Inflamation symptoms and conditions

I used prednisone for sinus inflammation and it gave me bad side effects such as: irregular heartbeat and stomach upset and anxiety. It actually did help with the inflammation but I stopped using it because of the side effects. It made my lip puff out too, which i did not mind because i have small lips and i looked better with a bigger lip, lol! I am thin so if it made me swollen i did not care because i need to gain weight, i am only 105 lbs. I just started taking methylprednisolone tablets packet and they seem to work better and if it causes increased appetite that would be good for me because i lost so much weight because of my teeth and sinus pain i had everyday for four months. So far it is working but i just started it and will keep you posted. It does seem milder than plain prednisone I suggest you switch to this if the prednisone is not working for you. It sounds like most people are on too high of a dosage and take with food and a lot of water. Hope everyone feels better soon.

I was on Prednisone 10 mg. per day for sinus inflammation which helped with that but gave me some bad side effects such as: loss of appetite, fast heartbeat and the worst being nervousness, anxiety, and nausea. I got rid of my pain but the side effects, ugghh!! I am not going to take it anymore. There are other things to take for inflammation.

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?

They think that I have either crohns or ulcerative colitis. I have tried antibiotics, lialda, mesalamine enemas, with no improvement. After another colonoscopy they put me on prednisone at 40mgs, 30, 20, 10, then 5 decreasing weekly. Well the first week was okay. I had some of the side affects, insomnia, extreme hunger, and crazy. I could deal with that. But then when I decreased down to 30mg, my body flipped. I awoke from the middle of the night with burning pain in the knees. So bad I took 4 ibuprofen and threw myself in the tub with epsom salt. I thought okay that was weird because I have never had a joint pain in my life. I saw the gastroenterologist that day bc I was still having abdominal pain. He totally blew off the knee pain and said he had no idea what that was. I thought okay maybe it will go away. A few days went by and nothing. 3 days later and I awoke one morning crying in pain because of my legs. I called the on call doctor who also said he had no idea and go to the er. So I went crying hysterically for 4 hours. Even after 3 rounds of dilaudid I was still in pain. They suggested a Rheumatologist. So I went to one a week later who said I was going through steroid withdrawals. And there is nothing we can do but treat the symptoms of pain. I am now down to 10mgs have been out of work for 2 weeks and am absolutely miserable with severe leg pain, muscle weakness and fatigue. He also adjusted the drop down increments to 5 instead of 10. Anyway I will never take this drug again and I think they rushed to this one. Just wanted to share. I am glad I found this website because I went from a fully functioning physically fit 28 year old to a crippled crying crazy person. I think I was scaring my husband, honestly, until we both read some of your postings which were similar.

My mother, who is in her early 70's, is diabetic and had high cholesterol. She had been taking Lipitor and the doctor increased her dosage. She was experiencing muscle pain for some time, especially when she woke in the morning. The muscle pain worsened and her muscles became very weak. She had been complaining to her doctor for some time. It took a chiropractor to suggest it was the Lipitor. Her doctor finally ordered blood work and her enzyme levels were at 9500. She was immediately hospitalized, tests run and IV's given to flush the Lipitor from her system. She was expected to slowly recover. After weeks, her levels dropped to 6500 then began to rise. Her doctor now says her muscle damage is permanent and plans to give her prednisone to stop the inflammation. This muscle damage is a terrible "side effect" for a drug that was supposed to help her. She can hardly get up or down from a sitting or lying position, can hardly walk and her lifestyle has been severely curtailed. She is also exhausted all the time.

16 days ago on Jan 17, 2009 by chris555, #16131
Sorry to disappoint you, but I have no vested interest in Merck or any other pharmaceutical company for that matter. What I have a vested interest in is providing some balance to those parents who come to this blog site and are scared to death. That is what happened to a very good friend of mine. After reading the posts here, she was so panicked she took her 12 year old off Singulair. A kid who had no problems on it by the way. A few days later my friends kid was rushed to the ER and almost died from an asthma attack. That is what I have a problem with. People here telling others the side effects will creep up, that kids should stop their medication right away, etc.

Reply 8 minutes ago on Feb 03, 2009 by concernedcitizen, #16701
To chris555:

Merck warns on it's Singulair website that Singulair is not an effective replacement for fast acting inhalers in the event of sudden symptoms. Originally when Singulair was developed it's purpose was to prevent damage and inflammation that is caused by excessive number of eosinophils in respiratory tissue. There is no evidence at all that Singulair is effective as the only treatment for asthma to prevent or treat acute asthma attacks. And, Merck makes this very clear in the warning notice.

