Chest congestion symptoms and conditions

My husband developed a bad, really red rash on arms, legs, back chest and face after 3 days of being on Avelox. I did not know what this was from as he takes several medications, but this was a new one prescribed for chest congestion so I decided to look it up on the internet. Lo and behold, lots of other people have had this problem as well. He took another Avelox today before I found out this info.... hope he does not get worse! Looks like this is a common side effect of this drug. He won't take another one ever again!

I am on Biaxin for Laryngitis and an upper respiratory infection. I went to the ER because I felt I couldn't clear my chest congestion and I was miserable. He prescribed me 500mg of Biaxin twice daily. I have just taken my 4th pill. Day 2 over. I have the stomach aches like everyone talks about. They feel like im starving, but I know im not because I just ate. Strange. The taste in my mouth is disgusting no doubt. It's a metallic taste, but not too bad. I keep drinking flavored waters and sucking on candies and that helps with the taste. I have had mild diarrhea today, twice. I actually have, previous to taking this medicine, a heart racing condition known as PSVT. I take medication for it to slow my heart down and lower my blood pressure. So far, thankfully, I have had no reaction in my heart to this medication but I am worried. I will keep this updated as it seems that most people started having more problems in days 3 and 4. hmmm. I have taken the Z-pack several times, (im always sick it seems like) and have never had any problems with it. I used to take amoxicillin, but it never seems to work on me. I think my body is now resistant do to taking it so often. I also take Zoloft for anxiety, so im pretty worried, ha ha, that I might have this severe depression or anxiety attack problem a lot of people seem to be having. Ill wait and see. I called the pharmacist tonight to tell him about my stomach problems and he said (Walgreens Pharmacy) that it was not an allergic reaction and would probably be fine, but to consult my doctor just in case. I will call tomorrow and update this if I end up having any other reactions or if he prescribes me something different.

In skimming through these posts, I think I only saw one other that mentioned nasal problems. I have been on NR for almost two years, and it only recently occurred to me that that may be around the time my congestion problems started. I have chronic sinus congestion and fluid in my ears, and am on Flonase and Singulair. The worst thing is that I have constant chest congestion and have to clear my thoat constantly...I drive myself and my family crazy! I have had a chest x-ray with normal results, but sometimes I feel like my lungs are drowning in mucus! Oh, and after reading these posts, my husband will be very glad to know that NR apparently kills the sex drive. I have had no interest for quite awhile now and just thought it was my age. (I'm 47).

started Zpak last week for a lingering sinus infection. I live in an area where the weather changes constantly. Two days after I finished the 5day Zpak I began experiencing horrible and flu-like symptoms and worse. I can hardly breathe out of my nose. Heavy chest congestion. Lots of diarrhea and even blood in the stool one day. Taste buds are gone. Here I am a week after finishing the Zpak feeling HORRIBLE. I'm afraid to go back to the doctor (uninsured) only to be prescribed something else that might bring on more side effects. Right now I'm taking Sudafed PE and hoping that kicks it. I've been on a Zpak before but NEVER had side effects like this. I don't wish this on anyone. and I'm wondering how long the Zpak stays in your system? It is possible to make you sicker? Seems so in my case and many others here.

I've not experienced any of the horror stories listed here, but I've had two side-effects that I've isolated. The first is the upper respiratory tract infection. That's a known side-effect. The second I believe was caused by an interaction between Januvia and Splenda. I use a lot of Splenda in my oatmeal. I've been having to urinate in the middle of the night (not like me) and I've experienced urinary tract irritation. Since stopping Splenda I've stopped getting up in the middle of the night and my tract irritation is subsiding. But, all this could be incidental and I would like to hear if other people are experiencing these symptoms while on Januvia and using Splenda. It appears, APPEARS, that, while on Januvia, that I experience the published side effect of losing a little bit of my appetite (good!) but that I have an increased appetite (bad!) using Splenda while on Januvia. I did not experience these symptoms while using Splenda before I was on Januvia. Please write to me if you have similar symptoms and situation at ******

