Ct scan symptoms and conditions

The first time I heard the word prednisone was late Dec 07 when I was hospitalized for severe pneumonia. I started off with a bad sinus infection that quickly advanced into pneumonia in a matter of a couple weeks. I tried 3 courses of antibiotics but I continued to get worse and got to the point where I was unable to breath on my own. Within a day of being at the hospital I felt like I was living in a dream world and from there I continued to get more stoned by the minute. I had no idea I was being pumped full of prednisone intravenously, along with my antibiotics. I was given a dose of 250 mgs daily, and obviously it was way too much for me. As I progressed into my dream world, I had a couple of “episodes” where I acted completely out of character, and got really paranoid and highly emotional. I pulled my IV out of my arm the one night and sat and watched the blood dripping from my hand, not really understanding where I was or what was going on. Later on I got really paranoid that the nursing staff was conspiring against me and talking about me behind my back (lol) , which I normally would not care about, but for some reason it made me really upset and I sobbed uncontrollably at times. I also tried to leave my room in intensive care a few times, as I was convinced that I was not supposed to be there and wanted to go home. My doctors were really freaked out so they gradually lowed my dose over the last few days I was in the hospital, even sent me for a CT scan of my brain in case I was going crazy. Prednisone is an extremely strong and evil drug – that is why I had the adverse reaction!! Not because I’m crazy! And one should never be given a drug like prednisone without their knowledge!! A few weeks after leaving the hospital I started going down hill again and the doctors realized that what I had was an immune disorder and not just pneumonia per se. After a few months of on again off again prednisone (never longer than a week at a time), I was put on a daily regiment (50 mgs) of it starting in May. Since then I have experienced all of the same side effects noted by everyone on here, weight gain, sleeplessness, anxiety, hair growth (the worst is on my face and fingers!!) dizziness, confusion, trembling hands, tooth aches, and the worst of all , big time MOON FACE! I feel like a complete freak most days. I am now tapering and am down to 10 mgs. So far I have seen no improvement in the side effects, accept now I have withdrawal side effects on top of everything - nausea, headaches, flu like symptoms and trouble breathing. I HATE this drug, even though I know it ultimately saved my life in the hospital and my kidneys – as I had complications caused by the autoimmune disorder. I see my doctor next week and I want off this drug completely. I am not sure the benefits out weigh the side effects to be honest. I want to feel normal again and be able to recognize my own face in the mirror  People should use extreme caution when using this drug and it should only be used to save people’s lives, not used for minor things like poison ivy. That is unconscionable!!!! Good luck to all who are on this drug.

I'm experiencing some VERY concerning symptoms and have a feeling it might be from the Mirena. And my doctors think it's just stress! SOMEBODY HELP!

I had a baby 4 months ago and at my postpardom appointment I was talked into getting the Mirena. After I had it inserted it all started with severe cramping and light bleeding that still has not subsided. I have been suffering with chronic headaches, dizziness, and facial numbness. I've also had bouts of anxiety and leg cramping and recently starting to have pain in my neck and one of my lymph nodes on my left side has become present and tender to the touch.

I mentioned all the these symptoms to my OB/GYN and he said "it's NOT related to the Mirena, go to your Primary Care Dr. and get some tests done" Well, I did that, got a full CBC and had my thyroid checked and all of my blood work came back normal. My Dr. said I am stressed after having the baby and to get some rest. I really wanted to have a CT done but after reading this I am beginning to think it's the Mirena as I had not had any of these symptoms prior to the IUD. I think i'll make an appointment to have it removed.

Anyone ot there have any of my exact same symptoms???

I had Mirena inserted after the birth of my 2nd daughter - November 07. Things were going ok (at least that was what I thought) until about two months ago. I really did not think about the Mirena much. Maybe that was because my sex drive has been soooo gone that I have only used the benefit of the Mirena about 3 times. The problems I guess really started when my period disappeared. That happened 3 months after I got in inserted. I thought that was going to be great because my periods usually last 7 days from start to fully finished. But with this thing, I did not bleed but I definitely was still having a period. Bach aches, mood swings, headaches, bloating, etc. I started to think something was really wrong when I got a headache that lasted about a week, and I don't normally get headaches that last longer than a few hours. I could not figure out what was wrong with me. I even went to the emergency room to have them tell me that there was nothing wrong and it was probably just stress. I started to think that maybe it is the Mirena. I started doing searches on the adverse side effects of the Mirena and thank God I found you guys. I have most of the symptoms described here and other Mirena side effect pages. I will be having this awful thing removed in about two weeks. I don't know what my husband and I are going to do about birth control. We both do not want anymore kids but I am only 28 and do not want to have my tubes tied.
Headaches
Joint Pains
Low Back Pain
Mood Swings
No Sex Drive
Massive weight Gain (I have not lost any of my baby weight plus i put on a few more pounds)
Breasts Double in Size
Fatigue
Dizziness
Depression (low self-esteem)
My feet have even grown (probably because of the weight gain)

