Biopsy symptoms and conditions

took avelox for 5 days, and developed "drug induced hepatitis", which hospitalized me for several days, and been sick with severe jaundice for 9 weeks, unable to eat, or be around food.
this has been confirmed by many tests, including biopsy's, ultra sounds, and cat scans.
no "liver" side effects noted but they can be severe.........................and should be noted !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!

I had the Mirena inserted when my daughter was 6 weeks old, August 2007. I had no problems (that I THOUGHT were related to it) until end of July this year. I had next to no period up until then and then bled for nearly 3 weeks straight. Went to the doctor who said I had a miscarriage...ok so let's take it out, it obviously doesn't work for me and go back to the pill which I had been on most of my life when I wasn't pregnant with any of my 5 children. After 3 weeks of being on the pill I had it removed on 9/10. No pain at all actually but haven't stopped bleeding since! Went back to the Dr on 9/23, felt my uterus and said seemed fine. No fibroids or polyps that he could feel. Changed my pill Rx and said it should straighten out within the next 2 cycles, if not come back...on 10/5 I went back without an appt and was told by the nurse to double up on my pills to try and stop the bleeding. I scheduled an appt to see the Dr the following am. Had an internal ultrasound done and a biopsy of the lining of my uterus. Results should be back on Tuesday... my Mom & Sister told me to look online about side effects with the Mirena and I found this page. I am comparing many of the things I have been experiencing and now realize perhaps they were ALL related to the IUD. I gained weight (am actually heavier then I was after my daughter was born and I lost all my pregnancy weight within the first month), I had terrible acne, headaches, back & neck pain, constant fatigue, emotional, decreased sex drive. It has been out 4 weeks today and although my acne has improved slightly, I feel like I have been on the brink of the flu since last Saturday, no motivation, pure exhaustion, and emotional roller coaster not to mention the cramping from my biopsy that probably wasn't necessary now I'm thinking and 4 days in a row home from work... I am hoping time will heal the way I feel once the hormones adjust themselves. The pill always helped me more then it ever hurt me. I'm glad I got the Mirena out as soon as I did. Just wish I would have known sooner what it was really doing to me!

I have been on Yasmin for over 5 years, and just thought that I was a hypochondriac. After starting Yasmin I experienced severe nausea and unrelieved hunger pains. I saw a gastroenterologist who performed an EGD and Colonoscopy at the age of 20. It was normal and I was placed on Protonix to help with the GI issues. Also I have severe joint pains in my knees, hips, elbows and shoulders. I have been tested for everything from Lupus to Rheumatoid Arthritis, and it was all negative. I get headaches, have little sex drive if any, my skin is not clearer than usual and nor has it been since starting Yasmin. Thanks to all those people who have voiced their concerns and shared their stories, it makes us feel less crazy. I threw out all my birth control pills last night and I am going to try another form of contraceptive. I mean my headaches and chest pains have gotten so bad that they have forced me to go to the ER on several occasions. I DO NOT THINK THE BENEFITS OF YASMIN OUTWEIGH THE RISKS ASSOCIATED.

My mother took lisinopril and she developed the persistent cough many experience. It was so severe that she went to the ER. While she was there, they told her she had fluid retention in both lungs and didn't link this drug to the fluid retention. Instead, they told her to get a biopsy for the possibility of lung cancer. More money in their pockets for tests and biopsies? Definitely!
I definitely see the link between the drug and the cough and the fluids in her lungs. Now,she's not on that medication but she is still dealing with side effects and I feel that all these medications they tell her to take are just making her worse. Has anyone just stopped all the conventional medications of high blood pressure and perused alternative treatments with success? I'm hopeful to find out what options i have that can cure her situation instead of leaving her at the same hopeless stage of dealing with terrible side effects.

