Oxygen symptoms and conditions

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.

I have been taking this medicine for three years. This morning I woke up and my right upper lip was completely swollen. While at the ER, the doctor said that it was a common side effect--even if the person had taken it for a prolonged period of time. I had to go back to the ER about 3 hours later because my mouth became even bigger! As I was checking in, a nurse looked at my mouth and said, "Oh, you take Lisinopril, right? I see that reaction all the time here, plus, I had it myself." The second Dr. came out and told me my airwaves and oxygen were okay and that I was just going to have to wait it out (they had earlier prescribed me Benadryl and a steroid). Then he explained he had to stop using the medicine himself because is tongue became swollen. This is a common occurrence. And if you are like me, you assume if you are going to have a reaction to a medicine, it's going to be rather early. This side effect can take time before it shows. Be careful, apparently it is a very common incident with this drug.

I had a cortisone injection into my left knee on Friday, June 5th and immediately started to react. Within an hour, I had extreme redness and heat in my face, neck and upper chest. Wheezing, hives in throat and mouth and behind my ears. Extreme headache that came on suddenly and started in the back of my head and stretched to the front. Dizziness, chest discomfort. I went to the ER and was given a nebulizer treatment, benadryl IV and prednisone because the doctors at the ER felt that I must have had an allergic reaction to some medication that was mixed with the cortisone injection, because they said that to be allergic to cortisone is very rare. About 20 minutes after they gave me 60mg of oral prednisone, they started my benadryl IV. I felt such a hot rush to my face, my ears were burning. Eventually, the reaction calmed down and they sent me home with a prednisone taper and benadryl every 4 to 6 hrs. Sunday morning, I took 60mg of the prednisone and within 20 minutes I knew that I was in trouble so I took 50mg of benadryl and on the advice of my doctor, called an ambulance. In the ambulance, I was given oxygen, a nebulizer and more benadryl IV. After that morning, I knew that my problem was the steroid. I hadn't had any sleep since Thursday, I had been nauseous ands been battling chest discomfort and a very bad headache. I spoke with my doctor on Monday and he wanted me to take Atarax,25mg, every 3 to 4 hours. I saw him on Tuesday and I went to an allergist on Wednesday. She started me on 50 mg of zyrtec twica a day and 25mg of Atarax at night to see if this would help the reaction that I continue to have. She said that it could be several weeks, at least, that I will continue to react, until the injectable steroid is out of my system. It had been 13 days, and Im still reacting.

I am allergic to Prednisone. My primary Dr. does not believe me nor does most of the medical profession. The arrogance and assumptions that Dr.'s make has me at my wits end as I am allergic to many things. The 2 main things are any form of Ibuprofen and Prednisone.
I had an LAVH and oophorectomy performed last Tuesday.
To make a long story short, after surgery the attending Dr. ordered Motrin. I went into anaphylactic shock and was aware that I was in serious trouble but didn't know why. I thought I had developed a new allergy as all my known allergies were clearly listed on my chart. As they were moving me to ICU he stated he was going to give me Prednisone and my family told him no, you cannot give her that, she is allergic to it. Once inside ICU I became aware that I was in a fight for my life as they were going to keep experimenting on me like a guinea pig until they killed me. The Dr. came to me and said he was going to give me Prednisone and I fought back. I told him l would NOT take the Prednisone. I told him I did not want him or anyone else there to administer one more thing to me. I would not take anything except Benadryl and I demanded to be discharged. (IV/Oxygen/Catheter/everything still hooked up to me) Luckily, my surgeon showed back up at that point and took charge of the situation, immediately administered the Benadryl I had been asking for and I did indeed leave the hospital later that night with her blessing.
I believe in my heart that had they given me the Prednisone there is a good probability it would have turned tragic.
You have to fight for yourself because sometimes the Dr.'s think they know more than you do about your own body.

I was on remicade for 2 months and contracted pneumonia. It kept getting worse for 8 weeks until I had to go hospital. None of the antibiotics were working. I almost was dead and they considered a heart and lung transplant and I was on a respirator in a coma. Finally somebody figured out I had eosinophilic pneumonia and treated it with cortisone. I began to improve but was still in hospital 4 months and after almost 2 years I'm still on oxygen and can't walk right. Many people develop this and die without a diagnosis. I won't take remicade ever again.