I am so glad I ran across this site. I had got the Mirena in April 08 and started having leg cramps and foot cramps all day, as if I had just run a marathon, but trust me I couldn't even run a block. I am so tired all the time and recently started having headaches lasting for over 3 weeks, they have caused me to be dizzy and "not focused". I actually went to a MRI clinic today for a CT scan because I was convinced I had something going on. I also had my doctor run blood work today. After reading these posts, I am thinking it could possibly be the Mirena, I hope so, at least I can have that removed.

within two days of taking metronidazole for a gum infection i had horrible pins and needles the worst crushing headace ive ever had anxiaty panic attacks and couldt sleep for a week this medicine is the nastiest side effects ive ever had .i just got back from hospital where ive been for two days as my symptoms were so bad docs thought the infection in my gum had traveled to my brain, but after a ct scan,lumber puntcture, blood tests all came back clear they decided it was the tablets. it will take me a long time to get over this , i would advise anyone with a history of panic attacks,depression or headaches not to take metronidazole.

I had Mirena inserted on June 19th at my 6 week follow up from giving birth. He presented it like it was the best contraception to get, so I thought "Why not?" I had it inserted right then and it didn't quite go in right the first time, so he tried again. And, yes, it is quite uncomfortable! Well, he thought it was in there correct (99% sure) but decided to send my for an ultrasound the next day to be 100% sure. So I had some cramps the rest of the day and night, nothing I couldn't stand, and went for my US the next day. Sure enough, the IUD had been pushed through my uterine wall and was now somewhere in my pelvic cavity roaming free. I went for a CT Scan because they couldn't find it with the US, and then had to get it laparoscopically removed the same day. So much for trying to be cost efficient with the Mirena! I had some cramps that lasted a few days and continue to have some slight vaginal discharge, but at least it's out. Of course my doc said that was the first time he had encountered the Mirena going through the uterine wall. (Great to hear) Depo worked great for me before, and that's what I'm doing now.

Well, I am so glad that I read these responses. I have had the absolute worst headache for 1 week now. It is miserable. It is on the right side of my head and goes down behind my right ear. I have even been so concerned about it that I had a CT scan of my head done. It was a pain like I have never had before. I was on the NuvaRing for two weeks and when I went for my yearly, after complaining of the headache, she yanked that sucker out. I have still yet to start a period 4 days after the fact, and welcome it with open arms. Hopefully when this hormone is out of my body, my so called "hormone induced migraine" will leave me. Lortab doesn't even subside the pain. UGH>

Last Christmas (07) I was diagnosed with pneumonia in the the right lung and x rays ordered. Xrays revealed an "unknown mass", or so they thought... they decided to redo - confirmed them and ordered CT scan... mass was gone, but there was PE in both lungs... so started the coumadin. I am type 2 diabetic as of Jan 07... have been managing my diabetes with healthy diet and regular exercise (A1C 7.4 to 5.4 in 9 months) ... no drugs... so the prospect of coumadin for life bothered me. However, my doctors all made a great case about how safe it is compared to other drugs... I lost 35 lbs in 07 after changing my lifestyle... and felt great. I am here today because I gained 20 lbs in 4 months of coumadin therapy (no change in how I was living), have aching muscles, chest pain and shortness of breath, and thinning hair.

After 2 days on the web I find only doctors and pharmacies say no side effects, but the hundreds of testimonials of actual coumadin guinee pigs like myself are finding a lot in common. For me, Im off it tonight.

Severe headache, fatigue, diarrhea, and nausea, stomach pain that you wouldn't believe. I have common side-effects to most antibiotics so I wasn't worried at first but now that I have read all these posts I am getting pretty nervous. Last night I was back in the ER for the second time in three days because the lymph nodes and glands in my neck were swollen. The doctor gave me a CT scan and discovered that I had acute bilateral infections in my lymphnodes. An infection that I didn't have before I started taking the medication. This drug is horrible and I don't recommend it to anyone.

