Ulcers symptoms and conditions

I have been on the NuvaRing for about 3 months. Just after I started it...maybe two weeks later I got the worst case of heartburn ever. I had never had heart burn before. I had just eaten a big meal so I thought it was that. Then a few weeks later I had another severe case of heartburn that lasted all day. I threw up and by night time my back was in so much pain I almost went to the ER. Finally fell asleep and woke up the next day and it was as if nothing had happened.
Went to the doctor and they tested for ulcers and found nothing. Had a few more minor bouts of heartburn in the next 2 weeks. Then this morning...same thing. Strong heartburn which has gotten worse through out the day and not my back is in serious pain. Just hoping to get to sleep. Called my doctor and told her about this possibility and she had never heard of this. She told me to remove the ring to see if there is a correlation. Removed it a few hours ago. If the heartburn goes away and doesn't come back I will have an answer.
I eat quite healthy and am not overweight. I exercise regularly and don't take any other medication. Has anyone else experienced this with the nuvaring?

Well, I got a call from my daughter's doctor's nurse and they found ulcers all over her small intestine. Now, the nurse procedes to tell me that they are so bad that they pill cam that she had to swallow to find them had a hard time even getting through the small intestine because it was so inflamed! I don't know if anyone else has had this problem or if they have found any articles about someone else going through this after the shot, but please let me know if you have, thank you!

I went to this web site because I want to help my wife. She's been on Jolessa for 8 weeks now. As of this week, her heart has been "fluttering" for lack of a better word. She went to the ER room and they said basically that nothing's wrong with her but she is experiencing premature ventricular contractions (PVC's) which are not dangerous (according to the doctors). She asked the doc's if she should stop taking Jolessa and of course they said,"no."

We're wondering if anyone else is experiencing this feeling with this junk? My wife is 38 years old, healthy, never had heart problems or disorders. As of the past few weeks though,she's been feeling down in the dumps, sluggish and has a slight mode change.

If anyone is experiencing a change in heart rhythm, since taking Jolessa, please post it here. Thank you.

Has anyone developed tartive dyskenisia. It is involuntary body movements. Mine are in the mouth, like I am sucking on my teeth . It is very disturbing and listed as one of the side effects. It can occur in other parts of the body, like tapping.

I have waited long enough to tell my story. I am a 29 yr old single mother of 3. I started YAZ in Feb of 2008. I took it for 11 days. ELEVEN DAYS. It was about 4 days in that the headaches started. I couldn't stand light, I wore hoodies and sunglasses. I was nauseated. Saw double, black spots. Motion sickness.I could barely make it to work. I was out of control. I did not have control over my mind. I was crazy. My friend almost took me to the hospital to have me committed. There is no history of this in me or my family. The headaches would last from the time I woke up til the time I would go to sleep. Painkillers was the only thing that would keep me asleep through the pain. My dr immediately stop the the pills. I saw an eye doctor and they found nothing. They ordered an MRI. They found T2 Foci scattered throughout my brain. VERY unusual in someone my age. What that is, is my protective covering of my brain cells had been damaged there were gaps in its covering. I soon developed a stutter and a slur in my speech. The pain then moved throughout my whole body. They said fibromyalga and daily migraines. I'm now on topamax daily which gives me breaks in my headaches. I still get them daily. I still have pain in my body daily and I'm on painkillers daily. I have found a new dr who is wonderful. Who has recently taken blood. Who thinks that maybe it could be lupus. So I started researching Lupus...my symptoms and rashes match up. There is also a DRUG INDUCED LUPUS. and ORAL CONTRACEPTIVES is a KNOWN drug that can cause this!!! BUT IS THAT ON THE LABEL???? NOOOOOOOO!!! I was perfectly healthy before yaz, in kick boxing and now I walk and have the memory of a 60 yr old and my brain is permanently damaged. I have another MRI coming up to find out if there is more damage and I will find out the results of the blood work to find out what is wrong with me...but I blame all of this on YAZ and I hold them responsible. I SAY CLASS ACTION LAW SUIT....just have to find a firm with big enough BALLS to do it!!!

