Oxygen symptoms and conditions

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.

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!!!!!!!

I had my parotid glands washed out with saline and because they were still dirty the surgeon decided to swab them with Betadine. When I came around from the operation I was panicking in the recovery room. Later, I was put into a side ward, luckily with my sister in attendance, and took a minute sip of water. This caused me to choke and I could not catch my breath. Assistance was sought and I was taken away to get help with my breathing. My whole face swelled up and my eyes had huge sort of blisters under them, which affected my sight for about 3 days; my hearing was also affected temporarily. The sides of my face, where the parotid glands are, were absolutely solid, my lips were distorted and I looked like I had been in a fight. My vocal cords were also swollen, which resulted in very poor speech for 24/36 hours. I had to be put on continuous oxygen, and have frequent nebulisers. I was given steroids, antihistamines, antibiotics and other treatments which I am not sure of. What should have been a 45 minute operation and 2-3 hour recovery resulted in a week's stay in hospital. When I was discharged, I had to return the following day, as the swelling had come back up again and I had to have the steroid medication I was sent home with doubled and Piriton and Omeprazole prescribed as well. I had intense pain at the top of my head, over my left ear, at various times during the week, resulting in me having to take Oramorph. All of these effects caused my diabetes to go out of control, with my blood sugars running over 20 for the first 2 days and well over 10 for the rest of the week. All in all I was very unwell.

Dealing leg pain and swelling fpr over 6 months - having 2 DVT test and 3 MRI's they finally found that I did have a DVT in my left leg and now I am taking Warfarin as of May 30th 2008. I now have severe joint pain, sore skin/sensitivity, my vision is going I can hardly read anything all of a sudden, so exhausted, sleeplessness - even after taking an ambien and getting some sleep, I can take a shower dry my hair and I am ready to go back and lay down because I am so tired. the doctor says thin blood does not carry oxygen as well so this is why I am tired. I am not anemic as I just had that checked. I can feel my muscles getting weaker. From reading what everyone else says it must be this drug, but I don't think I could live without it since my clot is so massive. I feel like my life will end soon I am getting weaker by the day...is this just my imagination? I know I am depressed but I do think all of the symptoms I am having is from the warfarin(besides the pain from the DVT which is still very painful)

MY mother of 73, who was just put on lisinopril and had a pace maker put in do to heart rate of 38per minute. She was also coded and we were kicked out of the room when her heart rate dropped past 7. A emergency pace maker was put in ...then her permanent one followed 2 days later. She was released from the hospital on Sat. the 21st and since she has been home, she cant sleep properly and when she does she wakes up gasping for air. Could this be a cause of the drug? lack of the oxygen that she was on in the hospital? We have put a call into the doctor, but still haven't heard a replay....wondering if anyone can give us some info...Thanks

I have had 1 remicade infusion so far for ulcerative colitis. The next day a bunch of spots appeared on my lower legs. There were 30-40 of them, small, roundish, purple/dark red. They looked like blood spots under the skin.
It wasn't a rash and they didn't itch or hurt. My doc had no explanation, and I haven't heard of anyone else having this reaction. They checked my blood for a clotting problem and didn't find anything. The spots faded away over a week or so. My next infusion is in 2 days, so we'll see if they reappear.
I have also been experiencing a weird kind of insomnia where I am so physically antsy I CANNOT keep lying still, I have to shake my body or kick my legs or something. I read up on restless legs syndrome and the symptoms sure sound like what I am experiencing. I don't know if it's connected to the Remicade - I read that iron deficiency can also cause it and I am anemic due to the UC. But since Remicade can disturb the central nervous syndrome, it seems possible. Anyone else experience RLS with Remicade?

