Cortisone symptoms and conditions

On Sept. 2, 2009 I had a cortisone shot in my back for L4, L5, C1 disc problems. The shot was painful but brief and I went out of there with no particular symptoms. It was done in a hospital by a neurologist. On Sept. 4th I woke up and the whole room was spinning. I threw up and this continued for awhile. I could hardly stand and went to the hospital emergency room where I spent the next twelve hours getting all kinds of tests. My blood pressure was 185 over 110. Finally, they told me they could find nothing physically wrong and dismissed me with meclizine for dizziness. This is now Oct.27th and I had these vertigo symptoms for seven weeks! I was sent to an ear specialist and underwent vesicular therapy for benign position vertigo several times a week at a rehabilitation center. I had brain MRI and a neck MRA which showed nothing. Last Saturday I passed out for a few seconds. Every medical specialist insists that the Cortisone shot had nothing to do with all this but I am still undiagnosed. Yesterday (Oct. 26th) the dizziness ended (7 weeks). I don't know if it is gone for good. I cannot believe that it is just a coincidence that all this happened two days after the cortizone shot. Does this strike a bell with any of you?

I had that Kenalog and it's been a total nightmare...My doctor Dermatologist injected into my two index fingers on each hand. The itching has been insurmountable and absolutely horrible....I haven't been able to sleep, wash dishes, do anything with my hands....I am telling you I am about to go out of my mind. I went back to her..and now she put me on Prednisone and Singular...now I am reading the side effects of Singular. She never told me what type of shot she was giving me for the pains in my hands that i was getting. I have had cortisone shots for joint pain before...for I figured that what it was that she was giving me...later to find out it was this damn Kenalog. I would have never agreed to such a thing until I had looked up the side effects. This has been a night mare completely...

The itching is so bad, that I have broken the skin, I have a rash completely on both fingers. It so sad...and she's charged me a fortune for it too, and the second time I had to come back for help. What the hell is wrong with people..?

DON'T TAKE THIS DRUG...UNLESS YOU DO CAREFUL CONSIDERATION..!!!PLEASE

ive been on prednisone and cortisone..2 doses i woke up and couldn't move my legs at all. the more i walked the more it hurt..the more i sat the worse it was to stand up and walk..idk what to do..i have to take this for the rest of my life..its just terrible to move.and my doctor wont be around for 3 days.

I have been taking Lipitor for about 6 years suddenly developed a rash on my shoulders and chest. My doctor diagnosed SCABIES!!so I treated myself for that then the rash progressed so I had a biopsy done and after 3 months of agony my slin specialist had taken me off Lipitor as theh test showed a reaction to a drug. I am still itchy prickly and burning on arms legs and hands and cannot tolerate cortisone cream so am on tablets for a week..can anyone relate to this condition? My scalp is also very dry and scaly.

I was on prednisone for 1 year for chronic pericarditis, finally weaned off and no problem with my heart since. It now been 5 month and I now have chronic shoulder and foot pain, I've read that it can take up to a year for your body to adjust and produce the correct levels of cortisone, I'm taking voltaren when the pain is too much, I feel like a 75 year old in the morning and I'm only 48. I feel so sorry for everyone who has had issues as well.

I started feeling much better very quickly after being off Lipitor now 7 months. However, the symptoms I had using the RX has cause significant problems. I fell so many times with my weak joints and muscles, that I had severe problems. I now need to have knee replacement surgery after falling so many times injuring my knees and weakened muscles to support myself. I am getting cortisone shots in that knee, as well as physical therapy. My MRI shows a torn meniscus, stretch PCL very thin, cartlidge loss and debris, still swollen with csyt after all these months. With no meds, and lack of being able to exercise, I now have hig-chol back. On and on it goes.... a real catch 22. Take care of yourself, watch out for symptoms. I ignored sx's thinking it was stress but after reading adverse reactions, it fit me to the T.
My original posting re: Lipitor is Forestseaski on Jan. 2, 2009

C.

I am a 48 year old woman, 5'1" (now 145 pounds). I had Mirena inserted almost exactly 5 years ago, and am scheduled to have it removed in 2 weeks. I gained 25 pounds over the course of the last three years; prior to that, my maximum weight for my whole (non pregnant) life was 123 (I was at 120 when Mirena was inserted, four years after the birth of my second child). I have always been very healthy, never abnormal blood tests except during my two pregnancies was tested as pre-gestational diabetic and had to watch my carbs.