I have been taking lisinopril for about 2 1/2 years now. About 4 weeks ago I was having trouble sleeping, my legs hurt real bad and when I would wake up I would have a numbing tingling sensation in my legs and feet. Went to the doctor asked her if it could be the meds and she said she didn't think so and to continue to take it. I still continue to have problems, tired, weak muscles, hurt and a raw lump in the throat feeling. She sent me for a brain mri that showed white lesions on the brain. She said it could be from high blood pressure but said my has never really been that high or it could be MS. I am right now waiting to see a neuro dr to see if I have ms but after reading all these post I am wondering if it is the lisinopril. Has any one else had these types of symptoms?

I was given Advair by the doctor's office they started it there at about 1:00 PM in the afternoon and I started have chest pain, coughing, wheezing etc. by 6:00 PM at night. I was not even given a rescue inhaler. They "think" I may have asthma again but I have not been on an inhaler for years. I am not getting enough oxygen in my blood, especially during the night. Needless to say, I quit taking it and called the doctor's office the next morning. It has taken 12 days for the nurse to get back to me. She said the doctor recommended that I start taking it again but did not offer any rescue inhaler. I told her that I live in a remote location, no street signs even and that my nearest neighbor is on vacation. We all have 20+ acres each so no one is close and I am alone. She brushed aside my comments and said of course, it was up to me if I wanted to continue it. After reading many of these comments, I am not sure I want to even try it again.

I've been taking Niaspan for about six weeks now; I started out at 500mg for the first three and I'm now on week three of 1000mg. I hadn't had any side effects and I was thrilled because I can't take statins (though I do take Lovaza with success). My doctor mentioned -- but did not stress -- the "take an aspirin ahead of time" or "eat something with it) thing, so I haven't been. Three nights ago I work up from a very weird dream about my house being on fire and couldn't go back to sleep, partly because I felt hot. I got up and looked in the mirror, and as others have described, I was beet red on my neck, chest, and arms, and very itchy and hot. The "rash" was mottled at the edges. It reminded me of sun poisoning. I wasn't sure what to do; it was 5 am and I knew my partner had a bad night with sleeping already, so I didn't want to wake her. I took a Benadryl. I was wide awake, so I got onto the computer to do some stuff (never thinking I should research the damn thing!), but about 20 minutes later, I felt itchy on my stomach. I went into the bathroom and looked again. My stomach and lower back were now getting it! Interesting. I went back to what I was doing, then about 10 minutes later, my stomach was hot, so I looked again. Now my stomach and all of my back were covered, and I noticed that my neck wasn't as red. Hmmmm... 20 minutes later I looked again, and now my neck and chest were pretty clear (but still itchy) and my butt and upper thighs were getting it (stomach and back still had it). I could actually feel it breaking out on my legs! 20 minutes later, my stomach and back were clear, and my legs were covered. about a half hour later, it was completely gone. I wracked by brain trying to figure out if it was something I ate, a new detergent, a drug interaction gone wrong, but I could think of nothing. I never associated it with the "flush" my doctor told me I could get. This was so much more than a flush. The next night I was so tired that I took a half an Ambien and slept through with no problems (and remember, I had no issues before this, at least that I could remember). I thought it was a fluke. I then spoke to my father yesterday about The Rash, and he asked if it could the the Niaspan, as he had taken it before (but the flushing had been too much and he stopped). I did some research and through that I found this page. Bingo! I had already taken the Niaspan, so I couldn't try the aspirin first. Last night, I woke up at 3 feeling hot and looked, and sure enough, it was starting on my face and neck. I took a Benadryl and went back to bed. I finally fell back to sleep. I'm still a little itchy, though nothing unbearable. Tonight I will try the aspirin a half hour before and eating something non-fatty with the Niaspan. I'll give it a week to help, then I'll call my doctor. I hate to give it up if it works because I am just about out of other options to lower my cholesterol.

I am recently out of the hosp after 9 days with COPD exas, pneumonia, flu. I have been on heavy antibiotics, steroids--home now for 1st time with oxygen---I feel GREAT.First time in years I feel like I have a life to live. Like a veil has been lifted. I'm scared for this feeling to go away--what is it? the steroids?? the oxygen?? Whatever it is I need to know so I can fight for it and stop just waiting to die.

