. However, about a month ago, I noticed this small indentation in my left buttock cheek - I wondered what on earth it could be (cellulite, weight gain/loss from going to the gym I started going to, who knew?) It got bigger and hasn't gone away over these past few weeks, instead getting larger and my skin becoming ever whiter than I already am and the area is sensitive. I had no idea what it was until I stumbled onto this site - I now realize that indentation is the same spot where I received my allergy shot eight months ago!!! I checked my online medical record and sure enough, Tricyclamide Kenalog injection! NOBODY told me that this indentation/muscle atrophy at the injection site was a possible side effect! They warned me about allergic reactions, drug interactions, buildup of steroids in the system, etc, but absolutely nothing about this awful indentation - it is sensitive and unattractive and I really, really hope it goes away or at least shrinks. Not that I am super vain, but it's not all that cute to have a big "hole" in your cheek, especially when that was one of my body areas I actually felt okay about. Just be forewarned allergy sufferers - just because you haven't had a reaction the first time you get the shot, it could happen the second or third or fortieth time. I wish someone had said something about this, so at least I would have been able to make a more educated decision and choose whether to suffer through a few months of allergies or a lifetime butt indentation!

My mom just passed away 2 months ago from taking this ace inhibitor and she had been on the medication for years. The explanation we received is that "in African Americans, we are proned to have allergic reactions while on this medication and it could happen at anytime...even if you took the medication for 10 years, u could just all of a sudden have a reaction." My mom took it at least since 2004, I seen an old prescription bottle while cleaning her house. I am very torn about what i should do. I cant bring my mom back and I miss her dearly. Is there something I can do about this? Contact the makers? Who are they? Warn others? My mom was only 57 and if I can help someone else, then that could also help me heal.

I to experienced an allergic reaction but not to the sulfa-based compounds but to the filler used. Everyone, please review all seemingly allergic reactions when taking any drugs as the reaction may be from the filler ingredients.

I have been taking Doxycycl 100 Mgt twice a day for 9 days. I'm experiencing some nausea..what I didn't expect is the extreme fatigue and dizziness. I tested positive for Lyme disease and definitely want to get over that.

Not sure what to do..is this is a normal side effect of the drug? Should I contact the doctor? Don't know what to do?..
I have had other allergic reactions to Cipro and Biaxin (but I know there are a different class of drug. I seem to do better when I eat and drink a lot of water throughout the day. JFJ 7/25/09

Alright, listen. There is a light at the end of the tunnel for those who have found this site. My story was posted on June 20th. I would have to say that I cannot trust any doctors for anything since then. This web site has saved me money from the idiot doctors and my insanity. Really. It is so scary that when you go to the doctor they will never investigate your meds you are taking and will send you through many tests and prescribe you medicine that you don't need. I went through 4 different doctors multiple times that prescribed many different things with no effect to my condition. I went off Lisinopril and went back on Diovan and it took 8 days before I noticed any improvement. During those 8 days I got more depressed because I didn't feel any better. Then my symptoms started going away. My anxiety and coughing started to decrease. By the second week i did not need the help of sleeping pills to knock me out due to the anxiety at night and the gagging and coughing decreased.Since then I am almost back to normal. I still though have some symptoms of coughing, but not that bad. If you found this site and taking Lisinopril, please take note that your doctor is probably wrong. You are not going to die. Get off the da#m med and start living again. It may take longer than me. Don't get discouraged.It may take more than a month or so. Stay strong. I am pissed off and would love to beat the s&it out of the ones that created Lisinopril. I know we are the small % that has the effects, but get it off the market. People are dead from this med and the others are going though Hell......I feel for the ones who have had family members that have died from allergic reactions. I had an undiagnosed throat swelling that took me to the ER. I know what it was now...Take care, stay strong, get off Lisinopril, enjoy the rest of your life...