I got sick on 1/21 I went to the doctor, I was starting to see yellow phlegm every morning for the past 3 days. The next day I was really messed up. My chest started to hurt and I was all congested, accompanied by lots of phlegm and loss of appetite. I called the doctor and she ordered amoxicillin because it works better for me. She wanted to order zpack, but I was reluctant because in the past I have gotten yeast infections from taking it. I felt worst with the asthma, chest congestion that I just wanted immediate relief. By the 3rd day, my throat irritation began, so I went to the emergency room. They order zpack and prednisone and as a precaution gave me a pill for a yeast infection. I started both meds and by the 4th day, the chest congestion was clearing and it was the first day I started feeling a bit better. I went back to the doctor, but I went back and still needed a treatment in the office. I was making a turn for the best. I finished the zpack on Friday and by Saturday, I was noticing a tinge of pain in my left side on Saturday. By Sunday, this pain was constant and stabbing accompanied by a yeast infection. The pill did not clear it up completely yet. Monday, the pain on my left side was unbearable, so I took a Tylenol which had no effect. So I went to the Emergency Room again and now they did an exam, touched my side and ran a ct scan, chest xray and blood test.

Get this, the results showed that I have gallstones on the right which were not causing my pain, a UTI and possibly passed a kidney stone. They gave me morphine and a nausea pill. Ultimately, they said they do not know what was causing my pain, so they gave me levaquin for the UTI and hydrocodine for the pain. I know the UTI came from not drinking enough fluids, but I would like to know where this pain is coming from. For Tuesday and Wednesday after leaving the ER, I could not use the bathroom with a bowel movement. I took a laxative today and used it fine this afternoon, Now my right ear feels like I have to swallow to open it. but the pain is still there and without the hydrocodine, it is unbearable. I have never had gallstone, kidney stones or pain like this. I called the doctor today and will see the doctor on Friday. This pain is unbearable, but the chest congestion, throat irritation are all gone. Why are the side effects so severe for a medication that seems to heal immediately.

HA! And I just thought I was allergic to the crud. I was given Levaquin for head and chest congestion. The first dose of 10 days didn't seem to help. I felt so bad from what I had I didn't notice anything else wrong. So my doctor gave me a second round of it. One day before it was gone, I realized that flu like pain all over my body should not still be there, and was terrified to find I could barely swallow. My husband rushed me to the emergency clinic, and my doctor there told me I was allergic to it and going into anaphalactic shock and that I was lucky I didn't die. What I thought was me getting sicker from the sickness, was actually me getting deathly ill from the drug. My throat was beginning to close off. This is a deadly drug.

Oh my God, where to start. The past few months I have gone through some crazy things from prostitis to having 2 cystoscopy's performed. This past weekend the scab came off the biopsy location in my bladder and blad pretty badly. It caused a large clot to block off my bladder and I could not urinate. In the ER they found a lot of bacteria in my urine and prescribed Bactrim.

Let me just say the past few months have been NOTHING last the past few days on Bactrim. First it was the crazy dreaming. Dreams that were so outlandish, yet so real it was quite frightening.

On day 2 of taking Bactrim I started to itch. It has been quite cold here in Jersey so I chalked it up to the usual dry winter skin. On day 3 I woke up (after minimal sleep) with a sore throat and chest congestion. I then found that the itching grew immensely in intensity and now was adorned with red bumps.

This rash was mainly on my upper arms and lower legs. I scratched at it so badly I drew blood, I have never felt itchy like this. This is ITCHY....EVIL ITCHY!

I woke up on day 4 the same, took another dose of Bactrim (dose #8). As I swallowed the pill something told me "Hey, I bet this pill is causing all your problems." After some research, viola! I found information online that pretty much assured me I was correct.

I went to the doc today and he advised me to take 1 Zyrtec a day and prescribed me Prednisone. I just hope this itching stops soon because I am making a mess of myself with all this scratching.

How could a pill like this be on the market and be utilized as much as it is. The testaments on this site are amazing and stunningly all similar.