I am a 61 yr. old female former smoker diagnosed with COPD/emphysema. I was put on ADVAIR 500, along with using a nebulizer with albuterol and bromide to "inhale" several times a day.I also was on oxygen. I quit smoking and worked at getting my health back and to the surprise of the doctors went back to playing tennis several times a week.After reading about the side effects of the high dose Advair I had my Dr. reduce the amount to 250. It has been almost a year now that I have been on Advair. I have noticed some of the side effects mentioned here. The leg cramps, and leg spasms have been horrid. I also have had blurry vision. And lately I seem to not be able to sleep even if I am tired.I am going to see if my Dr. will let me drop to the 100 Advair level. Lately I have been intentionally skipping Advair doses to see if I notice any difference in my breathing. I almost forgot- since going on the meds listed above I have had kidney stones, an emergency appendix surgery and now high bilirubin count. I cannot find any info on those problems if result of medication ADVAIR. Even though I smoked for a number of yrs. I was very active and not over weight. The Dr. thinks thats why I am back to playing tennis. Has anyone else had a gastro problems ??Thanks A.

I have been on Lamictal for approximately 7 years. The product initially seemed to work a bit on controlling my seizure activity, and did provide a bit more confidence in social situations. At this point I was taking 400mg per day, and had little side effects other than the absent mindedness, and occasional problems with vertigo.
Briefly, about a year ago, I began having an increasing number of partial and general seizures, and was brought up to a dosage of 700mg per day. It was at this point that I began noticing what could only be called "hard-core" side effects. These included days where I was just totally confused, paranoid, suicidal, having an unrelenting feeling of not being able to breath, feeling bloated in my abdomen, and regularly being struck with a very irregular, very scary, rapid heart beat.
At this point, I am taking 600mg per day, and am still having most of these side-effects, but in decreased frequency. My neurologist never mentioned any of these possible symptoms, and doesn't seem overly concerned about any of the problems that I have mentioned in the past. With this in mind, it is somewhat relieving to see that there are others out there who are noticing similar effects.
If anyone can explain the difficulty breathing thing a bit more, it might help me wrap my brain (no pun intended) around this whole mess. I'm not sure if it's related to a decrease in blood pressure - I've been monitoring mine and haven't seen any irregularities. Or if it's related to a decrease in the amount of oxygen in the circulatory system due to the drug itself, or as a side-effect of the shallow breathing I have read about in other posts here.

I have been on Synth since june of last year and have steadily gained weight to the tune of 22 lb! Most of my symptoms ( Fatigue, joint pain, dizziness, foggy thinking) have gone away, but the heavy ever lasting periods are still here, as is my extremely terrible acne and the numbness in my hands.Also have daily headaches that never subside. I just went off the synthroid all together yesterday and am hoping that I start to lose this weight. I have been diagnosed with asthma and am now on Advair, so I am hoping that it will make me feel better, maybe all of my symptoms were related to lack of oxygen! Cross your fingers that all of the bad symptoms don't return, I will post back when I notice a difference, either way.

I love that you all have the courage to post here. We must self diagnose, most dr's don't care, we are but numbers to them

Thanks to all

I am 21yrs old and was just diagnosed with Bipolar 2 disorder. My doc put me on Lamictal,Prozac and Geodon. I take 80mg at night. I feel pretty manic after being on it for only 2 days. I have enough energy for 3 people and my hands shake and my vision is quite blurred which isn't good because I'm legally blind in one eye anyways. The only real side effect that I find troublesome is when I feel like I can't breathe. It only happened when I took it the 2nd time though. It felt like I couldn't get enough oxygen in my body. It was literally hell. My mom finally gave me benadryl thinking that maybe it was allergies and I fell asleep when the benadryl kicked in.

Its me again, the next statistic for GSK, I just also wanted to say if anyone feels like joining me on my takedown of the purple beast please feel free to contact me via e-mail. I Also, I read alot about nebulizers (sp?) and am not familar. Can anyone please explain? Can it help me not die from not taking my meds? That would be helpful. Thanks in advance!

