Medications symptoms and conditions

I was diagnosed with a bronchial infection 1 week ago today. I was prescribed Clarithromycin (500 MG tablets) and Advair. About 3 days into treatment, I started having a bad taste in my mouth. In the last 4 days, the taste seems to be getting worse. I've also been feeling jittery, my heart feels like it's racing and I keep a dull headache. On the 3rd day of taking this combo, I ran a fever between 101.3 and 102.3. I thought I had the flu, but the fever broke with some Tylenol and never came back. I was told I did not have the flu, although my husband and son both got it 2 and 3 days later. After a week of taking medications for an infection, I would think I'd be feeling better, but I'm not. I have 2 more days left of the Clarithromycin, but I'm not sure I want to continue. I think I'll probably cut out the Advair first and see what effect that has on me.

I had a sudden onset of tinnitus in my left ear about 2 weeks after starting to take singulair nearly a year ago.. I had not made the connection until I read about ototoxic medications on Wikipedia. I will try stopping Singulair and see if my tinnitus improves. I'll report back.

I have been on Paroxetine which is the generic for Paxil, I was put on it for panic, anxiety and depression..I have been on since about sometime in March. Now if anyone can avoid running out of their medications it would be a good thing to make you don't.
I have recently ran out of my medication and I have noticed today mostly of the two days I have been without it some differences in my moods, and attitude. Today I have really noticed that I have been very impatient myself with family, husband, and pets, I get angry quicker about anything. I just don't feel right at all..
I am exhausted, I have no concentration, no focus at all. I am having a hard time right now. I go to a clinic to get my prescriptions and lately with what I have going on in my life,my needs get pushed aside.I am a full time student and now my husband goes to school so he can get a better job, and he has to be driven there two days a week by me, so that takes time out of that day to go and see the doctor.

I was prescribed 7 days of Avelox 400 mg for bronchitis. On my fourth day of taking this medication, I began to suffer from severe abdominal pain, cramps and debilitating diarrhea. These symptoms were so bad that I missed a whole week of work. I was taking each pill with dinner in the evening and then I was up all night back and forth to the bathroom. I took 6 of the 7 pills and then refused to take the last one when it became obvious that Avelox was the cause of these symptoms (the only side effect listed on the bottle was dizziness, which I did not experience). I have now been off Avelox for 2 days and I am still suffering from severe abdominal pain and diarrhea. I am afraid to eat anything because it goes right through me and it is very painful.

I am taking probiotics now to regain the good bacteria in my digestive tract, but I am still in a lot of pain. My sister, who is a physician assistant, told me that it should take from 48 hours to a week for this to flush out of my system. She said that Avelox is an extremely strong antibiotic that she only prescribes for confirmed pneumonia.

I am otherwise a very healthy 42 year-old woman with no allergic reactions to any medications which is why it took me so long to make the connection. I would not recommend this medication to anyone and have told my sister that she should not prescribe it either.

These postings have really helped me. I feel lucky that I did not suffer more severe symptoms.

I was on YAZ for about 4 months. And like all medications, i gave it time. In the beginning i experienced a lot of nausea, fatigue, headaches, and severe diarrhea. And instead of clearing my skin, it made my skin absolutely terrible. i stuck it out in hopes that my body would change, and begin to get use to the hormone but it didn't. I have been having GI issues August, have been through a Colonoscopy, and everything came back normal. Ever since stopping this pill, my body has felt so much better overall, but the GI issues are still there which concerns me greatly. Has anyone else ever experienced this? My bowel movements have changed completely, and all of the specialist i have seen, say that the pill wouldn't do this. I do not believe it. I believe that the pill has messed up my GI tract so much, that i can't have a normal bowel movement. I honestly do not recommended this pill to anyone. I am 18, and to be experiencing what i am especially going to school, is so not fun. Could YAZ have been the cause of all of this?

