Steroids symptoms and conditions

I had Mirena put in January of this year, I am 49 years old. I did not need it for birth control as my tubes are tied. I was having very bad perimenopausal symptoms so my doctor suggested I try it for the hormones. I was still having heavy periods 8 months later. A little over two weeks ago I had a complete hysterectomy so obviously the Mirena is gone! I was and am having HORRIBLE joint pain as others have posted. I feel like I am 100 years old some days, my legs and shoulders and hips hurt the most. I read that the Mirena hormones are contained in a steroid reservoir, whatever that means,does anybody know? I have been on steroids before and this is exactly the same reaction I had, hip and joint pain so bad they had to take me off. Well anyways, I am glad it is out of my body but my question to anyone is, once you had it removed, how long did it take for the joint pain to subside????

Today is 10/28. I am Weezie1 and I posted on 10/26 about my severe drug reactions. They have gotten worse since I wrote my first post. The fever and chills are gone. But now I have been dealing with a rash/hives over all parts of my body. They are worse where close contact to sleeping clothing are - back, chest, neck. The one side of my face that I usually sleep on is purple every morning, along with that same side of my neck. I managed to get myself back to the doctor on 10/26 and am now on a 6 day dosage of steroids for the rash/hives. The steroids have stopped the hives from getting any worse. But it is taking awhile to go away. Any heat, anxiety, frustration brings them out again. I see I will be dealing with this for awhile. I go back to the doctor on 10/29 for a recheck. I lost 2 days from work because of this. My skin felt like it was on fire with hundreds of bee stings. Now I feel like I have a severe case of poison ivy. I have found some relief using Aveeno's oatmeal powder to do a bathtub soaking at night. Then I follow that with Aveeno's rich moisturizing lotion. The doctor may want me on steroids for longer than first prescribed.....not a med you want to be on for too long. All because of an UTI last week that could have been simply treated with a regular antibiotic if my doctor was not able to prescribe this sulfa drug to me on 10/19. Next time I will go with my initial gut feeling and refuse to take a medication when I see its extensive side effect list. I wish I had done so last week. I am suffering much more now than I was last week with my UTI. I filed an online complaint at the FDA's website. They mention it at their phone number that Weezie1 reported in my 10/26 posting here. I, unfortunately, expect to see additional patient complaints here every few days when I check back at this great medications site. And now I see that someone has internal bleeding. What next? A death? My blood pressure and heart rate were both increased for several days due to this drug. I could feel my heart pounding when I was sitting still and laying in bed. Thankfully, my BP is normally on the low side, but all the numbers went up by 10. We have to band together to get this crap off the market and out of the hands of doctors and unsuspecting innocent patients. Our voices will be heard if we speak in large numbers. Keep talking!Good luck to all.

Hi all, im so glad i found this site as many are too. Im 22 years old and was diagnosed with colitis at 14 and was put on 40 mg of prednisone to combat it. I can honestly say it generated the worst time in my life.. I went back to school and was overwhelmed with massive panic attacks feeling like my heart was gonna rip through my chest. Big moon face etc. I recently have had an attack and was put back on steroids its always my last last resort. I just feel very detached and anxious all the time constantly feel like im lost. I am now in the process of stopping them first day without 1 and I feel as explained. The worst thing is that no one seems to understand the effects, they cant understand why you'd rather be ill than go through with them. its not good for you on the whole. Good health is the unity and prosperity of all aspects; Body Mind Soul. Hope the best to all.

This is further to what I has posted here below on the 16th of October.(you may look at it for symptoms). My dad passed away last night. The doctors had administered steroids to him saying it is the only solution to healing him out of this in order to save his eyesight.I am crying to myself now remembering how he suffered those last 10 days of his life due to this drug. He had never experienced anything more horrible in suffering like this during his life. His death report says, cause of death: Steven Johnson's Syndrome.

