Ct scan symptoms and conditions

One week ago , i have read in newspapers that a child 9 year old got high fever(40 C) , he was seen by a pediatrician , who gave him voltaren shot i.m , after that the child condition deteriorated rapidly and he became unconscious , he was rushed to the ER in another hospital where he has had CT scan head that revealed bleeding inside his brain with an associated bleeding from his nose and mouth, after being in intensive care unit for sometime the child died .
There was a suspicion that H1N1is behind his fever and till now the cause of his internal bleeding that led to his death is unknown , could be this linked to voltaren shot he got in his ped. clinc as what the preliminary reports stated ?

I finally stopped taking Topamax because of the side effects. But the worst was getting kidney stones from it. I only drink water and drink a lot, but I still got stones. The first time I was in so much pain that I could barely stand it. The second time, I had the pain and with it a kidney stone that was too big to pass. I could barely urinate. Had to have emergency lithotripsy to remove it. The doctor did a CT scan recently and it showed I still have many stones in both kidneys. I can't take another one of these attacks because they are so painful. My neurologist gave me a natural remedy for migraines called Petadolex. This stuff works! It has made my headaches much less severe when I have them which is not very often and my daily low level headaches are gone. This stuff is made in Germany and can be found in most health food stores and pharmacies. It also cost a lot less than Topamax.

When the generic Topamax (topiramate) came out, my insurance company wouldn't cover the real Topamax and it was costing me $400 a month if I wanted it over the generic. The generic was the worst drug I have ever taken. It is NOT the same as Topamax. I got so ill off of it that I had to get back on Topamax. I am finally off of Topamax completely after decreasing the dosage over many weeks. I was on 200 mg a day. I had all the side effects too like tingling hands, cognitive impairment and depression along with some others. This drug is poison and I am so angry the manufacturer didn't state all the possible side effects when they knew damn well it had them. There is a class action lawsuit against this manufacturer for not disclosing some of the horrible side effects.

I was literally in tears when I found this site and read all of your posts. It was as if I was reading something I HAD WRITTEN. Having just returned from getting a CT scan of my head, I started researching "causes of severe headaches not related to migraines" and lo and behold this site popped up in my search. What caught my attention was the word "Mirena". Up until today I had never even considered that all of the issues I have been having since the birth of my daughter in August 2008, were in any way related to Mirena. When my daughter was about 2 months old (after my 8 week check up and insertion of the implant) I became extremely moody, sad, social anxiety kicked in, I cried for no reason, had no desire to talk to anyone, not even my husband - VERY unlike my personality. After talking to my doctor it was determined I had post partum depression so I was prescribed zoloft. Didn't work. Was still irritable and lethargic but maternity leave was up so I went back to work. I was exhausted, couldn't process my thoughts, was constantly dizzy and had blurred vision and it was all attributed to the "baby schedule (nightly feedings, no solid sleep, adjusting to schedule, etc.). My mood swings were out of control and it got to the point that I even through a knive (albeit a butter knife) at my husband. I began seeing a psychiatrist who determined I had mild bipolar disorder so he put me on medication for that. It has helped some but still doesn't control my crying spells or occasional outbursts. Recently I was so dizzy that I saw my ENT doctor who said I had vertigo. I was prescribed something for that. Still, I am dizzy and feel off balance. Most recently, I have had severe, severe, severe headaches and though there is a great possibility it is a viral issue, I was ordered to have blood drawn and to obtain a CT scan. Nothing much revealed so we set an appointment to see an neurologist next week. So, because of the worry over it, I started doing an internet search and her I am. Reading these posts brought on an overwhelming sadness because my poor family has had to endure my wrath for past 12 months. I am so angry that I didn't see this sooner and moreso that their !@#@#$% side effects didn't list ANY OF THESE discussed here. Additionally, my hair has been falling out in clumps and I can't seem to lose weight despite my 1500 calorie diet and exercise.
I made an appointment TODAY to have it removed. If I could yank it out myself I would. Thank you all for your posts. You may have just saved my marriage and my life.

within about one or so hours after having been injected for a Ct Scan I began to shake uncontrollably and feel very ill and also had severe pain in my coccyx. I had to be admitted to hospital where I was treated with an IV drip containing about 100 mg of prednisone.My creatinine level increased above the normal limits but reverted to normal after about 2 days.I was very listless for about 3 days.

this is probably the worst thing Avelox caused, besides death, which would have happened without help..

7th day on Avelox for sinusitus - massive pain back of my head, sweating so much my clothes were soaked, threw up 2 times, legs were uncoordinated when trying to walk

Called 911 - paramedics took blood pressure - guess what.. 210/180.. something was definitely wrong. Rushed to hospital - passed out in ER - woke up with wife and family present - CT scan found my brain bleeding and brain surgery was performed to remove the clot..