The efficacy and safety of Singulair has a genetic component. That means that it is entirely possible that some people are not compatible with the way in which Singulair works. Adverse side effects are very possibly the result of compatibility problems.

Sadly, Merck has succumbed to the disease of "corporate greed." Meaning that they care more about profitability and the shareholders than they do about the patients. For this callousness, some day this corporation will suffer the punishment. Merck has always known that the cysLT1 receptor is a gene with more than several variations. If they told doctors to watch out for side effects due to genetic variations, then they wouldn't be able to sell this drug like it's harmless - cherry chewable - candy. The adverse side effects are real. Patients started reporting them immediately when the drug was released. Singulair is dangerous to people with gene variations and it causes unnatural biochemical events to take place.

IMPORTANT SAFETY INFORMATION
SINGULAIR will NOT replace fast-acting inhalers for sudden symptoms. You should still have rescue medication available and continue to take your other asthma medications unless your doctor tells you to stop.

To get the real information in regards to what level of research that is going into this investigation is.go to the Institute for Safe medicine practices click on Quarter watch.
To people like chris555, I believe you are engaging people for sport and say very hurtful things,your day will come and it may just be in the unemployment line.I can only imagine that you must work for Merck or you would not feel so threatened by the good that has come from Parents advocating for their childrens safety.I want you to know, that all who knew our family and our child understand what took place and our reasons for trying to get the proper information where it should have been," on the label". When our child died no one knew about all the added side effects from post marketing reports,which is "a reliable way to track a drugs adverse events".Maybe you should do more research on the legitimate information of causal relationship. Don't be so afraid of a possible drop in revenue for the drug company that I believe you might be an employee of.K. M.

My daughter was 16 when her GYN started her on Yaz. She was 5 ft 3 and 100 lbs. Non smoker. No risks. She went on the pill because she was having heart palpitations and extreme fatigue that correlated with her menstrual cycle. The idea was to level her hormones and see if that would level off the physical problems. Within 6 weeks she suffered from a pulmonary embolism. Because she was young, everybody though it was just pneumonia or inflammation of the lining of the lungs (pleurisy). Then her leg swelled up and turned blue from a clot (DVT). I found it fascinating that everybody at the first hospital, during the helicopter ride and at the second hospital all had EXACTLY the same reaction . . . They all said, "you just started taking the pill, didn't you? Probably one of the new ones like Yaz." Apparently, these new 'third generation' pills are worse than the old ones when it comes to clots. It turns out that my hubby's history of blood clots should have been a clue that my daughter has a common clotting disorder and YAZ triggered it into action. The clotting disorder affects up to 10% of Swedes and that is where my hubby's family comes from. Up to 5% of all Caucasians in the United States have Factor V Leiden as well. I notified the FDA and highly encourage everybody else to do so as well. The doctor are not required to file a report unless a patient dies. My daughter is doing better now. If any reporters are reading this, please contact me. B. A. ***** If you have ANY family history of problems that might be due to clots, avoid the third generation pills.

I was given a shot in I think January of 2008, not knowing exactly what it was, because I had a fever and the doctor said it would jump start my recovery. At first there seemed to be no problem with the injection site and I felt great just days after.

A couple of months later, when I was working out and losing weight and keeping a very close eye on my body because of it. Suddenly, I noticed that I had a deep indentation and discoloration on the left side of my lower back - right where they gave me the shot. It seemed like it appeared over night. It got deeper, and darker as time passed.. I was scared to press my finger in it because when I did, it just kept going in..as if there was no fat OR muscle in that spot.. I was FREAKED out. I'm a model so this fact that there was a bottomless whole in my lower back was devastating. I also feared that there may be something life threatening going on. I mean, a chunk of you just doesn't disappear overnight..Unless someone stole your kidney, but, I didn't wake up in a bath tub full of ice.

I typed in "Injection that causes Indentation in the lower back" and I found this board. Everyone here suffered the same exact symptoms from this shot and worse. I was certain that it had to be Kenalog. It seemed to cause death of all tissue at the injection site, depression, lethargy, moodiness, insomnia, pain and all sorts of other symptoms after this shot. I started to suffer from all of them soon after the shot and I didn't really know why or where it came from. I was in so much pain and was so tired.. I stopped doing everything I loved and I could barely sleep because of the pain.