I am diabetic and have chronic ear infections. Just wanted to say that I have never had ANY side effects from taking this drug.. I have had allergic reactions to other drugs, but that is not the drug companies fault. It is unfortunate, but unpredictable, who will have a reaction and who won't. Neither the drug companies or your doctor knows your exact genetic make up and how you will respond to everything that is prescribed to you. ANY time you are on prescribed medication and have unusual effects call your doctor immediately instead of continuing to take it and assume it is a part of your illness. I hope that those folks out there currently experiencing the mentioned symptoms heal quickly

After taking a 500mg Niaspan last night 1/2 hour after taking it I had this reaction: Hot flush in my upper body, face,neck and arms.
Happened out of the blue. got scared.
Went to the bathroom and washed my face with cold water.
Came over to the iMac (computer) Googled Niaspan allergic reactions, found this site and was mentally relieved to note that this was a common side effect of this drug.
Consumed 10 oz of water calmed down and fell better within 6 or 7 minutes.
While some people curse the amount of info on the net I am not one of them.
I am really glad that people share info like I am doing.
I suggest though if any of the side effects are worse then mine yo go to the ER and if you cant hit 911.

First off, let me say that I have been on Depo for 3 years now. I actually like it but I realize that I may be doing something potentially dangerous. I have no idea what else to do though because like many on here, I have atrocious periods and cramps. I am a small petite 95 lb woman, but I would have heavy periods in which I would have to go through a super plus tampon every two hours at some points. I had ulcerative colitis in high school which made me anemic for a while so I decided it wasn't good to be having such a heavy period and losing so much blood. But really it was the cramps that were the worst, they would keep me from work/school. I have had no periods in about two years now which is awesome. I had tried one of the pills back in my past and I seemed to have allergic reactions to it, but the depo seems to work BUT......

There are some things you should know about before you go on this. It DOES decrease sex drive. For the first two years I was on my depo I was still having sex, but for the past year I'm like Meh. I think it partially has to do with the fact that my last relationship was HORRID (I'm paranoid of men now and their intentions), but I also think its the shot contributing to the lack of sex drive. Also, if you are skinny/slender and you get on the shot, its likely that you will remain the same (at least I did), but if you are normal sized or on the heavier side, you will gain weight. I know some women who gained 40 lbs off of it. I also know some who have had worse side effects from it, like, nearly fatal, so I had to think a lot about things before I got on it.

I do have to say the worst side effect for me, and this is embarrassing, but hey, its the internet, right?.... was it made me smell not so good down there. I had never had a problem like that before, I had never even had a yeast infection or anything weird, and from the 4th month or so of being on the shot up to the 10th month (a 6 month time), lets just say it was horrible. I think that also decreased my sex drive because a guy DID say something about it and you can try to explain to them that its your hormones trying to adjust to B.C. but they don't understand. I stuck with the depo because I had a feeling that it would eventually go away, and it did, but good God that was horrible.

The mental side effects didn't really affect me. In fact, I feel that depo made me more sane. It seems that for me, the side effects level out after a year or so, but for the first year it may be hell at times. It's completely possible to be a positive, happy person on depo. I have learned as I have gotten older that happiness is sometimes a choice that isn't easy to make, but is necessary. Usually I find that if I am depressed its because I'm spiritually dead or I just went through a time of emotional trauma, but then again I guess thats situational depression and not clinical depression. I did suffer I guess what you would call an emotional breakdown while I was on depo, I don't think it was the depo, it may have had a little to do with it but it was mostly a bunch of stuff that happened to me a while back. During this breakdown I realized that I either had an impetus to change for the better or I could keep fading and negating myself, and I chose the better option. Sometimes a change in mindset will make all the difference in the world.

I'm in my 5th month of taking Yasmin, and in my 4th month I developed rashes on my face and all over my body. They look like inflamed skin with heads of pus, and very itchy. I first thought it was some severe skin reaction unrelated to the pill because I've taken bc before (ortho-tricyclen) for many years and that never happened. But after reading this forum, I think the cause is Yasmin. I've never had any skin issues like this before, and what's worse is that my immune system has been weakened and I got a bad flu-like illness with high fever in my 4th month of taking this pill. In fact, I'm experiencing my second rash reaction right now, and I'm in my 5th month. This time I'm heaving as well. I think I will stop this drug tonight. I'm so glad you are sharing your experiences on this forum because reading this helped me figure out why I've been so sick. From what I'm hearing, this drug is awful! Nobody should risk taking it because it is even worse than high dose pills, in my experience.