But wait, it gets better... 2 days in the ICU my brain swelled from the surgery and the fluid stopped circulating.. I was semi conscious in the ICU for probably 4-5 hours and nothing was done. My wife came in early in the morning and thought I was sleeping, but could not wake me.. The nurse said that a doctor was called and will be there later. I'm DYING right before their eyes in the ICU!!! My wife demanded I get a CT scan immediately. If she didn't I would have stopped breathing. Later CT showed my ventricles enlarged with fluid backed up so much that my brain and brainstem was ridiculously squeezed so much, my head was all ventricles and barely any brain showing in the CT. I attribute my current brain damage to this episode.

A shunt was placed in my head for about 3 days.. basically a needle is inserted into my brain and left there to drain the excess fluid.. After my condition stabilized, the shunt was removed.

Spent 1 week in the hospital, then transferred to another hospital to stay in for inpatient PT and treatment. I didn't know left from right, had double vision, was throwing up constantly, was hot, then very cold, my legs hurt, had hallucinations (was believing certain things were happening, that really weren't) was incontinent, had a new catheter inserted every single day, was taught to walk again, had to use a wheelchair.

I had always been healthy, was vegetarian and did not smoke cigarettes.. I exercised regularly, did not use drugs (i.e. - cocaine or methamphetamine which can cause high blood pressure leading to a stroke)

Didn't know what happened to me, but realized I had to be there.. After 1 month, decided to go home (the hospital was becoming too stressful, somebody was always screaming and yelling at night and the daily catheters were uncomfortable), to be back in the lifestyle I knew.. my wife, my granddaughter, my house, my dog, cats, and other pets were sorely missed.

Once home I found that I couldn't do what I used to anymore - could not mow the lawn, drive, speak well, walk properly, had double vision, a tingling on my face, a metallic taste in my mouth so bad that good food tasted bad.

My wife set me up for physical therapy three times a week daily outpatient at the hospital I was at. Vomited regularly from the daily dizziness.

This was most disturbing, I developed a pain in my left hand and left shoulder, to the point where I could not raise my arm above my head and had to sleep with my arm straight down for at least a year. After playing guitar for 30 years, I found myself unable to play my guitar anymore. My left hand had lost all its dexterity and was not usable. I did not realize what happened to me until my wife explained the entire thing to me.

In the next few weeks I spent each day trying to put "2 and 2 together" and figure out why this happened to me. When doing research on strokes, I realized that certain things happened to me that were not consistent with having a stroke. In my brain damaged condition, I remembered taking the antibiotic Avelox, based on a physicians prescription. I researched the adverse effects and to my amazement, the listed side effects were consistent with what happened to me.

I began a quest to file a lawsuit - was unable to find a lawyer willing to tackle such a huge case.. although one lawyer did file before the 2 year time limit expired.. I had MRI's performed on my hand and shoulder which revealed scarring and previous ligament tearing.

During the time of having more outpatient and in home therapy, I regularly visited a psychologist and my physician confirmed that the Avelox most likely caused the brain bleed, tendon tears, and other mysterious symptoms when I presented him with my research. I was unable to work and my only income was from monthly Social Security Disability benefits that didn't begin until 6 months after the incident.. leaving me with no income and unpaid bills for 6 months. The mortgage payments fell behind and soon foreclosure notices arrived. We decided that an alternative would be to sell the house.. it could not be sold after 1 years attempt, so my wife and I moved to an affordable apartment. I put household items in a storage facility. I either sold to pay bills or threw away much of my personal things,since I was devastated by what happened to me, I didn't think I was going to survive long after reading statistics on strokes.

While in the apartment, I needed an income and was forced to take what was in the scpoe of my limited ability. I accepted an early morning paper route and then made deliveries for a courier company using my own vehicle.. That was a 12 hour work day. Being completely upset over what happened, losing everything including my house.. I decided to attempt to escape the overwhelming things that happened and were still happening. I found a house for rent that was less than the apartments rent, except it was in North Carolina. At the time that seemed perfect, a 3 bedroom house located in a far away place where I could forget everything that happened and make a fresh start. Only problem is my wife not want to go, but I was adamant upon doing it. She helped me move everything, including all storage items.. I had moved to North Carolina, but soon found being alone and unable to find suitable employment unbearable. I was being contacted for back rent owed, but could not do everything alone - I became more depressed to the point of feeling suicidal, so I called my aunt in NY and she said just leave everything and get myself to her house. I did, leaving everything behind, and stayed with her for a month until my cousin invited me to stay with him.. which I did. I stayed with him for 3 months, all the while searching for employment.