I never put it together with Mirena until just recently, when I started doing research on hypothyroidism after a friend told me that my symptoms could be due to that problem. Depression, hair loss, acne on my back, and the terrible weight gain. I went to see my G.P. who referred me for blood work. I hoped to see evidence of low thyroid function (actual TSH value, 3.12 -- I was told this is normal on a range of .4 to 4.5). I also discovered that I now have high cholesterol (269 triglycerides, 251 total cholesterol, 46 HDL, and 151 LDL). My fasting (14 hours) glucose # is 99 (I was told this is normal on a range of 65-99 mg/dL), and my vitamin D, 25-OH is 21 (also was told this is still normal but low on a range of 20-100 ng/mL). I tried to give blood six months ago, and was turned down because of anemia, so I've been eating a lot of spinach, greens, and more red meat than I normally would, so I was interested to see if I am still anemic -- the red blood cell count is 3.8 (told it was normal on a range of 3.8-5.1 mill/uL). I mention these specific results because although I was told they were normal (except for cholesterol), when I physically went to the doctor's office and requested a copy of the results and did some research online I see that my thyroid IS actually low-functioning -- according to guidelines revised six years ago, anything over 3.0 is considered hypothyroid and should be treated. Plus, isn't a fasting glucose of 99 pretty high? Yet my doctor's only suggestion: diet and exercise. Good grief, I've been on a diet since I had my first child, 13 years ago. True, I don't exercise regularly (I'm a teacher and mom of 2; I never seem to have the me time.) I guess I have an excuse to get a gym membership now.

Also, for the last year I've had increasing pain in my shoulder (I couldn't lay on my side, for example, and lately I can't reach behind me or over my head). An x-ray turned up mild bone degeneration, but not enough to cause the pain I've been having. I was referred to an orthopedist, who today diagnosed a shoulder rotator cuff injury (I've had no injury; he says it is a common degenerative complaint in the over-40 crowd). He gave me a cortisone injection and I'll be on PT for a while to see if the pain goes away. If not, I'll have to have an MRI and surgery to correct the tear.

I'm posting all of this in case it might be useful to someone out there who might be going through the same thing. I had a thyroid test done about six years ago at my OB/GYN, and it was normal then (though I don't have the number; I'll get it in 2 weeks at the OB/GYN). It will be interesting to learn whether my thyroid level has gone up since Mirena. Also, although my research suggests that the effects of these synthetic hormones do not wear off for some time, possibly even years, I will finally feel like there may be hope if my symptoms improve over the next few months when Mirena is gone. If so, I will share it with you.

If you are reading this, perhaps you have a similar story. I wish I had been more aggressive about checking out the possible causes of my many symptoms, but I let them go for years because, I guess, I just figured I'm a healthy woman who is no longer young. (Oh, one more thing: for the first year or even two years that I had Mirena, I had incredibly heavy periods. The blood flow was similar to that during the day or two after the vaginal births of my daughters. Don't know if that's significant, but it took a couple of years for my periods to get fairly normal on Mirena.)

I have read the posts below and thank goodness I found this site! I got an injection on Wednesday, 6/17, in my right knee and for the first 24 hours it hurt like heck - more stiff and painful than prior to the injection. On Friday I woke up shaky and started to feel anxious. My face and chest flushed a bright red which lasted all day. Saturday was worse; shaky, heart racing or palpitating, head/neck pressure with headache, hot flashes, nausea and stomach cramping/pain. I even actually had a panic attack (already a predisposition for me). I became uncontrollably weepy and depressed! Today, Sunday, I STILL have major anxiety and headache/pressure. I'm convinced the injection brought all of this on because before this, all I had was knee pain. So, WHEN will these icky symptoms start to subside? I was told the cortisone was good for 4-6 months. I can't live feeling like this everyday for that long!!! Any suggestions or encouragement?

