Diarrea symptoms and conditions

I have just taken my sixth and FINAL Lupron shot. I was unaware of many of the side effects, like IBS. I am a lot different than most women. I was born with a birth defect called cloacal exstrophy. I am 41 years old and have lived my life with no bladder or rectum, due to extreme reconstructive surgery at birth. I have a permanent Colostomy and urinary diversion (ileal conduit). I do not have a very large amount of intestine, which creates an absorption problem of certain things, one of them being Calcium. I have also had severe orthopedic reconstruction since birth.

In December of 2008 they found a mass on the right side of my abdomen along with a hydrosalpinx. The hydrosalpinx was drained and I was then urged to start a 6 month cycle of monthly Lupron shots. There is a long history of endo in my maternal family. I have been advised that because of existing scar tissue from so many past surgeries a hysterectomy was not possible. I can not even have a laproscopy to determine that the growth is actually endo.

3 months into the shots I started to suffer extreme diarrhea, lasting from 1 to 3 weeks at a time post the Lupron shot...it was blamed on overgrowth from past surgeries, etc. It has become a terrifying experience for me. Due to my inability to absorb calcium well I now have several calcium kidney stones that must be broken apart with a laser. I have no idea what will happen with the GI symptoms or if they will continue once the Lupron "wears off".

I have no concerns about fertility, since having children has NEVER been an option for me. My concerns are surviving my life longer without additional risk to it from taking this drug.

I have had the usual symptoms of sweating, night sweats, fatigue, Hair loss, loss of appetite and occasional insomnia. Again, the most concerning to me are the kidney stones and GI problems I have been experiencing, including "sludge" in my gallbladder.

I am severely disheartened by the lack of looking at the whole picture, at least midway through this treatment. This is compounded by the fact that my treatment stems from one of the country's "top 10 Hospitals", which is a direct affiliate of the Children's hospital that did an AMAZING job of successful reconstruction in 1968. It is 2009 and I have fewer options to improve this situation than I did the issues from the original reconstruction in 1968.

I feel I never should have been put on this medication and am deeply concerned about my survival from here. If I could go back 6 months, as informed as I am now.....this IS NOT the path I would have chosen. I no longer know which Doctor to trust, what decision is best for me or how much more I can take.

If there are any AMAZING Dr.s reading this, please feel free to contact me...I am desperate, I do not feel that this should affect my survival rate and am willing to listen to alternative solutions IN THEIR ENTIRETY.

Anyone with a shortened GI tract, absorption issues, or previous health conditions should WEIGH ALL OPTIONS and do AS MUCH RESEARCH AS POSSIBLE before agreeing to this treatment. I placed trust and confidence first, not one of my better decisions concerning my health. I will not continue treatment with Lupron.

My 62 year old husband has had Parkinson's for about 10 years now. The other day he was prescribed Prednisone (20 mg tablets, twice a day) for 5 days. After the first day his pinched nerve problem was greatly improved, and as a side effect, his Parkinson's symptoms disappeared completely and he was like normal again! This is a miracle to us and we are looking for medical research to help prescribe Prednisone for Parkinson's', or some agent similar. Did the Prednisone make the other Parkinson's drugs more effective; or did the Prednisone fix the Parkinson's on its own. We don't know. For 5 days, it was bliss; I hope we can get someone to weigh the side effects against the miracle of being normal without any Parkinson's symptoms!

Glad I found this site...I have been on the NR for 1 1/2 months, this is my second attempt. First time I had it in after attempting an IUD (Murina), which gave me intense cramping (I have a tilted uterus) and bled for 7 weeks. I thought that the cramping from the NR was due to my body healing from the IUD, so I left it in for a month until I couldn't stand it anymore and took it out.

Now my second attempt at the NR, I have cramping on a daily basis, spotting to the point where I will be walking along and splat in my underwear major discharge (yuck!), heartburn, diarrhea (IBS), headache, unexplainable crying, little weight gain, I go to the gym 3 times a week and do yoga and pilates at home, my body responds really well to workouts and the scale has not budged to any weight loss.

My body is very sensitive to BC and was told by my gyno that NR has a low dosage and will not affect me like YAZ (made me a crazy person), Ortho Tri-Cyclene, Ortho-LO, which gave me migraines for 9 days out of the month.

