911 symptoms and conditions

thank you so much !i read your blog when my 79 year old dad was taking his first dose of avelox, 30 minutes later he went into a seizure i called 911 and they rushed him to emergency room.he is doing good now.it is a very bad drug.

I have an 8 yr old son that has allergies and asthma. The allergist recently prescribed Singulair which my son had taken when he was 5. We took him off of it back then due to anger outbursts. By the way, the Dr. said that was not a side effect, but nonetheless the issues subsided. When it was recently added back to his medication list, within 3 days he had anaphylactic type episodes 2 days in a row. The attack started with stomach pains, chest pains and then he couldn't breath AT ALL and turned blue! There was no time to call 911 so I gave him an Epi Pen. The attacks are still occurring yet milder and all his Dr.'s swear by Singulair and think I am crazy. I took him off Singulair immediately and we are still waiting for it to leave his system. I think that is why the recent episodes have been milder. He has been tested for all sorts of allergens which he did not come in to contact with prior to the anaphylactic events. We still have no answers and if I hear one more Dr. talk about how great Singulair is, I am going to freak out!! To heck with these drug companies and doctor's who get perks for prescribing medications without informing us of side effects.

Approximately 1 1/2 years ago I was given Avelox for Bronchitis. I had taken the drug several times without any Side Effects. Within 15 minutes of taking that dose I got a flush that started at my toes and went up to my head in seconds. Then I started to itch and broke out in hives. At this point my mouth started to swell and I knew this was bad. At this point I called my doctor's office and told them I had an EPI Pen at home should I use it. The nurse told me to take a Benadryl and that she would check with the DR and call me back. She said if the reaction got worse to just call the squad and go to the ED. The nurse called me back and told me to use the EpiPen and if this didn't help to call 911. It was pretty scary.

I recently had a severe Drug Reation to Avelox in April 2009. Within 5 minutes after taking it, I started with heart palpitations, very similar to an anxiety attack. My thinking started to get out control, my breathing became shortened and rapid, much like a panic attack. I started to itch, couldn't think and felt like I was losing control of everything. Within 10 minutes I knew it was getting worse. I had my husband call 911 and the operator told me to take benadryl while I was waiting for the squad, and I did. The squad was there in a reasonable amount of time. However, at this point I was so short of breath, I could barely walk & talk. I just collapsed as soon as I reached my porch steps. It nearly took me 1/2 hr before I could walk to the squad, only taking a few steps at a time and waiting about 5 minutes or more, before walking again. I hardly remember walking out to the squad and the ride to hospital. I remember being totally limp, and was
carried down my porch steps. I barely remember getting into the squad. I had to answer questions in short phrases, pausing several times to get enough breath to do so. I was told by the time I got to the hospital I was purple. After about an hour things started to calm down. I came very close to "buying the farm" that night and never want to experience anything like it again. I spent the next 7 days in the hospital, on oxygen and several medications to help me breath and clear the tracheal bronchitis.

this is probably the worst thing Avelox caused, besides death, which would have happened without help..

7th day on Avelox for sinusitus - massive pain back of my head, sweating so much my clothes were soaked, threw up 2 times, legs were uncoordinated when trying to walk

Called 911 - paramedics took blood pressure - guess what.. 210/180.. something was definitely wrong. Rushed to hospital - passed out in ER - woke up with wife and family present - CT scan found my brain bleeding and brain surgery was performed to remove the clot..

But wait, it gets better... 2 days in the ICU my brain swelled from the surgery and the fluid stopped circulating.. I was semi conscious in the ICU for probably 4-5 hours and nothing was done. My wife came in early in the morning and thought I was sleeping, but could not wake me.. The nurse said that a doctor was called and will be there later. I'm DYING right before their eyes in the ICU!!! My wife demanded I get a CT scan immediately. If she didn't I would have stopped breathing. Later CT showed my ventricles enlarged with fluid backed up so much that my brain and brainstem was ridiculously squeezed so much, my head was all ventricles and barely any brain showing in the CT. I attribute my current brain damage to this episode.

