Steroids symptoms and conditions

I wrote a post few days ago about Singulair and how great my daughter is doing since she started to take this medication three months ago.
Then I started reading about all the side effects that other children had because of Singulair. I GOT SO SCARED!
So scared that last night I stopped giving Singulair to my daughter.

From January to September my daughter had asthma every other week. She was put on steroids (prednisolone) every time she couldn't breath. Then in September the pulmonologist said we have to take control of the situation because so much steroids can damage a little body.
She made me feel I had been a terrible mothers since I always refused to give her singulair.
She convinced me and then I started Singulair, but now I feel worst because I have the feeling I am giving poison to my daughter even if her asthma is under control.

My 7 years old stopped Singulair 12 hours ago, I do not know what is going to happen now. Of course I cannot call the pulmonologist anymore in case my ds gets bad.
Somebody here said that she is giving her son Nordic Naturals Fish Oil, Culturelle probiotics, vitamin c, and changing his diet - increased magnesium and decreased dairy.I will love to have more information about this alternative way of controlling asthma. I do not remember who wrote this post. If there is a web site of a doctor I can contact i will do right away. I live in New York.

I need help. Thank you so much.

Have had two back to back ER visits because of severe hives on Buproprion (generic wellbutrin). Had been taking it for a little over two weeks. Was told that the wellbutrin couldn't be the cause (is the only drug I was taking) and it must be due to my CHRISTMAS TREE...uh-huh. But I'm a good sport, kept taking the drug even on the day I was in the ER. Hives go down by the first evening but after a shot of benadryl and steroids which knocks me out for the rest of the day. Next day I take oral benadryl, clariton, prescribed steroids, and use hydrocortizone cream (all recommended in ER), new hives but little...end of day, can barely walk because feet and thighs are one big hive. Ears, mouth, shoulders, arms, in between fingers....hives. BACK to the ER (lovely Christmas eve) and am told by a new Doc that it was stupid to keep taking the buproprion. This time more shots don't help. The hives keep coming for several more hours. It's the next day and they have gone down some but were so bad that I have been left with dark bruises in various locations. Yuck.

I had had some initial side effects that were pretty mild and all went away after the first nine days (insomnia, headache, dry mouth) but I will not be waiting to see if my airway stops constricting after a few more days of treatment. So...ouch.

hi got put on prednisone 6 days ago for breathing difficulty was on 30 mgs, after day 3 had to stop taking them , felt like i was going crazy couldn't sleep and the thoughts going through my mind are frightening been off them three days and still having to focus on not thinking these horrible thoughts , been down the road of severe depression before and just hope this hasn't triggered it again will i go back to normal????

Hello, I have read over most of these side effects and i would have to agree and be afraid of most of it. See I was diagnosed with bronchitis/pneumonia, they prescribed me these pills along with steroids. I have not taken the steroids yet but I did take my first dose of levaquin about 12 hours ago around 8 pm. With my dinner and plenty of water and fluids. I went to bed late with my fiance but not cause of the medicine, we decided to stay up and watch movies. Although, it did help my coughing and breathing, I felt bloated or ballooned up all of a sudden and it was starting to hurt my stomach. I figured it was the food I ate and all the water I have been drinking. So, next I noticed some minor vaginal discharge of which looks like when I'm ovulation so I pasted that as that. Now I woke up at 5:30 in the morning when I went to bed at 2 am and I can't go back to sleep! I woke up from a nightmare to see things in the dark to scare the %$^* out of me. I had this really bad taste and dryness to my mouth I felt like it was suffocating me. I cant seem to think straight or type well (I had to go back and review what I wrote but I might not have gotten all my mistakes) I feel like I have ADD I keep forgetting how to spell simple words... I mean the list keeps going and going. I am writing now because I am currently on it. I will not be taking this medication anymore much less the steroids but if anyone reads this, I hope you read first then take.

My three year old daughter was on in as a baby and it was great for her asthma. I stopped it for a year and now she is 3 and has started it again about two weeks. She sleeps at least 12hrs a night and has a nap. This is someone who slept maybe 8hrs a night and never a nap. Actual the sleep is so much its kinda worrying me. I have a hard time even waking her up. What should I do?

