Catheter symptoms and conditions

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

A year ago I was misdiagnosed with Sinus Tachy. I did have HBP though and did not know it. We just moved across country, looking for a house to buy, living in a hotel until we closed on the house, and then moved in and started renovating it. Lots of stress...on top of that i was not eating right. i went to a new doctor in our new town. I had an echo, stress test, and holter. the only test she used to diagnose me with tachy was 1 time of having a heart rate of 148 for a second or two. after being put on toprol i started having crazy symptoms. i changed doctors and the new doctor sent me to a cardio. i had a catheter done. the cardio didn't find anything that he said was alarming and wished his heart was like mine. the results were sent to my primary doc. my new doctor sort of listened to me and when i took the results of the initially holter that showed the tachy, i asked him if i indeed had sinus tachy. he looked at the results and said NO. i asked him if i can get off toprol xl...and he was hesitant. after telling him my symptoms he relented. he told me to go to 75 mg and then check with my cardiologist in a month and see if he wanted me to go down further. my bp and hr prior to lowering the dose averaged 100/110- 55/72 with hr averaging 65-70. July 5 was my first day of tapering my 100 mg tablet to 75 mg tablet. the first couple of days were pretty rough. my heart rate would spike to 110 with activity (taking a shower and walking very slowly around the house) and during an "episode" while sitting down would be 75-90. the BP spikes would go up to 140/90 during the "episodes" but would come back down with lots of deep breathing. i had chest discomfort, weird headaches and just an overall feeling of like i might die of a heart attack. around the 5 and 6 days...i was able to slowly move around without the above mentioned symptoms being less severe and by the day 7 and onward my heart rate had re-stabilized back down to around 105/118 over 65/80 with h.rate hovering around 70-80. after 2 weeks on 75 mg...i decided to lower it even further, down to 50 mg. the first 2 days of 50mg, there didn't seem to be any serious things happening but on the 3rd day it hit me. my pulse upon getting out of bed was 100-105 bpm. when i walked around slowly around my house, it stayed elevated..high 90's. it sort of settled in between high 80's and low 90's. my BP was now hovering around 118/125 over 79-89...sometimes spiking as high as 132/90 a couple of times. after the day progressed, the heart rate settled back down to around 80 ish and was in the upper 60's and 70's when i was reading in bed last night. my blood pressure last night was 116/78 with pulse at 66. i thought ...not too bad. Well this morning at 4am i woke up feeling hot and scared. i checked my BP and it was 109/74. a few minutes later i checked it again and it shot up to 126/83 pulse ranging anywhere in the 110-135 range. it finally settled around upper 80's. this spike occurred with me still lying in bed...not moving a muscle. i had my husband to get my toprol 50 mg tablet and a banana and once i took this my blood pressure lowered a little with occasional spikes along with erratic pulse as well. my blood pressure today has been ok....anywhere from 123/75 down to 108/69. my pulse on the other hand if hovering around upper 80's at rest (rest meaning sitting down on computer or driving) and it shoots up to mid to upper 90's while moving around..like going to the bathroom or walking from room to room. while i was making lunch it was in the low 100's. I guess all this to say that this is a roller coaster ride. i want off this med. once i have realized how potent it is, makes me more determined to get off....it is scary though. last night i swear i thought i was having a heart attack. my chest started constricting and my right leg became heavy...like it was losing blood flow...weird.. i know. i know that its rebound effects will occur, but when they are happening, i begin to think ...ok...do i need to stay on this med???? what i found interesting is that when i dropped the first 25 mg the rebound symptoms would occur around 11 am and last until 4 or 5pm. I attributed this to when i take my med...i take it right after breakfast around 8am. when i was on the full 100 mg these were the times i would feel the MOST fatigued....like a walking dead person going thru the motions of life..pretending to be ok. And im a homeschool mom so you can imagine how hard it was to pretend. i wasn't that surprised to find that my rebound effects occurred during this time. This last drop in dosage was different. The first 2 days i did not have the mid day rebound effects...they seemed to be elevated continuously throughout the day with the less rebound effects being right before bed. What was even more alarming was the middle of the night scare that woke me up..... i just wanted to share my current experience with withdrawing/tapering from Toprol Xl 100 mg down to 75 and then now currently at 50. i see my cardiologist in a few weeks and don't think i will taper down anymore until then. he is going to redo all the heart tests...and if i have a green light then i will continue to taper down until im off. For the record, my side effects while on the 100mg XL tab were......frequent...and i mean frequent urination, hair loss, (i have long very thick curly hair that i wear in a ponytail and i had to figure out how to hide the side bald patches..im only 38) seeing spots and floatys daily that i thought i kept seeing spiders move across my floor or walls, upper back/should pain that was very debilitating, vision focus problems, ankle joint pain...(i would wake up with a limp cuz the pain in my ankle joint was bad then the next day it would be gone only to return a few days later), hands and feet tingly all the time. i have also had thyroid tests... Weight gain or stubborn pounds that would not budge...even with daily exercise and a diet that consisted of fish 3-5 times a week cooked without oil or fats and eating only sauteed veggies and fruit. i have not had a piece of bread or processed carb in months relying on an occasional small baked potato with no condiments. i have calculated my nutrition so precise that i making sure i consumed 4500 mg in potassium, 2-300 mg magnesium, less than 600 mg sodium daily, 1200-1300 calories with 50-80 grams of protein and less than 30 grams of fat. all this and my weight would not budge. after dropping my dosage down to 75mg from 100, i lost 4 pounds in a week without changing a thing..I was even sitting a lot due to the crazy spikes in BP and HR. During that second week of 75 mg...i lost 1 pound. now that i have dropped down to 50mg i have lost 2 pounds and its only been 4 days. I would like to know anyone else's experience with withdrawing from toprol xl.