I've been prescribed Prednisone since April and just recently experiencing hair loss (I'm Female)

I am so glad that I am not the only one who has experienced this - not that I want others to experience it, but you know what I mean, it is nice to have some answers!!! I went in to get an allergy shot for my horrible allergies about eight months ago - I have had one done previously a couple years ago, with no problems, and this second one seemed fine too. My allergies are so much better, i can breathe and am not sneezing constantly, etc. However, about a month ago, I noticed this small indentation in my left buttock cheek - I wondered what on earth it could be (cellulite, weight gain/loss from going to the gym I started going to, who knew?) It got bigger and hasn't gone away over these past few weeks, instead getting larger and my skin becoming ever whiter than I already am and the area is sensitive. I had no idea what it was until I stumbled onto this site - I now realize that indentation is the same spot where I received my allergy shot eight months ago!!! I checked my online medical record and sure enough, Tricyclamide Kenalog injection! NOBODY told me that this indentation/muscle atrophy at the injection site was a possible side effect! They warned me about allergic reactions, drug interactions, buildup of steroids in the system, etc, but absolutely nothing about this awful indentation - it is sensitive and unattractive and I really, really hope it goes away or at least shrinks. Not that I am super vain, but it's not all that cute to have a big "hole" in your cheek, especially when that was one of my body areas I actually felt okay about. Just be forewarned allergy sufferers - just because you haven't had a reaction the first time you get the shot, it could happen the second or third or fortieth time. I wish someone had said something about this, so at least I would have been able to make a more educated decision and choose whether to suffer through a few months of allergies or a lifetime butt indentation!

I have MS and had to do a course of prednisone steroids. I was very irritable and just felt plain crazy. I have been off of them for ten days and am experiencing really bad shaking in my hands and am often tongue tied. I guess it could from the MS attack but was wondering if anyone else was having these side effects.

My 18 year old daughter had a terrible allergic reaction to omnicef 2 weeks ago after a 10 day regimen. Sadly, it happened 2 weeks after my nephew had an allergic reaction to the same medicine. His situation did not end so well. He was taking the medicine for strep. The allergic reaction started with hives and got worse. After some aggressive research on my brother and sister-in-law's part, my nephew was diagnosed with an allergic reaction to omnicef followed by rheumatic fever. I should have refused the omnicef for my daughter, but who knew.
My daughter is 2 weeks into annoying hives that continue to pop up in different places. Her feet are swollen and we are very concerned. She has taken steroids, Kenelog cream, benadryl, as well as prescription strength antihistamines. Tomorrow she is going to see another doctor to find out what is going on. Cefdinir/omnicef is no longer welcome in our extended family.

I was started on Bactrim 7 days ago. The first two days I felt fine, but the 3rd night I got cold...very cold and could not stop shaking for about two hours. My heart was racing and I was nauseated and couldn't focus. This went on for about 8 hours before going to the ER. Upon arrival I had elevated BP and pulse, but after a couple of hours it went down to normal. I saw a new doctor who said it sounded like I had a hypoglycemic attack!! I never had one of those before!! So, I'm figuring I'm getting sicker and maybe it is not from the Bactrim so I take it again and last night was another horrible night!! Racing heart, confusion, and urinating every 30 minutes. Thinking maybe I'm having another attack I get up and eat some applesauce and my husband gives me some sweet tea. I promptly threw up a few times and then we went to the computer to look for ourselves the side effects of this drug. Guess what? It causes hypoglycemia, racing heart, confusion and does something to your kidneys and makes you urinate too much and could be very dangerous!! That was it for me!! I didn't sleep the rest of the night but slept on and off during the day and felt like myself today for the first time since taking the drug. I don't know if it has done any permanent damage, but I will let everyone I know about this awful awful drug!!

Hi All, we definitely need a lawsuit. I am finally my old self again after 2 years of hell. My nose shut down after moving into my new house 2 years ago. Went to a local clinic here. My Dr. gave me the Kenalog shot for "inflammation", she did not tell that it was a steroid. I am allergic to steroids. I was suicidal, depressed, had a breakdown, lost 10 lbs. in one week from not eating. Menstrual cycle went from 3 days for 35+# years to every other week for 7 days. OMG, I went thru 2 years of sheer hell. Finally had to have a partial hysterectomy this past May I AM SO ME AGAIN! WE NEED A LAWSUIT against Bristol Meyers. Thank God my husband was beside me, or we would have divorced. Poor Guy.

