X ray symptoms and conditions

I started taking 20mg of Simvastatin on 10/17 due to high cholesterol. Five days later I came home from work feeling very tired and fell asleep. I woke up feeling severe flu like aches and pains in places I didn't know could hurt and then got the chills. I stayed home from work the next day and it's a good thing I did. I awoke with a severe cramp in my upper right thigh. I have always been prone to calf cramps so wasn't too concerned. However I stopped the meds on 10/22. This continued on a daily basis and I went to the dr on 10/27. I had an x-ray done which showed a bulging disc and some uncushioned discs. She put me back on the meds BUT with a COq10 am and pm and cut the pill in half. Do you think she knew it could be from the med? I foolishly restarted and by 11/4 took myself back off, had an MRI and such severe nerve pain in my right leg that I thought I would die. It was a bolt of lightening starting at my upper thigh and coming out the bottom of my foot. It felt like a hot poker running down my leg. The episodes were on a daily basis, would come every two hours, and could last as long as 45 minutes with no relief. I am now going for pain management and had an epidural a week ago which got rid of the nerve pain but I am still numb down my right leg to my right ankle. I have been healthy for years and feel that this was all brought on by Simvastatin. Any idiot can figure out that your nerves are running through your muscles. I am angry to think that this could have caused me permanent damage.

I am 56 years old and I was put on Lisonpril about three months ago.

We had just moved to a different town with a new doctor. The reason I went to the doctors was that I had a bicycle accident where I went over the handle bars (front brakes locked up on me). I was also due for a periodic check up. I was sore from my bike accident (jammed my LH wrist, RH elbow, both shoulders and knees). The doctor had no x-ray machines so he sent me to the urgent care, nothing was broken. My doctor said that I would be sore for awhile and gave me some Vicaden pain medicine.

Due my periodic exam the doctor suggested that I go on Lisopril because I am a diabetic, even though my blood pressure is OK. He said that he actually takes it because of the preventive nature of the drug.

Well, as the weeks went on I continued to have aches and pains in my joints (wrist, elbow, shoulders and shoulders), wch I thought was from my bike accident. I also play seniors softball which is not a very agressive sport. Well I've had a pulled hamstrin and archilles tendon pull during playing. Thought this was normal but these injuries continued to plague me.

At nights sleeping my shoulders & neck would ach. My knees would shoot pains. My ankles constaintly ache, day & night.

A friend of mine told me about taking black cherry juice for joint pains, maybe from gout. After taking this black cherry juice it seemed to help, but still not normal.

Today I stopped at our local taven to have a berr and talk softball with the guys. I broke out in a heavy cold sweat and almost pasted out, lightheaded. I thought I was having a heart attack or something. Being very concerned I told my wife who is an RN. She read the side effects of Lisonpril and it clicked. This web site helped me figure it out also.

I am taking myself off Lisonpril today and expect improvement and my life back. I thought all this was from my accident and getting older. I am excited to see the results, which I feel very positive about.

I am so happy to have found that many others are experiencing the same things...I have gone CRAZY!!!! I almost started anti-depressants and was scheduled to see a psychiatrist next week because I have totally changed emotionally and sexually. I had a great sex drive and was always happy go lucky....after some thought I starting researching this Mirena...and I think this may be the root of my unhappiness. Plus all these other side effects!....

~Tired all the time
~ Depression
~ Hungry all the time
~ leg cramps
~ hair loss
~ oily skin and bad breakouts
~ No period ..ever
~ Mood swings (huge...yelling fits at my husband and the kids)
~ light stomach & back cramps for weeks at a time

Best of Luck to all of you~I am getting this thing taken out ASAP!

How is this still on the market? I have had migraines which I have never had before. I have been to the hospital twice, had to have 2 cat scans because my Dr. was afraid I had an aneurysm (sp?). I thought there was really something wrong with me. I am having the Mirena out tomorrow, hopefully I will feel normal again. DO NOT USE THIS form of birth control. I would rather have 10 kids!!!!!!!!!!!!!!

There is a class action lawsuit for anyone that took Yaz/Yasmin birth control. I just saw the commercial the other day from an attorney in Denver and it's nationwide. Please call Nolan Law Group - Valerie Romo at 888-630-9340. They are handling it nationwide.