I don't know what to do about this. I'm extremely broke and I don't have health insurance(and they wouldn't fix anything considered to them as "cosmetic" anyways).. My parents are in no position to help me anymore and I could never afford an attorney to try to claim against this.

How can I go about fixing this with no money? Is there any way to fix this to begin with?

Any advice, insight or experiences would be GREATLY appreciated!

I would just like to say that I was prescribed Prednisone for inflammation. I know that some medications are used for different conditions but felt the need to comment due to the instructions I was given while on this medication. I had a total of 15 20mg pills and was to take 3 per day for 5 days. The doctor stated that it was very important not to take more then the above dose for my condition because it would be possible to shut down the " the steroid making system" thats already in our body. So be careful with this one all. This medication made me extremely sick to my stomach as well.

Thank God for each and every one of you'll who posted!! I am a 31 year old female who has consumed this poison since March 08. My PCP had started me on the Lisinopril 40mg and eventually increased it to 80mg per day.
OCTOBER 2008-
I begin having "flu like" symptoms which I started taking over the counter medicine for.

NOVEMBER 2008-
I was becoming worst so I went to my doctor (the one who prescribed this mess) and was told it sounds like bronchitis so she prescribed a "z-pack" (which is a 5 day course), "cough syrup", and stated to "quit smoking".

FIVE DAYS LATER-
I went back to my doctor with the same complaint chronic cough and now shortness of breath. I was told that since the "z-pac" didn't work it may be "asthma"!! SO of course I was prescribed more drugs one being one called "Augmentin" (which is a 10 day course), and an inhaler now for asthma!! I was ordered to have a "chest x-ray", and another script for more cough syrup with codeine!!!!

SEVEN DAYS LATER I WAS IN THE ER-
I felt as if I was dying! I was so scared and did not know what to do. I couldn't even go to work all I could do was cough, gag (sometimes vomit), and gasp for air!! I knew something was terribly wrong. The chest x-ray was clear other then a small amount of inflammation. I was prescribed yet more pills this time a 5 day course of "steroids" for the inflammation, more cough syrup, and was told I didn't need the inhaler!!!

1 WEEK LATER IM STILL COUGHING-
I was beginning to think that this condition was smoke related and begin to feel depressed as if my life was over. I decided to quit smoking as of 12/19/08, however the gagging cough and shortness of breath is still present.

I GOT A 3RD OPINION
I went to an internal medicine doctor (just 6 days ago) who stated that it appeared to be the Lisinopril the whole time and to stop taking it immediately. I was prescribed a medication called "Diltiazem" generic for " Tiazac" but the insert mentions cough as a possible side effect for this medicine as well. I am to weak, broke, and cautious to take another one so quickly. I'm still coughing as I type this!! I think I will just stick to my fluid pill and a better way of living before I continue to put this stuff in my body. To sum up this whole coughy blog, please, please think twice before taking this or any other medicine, trust me it will save you a lot of health problems and medical bills. And finally if your doctor wont listen, don't hesitate to get a 2ND OR EVEN 3RD OPINION IF NEEDED!!!!!

I had been taking singulair for over two years. I am 70 yrs old and in good health except for light asthma, allergy problems. My doctor took me off it. It did some good in the beginning but the last four mts I was continuing to get wheezing and bronchitis infections. I also had a lot of leg pain and was tested for all kinds of blockage, etc. I experienced very painful leg cramping, toes twitching, etc. The only way I could stop it was to pull my toes forward as the worst happened at night and woke me up. I finally found Leg Cramps with Quinine an all natural homeopathic med. It worked like a charm. I didn't know that this was a side effect of Singulair. Since I am off singulair just two weeks. It was replaced with Flovent an inhaler ( 2 puffs 2 x a day to begin and then later it will be 1 puff as the inflammation gets better. It also comes in granules. I am feeling much better and now I am ready to stop Leg Cramps as I feel the singulair may have been causing the problem. While taking Singulair I also had stomach cramps with diarrhea. I will not go back on Singulair. If the cramping returns, I will definitely go back on Leg Cramps with Quinine (available in any pharmacy over the counter and very inexpensive.