Hi, njcukett posted 2 days ago asking if anyone is still having abdominal pain after being off singuliar awhile.My 7 yr.old (on singuliar at least 3 yrs.) is still having pain.She also had bladder issues for the past 2 yrs.(Frequent dripping and urgency to void).This went unexplained by doctors.Over the past 6 weeks since she stopped taking singuliar,I have noticed a complete change in her stools.While on singuliar they had become grayish in color.She would have 2-3 of these movements a day.The color of her stools are now normal,but the lower abdominal pain is still present.So I am wondering if the pain is coming from the bladder, not the stomach.I am going in(without my daughter) to discuss this with her pediatrician next week.Singuliar also made her very anxious,do not want to add to that,by discussing this in front of her.For the people having abdominal pain,did the stools change while on singuliar compared to when off?Just curious.

I spent the weekend reading about the development of Singulair. The early studies recognized that the first phase of the acute asthma response bronco-constriction was probably not caused by leukotrienes. They identified histamines and prostaglandins as the probable sources. I don't think that changed because the Singulair literature states that it should not be considered as a treatment for that. Leukotrienes were a source of inflammation caused by eosinophils and mast cells present in greater numbers (than normal) in airway tissue. So, it was beneficial to find a way to decrease that.

The cysLT1 receptor was identified as source of the signals that tell the cells to produce leukotriene. The receptor, a gene, consist of 337 (they think) amino acids. They modified a compound that would bind to that receptor thus blocking the cells ability to produce leukotrienes. This compound is very specific. It was formulated to bind to the "model" receptor. This compound will not even bind to cysLT receptor sub-types. (That is the good thing.) There is an enormous amount of research that discusses the genetic variability of the chemical reactions that occur in the leukotriene (calling it this for simplicity) pathway. We are also seeing that a number of researchers would like to use gene profiles to predict whether patients will respond favorably to different asthma/allergy drugs. ALL PATIENTS HAVE A RIGHT TO KNOW IF IT IS INHERENT THAT SOME PEOPLE WILL NOT RESPOND TO SINGULAIR OR RESPOND ADVERSELY.

There are many studies from the 1998 era that conclude that montelukast is not effective for everyone. Those researchers stated that it can be predicted that those people who are going to respond favorably will do that within the first 14 days or so. That conclusion would be consistent with a genetic component for efficacy and safety of Singulair. Those doctors concluded that those who did not respond within that time frame should not take Singulair for fear of harming them. That makes good sense.

The Italian researchers wanted to know if there was more going on than blocking leukotrienes in the action of montelukast. They set up a "test tube" study regarding montelukast, the cysLT1 receptor, and some t-cells that they selected. Why? Researchers always have something on their minds. They observed the death of these particular t-cells.

Montelukast is a quinoline. We basically know of quinilines and quinolones as compounds that were invented as broad spectrum antibiotics. They work because they interference with bacterial DNA so they cannot replicate themselves. Montelukast is a quinoline modified to bind with the cysLT1 receptor (a gene) and prevent that gene from activating. That's consistent with what a quinoline/quinolone does.

So what does montelukast do in blood plasma if it does not bind to the receptor because of genetic mis-match? (If montelukast does bind, then a chemical reaction has occurred and the liver will break down the by-products. Montelukast metabolized in 10-12 hours.) What happens if it doesn't bind? How long before it breaks down? Does it produce toxic by-products?

I want to know what happens to lymphocytes such as t-cells just because montelukast is a quinoline. Maybe nothing but what's up with the Italians researchers? I want to know if montelukast has the capability to interfere with lymphocytes who can clone themselves. That could be a good thing under circumstances when these lymphocytes are causing inflammation. But it could be a bad thing in the case of normal individuals with no problems.

I want to know if the bad side effects are due to the fact that the body has to break down and metabolize a quinoline that did not bind to the receptor for which it was created. The side effects of Singulair are strangely similar to what is observed in the quinolones such as levaquin. I have not as yet been able to compare montelukast as a quinoline to levaquin as a quinolone. I am hoping to find something on these categories. There may be no reason to worry that they cause similar damage. But frankly, I think that there is. There is some terrible chit happening to some people. The scariest is the neurological damage.