I am allergic to Prednisone. My primary Dr. does not believe me nor does most of the medical profession. The arrogance and assumptions that Dr.'s make has me at my wits end as I am allergic to many things. The 2 main things are any form of Ibuprofen and Prednisone.
I had an LAVH and oophorectomy performed last Tuesday.
To make a long story short, after surgery the attending Dr. ordered Motrin. I went into anaphylactic shock and was aware that I was in serious trouble but didn't know why. I thought I had developed a new allergy as all my known allergies were clearly listed on my chart. As they were moving me to ICU he stated he was going to give me Prednisone and my family told him no, you cannot give her that, she is allergic to it. Once inside ICU I became aware that I was in a fight for my life as they were going to keep experimenting on me like a guinea pig until they killed me. The Dr. came to me and said he was going to give me Prednisone and I fought back. I told him l would NOT take the Prednisone. I told him I did not want him or anyone else there to administer one more thing to me. I would not take anything except Benadryl and I demanded to be discharged. (IV/Oxygen/Catheter/everything still hooked up to me) Luckily, my surgeon showed back up at that point and took charge of the situation, immediately administered the Benadryl I had been asking for and I did indeed leave the hospital later that night with her blessing.
I believe in my heart that had they given me the Prednisone there is a good probability it would have turned tragic.
You have to fight for yourself because sometimes the Dr.'s think they know more than you do about your own body.

I am glad to have found this information after deciding to google Yasmin and heart palpitations. I started having palpitations last night (I had them years ago when I was having anxiety attacks but not since and I am not under any stress right now). I just started taking Yasmin less than two weeks ago and will not be taking it any more (I started it for PMDD). I have also noticed pain in my right breast and I was on the verge of a bladder infection a few days ago since I did not drink enough water for a few hours (I have only had one bladder infection in my life and that was after delivering my third child and having a catheter). I have also had blurred vision twice since I started it (I have experienced that before but very, very sporadically - not 2 episodes within days, I have migraines and my dr. thinks the blurred vision is somehow related). I had chest pain for 2 days, granted, it happened after a tough workout, but that is still unusual for me. I've always had pluses and minuses with any form of bcp, but these cons don't outweigh the pros (which I have not experienced yet anyway).

I am a 55 year old female. I had a heart attack in July -08. I had a stent placed. Since then I have been on Plavix, Lopressor, Lisinopril and Lipitor. I have been back to the Hospital 2 times since then. The first time they found nothing. The second time I had to have another stent place because the first one didn't work. This last time they did another catheter and found nothing. I have episodes every couple days of Light headedness, heart pounding, stomach upset, confusion , really bad burping and sometimes diarrhea. I am at my wits end. I have lost 30 lbs and am weak most of the time. I was very active before all this and can't get back on my feet. When I ask about the medicines, the doctors say I don't think it's that. Someone please help!