500mg 3 times a day for 10 days, vomited once, have had a horrible headache that started day b4 yesterday, still kinda have it, comes in waves, sux real bad lol

i have Sinusitis, Bronchitis, and a severe respiratory infection.

i see some guy on here mad cuz the doctor didn't tell him he would have bad headaches, like the doctor was going to know in advance he would. this anti-biotic affects different ppl different ways, its really not his responsibility to go over every single side-effect this very common anti-biotic is going to have, thats why the pharmacy gives you a huge pamphlet informing you on the medication, if you would had read it then you would see that headache, diarrhea, and constipation are all common side-effects

i didn't read it however, until i came here and read what i read, which is comforting really cuz at least i know why i have the headache so bad, and why i lost my lunch yesterday, was actually worried maybe i had an infection in my brain and thats why i had it, i know, sounds dumb, but what can i say, im paranoid lol

I am 40 years old and was prescribed lisinopril/HCTZ 20-25 a little over two weeks ago. I went in for a little congestion and low grade fever. I am a teacher and have many kids out with the flu, swine flu, etc. and felt that I needed to get checked. I came out with 5 medications, one of which was lisinopril. I have never had bp problems in my life. I am almost certain that the nurse practicioner wrote me down for something else and the dr came in and changed. I am usually a very calm person but in the last two days have experienced what I thought was a panic attack and anxiety, horrible anxiety. I haven't been able to face my students which isn't like me at all. During the first week I took my students on a field trip and had a really great day with them- much less stress than a normal day. I got home and my bp was around 138/98. I thought that was kind of odd. It has been under control since I started taking it. On this same day, I got blistered on my face and wasn't outside much at all. I have Rosea and thought that it had been aggravated. I believe now that it was the lisinopril. I know that it has a diuretic in it, but it doesn't make me go frequently. Instead I get a sudden urge and have had two "accidents" recently. I have a sometimes dry, other times full of mucous, cough to the point of nearly gagging. My neck muscles were already stressed out and tight, but have gotten worse. I feel a tightness in my chest constently. My lips are so dry that they peel all the time. I have no appetite and when I do eat I get nauseous and almost feel like vomitting. I have been lightheaded and dizzy. I am not sleeping and feel extremely tired all the time. But these last two days have been awful. I love being around people and right now can't stand the thought of it. I am guessing that lisinopril has caused much of these problems. I am about to go see the doctor today and think they will want to put me on some sort of nerve pill. I hate that!!!! I have a plan to achieve everything that these meds are supposed to. Exercise, change my diet, go see the chiropractor, do more relaxing things for myself and take better care of me! After reading these blogs I believe that I am going to take myself off of lisinopril and see what happens. My hubby is also on it and just last week developed an oozing sore and his left cheek - could be the lisinopril. I will pray for all of you bloggers and those who are unaware. This is definitely a poison to our bodies. I think I even read that it contains snake venom. Is this true????? I will update in a few days. Good luck and God bless!

it's been about 2 months since my Mirena REMOVAL and I am just now starting to see a clearing up of my skin on my face and back. My skin was so bad. I had cystic acne on my back and arms and oily skin on my face and back. It's so nice to scratch my back without feeling thousands of bumps lining my neck and back.
*I feel better emotionally too. I am not getting irritated or angry as easily as i was when i had mirena in place.
*No more odor or discharge
*i'm still losing my hair but I think it's starting to slow down
*My knees don't hurt as bad as they used to.
In General I feel better and i'm getting better every week. I am sooo glad that i had it removed and that my life can continue now without such horrible side effects. It seems like it's taking a long time but that's ok as long as i'm making progress. I had it for 20 months so it will probably take a little longer to be cleaned out of my system .
Good Luck ladies.

I started on Ortho Tri Cyclen lo 4 1/2 years ago. About 3 months ago I went in to get my Ortho and was suddenly surprised by the low $7 charge since normally I pay $50(wonderful insurance). I was paying for the generic form(Tri-Sprintec) and for $7 I was all about it! Since taking it the only main side effect is HORRIBLE acne. I am 26 years old and have never experienced acne before.
My general doc told me to finish out the month and switch back to Ortho. He wrote a letter to my insurance company explaining his concerns for my acne and asked them to cover the cost of not only Ortho Tri Cyclen lo but Doxocycline and Defferin. Two medications that he prescribed in hopes to clear my face.
I have experienced larger ta-ta's too. Not that I'll complain about that one though. I've been an A my entire life....