I feel compelled to share my daughter's horrendous experience, which we (and some of our docs) believe was a reaction to Bactrim. Her chills, high, high fever, night sweats, itching and majorly swollen lymph nodes mimicked lymphoma. She had a biopsy of one of the swollen lymph nodes and it revealed Kikuchi' s Disease or Kikuchi-Fujimoto's Disease. Google it. Thankfully, it was benign and self-limited, but it made her very very sick and it was scary and most probably triggered by her allergic reaction to Bactrim - taken for acne. We will never take this drug again.

cannot believe how many stories I have read about mirena and hair loss etc..etc.. etc.. I have experienced many of the side effects that everyone is mentioning.. I actually feel I could live with most of them if it weren't for the hair loss. I have had ( copying from other post.. ridiculous right?)Tired all the time ~ Depression ~ Hungry all the time ~ leg cramps ~ HAIR LOSS TO THE POINT OF BALDING IN SEVERAL AREAS ~ oily skin and bad breakouts ~ Mood swings (huge...yelling fits at my husband and the kids) ~ fluttering in uterus~Sore breasts.. I have medium thick hair that is about 10 inches. I noticed a bald spot in June and now have discovered 4-5 others starting. I just had the iud removed today and my OB pretty much tried to convince me that there is no way that the IUD is causing my issues. I have never had any of these issues before. I got the Mirena on 4/30 of 08 and noticed slowly but surely all of the side effects mentioned. My OB told me that the progesterone could not be causing my issues because it is such a small dosage that it would be comparable to spitting in the ocean as far as the amount that is in my blood stream. She said because I am black and 35 that I may have an autoimmune disorder and that I should stop reading blogs. I told her that all of my research wasn't from a blog and that ALOPECIA is a side effect just not mentioned in my pamphlet that I can find. I understand what she is saying and that she is the one that is the dr. but nobody knows my body better than I do.. I am in it!! I have !never had any problems and have been healthy my entire life. There is no history of autoimmune disease in my family. I am going to my primary care doctor.. to have some blood tests done. I think that the mirena has caused an autoimmune response in my body.. it may not necessarily be the progesterone..although I don't rule it out no matter what she says . the progesterone is synthetic and has an androgynous like activity that is similar to testosterone the main thing that causes male pattern baldness. also Mirena is made out of Silicone.. perhaps those of us that are having hair loss are having it due to our body trying to fight off the foreign invader of the IUD itself. I was going to go and have the Paragard inserted.. because i was thinking it may just be the progesterone.. nope... I read that many women are complaining of ACNE and HAIRLOSS even with that because its made out of copper. So with that being said.. not sure what to do.. may have to go back on Yasmin.. didn't seem to have any problems with that.. I really just don't want to risk putting another hormone in my body.. We all need to get together and look into a class action suit because I am tired of being made to feel crazy by doctors.. sometimes what seems to not be possible is .. especially when there are so many women having the same problem. Feel free to e-mail me re: a class action suit.. if they took depo off Mirena needs to come of too. It seems like it has really screwed a lot of peoples system up.. Hopefully I won't find out I know have a thyroid problem etc.. etc..

I have been taking Lipitor for about 6 years suddenly developed a rash on my shoulders and chest. My doctor diagnosed SCABIES!!so I treated myself for that then the rash progressed so I had a biopsy done and after 3 months of agony my slin specialist had taken me off Lipitor as theh test showed a reaction to a drug. I am still itchy prickly and burning on arms legs and hands and cannot tolerate cortisone cream so am on tablets for a week..can anyone relate to this condition? My scalp is also very dry and scaly.

I have had a TERRIBLE time. 3 months-of almost non stop bleeding (3 1/2 weeks, 2 1/2 weeks and 16 days and counting )and I do already have overactive bladder but now all the sudden if I don't run to the bathroom as soon as I have to pee(even if my ladder is not full) or if i sneeze I pee myself and i am 29!!-this never used to happen!! My obgyn finally decided to switch me to the pill thats 3 months of active and 1 week of sugar. The whole reason i tried this was bc my periods were beginning to get longer (7-8 days) and this made them so much worse. She did a biopsy and an ultrasound both of which were normal. I already have a non-hormonal iud (which i have had for 3 years) but we left it in bc i take topamax (which decreased the effectiveness of birth control) for migraines so i need the iud for birth control. im just trying something else to improve my periods and obviously this is not it! i am beginning to wonder if the topomax also causes an increase in bleeding too...

