Nexium symptoms and conditions

Ive had the mirena for 4 months.My doctor thought it would help with my painful,heavy periods,well I been bleeding since and it just getting worse.I want to know if anyone has had stomach issues,like acid reflex,heartburn,gas,or just pain in your stomach.cuz im thinking I have a ulcer or is it this device????Lisa

i have had problems with acid reflux for approx 5 years now and have tried everything pretty much. i first went for tests and they did the one where you swallow the liquid metal stuff (barium?) and then a endoscopy. my regular doctor said i had a slight hiatal hernia after the barium test and after the endoscopy my stomach dr said i had acid reflux and didn't have a hernia so he started me off with nexium which worked good for a while but i began to have side effects . i would just feel not right mentally cloudy all day, extremely dizzy.after that it seemed like every drug he put me on (prilosec,aciphex,prevacid) seemed to have the same results. so i decided to see if i stopped completely if these feelings would go away and sure enough they did but the acid was soon to follow. i started taking zantac 150's and they worked but now i feel like i cant sleep at night and sure enough thats one of the side effects. i also read not to drink alcohol when using these drugs. so now i pretty much sit here not knowing what move to make next

I have read a lot of these responses and here and have noticed a common thread among all responses. This may or may not help.

You need to give any new pill a full 3 months before judging it. Your body needs to stabilize with the new hormones that you are giving it. It generally takes about 3 cycles to do so. ANY pill, whether it is Femcon, Loestrin, Yaz, Yasmin, or any other will have the same side effects. So, for that matter, will Nuvaring or other hormonal based birth control methods.

I had problems with Femcon during the first month as well, just like I did with Yasmin. The solution to the problem is giving it a full three months before making your decision. Anything else, and you are simply not making an education decision. Good luck ladies!

Hello everyone. My name is Michael, and my experiences with Advair were so horrific, I thought I would post here as a both a cautionary to those who would use this product, and to validate those who thought "they were crazy" while using it.

I was diagnosed with "World Trade cough" as a result of my four month exposure from that disaster. It finally culminated in frequent walking pneumonias and a sinus-drip initiated cough, which is really part of a complicated process from GERD, also World Trade related. Finally, the pulmonologist diagnosed the obvious "RADS", Reactive Airway Disease.

I was prescribed Aidvair Diskus inhaler 500/250 twice a day, along with Nasonex and Nexium. The first two months seemed uneventful. As my cough cleared, I saw no reason to take the medication anymore and slowly titrated its discontinuation.

Then everything went awfully wrong and my nightmare started. First, panic and anxiety attacks, which I hadn't suffered since World Trade overtook me at different times of the day. Only the Toprol for my high blood pressure kept me under control and out of the E/R with uncontrollable tachycardia. Next, the Depression which also was overwhelming, and the compounded fears from physical symptoms. Then the "TRUSH" came in my mouth and a concomitant fungal infection in my groin. Swollen glands in my neck. Fever, fatigue, listlessness joined the symptoms.

Though a committed heterosexual, a bachelor party a month ago raised spectre's too awful to contemplate and I insisted on the most ultra-sensitive diagnostic blood tests to rule out dreaded disease ( I did responsibly use a condom ). The 24 hours from yesterday to today were like sitting on death row, awaiting an answer. ALL NEGATIVE, including Diabetes.

Then I saw this site and had to enroll to tell this story. All of it was here from the THRUSH, which scared me the most, to the Depression and anxiety attacks, which made my fears really get out of control. The Advair had nearly destroyed my immune system.

I am taking "CLORIMAZOLE" for the fungus, which is no bargain...liver toxicity and nausea. Still, far preferable to the feared diseases.

I learned that so-called "modern medicine" is little advanced from the witch doctor. If you read the Pharmacology inserts, half the time they don't even know why something works, and they can't isolate the good effect from the bad. Then, they assault your body with another extreme ( anti-fungal ) to combat what they caused from the first medicine.