I started off taking Tenormin 50 mg 1 x a day and Lanoxin 25 mg 1 x a day about 21 years ago. I continued to have constant palps and skipped beats even though I was on these meds. I wound up developing vertigo after about 5 years that got so bad I had it daily. I ended up with severe sinus problems and was given a cortisone packet of pills (the kind that decrease each day you take them) to take. The vertigo left for 6 months, coming back again with a vengeance. I begged the docs to put me back on cortisone pills again, once more helping to stop the vertigo. However, at the same time I also stopped the Lanoxin. ??? I totally believe that Lanoxin was part of the problem causing the vertigo. I now only have it from time to time, maybe only a few times a year. I still blame the Toprol that I now take for the left-over vertigo. I was taken off of the Tenormin after about 10 years of taking it and put on the Toprol at that time and have been on the Toprol xl for the last 11 years. The docs said that I needed to be on Toprol XL, as it was an extended release and would help me much more around the clock. I did not notice much difference throughout the switch, but looking back I do believe that a lot of the things that I have been dealing with through the years are side-effects of the medicines. I have had irritable bowel syndrome, told I have fybromyalgia, then told I did not have fybromyalgia, hip and back pain, skin problems on one of my hands that started with the Toprol, headaches, tiredness, horrible weight-gain (without overeating!! Honestly.), I have averaged 5 lbs. a year and the docs never even listen to me when I voice my concerns, I have been diagnosed with anxiety, joints ache, ankels, feet, face and hands swell, stomach bloats something terrible, acid reflux, hiatial hernia, and I had a tumor removed that could have been a problem off my rectum (who knows what caused it), I have had CTs and MRIs of my head, twice, for the vertigo and what I was told was probably psuedo-tumor cerbri (because of months of severe headaches), told by my eye doctor that he wonders if I have beginning MS, everything came back fine and things seem to resolve and go into something else. I have been passed from my general physician, to a cardiologist, to a ENT, and a neurologist. No one can ever find anything physically wrong, but they did conclude that I definitely had benign positional vertigo. LOL, that means they could not tell me why I had it. I put a stop to testing when they wanted to do the spinal taps.

Now I am experiencing tightness around my lower rib-cage and feel as though I am sucking for breath, I have a terrible time falling asleep at night, I wake up gasping and swearing that I am dying. My rib-cage is numb around my right side, not so much the left side when I lay down to go to sleep at night. After a few bouts of this I finally fall asleep and sleep all night most times. My blood pressure is now on the rise 150/99 at the highest. I have been working out lately with a few positive effects, more energy, more endurance, less aches and pains, muscles are starting to tone up, however, no weight loss. I thought my bp was starting to lower, but found out it was actually up. I went to my family doc and she listened to me really good, realized at last that I was not shedding the weight despite the efforts I was making. She cut my toprol to 25 mg 1 x a day and put me on lisinopril, I did not tolerate the lisinopril so she switched me to dyazide, lowest dose 1 x a day. I have great positives ...no more swelling, weight loss, lower bp, HOWEVER, I am now having jitters, anxiety (somewhat), no appetite at all, a few muscle spasms in my arms and legs, nothing painful or severe, dizziness, slight headache that comes and goes especially through my eyes. I am also experiencing coughing, and raspiness...but I am also coming out of a bout of bronchitis, which got really bad with the lisinopril. I believe it is partly due to the meds.

I called my doc today to tell her about the twitching and buzzing feeling and to ask about the dyazide. My feelings are that I am experiencing a lot of different things, first the bronchitis, and all the meds I was taking for that...albuterol, musinex, tylenol w/codeine, and biaxin, then the decrease of my toprol xl, the bad effects of lisinopril (coughing and raspiness), and now starting the new drug dyazide (generic form). I really want this to all settle down and work out for the best, but it is getting to me now (after 2 weeks). Last Saturday I would up in the ER with shooting pains through my chest that left me very pale and lightheaded when it happened as well as very tight throug my chest and sucking for air. The ER did chest xray, chest CT w/contrast, bloodtests, urine test, bp's sitting, standing and lying down (it is highest while sitting), everything came back good. No heart attacks, no blood clots, no bronchitis anymore, nothing. Blood work was good, urine was good. I am beginning to think that perhaps my body is reacting to cutting the Toprol xl in half. Sort of a withdrawal. There is really nothing else it can be and I really don't think that the dyazide is that bad of a drug and probably not causing all of my problems now, maybe just a part. Which are the tingling, dizziness, anxiety, twitching, and coughing. I have only had 3 of the dyazide medication. But have read that withdrawal symptoms of Toprol can cause these problems for a while. I am also thinking that the shooting chest pains last week were also withdrawal of the Toprol as it had been 1 week at that point that it had been cut in half.