I've been on Advair for 12 years.I'm 27 years old and fed up with all this medications that doctors prescribe.We are so brainwashed into thinking that we misbehave if we don't see a doctor.Let me tell you what: The majority of the doctors, only know to prescribe medication.They get bonuses from the pharma industries every time they prescribe their "new discovered"medicine.
Advair is supposed to be preventive, what you don't know it's for how long.Exactly!!!.....'cause it's not meant to cure Asthma, it's meant to keep you hooked for the rest of your life.
My worse symptom is a very fast heart beating.I'm a martial artist and every time i exert a fast burst of energy(while i'm sparring for example), my heart goes into pumped up mode.It beats very, very fast and i have to stop because it hurts.Sometimes i keep going no matter what and feel like i'm exercising for two people.When i stop, i breath very deeply for 5 minutes and all of a sudden it stops and beats regularly.
It's not fun, and one more thing: I'm from Argentina and my mom sends me the medicine from there cause it's way cheaper, sometimes i run out(i procrastinate sometimes), i'm left off with no medicine for a few days and boy.....I'm a wreck.The time you stop you go right back to where you started.I've been researching about an alternative to this "S***".I'm afraid 'cause i don't want to feel discomfort with my lungs anymore, but i strongly believe that there should be a natural alternative to all this laboratory drugs and i'm on a mission to find it.

I received prednisone intravenously at the hospital to prevent a severe reaction from receiving platelet transfusion. I have a bleeding disorder and IgA deficiency. Because of my bleeding disorder I have to receive platelet transfusion before any surgical procedures. When I receive the platelet transfusion 20 mins into receiving the platelets my face feels flush and a tightness and pain in my facial bones. I get a sudden headache with severe pressure pain in my head so severe that you feel as if your head is going to explode. My doctor recommended the use of prednisone to prevent me from having this reaction. 20 minutes after receiving the prednisone intravenously I felt my face turn flush with facial bone pain and a pressure around my face and top of my head. I felt the pressure in my head, but not the pain which I would get from the platelet transfusion. That night I had dizziness,severe headache,nausea,stomach pains,severe sweating,over heated,weakness and unable to concentrate. This went on for 2 days straight. Today is the 3rd day and I still can feel a slight pressure on the top of my head. I also felt eye pressure and I still have the headaches. I am schedule to see my doctor in 3 weeks and I will tell him that I will not take Prednisone ever again. I am sure there are other medications that can be given.

I have been on Campral for over a year now for OCD (nothing to do with alcohol). Apparently Campral has been shown to work for OCD, so after many other medications didn't help me, my doctor suggested it.

I take 666 mg a day. I've been up much higher than that, but higher didn't seem to make a difference, so I went back down. I am also on 250 mg of Lamictal a day.

Campral works very well for my OCD, better than anything else has.

The most amazing part is that for me anyway, unlike every other medication I've tried, Campral has had no side effects on me. It's like it's transparent -- very weird.

Who knows -- we're all different -- but I'd recommend it to people who have OCD and not found success with other medications.

Today is 10/28. I am Weezie1 and I posted on 10/26 about my severe drug reactions. They have gotten worse since I wrote my first post. The fever and chills are gone. But now I have been dealing with a rash/hives over all parts of my body. They are worse where close contact to sleeping clothing are - back, chest, neck. The one side of my face that I usually sleep on is purple every morning, along with that same side of my neck. I managed to get myself back to the doctor on 10/26 and am now on a 6 day dosage of steroids for the rash/hives. The steroids have stopped the hives from getting any worse. But it is taking awhile to go away. Any heat, anxiety, frustration brings them out again. I see I will be dealing with this for awhile. I go back to the doctor on 10/29 for a recheck. I lost 2 days from work because of this. My skin felt like it was on fire with hundreds of bee stings. Now I feel like I have a severe case of poison ivy. I have found some relief using Aveeno's oatmeal powder to do a bathtub soaking at night. Then I follow that with Aveeno's rich moisturizing lotion. The doctor may want me on steroids for longer than first prescribed.....not a med you want to be on for too long. All because of an UTI last week that could have been simply treated with a regular antibiotic if my doctor was not able to prescribe this sulfa drug to me on 10/19. Next time I will go with my initial gut feeling and refuse to take a medication when I see its extensive side effect list. I wish I had done so last week. I am suffering much more now than I was last week with my UTI. I filed an online complaint at the FDA's website. They mention it at their phone number that Weezie1 reported in my 10/26 posting here. I, unfortunately, expect to see additional patient complaints here every few days when I check back at this great medications site. And now I see that someone has internal bleeding. What next? A death? My blood pressure and heart rate were both increased for several days due to this drug. I could feel my heart pounding when I was sitting still and laying in bed. Thankfully, my BP is normally on the low side, but all the numbers went up by 10. We have to band together to get this crap off the market and out of the hands of doctors and unsuspecting innocent patients. Our voices will be heard if we speak in large numbers. Keep talking!Good luck to all.