With help from my family I moved back to my familiar area in NJ in the summer of 2008. I had lost everything..unable to be physical with my wife and being seperated for 18 months, she has requested a divorce. Currently I live by myself and am still slowly recovering, yet my left arm and hand are uncoordinated, my talking is difficult, slurred and gravely (diagnosed with dysarthria), my balance is bad and am dizzy every single day for the past 4 years.. Although brain damaged, I am attempting to rejoin the computer support business again.

My entire past, everything I knew and did, everyone I knew, who I was, etc.. is all a strange hazy memory. If I don't take a sleep aid, I wake up around 4am with racing thoughts, unable to sleep.. My depression and anxiety are so bad, it is difficult to function and interact with others. My psychiatrist has diagnosed me with post-traumatic stress disorder and prescribed Zoloft and Xanax.

Upon proper research, I have to blame the prescription and subsequent use of Avelox for causing the brain bleed which led to my life being completely and utterly destroyed. My intentions are to file suit against the manufacturer Bayer and/or the hospital for allowing me to die in the ICU

To all the women still taking this drug: I beg you to stop taking this medication and read all of the posts on this site!!!! Here is my story... I was on Yasmin for 6 years. About 4 years into taking the drug, I noticed a mass on my right side. It was a painful mass that I could easily feel, and it eventually because so uncomfortable that I could no longer sleep on my right side, and it affected basic movement. At the same time, I was beginning to show some side effects of Cron's disease (which runs in my family), so my gastro doctor told me to get a CT scan and an MRI. The tests revealed a gigantic mass on my liver and I was told to see a liver specialist right away. I went to KU Med and was told that I had to have emergency surgery right away, and that I was basically a walking time bomb.... If I tripped and fell, it could cause this mass to rupture and I could bleed to death. He also told me that if I had gotten pregnant while I had the mass, it would almost certainly lead to death for me and the baby. Nonetheless, they cut me open from the middle of my chest clear down to my belly button. They did a liver resection and removed my gall bladder and several lymph nodes. The mass on the scan turned out to be 2 grapefruit-sized benign masses, called Focal Nodular Hyperplasia - most commonly caused from the hormones in birth control pills!!!! Ladies, this was major surgery.... I was in the hospital for 9 days and out of work recovering for nearly 2 months.... and this all took place 2 months before my wedding!!!!!! The MASSIVE stress I endured caused me to have panic attacks and I thought I was going to literally die. Keep in mind that my CT and MRI were purely coincidental. If my GI doctor had not ordered the tests, I would have never known about the masses, and God only knows what would have happened to me.... Anyway, this whole ordeal has DRASTICALLY changed my life and affected all of the people I love, my husband included, who has to endure all of my pain and anxiety. BOTTOM LINE - IT'S JUST NOT WORTH IT! TELL EVERY WOMAN YOU KNOW!

Have had the Mirena for a year due to needing some hormone therapy during menopause.I am 54yrs old and had my last period over 2 yrs ago-look physically like I am in my 30's. Had a breast reduction and weight reduction surgery over 10yrs ago VERY successfully lost 10# off my chest and 168# off of my body. SINCE having the Mirena I have gained over 30# and gained 2 cup sizes in my breasts! HELP!!! I have been treated by my regular doctor for mood swings with WellbutrinSR, Lexapro, Lamictal, Topamax and others-nothing has worked more than to ease some of the edge. I have gone from a size 2 to a size 10-12 in 9 months and am desperate for an answer! I feel as if all of the previous progress I had made with the weight reduction and breast reduction is all being undermined! I had a tummy tuck last September 08 and I swear my stomach was flatter before I had the surgery! I look pregnant! The surgeons have done a CT scan and can find nothing to indicate the surgery went bad. I don't know what to do as my OB-GYN tells me that "this IUD" is my best bet for hormone therapy and that it is ABSOLUTELY NOT the cause for the weight gain or breasts. Has anyone else "my age/menopausal" experienced this? Most of what I have read has been very helpful BUT all but a few are pre-menopausal and way younger. PLEASE let me know your thoughts!!

lower back pain, hair loss,joint pain, complicated migraines, vertigo, palpitation, hormonal imbalances (lowered DHEA, increased aldosterone-it affected my adrenal glands and kidneys), epigastric pain, bleeding, extreme fatigue, anxiety,pulmonary failure etc. I had to go through ER, 2 CT scans ( abdominal and brain), 2 MRIs, neurologist, endocrinologist, GI, gyno etc. I threw my Yaz pills in the trash after the first CT scan that revealed multiple tumors in my liver and left adrenal gland ( i took the pills for about 3 and 1/2 years)... the past 6 months have been a hell, but there are no more migraines, anxiety or other neurological symptoms at this point. By the way, one of my best friends who just started on Yaz recently ended up in the ER last week with a blood cloth in her left lung. Please stay away from that drug!