I stumbled on this site while doing research on DVT's. I am a nurse and was on YAZ continuously (skipping the inactive pills and going straight to a new pack) to control my migraines for about a year. I developed 3 DVT's in my left calf and behind my left knee. I have been having charlie horse cramps as well. I am now on lovenox injections 2 times a day and 7.5 mg. of coumadin to deal with the clots.I have also had the issues with heart palpitations, chest tightness, and feeling like i can't catch my breath. I read in one of the posts where it was described as she "had to think to catch her breath". I totally agree! I thought this drug was great, until now. I stopped it last wed 1/7/09 when they found the clots in my calf/knee. Can anyone with experience tell me how long it took them to recover from the palpitations and breathing issues. I am a very health person, non smoker, with no prior or family history of any clotting issues. Thanks for all the info on here and God Bless everyone who has suffered!

Tony Sapore
Too Everyone on this devil drug get the hell off it..My wife is Dead because if it.. Its happened so quick.We are from arizona(mesa) It pretty much happend in one day.I was at work My mother in law took sandra too go see a (her doctor) she was really white out of breath weak and coudnt breath ..Rite away they told her to go straight to the emergency room.They thought she was bleeding inside.They took care of her rite away. They started to take alot of test cool everything came back awesome. Then they said we are going to run a Kat scan.Bam that was it.Came back to us said she had Pulmonary Embolism .They said they can treat it.Never said you can past from it.So they took her to her own room in the hospital ..Started treating her for the blood clots in her lungs ..Everything was looking good getting color back and thinking positive.You know were like cool 3 4 days in the hospital eat good food alittle vacation dont have to take care of our son Nick 12 years old .Her mother was with us up until 1120 pm she was tired and told sandra that she was tired no problem go get some sleep and I will take care of her.She was resting pretty good then around 1220 pm about a hour later BAM stood up Cant breath and she was at white as ghost.She was suffering I could tell I called a nurse.THat when it happend so quickly They gave her oxygen nothing couldnt breath its was like she was having A CARDIAC ARREST her body couldnt function she was really tiny(her Nickname was peanut) 130 pounds then one doctor came then another like it was ER the show.I couldnt do a dam thing .Then the took me out of the room I knew something was up that was the last time I saw her alive suffering.I was sitting in a chair about 4 rooms over.Lights going off over the door.There was about 10 people in her room.Lights going off red white red.THen I heard them say Go GET A SOCIAL WORKER.I knew in my heart she was gone.They tried to give her CPR for about 20 min nothing.Then they said they want to call any family .They called her mom and Dad.and said they are going to try 10 min of cpr nothing they came out of the room and told me she died.Wow 35 years old both of us .Then her parents showed up and I had too tell them their daughter died all in one day..So know we know it was from yaz..All the signs losing hair cant breath always nervous lots of head aches .Every thing was their signs .Just because of that stupid pill.. Thank you so much and sorry it was so long have a good holiday.. always TONY

I had been with a cold for 2 months and could not see anything on the xray. I had chest pains in one lung and couldn't take in enough oxygen. My doctor after a third xray and seeing possible scaring on the right lung, couldn't identify pneumonia as the problem. Because it was the 24th of Dec., she prescribed Biaxin to try to get rid of the issue. It is now the 28th, I have been on the drug for 4 full days and can finally breath better. The pain is also decreasing. I can tough out the metal taste as this is the only side effect I have.

I am 41 and have been taking Yaz for about 6 months. My skin is much clearer and that is nice, but on the other hand I have had a continuous headache for two weeks now. Just in case, I took meds for a sinus infection but the headache has stayed... so now I am being treated for migraines. The problem is: the meds for migraines don't work. I am wondering now if it is the Yaz. When I first started taking it I got headaches at the beginning of each new packet, but now it's non-stop. After reading some of these posts, I am worried that coming off it will also have side effects, but it can't be anything (I hope) like the pain and fatigue associated with a long, drawn out headache. I am deeply scared that this headache will turn into a stroke or a tumor or something.

I have been on Advair since Feb. of this year, I have had a lot of these side effects but didn't really realize it was from this med. At first I was told to take it 2x a day, reading the directions it says it has to be 12 hours exactly apart. My work schedule didn't allow that so I just took it 1x....Working 2 jobs I just thought when I couldn't sleep and was always tired, it was from working a lot. When I told the Dr. about not being able to sleep more than 4 hours, I was told since I was taking the meds 1x a day that wasn't it. After a bad cold and bronchitis I was told I had to take the Advair 2x a day, now i'm more tired than ever, still can't sleep and have a headache that won't go away even with migraine medicine. I'm even jittery and forgetful--kinda ditsy now and itchy off and on all day...After reading this blog site I see its not in my mind and i'm going to stop taking this med. I think i'm going to the health food store and find something natural.