My 7 year old female Siberian Husky, Niceah is suffering with her second serious flare-up of IBD. She was taking 20 mgs. of prednisone every 12 hours for several days. We are now down to 12 mgs. daily and working towards 12mgs. every other day. She is lethargic and her body and belly have swollen frightfully to the point where it is difficult for her to lie down without grunting and sighing. She pants heavily. She drinks and eats constantly. Her nose is dry. Her tummy grumbles all day and night. I have been boiling chicken breast and mixing it with sweet potato and Enzymes & Probiotics. I am currently working with a holistic advisor concerning Niceah's diet once she has weened off the prednisone. The side effects of this drug are frightening and I am so worried that something more permanent and damaging will occur. Has anybody experienced this?? If so, I would appreciate any advise. Robin. copher370@aol.com

I was on prednisone while getting over pneumonia to help with my breathing. I was only on it for 7 days and the doctor didn't have me go off of it gradually. I missed the last dose on the 7th day and by bedtime, my muscles were sore enough it almost hurt to lay down. I took the last pill that night before I went to bed and had no muscle soreness in the morning. After that, the muscle soreness came back, along with dizziness. My pulse was also higher than normal. Two days later at night, I was still having muscle soreness and dizziness, although not nearly as but, but I was having a lot of trouble breathing and my pulse would refuse to go below 100 no matter what I did and the problems continued thought the night. The next morning I went to the clinic that prescribed me the predisone because the information they gave me said to see a doctor if these problems persisted. I told them I thought I might be having a predisone withdrawal because my mother, a nurse, said it was the most likely problem from experience. They completely ignored that saying it had been several days since I've stopped the steroid and kept asking me about my asthma (inhalers weren't working and it was definitely not an asthma attack -- I've had plenty of those, to all different degrees) and ended up giving me medicine for anxiety, which helped the closing of my throat, but none of my other symptoms. Three days later, my resting pulse is down to 80, but my breathing is so much worse than it would be with just my normal asthma and taking my inhalers as much as is allowed. I had no noticeable symptoms when I was on the prednisone except being less able to sleep. If it keeps up, I intend to go to a different doctor to see what is really happening, but I don't think it's 'normal' to have the withdrawal symptoms for this long after only having it for 7 days. I know I took it when I was younger (I'm 22), but I don't remember ever having issues going off of it before.

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!

I was diagnosed with Optic Neuritis in my left eye, at the time of diagnosis, I felt fine. Had an MRI to check for lesions on the brain, there were none. I was put on IV solu-medrol for 3 days, then 90 mg of prednisone for one week, with a rapid taper the second week. 6 days into the prednisone, I started have shortness of breath, etc. Went to the ER and my white count was 22,000. Had bronchitis and the beginnings of pneumonia. Because of the breathing problems, I only did 2 days of taper (doctor's advice). I have lost site completely in the left eye and now I have blurred vision in my right eye. Extreme fatigue, and a mental fog I just can't explain. A "twitch" in my left left hand and muscle weakness. I just don't feel "right". How long does it take for this drug to leave your system? Has anyone had a similar experience? My eye doctor was considering another round of prednisone for the optic neuritis, but I am not so sure I can survive it.

For me having the Mirena removed just last Thursday was the right decision. I was not using it for birth control but as hormone therapy for heavy, crampy periods. I had it inserted in July 2008 and bled every single day for the entire time, I had it removed last week and now I am bleeding very heavily but hopefully that will stop once all those hormones are out of my body.
While on Mirena I lost all sex drive, I became severely anemic and with that fatigued terribly, and moody, crying at nothing and screaming at my kids or husband for stupid reasons, I felt bloated and gassy and didn't have those problems before.
I am 42 years old and I hate my heavy bleeding in fact I want a hysterectomy, but not sure now what I will do.

For those of you who had the Mirena removed, how long did it take to stop bleeding afterwards? This is draining every last ounce of energy for me and I am taking iron supplements.

What sucks is the cost of this, Even with insurance I ended up paying a lot out of pocket to get this thing and then all the Dr. visits due to bleeding and side affects in the 4 months it was in and now the removal of it. I am wondering if there is any way that we can get a Class action lawsuit against Bayer for this horrible thing they are trying to sell to women.
I know there are some out there who have not suffered all these horrible side effects at least not yet or that they are aware of, but I truly believe that there is nothing good about this IUD and those of us and there are a lot of us who have suffered with this should be reimbursed or compensated for the pain and loss of parts of our lives and expenses with this. Does anyone else have any thoughts on this?