hi. just thought i might warn you for whatever it is worth. I have been on mirena for about 4 years. it was my answer from god sincerely because i had terrible periods. my period got so light it basically disappeared. yes!
then about 2 years ago, i started with terrible tension headaches, slowly they began to rule my life-- so that the only relief i got was going to sleep at night. only to awake with the same bandanna wrapped around my head so tight i could barely take it. but with 3 kids grown, a business to run, i figured it was stress. then i started with dizzy spells, almost falling over in the bathroom. A CT scan revealed that i had chronic sinusitis- but something i have lived with all my life. no tumor thank god. so what next-- guess what-- yes over the years the hormone from this drug has overloaded in my system. so make your own decision. was good while it lasted but it will take a while now for it to get out of my system. starting to subside. thanks.

My husband was taking coumadin and developed an infection in his leg. He was ordered Bactrim DS bid. By the third day of the Bactrim, his INR was 4.7 and he was having mental status changes and vomiting. A head CT Scan showed he was bleeding in his brain from the interaction of the coumadin and Bactrim. He had to have 2 bilateral crainiotomies to flush out the blood from his brain. He nearly died. He has severe headaches and short term memory loss.

My experience with Mirena has been awful. I had it inserted a little over a year ago (2 months after the birth of my younger son). Since then I had cramping ALL the time, significant hair loss, periods every three weeks, then every two, then every week and a half. They only last three days on average, but I go through a heavy tampon an hour. I lost a lot of weight while on Mirena, but I don't know if that can be attributed to it-just diet and exercise. I had severe bloating, depression and mood swings, complete lack of sex drive (very much unlike me), here's the kicker. When I went to get it out (last week), they couldn't find it. So after 3 ultrasounds, 2 xrays, and a CT scan, they found it. It's perforated my uterus and is floating around in my abdomen. The evil thing has gone rogue!!! I'm scheduled for a laproscopic surgery next week to find the damn thing, followed by a more in-depth surgery to remove the evil.

If you're thinking about getting it---DON'T!!!

I'm 25 years old and approx 5 weeks after my second Gardasil injection started feeling sick. It has been 6 months now and still no relief. I have been to the doctor 13 times in the past 6 months, before this vaccine that was how much I was there in 13 years. This experience has been a nightmare and everyday I wake up wishing it was. I have had numerous blood tests, a CT scan, an esophagram, seen multiple doctors and it is so frustrating having them not believe you. I used to be happy, healthy and a social butterfly. Went on a job interview today and felt like I was out-of-body not really knowing what was going on. It is absolutely horrible to know that no one can help and be completely unsure of how long this will last. I just graduated from college and I'm supposed to be starting my life and now it's not knowing if this nightmare will ever end. I have had dizzy spells, chronic sore throat, unbelievable headaches with no relief from any OTC drugs or prescription migraine meds, extreme fatigue, hot flashes, night sweats, dry/itchy/watery eyes, ear pain, side pain, jaw pain. I pray for everyone who is going through this nightmare. ALL I want is to be healthy, feeling like my old self. I would give up everything to just be healthy again, pre-Gardasil.

I am in shock and so glad that I came to this website. I have been taking simvastatin for about 5 months now and this morning I decided to do a web search with the words simvastatin and headaches. Everyday I for the last two months I have been asking myself why am I having these terrible headache. My Doctor did a CT scan, I had my eyes tested, I had my hearing tested, my blood tested and everything comes back good. I realized that I have to do something about this problem myself because my doctor prescribed another pill for the headache and that's that. Today I did not take the medication and I will not be taking it again. The symptoms that everyone described are so real to me but the headaches were the worst. I have to thank you all for posting this information. I now feel that I will get my life back.
Thanks verdul1

I have been on prednisone since I was two years old (I am now sixteen) because I have Autoimmune Hepatitis IIa. I would like to point out that there is still a life worth living being on prednisone, maybe I say this because I do not know life without it, but at least we're alive! Last year I had a flare up of the AIH and had to 6x my dose of prednisone. It sent me into a spiraling depression of constant sleep, crying, hopelessness etc....but I made it through. Just PLEASE keep hope that things would get better, because I know what it's like being on the dreaded drug better than most.