A shunt was placed in my head for about 3 days.. basically a needle is inserted into my brain and left there to drain the excess fluid.. After my condition stabilized, the shunt was removed.

Spent 1 week in the hospital, then transferred to another hospital to stay in for inpatient PT and treatment. I didn't know left from right, had double vision, was throwing up constantly, was hot, then very cold, my legs hurt, had hallucinations (was believing certain things were happening, that really weren't) was incontinent, had a new catheter inserted every single day, was taught to walk again, had to use a wheelchair.

I had always been healthy, was vegetarian and did not smoke cigarettes.. I exercised regularly, did not use drugs (i.e. - cocaine or methamphetamine which can cause high blood pressure leading to a stroke)

Didn't know what happened to me, but realized I had to be there.. After 1 month, decided to go home (the hospital was becoming too stressful, somebody was always screaming and yelling at night and the daily catheters were uncomfortable), to be back in the lifestyle I knew.. my wife, my granddaughter, my house, my dog, cats, and other pets were sorely missed.

Once home I found that I couldn't do what I used to anymore - could not mow the lawn, drive, speak well, walk properly, had double vision, a tingling on my face, a metallic taste in my mouth so bad that good food tasted bad.

My wife set me up for physical therapy three times a week daily outpatient at the hospital I was at. Vomited regularly from the daily dizziness.

This was most disturbing, I developed a pain in my left hand and left shoulder, to the point where I could not raise my arm above my head and had to sleep with my arm straight down for at least a year. After playing guitar for 30 years, I found myself unable to play my guitar anymore. My left hand had lost all its dexterity and was not usable. I did not realize what happened to me until my wife explained the entire thing to me.

In the next few weeks I spent each day trying to put "2 and 2 together" and figure out why this happened to me. When doing research on strokes, I realized that certain things happened to me that were not consistent with having a stroke. In my brain damaged condition, I remembered taking the antibiotic Avelox, based on a physicians prescription. I researched the adverse effects and to my amazement, the listed side effects were consistent with what happened to me.

I began a quest to file a lawsuit - was unable to find a lawyer willing to tackle such a huge case.. although one lawyer did file before the 2 year time limit expired.. I had MRI's performed on my hand and shoulder which revealed scarring and previous ligament tearing.

During the time of having more outpatient and in home therapy, I regularly visited a psychologist and my physician confirmed that the Avelox most likely caused the brain bleed, tendon tears, and other mysterious symptoms when I presented him with my research. I was unable to work and my only income was from monthly Social Security Disability benefits that didn't begin until 6 months after the incident.. leaving me with no income and unpaid bills for 6 months. The mortgage payments fell behind and soon foreclosure notices arrived. We decided that an alternative would be to sell the house.. it could not be sold after 1 years attempt, so my wife and I moved to an affordable apartment. I put household items in a storage facility. I either sold to pay bills or threw away much of my personal things,since I was devastated by what happened to me, I didn't think I was going to survive long after reading statistics on strokes.

While in the apartment, I needed an income and was forced to take what was in the scpoe of my limited ability. I accepted an early morning paper route and then made deliveries for a courier company using my own vehicle.. That was a 12 hour work day. Being completely upset over what happened, losing everything including my house.. I decided to attempt to escape the overwhelming things that happened and were still happening. I found a house for rent that was less than the apartments rent, except it was in North Carolina. At the time that seemed perfect, a 3 bedroom house located in a far away place where I could forget everything that happened and make a fresh start. Only problem is my wife not want to go, but I was adamant upon doing it. She helped me move everything, including all storage items.. I had moved to North Carolina, but soon found being alone and unable to find suitable employment unbearable. I was being contacted for back rent owed, but could not do everything alone - I became more depressed to the point of feeling suicidal, so I called my aunt in NY and she said just leave everything and get myself to her house. I did, leaving everything behind, and stayed with her for a month until my cousin invited me to stay with him.. which I did. I stayed with him for 3 months, all the while searching for employment.