I have no idea if these are side effects from Remicade or not- because doctors always dismiss it as "probably just you". Definitely HEADACHES. I would occasionally get headaches before, but since being on Remicade the past year, I get really bad headaches. Neck/scapula pain/strain. I have woken up with immobile neck 3 times now in past 2 months. It's getting ridiculous. The doctors just say I need PT or to stretch. But I really wonder what's up and why I've never had that in my life until now. Also flushing with inital infusion, but that really is no biggie. I definitely feel STUPID. I've heard of "chemo brain"- does the same thing happen with Remicade?
I am 31 and taking this for inflammatory condition NOS. I have an autoimmune/inflammatory eye condition NOS that left me with significant Retinopathy. I did Prednisone, Methotrexate, Humira, Cyclosporine, Tacrolimus, Cellcept all for a few years- and nothing helped except steroids. Which obviously you shouldn't take long-term. Plus I HATE them, they make me fat, hairy and psycho! So Remicade has been a god-send in some ways. But I am a mother of 2 and love my husband, and worry that I may not go blind but will die young from side effects of this medicine. But why should I worry? Every health care professional says there are "NO" side effects. What's the deal?

Warning: I do not know if this is related at all (or if there is anyway to know for sure). I accidentally saw a connection looking up conspiracy theories, and I can't seem to find any "real" information about it at all.

My daughter at 14 years of age had this shot. She didn't feel good after, but I thought "normal" vaccination reaction and haven't thought about it since. Feeling a bit faint, a fever, and such.

However, last September (a few months later) she was diagnosed with autoimmune hemolytic anemia. It started with her heart racing, she looked pale (and sometimes even yellowish), tired all the time, her urine turned a dark color, and fainting. Not knowing anything about this I assumed that she was dehydrated, and had her drink lots of water. Until she started fainting, at which time I took her straight to our family doctor. (Another reason that I wasn't to worried is she actually had been to many doctors who didn't seem to think this was abnormal.)

She started on high doses of prednisone to keep her immune system depressed, and has now moved on to mercaptopurine (as the steroids made her suicidal.)

I plan on bringing this "possible" connection up to her hematologist and I will report back (she has an appointment on the 11th.). However, I think it is better to do a little scare here, and possibly help someone rather than take for granted that I am not sure... (So take this information with a grain of salt.)

Also note that this was sudden onset, they can find no cause, and we have no family history nor any of the other typical reasons (sometimes can be "medicine" induced.) 10 months later she is still testing positive on her combs test though.

While in the 1st month on the NuvaRing, I experienced small bumps on my stomach area (bellow breast & above the belly button). I thought it was heat rash. However, while in the 2nd month on the NuvaRing, I experienced sunburn/welting hives (range from 1/2 to 4 inches) all over my body, swollen fingers/hands, swollen lips, swollen left side of my face (including eyes), heartburn feeling in my chest. This landed me in the ER because I had a hard time breathing. The ER doctor immediately administered Diphenhydramine (Benadryl) via an IV. I was also given Prednisone (steroids) Famotidine (Pepcid). The next day--I still have hives that pop up of I don't take the Diphenhydramine & Prednisone pills on schedule. The chemical/NuvaRing has to get out of my system!!! Beware Ladies!!!

I started on the Wellbutrin almost 3 weeks ago. Other than a little problem with insomnia, I really liked the medication. It seemed to be helping me control my binge eating which definitely a plus and also the depression. One morning, I woke up with hives all over my body. A few hours later, they had become very severe. I had hives there were 8 inches long and hive patches about 8X12. They were in my scalp, neck, arms, upper legs, back, stomach. Went to family doctor who gave me shot and started on prednisone and was also taking benadryl. That night the itching was so severe, had to go to ER for IV steroids. This calmed things down tremendously. Haven't gone totally away yet, but much better and more bearable. It's a shame because I was feeling very hopeful on the medication. I was taking the generic form at 150 mg 2x day.

I am so relieved to see these posts. My husband started Wellbutrin 2 weeks ago. We are at the beach and yesterday he started experiencing itchiness followed by rash and welts that have spread and are huge now. He has them on his legs, under arms, around waist and on feet. This morning his right eye became extremely swollen and now his lips are HUGE.. At first we though an allergic reaction to seaweed until it started getting worse. I googled benadryl and wellbutrin to see if they could be taken together and found this sight. He has also been complaining the last week with chest pains and I see some people also experienced that. Thank you all for sharing for now I can see what is causing it and we are stopping Wellbutrin now.

