Gi symptoms symptoms and conditions

I am taking omeprezole & blood pressure medication & am having muscle cramps in my legs & feet mostly, but even in my chest (Thought I was having a heart attack).I am experiencing severe fatigue & like one of the previous posts, I'm having difficulty even holding the steering wheel of my truck.It's difficult for me to stay awake ,especially if I relax for more than 5 minutes.I assumed it was the blood pressure meds, & stopped taking them recently to see if that would help.(It didn't) I'm going to stop all synthetic meds ASAP & hope for recovery.I've been taking these for 3 years & am experiencing many of the same symptoms as other posts,including swollen breasts (I'm a male)...THANK GOD FOR THIS SITE!!! I'll keep you posted on my progress. Best to all fellow sufferers.P.S: My doctor thinks I have more symptoms than "a 90 year old lady" (I'm 54)God Bless, & I'm praying for you all.

I think that I finally figured out why I am so physically and mentally sick. I received the mirena almost 2 years ago and I was a true advocate of the product...I love it!! About 6 months ago I started to have panic attacks and anxiety (i have never experienced this before) it was so bad that I barely made it to work everyday and could no longer handle being out in public. My PCP placed me on different types of anti-depressants (which made me depressed). Currently I take Budeprion which has decreased my anxiety but I do not feel like myself. The past month and a half I wake up with the feeling of morning sickness (the numerous pregnancy test say that I am not), have headaches, low energy levels and little motivation. I was pretty sure that my hormones levels must be "off" but my PCP and OB insisted that there is no way that my symptoms have anything to do with my hormones because my child is almost 2 years old and I am 29 years old. I have gone through numerous tests on my gallbladder and other organs to find the cause of these symptoms that I have and Everything is Fine. After reading the stories on this website I now know that I do not need anti-depressants and I am not going crazy...I just need to get the Mirena removed.

Been off omeprazole for approx 2 weeks now, very gassy, burning feeling & burping mostly at night. Apple cider vinegar (2-3tsp in 8 oz water) seems to help. Still feeling a little "anxious" at times but much better than before stopping omeprazole. Anyone else having the GI symptoms after stopping?

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.

Was prescribed Sulfamethoxazole-Trimethoprim 3 days ago for a bacterial skin infection. At the same time, I also had an apparent allergic reaction going on (unknown source, had never had one before) where my arms were both covered with hives/welts. So my skin was peeling and hive covered BEFORE even starting the meds, which is making the evaluating of the drug side effects a bit trickier. So far, the skin seems to be improving but the hives/rash has not improved, despite taking prescribed allergy meds during the same time. So this could be the current source of the rash, but I can't tell.
On the plus side, have not had any stomach upset (I took all doses w/ food) or other GI symptoms other than increased frequency in BMs. I only seemed to get a headache after not drinking water for a couple of hours. If online sources are to be believed, the "sulfa" portion of this is the culprit behind the worst side effects, AND food may interfere with absorption/effectiveness. Based on that, I'm planning on taking my remaining doses w/ food since the skin infection is already clearing up after 2 days and I've got 10 days to go. Hoping to avoid the reactions folks described here where they starting rashes late in the treatment cycle.

My son (now 6) was put on Singulair at 8 months old for asthma and has been o it since. He has never had an appetite and is quite underweight. He complains of stomach pains and headaches daily. At age 4 he was sent to a pediatric GI and neurologist and any brain or gastro issues were ruled out. No one could figure out what was wrong. He has sensory issues and just recently was referred to a psychiatrist for occupational therapy. It was at this appointment that it was suggested that the Singulair is responsible and since he has been on it for the majority of his life we were unable to make the connection. He has been off of it for 2 weeks now and has not complained of headaches or stomach pain at all. His eating habits are slightly better, but not great. Hopefully his appetite will improve over time. I wish we had only known sooner. I feel like such a terrible mother!

I'm an 81yo Caucasian male who has been taking Lisinopril for two years ago. I have suffered through the aches and pains , dry cough lightheadedness , associated with this drug. When I first took 20mg/day, I tracked my BP as frequently as 20 times per day. Some of my symptoms were a result of my BP dropping down to s practice of medicine, MDs do not always have the time to experiment with each patient, so the patient must do some of the logical investigations independently.
Remember, no one knows your body better than you, and your PCP or Cardio MD only sees you for a short period of time. I have tried five statin drugs and cannot tolerate any of them. Alternate, naturally-occurring substances are available.

I am almost 41, and have had migraine headaches most of my life which I could manage with 800mg of Naproxen Sodium, or a Norgesic Forte, and when Imitrex came out, I could just administer that. Six months ago, my headaches got so frequent that I had to start taking my Relpax (similar to Imitrex) and/or Fioricet more than 2X per week. According to my neurologist, this is a no no, as both of those meds can couse rebound headaches. He started me on Topamax, 50mg per day. It did nothing. He bumped it to a 100, nothing. Now I'm a 200 mgs, I am still have a migraine in left temple as I write this. I have the tingling, the daytime sleepiness, but my mind is fine, and my appetite is just swell (regretfully). What the hell am I going to do now? Ask him to bump me up to 400 mg? Now I have these headaches every "F"ing day, and I can't take anything. I just have to suffer.

Topamax is NOT working!!!!!

I have been taking OMEPROZOLE for around 9 months for Barretts Asophegus reflux.
In general I was beginning to feel I was very ill with symptoms mainly: hot flushes, my face was burning for a few seconds, dizziness, stomach cramps top right mainly, feelings of diareah, and dry mouth.
Has anybody else experienced any of these symptoms... my GP is sending me for a scan on my Gall Bladder, but in my mind all these cramps are associated with Omeprozole... I cannot stop taking it or I get severe pain between my shoulder blades with reflux burning.
Maureen.

I am a healthy 55 year-old menopausal woman who started taking Vagifem in May 2007. By early July 2007, I experienced my first gallbladder attack. Both Ultrasound and CCK Gallbladder Ejection Fraction (70%) were normal, but I continued to experience gallbladder symptoms (nausea and right upper quadrant tenderness but no pain). My gastroenterologist and GI surgeon recommended gallbladder removal.

Neither my doctors nor I have linked Vagifem to these symptoms. I am thankful to have access to this website and learn that Vagifem may be the cause. My plan is to stop Vagifem altogether and note any improvement in my GI symptoms.

I wanted to give you an update. I wrote on this forum about a year ago. I have been off yasmine for 15 months, it has taken this long to be just about totally back to normal. I am 48 years old, still menstruating, but yasmine had hit me in a particuarly bad way.

In that, I mean, after two years of being on the pill it triggered Inflammatory bowel disease, IBS, terrible GI problems, and worst of all panic attacks and anxiety. At first, getting off of yasmine made it all worse, for about 3 months, but then gradually it began to get better each month.

But it has taken all of these 15 months for me to finally report a very normal menstrual cycle, normal PMS, bad periods (but that is welcome, it tells me everything is like it as before), a normal sex drive, and normal gastro intestinal function. The only thing that still lingers is anxiety in the couple of days preceeding ovulation and a few days preceeding my period. This anxiety is worse than it was in my pre-yasmine days, but nothing compared to how it was when I was on the pill.

All I can say, is for those of you that have stopped taking it, be patient. Eventually you too will feel back to your old selves. For those of you who are still taking it, be wary of any odd symptoms, especially anxiety and GI symptoms. I have filed a report with the FDA, as I believe this is a very dangerous drug that was approved too soon, and all of us have been guinea pigs for the pharmaceutical industry. Good luck to all the other recovering victims. If you are off it, you will eventally be OK>