With help from my family I moved back to my familiar area in NJ in the summer of 2008. I had lost everything..unable to be physical with my wife and being seperated for 18 months, she has requested a divorce. Currently I live by myself and am still slowly recovering, yet my left arm and hand are uncoordinated, my talking is difficult, slurred and gravely (diagnosed with dysarthria), my balance is bad and am dizzy every single day for the past 4 years.. Although brain damaged, I am attempting to rejoin the computer support business again.

My entire past, everything I knew and did, everyone I knew, who I was, etc.. is all a strange hazy memory. If I don't take a sleep aid, I wake up around 4am with racing thoughts, unable to sleep.. My depression and anxiety are so bad, it is difficult to function and interact with others. My psychiatrist has diagnosed me with post-traumatic stress disorder and prescribed Zoloft and Xanax.

Upon proper research, I have to blame the prescription and subsequent use of Avelox for causing the brain bleed which led to my life being completely and utterly destroyed. My intentions are to file suit against the manufacturer Bayer and/or the hospital for allowing me to die in the ICU

I can't even get up to go to church. I feel so weak and so sick. I have been off this awful stuff for 2 days and still feel so ill, I can't function. i just want to throw up. I have no support and no help whatsoever. How can this be happening. Will I make it through this horrific feeling. I can't do anything, not even eat. My whole body feels like someone has punched it all over. I don't know if I can hang in there. Please post, post, post.

Please help me. I have had the Mirena for a little over a year now and I have been miserable ever since. I just yesterday one of my very frequent depressive states. I has become so bad that I often think about hurting myself. I am very petite, 4'11 to be exact and I have never weighed anything over 115lbs. I just recently went to the doctor and I weigh 147lbs. I have always eaten healthy and I couldn't explain my weight gain. It has become so depressing I refuse to take pictures and I no longer want to look in the mirror. I have horrible headaches and my periods are longer. I am now going through a divorce and I don't have a job or health insurance. I really need to take the Mirena off but I don't know what to do!! Every day that passes by I keep getting more and more depressed. I am afraid for myself...help me

My healthy, active 55 yr old husband of 30 yrs was prescribed SIMVASTATIN in Aug. of last year. He started having pains in his legs & back and had an appointment in Oct. with the dr. to check on how he was doing with the new drug. When he went in to the office, he was having terrible pains in his chest, legs & back. The dr. immediately called 911 thinking he was having a heart attack. He was in the hospital for a week while they ran a multitude of tests. All came back clear for his heart. He kept telling the dr. that the back & leg pains were still there. They didn't seem to be concerned about anything except his heart. He was dismissed continuing to have pain. The pain steadly increased over his whole body, then in Feb. of this year, he suffered a major seizure and spent another week in the hospital. This time they wrote it off as epilepsy and put him on anti-seziure pills. After he was released, the symptoms increased, his memory, vision & balance are all effected, he has chest pains, depression, and is in constant pain. He's been sent for numerous MRI's, bone scans, blood tests,etc. He has been to neurologists, neurosurgeons, chiropractors, physical therapists, etc. The entire time, his health has declined because he was being poisoned by Simvastatin. Finally, after doing our own research, we found a neurologist that recognized the problem. He told us that this drug distroys muscle tissue and that the damage may be irreversible. My husband can no longer work, drive, or enjoy life. He walks without a cane or walker, and depends on pain pills because the pain is so severe. He stays in bed most of the time due to the pain and lack of energy. He has been off Simvastatin for a week now with no change. We are hoping & praying for improvement over time. PLEASE, if you are your loved one are taking this drug-STOP IMMEDIATELY. The results can be devastating. I can't imagine why the FDA would approve a drug like this that destroys quality of life.

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.