I am 20 years old and have been on Yasmin for PCOS/mood swings/irregular periods since I was about 16 or 17. This past December, I was out with friends when I suddenly had this awful, all-over terrible shaky feeling, thinking I was going to pass out, die, or vomit. I had pressure all over and my tongue felt thick in my mouth, lump in throat and had to go home immediately. I thought I was getting some kind of flu. Weird feelings kept continually happening to me every day since then and the symptoms change over time and last for different lengths. I've mostly experienced tightness/strain/pressure in my throat, lump of pressure caught there, almost numb pressure sensation under my tongue, jaw, and up into my ears, an ache/pressure in chest and sternum. I stopped taking Yasmin, switched to Aviane which made me nauseous constantly and have been off BC over a month now. I have been told it's anxiety constantly by two different doctors, gone to ER, had blood work, thyroid checked, ENT stuck scope down my throat, everything. I was given Klonopin which never seemed to do anything to me, was given meds for acid reflux which did nothing. Even after getting off BC my emotions have also gone haywire and I feel at an all-time low and this is ruining my life and my relationship with my boyfriend. I finally gave in and tried Xanax. The first two times I've taken it, I felt great for the rest of the evening and slept well. Today was the third day and I felt fine for about two or three hours and the pressure in my throat and under my jaw is back again. Does anyone think this could be anxiety or something else, or does it truly seem to be Yasmin?? I'm at my wits end and would like to go back on the pill for my emotions/periods if possible but I'm so afraid in case that caused my problems. I feel helpless and always in pain and discomfort.

I 've had Mirena for 17 days my first symptom in the 1st week was i woke up with my eye lids full of fluid,it has been that way everyday .now their itchy,red and peeling.I also feel like i have to urinate frequently and my scalp itches like crazy,I think i'm having allergic reactions to this thing,it coming out.I wish i would have seen this sight before i got this.

I am extremely allergic to petroleum. I found out when I applied Petroleum Jelly all over my face for four day in order to endure the harsh cold winter weather in the North East. I developed an extreme rash immediately after applying the product the third day. My face hyperpigmented to a dirty complexion. I am now two months after the initial reaction. The rash is now finally no longer itchy and irritated and my skin has started to heal. I am advised that the healing process will take a few months and that the hypepigmentation will eventually slowly, very slowly resolve.

Hello all, I am feeling the bactrim pain. I came in for a staph infection which turned out to be the pesky MSRA. I have been taking 2 800mg tablets/day for about 5 days until I went back for a check up. My dosage was then doubled and to be continued for another 10 days. Also I was given 8 tablets of 150MG Cleocin because the staph wasn't clearing. All seems fine until about the 10th day of the continuation. I started tingling, iching from the ears then later noticed a rash developing down my arms, and back and chest. Now it is everywhere, even on more severely my legs and knees. Seems also folliculitis(infected hair follicles) are popping up with the hellish itchy red spotty rash that is everywhere. I went to the doctor for the rash today(day 2=much worse than day 1). The Doctor said it was an allergic reaction to the Bactrim. I remembered already asking the doctor from the last visit about 10 days earlier if i should be concerned with any allergic reactions. He laughed and said 'why". Well, this time I was give 10 more days of 4 dosages 300MG of Cleocin for the staph and steroid shot for the rash. Also I have this nose stuff for the staph to put in my nostrils twice/day for 5 days to help kill the staph which resides in my nose. OMG, i itch. I really appreciate all the information given here. It is somewhat comforting. I had just taken some benadryl from reading this forum in hopes of combating the rash. Finally, I can't sleep and just want to cut off all my skin.
Take care all and have a happy life.