Bactrim is undoubtedly the worst prescription I have ever taken or have read up on. To whoever reads this, if you are prescribed Bactrim use one of the rubber test gloves in your doctors office and slap him/her across the face with it. Dealing with the pending lawsuit would be better on you than dealing with the side effects of this drug.

I had the Mirena for over 5 yrs. I also had it for bad periods. I spotted constantly for the first couple of years but I left it in because I figured the annoying spotting was better than the alternatives (hysterectomy, ablation, etc) Finally, I was having some months with no bleeding for the rest of the time. What I didn't realize until after I was due to get it "switched" after the 5 yrs was up, was that I have been having so many of these side effects as everyone else. ( I stumbled across this and another site while looking for codes for the mirena to see if my new insurance would cover it). I have gerd, weight gain, back pain, UTI's, chest congestion, just to name a few. I always blamed it on me being overweight and getting older. One good thing about it was I didn't have pms anymore and I didn't feel so drained from the heavy periods. Oh yeah and I had INCREASED sex drive. I spoke with my doctor about how other women were complaining of the same side effects and she said she did not think it would cause all of that because only a little of the hormone gets into the bloodstream and it is less than the amount of bc pills. I decided not to have a new one put in right now and see if it was the Mirena that was causing me all of the extra problems. I had it out in September and I spotted for a week or so then I did not bleed for 1 month. I even went out and got a pregnancy test because I couldn't understand it. Then I started bleeding and it has been HORRIBLE. I have the most disgusting "period" I have ever had in my life. Not much pain though. I am still suffering and it has been over 1 month with no let up. I finally called the doctor's office and they want me to have another Mirena. I told them no. I do not want it. I do not know what I am going to do. I am waiting for some suggestion from my doc. I need some relief soon, though.

I am writing on behalf of my elderly parent, Carmela, who has been diagnosed with Lupus since 1991. She has been on a small dose of prednisone since her diagnosis in 1991. In the last several months she has developed very many odd hazey type grey spots all over her body. Dermatologists and doctors are not giving her any answers. They took her off predisone because they THINK this may be the cause. She is on an inhaler and does not like it. She wants to go back on the prednisone as she is feeling chest congestion and lethargy. I read an article on the internet that describes prednisone may cause unusual bruising. I'm not sure if this is what her spots are. They are only the color grey and appear to be beneath the skins surface. They are soft or hazy looking. They are small, about the size of a dime. Has anyone heard of this before in Lupus (prednisone) patience. Any info you have is sure appreciated. S. ******

Like many patients, I started out on a low dose of Lamictal. Eventually, I was taking 300 mg. This seemed fine for awhile. Then, I started feeling a bit down, so the doctor increased the dose to 400 mg. Increased dosage does not necessarily mean improvement in mood (bipolar). I began to experience a good number of the adverse side effects reported here, including excessive fatigue, gastrointestinal disturbances, cotton mouth and very bad taste in my mouth, muscle tension (particularly in my legs), forgetfulness and confusion, and sinus and chest congestion. At one point in time, I even had difficulty articulating words.

Though I did not suffer from rash, I have been up in the middle of the night with itching all over my body. I had a few episodes of mouth sores and one pimple on my chin. Many of these have improved since the doctor brought me back to 300 mg. However, they have not entirely disappeared. I continue to suffer from the excessive fatigue many of you have reported here.

I recently had a blood test and learned I have very low levels of Vitamin D and Vitamin B-12. I do not know if there is any relationship between long-term use of Lamical and these test results. However, I do know that low levels of Vitamin D can cause fatigue.

Though I am willing to follow through with further blood tests, I am beginning to understand why some people are tempted to discontinue their medications. I am so tired of being so tired and sleeping so much. When I finally get up, I am still tired and drag through the day.

Sometimes, I think I'd rather have a down day or two than take this medication. I should add, though, that my bipolar is not severe, and that I am only reporting how I feel. I'm certainly not recommending anyone discontinue medications for this or any other condition they may be suffering from. If I were to recommend anything, it would be to get a second opinion if one is concerned about his or her treatment.
If I were to make any suggestion to doctors, it would be this: more is not necessarily better. Send your patients for blood tests (mine were ordered by my M.D. and not by my psychiatrist). Increasing the dosage--at least of Lamictal--might result in a host of negative side effects. Your patients might then become disillusioned with their treatment and give up.