I have been on this for 6 days for a UTI. I personally am not allergic to sulfa drugs and have had absolutely no problem while on it so I can't speak to specific side effects but I do have something to say about it. I'm a little confused as to why so many of you believe that this drug should be taken off the market. Surprise, a lot of people are allergic to sulfa drugs which accounts for the vast majority of adverse events described by nearly everyone on this post. And guess what, every single drug comes with side effects (Tylenol, Advil, Tums, etc. are no exception) and you accept the risk of those side effects when you put it in your body and weigh that risk against the possible benefits. It's not your doctor's or the drug company's fault you're allergic! Antibiotics, including this one, have saved millions upon millions of lives. It seems intuitive but it evidently must be said: if you're allergic to it STOP TAKING IT and call your doctor so he can prescribe a different antibiotic. Seriously people, it's not rocket science. Hives are a pretty straight- forward symptom of an allergy and one that can be diagnosed by the lay person. I am a medical professional, but even if I wasn't, you don't need an MD behind your name to figure that one out. Why would you continue to take it after having an obvious reaction? (a reaction that, by the way, is a well documented, clearly stated possible side effect of this particular medication if you'd taken the time to ask any questions whatsoever regarding your own health, not a surprise adverse event of a bad drug) It's not rocket science, it's common sense people. When I'm prescribed something I'm not familiar with, my first question is, "What do I need to know about this." Even after a satisfactory explanation, I look it up before taking it. In fact, that's how I found this post. Which brings me to my last point, why is it that people blindly put things into their bodies that they know nothing about. If the pharmacist doesn't explain drug information to you in person, that's what the little drug safety pamphlet attached to your Rx is for. Read it, that's why it's there. OR, there's always the option of using this wonderful resource called the internet. Use your brains for god sake and take a more active, responsible, and informed role in your own healthcare process. You are ultimately responsible for your own health, and to be completely honest, you're one of the only people who actually cares about it (guess what, your doctor probably isn't one of them because he has a hundred other pain in the ass patients with no common sense to keep track of). Think people...

This is my less than 24 hour update from yesterday since I had my Mirena removed. I had my yearly appt. yesterday and explained to my dr. all the problems I've been having over the last year. I thought he would try to talk me out of having it removed but he was very sympathetic and removed it without question. So, I'm definitely relieved about having it out. I'm sure it will be a while before I will be able to notice any changes that I can directly relate to the Mirena coming out. But, I can tell you that my husband and I can already tell the difference during intercourse without the Mirena. It is so much more comfortable so, we are very excited about that! I requested Yaz for birth control since I've been on it before and never had these emotional issues while on it. He also gave me a brochure and DVD on the Essure which is the in-office permanent sterilization procedure. So, I'll be doing research on that to see if that will be a good thing for me to do.
Another thing, too, during my gyno exam, he found a lump in my left breast. I have never had any problems and definitely no history of any kind of cysts. I'm not blaming the Mirena but all of this is just way too coincidental. Now at 35, I'll be having a mammogram and ultrasound to determine what this lump is. I'm just praying hard that it won't be anything and definitely trying to stay positive. I'm just very relieved to have the Mirena out and I will stay posted as to any additional changes in the future.

