Cat scans symptoms and conditions

My daughter was on Yasmin for about a year approximately 3 years ago.She constantly felt ill and was always at her regular doctor with excruciating head aches, dizziness, respiratory problems, bladder infections, kidney infections etc etc.A battery of tests including CAT scans etc showed nothing.Then came the manic mood swings, depression, rage and severe panic anxiety attacks which grew worse over time.(We are talking about a former gymnast who lead her team to the State finals in H.S. and used to be cool, calm and collected tumbling on a 4inch wide balance beam 4 feet off the floor!) She finally stopped taking Yasmin after I spoke with a gynecologist I met during mutual sports activities our children shared. He told me to get my daughter off of Yasmin immediately. It took about 6 mos. before she was close to being back to normal. Taking Yasmin caused a number of issues for my daughter - some of which I believe she still deals with today in the aftermath of the effects of this drug. PLEASE if there is a class action lawsuit against these people for putting this out there, she DEFINITELY needs to be a part of it and retrieve some sort of compensation. Thank you!

I am 44 years old and began taking Yaz about three months ago. I now have a very high level of Potassium. I have very bad stomach aches after eating or when any thing is in my tummy. I have had all kinds of test from Scopings to CAT Scans and nothing was found. My doctors advised me to stop taking Yaz. I have stopped for about a week now and have started to feel a little better. I started taking Yaz to help with crapping and irregular periods. It helped with those symptoms. I did not have weight gain, but felt nauseous and blotted all the time.

For me having the Mirena removed just last Thursday was the right decision. I was not using it for birth control but as hormone therapy for heavy, crampy periods. I had it inserted in July 2008 and bled every single day for the entire time, I had it removed last week and now I am bleeding very heavily but hopefully that will stop once all those hormones are out of my body.
While on Mirena I lost all sex drive, I became severely anemic and with that fatigued terribly, and moody, crying at nothing and screaming at my kids or husband for stupid reasons, I felt bloated and gassy and didn't have those problems before.
I am 42 years old and I hate my heavy bleeding in fact I want a hysterectomy, but not sure now what I will do.

For those of you who had the Mirena removed, how long did it take to stop bleeding afterwards? This is draining every last ounce of energy for me and I am taking iron supplements.

What sucks is the cost of this, Even with insurance I ended up paying a lot out of pocket to get this thing and then all the Dr. visits due to bleeding and side affects in the 4 months it was in and now the removal of it. I am wondering if there is any way that we can get a Class action lawsuit against Bayer for this horrible thing they are trying to sell to women.
I know there are some out there who have not suffered all these horrible side effects at least not yet or that they are aware of, but I truly believe that there is nothing good about this IUD and those of us and there are a lot of us who have suffered with this should be reimbursed or compensated for the pain and loss of parts of our lives and expenses with this. Does anyone else have any thoughts on this?

I have some of everything above and am in so much pain that I feel as if I am dying a slow, painful death. I am on heavy pain meds and even with those I have severe abdominal cramping. I don't know what I would do if I didn't have this pain relief. I am very worried as to what is happening to me internally. They are scheduling cat scans and I am awaiting a phone call to get something diagnostic done. This all started 8/15 and not only are things not easing up, but I think this is getting worse. I also have a urethral discharge, UTI, and alternating constipation and diarrhea. Initially, I had a 102 degree fever and now my temp is low, only 97.1! my husband plans on calling a lawyer today, 8/26. One day I passed brown urine and it shocked me! I'd appreciate hearing from others as I feel so alone in this horrible nightmare which is unfolding! FYI, my doctor feels that my muscle tissue is breaking down...has anyone heard anything like this from their doctor? The stomach and abdominal pains are like labor!

