Omeprazole :: Side Effects - Muscle Spasms And Pain?
Jan 12, 2009
Hi my name is Michele and i am wondering if there is anyone out there who has suffered as much as my grandmother...she has been in really bad shape here is what happened..My grandma was prescribed omeprazole back in July of 2008 for acid reflux...She seemed to be doing fine until the first part of december when she was getting muscle spasms so bad she could hardly walk and is still dealing with the muscle pain, pain in the middle of her chest and her right shoulder so bad that she has to stop what she is doing to catch her breath, this chest pain also came with a rash that was very itchy and dry between the breasts, she couldn't figure out what to do until it dawned on her that it must be these pills...she stopped taking them the beginning of december and is slowly getting better but is getting frustrated with the pain that she is still enduring...is there anyone who has hope for her who has taken this medication who had the same symptoms as her..we do not know what to do to make it easier!!
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I'm on my 12th week. I've been diagnosed before with GERD. Now due to the pregnancy, it seemed to worsen as I experience painful heartburns. My doctor recommends I take omeprazole along with antacids. I've been taking antacids because I know they don't bare side effects on pregnancy. I am not sure though with omeprazole. I'm scared. I am afraid it might harm the baby. Anyone here experienced the same?
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My husband has been taking omeprazole for the last few months. He has complained about dizziness and nausea and a heavy feeling in his chest for about 6 weeks. Last week he became very anxious about a 2 hour drive. He is usually a very confident person. Then last night he broke down when I said that he was slurring his words and becoming very forgetful.We read the side effects of the drug and he has stopped taking them. It may be psychological but he says he feels better already.
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For those of you who are just starting to take omeprazole, please stop and find other alternatives!!! I have endured so much agony from this medication since I first started taking it last year. You might feel better initially but if you take it for longer than 2 weeks, you will find it extremely difficult, if not impossible to get off of it because the rebound acid is a killer.
On top of that, I've experienced some horrible side effects (which I've never had before):
- exercise-induced tachycardia: extremely fast and uncontrollable heartbeat (over 200 bpm).
- heart palpitations and irregular heartbeat
- anxiety
- chest pains
- extreme fatigue
- depression
I am a healthy, physically active 34 yr old female and was prescribed omeprazole for a mild stomach irritation or suspected ulcer. I stayed on it for several months with few symptoms at the time. However, going off of it was another story. Because these pills stop your stomach from producing acid, it burns and hurts enormously when you try to go off of it. As well, after I managed to wean myself off (I had to go through a juice fast in order to do it), I started developing digestive issues I'd never had before like heartburn and reflux. I believe it is these pills which have caused it as I'd never had heartburn until taking it.
And now, having been on it a 2nd time, I've developed the list of symptoms above which have caused me endless grief!
I've read other stories of people having the same symptoms as well as a host of other problems like osteoporosis because it drains your body of calcium.
More people need to know about the dangers of this medication. I read about people staying on this for years and developing even more conditions!
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Are there any side effect of taking vitamins(e.g. vitamin D+calcium) for long time as 3 months or more.
Does "Omeprazole 20mg" cause any harmful effect in long term use ?
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I have a friend who has been taking oxycodone 5/325 3 a day for about 2 years without issues for severe back pain.
Recently he has had a big problem with muscle strength/weakness exercise intolerance and fatigue. He has been to physical therapy with no improvement.
Could this be from using the medication for so long, has anyone experienced such a thing.
He has been tested for MS,ALS and is now seeing a Neuromuscular specialists.
Any thoughts would be appreciated
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I know that it's known that lipitor has the side-effect of muscle tiredness and aches. Has anyone else have to deal with this? Man it's off the hook. I almost am paralyzed fro, lipitor. This horrible and I would like to talk to someone who's been through it. This is a very under-rated affliction IMO. I've been tested and it doesn't look like I have the Rabadolosis<sp? That spelling isn't even close. I was very scared before I realized what was causing this severe problem.. Now I know that lipitor has helped a lot of people, it brought my cholesterol down a bunch very quickly. Frankly i would rather have high cholesterol. I did have a stroke at the end of November, small, deep in the cerebellum. Hence the lipitor.