All of these questions would be in the everybody pharma knows to ask category. I don't know where the answers are. I haven't found them as of yet. Maybe there are no answers. We have to remember that Singulair and Vioxx were released in the same year. They have continued to be drugs under the current executive management of Merck. If the Vioxx marketing promoters had their ghost writers, why not the Singulair marketing promoters. The genetic component appears to be widely accepted but we haven't heard one thing about even that.

I think that it is sad that maybe the marketing of Singulair as one stop shopping for asthma/allergies may have destroyed the original concept. I really think from reading the original work that they knew that they couldn't engineer a drug for one size fits all. Everybody gets harmed when information is withheld.

Shame on the allergist who yelled at the mother who wanted to discuss issues. Does he know exactly who is allergic to Singulair and who isn't? Get him a dunce hat. Just because Singulair is marketed for allergies does not mean that you cannot be allergic to it. See the power of Madison Avenue? The ad agencies focus group these drugs to death. The ad agencies cleverly craft the product information. A good piece of legislation would be to prohibit consumer drugs ads.

Update: My daughter has been off Singulair for 3 months and is doing so much better. She is not having anymore nightmares, heart racing, anxiety attacks. No more itching, headaches, stomach pains, depression. She is so much happier now. She is 7 years old and acting like a happy child now. I am so glad that I took her off it in December. She is not crying and upset like she used to be. We could tell that she improved within one week and is still improving. Hope everyone else improves like my daughter has.

Here is some perspective for you all. I take Singulair and do well on it and in ACTUAL studies it has one of the safest safety records. Understand that post marketing reporting does not mean there is a correlation between the event and the product. Throughout the life of a drug the companies must disclose any report of side effects reported to them REGARDLESS of causality. A popular antihistamine that is OVER THE COUNTER also has suicidal thinking/behavior listed in its post marketing section. However, just because patients who had reported having these thoughts while taking the product doesn't mean it was a result of the product! Maybe they had a depressive personality and were also on multiple other medicines to treat that. You must look at the "Adverse Reactions, Warnings and Precautions" sections of package inserts to see the side effects that were actually seen in studies. You can die from ulcers derived from over use of aspirin or ibuprofen. Decongestants can throw off your blood pressure and these events are documented in actual studies! Listen to your bodies when taking any med. If you feel differently report it to your doctor.

These are all drugs people, there are potential side effects. There are also side effects to those "natural" over the counter remedies that are not nearly as regulated by the FDA or studies by the drug companies.

To anyone out there who has experienced side effects to singulair timed to when you started it, talk to your doctor, stop taking it and see if it goes away. Same advice for any product prescription or over the counter medicine. Side effects can be a combination of many factors (what other meds are you taking?) But understand for many people this product is the safest and most effective treatment for them. The FDA and Merck are reviewing all information to see if there is any correlation to the reporting. But singulair been around for about 10 years and prescibed to billions of people and is known to be one of the safer medicines out there overall.

In between the legitimate posts on this site I get the sense there is a lot of ambulance chasing going on. People looking to cash in on this big drug companies. We want drugs, we want them cheap and with no side effects which is not a reality. Keep stepping up the regulation and make the companies hire more lawers to protect themselves and jump through even more hoops and see what happens to the price and access to new meds. Even better, see how regulation has impacted the development of new medicines around the world (here's a tip, it will dramatically decrease). Drug companies certainly aren't perfect but which industry is?

Please, when taking any medicine over the counter, prescription or herbal supplement listen to your bodies to see if the potential benefits of the product outway the risks or side effects. Report any changes to your doctor.

I have been crying for almost 24 hours now. I cannot believe what I am reading and hearing about Singulair. My son has been to hell and back again and again. I cannot say for sure the Singulair is the culprit. But after reading all of the other stories on this website, I am convinced it is a strong possibility.

My son is 11 years old. He has severe allergies and asthma. He takes many, many medications for this including Singulair. He as been on Singulair for about 8 years now (my best guess because he has been on it for sooooo long.)

My son was diagnosed with ADHD in pre-school. He has taken many medications for the ADHD, but none have ever done any good at all. We thought some of the medications even made things worse. Now, I'm not so sure.