My new girlfriend is Chinese. Next time I am sick, I am trying alternative medicine. In the meantime, for anyone prescribed or handed a sample by their doctor, AVOID THIS MEDICATION IF YOU CAN!

I've been on Abilify for over a year...first 10mg. I'd take it in the am, get the kids to school, then sleep....but not sound....like a stoned sleep...in and out while I watched tv on the couch...I guess like in the 70's....doing acid or something lol. I couldn't function all day til it wore off in the afternoon when it was time to pick them up. Then down to 5mg. Oh, I'm taking it for migraines, but I'm borderline bipolar II. I don't get manic. I just get depressed. So this ability has taken away all I like to do. No more crocheting for cancer patients or for baby gifts, no more craft shows, no more aerobics......no energy......period. I don't laugh. I've lost all my personality. All for what? To get rid of migraines? Oh, it made me gain weight, too. And it worsened my acne. I'M 43! I take Topamax, too, so btwn what I learned about the side effects from that and this....I'm done! My snap at the kids attitude and the hair falling out and the acne and weight gain are too much for me.....better find some new meds for depression and migraines.......anticonvulsants are out for me. I hope you all have better luck than I did with Abilify.

I am a 56 y/o female who started on Fosamax last Sunday. I have a dx of osteopenia. I followed the directions of taking pill with full glass of water and remained upright for 30 minutes before having anything to eat. I was fine on Sunday but on Monday I woke with SEVERE bone pain! My whole rib cage, back, knees and heels were hurting so bad. It felt like I had pain in every bone in my body. I could not take in a full deap breath as my rib cage was hurting so bad. I could not bend or turn without terrible pain. My energy level was zero. I immediately called my doctor who told me to hold the Fosamax (ya think?) and ordered Vit D lab levels. Apparently when you Vit D levels are off (don't know if too high or too low) you can suffer this bone pain. I am awaiting the results. The pain is better today and I was told it takes 5 days to get out of your system. I only wish I had done my homework and found this site before taking this poison. I have to say I'm a registered nurse and know that ALL medications have side effects and everyone responds to meds differently. Some side effects subside as your body gets use to it and some can experience severe allergic reactions. But it's important to weigh the risk vs the benefit. I would rather deal with osteopenia in another way. So my search begins for alternatives to Fosamax for good bone health. Has anyone had good results with other supplements/meds?

My wife started taking Reglan last year one week before she committed suicide at the age of 57. She had never been diagnosed in her life as depressed, but obviously she was at the end. Two years previous she had a hysterectomy as part of treatment for uterin cancer. Five months previous to her suicide she got sick and after many weeks was diagnosed with acid reflux. She was given Nexium for this, but continued to suffer from the reflux. I believe somewhere in this time she became depressed though she continued to deny it right up to the day she took her own life. I really do not know if the Reglan or the Nexium was behind her suicide, but I believe it is quite possible. I should be mad as hell about this, but for now I just can not get beyond the grief. I am putting this out here just to say you may want to be very careful with Reglan!!!

My husband has been taking Omeprazole for about ten years now. About nine months ago he went in for a endoscopy and the doctor said she wanted to increase the omeprazole of 20mg 2xdaily because of the acid reflux. Several weeks after increasing this drug, my husband began getting very depressed. He losted all interest in our business and started having severe mood swings. He couldn't sleep at night, screaming with cramps in his legs, heart palpitations, blurred vision, ringing in ears, hot flashes, headaches behind the eyes. Some night I thought he was having a heart attack. It only got worse, hallucination began and horrible nightmares. He thought I was putting drugs and poison in his food. and felt like the world was against him. He became very violent toward me because of the hallucinations. We went for a follow up at his doctor and she suggested a psychiatry. Of course, my husband refused because he felt nothing was wrong, it was everyone else with the problem. His attacks got so bad, it was happen everyday, all day. We have two small children and we decided to split up for the children sake. My husband left for a week and when he left he refused to take the Omeprazole. He called me during that week and said he has felt great, he was able to sleep, no anxiety. He said to me if you are not putting drugs in my drink and food..it's got to be the omerprazole.
Of course the doctors said it's not possible...he has been off these pills for 8 days and it's unreal how this symptoms has disappeared. He is still having some side effects and withdraws. I don't know how long this will be in his system but I hope it goes away soon. THIS IS A DEVIL DRUG. He almost took his life and my too over OMEPRAZOLE. My doctor recently wrote this drug for me but I will not take it... We would never know about how serious this little pill for heartburn was if we didn't research it. When you get this drug from the pharmacy, they only list some side effects and not the serious one...How many more people out in the world is dealing with this same problem and not aware of these serious side effect. This almost destroyed our lives. WE NEED TO TAKE SOME KIND OF ACTION, SO THESE SERIOUS SIDE EFFECT HAVE TO BE LISTED..