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 had a lot of trouble from it anyway, the mood swings depression, cramping and discomfort during sex. i had mine for 2 years and 3 days ago i was at work and and i started getting extremely bad cramping. I went to the ER and they did an X-ray..then they TRIED to do a pelvic exam and couldn't because i was screaming in pain. Come to find out the mirena was hard to find cause it went sideways and was poking all sides if my uterus wall! The nurse had to give me narcotics through an IV just so they could remove it. Now i feel normal again in only days time, i don't know what i was thinking getting that man-made device inside something so fragile. I DO NOT recommend the Mirena to ANY woman out there........

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.

PERFORATED MY UTERUS --- The placement of the Mirena was extremely painful. I could barely drive afterwards. I was sure that something was wrong, but the doctor assured me that everything was fine. I breastfed my son for a year (I had it placed 6 weeks post-partem) which is why I had it placed in the first place. It was considered safe for breastfeeding mothers (please research side-effects of the active hormone it releases on infants. We now know why our 13 month old has had respiratory issues since he was 5 months old). Over the year, I had radial stabbing pains up my back and down my legs. It hurt during sex. At my year check up, I asked the doctor to remove it, but he could not find the strings to remove it. After an x-ray confirmed that it was still in my abdomen, he scheduled a hystoscope to find it and remove it (he assumed that it was still in my uterus). During the procedure, he could not find the Mirena in my uterus and had to perform emergency laparoscopic surgery to remove it from MY ABDOMEN. It had PERFORATED MY UTERUS. My husband and I now know of 4 women that this has happened to just by telling people our story. WE LIVE IN A SMALL TOWN!!!! THE NEGATIVE SIDE EFFECTS ARE UNDER REPORTED!!! PLEASE INFORM YOURSELF BEFORE GETTING THIS DEVICE.

I absolutely hate this thing. I have had 2 ob's recommend this thing to me instead of me having my tubes tied. They made it sound like it's wonderful and will save lots of money in the long run. Months ago I started having really bad back pain, so bad I can't bend over to pick something up. I saw my family doctor and he ordered an X-Ray. Nothing came of it. I went and saw my ob and she checked the IUD's placement and examined me and came up with nothing. A few weeks ago I noticed sharp and at times severe pelvic cramping and burning. I went to my family doctor who ordered a CT scan with contrast. He discovered that I have an enlarged ovary. Next I had to have a pelvic ultrasound and I learned that I have an ovarian cyst. All that time and money for a cyst!!!! After telling my ob everything my family doctor had discovered, she thinks I should take the pill. I cannot believe all the time and money I've spent on this darn thing, only to find that NOW I should take the pill. If anyone is reading this forum to decide whether or not she should get this thing.... the only advice I have is to save up lots of money because you're going to need it. I have spent 4,000.00 on unnecessary testing on things that I thought were serious health problems, but were nothing more than side effects. I wanted this thing to be removed months ago but my ob insisted that I wait just a little longer. Now, I'm stuck with a bill for thousands of dollars and it's all because of this damn thing. Wish I would've went to Planned Parenthood... they would've removed it for $150.00, but at least I wouldn't have been out $4000.00!!!

I started Lipitor 2 months ago, today is April 23, 2009.
1 month ago I started with Vertigo, doctors have tried many things to get rid of it but can't.
! week ago I started having trouble breathing, talking very short walks, problems still with vertigo, pain (headaches) on my left side, and I never have had headaches, pain in my neck left of the c-7 vertebrae.
Now 2 days ago I have problems swallowing food in the center of my chest, it really hurts, so now I am on an ice cream diet to figure things out.
I went to my doctor yesterday due to all my problems, which are all new in the past 7 weeks, and she did an x-ray, and blood work thinking I had a blood clot in my lungs.
At 6:30 pm last night 4-22-2009 she called me to go to the emergency room and have a cat scan done, and the results were I am loaded with lip-nodes in my chest and arm pits, and it look like cancer, so I have an appointment today at 2:00 pm to see what the plan of attack is.
God Bless,
L. G.
Biddeford, Maine

******

Had the Mirena 12 weeks after the birth of my child. Insertion was very painful, just didn't feel right. I checked out this website and thought i had to go have it checked. As other listings here, the doctor couldn't find the string, did the ultrasound, there was no Mirena in the uterus. Did the abdominal X-ray and there it was somewhere in the pelvic cavity. Had to do Laparascopic surgery to get it out, under GA. I wanted to do do it ASAP before it perforated my bowel. Surgery went well, little morbidity, but still a surgery with 2 wounds to heal. A message for any lady considering the Mirena, if it didn't feel right, go get yourself checked, and make sure it's alright. Good luck to all.