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After seeing my GP and a specialist about ED, they've prescribed me 5mg cialis to take every day. I'm on day 3 and i'm getting side-effects, flushing (warm feeling in the face), muscle aches and also feeling fatigued and drowsy.
Has anyone else here taken it daily? do the side effects wear off or is this what I should expect now? if they wear off, i can tough it out - but if this is just how-im-going-to-feel-now.
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i have been taken ezetrol for a long time now and have complained about muscle pains especially in my legs and as a runner it has restricted the amount of exercise i can do. I have had blood test and the enzymes seem to be ok. I have stopped taking them and the symptoms get better and i can run for longer but have restarted taking them. Also i have been told and am in the process of trying it out that the most effective amount to take is the first 10-20 mg after that the reduction is very limited and is not worth taking any higher dose. I was on 40mg and level was 4.6 am now on 20mg and level is 4.9 but the side effects have got slightly better. Overall i feel that these drugs have had a detrimental effect on my fitness
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2wks ago, I had a very large herniation removed and I did great the first week, but I think that I am now having muscle spasms. I see my doctor for my first post op visit this week. I have been in a back brace since the surgery and only take it off to sleep (am a side sleeper). This week, I think that I have been having spasms at night. I know that it's not nerve pain b/c I know what that feels like. It feels like a tightening and ache and is scaring me b/c it's in my back and leg, where I had the previous nerve pain. Are these spasms? I have not slept all night. I got up and walked around, but I don't know if I should be walking while in pain. I do have Valium, which was giving to me as a muscle relaxer upon release from hospital, but am getting no relief. Is this common and are there any tips?
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My mom (40-50yrs) has had MS for about 13 years now. She has had muscle spasms for a while now, but medication would usually help. I know infections, colds, and any other types of illnesses will make them flare up, but lately the muscle spasms don't stop with the meds. They have gotten so bad that her knees get sprained, from time to time. The doctors push for baclofen but she took that for 8 years and doesn't help her anymore. She is currently taking tiZANidine which helped for the last couple of years but no longer. At the emergency room they have also given her volume and tried morphine but they don't help either. Anybody Using something for severe muscle spasms or have some routine or method of getting rid of them that might help?
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For the past week, I've had a headache. It started out with being one of the worst headaches ever. I've been dizzy and lightheaded with ears ringing for the past week and a constant headache that varies in pain. Yesterday, I found my occipital node is swollen and if I push anywhere on it or on the left side of my head, I feel pressure and it hurts in my face all through the left side of my face and in my eye. I've been having awful muscle spasms in my neck and body, and now there is a constant dull pain still in the left side of my head that will not go away. I hear cracking and popping in my head often since it started too. Please help! This is killing me. What could it be? The headaches get to almost unbearable and sometimes it's just a dull agitation.
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I started last week noticing shooting leg and butt pain went to Chiropractor and seemed fine.
Then about 2 days ago went into bad wicked leg cramp(left side of body)and very bad stabbing back pain .
went to dr who says it's pinched she has me on cyclobenzaprine aka Flexeril hcl 10 mg 2 per day I took it at 4pm and Tramadol hcl 50i took at 6pm mg every 6 hrs have done that today plus bath/heat pad , icy hot spray, mineral ice and cold ice pack, everything I've done seems to make it worst or just not help . The heat and cold treatments seem to make it worst and aggravate the pain into cramp like symptoms
Wondering how normal that is have tossed out back before and muscle relaxers put me to sleep and make it go away this isn't even helping. I find laying painful standing walking are near in possible and extremely painful to the point it makes me want to cry literately like a throbbing stabbing pain ,sitting seems to be better then laying but not buy much.
unsure how to describe this part but when walking what little bit I do back has a odd pop sensation and leg and back starts to spasm to the point i can't put weight on leg or move.
Wondering if anyone has any home treatments or advice.
As i find this can't be normal after that many pills to feel still worse then when I went to the doctor. i'm in central time so pills are still hrs away from me taking more
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I have joint pain and my doctor prescribed me Cataflam. I know that Cataflam is strong medicine and I am not sure should I take it. I want to know more, also, about Cataflam side effects. My friend told me that Cataflam is strong and dangerous medicine. Is she right?
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Hi everyone! I know that kidney stones are terribly painful and that there are various unpleasant treatments to get rid them. In other words, kidney stones are not something you would aim to acquire :-). But, my question is, other pain, what are the consequences of kidney stones? Are there any side effects?