My 3 year old daughter was put on Singulair for her asthma and supposed allergies. I did not notice any behavior issues, but when I read the very very fine print saying that it could cause stunted growth AND had had no clinical trials in children, I took her off. I have cured her asthma with herbal supplements (a combo that fights bronchial inflammation ans desensitizes the liver to minimize/eliminate allergic reactions - from GAIA labs, look up asthma/bronchitis / allergy). She is now 11 and has not needed any treatment of any kind for at least 6 years now.

I've been on Yaz for about 2+ years now. I'm a healthy 23 year old. Recently I started breaking out in hives and itching all over constantly. After listing every possible allergy it could be, something brought my attention to the one everyday constant thing- Yaz. I went to read about allergic reactions to this medicine and noticed I have at least TEN side effects! Headaches daily as if on a schedule, intolerance to wearing contact lenses (of which I wore well before starting Yaz just fine), weight gain (I eat moderately but crave junk food even when i'm not hungry!), moodiness (yikes.. this one is really horrible.. I owe my friends and fiance a huge apology!) and irritability unlike anything I've ever known. I break at the smallest thing. I've been looking at changing methods for a few weeks now, but now I know it's making me go crazy, I'm stopping immediately! My fiance and I have discussed this and we both think it has to be done. I'm ready to get back to my old, sane self!!!!! Reading other users posts and the Yaz website has really confirmed my decision. I am sensitive to medicines and don't know why it's just now affecting my body. I'm ready to find something else, even it if means longer periods! Do your research before taking this drug!!

i have been taking this medication and ive been itching .
nearly scratching my arms off
and making me throw up .
and get sicker than i was

Cymbalta has been a lifesaver for me. There is one annoying thing though... constipation. It's probably due to my other meds. as well but it is well worth the "effort" to stay on it. I have tried virtually every anti-depressant out there. I've had allergic reactions to many medications that have left me with proximal muscle damage (muscles closest to your body) and during the 10 years I was on Lithium (the first and major cause),. then cholesterol meds. such as statins, I had to have several surgeries to fix what muscles were breaking down (total rotator tear from simple exercise). Anyway, all this to say I had severe depression, was officially un-diagnosed bipolar, got off the statins, Lithium and got somewhat better. Then three other meds. did this to me so my body really reacts strangely to meds. Cymbalta has really helped me to function and not want to just die. Stay on it if you can. There aren't many better choices out there.(I asked to be put on the highest dose 300 mg 1 per day to see if I'd get the muscle pains that start at the top of the thigh and shoulders)

For Medications.com October 18th
Earlier this past summer I took this drug for ninety two days after I was prescribed this medication when I visited the doctor for a bladder infection and I was told I also had high blood pressure. No tests were done except for a urine test at that time and no follow up tests were done later. This drug not only gave me a slew of other side effects but pushed my simple bladder infection to where I no longer urinated in a normal manner regardless of the amount of fluid I added. Only after discontinuing this drug did normal urination return after a few days.
Allergic reactions were as follows. Severe debilitating stomach cramping resulting in swelling of the abdomen, and all digestive organs. Angioedema. (no pre history of this) Urine flow continued to lessen even with increased fluid intake, resulting in bladder pain and a sensation of bladder being pushed from the body. Lack of energy, flu like symptoms, insomnia, leg cramps, many bouts of rapid heart beat, some lasting for awhile, even after stopping the drug. Lack of appetite and a change in taste buds. I had several bouts of angioedema but thought it was 'something I ate, stress etc', as within a month of my diagnosis, my daughter had an extreme reaction to Ciprofloxin (see floxintoxin under that medication) and anything that was going on with me was put aside. She was debilitated by her drug reaction and was unable to walk etc, so I thought I wasn't handling stress too well as I was getting older. Each bout increased in severity leaving me lying debilitated on the couch for four days, eventually for a full week until luckily by that time my daughter was able to take care of herself and began thoroughly investigating this drug only to discover that Lisinopril was the true cause. The warnings with this drug are not very explanatory and leave so much out that should be for patients to read and digest to make their own health decisions and it takes a lot to dig deeper on the Internet to find the true adverse reactions.
We thought by stopping the drug I would get back to normal quickly and I did with the help of a herb called marshmallow which reduced the swelling after a couple of days. However after I thought I was cured I stopped marshmallow and within a couple of days had another angiodema reaction and I thought it was because there must be traces of this drug left in my system. I then took marshmallow for over two weeks and feeling fine I stopped again. Then another episode hit me with not only the stomach problems but a severe bout of coughing that lasted a couple of hours and trickled into a few days. It was then I began digging on the Internet to find the words I wanted to hear, that this drug caused long term problems. I found it by adding UK after other words and found this and much more.
ACE-INHIBITORS
A particular group of heart pills called ACE-inhibitors (the chemical names end in -pril, e.g. enalapril, lisinopril, ramipril) can occasionally cause urticaria, although they more commonly cause angioedema; about one person in 100 who takes an ACE inhibitor is likely to get this problem.  
The reaction is not caused by true allergy, allergy skin and blood tests do not show it, so why does it happen?  Reactions are thought to occur because an unwanted pharmacological effect of the drug causes the release of compounds similar to those released in an allergic reaction.  The only way of showing that a regular medication is the true cause is by stopping or changing the treatment.
To complicate matters, the angioedema attacks may not start until the individual has been taking the ACE inhibitor for months or even years making it difficult to spot the relationship. Also, attacks may continue for several weeks after the drug has been stopped.
I could not find anyone doing following to patients with adverse reactions and I think that is a very bad problem. We are on our own. I do hope this helps others and if you want copies of all my research let me know.
Now I am hoping there won't be any more bouts but I'm still taking marshmallow and when I think I have the courage I will wean myself off it slowly and watch for signs. Believe me angiodema isn't fun and you can't see it on the outside of the body which makes it difficult to understand.