About 2 and 1/2 months ago I went to an urgent care facility since I felt like I was suffocating. I am a long time smoker (30 years) and have not had any problems with breathing accept for the occasional morning cough. Long story short, the doctor after hearing my breathing and taking 2 xrays said "you have a pocket of infection in your lung and COPD". I didn't realize it was that quick and easy to diagnose COPD and thought there were more extensive tests to prove that, but I went along with the doctor. The doctor prescribed Advair, an antibiotic, ProAir HFA (albuterol pump rescue inhaler), a decongestant and prednisone. I thought that was an extreme amount of medication but the doctor said she was being proactive. After a couple albuterol breathing treatments and a shot of steroids at the urgent care center I was on my way.

I finished the treatments of antibiotics and steroids as prescribed, but I never took the decongestant (did not want to over-medicate myself). Immediately after starting Advair my joints ached and I felt over all like I had the flu. With my 1 weeks checkup with the doc I mentioned this and she just smiled. About a week after that the achy joints starting easing up, but I started cramping in different muscles. For instance one week I would have a dull cramping in my leg that was persistent during the day and worsened at night. Then the leg stopped cramping, then the lower part of my back started in to a point it was hard to get out of bed, walk or bend over. Then when that stopped something else started up. Then during the last two weeks that I was on Advair I was having periodic chest pains, tightness in my chest, (once again) difficulty breathing, and my vision started to go (blurring)...that with the lower back pain. I am almost 50 years old and have been in excellent health my whole life, and honestly I have never felt as bad as I did while on Advair.

I stopped taking Advair 6 days ago. No, I did not call and ask the doctor's advice because I knew what the doc would say. The first day after quitting Advair I had restricted breathing so I used the rescue inhaler once. The breathing issue became better during the remainder of the day. Slowly the cramping in my body and chest eased up. Today (6 days later) my vision is back to what it was, no chest pains, occasional restricted breathing and will use the rescue inhaler during those times.

I think it's too early to know the long lasting affects of Advair, but at this stage in my life (unless I am worse off with my breathing than I am right now) I don't care to use the medication.

54 year old Male, Retired Marine, Very physically active, with Type II Diabetes; 5mg. Thanks for this Website. Started Lisinopril 3/25/09. Took it for 25 days, found this website and stopped taking it immediately. I had severe JOINT PAIN. It started in my hands, then feet, knees were next, then moved into my shoulders. The pain was the worst I've ever felt. Approximately 60 days after stopping the drug I went to see the Dr. after the Pharmacist told me Lisinopril should have been out of my system after 2 weeks. The Dr gave me Steroids (Prednisol) which completely eliminated ALL pain in 2 days . I was tested for Polymyalgia Rheumatica, however the my Sed Rate was normal. The blood tests did reveal that my RHEUMATIOD FACTOR is elevated (34.3 where the normal range is 0.0-20.1 IU/ML). Was told that if the pain returned, then I would be referred to a Rheumatologist. 3 Days after finishing the dosage pack of Prednisol, the pain/swelling in my hands and shoulder has returned. Going back to see the Dr today to discuss next steps.

Although the doctors don't agree, I believe Lisinopril caused this pain, and although out of my system now, triggered something that isn't going away.

The rest of this describes the roving pains I experienced.

Hand pain included swollen fingers, inability to make a fist or type on a keyboard. After light yard work on Sat., shooting burning pain up the inside of both arms. Trying to close your hands into a fist, you can feel the tendons up your arm burn with pain. Motrin did not alleviate the pain. Hot water did not help.

Pain in my knees each morning. The pain worsened over night and frequently causes you to wake up. The pain was like your knees were being squeezed in a vice. No position is comfortable. Motrin sometimes helped, but after awoken, getting back to sleep was impossible.

Feet swollen. Couldn't wear any shoes for extended periods. Loosening the laces helps, but still caused pressure which becomes unbearable and the shoes have to come off.

Shoulders; This is the strangest one. First pain was in the left shoulder, like I had impacted a brick wall at a full run (actually no trauma occurred). The pain felt like someone had stabbed it in my shoulder in the socket. At it's worst, no position is comfortable. Had to put my arm in a sling. 5 Days later, the same type pain moved to the right shoulder.