I took aviane that is supposedly the generic version of Aleese.. which its NOT. Aleese was taken off the market and replaced with pill and they called it generic.
Well Aleese has don't wonders for some but when Aviane was introduced it was slightly different. Well, anyways..

I took it for a few days and don't say its not long enough. EVERYONE'S body reacts differently to ALL MEDICATIONS!
After my few days I was biting my fiance's head off and handing it back to him. Next day I was happy as a cucumber and days following I started to get a weird feeling. I felt itchy ALL OVER! And I felt short of breath a little bit and I HAD MASSIVE INCREASED ANXIETY!
I went to the doctor and they said I was having an allergic reaction to something. They couldn't figure out if it was the hormone in the pill or if it was the dye covering it.
NOW I have to go on the nuvaring to see if that does the something.

A few months ago I was diagnosed with a UTI and was prescribed Sulfamethoxazole (1 pill twice a day for 10 days). After a few days, my UTI was cured, but I continued to use the medication as I was instructed by my doctor and pharmacist. I had no side effects or allergic reaction for the entire period. However, on day 11 I noticed a small splotchy red rash on the right side of my body near my armpit. The next day the rash had spread to my legs, stomach and other side of my body. It was not raised and did not itch, so it didn't worry me. My boyfriends suggested that it might be a reaction to the medication, but the rash did not appear until at least 24 hours after taking my last pill. Five days ago, I became worried that I had contracted another UTI, so yesterday I visited the doctor again (a different one). She asked if I was allergic to any medications and I told her that I wasn't aware if I was. I did not think about the rash from a few months ago because I did not believe it was related to sulfamethoxazole. So she wrote me another prescription for the medication, but this time I was instructed to take 1 pill twice a day for 3 days. I took one pill around 4 PM yesterday and within 30 mins my entire body began to tingle and itch slightly. 2.5 hours later my face was bright red and severely hot and puffy. My eyes were as red and puffy as my face. Around 9 PM I began to chill and shake severely and I took Excedrin for a mild, dull headache. I took a warm shower, but I felt extremely fatigued and became nauseated simply from standing. So I got out with intentions of vomiting, but when I sat down in my bathroom floor I no longer felt nauseated. But my shaking became even more severe. I was cold, but also I was nervous and anxious because I felt mentally unstable. I have never battled depression, but I felt a slight bit of depression last night. I was very irritable and short tempered, which is very unlike me. My skin became so sensitive that I could not even stand feeling my boyfriend's breath on my shoulder. My body began to ache, specifically my ankle and knee joints, and it hurt to walk. I woke up around 2:30 AM with a fever of 100.4, so I took two Tylenol and the fever broke quickly, but I did not feel much better. This morning I feel a little better with no fever, but I still have slight chills and my whole body is red and itchy. Yesterday evening was a nightmare.

I have been reading all of your posts and I am surprised by what I am hearing. Especially the depression, loss of sex drive, and hair loss. I did check out their website (http://www.nuvaring.com/Consumer/aboutNuvaRing/possibleSideEffects/index.asp) and it seems they are actually pretty honest about the possible side effects. HOWEVER... although I checked the site before I started taking the ring 2 years ago, I kind of ignored the "possible" side effects as just that, "possible." Because I've never had any problems with medications or birth control before I didn't think they would happen to me.

Last week I 2 days late in putting in the ring and since then my breasts have been SO tender I can barely walk. Seriously, it's awful and I know it is the hormones from the ring. Until this point, I have had no problems with it, in fact I have really enjoyed its convenience and effectiveness. But after reading all of your posts I am wondering if I should rethink using it... I have been feeling really down, angry and anxious over the last few months and not really craving sex with my boyfriend like a 22 year old women should!! I don't want to over react and blame it on the NuvaRing if it could be other things in my life, but I also don't want to ignore it either because if taking the ring out would make me feel better, more healthy, less angry, etc...