Jen
Washington State

It has been 18 days since my 9 year old daughter has taken Singulair. Our daughter had been taking Singulair for approximately 2 years. It was in the last year that we started to notice some behavior changes and mood swings that were so often unprovoked. We were somewhat concerned and thought like so many other parents that it was a phase. Then in December 2007 she came home from school with a tummy ache and had several episodes of vomiting. She seemed better the following day, but we took her to the pediatrician to be sure that this was a virus. The stomach pains continued, and then anxiety attacks began. Over the next month she began to wake up each day with stomach aches and we began more visits to doctors and more testing. She had abdominal X-rays, CT scan, mekel scan, GI consult and endoscopy. All were ok except she did have some small amounts of acid in her stomach. She was treated with Prevacid with really no significant changes. As weeks passed she missed more and more school, she just could not make it through the day. She had intense separation anxiety, and developed OCD about being sick again and vomiting, fears that she may stop breathing; fear of dying and the list goes on. She was refusing to ride the bus to school, and was having more and more panic attacks that would last for hours. We finally took her to a psychiatrist after we had done every test we could possibly do and all were normal. She woke up with the fear and anxiety, and fell asleep each night the same way. The doctor said she had "OCD" which she believes was triggered by the fear from vomiting. "This was the first time she had vomited since she was an infant.” She was treated with Lexapro, and Klonopin. The symptoms worsened over the next few days even with the new medications. After many calls to the doctor we were finally advised to have her admitted to a children’s psychiatric hospital for closer evaluation where higher doses of medications could be administered. She was there for 4 horrible days with slight improvements. Over the next few weeks the medication did begin to help some and she was able to make it through school each day as long as she was able to call me a few times a day for re-assurance. I thank God each day for her wonderful teacher and staff that have helped us through this. They all have known her for 3 years and knew this was just not her character at all and she was truly struggling. She was always known as "Smiley" to everyone because she always wears a grin. We began therapy with a psychologist as well and she has good and bad days. Then we heard the news about Singulair and I began to trace back other issues she had with focusing in 2nd grade and how things just seemed to progress from there. It all happened so gradually that I would never have put two & two together. She is showing improvements every day with personality, mood, attitude, fears, and the "OCD". She told me today that this was the best day ever!! I have made all the Doctor's involved aware of this information and the progress she has made in the last 2 1/2 weeks. Her doctor did cut her meds in half this week as well. Thanks to everyone that has posted their nightmares as well, and we will pray for you and for full recovery for all those that have suffered.

I was put on Yaz (same as Yasmin but with a smaller estrogen dose) due to irregular periods and a presumed hormonal imbalance. That was in September '07. Four month later, on Jan 1, '08, I went to the ER with breathing difficulties, and weakness in my arms and legs. I had been having muscle cramps/ charley horses in my right calf, but that was the only other health problem I had experienced. I thought I was having an asthma attack. So did the ER - at first. After I did not respond to the breathing treatments, and I became completely out of breath and exhausted after walking across the hall to the restroom, the ER doc checked my D-Dimer level to see if I was at risk for blood clots. He said if it came back over 500, he would have to do further testing for clots. It came back 4500!! I was sent immediately down for a CT Scan which showed mulitple clots in both lungs, mostly small, but several of significant size. I was immediately put on oxygen and a heart monitor, and an IV drip of heparin was started. I was in the hospital for 4 days, had to learn to give myself shots of Lovenol in my stomach until my pill form of blood thinner had time to kick in. I am now taking Coumadin blood thinner every day until July, when my D-Dimer will be checked again. Depending on the results, I may come off the Coumadin, or I may have to commit to it for 3 years. However, I was tested for all the hereditary blood clotting disorders and all came back negative, so my doctor feels as though the cause has to be the YAZ! Everyone tells me I was very lucky and that I could have easily died, especially when I was just thinking I was having an asthma attack and put off going to the ER for a few days. If you are taking Yaz or Yasmin, and you begin to have difficulty breathing, any kind of leg cramps, weakness, or tightness in your chest (I had also been having severe heart burn) - go have yourself checked out!!!!!