I have been taking 40mg Omeprazole (by APOTEX) for one week. At 3am Saturday 6/20/2009, I woke up with a severe itchy rash from head to foot. Over four hours, I took 125mg of Benadryl, but the rash got worse, At noon, I went to the Emergency Room at UPMC Shady side. They gave me intravenous steroids, but this had no immediate effect, After three more hours, they admitted me to the hospital. It wasn't until almost midnight before I began to have relief. I was discharged the next day. I have been instructed to never take Omeprazole again.

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 was prescribed Simcor and had started taking it 4 days prior to an "attack". Out of the blue, the flushing, redness etc. No worries that is common I told myself. However, the severe burning and swelling set in. I had a splotchy rash that covered entire body and my face was the worst as it was swelling, effecting my neck, eyes etc. I did not wait to see what happens next. Straight to ER. Dr advised a good thing because it is potentially life threatening side effects for some. An IV with meds including steroids and 4 hours later the rash had subsided. Will not be taking this medicine again. Hope this helps.

A year ago I was diagnosed with Sarcoidosis and began taking 50mg Prednisone per day. The worst side effects in the beginning were weight gain, moon face, facial hair, hump-back neck, bruising (for example, just by my knees being together while I sleep,) excruciating joint pain and water retention to the point I felt my skin would split open. And poor vision which could have led to glaucoma, but an eye specialist put me on eye drops to reduce the pressure to normal levels. I've felt horrified and embarrassed by the change in my appearance but relieved that my sarcoid was being treated.
I feel confident in my case that Prednisone was the necessary treatment. My pulmonologist, opthamologist and regular doctor all agreed on a course of treatment. But I really advise people to get a second or third opinion before they take it. A friend of mine was prescribed a weeks course of Prednisone for a severe sinus infection. Luckily she didn't have any side effects but I really question if it was necessary. I'd also like to stress that if you're on Prednisone and experience worsening vision, please see an opthamologist who is a glaucoma specialist because it can lead to blindness if not treated.
And lastly, sorry this became a novel! I have been tapering off and I'm down to 20mg. But recently I've noticed my hair is thinning so much. I lose a ton when I brush it and it clogs the drain when I shower. Also my skin is shedding. When I shower and use a loofah sponge like I've always done and I lose layers of skin like a snake. I would really like to know if my hair will start to grow back when I'm finally off the Prednisone or am I going to lose it completely??

I am a 48 year old female who had just recovered from pneumonia and was prescribed avelox for a lingering sinus infection. Within hours after taking just 1 400 mg pill, I began experiencing a severe reaction. First there was a rash all over my body, with swelling and flushing all over. Then I became nauseated to the point of dry heaves and my temp went to 104 digress. My body then had neurological shakes, I could not control them -- just like Parkinson. I had no energy to move. My husband rushed me to the ER where I was treated with steroids, liquid benadryl, nausea medicine and IV fluids. After a few hours, I was released. Two days later, after another trip to the ER because of tingling, rash and no blood flow to extremities the same treatment was given. It has now been two weeks and I am just now feeling like I am coming out of this and getting back to normal. I have just spent over 10 days in bed, untold amount of money at ER and lost two weeks of my life.. BTW, the ER Doc said he would never prescribe Avelox to anyone due to the numerous reactions he has seen. If there is a class action suit, count me in.. Never let anyone take this drug..