If anyone out there has suffered from B-12 and D deficiencies, let me know. I'll let you know what I find out.

And remember, most doctors are really trying to help us.

Hi everyone, I just want to say thank you for all who shared on this site. I am a 47 year old woman. I have spent several hours reading posts last night and today, and discontinued my Singulair last night. I have been taking it for approximately 4-5 years for mild asthma. Since then my health has gotten worse and deteriorated rapidly in the past year. I have had chronic chest congestion leading to frequent infections. Have had pneumonia three times in the last three years and frequent bronchitis. In the last eight months I have been on antibiotics more often than not, along with Singulair and Advair and frequent rounds of prednisone. Still I continued to worsen. I have had a rash on both legs since March which clears up with a shot of prednisone, but comes back within a few weeks. I've been going to bed nights by 7:30 and still find it hard to get up and go to work. Energy levels would vary, but some days I literally felt as if I could not keep putting one foot in front of the other. I have always been the quiet, serious type and prone to depression, but this past year it has been getting progressively worse. I have become very antisocial and even missed my son's wedding because I was so stressed out about it. I have also had alarming hair loss and just feel that my body is in a very depleted state.
My doctor, an allergist, ran a number of tests, but could find nothing. He finally referred me to a specialist at a University. He did a bronchoscopy and tested for tuberculosis and sarcoidosis because I had very similar symptoms to both of those diseases. They were both negative, but they found a rare form of bacteria in my lungs that doesn't respond well to medication. They felt that it should run its course eventually. I'm sure all of the immune suppressing drugs I have been on have made it difficult to recover from this. Aside from a two week prescription for a form of sulfa which they felt the bacteria may respond to, I am off all other drugs. For congestion they have prescribed a therapy vest instead of medication. I am very anxious to see if being free of Singulair and Advair helps me to recover more quickly. Already on day one I feel a better outlook on life and even went on a shopping trip with my mother today :-) I can't say at this time what role Singulair has played in all of this, but am anticipating an improvement after reading all of your posts. Thank you.

I took Albuterol for my chest congestion. My daughter was given the prescription for pneumonia and slight asthmatic tendencies during colds.

OK, I thought if it was safe for a young child, it would be safe for me. After only one dosage (using a Nebulizer) I experienced tremors and heart palpitations. I had to stop because my heart was beating so fast! And it's 10 minutes later and I still have some tremors. According to the package, 20% of 135 patients in a clinical trial experienced tremors. That is a lot! Needless to say, I will not take it again. I question whether my daughter should, too.

Had used it in the past without a problem. Then developed rash on abdomen, face, and scalp with single dose. Didn't make connection. Rash went away in a day or so. Used Doxy again three weeks later. Again, had severe rash plus some chest congestion with one dose.

I was put on Avelox 6 days ago along with methylprednisolone for a severe sore throat, chest congestion, and cough. Since taking the medication, I have had episodes of anxiety, panic (hard to catch my breath which leads to the feeling of panic), restlessness, trouble sleeping at night, nausea, and problems with my memory (I have had numerous episodes where my mind blanks and I forget what I was going to do or what I was in the middle of doing). My emotions have been all over the place since taking this. I have had episodes where my body just feels very strange. I also have had bursts of pain in my left hip. I am only 41 and have never had this happen before. I was attributing it to my illness because I was very sick at first but now the illness is gone (except for a little congestion that is left) and I am stilling having side effects. It didn't occur to me until today that it could be the medication because I've never had any bad side effects from medication except getting sick to my stomach with codeine. I decided to research Avelox and now am convinced about its side effects. I won't be taking my last pill and will call the doctor tomorrow.

I wonder if mixing Avelox and methylprednisolone caused any effects? Haven't researched that yet.