I had a Mirena put in originally to avoid surg for excessive bleeding. That was almost 6 yrs ago. It was wonderful and during the first 5 yrs, I had only one period! The insertion was terrible and the pain was like a very hard contraction. I passed out when it was put in. When it was time to take it out, the MD couldn't get to my cervix (very high and tilted) so I had it surgically removed and another put in Sept 2008. This time has been very different. I have bled every 10 days or so for about a week. I have had PMS like I used to have before any Mirena. Now I have been bleeding for a total of 20 days and the MD just took out the Mirena and did a biopsy. We will see what happens now, when will I stop bleeding? I am gonna enter the World Records ....btw...lots of chin hairs over the past 6 yrs, pluck daily so maybe that too will stop.

I was injected with Lupron and the shot last for three months. I had the shot in order to stop my periods to increase my blood count for surgery to remove fibroids. The first two weeks, I spent having a very light cycle. I'm 2 1/2 months in and haven't had one since. I have, however, had menstrual cycles and never had them when I had my cycles before Lupron. I have a high tolerance for pain, but I was constantly popping Motrin to deal with the cramps. I experience pressure in my head during the second month, but it has gone away. My sex drive sky rocketed since I've been on the shot, but I have some vaginal dryness. My energy has also decreased since being on the shot and I don't work out like I use to. The three months is almost up so hopefully I can get back to normal once it's over.

I am on two 500 mg doses of cephalexin daily to help heal a bug bite..Still waiting for the biopsy to come back. Doctor suggested could be a brown spider bite. Definitely want to stop the skin deterioration and get the wound from where the bite was removed healed but the itching started on day 3 on my stomach and has now spread to entire torso, back, insides of arms and legs. I have tried aveeno baths, benadryl (knocks me out) and eucerin itch-relief. Today I coated my entire body with 1% hydrocortisone with little relief. HELP - I am scratching to the point of bleeding and now that I have read these other comments will NOT take another one of these pills. Any other OTC relief anyone has found?

I took yaz for maybe two weeks. after one week my breast blew up a cup size. they were so swollen! then i started noticing i was gaining weight but my diet hadn't changed. i started to swell all over within the next week. but what made me quit taking this pill was that i started getting these sharp intense pain in my upper abdominal region. it would come and gnaw at me for like 2-5 seconds then it would just go away. there was also like this temperature sensation anytime i would eat or drink anything. i've been off of it now for 5 days! i still have not got my period, my breast are still swollen, and my stomach pains are still there. i know im not pregnant, because i haven't had any sex! when is this going to get out of system or has it done something to me? i would imagine if you skip your period in one day and you can get pregnant in that one day... the pill should be out of your system! anyway- anyone else have this same situation?

Hi, I am new at this, I have been so frustrated. I too was told this was the best thing out there, and the benefits looked great so I got the IUD Mirena inserted. Cramping when I first got it for a few days then nothing for a while. Seemed ok, then one day I noticed my hair was thinning then more and more. So I made a appt with my gyno and she said basically it was in my head. I also mentioned a memory issue, kinda foggy feeling. She dismissed me and ushered me out by wave of her hand. I then go to a dermatologist to see if there was something there, maybe a sign something was definitely wrong. He noticed it was profuse and in the back of my head. He had my blood checked for vitamin deficiency and my thyroid, came back normal. Told me it looked like a pelican and had me use Rogaine and special shampoo and biotin. He also told me of an option to do a biopsy, which scared me. I waited a few weeks and decided to do it. It came back normal, no hereditary or any other abnormalities. He suggested removing IUD. I talked to him once more to see if anything else can be tested, he sent me to an endocrinologist. Did another blood test and all normal. He also did thyroid all over again. By this time, I was devastated. I felt hopeless. I was still thinking it wasn't possible. That’s when I hoped online and saw so much more others had the same problem!! I couldn’t believe my eyes! I am 32 and had this damn thing in me for a year and a half. I only wished I would of taken it out by that same doctor who told me was all in my head. It would of saved me so much aggravation. Mind you I was feeling a bit depressed and I noticed I was uptight and yelled at the kids a lot. The good news in all of this, I had it removed today and again they tried to talk me out of it. I told her, if I didn't have all these tests done, I would probably kept it in. I did my share of making sure nothing else was wrong with me. I even talked to my regular doctor and had a heart to heart; he explained everything that the others would not, including lab results. I am hoping that my hair will come back. I love my Dad, I just don't want to look like him....