I took Levaquin as a treatment for pneumonia. After 3 days on the drug, all my joints were stiff and I had difficulty breathing. I called my doctor and I was told to continue the medicine. After a week, the reaction continued to get worse, I could hardly move, my breathing got worse and I had to be put on oxygen. My hands were like clubs and I couldn't open anything. I sat in a chair all day. It took me a half hour to get out of the chair to go to the bathroom. My hands were so swollen that I could not flush the toilet with my hands. I had to use my elbow to flush it. I saw doctors thinking I had rheumatoid arthritis. I saw pulmonary specialist and my lung capacity was at 48%. They sent me for many blood tests, cat scans, and I even had an MRI to try to find the cause. Finally, my heart doctor found out that some people were having adverse reactions to Levaquin. She found out that it caused severe anemia, breathing problems, and joint pain. She dosed me iron and within a week I was finally beginning to see the swelling in my hands start to decrease. I was out of work for 3 months.

About 4 months ago I was put on a 10 day treatment of 500 mg Levaquin, because of an on going sinus infection. I took the pills for 5 days and experienced muscle twitching, weakness, dizzyness, upset stomache, irregular fast heart beat, extreme anxiety, I had this weird tingling numb feeling from my knees down and couldnt sleep at all. I called my doctor after 2 days of the medication and told her about my side affects and she told me to continue the medication. After 5 days went by I looked up this web site and was shocked to hear that I wasnt alone. I threw away the rest of the medicine and prayed I wouldnt have long lasting affects. I continued to have muscle twitching, cramping, and weakness for the next 3 months and my leg muscles would ache and tighten by themselves. I have played sports my entire life and had just gotten done my season of college basketball before I got sick and after I took this medication I could barely walk up the stairs without feeling like I was going to pass out. I was in and out of the hospital having blood tests they tested me for lyme disease, and did 2 cat scans of my head. I went to a neurologist and had tests done worrying it was ms or als and they sent me to have an MRI of the brain and my neuroligist asked me if I had been on any medications and I told him levaquin. After 3 months of crying myself to sleep being put on about 8 different medications to control my anxiety my neurologist diagnosed me with BFS. BFS is a neaurological disease that affects your nerves. It is not life threatening but many people suffer because of the anxiety that comes along with the disease and I get muscle twitching all over my body and feel tired most of the time. It took me to get a long time to feel even a bit better but I began taking magnesiun, B12, Potassium, and other ones to help nerve function and a mild anxiety medication and I have felt a little better. Nobody believed me when I told them my illness was from levaquin but after I was diagnosed I realized that just 5 pills may have ruined my life. Now today I have my good days and bad. I just turned 21 but I cant drink or have caffiene because of BFS. I met the love of my life about 3 weeks after I got out of the hospital and I knew we were meant to meet because his step father had passed away a month before. His step father took levaquin for an infection and his kidneys and liver failed 11 days later and he passed away. I was so devastated when my boyfriend told me about this and called my parents to tell them how SCARED I WAS. I am dealing with what this medication has done to me by staying positive, and telling as many people as possible about how bad this medication is. I wish I would have rad this site before I took those 5 pills but I didnt. Levaquin should not be on the market and I will pray for those who have had the same heartbreaking experience as myself.

Hello,

I read about how YAZ birth control pill affects the body and psych and I am now scared. This is my 2nd day of YAZ (I've never been on birth control pills ever and I am 27 years old), it's all new to me but after reading all these negative posts about Yaz I don't know what to do. Before the birth control pills, I was depressed, annoying, serious weight problems - 210 lbs :~~((, low energy, low libido, always tired, terrible migraines every 2nd day, ridiculously increased appetite and excessive hunger, hair where it shouldn't be, menstrual blood clots, excessive cramping etc
I have all these problems for 3 years now and now that the family doc. put me on YAZ birth control pill I am even more scared - mainly of more weight gain, it would be a tragedy for me, I am fat enough already and what's worse I can't lose the weight, exercise doesn't help, diet doesn't help, NOTHING. Will YAZ birth control pill worsen my already tragic condition? I just don't know what to do and what to believe ... I appreciate any advice or help you can give me ... Thank You to all!