I have had the Mirena since October, 07, right after my daughter was born. Very easy insertion. I have had the usual problems with weight gain, acne, moodiness. I went to get my IUD out on Monday, 3/23. My doctor couldn't find it and I was in agony as he tried to "tease" the string back down out of my uterus. I had always heard the removal was the easy part. I went back today after doping up for the pain, and after thirty minutes, my doc still couldn't find it. Now I have to have an x-ray and surgery done to remove the stupid thing, which has either imbedded in my uterus or perforated into my stomach cavity. It is supposed to be very rare, but it has happened to me, and I just want the thing out of me. I want to get pregnant later this year, and am fearful for my fertility. Think about that very carefully, anyone contemplating it. I had no idea that could happen or I would have NEVER gotten it to begin with.

Well I had the mirena inserted in January and went for my 6 week checkup last week, Now let me tell you I thought that getting it was one of the most painful things I have ever gone through, it felt like i was in labor again, the midwife that inserted it even told me that she never had that much trouble trying to put it in...Anyway when I went back for my check up she said she couldn't find the strings so they sent me for a ultra sound and still could not see it, They then sent me to the hospital for a x-ray and saw that it was somewhere in my pelvic area....I had to go back this week on Wednesday so they could stick a little camra in my uterus and see if the mirena was there and if it wasn't then i would have to have laparscopic surgery to get it removed because it would have had to went through my uterus walls..well guess what ladies I'm scheduled for laparscopic surgery on april 6th because once again it wasnt there, as you can see i have not had the best of luck and i hate how bad things happen to good people, I'm not sayinf mirena is a bad thing but I really wish this wouldn't have happened, so those of you who have had bad luck I feel your pain, for now on the only birth control I'll be using if the kind you can see and take everyday

My Mirena has actually gone through my uterus wall and attached to my intestines, after experiencing server cramping (worst than labor) and going back and forth to the doctor they couldn't find the Mirena and had to x-ray to discover it was in my intestines, this explained the excoriating pain i had as i am sure it is quite a big task for the Mirena to work its way through my uterus wall!. I was going to get it removed but the specialist said that it was more risky to take out than leave in. I used to get sever migraines until they found out the mirena was no longer in my uterus so i had to go back on the pill and this has stopped the migraines, however i am constantly still experiencing headaches, lower back pain, server anxiety, panic attacks, tiredness, feel sick and unwell a lot of the time. After discovering this site I am so getting this thing removed and hopefully will be able to get back to my normal self.

During my 6 months on Warfarin (Coumidin) I experienced tremendous lethargy and short term memory loss. No issues with other commonly reported symptoms of hair loss, heavy legs,…
I am a 49 year old male. In January 2008 I was diagnosed with DVT's in my right lung. Interestingly I experienced 100% of the pain on my left side though the DVT’s were on the right. The onset of symptoms was a pain in my chest like I pulled a muscle lifting something. The pain progressed from "notable" to progressively uncomfortable, where I was restless in bed to the point of not sleeping. On the 3rd day after fitful sleeping and progressively more painful breathing, I made a doctor's appointment for that afternoon. By the time I got to the Dr. I was sure I had made the right decision (I am male and avoid these things).
My primary care did an EKG to rule out a heart attack which the symptoms were identical to; sharp pain in chest toward left shoulder and arm, trouble breathing. I was sent for an X-ray and was very uncomfortable laying still on the Xray bed as the pain as I inhaled had gotten sharper. I went home and resumed office work but soon was in extreme pain with each breath. So much pain that I could not lay or sit, but collapsed to my knees where I stayed for 20 minutes until I could move again. I called the doctor's office and was advised to go directly to the ER. Duh. The ER again ran an EKG and ruled out cardiac issues.
Three ER Attendings pondered my condition for an hour or so and then began asking as series of questions and at the 3rd question – had I flown any long flights recently? Yes, several transatlantic – at which I saw their glances and was whisked off to a CAT scan which confirmed DVT’s. I was put on morphine and some IV’s and admitted for 5 days. I started Lovenox shots and by the 4th day was feeling better.
Blood tests did not revel any genetic disposition (factor V) for clots and no family history so it was recorded as “Coach Class Syndrome”. I was put on Warfarin for (5mg/day) for 6 months. I was able to keep relatively good INR’s. I came off Warfarin (12 August 2008). I will have to take Lovenox shots before long flights. I am happy to come off the Warfarin as I experienced tremendous lethargy and short term memory loss. No issues and I have been off coumadim for 6 months now. Glad to have that behind me… hopefully.