Any opinions, if anyone can make heads or tails of anything that I have wrote. Sorry for the length and if it is confusing.

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

I was given Levaquin on February 14, 2001 for a sinus infection. I had taken a Claritin ready tab before I took the Levaquin. Within 5 minutes of taking Levaquin, I literally felt as if ants were crawling all over the inside of my skin. I was in the bathroom when this happened and I remember that I started to sneeze non-stop. It got to the point that every time I sneezed, I could feel my throat closing and blood would come out of my nose. I knew I was in trouble. I didn't have time to wait for an ambulance and my mom, who has epilepsy and doesn't drive went with me to the ER. By the time I got there, 5 min drive away from my house, I was covered in huge hives. My hands, feet and face were also blue and I couldn't speak! I had gotten there just in time. I got 3 shots of antihistamine (benadryl) and 3 of hydro cortisone. My doctor was in disbelief when I went to see him the next day to tell him what had happened. Apparently my reaction was "rare", but by the other stories on this page-I don't think it is. It was a horrible experience going into Anaphylaxis shock. I now watch everything that is an RX and ask a lot of questions. I found out a few years later that I was also allergic to sulfa based drugs, almost the same reaction (not as severe) but I was ready and I knew what to do. Thank God for Benadryl!!!

Wow, who should I believe? Placebo controlled studies which suggest Avelox is a perfectly safe drug or a bunch of crazy people who like to TYPE every OTHER word IN all CAPS who are probably all middle aged women with psychological problems and/or fibromyalgia, irritable bowel syndrome, or other made up diagnoses.

Here's a hint morons: The reason why every drug in existence now lists every possible side effect is because of crazies like you. This way, the drug company can protect themselves from litigious idiots like the poster below who wants to join a class action lawsuit. This only compounds the problem, though, because then more crazies look at the side effect profile and when they see that "Oh my gosh, it says right here it causes x, y, and z" it just validates in there mind that this is somehow a dangerous drug.

I swear, if all of the pampered babies in this country were put to work in a rice field in Cambodia, there would be a lot less nonsense in the world. You would see what true pain and suffering is about.

My Mom was prescribed Levofloxacin ( AKA Levaquin) by her retarded doc for a mild cold and a sore throat.
After taking 2 tablets of 500mg each my mom is down is severe pain all over her body! she has joint pains, neck pain, arms, palms shes got severe pain all over her body!
She also has severe itching on the palms and her arms as well..
Headaches,
Things aren't looking good.

She in real pain! She tells me she just wants the pain to stop and that she was better off with the cold and sore throat.

She has stopped taking Levaquin.

Anyone got anyway to help her? something?? She is asleep now but tmr Im going to ask her to drink some kefir..

Thanks

I have been taking 40mg lipitor for over 9 years now.

I have had back issues since an injury to one disc (L4?), and had microdiscectomy in 2001? Took about two years to actually get close to normal.

The last few years, I have had multiple issues with shoulder pain, wrist pain, elbow pain, lower back pain, Upper rump muscle pain , and now both hips are killing me (the shoulder, upper rump muscles and hips are by far the worst). And I am now so weak in my lower back muscles, that it feels like I will (and do) pull out my back.

I have seen NO many doctors I can't even name them all. I have had operations, multiple injections (cortisone) taken pain meds, etc. Nothing has helped and in the last year and a half, I have gotten steadily worse. To the point where I can't really do much of any activity. Sleeping at night is painful. Can't lie on left shoulder, and can't lie on either hip for more than a few minutes. If I fall asleep on my side, the pain wakes me up. When I try to walk, 80% of the time, I end up with a pain in my upper right rump (sacroiliac area), that I MUST sit down to get the intense pain to go away, which it does. But comes right back when I walk again.

I have had x-rays, MRIs etc, and never reveals all that much. Disc issues, yes. NOt much else.

Recently, I have begun to get a nasty clicking (catching) on my left jaw (joint?). Not really painful, but something definitely wrong. My dentist sent me to his Chiro. I went and liked him right away. I had gone to another chiro for years and I believe in them. But this one is the best I have seen.