MY APOLOGIES TO ALL FOR AN ERROR IN MY PRIOR POST. WHEN I CUT AND PASTED THE INFORMATION FROM MERCK'S WEBSITE NOT ALL OF IT APPEARED IN MY POST FOR SOME REASON. THE CORRECTED INFORMATION IS BELOW. CHECK THEIR WEBSITE FOR YOURSELVES TO VERIFY THIS.

THIS IS FROM THE PATIENT INFORMATION:

"What are the possible side effects of SINGULAIR?

The side effects of SINGULAIR are usually mild, and generally did not cause patients to stop taking their medicine. The side effects in patients treated with SINGULAIR were similar in type and frequency to side
effects in patients who were given a placebo (a pill containing no medicine).
The most common side effects with SINGULAIR include:
• stomach pain
• stomach or intestinal upset
• heartburn
• tiredness
• fever
• stuffy nose
• cough
• flu
• upper respiratory infection
• dizziness
• headache
• rash

Less common side effects that have happened with SINGULAIR include:
• increased bleeding tendency
• allergic reactions
• behavior and mood related changes
• drowsiness, pins and needles/numbness, seizures (convulsions or fits)
• palpitations
• nose bleed
• diarrhea, indigestion, inflammation of the pancreas, nausea, vomiting
• hepatitis
• bruising
• joint pain, muscle aches and muscle cramps
• swelling

Rarely, asthmatic patients taking SINGULAIR have experienced Rarely, asthmatic patients taking SINGULAIR have experienced a condition that includes certain symptoms that do not go away or that get worse. These occur usually, but not always, in patients who were taking steroid pills by mouth for asthma and those steroids were being slowly lowered or stopped.
Although SINGULAIR has not been shown to cause this condition, you must tell your doctor right away if you get one or more of these symptoms:
• a feeling of pins and needles or numbness of arms or legs
• a flu-like illness
• rash
• severe inflammation (pain and swelling) of the sinuses (sinusitis)
These are not all the possible side effects of SINGULAIR. For more information ask your doctor or pharmacist.
Talk to your doctor if you think you have side effects from taking SINGULAIR."

d27gayle POSTED INCORRECT INFORMATION ABOUT THE SIDE EFFECTS OF SINGULAIR. I JUST COPIED THIS FROM MERCK'S SINGULAIR WEBSITE. THIS IS THE CORRECT AND UPDATED INFORMATION. THIS INFORMATION DOES LIST DEPRESSION AND SUICIDAL BEHAVIOR AS SIDE EFFECTS.