Thanks to all the women out there (YOU ROCK!) who are posting their experiences, as of today this ring is out of my body!

withdrawal symptoms after being on it for a few months...severe diarrhea!! And bad headaches

Pain in right side lower back (around waist area). Like you have gas in your back. Constipation...dizziness.
lizzy

I've been taking Macrobid for almost 2 days now for a UTI and I now have severe, burning, watery diarrhea, stomach pains that almost feel like extreme heartburn, back pain, nausea and recently tonight I have just began spotting. I am 2 months pregnant and I am pissed! If I miscarry and this medication turns up to be the reason why, god help me because my husband and I have been trying to have a baby since last year.

I am a 40 year old female and both my husband and I are taking Lisinopril 40 mg. I have mild tingling in my arms at night, however the tingling/ burning sensation is so great in my husband's arms that he can't sleep at night. His rest is continually interrupted by this uncomfortable sensation. I have noticed a host of things like tiredness, an occasional dry cough, feelings of depression, rapid heart beat, and lack of energy in myself. My husband has experienced all of the above and muscle pain and irritability. I thought his irritability was being caused by lack of sleep, but I have learned from this website that it may be yet another side effect of the medication. We both have to get off this. Thanks for all of your helpful comments.

I started taking Yaz 3 weeks ago and I am feeling very sick, this headache wont go away ,stomach pain that's constant and dizziness and diarrhea I did not have this pain before, it just started when I started taking Yaz I should have research this Birth Control before I started taking it .Does anyone know how long it takes for this Birth control to be out of your system.

My wife and I both on 14-day Biaxin XL for bad flus. We both have an absolutely completely disgusting tastes in our mouths. Have tried everything drinkable & edible for relief to no avail! My wife with some diarrhea, myself some sleeplessness. The worst is this taste! We are both hoping that we can last another 6 days until we finish. Will never take this med again if we can take an alternative!

I have been taking Nexium for over 7 years. I started on Prilosec but when that became available over-the -counter my doctor switched me to Nexium, 20mg once per day. Not long after that I started seeing a new doctor. I was still taking the Nexium, 20mg, one per day. But I was still having a little of that burning pain just below my sternum. I told my new doctor about this thinking he would probably increase my dosage to 20mg twice a day or switch me to the 40mg capsules once a day. Instead he switched me from the 20mg Nexium to the 30mg Prevacid capsules. I had horrible side effects immediately. I would have sudden and unpredictable loss of appetite. Not just loss of appetite but the sight of food would actually make me feel queasy. I lost over 10 pounds in a week and wasn't even trying. But the worst, and most frightening, side effect was the severe shortness of breath. I was in the Navy for 10 years and kept myself in pretty good shape. At one time I was even running 3 miles a day. Immediately after starting on the Prevacid I got so short of breath I could not climb a flight of a dozen stairs. It made me feel like I was 80 or 90 years old. And I was only 48 or 49 at the time. My chest would heave up and down. Air was going in and out. But it felt like my lungs weren't getting any oxygen from the air that was going in and out of them. I wanted to trust my doctor but I was actually becoming afraid of going home from work and taking the Prevacid. I got back in to see my doctor as soon as I could and he put me back on Nexium. Not long after this he took a job at another practice/clinic to be closer to home and family. I had to find another doctor. When I went to see my new doctor (the 3rd I've had since the reflux started) I told him about the Prevacid and the shortness of breath. It wasn't as bad since I stopped taking the Prevacid but I still had some shortness of breath and burning pain in my chest when I exercised. He said he had never heard anything about the Prevacid and breathing problems. He sent me to the hospital for the treadmill stress test to make sure it wasn't my heart. It wasn't my heart, but then again I knew that. Even after complaining about the shortness of breath during several visits over the years he never said or did anything about it. About 2 years ago I had a bout of bronchitis. My doctor was busy all day so I took an appointment with another doctor at the same clinic. (I've had to do this several times) While seeing this other doctor for my bronchitis I mentioned to him the whole shortness of breath story. He said I should consider having a pulmonary function test because "you're not too young to have emphysema". Then early in January, 2008 I had to see another doctor at the same clinic, again for bronchitis. I told her about the Prevacid and the shortness of breath. Finally someone sent me to the hospital for the pulmonary function test (PFT). Two weeks later I had an appointment with my PCP for an annual physical check-up. I asked him about the results of the PFT. He said he hadn't seen them but he would check on it while the nurse was giving me and EKG test. Some time later he comes back into the exam room and says "yep, you have a little emphysema". The nurse-practitioner who sent me for the PFT had already started me on Advair. Besides that my doctor seemed to have little to say about my newly discovered condition. I'm not sure if the Prevacid or continued use of Nexium had anything to do with me developing emphysema. But I do know that after complaining to MY DOCTOR of shortness of breath for 3 or 4 years it shouldn't have been someone else that discovered that I have emphysema. Anyway, I guess my real question is has anyone else had a problem with SEVERE shortness of breath on Prevacid, Nexium, or any of the other PPIs?