What should I do?

i have a friend who went after her husband in a ctalsudden rage after starting the Lamital, she loss huge amounts of hair and it conytinues to fall out , was put out of her house,broke up her family and is a complete mess. She was on adderall, suboxone and the n the dr gave her this,i was trying to figure out what was going on with her and i looked up the newest of her drugs lamital and found out what was going on . Mt advice to all you bipolar people find GOD no one is ever happy all the time and we all go through really hard times . I am sober and take nothing for the last 20 yrs. When i first got sober doctor tried to tell me to take antidepressant, I said ," the difference between us is when all else fails i go to GOD and you go to meds"" YOU wont break. We live in a society run by drug companies that you are not allowed to have emotion, they flat line everyone.and when it doesn't work they give you more drugs till you are a blob of a person. Get off everything{ except if you need it for ceisures } It could take a yr to completely detox, be patient and go to na meetings

Just had to comment on these side effects I'm reading about Lipitor and other Statin drugs. I don't take anything and I never will after finding this site. Guess what, I have had high cholesterol since I was in my early 20's. When I say high... it ranged from 240 - 260...remember when 250 was OK? Well folks, it's 30 years later, my cholesterol is just about the same range, and Oh My GOD...I'm still here without any drugs.!!! They lowered the range so they could pass out the pills!!! Greed, greed, greed. Do you wonder why our Healthcare system is out of control? Well, when you keep feeding people medications that are presenting the side effects they do, making them sicker, they just keep testing and testing and testing for other things. Let's do blood work, MRI's, CAT Scans, Spect Scans, Pet Scans...Scan away...and guess what...all comes back OK...hmmmm why not look at the drugs you're prescribing. We need to see "all the side effects" listed. Not just some. They're misdiagnosing, Alzheimers, Fibromyalgia, MS, Lupus, Dementia, Arthritis, and on and on when it's been the drugs causing the diseases!
Ween off everything and anything you can...take your chances...when God wants you, he's going to come and get you no matter what you're doing...right or wrong!

I started taking 5 mg of abilify a few weeks ago. Before that I was taking 2 mg for 3 to 4 months. I also take 400 mg of lamictal and 20 mg of prozac. The prozac was very recently added.

Anyway, I have tried many different medications and apparently my depression is treatment resistant. Abilify has made me a cold, emotionless person. I have not cried in months. It is terrible when you feel so sad inside and you can't even cry. I have also developed a twitch in my eyebrow which is very hard to control. Most recently I have discovered, on my own and with the help of my mother, that I have akathisia. Although I mentioned a lot of symptoms to my doctor before, she claimed it was just anxiety.

But this is so much worse than anxiety. This is extreme anxiety, being unable to sit or stand still, getting anxiety with just the thought of having to sit still, getting urges to kick, feeling terribly restless inside unlike anything I've felt before, feeling like something terrible is about to happen...

I hate this. I don't know what to do. I'm seeing my doctor in a couple days and I'm just wondering what she will do. Will she take me off or will I get something even worse... will this go away..

My 16 yr old daughter had her series on Gardasil shots completed in March 09. I don't recall any major side effects right away. In the past three months, she has been throwing up after taking a few bites of food. She drinks a lot of Pepsi and has a lot of stress, so I thought she was developing an ulcer, so I told her to stop drinking pop for awhile to see if that helps. The symptoms have subsided, but now that I am reading this website, I am worried. Before the shots she had headaches or migraines, they run in our family, but I have noticed that she has them more often now. Another thing is her hair is everywhere. I thought she was damaging her hair with the straight iron, but geeze, now I don't know. All these problems might be tied to the Gardasil shot.

I have been on Methotrexate for about 1 year to treat RA. It has worked great for pain BUT I have noticed a lot of things going on that I've simply contributed to life. I have severe headaches, dizziness, extreme fatigue and major mood swings (depression and anxiety). I've seen some things posted on the internet about these being side effects. I am going to talk to my RA doctor and see if there is something we can do. I have been so bothered by these symptoms that I would just about prefer the pain to the constant feelings of irritability and depression. What are some other medications people are finding useful of RA with out the side effects????