When I started my little emotional rollercoaster @ age 35, they classified me as being bi-polar with generalized anxiety disorder. I put myself into a treatment center after feeling like I was going to go crazy. I used to work in the medical field and I should have known better. They doped me up on 1000mg of Lithium, and 9oomg of Depakote. Lithium can be hard to regulate and dangerous; coming from a person who can sneeze and lose two pounds Depakote just turned out to be a fat pill (180 to 210 in three months). I went through the guinea pig stage Every SSR they put me on had a very bad side effect, Paxil being the worst. After two days of taking it the racing thoughts and feeling out being out of control made me want to jump out the window. I could not even call 911 as I felt I would go even more insane. I really almost did not make it through it. I discussed it with my new Dr. and he suggested Lamictal. I have been on Lamictal for over 4 years at 300mg a day. It has stabilized my moods but I still argue with the doctor about my diagnosis as I feel I am more Cyclothymic , my mood swings are not as pronounced and can last from a few hours to a few days. Since first taking the med I noticed the memory loss, my train of thought going out the window, bloated, the feeling of having a fever, but not. One of the most important affects, if I am an hour or so late from my regular scheduled dose I get dizzy and my shoulders and neck start to tingle and get numb. Just two weeks I requested an increase in the dosage to 400mg to see if it would help with my underlying depression that every other combo has not addressed. Since then I have been a bit more of a whack job. (Emotionally)Two days after the increase I had a very hyper mania day, I had to leave work early for fear I would lose control of my mouth, do or say something very ADHD. I took two days off and seemed to be fine after that. This Sunday I went downhill as soon as I woke up. I wanted to cry, but couldn’t and I did not know why; I felt void of emotions except for sadness, lacked the energy to want to deal with people, even my other half, wondering why I was even here. (Physically) I have noticed heart palpitations and muscle spasms in my face and arms. I looked up side effects and found this site and wanted to add to it. I have tried just about everything out there that I can and nothing will really work as good as this one. Combos with it do nothing for me either. It really freaks me out that the thing I am taking so I do not feel the way I do is making me feel that way to the extreme. I am letting my Dr. know that I will be taking myself off this dosage.

First I want to say, after reading several posts, that it seems a lot of you are taking Topamax without food, which may be causing your "spaciness." My doctor suggested always taking it with food, even though it says with or without food, and I only experienced spaciness the few times I took it at bedtime without food. Once I started taking it with breakfast and dinner, that never happened again.

I am a 48 year old woman, prescribed Topamax in September of 08 for migraine associated vertigo without headaches, with facial numbness. The first thing I noticed was I immediately had headaches, which to me indicated it was dehydrating me as that is the only time I get a "normal" headache. So I knew I had to drink a lot of water. Soon after starting Topamax I developed a dry cough that lasted the entire time I was on the med. I did not relate it to the drug at the time, however. It never even occurred to me. After about two months on the drug I started having trouble breathing with extreme dryness in my airways. I was prescribed an albuterol inhaler which did not help. I was then prescribed a corticosteroid inhaler which also did not help. I thought the trouble breathing was from taking Nadolol which I was prescribed for occasional heart fluttering - the neurologist said this was a normal side effect of Topamax. I stopped taking the Nadolol but the trouble breathing continued. I also had more migraines with vertigo and facial numbness than before I started taking the drug. I hoped it would eventually stop and the drug would kick in to help the vertigo, so I stayed on the drug. I had very minor tingling in my feet, but it was tolerable. I became very stressed out, had trouble sleeping, depression, my face started breaking out in November (and still is), I lost interest in everything that I normally enjoy - reading, photography, following politics in the news (sort of an obsession of mine). In December I was so depressed that for the first time in my 11 year career I started canceling appointments and eventually took three weeks off from work to "re-group." In January the neurologist decided that we would increase the dose from 100 mg to 150 mg for one more month, and if it did not get rid of my migraines with vertigo, we would discontinue the drug. The first day on the increased dose I had a killer headache, and I drank 150 ounces of water before it went away. That night I did not have to go to the bathroom during the night, unheard of for me. That's a lot of water to drink and not have to pee. Within two days of increasing the dose, my cough became much worse, and within three days, the breathing became more difficult. Within five days, I was having trouble speaking because my airways felt so dry. I called the doctor the next morning and he said it was not the drug, but if I wanted to, stop taking it. So I went off it cold turkey, per his instructions. I had rebound migraines every day for a week or two and my heart was pounding, sometimes for three or four hours at a time. Eventually the cough and trouble breathing went away, however, I had to continue drinking lots of water or I would notice that I didn't have to urinate, sometimes not at all. Again, unheard of for me. I saw a cardiologist at the neurologist's urging and they said the heart pounding was just anxiety. I disagree, as did another doctor of mine. We both believe it was withdrawal. I have now found out (by getting copies of my medical records) that the neurologist is now attributing all of my side effects from the Topamax to "somatization." In other words, psychosomatic - not a side effect, but just a way of getting medical attention. I am seeing a few people on this board who have also experienced a dry cough and trouble breathing. Can I have the same side effects as other people and have them still be psychosomatic, even though I had no idea those side effects could occur? I don't think so.