I am not sure if the Lisinopril is my problem. I have been on it for 3 yrs now. I do not have HBP -never had it. I developed Type II diabetes and am on Metformin. In the last two months, I have developed dizziness and light headedness. Also, last two months, heart palpations - and the itching is driving me crazy. Skin has developed tender sites - like the skin feels like very thin paper. I think I am going to stop it - even reading what's on this page - it may be what's causing these strange things. I did not know it was from viper venom. I also have dry mouth, but no consistent cough. Every now and then.

I was prescribed Lisinopril and have taken it for 4 days now. I am so bloated. I have shortness of breath. I will call my doctor to see what she says but at this point I am stopping the meds. I would rather die than have this horrible bloating with diarrea. I can hardly breath.

I am sitting here is shock as I read the posts here. I have been taking Toprol XL for about 5 years now. It was 50MG and went up to 100MG when I had some heart arrythmias. Except for some dizziness at first no other side effects were noticed. For some reason my cardiologist switched me to me metprolol. I am currently scheduled for colonoscopy, a look into my stomach as well as blood test and stool test and on a strict diet.. why?, because I have been having serious gastro problems for 2 months now. (Diarrea, gas, stomach pain, blood )I told m first gastro guy about my meds and he said Metoprolol would not cause it. Yet I have just read here and on a side affect site, that gastro problems happen to 5 out of 100 people!!! This problem started very soon after I switched meds. Yesterday I skipped m meds accident. I went 48 hours without meds. NO problems! I took m meds last night and this morning my stomach is in turmoil. Tomorrow I cut my meds in half. Then call my cardio guy and change back to Toprol. There is an obvious difference in the drugs.

i have been taking the nuva ring since april of 07 , i have recently been waking up in the middle of the night with severe back pain and durning the day gettting headaches this has been happening for two weeks now and all the other comments i have read dont match my symptoms except the diarrea i have that sometimes usually when i first put it in and i also have vertigo sometimes and am breaking out in pimples just about the time i get my period and take it out but see the thing is i still have these symptoms even when the ring is out . Does any one else have these symptoms please email me , i also have the nausea alot of you have talked about but does anyone else have the back pain?

OMIGOD!!! I totally thought I was going crazy too and I have only been on yasmin for 2 months! I have been unbelievably miserable, or have wanted to cry for no apparent reason. I have super bad cramps, and crazy migranes as well. I haven't been able to sleep, been getting hot flashes (and i am only 22), and been overall exhausted. I get dizzy really easily, and my sight keeps blurring. I have also suffered from nausea, heartburn, diarrea, and have been super depressed. I am going to the doctor tomorrow to get off this pill. It isnt worth ruining my 3 week old marriage over, that is for sure!