I'm sitting here in tears reading all of your posts because I've also been on prednisone and have horrible side effects. I was diagnosed with metastatic breast cancer in my lungs in June of 2002 and, after starting at 60 mg/day then, I have been on 20 mg/day for years now. The very first posting that I read mentioned problems with the femur bone. Besides all of the other problems associated with this devastating drug, in December, 2007, I broke a bone in my left foot with no known cause for it. Then I started experiencing pain standing or walking in my left leg and was diagnosed with a fractured femur bone and after several months of trying to get it to heal (including an ultrasonic bone healing system), it just kept getting worse until an orthopedic surgeon recommended that I have a 16 inch rod put into my leg which I did and it ended up to be one of the worst decisions that I have ever made. After experiencing all of the prednisone side effects for almost seven years including depression, severe fatigue, weight gain, moon face, thin skin, cataract surgery on both eyes, hump on my back, mood swings, etc., the pain and suffering that were caused by that operation brought me to seriously consider suicide. I was also diagnosed with chemical neuropathy in both of my legs also which makes my legs so weak that I have to crawl up any steps and have trouble just standing. I actually have an appointment for this evening to have an x-ray done to see what is wrong with my knees and did not realize that this also is yet another side effect. I never make it through the night without waking up in pain and getting a pain pill and then getting up in the morning is almost unbearable with that "burning" pain. I am now on Cymbalta for depression, Xanax for anxiety, Percocet for pain, and of course 20 mg of Prednisone. I was told that I would have to remain on Prednisone for the rest of my life because of the lung scarring and COPD. After reading all of your comments, I have decided that I would rather put up with any breathing problems (and I don't even know how slight they may be at this point) than to remain on the Prednisone. I have tried weaning off several times but get so fatigued that I can't move and that's dropping one mg every week. I'm affected by the decrease but it gets out of hand when I get to 14 mg and I get so frustrated and depressed at not being able to do anything that I just go back up to the 20 mg/day. If you have been able to wean off of it, would you please let me know how you did it and what you had to go through? I'm 65 years old now but I have two wonderful granddaughters (ages 4 and 6) who I can't do any normal "Grammy" things with anymore at this point and I have to change this condition for them and for me. Obviously, the doctors don't recognize the severity of the drug because they just keep prescribing it and out of a regular doctor, an oncologist, an orthopedic surgeon and a neurologist, they can't seem to get together to come up with a solution. I have to say that I haven't considered suicide lately but I do wish that I would just die and be out of this pain. My family and definitely my granddaughters and wanting to see them grow up are the only things that keep me going. There are probably things that I'm forgetting but I'm sure that one of you have covered it in our posting. Although my family is so supportive, no one and I really mean not one of them, realizes knows what we all go through because of this drug. How could they know that something that is supposed to help you could cause these problems? My life is a living hell, all because a pulmonary doctor prescribed prednisone seven years ago and I trusted him to only do what was right without informing me of what was to come. I more than sympathasize with all of you. I sincerely appreciate the time that you took to post to this site and so thankful to know now that this knee pain is not something new that I have but another side effect of the prednisone. I wouldn't have known that if it wasn't for this site because I'd be willing to bet that after I would have had this x-ray done, one of my doctors would have just prescribed another medication to take. Please feel free to contact me directly with any comments or especially any help that you can give me. I know that all of you are going through the same thing so if I can do anything for you, even just listen and understand, please contact me also. Sometimes that's the only thing that people can do is to listen and someone who is in the same situation can always understand. I'm here for anyone who needs a hug for the day.

Been taking this for the past ten years and it is the only thing that allows my skin to quickly recover from eczema. Eczema started at age 22. After my first injection I felt more powerful than Darth Vader and noticed an increase in energy and stamina. A few weeks later, a crash begins and I feel the side effect of lethargy. Consistently, after each Kenalog shot, my skin will develop several pimples around my buttocks area and sometimes on my back after a month or two. I would prefer never to use Kenalog, but it has been the only thing that relieves the patches of skin that become red and flaky due to stress, lack of sleep, and a poor diet. Ultimately, I did develop 'hypercutia' which is a skin condition which allows my dermis to bleed more easily. After stopping the Kenalog injections for a few years, my entire dermis still remains thin and more vulnerable to bleeding. I make my living as an actor and it is part of the reason i still rely on Kenalog whenever an audition comes up and I need to show my body. The pimples eventually become little scars, which eventually become little darker spots on my body. I still believe that in spite of all the side effects, it is worth it if you make your living as an actor or model.

I began prednisone May 20th for hives from a reaction to an antibiotic. After taking it for a few days I started having ringing in the ears, shortness of breath, tightness in the chest and sweating, dry mouth, puffy face and just a strange feeling like my blood pressure is up. I took it for 7 days out of the nine because the nurse told me to stop it after I called in about how I have been feeling. Today is the first day of not taking it but I see hardly no improvements. My husband tells me to drink a lot to flush this medication out of my system. Today I am experiencing some chest discomfort with slight aching. I feel the same as all of you. I wished I knew of this drug beforehand, and I hope to never see this drug again. I just hope it didn't cause much damage. I will be praying for all of you. No one knows any more what can happen after taking such medication. If you are on this call your Dr. to be taken off. This is not good, I have no idea why this is still on the market. Hope you all recover from your symptoms after taking this drug!