Howdy,

Mom from Wyoming who's daughter was a non-smoking, non-drinking 20 year old driving, full time college student and part time working young woman. She was diagnosed with polysistic ovary syndrome and she wanted to have "normal" cycles.

The OBGYN clinic gave her Yaz pack to take. After one month and a half, she developed severe headaches, began to throw up, abdominal pain, became covered in acne, anxiety at being alone, and her depression worsened. She could not sleep through the night and was fatigued for the next days activities.

On March 16th, she woke me screaming of a neck ache and demanding to go to the ER.

They did a CT scan and a MRI to confirm that they had discovered she had 2 blood clots one in each sinus area and one blood clot in the base of the brain drain. She was hospitalized for a week.

She has lost her quality of life and her independance. She will need to be on medications and blood thinners for the next 6 to 8 months (maybe the rest of her life) and NEVER use any form of birth control again.

She cannot drive, work or continue college due to the reactions of the blood clots and the pressure on the brain. Her short term memory was affected by the 2 blood clots in the sinus area. She is living in a survival mode and recalling things that happened when she was 13 years old as if they are happening today.

The doctors have informed us her sisters may be subject to the same effects if they take the same birth control.

We were lucky to have a radiologist that could read the CT scan and have us return to the ER and then a professional staff admit her to the hospital. I thank God I have my daughter and she is on the long road to recovery.

Hello, Ladies.. I am 33 yrs old.. I have suffered a stroke from taking these birth control pills yasmin.. I was only taken these pills for about 4 months.. I woke up one day with a serve headache.. I had taken all the amount of tyelnol I could take in a 8 hr day. And the headache did not go away.. I just thought it was the weather or something.. It lasted for 2 days.I am a single parent of a 9 yr old daughter.. I woke up on monday morning still not feeling good. I got up and was going to start the day like I normally would.. Well I got in the shower and then got out and felt very dizzy. Then the next thing i remember was that my arm was shaking uncontollably and would not stop shaking.. I had to get my daughter up and she got dressed and got me dressed and called my dad.. Then she called 911. I was having a seizure.. Then by the time the ems got here my left side was completly numb.. Could not feel anything.. So then they did a ct scan.. I had a blood clot in the main vessel of my brain and it was bleeding.. Then they told me and my family that I may need brain surgery.. Then had to be transported to riverside methodist hospital.. Then I went into a full blown seizure.. I don't remember that at all. I remember curling into a ball and shaking and that is all that I remember.. Then I was at the hospital for 2 weeks.. Then when I came home about 4 days after that I went back.. My right side was going numb.. That was due to I was having more seizures.. I would love to get together with all of u and form a class action suit against this drug company. I am not like this but this is my life and the lives of other people.And not only that I have a daughter to raise and think about.. So if any of u would like to contact me..Please feel free to do so.. My email address is mcottrill2@verizon.net..

I had what I thought was a sinus infection for three months, I was treated with various antibiotics and Prednisone. Finally a CT Scan was done and I had clear sinuses. I was having pain/tingling under my eyes, extreme tension in my cheeks, jaw, neck and shoulders. It turned out that I was having "involuntary muscle contractions" related to the medication. I had to take muscle relaxers for several days after getting off Topamax. It has been 3 months since I've been off and I am still having some tingling/discomfort under my eyes. I am seeing a neurologist soon to see if this is permanent nerve damage.

I am 41 yrs old and have been suffering with very heavy, clotting periods for the past 5 years. During those 5 years, I tried several different hormone therapies to control the bleeding, but every one of them caused extended periods lasting 10-12 days with only a week or two of no bleeding in between. I went to the GYN and her recommendation was to try the IUD as a way to lessen the bleeding and help treat migraines I also have during my cycle. I had the IUD inserted on Feb 12, 2008 and have experienced the following ever since: very sharp pains in my abdomen, constant minor cramps, extreme bloating so that my clothes do not fit, nausea just enough to not want to eat, constant light bleeding forcing me to go through several pantyliners a day, and very sore and full-feeling breasts that remind me of the days of nursing my baby, night sweats which I've NEVER experienced before. I do not have any desire for sex, but that is partly due to the constant bleeding. I went to the ER for the sharp pains in the abdomen to check for IUD perforation, but all their x-rays and CT scans showed it was in place. The CT scan showed a small spot near one of my ovaries that was 'explained away' as probably a result of ovulation. In all my years, I've never felt ovulation to that degree, this pain was a stabbing feeling from the inside. I decided to follow the GYN's recommendation to keep the IUD in at the time, but I now have an appt in two weeks to have it removed. I thought I had researched all there was to find about this hormonal IUD before my decision to have it placed--if I had come across this forum at that time, I would have said no. I was a little hesitant to go this route, putting a foreign object inside my body, but didn't listen to my own instinct at the time. I wish I had now, and I will definitely share my story with others so that they will be well informed before making this decision. My next options (as I am finished with having babies) are either thermal ablation or hysterectomy--at this point, I would welcome the hysterectomy because it would make all this bleeding/cramping STOP!