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 daughter is 7 and was just put on Singular as a preventive medication for croup which she gets when she has an infection. She is not on a daily inhaler nor does she have asthma attacks at school. I asked the doctor for an alternative to the pulmicort breathing treatments b/c the prolonged use of this caused her to have dental issues (8 cavities) and he gave her singular. I am concerned of the side effects in the reviews of this medication but I need some relief for my child. She has been on the medication only 1 day is frequent urination a side effect and can it come on that quick? If there is another medication that doesn't have the side effects apparently singular has please let me know.

I made an appt. with my gyno. about six weeks ago because my period was going on for two weeks at a time. Around that time my husband noticed a dent in my butt cheek, and since then it has gotten worse. I was looking up indentation on the butt and came across this information. I JUST called my Dr. and asked them when I was in there for poison ivy what they gave me for a shot, you guessed it KENALOG 80MG. This was five months ago. The indentation is getting worse. Will it ever stop, and what kind of Dr. do I go see about this? Will my periods ever regulate?

I had one injection of Kenalog to treat anal itching. Doctor did not know how to treat it and used Kenalog as her last resort. It did not make any difference. Eventually another doctor diagnosed me with Herpes Cold Sore and treated me with Valtrex.
However, Kenalog messed up my menstrual cycle so badly and I haven't had ovulation for the last three months. What's upsetting is that my doctor knew that I was trying to get pregnant and did not inform me of such side effects. When I called the doctor later and told her what happened, she sounded very surprised and said that she had never heard of such a thing.
Doctors need to be better informed about side effects before recommending any medicine to their patients. And the lesson learned for me is to not trust doctors any more, always do research beforehand. Oh well, hopefully the ovulation will come back soon, it has been way too hard emotionally to deal with the overall situation.
Hope it's helpful.

I don't know if it was the two kenalog injections but I began to menstruate-three years post-menopause. I immediately was seen by my endocrinologist, trans-vaginal sonogram and endometrial biopsy done. i just received a call tonight informing me that a polyp was found and I will need to have a D & C. It sounds like endometrial hyperplasia and this is a very sudden onset - I had the same sonogram in February and all was fine.
I have now found out that steroids can "wreak havoc" with our hormones. I was schedule to have epidural injections of steroids for back and neck injuries. I will not have them now or ever- they are not as benign and helpful as many doctors would have you believe.

I took prednisone for 6 days ( the pack). Six the first day and five the next till day six I had one pill left. I have never experienced hair loss like this. I have a patch of hair that fell out in a circle the size of a 50 cent piece. I didn't notice it really falling out but noticed a bald spot and I freak out. I came on line to get info about this medication. This drug was ordered for me because I have severe pain in my back due to osteoarthritis, sciatica and back surgery. I was told taking this would help with the inflammation and might relieve some of the pain symptoms. Well, I think the pain would be better then the side effects that I suffer. I had loss of appetite and acne on my face. I feel dizzy and bloated. I pee all the time and seems like i visit the bathroom much more often for other reasons too. I have felt like a crazy lady and have less patience than normal. I hope that this does not last for ever. This is a small amount of the medication. I am sorry for those of you that have experienced a long period of time on this medication. I pray for you that they will find another alternative with less effects to your bodys.

I have been on Coreg for 1 year and switched to Coreg CR(time Release) for the last year. Since then, I have had bronchial inflammation that I have had to use antibiotics to recover from what starts out as a normal cold or flu. I have never had to use anything but over the counter meds in the past, and rarely got sick to begin with. This has occurred 3 times since Feb. My GP told me that this is a common side effect for this class of drugs. I work out 3 times a week and ride about 20 to 30 miles a week on my bike in addition and have had no other problems. Does this sound similar to anyone elses experiences

I'm a physician. Usually Kenalog injections can be avoided and oral steroids used like prednisone. The local dimpling effect may occur if the injection is too shallow, actually there is a temporary "disolving" of the subcutaneous tissue, the muscle and joints are not damaged. It is usually viewed as a "cosmetic" adverse effect. The Kenalog injections was primarily designed for joint injection and the kenalog or similar depo form stays active in the joint for a few weeks. All steroid medications can cause irritability and this is usually temporary for a few days. Steroids can cause muscle weakness- this is usually associated with high doses for prolonged use like being on prednisone for 3 or 4 months. Steroids can have an adverse effect on menstruation, but this is usually associated with chronic use. The most serious problems with the steroids result in bone weakness(osteoporosis) and serious damage to joints like the back and hip. Steroids can also result in weight gain, diabetes, high blood pressure and cataract formation. I don't think Kenalog is any different than other steroids such as Medrol or Prednisone in terms of the side effect profile. These are dangerous medications that can also be very helpful in saving lives and diminishing pain.