Sinus infection and chest congestion: doctor knew I was on HCTZ, a diuretic, as well as Zyrtec and Nasonex. The HCTZ I now known is an agent that should have triggered a modification of the treatment protocol. First night on the 400 mg Avelox, during conversation at the supper table, a black cloud of depression suddenly descended upon me like a curtain. Then I became extremely irritable and short-tempered. (Hard to blame on a drug, except that this came out of the blue right when I was feeling mentally and emotionally happy and relaxed, enjoying my husband's companionship. No reason for depression, irritability and short temper, especially to such an uncharacteristic degree. This was severe!) No sleep whatsoever that night due to shivering without getting warm, feeling like my whole body was crawling, feeling terrible frustration and anxiety and depression. Had taken the Avelox with my supper. Second night: unable to breathe through nose at all. Nasal passages so dry they hurt. I decided to abandon Nasonex and Zyrtic but never thought about stopping the HCTZ (the info insert from the drugstore never mentioned that). Insomnia and feeling electrified. Again, the feeling of total body crawling and restlessness. Irritable to the max. Frustration. Wound up sitting up most of the night to avoid waking loved one with my tossing and turning and misery. Third night, I took the Avelox early, at 5 p.m. Had been having to turn on the shower and steam up the bathroom to moisturize my nasal passages enough to bear the painful dryness. Also began using Ocean Mist to ease the pain. Despite the dryness, my nose was still too stopped up to breathe. Heavy sinus congestion and pain not any improved yet. Dozed some that night but a phone call came at midnight for my husband and after that I was wired awake again. I am desperate for rest. This is the fourth day and finally I'm coughing less and the congestion is coming up. But my sinuses are harder than ever to empty. Mucus extremely thick and sticky (sorry for the graphic quality of this post). One very severe side effect is that I am now incontinent. I never make it to the bathroom in time to urinate and so am wearing pads. Having to change them every time my bladder begins to fill. Leaking, dribbling and now gushing urine without any control whatsoever. I have just read the full prescribing info and wonder why on earth was I not given a safe antibiotic (I realize everything has some risks and side effects, but why was I exposed in this way to such a dangerous drug without a life-threatening disease to require its use?) This is an outrage. Now I"m stuck finishing the script or else my infection will be back worse than ever and then I'll be given yet another bad drug. I have only one clue to this question: I was asked what my Insurance company was just before the script was written. I cannot help wondering: what if I'd had no insurance, or another insurance? Would I then have been given a less-expensive and much safer, even safe drug? If you are ever asked just before the script is written what your insurance company is, ASK WHY THEY NEED TO KNOW. They will probably tell you it's so they can pick a Preferred drug. That would be a bogus answer, because after I told them what my insurance company was, they never went and looked for a list of preferred drugs! They simply swiftly wrote for Avelox! I was never told any of the bad effects. Now I fear getting the colitis, the tendonitis (no one told me not to exercise!). I even fear permanent incontinence. I also think that this depression, anxiety, and insomnia, and the horrible restlessness and whole body crawling sensation could be lasting and that really makes me feel very depressed. My husband has had to suffer with days and nights of my irritability and temper -- and he has cancer and I never wanted to ever be cross or complaining or to worry or burden him. This medicine is not worth it. THere are safer better options. DEMAND BETTER OPTIONS. I also wonder if the HCTC or Zyrtec or Nasonex taken on the same days could have damaged my kidneys or liver. I really think that antibiotic resistance is the ultimate bad side effect of this drug. What could be worse? Why is this being used for garden-variety sinus infections? Why is it not an option only for those who must have it or probably die of some life-threatening illness? This medicine needs more than a black box. This medicine should be available only to doctors treating patients who are in danger of dying of an illness. I have had doctors give me black box medicines before and I was spineless enough (and ill enough with severe, recurrent sinus infection) that I took the medicine. But from now on, never again. There are still better options and I deserve the safer options just as much as the next person -- no matter what my insurance coverage is! Doctors don't hesitate to use black box medicines anymore. Why do they hesitate so long to prescribe medicines without black boxes? They say it's because of the new resistance to antibiotics and the super bugs. Well now I'm susceptible to super bugs PLUS all these other severe side effects have to be endured. If anything else goes wrong, I'll come back and add another post. Meanwhile, I'm praying for each of you to make a full and speedy recovery.