After exhausting all the ADHD medications, our pediatrician sent my son to a psychiatrist and a counselor. The psychiatrist put him on 2 different antipsychotic medications. Again, neither one did any good and seemed to make matters worse. The psychiatrist sent my son to a psychologist to be tested for Asperger's. For those of you who don't know Asperger's is a high functioning form of autism. The psychologist ruled out Asperger's by diagnosed ADHD and Anxiety Disorder. He did not prescribe any medication.

For some unknown reason, I've only given my son the Singulair off and on for the last year. My son had the best year in school ever. However, his pediatrician was still not satisfied. He sent him to see another psychiatrist at Children's Hospital in Pittsburgh. We were told he is believed to have more than one disability. He is believed to have ADHD, Aspergers, Teurettes and a possible 4th medical problem that has not yet come to light.

We are scheduled to see a neurologist at Children's Hospital on the 15th of April to rule out any medical reasons for his tics. We see the psychiatrist again on the 18th of April.

I am so tormented by this recent news. Has all of these problems been caused from him taking the Singulair for so long? Although he has had his best year in school yet, he still has a lot of problems. Are the side effects of the Singulair permanent.

The other side of the coin is this: It is also very scary to watch my son not be able to breath. Asthma can also be life threatening. What is a parent supposed to do.

Also, I now don't know whether to keep these appointments that are coming up. I hate so much to put him through more. He has endured enough doctors and tests to last him a lifetime. However, what if it is not the Singulair and there is help out there for him that I am not aware of.

Please if anyone else has had a similar experiences e-mail me. I would love to hear from you.

God Bless everyone who has been through this kind of hell.

THIS IS MY 8TH DAY ON LAMICTAL 25MG AND I WOKE UP SO DIZZY THAT I ALMOST FELL OVER. I HAVE BEEN THIS WAY ALL DAY IT LIKE COMES AND GOES FAST. IM DIZZY NOW..
I HAVE NOTICED MUSCLE ACHES BUT I THOUGHT THAT IT WAS THE ATENONOL 25MG I TAKE FOR PALPITATIONS BECAUSE IT LOWERS YOUR POTASSIUM. IM THINKING THE LAMICTAL DOES THE SAME LOWERS YOUR POTASSIUM WHICH CAUSES THE MUSCLE PAIN AND ETC.. SO I BEGAN EATING BANANAS AND SEE HOW THAT GOES. MY DOC SAID THAT IF YOU TAKE A ANTIDEPRESSANT AND YOU ARE BI POLAR YOU CAN HAVE SERIOUS REACTIONS TO THE MEDS. SHE TOLD ME TO "NOT" TAKE A ANTIDEPRESSANT.
I WAS ON THIS MEDICINE BEFORE AND WAS UNSURE ABOUT A SIDE EFFECT OF ULCERS IN MY MOUTH AND STOPPED IT. I REALLY WANTED TO CONTINUE BECAUSE IT MADE ME FEEL GREAT(only got to 50mg then)
I HAVE ACTUALLY FELT PRETTY GOOD MORE GOOD DAYS THAN BAD EXCEPT YESTERDAY AND TODAY I HAVE BEEN REALLY TIRED ALONG WITH THE OTHER.
MY QUESTION IS WILL THESE SIDE EFFECTS GO AWAY???? AND I DON'T WANT TO REALLY EAT MUCH.
I REALLY LIKE THAT I AM NOT MOODY ANYMORE LIKE I WAS AND I GOT MY SEX DRIVE BACK AND I DON'T WANT TO GO OFF IF I DON'T HAVE TOO.. HOW LONG DO THE SIDE EFFECTS LAST??
AND IS IT WORTH STICKING IT OUT?