I went to the doctor yesterday for test results. I have had an ultrasound and xray to locate the Mirena which is not in my uterus. Now I have to have a ct scan to make sure it's not near my spine and I'm so scared and angry.
Has anyone else had this experience?
I continue to gain weight rapidly. Last week I could fit a size 20 and this week I need to buy a size 22. I've gone from a size 16 to size 22 in 5 months. I'm so sad and my skin is prickly and itchy and my feet swell something awful. My ob/gyn is not being supportive and she appears to minimize what I've experienced. I'm looking for another doctor so I can find out where this IUD has disappeared to.

I went to doctor because I thought I had an ear infection. He looked at me and said I have a little fluid in my ear. He prescribed Amox. Didn't work. I then went back and he prescribed Sulfameth. I began taking two pills a day for a probable sinus infection (never had one before Im 41 yrs. old). I immediately felt like my world was crashing down on me. Im am dizzy all day, my glands are swollen and have dry mouth. I cant sleep and have nausea which is probably why Im depressed. I however continue to take this medication hoping that it will eventually work. Im on day five and feel terrible. Today I go for a CT scan of my nasal area. Pray, Ive never been so miserable in my life!

I had mine taken out today for all of the same reasons. I've also had horrible headaches daily for at least two months. My headaches, nausea and depression have started getting worse every week. Fortunately, I only had Mirena three months before now when I started putting things together. I've never had a problem with birth control pills and I've taken all of them. I used to get heavy and long periods- it took a while to find one to regulate my period. I love, love, love my OB. He told me the same thing today he told me when I got Mirena- that it has less side effects than any birth control pills because the amount of hormones released is lower. Nonetheless, he did agree that it should come out to see if it has been the cause of all of my misery.

I hate to think about the women out there with Mirena who are feeling tired, sick, and depressed and don't know why. Honestly, I don't know how I put it together for myself because I thought, IUD- NO SIDE-EFFECTS, it's just a device right, thrown in with a tiny bit of hormones, but at first I thought maybe I wasn't taking good enough care of myself and that was why I felt so bad all the time. Then the headaches . . . I thought that was sinuses . . . had a CT scan, came back okay . . . thought it was migraines . . . went to the neurologist, had an eeg, treated for migraines . . . still having headaches with nausea.

I almost didn't realize how depressed I was until my husband said something to me. He told me, "you've been depressed for three months now". Eureka!! I got Mirena three months ago. Plus, I am always under the treatment of a psychiatrist who monitors my medicine and am currently taking high dosages of prozac and wellbutrin. I've always had depression/anxiety problems and actually had to continue taking my meds while pregnant, just at half dosage. I had NO problems with post-partum depression (which was very much planned between my psychiatrist and medications). If I were to have problems arise with depression I certainly think it would have been closer to post-partum. I really don't think that my meds just quit working either. I realized that nothing gets me excited. I exert all of my energy into being a decent human being by going to work, taking care of my child, and trying to keep a somewhat-neat house. There is never time, energy, or desire for anything else.

I'm anxious to see how the next couple of weeks go . . . keep posting your progress and I will do the same. I certainly hope my symptoms start to subside . . . if not, I'm in trouble because I know that something is wrong with my body!!

Also, a Naturopathic Doctor told me to take Evening Primrose and it should aid in getting my hormones back to a natural level more quickly.

After 2 years and 7 months, I had my Mirena removed on 5/4. I had it inserted 3 months after the birth of my first child in 2006. At the time, it seemed like my best option due to problems I’d had with the Pill. I was on the Pill for 6 years, the first year or 2 weren’t too bad, but things gradually got worse. Because it was so gradual, it took me years to realize the cause of my problems. My blood pressure slowly got higher, my heart would often race, and I had anxiety and mini-panic attacks to the point where I never wanted to go anywhere. (My heart rate got up to 160 while waiting for the Dr during an appointment and my blood pressure was up to ~145/99) I also started getting migraines that got more and more frequent. I had an EKG and stress test and everything came back normal. I stopped taking the Pill and within a couple months felt a million times better and my BP went back to normal. I had no idea how much it had affected me and it still makes me sick to think of the years I lost because I felt so awful. I didn’t take anything for 6 months before we started trying to get pregnant and they were the best months in a very long time.

After I got Mirena, I thought it was great. I bled for about 2 months, then never really had periods after that (just some occasionally spotting). Three months after it was inserted, I lost the final 10 pounds of baby weight just by dieting. If I was emotional or moody during the first year, I just thought it was my hormones after having a baby. Slowly over time, I began to get more and more irritable. Everything and anything would enrage me. Rage is the best word for it. It would take a split second for me to fly off the handle. Everything irritated me, particularly anything my husband did. The more it happened, the worse it got and I began to worry if I would eventually lose control completely. Meanwhile, I slowly lost my desire to do anything. I’ve never been a big housekeeper, but our house has become a wreck and I have to force myself to get things down when people are coming over. If it weren’t for family coming to visit frequently, we’d really be living in a mess. I just never feel like doing anything and I’ve lost my passion for everything.