I have suffered with chronic sinusitis for about 8 years, and concurrent asthma for about 6 years. I am a 46 year old male.

I have worked with highly noted ENT in the area, and he tried many (non-prescription) recommendations over the course of a few months, but nothing worked. I had a CT scan that showed profound sinusitis in all regions, especially the ones that nasal corticosteroids cannot reach. In an attempt to avoid surgery, which he described as risky and not particularly effective with the type of widespread sinusitis I had (my orbital lobes were involved), he then suggested I get a single intramuscular corticosteroid shot, which he administered about 10 days ago. I was not advised of any potential side effects.

I called today to ask what it was, and was told Kenalog 60mg - I was getting a prescription for something else and wanted to make sure the pharmacist knew what I already had in my system. No comment from the pharmacist.

First of all, the Kenalog has worked like a miracle drug on my sinusitis. I can breathe normally, I can fly without intense ear pain, my sense of smell and taste has returned after an absence of almost a year, and my asthma seems to have improved. Also, and perhaps strangely, I had a noticeably enlarged lymph node below my left ear on the lower part of my neck for many, many years. It felt like a pea under the skin. None of the doctors in any of my physicals expressed concern about it over the years. Since receiving the Kenalog, this node has returned to normal and I cannot feel it unless I really search for it. I thought it has just calcified and was going to remain that way forever, but perhaps it was permanently inflamed from permanent sinusitis.

The only side effect while on Kenalog that I have noticed is that following Albuterol inhalation (for the asthma), my lungs burn a little and I have a productive cough for a few hours. I suspect that two things are going on: the Kenalog has decreased bronchial inflammation, and increased a vast amount of sinus drainage, some of which is going into my lungs to be expectorated.

My doctor is an older, seasoned pro, and I trust him. I just found and read online the BMS prescribing leaflet (the one for doctors) and it is very explicit that unless the injection is given as a DEEP intramuscular injection, then local atrophy is LIKELY to occur (their words, not mine). It does appear, therefore, that the side effect of atrophy is potentially dependent on the skill of the administering doctor.

I know I will get about 2-3 months relief from this medication, but with all the very tragic tales of side effects listed here, with which I sympathize deeply, I will be reluctant to take it again.

I am hoping the skill of my doctor - and my body's own system - cope with injection without some of the more serious side effects that the people here have been experiencing, though I expect I will have to wait a couple of months to see what happens. For some of us, the drug has (so far) saved us from a life of constant misery and fatigue. I am keeping my fingers crossed and will report back.

Wishing you all well.

Hi! I've been on Wellbutrin XL since November 2007. It's late February 2008 and I just stopped taking it two days ago. I know I shouldn't go cold turkey, but like others...I'm afraid of the side effects.

I've been having headaches since December. After having my eyes checked (prescription barely changed) and returning to the chiropractor (thinking something may have been pinched in my neck), nothing helped. I have NEVER had migraines until I started taking this medication, which a friend brought to my attention. "When did you start having these headaches? Wasn't it around the time you started Wellbutrin?" He asked because he, too, has had issues finding an anti-depressant that worked for him. On many, he's experienced headaches.

My doctor ended up prescribing a CT Scan and an MRA w/contrast of the brain because I told her that, in addition to the migraines, I also had two occasions where it felt like I was going to have a stroke (like my head was just going to explode and I almost passed out).

I have yet to have the scans due to an insurance issue, but I have stopped taking the Wellbutrin to see if that will help. I'm not looking forward to the depression, but I'm hoping I can take other positive steps (exercise, proper diet, vitamins, etc.) to avoid taking any more anti-depressants. The side effects are NOT worth it, at least at this point. I'm just going to have to find another way to get myself out of bed in the morning! :)

I have been taking Omeprazole since December 2007 now so 2 and a half months.