Does anyone now how long the hormones stay in your body and how long till hair will stop falling out?

I had my mirena placed in march of 07 for heavy periods. It has been a little over 2 years. I have most of the same side effects as everyone else headaches, Extreme weight gain, fatigue and back pain. I also have not missed a period the whole time on mirena in fact it has not even helped a bit with the heavy bleeding and clotting.

I made an appointment to have my mirena removed on April 29th. I had a regular pap appointment then when it was time to remove the Mirena my Dr. could not find it. I was scheduled for an ultrasound the next day and they were able to find my mirena at the bottom of my uterus near the cervix opening. I was then scheduled tthe next day to try again to remove it. This process was40 minutes of torture and to no avil. Four days later I was back into try once more again nothing I am now scheduled for Surgery on June 1st to have the Mirena removed, do a biopsy to make sure everything is okay and to have the NovaSure procedure done to stop my Periods.

I will post once I have had everything done. This has just been a nightmare!!

My 15-year-old daughter experienced alopecia (bald patches) after the first injection. We didn't initially connect it to the vaccine. Then, after the second shot, her thick long hair thinned significantly. She will NOT be getting the third injection Gardasil is poison. Anyone else who has experienced hair loss, please post a comment with information on how long it took to come back. She cries daily about this and it breaks my heart.

Just wondering if anyone else has similar side effects ... I have had Gall Bladder symptoms but all the tests say my gall bladder is working well. (Blood, sono and MRI with contrast) It all started a few weeks after the mirena was inserted. Extremely Severe pain in my right side that last for 8 to 12 hrs. Seems to feel slightly better with a few crackers (unlike gall bladder) and seems to move lower as it gets better (also unlike gall bladder). It does not move around to my back like gall bladder should or usually does. Gall bladder made sense since I have the risk factors ( women over 30, just had a baby etc)

Anyway, Anyone else having the right side pain? Thanks!

Ran into friend at grocery store with mystery illness. Docs attribute it to Agent Orange exposure. Been at death's doorstep for a year. Hands were extremely cold and has little energy. Showed up one day at golf course with oxygen bottle! Asked him if he had taken Levaquin. Unfortunately had. Docs again fail to link antibiotic exposure to his ailments.
I wonder how many illnesses and deaths this poison has caused? Why does the FDA allow this crap? Do you people realize that the average person is clueless about the side effects of drugs like this. Put total confidence and their well being in the hands of ignorant docs and profit crazed drug companies.
Ignorant oncologist failed to link my dad's symptoms to Levaquin, instead attributed them to b-cell lymphoma which just happened to suddenly appear. Rituxan and numerous other drugs (Heparin, Lasix, Gamma globulin, Tylenol, antibiotics, Insulin, steroids, Flowmax, etc.) was too much. A fiasco, people think he died of lymphoma. Was walking three miles a day before taking Levaquin, for an undiagnosed lung infection.

I had the mirena placed about 2 months ago, a year after my daughter was born. i was ready to start dating again and i figured this was a safe second protection for me. 2-3 weeks later i had a yeast infection, i've never had a yeast infection in my life, i'm 29yrs old. I was so scared i thought i had an STD. I scheduled an apt ASAP with my primary care Dr. yes it was a yeast infection but i did not think it was the mirena. After that my "girl" hasn't been the same. ive had this slight burning sensation all the time. my "girl" is swollen and irritated and i now have another yeast infection. I became concerned and started to research yeast infection and came across this site and instantly I knew what was wrong. i'm getting this thing out my body instantly. I'm also hypothyroid because of thyroidectomy surgery and thought my new symptoms were because my synthroid doses were being adjusted once again but now it seems the mirena is also to blame. Either way i'm getting the mirena out because of the yeast infection alone. this is making me crazy.