I’ve always had bad skin and have taken everything made for acne, including Accutane. My skin was the best it’s ever been the weeks after my son was born. Over the past 2.5 years, it gotten worse and now it’s as bad as it’s ever been. As my 30th birthday approached, I began to wonder if I’d have zits when I’m 70, then began wondering if the IUD might be causing it.

Also in the past year, I have begun to struggle with my weight. It had slowly started to creep up even though my diet hadn’t really changed. The past 6 months have been the worst. I constantly have a desire to eat and crave anything sugary which I’m sure has contributed to my weight gain. I’ve tried dieting and exercising more than ever before and couldn’t lose anything. Then I gained 10 pounds in 2 weeks. If I diet and workout, my weight stays the same – if I eat normally, I gain weight, just as many others here have mentioned. I’d say 80-90% of my excess weight is on my stomach and I’ve been asked twice in the last 6 months by strangers about being pregnant. I now weigh what I did when I was 7-8 months pregnant (25lbs over my pre-preg weight) and I look 6-7 months preg.

All of these issues have gradually gotten worse over time, but significantly so in the past 6 months. My fits of rage began to scare me and I would feel like my head and/or chest were going to explode when I would yell. I started to realize from my previous experience with the Pill that my blood pressure was going up again. I had also begun to get migraines again which I hadn’t had since the Pill. Then I began to feel like I was living in a depression medicine commercial. I’ve never dealt with depression before even when my husband was gone for months at a time in the Navy. Yet all the sudden I felt like I could check off all the symptoms for depression. I started having irrational and scary thoughts that I had no control over and they would go as quickly as they came. I began to get frightened because I felt like I had no control over myself, my thoughts, or my emotions. For whatever reason, I decided to look up Mirena and depression and couldn’t believe what I found - pages and pages of people describing exactly how I felt with all the same symptoms. I had been contemplating it anyway, but I decided then that I was going to get it removed. I went to the doctor and my blood pressure was higher than I expected. She gave me BP meds and offered me meds for everything else. I got the impression that she probably thought I was blaming too much on the Mirena. I would have agreed if not for my experiences on the Pill. She had never removed one, so she referred me to an OB/GYN. They couldn’t see me for over a month and there was no way I could wait that long because I knew it would take a while for my body to get back to normal. Amazingly, I found someone who got me in 4 days later. I was so excited! As everyone says, it’s a lot easier coming out than going in – just a pinch that lasts a second. So far, I haven’t noticed a huge difference (it’s been about 3 days). I felt less bloated the second day, but it seems to have come back a little yesterday. I have been very thirsty since the evening after I got it removed and have been peeing as much as I did when I was pregnant. I slowly feel like my desire to constantly eat is going away and I am not craving sugar as much.

I also wanted to mention, I started the blood pressure meds the day after I got them. I will say that it has helped my irritability a little and I no longer feel like I’m going to explode when I get angry. Now that the IUD is gone, I’m sure it will go back to normal on its own in month or 2. It’s frustrating because I got Mirena because of my BP problems on the pill. I was under the impression that there wouldn’t be any side effects and now I’m back to where I was when I stopped the Pill. I lost several good years with my husband because of the Pill and now I’ve lost almost 3 more and the first 3 years of my son’s life because of this stupid IUD. If it weren’t for our son, I don’t know that our marriage would have survived the last 3 years. I just pray that I will get back to being me and will be able to be the mother that my son deserves.

A few other side effects I’ve noticed after reading all these posts that may also be related are greasy hair and skin, hair loss, facial hair, memory loss/lack of concentration, and the strange odors and various infections that others have mentioned. I used to not be able to wrap my fingers around my ponytail. Now I can almost wrap them around twice. Like most of the other side effects, I blamed it on aging, stress, etc. I’m interested to see if it starts coming back now.

I know this is a really long post, but I wanted to include as much info as possible in case it might help someone else. I probably would have gotten it out sooner, but I didn’t think there were any side effects. For now, I am not going to take anything. I want to know whether the side effects go away and not have to worry if something is caused by a new birth control. I may try something else in 6 months or so, but we’ll see. My husband doesn’t want me to take anything ever again, but I really don’t want to get pregnant. I don’t think I want any more kids, but I’m only 30 and not ready to do anything permanent yet. My new OB/GYN mentioned Implantation, which uses a different hormone, but I don’t have much faith that it won’t have the same effects. I will probably just try different pills and keep an eye on my blood pressure. I plan to post updates when I can to let you know if things get better. I hope that my story helps someone else.