I had the dose increased to 40mg 3 weeks ago as 20mg wasn't curing the burning in my throat.

For a few weeks now i have had increasing vertigo/dizziness and palpitations. I only linked the 2 to the medication just yesterday, googled it just now and confirmed my suspicions to the Omeprazole.

Other feeling i have had since taking this medication...

Severe dizziness
vertigo
palpitations
headaches/migraines
weakness
fatigue
sweating
nausea
bloating
stomach cramps
visual problems
intolerance to bright lights
aching joints
chest pain

Now my question to myself is do i come off the tablets and endure the misery of my acid reflux? surely there must be something else we can take for our stomach problems that don't cause these awful side effects.
Anyone tried anything else that worked and didn't make them unwell?

This is a total nightmare and i need advice! I was on Lamictal for a year and about six months into my health began to slowly deteriorate. It started with shortness of breath and heart palpitations and eventually attacked every system of my body. My symptoms are muscle pain, spasms and knots to the point that i can't turn my neck sometimes, joint pain (mostly knees), stabbing floating pain everywhere, headaches, frightening tingling in my extremities and a few times my entire body, sore throat, flu-like feelings, stomach cramps, bloating and heartburn. The list goes on. I have been off of it now for two weeks. My psychiatrist has never seen this type of reaction before and is not convinced it is the Lamictal. I have been to every single type of doctor and the ER twice, had extensive lab work, CT scan and two MRIs. I have been off Lamictal now for two weeks and am not feeling much relief. I am so scared and frustrated and please need advice. Has anyone else experienced this? Does it ever go away? I feel like I am literally living a nightmare with no-one to turn to for advice because no-one seems to know ANYTHING!!!!

This is the 3rd time I have been on Wellbutrin. Once in 1999, then in 2004, and just started taking it again 3 months ago. The first two times I took it I had joint pain and a lot of muscle inflammation. This go around is different... Just recently, within the past few weeks, I started breaking out with hives, after taking it with no problems for three months! Started on my head and progressively got worse. I break out all over my body, head, legs, back, hands, etc. For some reason it seems to happen more frequently when I lay down in my bed to go to sleep (weird!) One other scary side affect is, I frequently stop breathing when I start to fall asleep, and wake up gasping for air. Has anyone else experienced this?
Since I had never experienced problems with hives the first few times I was on Wellbutrin, I didn't think it was the medication causing the hives. So, I cut my dose in half (50mg/day). The hives didn't go away, so I stopped taking it all together 3 days ago, but still continue to get hives. Does anyone know how long it takes to get it out of your system?

I'm a woman, about to turn 50.....and have been experimenting with the statins for about two months(not by choice either). I tried Zocor and had a stop that after 10 days because of massive hair loss. Once stopped....the hair loss stopped immediately. Just a ill more than a month later I started on Lipitor. All seemed to be going ok. NO hair loss. BUT.......mannnnn I don't sleep hardly at all. I'm tired beyond all belief......and its that bone deep OMG I'm sooooo exhausted type tired. I often times don't eat an evening meal after work because I seriously don't think I cant stand long enough to make anything. My legs feel as though they cannot move another inch. I have horrible cramps in my fingers.....the calf of both legs and now in my rib area. Ive had horrible horrible blurred vision.....my attention span is about as long as a gnat!!!!! I seem to have an all over bone deep body ache. It gets to the point that if MOVING A MUSCLE would save my life........Id have to die sitting still....I cant do it. The every day you wake up in the morning headache is way beyond OLD. I also notice I'm nauseous and or have a gut ache almost all the time. Its effectively killing my appetite so maybe I'll lose weight, but damn..is this the way to do it?

WHY wont the doctors believe that this damn drug is responsible?