Anyway, one of the FIRST things he suggested, was that it was POSSIBLE that the Lipitor is causing all of my problems. Put me on COQ10, and doing multiple adjustments and treatments. I will be seeing my regular doctor 5/26, and my chiro wants me to see if he will take me off lipitor and put me on Niaspan instead.

I guess my question is: Can Lipitor be fine with me for so long, and then in such a short period of time, turn me into a compete wreck from the pain and wasting away of my body/muscles? I've told doctors for over a year now that there is SOME connection as to all these issues and pain. One Doctor, of course, gave me the "you are getting old" bull. Yes, I am 56 yrs old. But I understand the process of getting old, vs the complete failing of ones body.

Also, IF it is the Lipitor, can it possible all go away? Or should I expect some damage forever?

One more thing, the last ortho I went to the other day for a second opinion, wants me to do a EMG, to see if there is muscle damage. I was not planning on doing it, but wonder now, should I? He was not doing it because of lipitor, as he never even talked about that to me. I had shoulder operation and have not had the results I feel I should have had.

Hi everybody. I just happened to stumble upon this website. Today is my birthday and I'm home because of a new medication regime to counter act my terrible side effect from Bactrim. Last Saturday I went to the Emergency Room and found out I had a bladder infection, so the Doc prescribes this crap to me. I thought I was having a heat rash from being out in the sun too long (oh by the way, exposure to sun for a longtime is a big NO NO when on Bactrim). It started on a Sunday afternoon, fine little clustered prickly bumps all over my chest. THEN it began to spread on my back. THEN to my FACE! My shoulders, upper arms, forearms, back of my hands, thighs and knees....etc,etc, LOL EXCEPT for my pubic area, thank God! All of this progressed from Sunday night and finally ended up all over my body by Wednesday. The itching was unbearable. I tried everything from the Caladryl, Benedryl, Cortaid, Dermaplast, and absolutely nothing relieved me for more than 10 minutes. I finally went back to the ER when I realized I wasn't getting any better from my intial infection, because now I was running a temp of 100.3 degrees AND my lymph nodes in my groin had swollen to the size of walnuts. Talk about painful! After all that time taking that "poison." Okay, after for hours of waiting in the Lobby, being stared at while scratching and suffering the whole time, I finally went back into ED only to receive my first and most PAINFUL cortisone shot ever in the history of mankind., which did nothing for me but make my leg go numb. I also received Zantac (an acid reflux/heartburn med, I mean, WTF) and some Hydrocortisone pills? or something of that nature and I was on my way with four new prescriptions. Methylprednisolone (steroids! can we say weight gain and hirsutism) Hydroxyzine for itching (works a little, but still itching like hell), Ciprofloxacin I guess to knock out the rest of my infection, and Cimetidine aka Tagamet, which I don't know why heartburn medication is prescribed for me for a rash. Oh well, thats about it. All I've been able to do since is sleep, take meds, sleep, wake up, take meds etc. No new side effects..yet. What an ordeal, from taking one med for one problem to taking 4 new ones for this horrible rash. If you're ever in the southeastern region of N.C. don't ever go to South Eastern Regional Medical Center unless you feel as you're about to die (which if you do go, hell, you might just finish killing you) Sorry this was so long, but this was a very traumatic experience for me.

have been taking 20mg for about two weeks. a couple days after i started taking the stuff i started experiencing chest pains at night that would wake me up, coupled with leg pain. it's getting worse; now, after two weeks i am having severe lower back pain that radiates down both legs, similar to sciatica, happens at night but continues throughout the day. also leg spasms at night. i am stopping zocor today. can't face this pain anymore. i have bad knees, and recently had to have a cortisone injection, but this new pain is worse than the knees. owing to the chest pains, i had a stress test today at the heart group, and had such difficulty walking that i could barely make it down the hall with my cane. three of the nurses there said they hear this all the time about the statins, and that the doctors don't want to listen to the complaints but the nurses all agreed that the statins are the culprits. results on stress test were fine.

My 15-year-old daughter experienced alopecia (bald patches) after the first injection. We didn't initially connect it to the vaccine. Then, after the second shot, her thick long hair thinned significantly. She will NOT be getting the third injection Gardasil is poison. Anyone else who has experienced hair loss, please post a comment with information on how long it took to come back. She cries daily about this and it breaks my heart.