Hi, Reading all of your posts. I have been 100mg of Topamax for three years now and my side effects consist of tingle of the fingers/hands/feet,
oily T zone (face), short term memory loss, extreme fatigue, loss of taste. which I don't think is necessary a bad thing. haven't drank soda in three years due to the carbonation. Anything to sweet I can eat or drink. I have to water down my juices otherwise there to sweet. and I experience far less
migraines. from 2-4 a week or week long migraines where I would go to ER to get a shot of morphine and I was still feeling the pain. to only maybe 1 a month. But if I spot it fast enough a couple Tylenol will help before I have to take a Zomig to knock me out. It sucks being on meds for the rest of your life being young, this started for me age 30 I will be on migraine meds for life so my neurosurgeon says, and they don't think its related but I also ended up with 5 ulcers and a broken esophageal sphincter which now gave me GERD and requires life long meds which oh yeah I have constipation but is that from the GERD or the Topamax? So I don't take anything unless I absolutely have to. which includes my asthma inhaler or nebs. last thing I need is steroids on top of everything else. I drink coffee all day just to keep me awake but at the same time the min I stop I sleep hard and sound. Go figure.

I have been taking Omeprazole since December 2007 now so 2 and a half months.

I had the dose increased to 40mg 3 weeks ago as 20mg wasn't curing the burning in my throat.

For a few weeks now i have had increasing vertigo/dizziness and palpitations. I only linked the 2 to the medication just yesterday, googled it just now and confirmed my suspicions to the Omeprazole.

Other feeling i have had since taking this medication...

Severe dizziness
vertigo
palpitations
headaches/migraines
weakness
fatigue
sweating
nausea
bloating
stomach cramps
visual problems
intolerance to bright lights
aching joints
chest pain

Now my question to myself is do i come off the tablets and endure the misery of my acid reflux? surely there must be something else we can take for our stomach problems that don't cause these awful side effects.
Anyone tried anything else that worked and didn't make them unwell?

I started on Prilosec OTC 20MG 12/12/07 first thing in the morning (1 hour before eating) for ulcers and suspected Hiatal Hernia. At first it was great - took my acid reflux away - starting yesterday I developed a tickling feeling in my throat an hour or two after taking and a cough that accompanies the tickle - also after eating within an hour my nose gets stuffed up and I feel like mucous is running down the back of my throat. Also I have had a feeling of upper chest tightness off and on (especially within an hour of eating) almost like a cramping feeling in my chest.

I was put on Prilosec because the Dr. suspected that acid reflux was making my asthma much worse. Asthma has been better on the Prilosec but with the past two days of the dry tickling cough and chest tightness it is scaring me.

Anyone else have this??? Please help!!!!

I have been taking nexium for about 3 months and I decided to stop due to the development of severe pain in my heels, hip, shoulder, collar bone, and hands. Now looking for a natural way to heal my ulcers. I was told aloe vera liquid. Not sure about this so I will investagate.

My mother has been on Fosamax for years, and now at 79 she has been diagnosed with anemia and has had tests for ulcers and intestinal bleeding. All were negative. I suspect Fosamax. Has any one else experienced this.

I wish I could say that my symptoms are something new but they're not. I can only thank God that I found this site and finally feel like I'm not totally crazy! I received a cortisone shot (kenalog and Lidocaine) on June 15th. June 17th I started experiencing tingling down my arms,across my shoulders, serious heartburn, change in tastebuds (sour tasting all the time), which progressed with a sudden case of high blood pressure. My period also came a week late and has not left yet but only taken short vacations (3-5 days of light to no bleeding, followed by a regular flow with some gushes all over again). Two weeks ago I started having a tight sensation in my jaw and cheek with sensitivity right under my ears. I've had periods of dizziness, severe migraines as well as heart palpitations (fluttering in my throat). Added to this is swelling down one side at any given time, changing back and forth with no reasoning. I had severe gastritis and GERP as a result as well.

I too was living a healthy life and regret the moment I agreed to that shot. Does anyone know how long these side effects last? Who do you see to deal with them? Are they mimics of real situations (do heart palpitations turn into heart attacks? gastritis turn into ulcers?)

Wow. I posted about a month ago describing a list of symptoms that I've been dealing with for the past eight months. I was seeing a gastroenurologist to test for gallstones, pancreatitis, ulcers, IBS, etc... My blood tests showed that my Lipase was 400 (normal level is 60) and my Amalayse was just as high!--Dangerous levels! These both test your liver and pancreatic function, so my doctor concluded that I had pancreatitis due to something that he could not find. This made my doctor very nervous, so we ran a load of tests and he was stumped...