I have taken Avelox before with only minimal side effects nausea and diarrhea were the only ones I got but they were enough. I have been suffering from chronic sinus and ear infections for going on two years now. My doctor gave me samples again of avelox on Monday. Last night I had to be rushed to the hospital. After throwing up all day I got a severe headache. I felt dizzy and out of sorts all day but when I couldn't take the headache anymore I tried laying down. With this medicine you can't take any pain relievers so I thought if I just went to lay down maybe it would ease up some. Well it didn't, and before I knew it I was shaking uncontrollably with tremors and could no longer put sentences together. My head hurt so bad I just wanted to stab myself to make the pain go away. At the er they gave me an IV with something to help with the headache.Anyway after taking a Ct scan and not seeing anything on there the er doc gave me the ok to go home and gave me a script for pain meds. I was having hallucinations, anxieties, and could not speak correctly. I am still having trouble making sentences, I am stuttering, which I have never done before. And I can't get words to go together to make a sentence. The Er doctor wants me to follow up with a neurologist. My tremors still haven't stopped and now I sound like the guy from rain man when I am trying to make a sentence. This is pure torture and I feel like I am in someone else's body.

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.

First of all, a big thanks to all of you who have shared your experiences. I am a biochemist, with a background in pharmaceutical research...I chose the Mirena IUD after careful consideration of it's active ingredient, Levonorgestrel. The side effect profile seemed pretty acceptable...until I started to experience nearly ALL of them...I am 33 years old and had the Mirena IUD placed in October of 2008 after the birth of my second child in June of 2008. The initial reaction was to be expected...cramping, a little spotting etc...nothing to be alarmed about. I still have yet to have a period (which I really don't miss so no problem there) I never gave a second thought to this until now...for the past month or so (coinciding with the weening process, since I have been nursing the entire time, I believe the side effects were not as noticeable) I have been experiencing the following (that may or may not be related to Mirena as my OBGYN has so adamantly pointed out, but after reviewing your posts I'm willing to bet they're connected) and are in order of occurrence: Major, but temporary, hair loss after 2 months or so; Major respiratory infection lingering over a month with difficulty breathing, tightness and pain in the chest at around 6 mos; And in the past month, several instances of motion-like sickness/ nausea, dizziness, blurred vision, major impatience/ mood swings, loss of appetite (pregnancy-like symptoms...yep, I was thinking man I'd be pretty pissed if I was that 0.01% pregnant statistic), and as of this past weekend, my first aurora migraine with tunnel vision and serious nausea and vomiting, to the point where I went to Urgent Care...who referred me to the ER...who wants to perform a battery of tests including a head CT. I have an appointment with a trusted GP tomorrow to discuss possible root causes...but it is to coincidental that so many women are experiencing these same symptoms! I am certainly leaning towards having this removed. CAN THOSE OF YOU WHO HAVE HAD THIS REMOVED PLEASE RESPOND IF YOUR SYMPTOMS SIGNIFICANTLY IMPROVED OR WERE RESOLVED!!! THANK YOU!
These side effects seem to go well beyond a 5% rate of incidence according to all of you who have reported. I will investigate further and keep everyone posted. As someone who is highly experienced in the pharmaceutical industry, you bet your a$$ I'm going to get to the bottom of this! Good luck ladies!

I am 29, super fit and healthy. I'd been taking Yasmin for 6 months, in addition to having a high blood pressure 3 months into taking Yasmin, in the last month, in addition to a high blood pressure I started getting rings in my vision (lasting 5-20 mins and then returning to normal), i had problems with my hearing, i started getting dizzy after very light exercise and lost my breath, i found i was slurring in my speech or having trouble getting the words out, i felt pressure at the base of my head. The problems with my vision led me to getting a CT scan and the docs believed I had a small blood clot in my brain caused by Yasmin.

After finding out I had a thrombosis caused by the pill, the rest of my symptoms could be attributed to that. Yasmin has been taken off the market in many countries because of its side effects. Yasmin is indeed evil and I feel fortunate I had a doctor who referred me to a specialist to get checked out. So many doctors will say take pain killers and come back if it gets worse. I will never touch BC pills again.