My husband entered the hospital in Nov of 2005 for a surgery. He almost died in the recovery room and from there things went from bad to worse. They put him on a massive dosage of Prednisone. 95 days later we were able to come home. About 2 weeks later he started vomiting and lost all energy. We returned to the hospital and the diagnosis came down as acute adrenal insufficiency. He was pumped full of Prednisone again. From there he went to a very slow wean and he got completely off the drug. No problems. This year he suffered a fall resulting in extreme trauma and blood loss. Back to the hospital where it was determined that his adrenals were again in crisis. Got him all mended and on the way out the door when a nurse decided that he should have a pneumovax. Within 24 hours we were back in the hospital with my husband in critical condition with three life threatening situations. His kidneys were shutting down, his blood pressure was beyond the danger zone (low) and he had cellulitis. Back home again to another slow wean. We are down to 5mg now and are hopeful at the next appointment to be able to start weaning further and back to zero. We were given Dexamethasone Sodium Phosphate for injection in case of any trauma in the future. In addition, my husband now wears a MediAlert bracelet which notes his condition and that in case of accident/trauma Dexamethasone Sodium Phosphate is to be given. Anyone on steroids should register with MediAlert at ******

What everyone needs to know is that the adrenals are responsible for a person's feeling of well being. When you are on a steroid, you need to wean very, very slowly to let your adrenals start doing the job on their own. The reason Prednisone is often prescribed is that it comes in as low of a dosage as 1mg and can be split 4 ways for 1/4th mg per dosage. For those that cannot tolerate Prednisone, Hydrocortisone is available. 10 mg of Hydrocortisone is the same as 2.5 mg of Prednisone. Hydrocortisone can also be split.

So happy to find this site. I never noticed My son never had an eye tick until last month, ironically we started giving him Singular on a daily basis about the same time. My son just turned two and is has also been waking up screaming 3 times every night. Have others reported this same problem...also he is on Pulmicort too, have you read that it is linked to Glaucoma and Cataracts? Do you think that this could be causing the tick? Please HELP! I want a parent's opinion before bringing this up to the doctor...they are so quick to jump to more drugs it makes me sick! Thank you! Any other children with eye "ticks" like really quick consecutive blinks?

It made me bloated, excitable, moody, depressed, angry and most of all, lost my sense of smell. Not to mention, 2 weeks after I stared taking it I caught a horrible cold and I never get sick, accept for my allergies. I only took this medicine for about 3 weeks. I cannot wait until it is out of my system. I know it has steroids in it and they are powerful drugs and it can stay in your system for a long time.

October 22, 1998 I had resp. failure (with intubation). My new pulmonary doctor put me on Singulair 10 mg once a day, a few weeks after. Within time, I started to have numbing and tingling in my face, arms, and legs. March of 1999 the symptoms worsened and started causing pressure in my face, arms, and legs, and anxiety started to kick in. I was told I had neuropathy and to take mobic. Symptoms getting worse, and went to a rheumatologist in June 1999, and he was suspect of singulair. The doctor thought that what I was experiencing was due to the singulair. He (the rheumatologist) discussed this with the pulmonary doctor and the pulmonary doctor did not believe this to be the case. Not forgetting, in March of 1999, I had a ct of the sinus area, and low and behold 1/3 of the cavity was and probably still is full of polyps.

As time went on, symptoms getting worse, and not one bloody doctor could figure out why I was feeling this way. In addition, at times, I was put on steroids for my asthma (not including my inhalers).

Two years ago, my body went into shock, leaving my left side very different than my right side. Affecting: my head, my face, my eye, my ear, my esophogus, my lungs, my arm, my leg.

I have been depressed and anxious not knowing what the heck was going on with me.

Recently ruled out thyroid, and lupus, and possibly ms.

Last weekend, I reviewed the letter from the rheumatologist (dated 1999) and the ct report from March 1999 (regarding the sinus/ polyps) and made copies to present to a pulmonary doctor that I have recently been seeing.

This past Monday the 10th, I had my appt with him. He knew of my situation from the last few visits (in addition, I had met him this past March for a pulmonary rehab program, and thought he seemed to be knowledgeable and compassionate). While waiting for him to enter the exam room, he had read those reports before entering.