Hello, I was on Yaz 5 months and I had a few muscle pains, nothing horrible. One day I started having SEVERE stomach pains. I went to the ER, then my fam doctor and he diagnosed me with gastritis. He put me on Nexium which wasn't helping. I couldn't eat anything beside eggs and bread. I was out of work a few days before I figured out certain foods were irritating it. I saw a Yahoo Answers post from a woman who said Yaz caused gastritis. I took it upon myself to stop taking them and in 2 days it was gone! Something that went on 2 weeks, severe pain and it was gone almost immediately after I quit this pill!(It says gastroenteritis on the side effects in the pamphlet). I was on other pills for 9 yrs and never had a problem except PMS! BTW my muscles were better in a week after stopping! I know it was this pill. When I first started it I read the side effects people were posting I was like yeah yeah it'll work itself out. NO, THIS WAS A BAD PILL FOR ME! I f you notice a gnawing and sharp stomach pain that's intermittent and you're on this pill, stop or it won't go away!

Our son started taking Singulair when he was 2 for severe allergic rhinitis and cough variant asthma (in addition to Zyrtec, which didn’t control all of his symptoms). He is 5 now. For the last three years, he has been an increasingly violent, difficult, defiant, argumentative, volatile child who has intense mood swings--one minute he’s laughing uncontrollably, the next he’s weeping over nothing. His doctor and therapist recommended that we see a psychiatrist to have him evaluated for bipolar disorder, which used to be unknown in children. Because he has such chronic sleep problems, the doctor also suggested we take him off Singulair (and increase his Zyrtec dose) to see if it improved his sleep issues. Within a week, he was sleeping much better and was a calmer, happier, gentler boy. He suddenly could take “no” for an answer without flipping out and trying to hurt me. We thought that we were just in an unusual, calm window that would shift either to mania or intense sadness or both, any minute. We also thought that his behavior change might be due to sleeping better. We were enjoying the rare reprieve. Over the last weekend, his springtime allergies really flared up. We gave him Singulair on Monday and by noon, he was completely out of control. I had to strap him into his car seat at one point to keep him from hurting either me or himself. It finally occurred to me that Singulair might be causing his “bipolar” disorder. Of course, we stopped the Singulair. After two days he was a new boy. Yesterday, I Googled “Singulair bipolar children” and got a few hits. I am stunned to read how similar other families’ experiences have been to ours and I feel sick that we gave this drug to our child for three years.

I am disheartened but not surprised that so many doctors are dismissing these reports of symptoms that patients have had after taking Singulair. The only reports that I have found to share with you are from Europe and Canada. All of these reports pre-date the recent news stories regarding Singulair and suicide.

In addition to those reports, the most important thing that I have posted is the reference to the fact that Merck itself recognizes that there are genetics differences among patients that are directly linked to the potential efficacy of Singulair (montelukast). I posted a British reports on that subject and a reference to Merck's clinical trial where they studied genetical differences and montelukast.

The best thing that we can do is to try to convince our doctors that this is not politics -- the major does not have to rule. Why do European countries publish frequent reports on all adverse drugs reactions not just those of the majority of the people? One size does not fit all.