I will never put this drug in my body and I will never forget the levaquin night. Dad was already on an antibiotic. He’s been gone 8 years now so this is somewhat of a blur. His catheter sprung a leak so he had to go to the urologist. While there doc noticed a UTI and prescribed the levaquin. Even though dad was already on an antibiotic he was told to start the Levaquin once he was done with the other. Who knows if the infection was even there by the time he took the levaquin.
Dad was on drugs for seizures. (Unexplained seizures to this day)
I filled the prescription. I was the one down on him for being on so many drugs. I should have read and noticed it said not to take this drug if you’re taking seizure meds. I’d programmed myself by then that things are what they are and no one would listen to me about the drugs and side effects etc. They all see me as a witchdoctor as my husband would tell me. The doctor later told me he doesn’t have the staff to stand around checking drug interactions all day long…..
Dad took the levaquin. I said let’s get you out for a while and come down to my house. I drove the 2 miles to my house with him and by the time we arrived he could barely stand. It was all I could do to get him into the living room. He couldn’t get comfortable. He seemed out of sorts and agitated. I assumed it was his surroundings and he just wanted to be home in his chair. I struggled to get him to my car and back home. .
Once back to his house, we were talking, his eyes went off into a dead stair. He wasn’t aware of anything going on around him. They became fixated (seizure). This lasted a long minute or so and I watched his eyes come back and him come back to awareness. It was then I went to the printout info on taking this drug and saw to not take it with seizure drugs. I called the doctor and was told to immediately stop the drug. (if my memory serves me, he took one a day).
Later that evening, I went to check on him lying on the couch. He had this dopey smile on his face and when he spoke this really creepy gibberish came out. He wasn’t making any sense. I couldn’t understand a word he was saying. My sister and her boyfriend arrived. Dad was calling my husband by MY name and insisting he wanted to march. ( He used to march in the front of the parade every year in his sailor uniform) My sister and her boyfriend had to hold him up to march. His legs and muscles were too weak to hold himself up. He was like a noodle. He would not sit down or calm down. It was constant moving him from one place to another.
I offered to spend the night and sit with dad. It didn’t look like either of us was going to get much sleep that night. Dad laid awake most of the night. Occasionally he would speak to me and I could barely tell he was indeed in there ….. somewhere. He looked wired with a somewhat terrified look in his eyes. He could barely speak and just seemed to be on a bad trip. I moved him around the living room all night from couch to chair to chair. He finally fell asleep and I dozed. I woke to find he had slid out of the chair and was on the floor staring at me. Huge wide awake eyes looking at me when I woke. Mom woke up. We helped him to the kitchen for breakfast. He did really well walking. You could tell the drug was wearing off. I felt some relief. I went to work.
After work I went straight to dad’s to take him to the doctor. We all gathered in his office at the hospital to discuss trying to get dad off most or all of his drugs. We were grasping at anything to give him relief. Herbal remedies were finally being considered for some of his conditions. It was time for his next Levaquin dose. He went into what the dr. called a “life threatening” seizure.
He was rushed to ICU and pumped up on more drugs. It was said his seizure drug wasn’t working because…. He had a seizure. No one would even consider the Levaquin causing ANY of this. The “side effect” was simply treated with more heavy duty drugs. The new seizure drug was doing practically the same thing the Levaquin did! Or from what I’m reading and researching online now.. maybe it was the levaquin. Doctors would tell me it was long out of his system and wasn’t causing any adverse effects. You could watch them put the new seizure drug in him and watch him leave reality and his mind. I was later told he had a rare brain disease. They couldn’t explain why this was happening, nor would admit that dad was in there somewhere. I’d see him there when the drugs were wearing off, before the next dose would arrive. We’d hold normal conversations. My husband saw him too. All my other family members were FREEKING OUT at his condition and didn't have their minds about them... in my opinion. They couldn't and wouldn't believe a drug could cause any of this. I can’t recall the name of the seizure drug. I have this all written down somewhere around here!
I do believe though, they would have never changed the seizure drug if not for the levaquin causing a seizure by being prescribed because the doctor has no staff to check drug interactions. I will always believe it was the Levaquin that started him on his downhill climb to not being with us today. He was a strong man before Levaquin. He became weaker and weaker to the point of getting pneumonia and having a heart attack before leaving us 4 months later. Levaquin may not have been the end of him.. it was just the beginning of the end………….