After a year of battling effects from an eye injury, an optho-neurologist finally came to the conclusion that I had orbital inflammatory psuedo tumor. I was told to take 60 mg immediately and then take 2-40mg doses (AM and early afternoon). On Friday, July 18th I took 60 mg at 6:30 p.m. and was so nauseous and barely slept. That next day I took 40mg in the morning and another 40mg around 2:30 p.m.. Although I had been, throughout the year, experiencing pain in my left eye and cheek..what I experienced by 4:00p.m. that next day was more severe than ever. I started having shooting pain and a headache so excruciating that I was in tears. (I had two children naturally).
By 10:30 I had several hours of this pain when the worst happened. The left side of my face drooped and I had difficulty speaking. By the time I got to the hospital I could not move my left arm and left leg. After five days in the hospital and every test imaginable (cat scan, MRI, EKG, etc) they ruled out all stroke, MS and anything else that would show up on these tests. During the hospital stay (although they did not cite prednisone for this event), they started tapering me off. I went from 80 to 50 in one of these days and thought I would DIE. There was no pain reliever/narcotic strong enough to take away the headache. I spent ten days tapering and prayed every day for the end. Sweating, no sleep, crying and did I mention...my headache has still NOT gone away. I have a couple of hours here and there without this pain but for the most part I have been in this hell even after my taper. The clincher is that NO ONE at the hospital or afterwards would admit that this was a side effect but they also could not provide a response. It took three weeks for me to work my way back to walking and using the left side of my body. Has anyone heard of this before? Good luck to all of you, it has meant a lot to read your comments.

I was prescribed Adderall 30mg tablets 3X's daily. Right from the beginning I found that the Adderall caused a very very annoying agitation to my throat. The only way I know how to describe the sensation is that it feels almost like I have phlemgm stuck in my throat,it causes me to almost continuously cough and gag so that I can clear my throat,but, nothing ever comes up!?? I'm wondering, could the Adderall be causing minor swelling or inflammation causing my throat to feel this way. If so, does anyone know of anything that would counteract this reaction?? I would hate to have to discontinue this medication as it helps me so much as far as staying focused. If anyone has any idea as to what I could do to make this bad reaction go away or to at least make it subside somewhat, I would be so grateful!!!!

hi i had my mirena fitted in October 1999 extremely painful as i have a tilted womb apparently, and today i am having an ultrasound scan to find it.
i have been asking my gp to have it removed for past 3 years and have been fobbed off so many times, made to feel a time waster.
problems i have had are listed below
5 stone weight gain
IBS
GERD
PANIC ATTACKS
LOSS OF LIBIDO
PAINFUL SEX
CHEST PAIN
HEADACHES
DEPRESSIVE SYMPTOMS
MUSCLE PAIN AND FATIGUE
WEAK BLADDER
BLACK HAIRS ON CHIN
POOR FACIAL SKIN
BLOATED STOMACH (IBS)
MOOD SWINGS (PMT)
COSTOCHONDRITUS(inflammation of connective muscle tissue in chest wall)
and just recently diagnosed with diabetes 3 months now
on my last diabetic nurse check i asked her if she could check my coil for me as i hadn't been able to...... she couldn't find it ?
i have pain just from sitting and feel like something is pressing on my bladder.
reason for having it fitted was my very heavy periods with 1 week in between after having my only child in june 1998.
had no periods since dec 1999, but terrible pmt and mood swings am at wits end as i am so heavy do not think general anesthetic poss if coils embedded. very worried

my doctor put me prednisone 40 mg for 9 days to treat my inflammation of my neck and shoulders. I took my last dose 5 days ago. I'm still experiencing side effects like insomnia,anxiety,nervousness,fast heart rate and upset stomach. how long will side effects .

I was taking 500mg three times a day. After 1 week I developed severe joint pain and swelling in my fingers. I got an itchy rash on the bridge of my nose and over my eyes and inside my nose. The joint pain continued to my knees and toes. I have been off of the medication 3 weeks and I am just starting to feel a little normal. a different doctor put me on 800 mg of Ibupropen 3 times a day and after reading up on the side effects of Cephalexin I began taking Benadryl which has helped a lot.