The doctor looked at my hands (red as a beet and swollen) and said "You have Churg-Strauss Syndrome, and get off the singulair."

I had done my homework from a few weeks ago, where I looked up untreated polyps.
Untreated polyps, can turn into vasculitis. There are many types of vasculitis, to include Churg-Strauss Syndrome.

I then cross ref CSS and singulair, and low and behold, BINGO!

I have been suffering for ten years, physically and emotionally because of this drug!

There is also recent updates from the fda (fda.gov) regarding singulair, of which most recently includes anxiety and depression.

I suggest before taking singulair, be aware of the side effects. As soon as a side effect comes up, contact your doctor. Also, be aware of existing conditions (like me, sinus problems and asthma) for this could lead to churg-strauss syndrome.

This info is indicated on the actual disclosure (the paper insert that indicates studies, side effects, etc...) not the handout that is given with the drug.

By the way, I am now working with a new rheumatologist in Los Angeles (Cedar-Sinai affiliated) and a new neurologist.

mdklezmer

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

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

I was prescribed Avelox for a Sinus/ear infection. I was given 1 pill a day for 5 days. I took the first pill and within 30 minutes I was starting to feel very "out of it". I started to get very anxious and began pacing in my house. I couldn't sit still without becoming agitated and disorientated but I was feeling so spacey that I didn't really know what I was doing.

My arms and legs started to itch, then tense up and began to tremor. I even started arguing with myself OUT LOUD about whether or no I should go to the ER. Finally I just made myself lay down in bed and slept for about 14 hours.

The next morning I work up and felt like I had been in a fight. My muscles were sore and weak and I had flu like symptoms that kept me bed bound for 3 full days after taking only 1 pill.

Hi everyone well yesterday i started to to take Prednisone 2 hour later my heart is racing along with high blood pressure , so ill try to calm my self down blood pressure kind off got back to normal but heart still beating rapid, today i woke up my blood pressure was fine but my heart still pounding do ya know how long it t takes for my heart to go back to normal , and im sorry to hear about everybodys different reactions to this stupid pill hope everybody gets better.

I too have been injected previously with Kenalog shots for allergies. I never had the site indentation that most of you are commenting on. But I can tell you that the menstrual cycles did change considerably. Kenalog is a steroid, and like oral prednisone it is hormonal. It is just like taking birth control pills, you have the irregular or heavy periods, the excessive hunger, hair growth where you don't want it and weight gain. And as far as my allergies are concerned it never worked. I have excessive sinus disease that has been aggravated by living in a dry windy desert climate. After my second sinus surgery in 2 months the holes in my sinus cavity are starting to close up again. So yesterday my doctor tried a new therapy of injecting kenalog right into my sinus cavity. However it was not injected directly. A small piece of spongy foam was placed into my sinus cavity and the medicine was injected into the foam so my nose would absorb it naturally without the tissue being directly injected. I don't know if it will work or not. I have experienced some unpleasant side effects already, higher blood pressure and increased heart rate. Although the heart rate did come down after a few hours. Any kind of steroid causes this problem. I was hospitalized in January with a severe asthma attack and was given steroids thru a I.V. It was the only drug that opened up my lungs, however by the second day my heart temporarily went into v-tach because I was getting too much too often. As soon as it decreased I was fine. So dosage is a major concern. I can tell you from experience that Kenalog last realistically for about a month even though docs tell you it's good for 3. I would not have multiple injections for any reason. But when you are in pain and hurting and you have inflammation in your body, unfortunately steroids of some kind will always be the drug of choice. I have recently started acupuncture and will see if that helps my sinus problems. I have taken up yoga too to help my breathing. I highly recommend these alternatives to drug therapy. I have been on every kind of asthma and allergy drug out there and I do not trust any of them anymore. But ask the doctor lots of questions and refuse the meds if you are not comfortable. if your doctor is herding you in and out of his office or not willing to explain the meds completely then refuse it and go to someone else.