Prescribed Avelox after previous antibiotic could not clear up sinusitis. Avelox cleared it up within three days, but I feel worse now. Extreme agitation/anxiety, tremors, twitches, no appetite, boughts of depression, dizzy, lack of coordination, accelerated heart rate, leg shake, cold extremities, very strange, vivid dreams. Doctor told me to stop taking and side effects should clear up in a few days ( I hope). This is nuts. I feel like I am going insane. I could not go to work for three days due to side effects.

I got the Mirena in August 2008 after having our second child. We thought it was a great idea b/c I wasn't ready for my husband to have a vasectomy in case we ever did change our mind about having more children. Although, we definitely have decided that we won't have anymore. Anyways, I have had spotting ever since and the three months of spotting is a joke because it has been way longer than that! The last two days I have had SEVERE lower back pain through the tops of my legs aching. Reminded me of having back labor it was so terrible. I couldn't sleep at night good because it was awful. I called my doc today and I am having it removed tomorrow. Can't wait!!!! I just wished I had read this website before I had decided on Mirena. And the comment I read about the hurt you experience having it inserted is the darn truth! If I had knew that I wouldn't have gotten it either. Besides that, my doc had to clamp my cervix while trying to insert it...so needless to say it was horrible!!!!!!!

I was prescribed this about two weeks ago. I knew I had high blood pressure and decided to work on getting it lowered. I started taking this and immediately had headaches in my temple...then numbness up by my cheeks and something that felt like hot flashes. I would get dizzy, was extremely tired, couldn't concentrate and had one of the worst cases of diarrhea I had ever experienced. My distant vision became very blurred. However, I thankfully never got the cough.

I spoke with the doctor about this and she said that there was no way this drug was causing my headaches. I'm scheduled for an MRI tomorrow and she wanted me to have a temporal biopsy, which I think is drastic.

I read an article from a medical journal that low blood pressure can cause headaches. This was just published last spring of 2008. I started getting the 24/7 headaches 3 days after I took Lisinopril. Aspirin or pain relievers never helped.

I took myself off of it two days ago. Yesterday I was so weak and tired with headaches all day long ...however today, I'm beginning to feel much better with much more energy. The numbness is disappearing in my cheeks and the headaches have greatly reduced.

I am thinking about a natural alternative to this ...losing weight...exercising and going on the dash diet. Unless of course the MRI shows something. I also thought about cutting the dosage of the pills in half or to one quarter.

I was diagnosed with SLE (lupus) when I was 14, I'm 21 now, and I've had to be on prednisone all this while. The dosages alternate between 60mg (the highest) and 2.5mg (the lowest), I just went for a routine check up today and found out that my protein level in my urine is at an all time high. So the doctor is pushing me back up to 30mg of prednisone. Its 2 am, and I am sitting in bed crying because I don't want to have to go through everything again; the weight gain, the moon-face, everything. I know I may sound shallow, because ultimately, the medicine is keeping me alive, but the side effects are terrible. Very few people understand that its not fat that you're gaining, and the remarks that I know I am going to get are enough to drive me insane.Is there anyway the water retention or the weight gain can be stopped or decreased?

I received a shot of Demerol and Fennergin in my buttock when I went into labor more than 2 years ago. Approximately 2 months after receiving the shot, a small spot formed at the injection site. Over the years, the spot has rapidly grown. The spot is about the size of a tennis ball and there is another smaller spot underneath the big one that is the size of a quarter. I have noticed recently that the large spot is spreading. There is now an indented line forming from the large spot and going around my hip. I recently had a biopsy done and they confirmed that it is fat necrosis. I don't know what my doc. plans to do next. Some side effects I have had from this is loss of weight (15 lbs. in 2 months) and haywire periods (one every 2 weeks).