I am not currently using nuvaring anymore because of a side effect I haven't really found anyone else experiencing. I would like to share my story and if anyone has had the same or similar symptoms please let me know because I am totally bewildered about it. I started using nuvaring after the birth of my daughter in December. I was on the ring for about one to two weeks. At first everything was fine but I started to experience very unique chest pains. The best way I can describe them is they felt like they were in the tissue and flesh in between my skin and my rib cage, and it felt like the area was being squished in a vice, and then my back would start to hurt alot. They first started about once every other day, but then got more frequent to the point when I stopped they were constant. I could not sleep because the only comfortable position was to sit down hunched over with a pillow on my stomach, with my back up against my headboard. My husband brought up the point that it could be the ring, and at that point I was willing to consider anything. I quit using the ring, and the pain stopped, for a little while. But it is still ongoing to this day. Although it only happens about once or twice a month, the pain is no less severe. I am sure it was the nuvaring or the ingredients in it that has triggered this because I have never had this problem before using it. Please if anyone has any advice or ideas, your help would be very much appreciated.

I started SMZ/TMP DS 800-160 tab 2 days ago. I have bad feelings about this drug and today is 4th July and the weekend. I will quit it to get some other drug for my UTI. But it won't be for 3 days because the doctor is out till Monday to get another drug. Someone tell me a drug that does work for UTI. Someone mentioned Amoxicilln? Can that be used? The headaches are awful. I can't seem to empty my bladder at night so I never really sleep since I pee every 20 mins a few drizzles. I also was given that drug that makes the pee orange. It is Phenazopyrid 200mg. It relieves pain, burning or irritation of the lower urinary tract. Someone offer us info on a positive good drug they have used to help UTI. Thanks!

mmm, contrary to virtually all the previous comments, I don't seem to have any adverse reaction to Flomaxtra. I had complete urinary retention, that required insertion of a catheter. My psa is normal, and my prostate size is typical for age. Flomaxtra was suggested as an alternative to surgery. Flow has increased from zero prior to taking the medication, to 12-15cc/second after about 2 weeks . (I am 54 years old). I have been on Flomaxtra for 6 weeks now . The only physical change I have noticed, is an increase in penis size, likely due to relaxing of muscle. Ejaculation and erection is normal. I do not like taking drugs, and will monitor any changes, but life is one hell of a lot better than not being able to pee, and catheters are so dehumanizing.

My 13 yr old daughter was put on Singulair along with Asmanex and Clarinex for her asthma about 6 weeks ago. Everything seemed to be going very well at first and her symptoms were starting to get controlled. I started noticing after about 3 to 4 weeks that her temper and attitude were getting much worse. Anyone with children this age knows what I mean but this was like a 180 degree turn for her. Her actions were becoming totally out of character. Before I knew it she would cry and get highly upset over the least little thing. Week 5 came around and things totally bottomed out. She came home from school and WAS NOT HERSELF. Made comments about how she hated her life and it was not worth living. Later that evening we had a big argument because I was telling her nothing was worth saying that. She went totally out of control and I had to physically restrain her to calm her down. It appeared everything was better so she went to her room. I went down to check on her and she calmly told me that she had taken advil and tylenol pm and things would be better for her forever now. We went to the ER where they made us wait for at least an hour, then finally took her back. She had to drink two cups of charcoal and was poked and prodded repeatedly. They did a catheter to get a urine sample. She was very cooperative but also was in a complete daze so who knows. The poor child couldn't even lift her head up when she started the vomiting to get rid of the drugs. It was very upsetting and sad. Her heart rate and blood pressure went very low and I really thought in the back of my mind that this was it. Finally, after several hours she started coming out of it and they sent us home. The next evening when she was starting to really come around she proceeded to tell me how she had been seeing a man walking around in her bedroom at night and she was afraid to go down there. Breaking down and crying telling me about all of the horrible nightmares she had been having recently and didn't know why. I thought what am I dealing with here? This just isn't her. Three days ago I heard about singulair in the news and looked it up on the internet. OH MY GOD THIS SOUNDED LIKE US!!!!! I immediately had her stop taking it and the next day phoned her asthma specialist who agreed she should stop now. We are going to watch her for two weeks and see if any symptoms return and then decide if she needs something else or will be fine on just the Asmanex. As a side note, she also mentioned being unable to concentrate in school (unable to do even the simplest math problems) and that her brain felt confused or like something was missing. She said this had been bothering her for several weeks. I know it was this drug. They really need to take this off the market NOW and stop flirting with disaster. The only reason I posted this was to let others know they are not alone.