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

every time I have a cortisone shot, I get horrible body aches all over in joints and muscles and headache.It happens every time. My grandmother had the same thing. I thought everyone had this. I had the injection in my knee today and then went shopping. 5 hours later, I was aching so bad, I had to go to bed. Tylenol doesn't touch it. I hate cortisone shots. I was really disparate when I agreed to this one. The shot didn't hurt much as they used the freezing thing. The doc is an orthopedic doc and he is good. He replaced my hip and it is wonderful and quicker recovery than my first one on the other side. Next we do the synvisc shots, He already tried the meniscus surgery. We are just trying to postpone replacement as I am only 58.

I have coronary atery disease, have had one drug coated stent in my main atery and am on plavix and asprin. Had a shot of cortisone into my left shoulder yesterday (without lidocaine); pain was immense and was a shock
to my system; Immediately afterwards, I became pale, faint, and broke out
in sweat. Had to lay down on an exam table to keep from passing out. After a few minutes of lying still and being fanned by a nurse, I regained composure to leave. For the remainder of the day, my skin was pale grey, and I generally did not feel well. It was not until later that night, after two our three hours of rest, did i recover. From that point on, I had the typical restless night with limited sleep, and face began to turn red. I have never had a reaction to cortisone, and don't know if that is what occurred, but I would be curious if anyone else has had this same side affect.

I have been getting the cortisone shots on and off for about a year now, basically, whenever my ankle flares up. I had one earlier today (or yesterday as it may be), and now here I am at 2:45 am, deathly tired, but with my mind so active I cannot sleep. I noticed the same thing after an injection a couple of weeks ago. I can't believe I never noticed it before. I have always had the woozy/loopy feeling afterward, afraid to drive home, but thankful I live less than a mile from the doctor's office. This is usually followed by a day of nausea and other side effects. It's weird, though. The websites with info on this drug don't talk about the nausea, the dizziness, the "feeling out of it", the headaches. Only that the pain is worse before it is better (definitely true!). But do the docs not know about this or are they just turning a blind eye? I keep reading that such side effects aren't possible because cortisone occurs naturally in the body. But the stuff they are injecting us with is not produced by ur bodies. It is synthetic, and being that we are not producing the dose naturally, it is very likely overload. So, how can there not be side effects?

Had injection 2 pm today immediately had head spins like I was off my face (I am a 45 yo mum so no drugs here) heart racing very dizzy and hearing was distorted. Told doctor he was not concerned. I have had injections before and have experienced the burning skin sensation rashes and tummy aches and cramps. I try to hold off for months on getting another but the pain in my shoulder is so bad I have to eventually. ATM my shoulder pain has intensified 10 fold although eventually I will be pain free in a week or so this should last up to 3 months. I will be able to sleep better which I desperately need as I shift work and have a young family.

Was prescribed Cephalexin in the ER after stitches. Took it 4x a day for 5 days. After completed, I developed a rash all over my body -- I have been itching for 4 days now with no relief. Tried Benadryl, Claritin, Zyrtec, Cortisone cream and Calamine lotin. No relief in sight-- I will never take this antibiotic again.

A few years back I severely injured my back. As part of my treatment my doctor gave me prednisone. My joints, especially my knees hurt beyond belief. I even had go to my parents house because I couldn't move, it hurt too much. I called my doctor and you know what he told me?!?! it was all in my head.He accused me of trying to get pain pills from him. The joint pain got so bad that I had to be hospitalized. You know what they told me at the hospital. I was having a allergic reaction to prednisone. No S***t!??! anyway, since that time I have not taken prednisone. My concern now is that my doctor wants me to get a cortisone injection. . . I am scared I would get the same reaction. from the research I have done so far, it looks like it is from the same family. Does anybody know?

Thanks
B.

Received my very first Cortisone injection on March 24th,2009. Immediately felt weak and shakey. Anxious. Called MD office and they told me to eat something. This did help for awhile. On March 25th woke up feeling great. No knee pain. Knee stiffness gone. About 24 hours after receiving injection, my face became flaming hot with redness to follow. Some swelling to my left cheek. Anxious. Feeling like I want to cry. Fingers feel strange. Some nausea. Not eating great now. Ears feel plugged. Slight headache. Just took some Benadryl. Am applying ice to my face and lotion to prevent all the dryness from the heat radiating off it!
Don't think I'll be getting a second knee done. I'd rather be in pain. KJ