I have a theory that Topamax interferes with hormones which causes a lot of the side effects like lack of concentration, memory loss, anxiety, depression, insomnia, acne, and hair loss - all symptoms of peri-menopause and menopause. Ask any woman in her 40's or 50's if she has these symptoms and most of them will say yes. My face has not been this broken out since high school! My hair is falling out at a rapid rate. I won't even bother mentioning these to the neurologist. He'll just say it's not the drug.

I'm very frustrated and not sure what to do at this point. The neurologist has me taking a supplement called Migrelief now, but I think it takes three months to kick in, so I have no relief at this point.

Has anyone else experienced the trouble breathing with dry cough? I don't believe for a moment that it was psychosomatic.

I have always had and currently have the side of effect of extreme fatigue associated with the use of synthroid and now Armour thyroid replacement as well.
Whenever my tsh reaches normal levels I become increasingly fatigued. Now I an hardly stay out of the bed and yet my levels are normal.
I have Hashimoto's Disease and am menopausal with severe insomnia to cloud the issue. But the fatigue associated with thyroid replacement is longstanding and has occurred for about 15 yrs. For many years, I would stop taking the medication because of it. My doctors do not believe that the fatigue is related to Synthroid which I find utterly frustrating. Will be looking for another endocrinologist soon. Has anyone out there experienced this side effect of extreme fatigue?
Any input would be greatly appreciated.

have to agree with Mrsbarrett's post right below mine...I have been a lurker on this board for the past couple of months and thank God for it or who knows how crazy i'd be right now!! Here is a list of my side effects and pertinent information:
DOI: October 2008
Side effects were gradual and most evident around the Christmas Holidays:
Dizziness
Weird eye/vision disturbance where i'd lose focus for a moment and then be okay.
Constant spotting of "old blood" nothing much but did require pantiliners 24/7
Anxiety
Hypertension (more than ever, like when I was pregnant, 150-170s/100)
Panic Attacks
Face Dryness
ZERO SEX DRIVE
No "natural" lubrication, but who cares when you have no drive, are spotting all the time, and it hurts to have sex
Vaginal Odor
Mood Swings
Depression
FATIGUE to the point of wanting to stay in bed despite having to care for my 7.5 year old.
Chest pains (kept thinking maybe I had heart trouble, had cardiac workup that came up PERFECT and bloodwork was perfect, Thyroid test was perfect)
Nausea (morning sickness type, would get slightly better in evening but not so much)
IBS symptoms (diarrhea)

DOR: January 23, 2009
2 days later heavy bleeding for a couple of days.....had somewhat of a "crash" the first week where I was still not better. By the 2nd week post removal I was still nauseated in the morning but improved in the late afternoon and got energy boost in late afternoon.By the 3rd week I was totally back to normal!!!!! (well what's normal for crazy me! hahahahha)

My husband came with me to the doc, and she had no problem with removal. I went back for a follow up this past Friday and she saw how normal I am and that I have lost several pounds as well. She realizes I am extremely sensitive to hormone changes but says i'm the only one that she has seen like that. (how many have problems that don't think it is the Mirena...that's what I want to know???)