I have just posted about my experience with Avelox on 11 Mar 08 but forgot to mention that my blood pressure dropped to 80/40 in the ambulance on the way and I kept blacking out and have also experienced extreme urination about every 15 minutes but thought that was from the catheter the ER used that night while treating allergic reaction to same.
I had to return to family physican Wed for shot Depramedrol as the Avelox was still in my system and the hospital also told me to use Benadryl to couneract same. I am glad to find this site as I was doing some research to see what in the world happened but my throat totally closed up as stated in previious post so could not talk!!

I am a 43 year old female who, until I found this site, thought I was dying of bone cancer - I am not even kidding. I just finished the last of my 10 day prescription for Avelox (for bronchitis and sinusitis). And I feel like I have been beaten about the head and body. Honestly, every part of my body aches and I can barely walk. I have absolutely no energy; throbbing and shooting pains up and down my arms and legs. Not to mention sharp pains in my chest area periodically. I have very clouded and unclear thinking abilities; and my neck and head hurt so bad not even an 800 mg ibuprofen helps. Oh and let's not forget the chills which are right down to the bone - I cannot get warm and I have yucky night sweats to boot. I would most certainly be interested in a class action lawsuit. I really hate that I took 10 days worth and wonder when I will start feeling better. PLEASE DO NOT TAKE AVELOX - it is not worth the painful side effects! The prescription flyer I received with the medication did not mention any of the side effects I encountered.

Symptoms I have:
NOTES on health since day after I started the Lisinipril.
9-03-07 – started taking Lisinopril
9-05-07 – Saw Dr. for Bladder infection (left urinalysis with doctor). Prescribed a sulfite antibiotic for bladder infection.
9-06-07 – First symptoms began; trouble urinating
9-06-07 – Called Dr. Kuebals office to let them know that I was having trouble urinating. I also asked if they got the lab test (urinalysis) back yet. The nurse let me know that I had strep in my urine (very rare she said) but they will be prescribing me macrobid and to stop the first antibiotic.
9-06-07 – Began taking macrobid
9-11-07 – Unable to urinate at all
More symptoms after a few more days of taking this drug: Heart pounding in my chest, Achy skin, panic/anxiety attacks (hard to catch breath, heavy chest), Cold feet, hot sweats and chills, urinary retention, bladder infections, ultra sensativety (body to the touch), muscle cramps, arms, legs, back and neck feel heavy. I can't even lift my arms to fold clothes they get so heavy.
9-12-07 – went to the ER to get catheterized
9-14-07 – At hospitals request (doctor at hospital) saw a urologist although he thought that this was most likely a cause of the bladder infection and that I might have some swelling around the urethra or he also suggested that it might be caused by a tear or “stretch” in the urethra from not being able to urinate due to the pain of urinating. I didn’t not think that one, because as soon as I was not able to urinate, I knew that I would need a catheter until we figured out what was wrong.
9-14-07 – Removed catheter at urologist office
9-15-07 – Early am – went to ER again to get catheterized as I was still unable to urinate
9-19-07 – Went to CT Scan requested by Urologist
9-20-07 – Nurse removed 2nd Catheter at Urology Office and said to come back by four if I still could not urinate on my own.
9-20-07 – Researched Lisinopril to find UT could be caused by Lisinopril (medications.com) and saw the side effects that some people were having with this drug. Also learned that this was a derivative of venom from a Brazilian snake (thus the symptoms of feeling achy, sick, tired, muscle weakness and urinary retention
9-20-07 – Went back to urologist to let them know that I still could not urinate and they showed me how to self catheretize. Also, as of the evening of 9-19-07 stopped Lisinopril.
Between the ER doctors, my PCP and my Urologist, they have heard me complain about all of these symptoms but they refused to connect them to the Lisinopril.

anyone experience problems with urination,bladder or prostate