I started having problems with my voice cracking and throat aching after singing or talking alot. Went to Dr. and he said he thought it was reflux (of which I had no symptoms). Wtihin days I started experiencing fatique, headache, depression, dizziness, ringing in my ears, and my right leg went numb about 3 weeks into taking it. Then about 2 months into taking, my entire right side went numb (thought I was having a stroke). Since that time I have been through CAT scans, MRI's, lumbar punctures. Been to 2 Neurologists, a Neurosurgeon, Cardiologist, Endocrinologist. 3 different Doctors thought I had Multiple Sclerosis or a stroke. All tests negative for both. After researching Prilosec on my own I found that Prilosec and all like meds block the absorption of and strip vitamins out of your body. 2 1/2 months after stoppping it I had B-12 level checked and it was almost non-existent. Started taking B Complex and B-12 shots. Symptoms have tremendously improved but haven't completely left. I still have numbness even 14 months later. The problem is that B-12 deficiency can cause the numbness and if not treated quickly enough the problems can become permanent. IF YOU TAKE any acid reflux medicine have your vitamin levels checked ... especially B-12.

My daughter started singulair 2005 she has been taking it for 2yrs. She was 7 yrs old now 9yrs old. She get headache all the time and she started with her hands making a fist then making her fingers touch and rub her fingers. Now she has stop soing that and her eyes are blinking all the time. And a tic from her eyes she can not stop. I got on line to see if other kids have experience this yes so maybe it is the drug singulair that brought it on. I ask that doctors if this was a tic and she said it probably was, but now I feel that it is singulair.
cat

Thank God I'm not the only one! I was actually relieved when I found this site. I was an active 60 yr. old female until hit with blood clots in lt. leg that went to lungs. I've been on Warifin for almost four months these are my side effects: extreme fatigue, back and leg pain, over-all weakness,decrease in flexability of limbs, dizziness, vision changes even from day to day, memory loss( I've always been known for my great memory). I did mention these to my hemotologist last month and he sent me to ER. Cat scans of head, chest and abdomen all were normal. Every doctor I have seen says Warifin is not to blame but all this has developed since I began taking it.

I have been on Toprol XL (25 mg/daily) for 6 months (F/41). I was really glad to come across this message board in a frantic search of "weight gain with Toprol XL". Have gained 10 pounds in these 6 months and for the life of me I cannot get any weight off, my body is just stuck where it is at. My problem is I have to lose weight since I am overweight about 40 pounds right now so this is so frustrating to me. At least I am not alone, thanks for posting your problems also with weight gain. I take Toprol for my fast beating heart, was having bad palps last January. Toprol does work well in keeping my B/P down (tends to be just a bit high) and the palps are non existent for me on this drug. I do have swollen ankles (at night) ok in the mornings. But the weight gain is really making me go crazy especially when I need to lose weight. This just isn't going to work so this morning I am cutting that pill in half and getting the heck off of it. I do find that if I stay away from sugar/caffeine my palps really don't bother me nearly as much. I went on it because the job I had was very stressful and brought back my palps again after not having them (as bad) for several years. I just hate those "fluttering" heart beats, they are hard to deal with and Toprol takes them away and keeps me "calmer" so I will miss Toprol for those effects, but not the weight gain! Thank you for this message board, it's been so helpful.

I have had dizziness for 2 1/2 years...when wlaking or sitting. Could it be the beta blockers? How long would I have to be off Toprol to determine if this is causing my severe dizzy condition. I also have arrhthmias...not often but the toprol was given to me for that. It might be effecting my equilibrium. Yes? No? Please answer. No doctor has been able to find the cause of the dizziness. All my blood tests come out just fine...and so do the CAT scans and MRIs. I have seen too many doctors...and lost faith in them. Sorry about that.