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 just wanted to comment to all of you asthma sufferers. I grew up with bronchitis and my brother with asthma. We were always getting sick while young, about every 6 weeks. My nephew inherited asthma from my brother, and he had it very bad, was always getting sick, needing oxygen, etc. While in his teens, someone told him to start playing an instrument like the trumpet or trombone which really exercises your lungs. He started taking lessons in school and it didn't take very long at all to notice a remarkable difference. His other siblings would even get sick and he wouldn't! The exercise, being natural, is a far better and healthy prevention, and makes your lungs stronger. I can't believe doctors don't spread this amazingly helpful advice around. I'm VERY sure they must have heard this before. Wouldn't news like that spread like wildfire through the medical community? But they would probably lose some business!!! So I wanted to help pass it around. I hope it helps some of you!

My Mom (87) who was in great health given her age, was given Avelox for a urinary tract infection. She has developed severe side effects that include shortness of breath,chest pressure, (not chest pain)swelling of her esophagus & eye lids, confusion/agitation, dry mouth,complaints of twitching in her mouth.
The worse case of all the symptoms has been the swelling of the esophagus and eyelids. Her eyes are swollen shut and she labors to swallow & talk. Eating is a monumental task.
She is currently hospitalized and the medical team seems to be having a hard time accepting this as an allergic reaction to the Avelox. They have run series of tests to look for other things such as pnuenomina, heart issues and stroke issues. So far the tests have revealed nothing out of the ordinary. One would think that they would start treatment with steroids or another anti-allergic treatment but they seemed convinced that the Avelox is a non issue because she only took 2 doses @ 400 mg each starting Saturday & Sunday (11/29-30). This ordeal started Sunday early evening.
If anyone else has experienced specifically swelling of the throat & eyes please post!

My Dad has had colon surgery. Levaquin was prescribed. My Dad is 84. He was doing very well for several days, then went off the deep-end. He had hallucinations and aggressive behavior to name a few of many,many side effects. He thought they were trying to kill him. Unhooked all the intravenous and oxygen tubes and left. They caught him at the stairs. Had to sedate him and tie him down. My Dad did not know me nor my brother.

He has been off the intravenous drug for several days. While better, he is still working off the effects.

He has had many of the listed side effects, however, with the colon surgery how much is part surgery and part drug as far as nausea, stomach pains, bowel issues, vomiting, is a guess. However, he went from doing very well to a mess.

I have taken three 500mg doses of Levaquin since Saturday. They were prescribed by my urologist for a "possible" minor prostates that might be affecting my PSA (2.2). The very first night I was unable to sleep, tossing and turning all night. Thought nothing of it, and blamed it on diet or too much sleep the previous day. However, insomnia has continued for three straight nights and last night I woke at 4:30 AM with shortness of breath (had to take long deep breaths to feel like I was getting enough oxygen) that felt like an anxiety attack. Although there was no pain, I felt like my heart was pounding and rapid. Finally got a little more sleep and woke up feeling OK in the morning, but blood pressure was elevated. I continually feel like I'm on a caffeine high. I never associated it, but, I woke up second and third days with a sore throat and have had a few minor muscle twitches in arms, legs and abdomen.

I feel fortunate compared to others on this forum. I have stopped taking the Levaquin and have an appointment with my family doctor tomorrow. As a side note, I had an acute prostates this time last year and took Cipro for over one month with no similar side effects that I can recall. Does anyone know if two drugs from the same group can have such different side effects, or can I expect the same problems if I start taking Cipro again?