I decided to do a little experiment on my own. After reading your posts, I realized that all my symptoms started about when I started Yasmin. So I went off of it. Within days I started feeling better--and I had another blood test a month later and my levels are all NORMAL!

Yasmin caused me to have pancreatitis...that's really bad. And scary. What's in this stuff?

I took it without water once. Well, I actually drank a glass of water and then took the capsules without taking another sip. They lodged in my throat and led to 2 severe ulcers in my esophagus.

I didn't put the events together for some time and neither did the doc: Couldn't eat for a long while.

Please take with water as directed.

I was taking doxycycline for about a month and one night experienced really bad indegestion (or thats what it felt like). After that it got worse. It casued me to have such bad acid reflux that it had begun to destroy my esophogus. I couldn't eat anything with any type of acid or texture and finally had to go to the doctor and get on medication. Now I am having to have an upper GI done to look for ulcers that were created, and I still am not able to eat reguarly.

I was prescribed prednisone for a severe case of poison ivy. 60mg for 10 days, then tapering over 2 more weeks. Side effects were dizziness, sleeplessness, hunger, thirst, slow healing, pent up energy, acne, etc. My doctor also prescribed Ranitidine 300mg 2x day because it's a histamine blocker, and that helped with the all-over itching. Ranitidine is normally prescribed as a stomach aid (for ulcers/acid reflux I think), so that may have helped prevent any of the stomach/digestive side effects. I also tried to follow the recommended dietary suggestions that I learned about. I focused on potassium, calcium, protein, zinc rich foods, lots of healthy vegetables, vitamin E, etc. Try searching the internet for "prednisone diet" or "prednisone nutrition". I think all that helped! Good luck.

Two years ago in May I was hospitalized for an intestinal blockage. They put a combo of levaquin and flagyl into me with IVfeed. It is such a powerful drug that they kept having to move where the needle went into my arm because it became red and swollen after a day or so. The last time they put it in was at the left wrist outside. This caused the vein to eventually collapse all the way down my inner arm and over the heart.
I was released within 5 days and told to take levaquin for ten more days. I could hardly take it any longer and went to my local redi-care to find out what I could take to alleviate the stomach pain. The doc there said stop taking it.
After that episode I began to have pain in my lower spine and across the gluteals. Sometimes when I would sit down it felt as if everything was tearing loose.
This past Feb/March I was given this drug again for headaches which were thought to be sinuitis. The only way I could take it was to cut it in half and take that until it was gone.
Now I have 6 ulcers, a ruptured tendon in the right shoulder and pain in my lower left leg and ankle.
Where I live it is illegal to sue drug companies.
Don't take this stuff or any of its family members.
I can hardly walk and my left arm is scheduled for surgery which I may need to cancel.

I have taken Mobic for about a year. Now I have ulcers that the Doctors say were caused by taking Mobic.

I have been on 5mg of lisiniprol for 6 months now and although my BP has reduced I have really bad sore pain in the lower inestine, always worse through the night followed by very loose stools the next morning. I have a slight cough but i have noticed that when i get a common cold, the sore throat symptoms go on for weeks and have turned into ulcers.
I would love to find a BP tablet that didn't upset my digestive system

I received radiation for breast cancer in 2001 and a month after the radiation treatments I was hospitilized with radiation penumonitis. I was given 120mg prednisone. I had horrible mood swings, kissing ulcers, and lost 15 pounds - the doctor's couldn't belive it. I lost muscle mass in my right leg and had to have physical therapy to be able to walk again. It took 6 months to work my way down to 2.5mg at which time I was hospitalized again with cryptogenic organizing pneumonia aka BOOP in my other lung. I was put back on 60mg prednisone. I have been on various drugs to combat the side effects. I finally got off prednisone in May 2005 but the end of June I got pneumonia and another inflamed lung. I went back on 10mg prednisone which I am trying to get off of now. I have been experiencing depression since going back on my latest dose, but am not currently medicated for it. I have returned to my normal weight and continue to do weight training to combat osteoporosis due to the prednisone as well as strengthen my leg. I worry about the long term effects of long term steroid use.