Anyway, that's my story and i'm sticking to it!!! If anyone would like to chat or share please let me know. I will also add that I have a Masters in Physician Assistant Studies (just not practicing since becoming a SAHM) and so I looked up tons of information to figure out what was wrong with me, I really am thankful to have found this site....medical mumbo jumbo is NOTHING when you have your body telling you something and all you fine ladies......Thanks again!
~G

I was prescribed Avelox for a sinus infection yesterday. Within 1 hour of taking the first dose, I experienced a bad reaction: My entire body turned very red, my entire digestive system felt as if someone were crushing my insides with a vice, and I had trouble breathing. I called 911, got the Emergency Squad to my home, and they got me started on some benadryl and took me to the ER. I also nearly passed out from the pain, and I've never passed out in my life.

A few years ago, my doctor prescribed advair to better control my asthma. After a few days, I had an almost fatal reaction to the medication. I woke up feeling fine, took a shower, and got ready for work. I took a puff from the advair discus and immediately felt my throat closing. I started gasping for air and took my rescue inhaler which didn't work at all. The nebulizer didn't work either. Within minutes I collapsed and became unconscious.Luckily, my son was late for work that day so he called 911 and gave me mouth to mouth resuscitation until the paramedics arrived. My blood pressure dropped to 60/30 and I had to be intubated for the first time. I remained unconscious until I reached the hospital. The doctor said the only reason I survived was because my son saved me. If I had been alone that day I'm sure everyone would have assumed that I died from an asthma attack. I wonder how many other people that happened to. Since then, I have been very careful about taking new medications.

I am sooo glad that I found this website!!! I have had so many of these symptoms, unfortunately for a lot longer than some of you other women. I've been on Aviane for about a year. The pharmacy automatically gave it to me instead of Alesse. I have a very stressful job as a 911 dispatcher so I though most of the side effects were from stress. I read an article in a magazine about how birth control effects your sex drive and started doing some research..... come to find out its not from stress!!!! I called and made an appointment with my doctor immediately!!! Although she told me that the symptoms that I had aren't normally caused by birth control, she switched me to Ortho Tricyclen Lo. It has already made such a difference!!! The mood swings are gone, Im not overly emotional or angry or erratic. I don't explode at the drop of a hat, I feel soooo much more mellow and in control. My sex drive has come back in full force!! My husband and I have had more sex in the last month since I've switched pills than we've had in the past like 6 months. He too has noticed a lot of changes and definitely agrees with me that it is worth it to pay the extra money each month to have a good pill and have me feeling better. I wish I would have thought about switching birth controls sooner. Aviane is terrible!!! It will make you into a craaazzy person!!

The second day after I started to take Lotrel 5/20 my blood pressure lowered considerably (good news) The bad news was about 45 after taking
Lotrel I felt a gradual tightening in my lower neck that traveled up and increased in intesity until it felt like someone was tightening a noose around my neck! I could not inhale ANY air. Nothing. For about 30 seconds I struggled managed to croak air OUT not IN and say "anaphlactic shock 911" to my son. Just before I thought I was going to pass out I was able to get air in and gradually breath. I have never been so frightened in my life.

The medication I wish to post on is not listed. I know that Valerian root is in the pill, as well as a few other roots and melatonin.

Last night I took SleepMD for the 1st time. Within 15 minutes of taking the pill, I started feeling funny. I became very night leaded and my swallowing became difficult. After about 15 more minutes of trying to calm down, my breathing became difficult, and my throat felt more think inside. I started shaking uncontrollably as well. My roommate called 911, my vitals were a little high, but I was getting 100% oxygen. They took me to the hospital, where I received IV meds and breathing treatments to help.

I'm a nurse, and I know that the worst reactions come the second time you take/ingest something. The doc told me to stay away, stick with benadryl. I basically had a mild anaplylactic reaction, which would go full blow next time if I took it again.

If it works for you guys, awesome! But just be careful.