IF PEOPLE ARE GOING TO SHARE INFORMATION ON THIS SITE, PLEASE MAKE SURE IT IS CORRECT BEFORE POSTING!!!!!!!!!

What are the possible side effects of SINGULAIR?
The side effects of SINGULAIR are usually mild, and generally did not cause patients to stop taking their medicine. The side effects in patients treated with SINGULAIR were similar in type and frequency to side effects in patients who were given a placebo (a pill containing no medicine).
The most common side effects with SINGULAIR include:
• stomach pain
• stomach or intestinal upset
• heartburn
• tiredness
• fever
• stuffy nose
• cough
• flu
• upper respiratory infection
dizziness
• headache
• rash

Less common side effects that have happened with SINGULAIR include:
• increased bleeding tendency
• allergic reactions
• behavior and mood related changes
• drowsiness, pins and needles/numbness, seizures (convulsions or fits)
• palpitations
• nose bleed
• diarrhea, indigestion, inflammation of the pancreas, nausea, vomiting
• hepatitis
• bruising
• joint pain, muscle aches and muscle cramps
• swelling

Rarely, asthmatic patients taking SINGULAIR have experienced a condition that includes certain
symptoms that do not go away or that get worse. These occur usually, but not always, in patients who
were taking steroid pills by mouth for asthma and those steroids were being slowly lowered or stopped.
Although SINGULAIR has not been shown to cause this condition, you must tell your doctor right
away if you get one or more of these symptoms:
• a feeling of pins and needles or numbness of arms or legs
• a flu-like illness
• rash
• severe inflammation (pain and swelling) of the sinuses (sinusitis)

These are not all the possible side effects of SINGULAIR. For more information ask your doctor or pharmacist. Talk to your doctor if you think you have side effects from taking SINGULAIR.

THE FOLLOWING IS COPIED DIRECTLY FROM THE SINGULAIR WEBSITE.....

The side effects of SINGULAIR are usually mild, and generally did not cause patients to stop taking their medicine. The side effects in patients treated with SINGULAIR were similar in type and frequency to side effects in patients who were given a placebo (a pill containing no medicine).

The most common side effects with SINGULAIR include:

stomach pain
stomach or intestinal upset
heartburn
tiredness
fever
stuffy nose
cough
flu
upper respiratory infection
dizziness
headache
rash
Less common side effects that have happened with SINGULAIR include (listed alphabetically):

agitation including aggressive behavior, allergic reactions (including swelling of the face, lips, tongue, and/or throat, which may cause trouble breathing or swallowing), hives, and itching, bad/vivid dreams, increased bleeding tendency, bruising, diarrhea, drowsiness, hallucinations (seeing things that are not there), hepatitis, indigestion, inflammation of the pancreas, irritability, joint pain, muscle aches and muscle cramps, nausea, palpitations, pins and needles/numbness, restlessness, seizures (convulsions or fits), swelling, trouble sleeping, and vomiting.

Rarely, asthmatic patients taking SINGULAIR have experienced a condition that includes certain symptoms that do not go away or that get worse. These occur usually, but not always, in patients who were taking steroid pills by mouth for asthma and those steroids were being slowly lowered or stopped. Although SINGULAIR has not been shown to cause this condition, you must tell your doctor right away if you get one or more of these symptoms:

a feeling of pins and needles or numbness of arms or legs
a flu-like illness
rash
severe inflammation (pain and swelling) of the sinuses (sinusitis)
These are not all the possible side effects of SINGULAIR. For more information ask your doctor or pharmacist.
Talk to your doctor if you think you have side effects from taking SINGULAIR.

I have been getting allergic reactions to ibuprofen..(so it seems) Every time i play tournaments in soccer i get knee pain so i take an ibuprofen to ease the pain...though when i take it , it causes me even more trouble it starts with a long stomach ache followed by chest pain next comes the couching and now runny nose and constant sneezing and when all of the symptoms die down my eyes run and go bloodshot and or runny