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Would like to ask about anybody's experiences of side effects of Atorvastatin (as oppose to Simvastatin) I think the latter is mostly prescribed because of it's low cost - the one I am on is rather more "up-market" and I particularly requested to change from Simvastatin, and was "lucky" because it is far more expensive and considered the better drug of the two. However, like so many of your experiences on this forum - I can relate to almost all of them. I am breathless to the extent where I have to sit on a kitchen stool to carve a joint or dish up a meal I have leg pains, back pains and every other B***** pain!
I also suffer with anxiety disorder which the side effects of statins do nothing for that!
Please let me know if any other patients have problems with these ghastly drugs - I have stopped mine now and will tell the Doc when I go next week! I have missed about a week's worth of pills, but have not yet noticed any difference! Does anybody know how long it takes for the drug to leave your system?
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I have a question about possible side effects of allergy shots. I got 4 shots so far (shot per week). On the first 3 there were no side effects besides feeling a bit tired on the evening of the shot probably due to the antihistamines medication that i am taking before receiving the shot, but in the morning after getting my 4th shot I woke up with very strong pain in the heart area (this is roughly 16 hours after the receiving the shot), the pain slowly went away in the course of several hours. I went to a doctor and did echocardiogram on the same day which was OK. I am not in a stressed period or did anything special during the week.
I am 36 years old, healthy, exercise regularly and have no heart troubles.
My question is if this heart pain can be related to the allergy shots or it is just a coincidence ?
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Took Binosto (similar to Fosamax) for a few months beginning this past December. Was feeling well at that time. Since then, began experiencing terrible lower back pain, gas, lower left ab pain and have had a cough for a few weeks. I think that sums it up. Went to my doctor and told her everything. She checked me out. We decided to stop the Binosto thinking it could be causing these symptoms (don't know about the cough, though). She said to give it two weeks to get out of my system. It's been two weeks now and I still feel like crap! Could it take longer than two weeks to feel better? Maybe a month? Two? Do you think it could be the Binosto? I was feeling fine before starting it!
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I have had a lumbar L5S1 mico on feb 14 of this year. Now I am having sharp pain in my back under my right shoulder blade by the T7. Plus this makes my back tighten up and spasm. Any thoughts out there. I know it has to do with the injury but does anyone know what this is... btw not the gallbladder I don't have one anymore. This pain is at its worst when I am lying down and if I rotate to the right side the pain will be so sharp it stops me in my tracks...any help would be great. I also got my S! nerve checked and it is relieved from the surgery but I am left with the numbness in the foot, calf, and upper thigh and also told this might be permanent.
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From the age of 8-14 i was seen at hospital for Scoliosis for years i would have x rays and check ups, since then nothing? confused! because i was young i only know that i have a lower curve of my spine (sorry don't know technical words).
More recently i complained of lower back pain which my doctor agreed and gave me co codamol as nothing i was taking worked. I am also currently waiting for a physio appointment as my dr said that it may help? not sure but i will try it, however that has been 3 weeks and i still have heard nothing!
Since complaining of lower back pain though i am now having more problems, the spasms are becoming more frequent and shooting up my back and making me gasp when they are bad, these are slowly getting worse. Again i spoke with my doctor and he didn't seem concerned, i however am.
I am working and it is a desk job but i can walk around and split the length of sitting down. Also a hot water bottle does help when i am at home at work is slightly more difficult. I currently have to sleep with a pillow under my back so i am more comfortable. I am also sleeping separately from my hubby as his mattress is way too soft for me to sleep on.
This is driving me mad and i just need the pain to stop. Can anyone offer advice please?
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I came across this syndrome when searching the Internet about extreme pain I have when I take the first bite EVERY time I eat and sometimes drink. That this could be a symptom of this syndrome but I don't know. I do have some of the other symptoms, i.e. neuropathy, blurry vision, muscle pain, fatigue but these can also be associated with Type 1 Diabetes which I have. Also, came across parotid/salivary glands are affected which also can cause the jaw to ear pain I'm having. Has anyone heard that the Coxsackie virus can have anything to do with it? How do you know for sure if it is Sjogren's and what type of doctor do you see about it - a primary?
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