I got Mirena Feb 15 2008 which was five months after my first child. I thought this was going to be a blessing not to have the heavy bleeding and anymore kids for five years being that i was so young anyway. It seem like im losing my mind now i feel flurries in my stomach and back pains 911 and nowi even think im losing my hair. Im scared to get it removed b/c of the high risk of having another baby and im not sure what other method i can use. I've only had one problem before this and i was bleeding really heavy and my doctor gave me some medication but now i think the only medication is to REMOVE this.

Well it is 5:02 am and thanks to Advair I am still wide awake.
So here goes my experience of taking only two (2) doses of advair.
In my part of the world there is this cold virus that everyone wants to pass on. Seems this monster will stay with you for 3-6 weeks and no meds seem to help. I now am going into my third week dealing with this leach. So today I went to see my doc. He took a listen to my lungs and said wow you really are sick.....dah I was thinking. So he gave me advair and suggested I take a dose right then. I did thinking boy I hope this helps. He then told me to take my second dose in the evening. After I returned home I go the shakes. I just chalked it up to not eating breakfast and went on about my day. I did eat, but I still wasn't feeling right and of course thinking it was the cold virus taking it tole on me. I was nearing 6:00 and I knew I had to be out the door by 6 to go coach my girls basketball team. So before I headed out the door I took my second dose of advair. When I arrived at the gym I was really shaking and my vision was a bit off. I had my son get me a candy bar thinking I just might need some sugar. Now I haven't had a candy bar in years, it is just not my thing, but I was desperate at this time. I told my son as he helps me coach that I wasn't feeling right and if you see me start to go down, you better catch me before I hit the floor..Finally I made it through the ballgame and got home. It wasn't long until I started getting these super sharp chest pains, a pounding headache, and then my arms started feeling numb....I am thinking oh no....I told my hubbie you better call 911, but before he made the call we started discussing the meds the doc gave me today. I had no information on advair, because it was a sample and the doc threw the information in the trash. I never though one thing about it he has been my doc for years. I go to my computer and look for information and side effects for this drug and bingo it described all my symptoms right on the nose. In my reading also I found the FDA voted down the recall on this drug 12-0.
Anyway I voted to stay home, stay awake, sit by the phone, and let the family sleep. After reading the side effects I knew what was going on and in reading also the doctors do not have a magic pill to help, but they can give you a handful of pills to help each of your symptoms and oh boy just what I need more drugs with more side effects.
As I await for all the alarms to go off I still have a slight headache, still a little shaking, the muscles in my arms and legs are still a bit numb, and I still have some chest pain. I will go see another doctor today just for piece of mind or the kids will drag me there anyway.
Now, you have my story of what advair did to me in just one day. I wonder how many others it has effected and how many had to spend hundreds of dollars to find the answer...

I must go now and thanks for reading my story and also I hope everyone is doing well after your experience with advair.....

I was prescribed Avelox for bronchitis on Thursday the 6th....not feeling better in 2-3 days fill the Rx. Talked to on call doc Sunday morning, was advised to begin to medicine, plenty of water and rest. As I have a known allergy to sulfa, I confirmed with the pharmacy the RX was okay then took my first dose Sunday evening. Within 30 minutes I had severe stomach cramps followed by sudden and explosive diarrhea. As I was trying to rationalize these symptoms I was hit (and I mean HIT) just as suddenly with racing heart, tingling lips, shortness of breath, tightness in my chest, light-headedness....at this point I yelled for my husband to call 911 before I passed out. As he came in the room, I was on the floor gasping for air...don't remember much in the following events. I know that he administered my epi-pen (I was to disoriented to even think of this**and I have had to carry it at all times for about 6 years due to other allergies) saved my life as my son says EMS/fire /police did not arrive for another 4-5 minutes. This experience scared us all! I have had meds case panic attacks in the past THAT IS NOT what I experienced at all!! This was a life threatening reaction...I agree with the CLASS ACTION SUIT as until reading your postings I could not figure out why 3 days later my stomach still hurts and although the coughing is better my chest still feels like someone is compressing it (I had a chest film to confirm the bronchitis had not progressed * confirmed clear yesterday) and my sleep is totally messed up. I would not wish this on anyone. Thanks for sharing as now I know what is going on.....ALL THIS FROM ONE DOSE......JUST ONE PILL......