I took Yasmin for a year while in high school, and it cleared up my face and made me lose weight. However, it wasn't very good at relieving severe cramps. I stopped taking it and for the next three years tried many other pills. My acne got so bad it got to the point that I'd rather deal with the cramps than shying away from society because of my face, so a year or so ago I went back to the Yasmin. I had so many horrible side effects! I was nauseous all the time, and several times a week I was vomiting and had diarrea with stomach pain. It was so bad, last June while at a rest stop during a long drive to L.A. I passed out on the pavement, in pain, panting and drenched with sweat. I've missed work and social outings because of this. I was seeing my doctor every month and I kept getting passed around because none of them could figure out what was wrong with me. I had bloodwork and body scans and ultrasounds of my abdomen; nothing. After a year I was diagnosed with IBS (Irritable Bowel Syndrome) and they gave me some medicine for that, but it just made it worse. Soon after that there was a really busy week in my life when I forgot to take the Yasmin. I felt better than I had in months and months. I stopped taking it completely and I felt so much better. I gained a few pounds and my acne came back, but now I'd rather have that than be sick everyday. Now I don't get sick thinking about, looking at or smelling food. This pill also enlarged my right breast but not my left. I'm hoping after some time that they will even out. After this whole ordeal I'm sticking to condoms and spermacide.

I believe my son is having complex partial seizures. He went through all the others mentioned here. Still having some issues with anger, diarrea, nightmares, and rash. Its been 3 weeks. I would be interested to hear about anyone having seizures after the meds are discontinued. Thanks all.

(6 yr old boy)Its been 2.5 weeks off the Singulair and the side effects have become less frequent and less intense but are still there. He still has a bit of an explosive temper, still having these shaking fits where he says its like his hands and arms just do what they want. Diarrea, nightmares less frequent. It has been so hard for us to deal with, mainly the erratic movements because they are involuntary though this is only happening for 10 minutes at a time now where it was 2 hours (with arms and legs going and buzzing for those of you who hadn't read my previous post.).

If you get diarrea from Omnicef or other antibiotics, take 3 or 4 Lactobacillus tablets every day that you take the antibiotics. The antibiotics kill the good bacteria in your stomach, the Lactobacillus tablets restore the good bacteria in your stomach. Children can take them, too, they are chewable and really help. They are a form of active yogurt cultures. Ask your pharmacy for them, you do not need a prescription.

On april 16 I was prescribed omnicef by my dr. i reminded him and his assistant to all my allergies but his assistant assured me that no one had complained about this. Well guess i wont be going back to his office. I had an ear infection and sore throat. After taking the antibiotic, i had black loose stool and a rash all over my body. I stopped the medecine. I called the dr and was told to stop the medicine. I still have the rash .

omigod, its 5:30am and i've been awake for 3 hours w/ severe stomach pain. i woke up and almost passed out in a cold sweat. the z pac isnt worth it. ugh...... its only day 2 and im calling the dr to get off this crap! im not sticking around for the diarrea.......

I started taking Levaquin three days ago, I cannot stay out of the bathroom, diaherria like crazy, stomach feels bloated, and I am trying to work, any suggestions, I was taking this for an infection on my little toe, its clearing up, but oh boy my stomach.

I'm a 26 year old male and I'm on my 5th day of Omnicef (Cefdinir). As I have a Staph infection, there is no visability of improvement, but the following are my side affects so far.
Diarrea for the first three days, somewhat upset stomach, increased urge to urinate, somewhat decrease in moral, slight change in appetite and mild trouble sleeping. I noticed there were many children and older people postings so I wanted to represent my age bracket.

I have been reading a lot of these side effect stories since I gave my son his first dose of Singulair this morning. Our doctor suggested giving it to him during the day and his QVAR puff at night. My son hasn't used his Ventolin inhaler for over 18 months and the QVAR was reduced to a single daily dose over 6 months ago. At this moment he has just shown an increase in his shakiness and a mild bit of diarrea. But at this point I will not continue with another dose til I talk to my doctor after the weekend. With my son having an increasing amount of febrile seizures the past 3 years, I will not increase any risk of future seizures by keeping him on this medicine. He was going to be taken off the QVAR and Ventolin entirely at the last clinic but he had a mucasy cough this winter that lasted for almost a month. The only reason we got any meds was of the "asthma" my son had in our old apt(black mold etc.) but since we moved from that suite over 14 months ago we haven't had any problems. Thankyou all for your posts on this drug, I would never have known anything than just what warns us on the little side effects paper in the box.

I was prescribed Sulfameth/Trimethoprim 800/160 for acne over 30 days ago. I have only experienced slight diarrea and dry mouth. Other than that it has worked just fine for me and I will continue taking it for my ongoing acne problem. Oh, and the acne cleared up nicely within 1 week!