I got the Mirena September of 2007, after about a month or so of having it put in I started having problems going to sleep and then had problems getting up in the morning with my children cause I had no sleep the night before. I have been VERY moody to where it's ruining my marriage, I was never moody before I got the Mirena. My headaches started about 4 months ago, When I first started having them they were so bad I had to go to the ER and now I have had weekly visits to my Dr. They have done a CAT scan MRI and an X-RAY to try to figure out what is going on...and now I am thinking that the Mirena is what is causing all of these problems. I have crying spells now this has been going on for about a month, I am very depressed and sometimes feel like I hate life...again that was not me before. I am gaining weight...I am not intimate...and my bones just hurt so bad sometimes...I think it's about time to take out the IUD.

I first posted my problems with Mirena on Jan. 15. Sice then I have been to the doctor 3 times and am now scheduled for SURGERY!!!! It seems that the Mirena has turned sideways in my uterus and after several attempts to remove it, without success, the doctor I'm seeing now says she will have to sedate me and use x-ray guided equipment to remove it. Has this happened to anyone else? I just can't believe this. No where in anything I read before I had the Mirena put in did it say that this was even a possibility! I get so mad when I watch their commercials on TV. They really need to tell people the truth about the possible side effects. They make it sound like there aren't any. I just hope that the women who are considering getting it inserted find this web site before they make their finial decision. I wish I would have found it sooner!

Further update. I went to get my mirena taken out but the doctor couldn't find the threads, she fished about for a bit while I laid in agony, still couldn't find them. I was then given a scan and they couldn't see it on the scan so I was sent up for an x-ray. Thankfully it showed up on the xray, it has got lodged somewhere in my pelvis/groin. Been sent away to wait for the gyny to call me to get me in for surgery, she isn't there until Monday so I have to somehow get through the weekend, they didn't even give me any pain killers. Please let me know if you know of anyone who has experienced this. I do think I've just been unlucky with the whole mirena experience, sadly its not over yet though!

I just posted yesterday about my side effects and making a dr. appt., well I went in today to have it removed and they said it had gone up into my uterus and I now have to have surgery and be cut open because of it, I also may not be able to have any more children. This mirena has been a nightmare. The dr. I saw today, which wasn't the dr. that put it in, said he wont even put it in because of the side effects, which makes me mad because a dr. that works in the same practice there told me it was great and insisted it would not have any side effects and that there had never been any side effects. I am sooo stressed out about this, but want to thank you guys for your information, If I had not have found this sight and read this then I would still be getting bloodwork done trying to figure out what the hell is wrong with me!

I posted a short one, would like to add to it. My daughter was taken by ambulance twice last week to the ER, after having violent seizure like episodes. On second visit, she had several while we were waiting to be seen. She spent 5 days in the hospital, having these episodes as few as 10, as many as 30. lasting any where from 4 minutes to 40. She screams out in pain. It's like her entire back, including arms, legs, hands, feet are having a severe muscle spasm at that same time. If you look up dystonia, the definition fits. Dr. said it was too severe for that diagnosis. They ran EEG, EKG, Cat Scan, MRI, X-ray, extensive blood and urine work, video for 24 hours, with EEG. Everything was normal. DR decided it was stress and anxiety. Released from hospital still having episodes. I called a dystonia specialist in Maryland, she asked if she had the GARDASIL shots. Said it sounded like a side effect she had heard of. Well, after reading all these blogs, youtube, I believe it's the GARDASIL causing her problems. I knew it wasn't stress & anxiety. We are currently detoxing with ionizing foot baths, gluten free diet and meds from Health food store, called HMD-Heavy Metal Detox. I feel we are moving in the right direction. My daughter is a cheerleader, dancer and honor student. She just wants her life back. It has been on hold for 2 weeks now. I consider her one of the lucky girls, after reading many blogs. God Bless each and everyone of you. Sign the petition to stop hurting our girls.