I had been suffering from bronchitis for over a week; my doctor believed that it may have been developing into pneumonia so he prescribed a seven day supply of Avelox along with an inhaler (for my congested airways). About an hour after taking the second pill (day two) and a couple puffs from the inhaler, it felt as if my throat was spasming (possibly closing), my chest hurt, and I felt incredibly anxious. I actually called 911 (which I have never done before) and the EMS suggested I stop using the inhaler. So I did. I stupidly finished off the week's worth of Avelox (yesterday 11/9) and am still struggling with moderate to severe anxiety. My stomach has hurt almost all day today, and it still feels at times as if my throat is spasming. Has anyone else experienced this?? I thought it may be anxiety-related, but now I'm not so sure.

I'm seeing my doc again tomorrow and plan on telling him that I never want to use Avelox (or any fluoroquinolone) again!!

I, too, am lactose intolerant and have been taking Lactaid. Just three days ago, I had another attack of severe abdominal pain, constipation, then diarrhea, and the feeling that I needed to vomit. The severe pain lasted for two hours. I still have some discomfort. I nearly called 911. This episode is the third that I have had. I was hospitalized for four days last May. That time and the one previous to it, I was diagnosed with ischemic colitis. No firm explanation was given for the cause other than constipation could cause it. However, the first time that I experienced ischemic colitis, I was not constipated. I now suspect that Lactaid may have brought on all three episodes and will stop taking it. I would much rather have the side effects of milk then those of ischemic colitis!

Sorry to repeat this post, but I wanted to make sure people know about it. I replied to a 19 yo who sounded perfectly ok with being on this pill, and it made me shudder. Here's what I told her:

I was looking for information about class action suits against the makers of Aviane, and I ran across this web page. When I saw your post, I just had to respond. Who knows, it might save your life.

My 17 year old daughter was on Alesse, then Aviane ( the latter for over a year) for a total of about 2 1/2 years, for acne. On Nov. 19, 2007, she was alone at home, and did jump roping for exercise. After jumping for about 5 minutes, she collapsed. Over 2 hours later, her brother came home, found her barely responsive outside, and called 911. She had had a stroke. She was in the hospital for 1 month, in rehab for a month, and then came home. It's been a horrendous nightmare. She couldn't say more than 1 or 2 words for a few weeks, and spent about 3 weeks in a wheelchair. Gradually, she learned to walk again. Now she walks pretty well, but she still has almost no use of her right hand. She can't move her fingers at all except for a weak grip. For you medical folks, it was a left MCA stroke. Her cognitive function was massively affected. She is relearning speech,math skills, writing, etc. All of her friends left her, except for one who was very negative, and an alcoholic. Finally, we encouraged her to let that one go, and make room in her life for some quality friends.

There's much more to the terrifying journey that this has been. We feel fortunate that she continues to recover. I wish someone had warned me about the pill. I thought only fat, old, chain-smoking people got strokes. Now I know better.

If any of you find out about a class action suit against this company, please let me know.

Thanks,

WH
Send Private mail | Add as friend | Flag as inappropriate

I was recently prescribed Avelox for Lyme disease. I took on dose, 2- 400 mg tablets. Within an hour, i could not walk, could barely talk, i was severely dizzy, my body went limp, numbness from my head to my toes, muscle twitches and lost my eye sight for several minutes . My husband had to call 911 and have the squad pick me up and take me to the hospital. Before they got there the only thing we could think of doing was for me to take a Benadryl.....which is probably what saved me. It look over 3 hours for this to wear off and along with every thing else i had a terrible seizure.
Please be aware of this medication. If so many people have had terrible side effects from the med, why is it still on the market????
This is just CRAZY!!!!