My son 10, has been on Singulair since he was 4 yrs old for Asthma and allergies. His last dose was 3/26/08. He has always been my emotional child, he is 2yrs older than this younger brother. Some of his side effects included headaches, stomaches, leg cramps, emotional breakdowns, major mood swings, crying outbursts over small situations, night sweats, lack of motivation, weight gain, ADHD, wishing he were dead and the list goes on. His younger brother has always been involved in sports but he was always too afraid he would get hurt. This medication has robbed my 10 yr old son from 6 yrs of his childhood. Since he has been off Singulair he feels motivated and looks forward to joining the football team his younger brother plays for. I look forward to meeting this new young man who for so long has been hiding behind this so called allergy medicine. I am so thankful to know that my son can look forward to a bright future without these side effects. God Bless you all who are going through this as well.

Received script for 300mg 2x per day for 10 days to treat ear infection and sever chest congestion. At the time the only side effect was sensitive skin & lots of itching, combined with a very mild diarrhea. Here is the crazy thing: now that it has been 30-40 days since I was on the antibiotic, my toe nails have grown out and you can see that it has killed the old nail in front of the new growth. My brother is a physician & he said it is weird, but not out of the question.

Hello everyone,

Just like all of you, I too googled this strange indentation in my left buttocks and found this site. I suspected when it first showed up that it may have something to do with a shot from my Dr. because the indentation was strangely in the same spot as my last shot. I have received several Kenalog shots over the past couple years for chest congestion and sinus related symptoms that typically drive me to calling my family practice doctor. Although he regularly administers Kenalog, I have had know reason to doubt his treatment as my history with him has been relatively good. However, he is not the one administering the shots, his young nurse it the one (less than a year out of school). Anyway, I too, like many of you am going to look into a class action lawsuit and/or my own legal counsel. If there is anyone out there who has gotten any positive feedback from a lawyer willing to take this on, please contact me for testimonial. This is not flattering and moreover, after reading the many previous entries, I am downright scared. Also, please advise is there is any known treatment to help reduce further reduction of tissue in this area. Thank you very much for reading and for the continued entries after this one.

I have been taking Januvia for about 8 weeks. I have had severe bronchitis, and now can't get rid of chest congestion for two weeks. Seems like fluid build-up in my lungs. Before I started taking Januvia, I was so proud of the fact that I had not been ill in years. Now, can't seem to get well. I stopped taking it this morning and hope to regain my health.
I plan to see my doctor next week.

I went to my doctor on Monday December 17, 2007, because I was experiencing a fever, chest congestion, with an extremely painful cough. He gave me 7 sample blister packs of Levaquin 500mg, and a sample Pulmicort Flexhaler 180mcg. He also prescribed a cough medicine for night time if I needed it. He said I had bronchitis or a possible pneumonia he couldn’t hear. I also used a nebulizer with Abutrual.

On December 23, 2007 I awoke with the most intense pain I have ever experienced. My wrists, finger, toe, elbows, knees and ankle joints all hurt. My muscles in my legs and back burned. My hands, fingers, feet, toes, and shins felt like they were “asleep” or the worst pins and needles ever.

My husband went online and found out that is was most likely caused by the Levaquin. And thankful I was taking TWO steroids! So when I called the company that makes Levaquin they told me to stay in bed! When I asked them how long this could last they said 1 week to two months.

As of today, the pain in my fingers, toes, wrists, elbows, ankles and knees, which is like tendinitis is mild to moderate. The burning in my muscles in my legs and back is still intense. The “pins and needles” is affecting mostly my hands and feet and my left leg from the knee down. I also still have a deep pain under booth knees. I have also experienced a periodic facial twitch on the left side, below the eye about 1.5 inches.

I am weak, and completely unable to get around do to the pain in my legs and feet. I am furious that my doctor prescribed a medication that could cause these problems without warning me, as samples do not come with warnings. I feel disabled, angry, and would like to know what I am supposed to do now!! Has anyone found anything that helps with the pain?