I was prescribed Doxycycline Hyclate 100m for acne on January 20th 2009. Then, on February 6th, I took the medication at 11:00 only to wake up at 11:40pm with severe chest pains. I have never had anything wrong with me heath wise and the first thing that popped into my mind was the medicine. I went to the doctors the next day because the pain had become so severe and i could not eat or drink anything (even water) without feeling a sudden sharp pain. They did an x-ray and found nothing wrong. I was told it was probably anxiety and this medicine had nothing to do with the chest pains. I
went ahead and took it again last night only to still have chest pains so i decided to do research on this medicine and came to this where i found posts in which similar things were experienced upon taking the medication. I have just stopped taking the medication today and am hoping for the pains to go away.

Does anyone taking Loestrin 24 Fe have lower back pain. I have a feeling in my lower back area that I need to be very careful how I move as to not move the "wrong' way and my right hip hurts. I had the Mirena and with complications the Dr. put me on this pill for 3 months to try solve my bleeding problems with the Mirena. I started having back pain. i thought it was the Mirena. I have been off the pill for a month and I decided to have the Mirena removed last week. He started me back on the pill and i am having back pain again along with nausea and headaches. My back actually "caught" on me this morning and took me 2 hours to stand again. Thank God I was at home. I call the GYN and they say the back pain is not related to female problems. I originally went to my Primary doctor with the back problem and he did a CT scan and x-ray- all came back good. My back only seems to hurt when my stomach is cramping. Can't get my GYN to understand. anyone else having these back problems? ******

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 was diagnosed with 'a "spot" on my chest upper left, after doing an x-ray.I had 100.4 fever really bad chills and sweats, terrible loss of appetite. I am 41 years old. No diagnosis given at initial visit. After 5 days of Levaquin 500, I felt that the dose was too low as I was not improving. When I called my doctor he said, we usually given 750 mil. I thought, well why didn't you do that in the first place? I would be over this thing by then! I was hacking and plenty of phlegm greenish yellow was coming up. He said to use Mucinex DM and Ambien to sleep. Ambien didn't work so I discontinued it. Don't recommend Mucinex at night it keeps you awake, daytime fine. I felt depressed, super fatigue and very anxious, with difficulty sleeping, but thought that is the way everyone feels when sick. I had trouble having my twins jump on the bed to see me, do to the aches, again I thought that is from the illness, now I wonder if these symptoms were exacerbated by the Levaquin . I had the original script that Dr. told me to refill, it was for 500 mil, so he said do another course of that for another 5 days, 1 per day. I did, at that point 10 days total. Still wheezing, I called and said I was still not any better after 10 days of Levaquin 500 and in bed all of the time. Finally I asked him what was wrong, 'bronchitis' he said. I never had it before but I started looking it up before he told me as it had to be that! He said do another 5 days of Levaquin 750. Very hard to get rid of cough still there, however weird wheezing slowly getting better. It is weird though, I have incredible pain on my lower right ribcage from my back radiating to the front. I think it is from being in bed so long, but hope it is not from the tendon issues people are talking about on this forum. My friends who had same symptoms one week before me, (her family and I got bacterial bronchitis from her 4-1/2 son on a play date we had the week before Thanksgiving) was prescribed Amoxicillin 250 per day and was over it in 1 week! My doctor said he didn't like the way Amoxicillin worked over the gastro track. My opinion, stick with the tried and true meds. unless we all become immune to everything, Amoxicillin worked for me with other illnesses in the past and that is what I will be requesting next time! Hopefully there wont be a next time! Good luck everyone. I hope and pray we have not suffered permanent damage from Levaquin!