IF YOU FEEL/EXPERIENCE ANYTHING ABNORMAL FOR YOU OR DO NOT FEEL QUITE YOURSELF SEE YOUR G.P./NURSE AND SERIOUSLY CONSIDER GETTING THE MIRENA COIL REMOVED
This medication may be suitable for some people but if you experience any of the following, I urge you please, please please, 'demand' that you want the Mirena removed. My symptoms were noticeably worse around my time of ovulation. I've also found out that people previously treated for/suffering from depression should not be prescribed this medication. (I've been on Prozac in the past). I had it fitted in Aug 2007 to combat very heavy periods and severe PMT at the recommendation of my G.P.and had it removed Sept 2008. Symptoms I experienced :-

Dry/furry mouth
Headaches (over time these became migraines)
No concentration
Poor memory
Lethargy (constantly tired and drained)
Smelly discharge (still noticeable straight after washing)
Very heavy legs
Numbness in my legs
Joint pain and clicking (mainly in my shoulders and knees)
Developed facial hair (mainly under chin and jawline)
Hair loss
Weight gain around my stomach (without increasing my food intake)
Feeling constantly bloated.
Spotting randomly for duration of Mirena being fitted. (Brown spotting)

Panic Attacks ( awoken in the middle of the night with them) escalating to the following:-
Palpitations (for no apparent reason)
Clammy/sweating palms and feet
Aggitation ( during an episode if someone was talking to me I wanted to really yell at them 'Just shut the **** up! You're doing my head in!)
Feelings of madness (actually wanted to run away from my own mind)
Pins and needles/Tingling in my hands and feet
Electric shock like surges going through my body (my nerve endings were obviously suffering)
Muscle tremours/shaking (mainly arms and legs)
Eyes became extremely light sensitive
Heightened awareness of sound

Insomnia
Terrible nightmares
Depression
Feelings of detachment from the real world.
Visual disturbances
Episodes of blurred vision

These symptoms did not appear straight away but appeared gradually and with more veangance the longer I had the coil. The more concerning episodes I experienced happened after about 3 months and very erratically. I could not predict when or what time of day I was going to have an episode or pinpoint any reason for bringing on an attack. I had no control over the effects, was absolutely petrified when I experienced a panic attack and just had to ride it out.
All my G.P. did was prescribe me anti-depressants to which I reacted badly. Blood tests also failed to show anything abnormal.
I even tried herbal medicines as an alternative and experienced similar reactions to the prescription drugs. I've now become very pill-phobic and would rather ride out and get over symptoms myself. Paracetamol & Ibuprofen being the only medicine I trust to take now. I had a horrendous year and everyone suffered. Not only my family, but I was signed off of work for 3 months. It was a very worrying time for my husband and my children, who all had to keep an eye on me and witness the effects of my symptoms. On looking back now, I don't know how I managed to function at all and even do my job. Most of the time my energies were spent concentrating on trying to appear normal and held-together to the outside world.
Although I feel 100% better in myself, I noticeably experience more migraines and headaches than I ever did in the past, along with palpitations, usually during my week before. Two days before it I often really feeI like I'm losing the plot! I also really bloat up now a week before my period, feel sick and have a feeling of being ' very full', so am hungry but don't really want to eat. One of my big toe-nails has gone black over the past few months and not through injury. This has just been sent away for analysis. The one on the other foot is raised/ridged/thick/yellow, but normal growth has resumed half-way up now, which I feel co-incides with the state of my health on having Mirena removed. The nurse I saw recently explained that it is true that nails and hair show the history of our health so, for me, this would seem true.
I wish I'd been made fully aware of all possible side-effects of this medication and am now actually concerned that the effects I've suffered may have left some permanent damage.
In spite of all this, it's so good to be me.

ive had mirena since nov. 2008 i had it placed 6 weeks after having my 1st daughter in sept. it hurt going in and since then i have had nothing but bleeding since it was inserted. its put me in the hospital twice, 1st time doctors said it was a cyst on my ovaries ( i refused a pelvic exam) then last Thursday night i started having horrible cramps on my right side in my ovary area to the point where it hurt to walk. went to the ER they did an ultrasound CT scan and a pelvic exam turns out i have a bacterial infection in my uterus. and i remember my obgyn telling me that if it cause an infection i needed it removed so all in all i made an appointment to talk about removing it tomorrow.. i thought it was the best thing in the world but they don't really tell you every side affect. i cannot wait for it to be removed although im not going to like taking a pill everyday!

I started with Lisinopril and had severe isolated visceral angioedema. Thought I was going to die. The attacks felt worse than childbirth. Urine flow would totally stop and bladder would cramp. Bowels would not function. Over a 10 on the pain scale. Went off Lisinopril and 3 days later Dr. wanted me to start Benicar. Within 5 days I was in emergency room with visceral angioedema even worse than the Lisinopril. I have had CT scan, ultrasound, numerous blood and urine tests, PAP, colonoscopy and everything is negative. It has taken a full week for all symptoms to stop. I finally feel normal again after 2 months. I cannot take this family of drugs. And Dr.'s need to be more informed about this serious side effect. My Dr. never considered it could be the Lisinopril or the Benicar since I didn't exhibit any facial edema. More information about this rare, but serious side effect needs to be published.