I was given 500mg Capsule of Amoxicillin for sinus infection. After 4 days on this med I am now getting all over body aches and pains. Not sure if this is a side effect of Amoxicillin or from the sinus infection. Either way I feel like hell. The Dr ruled out anything else, but I have chest congestion and headache and nasal congestion as well. It has abated some but taking a long time to clear up.

Boy, after reading quite a few posts I wonder if my problems are linked to my advair use. I started about 2 years ago, 250/50 and have had to go to 500/50 during the spring-early fall because this is the time my allergies are the worst. I have year round allergies, highly allergic to weeds and grass pollen, also molds, cats, dust, etc. I started having problems when I was 15 with asthma, I am 30 now. I've been on multiple meds since I was about 20 for my asthma. During the winter I always have problems with chest congestion, coughing, and sinus problems. About 2 years ago these problems suddenly got a lot worse, and I could not get over sinus infections, I was referred to a specialist, they tried 3 different antibiotics, but as soon as I got off them my symptoms returned. I had a cat scan, and they found my sinus cavities were terrible, full, swollen, etc. He reffered me to another specialist, who I think is awsome. They changed my asthma meds, back to singular, q-var inhaller twice a day, and advair twice a day. My asthma is better, my sinus problems got better and I was able to have sinus surgery about 16 months ago which Greatly improved my problems. I started allergy shots about 1 year ago. Since July of this year I have been having strange problems, which I think are caused by the advair. Lots of times I shake for a few hours after taking my advair and q-var, for the last few months the shaking has gotten worse. In July I suddenly started having problems sleeping, my legs and arms move involuntarily - most of the time violently thrashing around while I am sleeping. I am always tired, and since July I now have severe tiredness in the day, especially while driving, I have to fight falling asleep! Very concerning to me since I have a 6 and 3 yr old, and the 3 yr old is always with me when I start to get to tired (exccessive daytime sleepiness). The leg and arm movements are called Periodic Limb Movement Disorder, similar to Restless Leg Syndrome, but PLMD is usually only during the night, and you don't feel like you have things crawling up your legs or the constant need to move. My symptoms have grown increasingly worse, I had all types of blood work done 2 months ago, nothing was found to be wrong. I've tried different chiropractors, stretching my back/legs before bed, less caffine, etc. But nothing has helped. I started taking Requip about 6 weeks ago, increased the dose about 2 weeks ago, but still having problems. I have had leg and feet cramps for the last month, almost daily, and have periodic leg shakiness during the day, like I have worked out really hard, but I have been sitting! I noticed that Advair lists sleep disorders as a side effect, but doesn't specify what types. I will definately be talking to my doctor about weaning off and stopping advair!
Thanks for having this site and for sharing!

I took this yesterday after suffering with asthma problems off and on the past couple of months. After two trips to the doctor, the final consensus was that I had a sinus infection, and that the continuous dripping into my chest was causing the chest congestion.
Anyway, within one hour of taking avelox, I had a full-blown anxiety attack ....I was dizzy, lightheaded, my head felt like it would explode, had diarrhea, couldn't breathe, and thought I was dying. I almost called 911. After about 4 hours of this I took half of a 1 mg lorazepam pill to calm down. I continue to feel completely unwell all evening, shaking and anxious. I finally took a hot bath, and a full lorazepam, which allowed me to sleep. I am telling you that the whole afternoon and evening was a harrowing experience. I am also wondering if the side effects were exacerbated by the Astiliin (nasal spray) I took, since this morning that drug made me feel extremely groggy and tight in the chest.
I will NEVER take this drug again,and now I am so afraid that I am scared to take the zithromax the doctor prescribed in place of Avonex, even though I have used zithromax in the past with no side effects.
At this point, I am ready to consult a naturopath or acupuncturist to help with my condition - most of these new-fangled drugs seem to cause more problems than they "cure".

33, Female - Been on Advair a while now, last disk is this month. I have had chest congestion similar to an upper respiratory infection every time I have had to take Advair. I made sure to follow the pharmacist's instructions and gargle with water after taking it to insure I don't get a yeast infection in my mouth, but the congestion really bugs me.