The actual incident of headache in all users according to European reports is 18-19%. So when I read that headache, adverse drug reaction to a leukotriene receptor antagonist (Singulair) is then treated by ibuprofen (a Cox-2 inhibitor), which of course gets treated for stomach inflammation or GERD by Nexium or another drug-histamine receptor antagonist, then I wonder what the hell is left to inhibit? So if a patient does not fit the profile of the 80%, do we have to make that patient catatonic (meant figuratively)? I realize that this leaves out all of the receptors that aren't affected by any of these drugs but I am just trying to make a point.

So why does Merck list headache as just one of the side effects in a category of side effects just listed as greater than 1%? And why do so many people believe that there is no scientific proof of any of the complaints that we see here at this site?

On Prednisone for Asthma (have an infection) I have taken Prednisone before and the only side effect was increased appetite (which I could do with out as I am already overweight) this time however I have the worse heartburn I can literly feel my insides burning from the back of my throat down to the bottom of my stomach. I have also been experiencing increase sweating -fun wow. I feel bad for those of you who have to take this ongoing.

The drug insert for Doxycycline says to take the medicine with a full glass of water, and it warns not to lie down for a half hour after taking the drug. IT IS VERY IMPORTANT TO FOLLOW THE INSTRUCTIONS. Doxycycline, along with a number of other drugs, is quite corrosive.

I was on doxy for about a week when I woke up with the feeling of something caught in my throat. I had taken it with a full glass of water, but I had laid down immediately. I guess the pill had found its way back up to my throat. That night, I went to the hospital, did a barium swallow, and I eventually had an endoscopy to check out the damage. Thankfully it subsided after a couple weeks, but I had horrible pill-induced Esophagitis. I couldn't even drink water without pain and a feeling that I was choking. I didn't eat solids for 2 weeks, took double-dose Nexium, and I had to sleep SITTING UP because I also have silent acid-reflux, but when this happened, I could feel it intensely. I was lucky it wasn't perforated.

Anyway, lesson learned. Always follow the instructions. This can also happen with NSAIDs like Advil, btw.

I took 25 mg of Elavil for about a week for insomnia and chronic pain. It did nothing to help me sleeper relieve the pain and I started getting a horrible taste in my mouth, like spoiled food. It also made my reflux worse which I had under control with Nexium. I had to stop taking it because the horrible taste in my mouth was keeping me awake.

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 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?

My son was taking this medication for about a month and had horrible headaches after taking it. Felt like he was in a fog and vision problems, couldn't concentrate, had to quit driving and going to work. After many visits to the emergency room and many doctors. we found it had burned his stomach. Now he is on Nexium and it is amazing the difference. His headaches are maybe 80% gone. It seems that this medication is bad on the GI track. He took it with food but it just is hard on the body. If your symptoms stay have an endoscopy to see if it has done any harm to your GI track.

I was treated for gastric reflux last year and took Lansoprazole but experienced severe burning mouth,lips and throat after 2 weeks. Then I went on Omeprazole 10mg for two months which suited me altho did burn sometimes. Had an endoscopy diagnose of an inflamed esophagus who suggested a higher dose. Doctors changed me to Nexium 20mg and after a few days experienced that burning sensation again. Went off drug after two weeks as unbearable but experienced acid asthma type symptoms so returned to Omeprazole 10mg but after 4 days the burning is back again and finding it intolerant now. Anyone else experience burning mouth throat and lips whilst on the drug? Doctors say keep on it and take Galveston as well but how can it be reflux when I no longer suffer from heartburn?

I have been experiencing a flu like symptom for over a year now. They started about 2 months after I began taking 350mg of lamictal a day. Symptoms include exhaustion, headache, soar/achy throat, post-nasal drip, TONS of nausea, lack of digestion & regurgitation of food. I am tired and feel warn out all the time... I have had everything checked by doctors and they've found no health reasons to explain these symptom's.

HAS ANYONE ELSE EXPERIENCED THIS????

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.