I just got my Mirena removed today. I am SO excited. I have had it in for 1 year and it has been the worst year of my life. My symptoms were :MIGRAINES!- for which I was admitted to the hospital, they did all kinds of tests, and found nothing-( they even gave me an IV of morphine, and the migraine was so intense, i still felt it with the morphine.), arthritis- (or EXTREME ACHING in all of my joints, especially my hips, knees and lower back area., pain in my chest- like unable to breath, pain in my neck, I was sleeping 9 hrs a day and still exhausted and lately its been severe insomnia, cramping in my lower stomach and bloating really bad. I am 5"3, 21 yrs old, originally 107 pounds, and have two kids. After my daughter I was on Seasonique and although it made me have mood swings it was NOTHING in comparison to this. After my daughter I lost all the baby weight and then some. Even after I had my son in the 6 weeks before I got the Mirena, I lost all of the baby weight and was back down to 107 pounds. Now I weigh 130 pounds- and thats doing the same exercises and eating the same that I have always done. I have also never had ANY UTI's and I have had consistent UTI's since I have had it in, that have NOT gone away with various medications. I have had NO sex drive. Absolutely NONE, and I am 21years old! I felt very fatigued every day and it took all my strength and energy and mostly motivation that I HAVE TO provide for my family, to get up and go to work everyday. I read the brochure for Mirena when I got it inserted, and there were NONE of these side effects. I found some of these side effects on the Canadian website, and found people's horror stories of having Mirena in. I am SO happy to have finally gotten it out and am looking forward to being a normal healthy person again.

I had the Mirena placed in 2004 after the birth of my second child. I had weight gain, mood swings, hungry all the time (i would sleep eat), depressed, joint pain and was tired all the time. I eventually got it removed 3 years later and my symptoms got even worse. I was severely depressed, my sleep pattern was abnormal, my mind was fuzzy, couldn't concentrate, joint pain worsened and had absolutely no energy. I started itching and having tingling sensations and "bug biting" pain/sensation especially in my extrementies. It was weird. It stimulated a hormonal response that affected my central nervous system. I know it did. I will never be convinced otherwise. It was a shock to my system. There needs to be studies done in this. I finally drug myself to the my general practitioner 3 months later and I thought that I would get admitted in a psych ward. I was hardly functioning. No kidding. I had no reason to be depressed. My life was better than ever. I was not admitted, but I was put through the ringer for tests and my healthcare bills became outrageous. I had tons of blood work, sleep studies, saw a neurologist, had a myelogram, mri, and put on several medications which added to the weight gain. It has been almost 2 years now and I am just now starting to feel like myself. All of the tests were inconclusive. The neurologist dx was something neuromuscular. I am not on any medication now, but am not 100%. But I know that damage was done and I am older. So I'm afraid that I will never feel great again. I wish I had never had the Mirena. Never. I know I miscarried once and suspect that it happened twice. I didn't have a period for those 3 years but it was not worth it. This product should be recalled.

I have been taking Geodon for about 4 months now and it has relieved my bipolar symptoms remarkably well but in the last month and a half I have experienced a "Shocking" feeling to my heart that goes down my arms and legs. I was referred to a cardiologist and had a not so good EKG. I am scheduled for a ecocardiograma and to wear a heart monitor for a few days and then follow up with a nuclear stress test on Friday. The feeling is scary and recently I have not been sleeping. At first the medication was a miracle and I had for once in my life a normal sleep pattern. I guess I am worried about my heart. I take 180 mg every night along with a sleeping pill that was prescribed by my doctor. He was running out of medications that would help me. I have lost 27 pounds since being on the medication which is on the good side but is the cost going to be my heart? I will post what the doctor finds so that all of you can know what to look for or be on the watch out for. Many thanks for listening. B.

I got the Mirena 1 year ago, at age 46, when my youngest child was 13. My doctor did not do anything to dilate my cervix and the insertion hurt very badly. I almost told them to forget it! I have a high threshold for pain and had both my children without any medical intervention, so it is saying a lot to say the Mirena insertion hurt. I decided to get it because of my heavy periods. My periods are much lighter, but last just as long (6+ days). Since May I've had a weird rash on my legs and tailbone. The one on my tailbone looks like a bruise. My shins are mottled and itchy. I've been to numerous doctors and tried many different medications. They have gotten better, but have not cleared up. It seems that my legs are not getting adequate circulation. Also, my belly and area below my navel are bright pink and itchy. I, too, feel bloated and pregnant all the time. Ugh! I experience heart flutters and once ended up in the emergency room because the school nurse, where I work, thought I was having a heart attack. Does anyone else have a rash like I describe? This darn think was so expensive, I hate to have it removed but, if it is causing this rash, I'll have it removed right away!