I am so glad that I stumbled on this page so I can warn others so they won't have to go through what I am going through. I began using NuvaRing in August 2007 because I couldn't remember to always take my pill at night. I noticed a change in my mood, I was having major mood swings which was affecting my home life and my work life (I teach middle school), I was having headaches that would last for days. Also, I began having nausea and a stabbing pain in my right side just under my ribs. I went back to my family doctor (who by the way suggested the ring because that is what she is on) and she set me up for gall bladder tests. I went through 2 inconclusive tests on my gall bladder and was still having pain and nausea. I was then sent to a gastroenterologist for stomach issues. I have had an upper GI, CT scan and MRI. The tests showed that the root of my problem was a tumor on my liver. I am now awaiting an appointment with a specialist to discuss the removal of the tumor or what I can do for it. The ring was the cause of the tumor. I am 29 years old and have always been active, working out, I have 2 small children whom I play with often, I used to play bass guitar at my church but I had to stop that because I was too tired to go to practice! The tumors are very fragile and can burst to cause internal bleeding which can be fatal! PLEASE, PLEASE, PLEASE DO NOT START THE RING OR TAKE IT OUT TODAY!!!! There is nothing worse than looking at your children and your husband thinking that you could have internal bleeding that could kill you and you would never be able to see them again because you just didn't want to get pregnant! I didn't read the pamphlet that came with it, I just trusted it because that was what my doctor used. This "rare" incident that happens to like one in a million has happened to me! I took it out the 30th of Dec and have had much more energy and felt better about myself. That doesn't change the fact that I have this tumor that I have to deal with now. I was only on it for 4 months!! Be careful

I had my Mirena IUD put in May 1st of 2007 and all the side effects that came along with it......the constant spotting, acne, itching breasts (which I thought was due to new bras that I had just purchased), nausea, depression (which I had to go back to taking Wellbutrin), no energy; tired all the time. My biggest side effect which I have not found any others to have is Allergies. I know it sounds crazy, but I have never had problems with allergies until a month and half after getting the IUD, extreme allergy symptoms, swollen glands, neck pain, very shortness of breath; to the point that I was down for a whole day here and there, I am having to take Allegra; had to get a steroid shot. Now that it is cold, I thought I would be getting break from the allergies, nope. I joined a gym hoping that it would help in giving me energy, nope.........I have talked to my Dr and the nurses that work with my gyno and they act as if I am making this stuff up. It is very frustrating when you know that your body has done a complete 360 in the wrong direction and everyone seems to think your crazy.

Well I am having my IUD taken out as soon as I can!

My Saga began years ago when I had high cholesterol at 25 years old.
At 39 my doctor started me on Lipitor and I didn't stay on it.(no reason)
Now at 45(200 LDL) and at the urging of my father I have been on Lipitor for 24 days. He is on crestor. My father had open heart surgery at 41 and a second bypass at 55. He takes about 30 nitros a day at age 74. His brother died at 55 and father at 56, both heart attacks. So you see his concern for me, though being a female does help me.
Anyway at the time of my physical a swollen lymph node was found
on my neck. It has been there for over a month now and we have done
CT scans, mammograms & blood work . I will have a biopsy in 2 weeks on my neck. Everything has come back normal, however the pain in my
stomach started two weeks into the Lipitor. Also difficulty swallowing
like a chest infection. I lost five pounds not being able to eat much and constantly would get so bloated eating just soup. I went back to my doctor she sent me for a CT scan because lymph node issue too. Scary.
I had a biopsy on one breast as well because we are doing all these test for the lymph node swelling.
Well I have been popping Ibuprofen 600mg at a time to stop what feels like liver pain. I had hepatitis A so I know what that feels like. The pain was all over my top abdomen. I am starting to worry even more thinking I may have lymphoma. I start getting pain running down the inside of my right leg and the calf also. I spent 10 years in the Army reserve and was always fairly in shape so this was so out of the blue. I decided to go to and internal doctor because I was getting nothing from the family doctor and we still have the lymph node issue (swollen) He immediately said
stop taking the Lipitor after hearing my symptons. I still have to have a
biopsy on my neck but I am convinced Lipitor caused all the pain in my
stomach and fatigue. My doctor seems to think so too. Don't stay with a doctor that isn't aware of a drugs side effects. Definitely shop around. I hope to post again when my symptons disappear and my lymph node comes back negative.!

I had a CT scan with Isovue 370. About one week to ten days later, I abruptly started with severe pain, burning and tingling in both legs from about 2 inches above my knees to my toes. Had 2 bouts of cystitis symptoms five days apart. Was checked for infection- had none but had blood in my urine. I have had an EMG, x-rays and an MRI and the doctors find no reason for all this. I have been on Neurontin for 7 mos for this condition and am getting no help from the medical profession. My GP says it couldn't be the Isovue 370 but a neurologist says- probably was but doesn't know any treatment. Please help- it is so painful and I am having trouble walking now.