My sister was prescribed Avelox on Tuesday, March 11, 2008. Within 15-20 minutes she began having breathing difficulties. Because she has asthma her initial thought was that she was having an asthma attack. She tried asthma treatment and it didn't help. She soon was unable to breath. Her husband called 911, they responded quickly but had to intubate her in the ambulance. They know that she was without oxygen to her brain for at least 3-5 minutes. This caused seizures that lasted 20 hours before I.C.U. could get them under control. Unfortunately it caused brain damage leaving her with no higher brain function (vegetative state). As she has worked in the medical field for over 14 years she did not wish to be kept alive by artificial means. On Tuesday, March 18, 2008 her ventilation tube and feeding tube were removed. It is now Thursday, March 20, 2008 and she is in a wonderful Hospice House awaiting her death.
She had taken the same class of antibiotic in the past with no reaction. Really not sure what caused this one. She was going through chemo for breast cancer, but had just finished and was scheduled to start her radiation treatment. Her chemo doctor told us that since her reaction, they have had another patient who went into anaphylactic shock after taking Avelox.
My sister is only 43 years old. This medication should be taken off the market.

I am currently taking advair and I feel horrible pain in my chest. I am having a hard time breathing and feel as though I am not gettin g enough oxygen to my brain. This is only my third or forth dose of advair. The really bad chest pain is when I cough. But I still feel the achiness without the cough. My muscles in my back hurt as though I have been lifting a ton of weights although I have done NO strenous activity. How long will this take to wear off?

Took Avelox for pharyngisis 3 wks ago but then went to take l for some
dental surgery night 11 March 08 and within one hour hands and feet burned and itched, then left side heat started swelling, lips swelled, and then breathing cut off and kept blacking out and coult not talk. Called 911 and spent most night there on oxygen and IV's/shots. Do not know if it contracdicted Lasix which I'm on or what as the lst time I took it only rapid heartbeat.

So nice to see that I'm not just imagining the adverse reactions. I've been taking Advair 250/50 for about 3 weeks now after being diagnosed with asthma/chronic bronchitis. I went back to my doctor the following week because I was still having chest pain, back pain, felt as if I still wasn't getting enough oxygen and mentioned that I was having a lot of difficulty with being jittery. He evaluated my breathing with a peak flow meter and since that seemed to be OK, he wanted to do an EKG - which he did and seemed to see something that warranted a referral to a cardiologist. So far the cardiologist has not seen anything out of the ordinary.
I'm thinking more and more that there is nothing wrong with my heart and that this is all being caused by the Advair. Has anyone else been referred to a cardiologist and found out nothing was wrong?

I love this page! I have been taking Levoxyl for about 6 months now and my joints are killing me. Especially my wrists and ankles. It hurts to even pick up a half gallon of milk or hold my kids. I am also so exhausted all the time. I was put on 50mcg when I started the medicine but I was not having any symptoms before I started taking the medicine. I am trying to wean myself off of the pills and am down to 25mcg. I am taking b12 and b6 to help fight the fatigue. I also am having a huge problem with my periods, I get them every 2 weeks, and they last a week. This is not fun at all. I am also getting cold sores like crazy. Before I started taking this medicine I would maybe get 1 a year, if that. Now I get at least 1 a month, sometimes 2. It is really frustrating. My skin has changed, so dry and I look like I have aged 10 years. My hair is brittle. I am looking into a more natural route to take, maybe the Armour thyroid would work.I have been to the Doctor who just tells me that it is not my medicine and could be something else. I know it is not something else. All of these symptoms started right after I started to take the medicine. I am going off of it to hopefully feel better. Thanks so much for all your posts out there!!!

I took Levaquin as a treatment for pneumonia. After 3 days on the drug, all my joints were stiff and I had difficulty breathing. I called my doctor and I was told to continue the medicine. After a week, the reaction continued to get worse, I could hardly move, my breathing got worse and I had to be put on oxygen. My hands were like clubs and I couldn't open anything. I sat in a chair all day. It took me a half hour to get out of the chair to go to the bathroom. My hands were so swollen that I could not flush the toilet with my hands. I had to use my elbow to flush it. I saw doctors thinking I had rheumatoid arthritis. I saw pulmonary specialist and my lung capacity was at 48%. They sent me for many blood tests, cat scans, and I even had an MRI to try to find the cause. Finally, my heart doctor found out that some people were having adverse reactions to Levaquin. She found out that it caused severe anemia, breathing problems, and joint pain. She dosed me iron and within a week I was finally beginning to see the swelling in my hands start to decrease. I was out of work for 3 months.