Very bad rash that a week later has not gone away. Nexium actually burned my skin! I look like I have color like I just came from the beach. This is a dangerous drug. it works for the reflux, but the side effects arent worth it. I also develiped hip pain, like it was sucking the calcium out of the bone! The hip pain is gone, but i still have burning, itchy skin, and red all over, less than a week later after stopping, about 5 days off it now. Be careful if you are sensitive to hives, this medicine brought me to the emergency room with swollen hands and feet. it is dangerous!

I was prescribed Cipro for a bacterial infection... 4 days ago. Almost immediately I felt like my stomach turned to stone. Zero appetite. I feel like I can't get out of bed in the morning, with a feeling of morning sickness as if I were pregnant. I had nightmares, but I wasn't sure if it was this or a combination of Cipro and Lomotil.
I was also given Nexium to counteract the burning feeling from the Cipro. The combo made it worse, making my entire stomach and esophagus turn to steel.
It has to be the Cipro that is making me feel this way. It has been 13 hours since the last dose and I still feel like my stomach is full. I find it uncomfortable to even sit down, if I do, I must sit up straight. Or I must stand, but then my back hurts and I have to sit again.
I am, for the most part, a healthy 39 year old woman .. Had an antibiotic one year ago after being spurred by a rooster and before that, 7 years ago, for a sinus infection. Pills just aren't for me. Especially this one.

Thanks

Yasmin gave me IBS (Irritable Bowel Syndrom for those of you who don't know.) I was on the pill for eight months. My pre-symptoms were I had 5 yeast infections in a row, in the second and third months of taking it...this didn't ring any bells, even though I had never had a yeast infection before in my life, and my doctor just said I had a yeast imbalance. So a month after those stopped the IBS started. I was in the bathroom about 8 times a day, I thought maybe it was a flu, so i didn't go to the doc right away. I eventually gave up on that thought and went to see my doc, who even he, thought that it was IBS, so he sent me to a specialist right away. I had a colonoscopy and nothing, so the specialist told me that I needed to stop searching and just accept that I had IBS (I told him that I had been trying to figure it all out, because you literally don't wake up one day, go to the bathroom and your life changes forever, I KNEW something else was going on.) Anyways, I had a dumb specialist, he said that I had to accept this, I asked if it could possibly be my birth control and he said no and prescribed my a whole bunch of other drugs. Well I still just couldn't believe my life just all of a sudden changed, so I went to my family doc, lied, told him i was getting moody off Yasmin, and he switched me onto another. IT WORKED no more IBS, the results were immediate, it took a while for my poor damaged bowls to fix themselves, a few months actually, but now things are getting back to normal. Oh, and I've stopped birth control pills, back to condoms for me...my doc put me on Alesse, which didn't work either - moody! and then he put me on Marvelon, which inflamed my gallbladder (had to go for an ultrasound to see if i had gallstones) I figured at this rate, in two years i'd be dead from taking b/c so I was done, I would recommend the same to anyone!!

I just recently found this site and am very thankful I did. Has anyone ever even heard of someone being prescribed 1000mg oral prednisone for 7 days, followed by 500 mg oral prednisone for 7 days for a one day occurance of optic neuritis. It happened to my father and he died 3 weeks later. I would appreciate hearing from anyone who can help me make sense of this dosage.

I'm 46 yr old female and have been taking Singulair for 5-7yrs. I have been treated for Asthma for the last 10 years. I was treated at first with pulmacort until I figured out it was causing a break out around my mouth after several years (4) of being on it. My Dr. switched me to Singulair. I never noticed any of these side effects, until after I've read some of yours. I work out 5 days a week( swim & cardio) and have noticed my ears sometimes bother me. I'm on the computer all day, but my right hand has some tingling occasionally and sometimes it's a conscious effort to open and close my hands. I went to this web site to find out the long term effects of this drug. I had my blood pressure taken today and normally it's around 100/60-70 and today it was 100/80. I know that's not terribly high, but for me it is. I only take two drugs nexium and singulair and was wondering if one could be causing a rise in my blood pressure. If anyone knows please advise. Thanks Sylvia