I have Autoimmune Hemolytic Anemia (AIHA), was diagnosed in Feb. 2008. Have been ill for several years and finally it came to a head in Feb. I had a blood transfusion and then in the hospital 6 days later with a hgb of 4.0. I was so toxic and my blood so screwed up I nearly died. I was given another transfusion then (total of 5 pints of packed red blood cells) and started on Prednisone. For 3 days given liquid Pred injections, starting at 1000mg, tapering down to 250mg., then on the pill form at 100mg. Sweat poured off of me dosing down. I was off work for 2 months. I am still tapering but am now at 1mg. DR. added another drug, Danazol, after getting to about 10mg because my blood started going crazy again. My side affects with Prednisone have been, Euphoria, no depression, LOTS of hyper brain activity, thoughts running a 100 miles an hour but body at slow speed.Visual problems and a feeling of being highly drugged. 2 to 3 hours of sleep each night, compulsive behaviors and a lot of pacing back and forth. Couldn't hold my concentration because my mind wandered so much. Extreme Tremors in my back, hands and head. Wanted to talk constantly, if no one was around I talked to my Chihuahua or the TV. My cheeks puffed up and became hard and had a fat pocket puffed up on left side of my neck. My dog thought I was crazy, she was tired of the lights being on at 3 or 4 in the morning. Legs looked skinny but didn't gain weight until I got to about 60mg. Gained 25 lbs total. Tapering caused bad spasms in my calves, feet and hands. Thigh muscles would get extremely weak each time I went down a dose. At 50mg I started getting sleepy and could hardly stay awake. Went back to work at 35mg and couldn't remember how to sign on to my computer. Some memory problems since I was in the hospital, couldn't remember how to spell words I knew as a young girl. Started having hip pain about 3 months into the Pred, that hasn't stopped. At 10mg feet, knees, shoulders hurt deep in the sockets, muscles below my neck knot up, may take a while to totally get off this. Read on a couple of blogs where people cut a 1mg tab into 4 pieces to taper off the Pred. because of side effects. Had thrush in the beginning and break outs of shingles. I hope to God I never have to get back on this drug again, it is so HARD on the body but it did do what it was given for, to repress my immune systems. My next step is Spleen surgery, hope this is a cure for me, am sick and tired of being sick and tired. Wouldn't advise anyone to take Pred unless it's a life or death situation. It's prescribed too liberally and people have multiple problems, worse than I have experienced. I've probably forgotten some things, but there's enough I've mentioned to give you an Idea it's not good, but if Pred is all you have then you do what you gotta do!! My puffy cheeks have went down though, now my hair has become curly but at least I have hair and my chihuahua stills loves me!!!

Prescribed Levaquin 750 mg for diverticulitis. This was a higher does than prescribed for a previous bout of diverticulitis. Experienced extreme nausea at each dose. Eventually developed a skin rash that burned so bad it felt like I was being skinned alive. I have had shingles in the past and they were less painful than this!!! After 5 days of antihistamines, steroids, oatmeal baths and pain killers I am finally able to put clothes on again!! The dermatologists diagnosis was delayed reaction to the Levaquin...never again!!!!!

As a Doctor myself I think drugs are NEVER the answer except in EMERGENT issues in Heroic life saving... YOU however and all individuals are and should be MORE accountable for your own health and STOP DEMANDING the Drugs and look to LIFESTYLE changes in DIET and EXERCISE to achieve the GOALS so necessary for quality and quantity of life.... The tools are at your fingertips ... The almighty internet ... And your OWN imaginative mentation is your TRUE limitation... So TAKE control of yourself and BE accountable .... Sorry so blunt but MORE tough love and Educating people is whats needed.... NOT more drugs....