I had started taking Lamasil for toe nail fungus infection for about 20 days. I came down with fevers, chills and sweats about 20 days into 30 day doseage. My doctor prescribed Levaquinn for the fevers. I had a blood test and found my liver was very effected by the Lamasil. I was to take about 8 day of Levaquinn which I did. After 4 days of the Levaquinn my fever was gone but muscle pain developed for which I took Ibuprofen even after the levaquinn ran out. The pain became excrutiating. My calves felt as if they had been kicked and charle horsed. My shoulders felt as if they had drills drilling into the scapulas, My blood vessles felt as if they had gasoline running through them. My right hip started to get a deadened spot on top of the front of my hip joint, Pain flashed at various spots as if stuck with a knife. about two days fter stopping the Levaquinn, I had a period of three nights I could not sleep or lay down the pain was so great. Three weeks after stopping Levaquinn I am still in pain. My hip joint feels like it is being stabed by 40 Ice pics at time, it is sensitive to pressure and quick movement, my calves are still sore and make it hard to walk at times. Over the period I was tested for hepatitus A, B, C, HIV Lyme disease, Shingles Herpes, had Cat scans of my head and Abdomen, I developed Bells Palsy on my left face. After 7 weeks of pure hell and none of my local doctors culd think of any more test to give me, I went to a Nurologist on my own at the Lahey Clinic who identified the culprit the Levequinn. He tells me the pain will eventually go away in 1 to 3 months it has gotten more bearable after the many weeks but I still take Celebrex to sleep. No one thought to read the contra indications including me, least of all my doctors-except the last one at Lahey Clinic. Two medications suposed to cure damn near did me in!
Stay far away from this stuff unless you are dying- or want to.

I've been on Topamax for over a year now for what my doc says were migraines. I went thinking I had sinus problems that caused confusion,and forgetfulness. Cat scans and MRIs showed cysts that docs say have nothing to do with anything and put me on topamax for headaches.I started 50 mg at night and stayed that way for a year. At first it seemed the headaches were better and I LOVED the weight loss. I was trying so hard for so long to shed the extra baby weight and over 15 lbs just like that. It caused me to over look what was happening to me. I was becoming an imbecile. Not saying I was a genius but I was a relativly smart woman who could hold a conversation. Now I can barely focus,I have to read things over and over again to try and comprehend them,my memory shot,I lose my words in mid sentence,spelling is horrendous,At times I stutter,my vision is worsening,my body gets achy,I have terrible mood swings ,thought about hurting myself. I cant believe I'm still on this med. All for 15 lbs that I'm gaining back anyway cause I quit smoking. I deserve it for putting my body thru this. I talked to my doctor and I'm weaning off. Nothing a little Tylenol and excercise can't fix hopefully.I just hope the side effects go away and this is not permanent. By the way be very careful drinking while taking this med. I had a very bad reaction to it. PRO-I sleep like a baby ,I will miss that.

Chronic sinus infctions. They started out occuring every so often, nothing to be alarmed about yet right before I stopped taking singulair I was in at the doctors at least every 4 weeks for sinus infections. I was on antibiotics for almost one month before I stopped taking it and it was a factor in my coming down with bronchitis. I have stopped taking the drug when I realized it was making me sick. It's been 8th months and I have been to the doctors for a regualr check up and one infection. It feels great to have figured out why I was so sick. I had undergone CAT scans and saw an ENT and I was about to undergo more tests and see another specialists. I have researched online about possible side effects and infamed sinuses and respiratory infections are listed as side effects. The ironic part was I was taking singulair to prevent the sinus infections which my doctor and I thought were caused by my severe allergies when in reality it was actually making me sick. I cannot describe how much I loath this drug and feel that Merck does not do a proper and good job in making all the possible side effects know. My life health wise was...I don't know how to describe it- I was constantly sick and missing school and work and feeling terrible- I guess the word would be terrible. I strongly reccomend a person who is new to taking this drug to research it and know all of the nasty side effects.

very interesting as I read the above side effects people have experienced. I was put on toprol - l00mg two years ago. I have always been a healthy female = only going to the Dr. for yearly check-ups. Never having the flu, colds, and always low blood pressure. I was exposed to a chemical that immediately increased my blood pressure. Had a clean bill of Health with low blood pressure two weeks prior. I was put on Tropol 50 mg and then l00 mg. I had dizziness, tired, etc. but never related it to the possibility of the medicine and neither did my doctor. I was sent for tests for the dizziness and ended up with a pace maker. After reading the above side effects people have written in about - I wonder what actually created my problems. I always have dry mouth and dry eyes, which I never had before. The reason for pacemaker is if I should go into a faint spell it will kick in and not allow me to faint as I had three episodes of fainting. I also was given every test imaginable prior to the pacemaker. My heart and arteries are fine, cat scans, my heart beats are fine, all arteries flow properly. I now wonder about the medication.