I was on Prozac for 6 years..during which my husband was dieing.
Four years before and 2 years after. He was on oxygen for 4 years during which I took care of him, kids, and worked full time.With in 3 days of first taking it I stopped crying. It did help me cope with everything. I didn't bring work home with me which was good as I am in a very stressful job.
The problem I found taking it was I had no emotions which I guess was a good thing at that time of my life. I was never happy, sad, never felt intense love, basically numb. I also was tired during day hours when I took it in the morning, so I took it before I went to bed.
Years after he passed I wanted to start a relationship but I had no interest in Sex. Which is not a good thing when getting into a relationship. I was told by my doctor that is included as a side effect for Prozac.
The doctor put me on Wellbutrin to see if that was any better, as I'm told you feel more like yourself. I do have emotions now, which after all those years of not having any, I had to learn how to deal with emotions.
When going off of Prozac I did notice a slight change in sexual desire. But anything helps.
I got married 2 years ago and now I'm dealing with the menopause symptoms. If its not one thing its another.

I have been taking Nexium for over 7 years. I started on Prilosec but when that became available over-the -counter my doctor switched me to Nexium, 20mg once per day. Not long after that I started seeing a new doctor. I was still taking the Nexium, 20mg, one per day. But I was still having a little of that burning pain just below my sternum. I told my new doctor about this thinking he would probably increase my dosage to 20mg twice a day or switch me to the 40mg capsules once a day. Instead he switched me from the 20mg Nexium to the 30mg Prevacid capsules. I had horrible side effects immediately. I would have sudden and unpredictable loss of appetite. Not just loss of appetite but the sight of food would actually make me feel queasy. I lost over 10 pounds in a week and wasn't even trying. But the worst, and most frightening, side effect was the severe shortness of breath. I was in the Navy for 10 years and kept myself in pretty good shape. At one time I was even running 3 miles a day. Immediately after starting on the Prevacid I got so short of breath I could not climb a flight of a dozen stairs. It made me feel like I was 80 or 90 years old. And I was only 48 or 49 at the time. My chest would heave up and down. Air was going in and out. But it felt like my lungs weren't getting any oxygen from the air that was going in and out of them. I wanted to trust my doctor but I was actually becoming afraid of going home from work and taking the Prevacid. I got back in to see my doctor as soon as I could and he put me back on Nexium. Not long after this he took a job at another practice/clinic to be closer to home and family. I had to find another doctor. When I went to see my new doctor (the 3rd I've had since the reflux started) I told him about the Prevacid and the shortness of breath. It wasn't as bad since I stopped taking the Prevacid but I still had some shortness of breath and burning pain in my chest when I exercised. He said he had never heard anything about the Prevacid and breathing problems. He sent me to the hospital for the treadmill stress test to make sure it wasn't my heart. It wasn't my heart, but then again I knew that. Even after complaining about the shortness of breath during several visits over the years he never said or did anything about it. About 2 years ago I had a bout of bronchitis. My doctor was busy all day so I took an appointment with another doctor at the same clinic. (I've had to do this several times) While seeing this other doctor for my bronchitis I mentioned to him the whole shortness of breath story. He said I should consider having a pulmonary function test because "you're not too young to have emphysema". Then early in January, 2008 I had to see another doctor at the same clinic, again for bronchitis. I told her about the Prevacid and the shortness of breath. Finally someone sent me to the hospital for the pulmonary function test (PFT). Two weeks later I had an appointment with my PCP for an annual physical check-up. I asked him about the results of the PFT. He said he hadn't seen them but he would check on it while the nurse was giving me and EKG test. Some time later he comes back into the exam room and says "yep, you have a little emphysema". The nurse-practitioner who sent me for the PFT had already started me on Advair. Besides that my doctor seemed to have little to say about my newly discovered condition. I'm not sure if the Prevacid or continued use of Nexium had anything to do with me developing emphysema. But I do know that after complaining to MY DOCTOR of shortness of breath for 3 or 4 years it shouldn't have been someone else that discovered that I have emphysema. Anyway, I guess my real question is has anyone else had a problem with SEVERE shortness of breath on Prevacid, Nexium, or any of the other PPIs?