MDG

I am a loving mother of a 5 1/2 year old boy. He has been on Singulair for over 3 years. In this past 3 years my son has suffered in an unspeakable amount. He came down with Rota Virus and was hospitalized at 2. He then came in contact with Pneumonia in the hospital while he was there. They automatically put him on Singulair, Zyrtec, Prednisone, and antibiotics to treat the pneumonia. Since that day, my son has gone though more tests than I have in my entire life. He has had asthma, sinusitis, leg cramping ( to the point he cannot walk for 2 years), IBS, Acid reflux,(they gave him laxatives for a year that made things worse and addicted to them also), stomach pain, constipation and diarrhea back and forth. He also got Erythema Mulitforme TWICE, while on this drug. All of which the doctors said could NOT be caused by Singulair. He has had several Upper GI's and CT scans. Along with Barium enemas, several hundreds of blood tests, and many many pokes and prodded that were not necessary. All since he has been on Singulair. He now has frequent bathroom trips, depression, confusion, and anger outbursts. He also has to go to the restroom every 5 minutes. He has had genital swelling, and many other aches and pains. None of which his "doctor" ever said could be a result of Singulair. I am 100% sure it was!!!! He currently has anxiety and emotional sporadic issues causing problems in school The teachers and counselors say that it is so strange because there is no TRIGGER and the outbursts are completely inconsistent. His preschool teacher and director are sure he has ADHD. Well, we had him tested and he does not have any part of it. He has no learning disability what-so-ever. So that brought me back to square one. He is in a positive loving enviroment. How could he be depressed and want to hurt everyone around him? He cannot sit still. He cries and says he is 'stupid" and "can't think" like the other boys. He has nightmares and cannot sleep alone. He is scared of everyone and everything. So, as I sit here crying, I realized that this has all been a reaction of his "medicine" Singulair. He never should have gone through all of those painful tests, only to prove they couldn't find anything. So many treatments and sound full advice speeches from his doctors. How could they be so naive and selfish in the life of my son?

When I called my pediatrician of 5 years, she told me that " parents that have children with behavioral problems will LOOK for something to blame their problems on." She also said "drug companies only put side effects on their labels to PROTECT the drug companies. (as she laughed at me) They are not always valid". Then she said "if you take you child off of Singulair you will be playing Russian Roulette in his life." Then she said that all children around 5 or 6 go though this emotional time in their lives." She told me that if I take my child off of Singulair that she would no longer be a part of his health regimen for his asthma. She told me to see a Pulmonologist for further treatment.
Who is paying who? This is my son's life???????? I decided to go with my mother-gut instinct and get him off of this medicine. No matter what. He has been a different person since. He is currently going though a lot of side effects and withdrawals (leg pain, insomnia, hic-ups, emotional distress) but every day is getting better. How can the drug companies say that this is a "wonder drug?" There are more reported side effected patients then clinical studied patients! How can a "medication" that stimulates the brain not be connected to other problems? This "medication" interferes with the bio synthesis and action of LTs and has been marketed as NOVEL medication against asthma and allergic rhinitis. Who the hell is playing God here??? The pocket books of Merck or our over PAID "doctors?" Who pays the price? Our children? Or us. Thank god I found this before it was too late. I would not be able to withstand the pain of losing my son due to their lack of scientific evidence. They are lucky I am one of the smart ones. I will not settle for less than Justice for the drug companies and their paid "doctors?" You all end up in the same place. HELL

There are 18 million people on this drug. Most of them are children. Please save a life if not your own child's life. Thank You

I have asthma and have been prescribed prednisone several times for it. Every time i take it i break out in an awful acne looking rash all over my arms and my chest and sometimes even my face. it doesn't start until about 3 days after i have started the medicine and it doesn't go away for about 2 weeks and it itches the whole time. I told my doctors that every time they would try to prescribe it and they did not believe me they said no one could be allergic to prednisone but it has happened to me 6 times now and it has never happened before i had prednisone or on many other medicine since then.i finally got them to switch the steroid to a different kind but every kind seems to do it. i had to refuse steroids the last time i was in the hospital for my asthma they just would not accept that i could not take the medicine.

I am a healthy female with little to no history of adverse reactions to medications. I was prescribed a 10 day dose of Levequin (500 mg) for a minor but stubborn skin abscess. After the third day, I woke up with significant joint soreness in my fingers. Progressively the soreness spread daily to my wrists, elbows, ankles, knees, hips, etc. I did not suspect the antibiotic at first, but I know my body, and I know something was WRONG.
After my 8th dose I decided to look online...it is at least good to know that what I'm experiencing is definitely from Levequin. Thank you all for sharing your stories.

I especially found MERCEDESLANE posting on April 15th interesting. I guess this person works in the health care system. Considering this uncompassionate individual, who apparently wants everythone to know he has a Mercedes, can't spell (whine), and does not have basic grammar skills. Wow...my faith in the our health care system is stronger than ever. But what do I know, I'm just an "IDIOT" with shingles that needs to have a couple of glasses of whine while I pop my remaining Levequin.