My name is Heather I am now 32 years old I took levaquin when i was 29. After i took levaquin I went on a roller coaster ride I have yet to be able to get off of. First when i took it I had the worst night mares i have ever had only to wake up to a splitting headache and a very sore body. took another one the next day same reaction.I figured it was the bronchitis that was causing the problem. on the third day i was worse still I could hardly move. I stopped taking the drug. after another two days i felt better. two weeks later I was out with my father and he noticed a rash on my legs. I was also starting to get little blood blisters. I started to become concerned and the next day after going to the zoo with my family i came home and my legs were swollen three times there normal size and very sore. I put them up just to find the felt like play dough had been stuffed in to them and I had blood blisters the size of pencil erasers. I made an appointment to see the doctor. he said and i Quote " Heather I have No idea what the Hell you have" he sent me to a specialist. between the time of my first appointment and the appointment with the specialist my legs stopped working from the hips down i was 90% paralyzed (not spelled right ) they just wouldn't work right. My ten year old daughter was helping me get to the bathroom. I was soooo sick i had a headache all the time couldn't eat or sleep and when i did it was only for a few hours I couldn't move very well and to get up out of bed hurt so bad i almost fell every morning. by the time i had gotten to the specialist I had gone to the E.R. three times for the pain.and the last time was because my toes stopped moving altogether. at the appointment the doctor ran all kinds of tests checking me for everything from S.T.D.s (which i have been happily married for years) to Lupus. I felt Like and 80 year old Lady And like i said i was only 29. after the extensive tests and everything coming back normal the doctor put me on a steriod. for 4 months i was told i had to take prednisone After the first dose i could move again I still hurt but i could move.But now i had the side effect from that. i was gaining weight like it was going out of style, but at least i could move. after the 4 months things seemed normal kinda. I could move but if i sit still to long my legs go numb not fall sleep go completely numb even if i am standing to long. I am still afraid that i will wake up again feeling like i did that Fall three years ago. I still have problems but im not sure they are tied in but it wouldn't surprise me in the least. I only took three Pills of Levaquin three years ago!!!! How long does this stuff hang on really??????

My uncle has COPD and takes Spiriva and Advair. He has had pneumonia since June 08 off and on through Sept. I've been concerned about this and have been reading up on Advair for people with COPD causing pneumonia. My question is what other choices does he have for medication if he stops taking the Advair? Does anyone know that has been through this? He is on oxygen all the time and his dose of Spiriva is 100/50. After reading the posts, I'm convinced his pneumonia is a result of the Advair.

Hi all, I'm hoping someone here with Seroquel-experience can help us with some information. My wife has been on Seroquel for approximately 5 weeks (ramping up to 200mg per day during the first 10 days, approximately). After 4 weeks, the severe breathing problems started. Physicians have verified the oxygen level in her blood to be excellent, her lungs and heart are in perfect shape, she has no fever and no indication of bacteria-infections. All indications are that this is caused by the Seroquel. She explains the intense sensation as drowning, almost passing out while gasping for air. She's feeling very dizzy, probably due to breathing too much as a result. Occasionally her breathing is not so deep, but more like hyper-ventilation. The problem became unbearable (and my wife endures a lot) after approximately 1 week, so 5 weeks into the Seroquel scheme she quit cold-turkey two days ago. The breathing problems are still the same. We are hoping someone could tell us how much time these breathing problems can be expected to remain, as I've googled my eyes out without finding any information on this. A week? - Two weeks? -Even more? - please respond, and in advance, thank you for your help!

Immediately following the infusion (I was still in the chair), which was administered over 3 hours, my blood pressure dropped to 42/27, with the predictable result - loss of consciousness. This was preceded by extreme joint stiffness (fingers of both hands and both knee joints, elbows, everything). I was put on oxygen and administered IV bolus of fluid. On Day 2 the same thing happened, but it took longer to recover. Infusion 3 was canceled.

I am almost 41, and have had migraine headaches most of my life which I could manage with 800mg of Naproxen Sodium, or a Norgesic Forte, and when Imitrex came out, I could just administer that. Six months ago, my headaches got so frequent that I had to start taking my Relpax (similar to Imitrex) and/or Fioricet more than 2X per week. According to my neurologist, this is a no no, as both of those meds can couse rebound headaches. He started me on Topamax, 50mg per day. It did nothing. He bumped it to a 100, nothing. Now I'm a 200 mgs, I am still have a migraine in left temple as I write this. I have the tingling, the daytime sleepiness, but my mind is fine, and my appetite is just swell (regretfully). What the hell am I going to do now? Ask him to bump me up to 400 mg? Now I have these headaches every "F"ing day, and I can't take anything. I just have to suffer.

Topamax is NOT working!!!!!

please everyone who is on lisinopril be warned!!!! my mother was on this medication for a month and began having hives. she went to the emergency room and they gave her antihistamines. a few days later she woke up with facial swelling and a sense of not being able to breath. she went back to the emergency room where she was treated as above. twenty minutes after discharge she began swelling and her throat closed. she suffered cardiac arrest due to lack of oxygen from the swelling in her face and throat.she was stabilized, but unfortunately did not survive this ordeal. please, everyone on this medication, if you experience hives, facial swelling, or lip swelling, see your doctor immediately and push to have medication switched!!!!!!!