I experienced a hike in b/p after taking benedryl. I was placed on Lisonpril. After two weeks, I experienced extreme difficulty walking, weakness and fatigue, vertigo, persistent cough, panic attacks and anxiety. My skin felt like I was bathed in menthol or vicks vapor rub. I am not sure if it is the same "tingling" or "burning" that has been reported by others. E/r visits, ekg, cat scans, blood tests came back normal. I received inconsistent medical advice from e/r docs, cardiologist and internist (i.e. stay on the med, but change it, take it only if your b/p is high, get off of it completely- you dont have high b/p and dont need it). I decided to get off of it. Its been three weeks off the Lisinopril. I have improved daily; however, I am not back to normal. Anxiety and "menthol-like" skin sensations still remain. This web site has helped tremendously with jsut knowing that I am not crazy or alone. Thanks.

Sat, 19 Feb 2005 09:39:48 -0500 by Guest, #9575

Any idea on how to start a lawsuit against a medication? Any one heard of a lawsuit being started or interested in starting one? I just think that this pill is so unsafe, and think that people are going to be hurt by this.

RE: I would love to file a class action suite. If anyone knows how to go about doing that, lets do it. I have doctors bills up the ying yang. Cat Scans, Check ups, MRI's..etc. All were nothing and ended up leading to be becasue of Yasmin! I have several post on here, and I'm so glad I found it becasue I went off the pill right away! I hope to feel better soon.

In Aug I was on levaquin for 4 days and experiencing subtle side effects (nausea, fatigue) until day 4 when i woke up with severe abdominal pain and called 911. I later reread the prescriptions notes and figured it was a side effect from levaquin. But now i am sitting on $15,000 of medical bills because i don't feel the ER physician caught this connections and ran every test possible including 2 CAT scans and an MRI and still never mentioned that it could be a side effect. It seems obvious to me and I am not even a doctor. If anyone else has been to the ER or doctor because of these side effects or if there is a doctor out there that can help me build a case against the physician who I believe missed on diagnosing me correctly and administered several unnecessary exams, I would greatly appreciate it. I need alot of evidence and resources.

On the stuff for 7 weeks. Started at 60 mg for 4 wks now at 30mg for a few days then tapering to 5 in a few weeks. Moon face, insomnia, lots of food, seem to be in some kind of "zone" most of the time. It is a good and ba d durg but it is keeping me out of the hospital. Quit smoking in April (after 30 yrs). Started with chills and fever (up to 104) then pericarditis, the pyoderma ganrenosum. After tons of tests (blood, bone scan, bone marrow,cat scans, mri's,cultures, etc.) doctors can not come up with diagnosis. Scared to get off the drug but will.

Hello. My mom is 86 and has macular degeration and a bad back, but there was nothing wrong with her faculties. About a month ago she had severe pain in her back. We went to the emergency room and she was admitted. After a week and numerous MRI's CAT scans, bone scans, and Xrays it was determied she had a compression fracture of the T9 vertabrae. She had on previously.They had her on anhuge amt. of meds. She was being given ms contin, percoset and flexoril. They seemed to sort of work and didn't have any severe side effects, except the flexoril made her groggy. She was sent to a sub-accute center for physical therapy. She did fairly well there and was in for 2 weeks. When she was released ( a week ago Wed.) we had hwe ms contin rx filled. I was giving her her meds (her usual ones she was taking prior) and the morphine. Within 2 days she was getting strange. She wouldn't get out of bed (HIGHLY unusual for her)she was very disoriented, wouldn't eat all the usual side effects I found out about. I have stopped the pills as of Thurs morn. I have seen a pretty good changeEXCEPT for lingering confusion. She can't rember how to use her TV remotes. Since her eyes were bad she used the before by memory for the buttons but now she can't remember where the up/down buttons are. She realizes she is confused. Can you let me know what kind of time table if any there is to this medicines effects leaving the body. Even though she is 86 before she went into the hospital she had NO mental deterioration. I realize that it is only 72 hrs but I wan't to have some idea what to look for.
Thank you
Linda