Review: could Ms contin cause Heartburn (Gastroesophageal reflux disease)?
Summary: Heartburn is found among people who take Ms contin, especially for people who are female, 40-49 old, have been taking the drug for 5 - 10 years, also take medication Percocet, and have Muscle spasms.
We study 8,078 people who have side effects while taking Ms contin from FDA and social media. Among them, 12 have Heartburn. Find out below who they are, when they have Heartburn and more.
You are not alone: join a mobile support group for people who take Ms contin and have Heartburn >>>
Ms contin has active ingredients of morphine sulfate. It is often used in pain. (latest outcomes from 8,257 Ms contin users)
Heartburn (a condition in which stomach contents leak backward from the stomach into the oesophagus) has been reported by people with high blood pressure, depression, osteoporosis, pain, high blood cholesterol. (latest reports from 19,134 Heartburn patients)
On Feb, 12, 2015: 8,078 people reported to have side effects when taking Ms contin. Among them, 12 people (0.15%) have Heartburn.
Time on Ms contin when people have Heartburn * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
Gender of people who have Heartburn when taking Ms contin * :
Age of people who have Heartburn when taking Ms contin * :
Severity of Heartburn when taking Ms contin ** :
|least||moderate||severe||most severe |
How people recovered from Heartburn ** :
Top conditions involved for these people * :
- Muscle spasms (3 people, 25.00%)
- Anxiety (3 people, 25.00%)
- Stress (3 people, 25.00%)
- Neuralgia (3 people, 25.00%)
- Diabetes mellitus non-insulin-dependent (1 people, 8.33%)
Top co-used drugs for these people * :
- Percocet (5 people, 41.67%)
- Lactulose (4 people, 33.33%)
- Prilosec (4 people, 33.33%)
- Promethazine (4 people, 33.33%)
- Diazepam (4 people, 33.33%)
* Approximation only. Some reports may have incomplete information.
** Reports from social media are used.
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Do you have Heartburn while taking Ms Contin?
You are not alone! Join a mobile support group:
- support group for people who take Ms contin and have Heartburn
- support group for people who take Ms contin
- support group for people who have Heartburn
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- Can i take zantac with 20mg of rivaroxaban?
I was wondering if anybody could help me on this i'm currently taking Rivaroxaban Zantac with Rivaroxaban(20mg)(Daily)to treat DVT.
The thing is whilst doing this i'm suffering greatly with Heartburn, Acid Reflux.
Can i take the Zantac to soothe my pain with Rivaroxaban?
- Side effects of cimetidine(tagamet)? should i worry?
Hello, I'm 17 years old, I have taken Tri-nessa(Birth control) since January of last year(2014) with no side effects.
I've been having an Acid Reflux problem for a few years(Since I got my Gallbladder removed in 2011). It got really bad by the end of last year (2014) and I've been having multiple problems since Urgent Care diagnosed me with Gastritis. I then assumed I had heart problems due to a lot of issues/deaths with other people and their hearts. Got an EKG, it came out fine. Now, for Gastritis, they put me on Protonix, I was taking it up until this past Wednesday when my Doctor put me on Cimetidine(Tagamet), she also gave me info to go see a GI doctor. Thursday afternoon (Around 1:50-2:50)I had gotten really dizzy like my blood sugar dropped immensely. Ate some candy in hopes to make it better, didn't help (My family has a history of Diabetes). I begged my school to rush me to the ER, but they didn't see anything physically wrong with me, therefore, they said no.
And so, I went home with my friend and relaxed. Since then, I've been having these 'Tension headaches' that start in my left sided neck and travel up into my head(It switches sides sometimes, or just wraps all around and into the back) for about 3 to 5 hours putting a really hard pressure on my head like someone is crushing it under a wheel, sometimes it feels like I'm being jabbed with a small needle in random spots too. I tried taking Ibuprofen to remove some pressure of the headache, but to no avail. Friday, I went into the ER. They did bloodwork, took a urine sample, did a chest x-ray, and did three EKGs on me. They didn't find much else but a teeny hiccup in my EKG - nothing to panic about - they said, but if I want to feel comforted that my heart is fine, I can see a cardiologist (Going to see one tomorrow). Saturday, I started noticing a swelling over my left breast, next to my armpit. It, and my breasts, have little pains that surge through them every now and again. I also noticed that around my throat to my collarbone, on my chest (left & right), over my shoulder and to my back neck has started to burn and ache as well. The aching will send pains down my spine and make doing anything seem annoying. ON TOP of that, I've been having random coughs, sometimes my face has pressure on it, and Sunday morning I couldn't stop sweating in my sleep. I suspect I slept the wrong way on my neck and the nerves are causing the pain in my chest area, or my acid reflux is causing severe heartburn.
My big question is, should I go back into the ER and have them test my breasts and neck/spine, or should I kick back and relax in knowing it's just a few side effects from my Cimetidine and a little ache in my neck from sleeping wrong that will go away shortly? (I read it can cause tenderness in the breasts, usually for guys, but maybe girls too?)
My family doesn't have much money, and my father thinks I'm being a hypochondriac, but I know I have a lot to live for so I'm praying it's really just nothing.
- Does morphine cause mouth ulcerations
one month after beginning the drug morphine I developed mouth ulcerations on my mouth palate. My mouth and face has developed soreness and painful pressure.
More questions for: Ms contin, Heartburn
You may be interested at these reviews (Write a review):
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For over ten years I have been taking high doses of morphine for chronic pain nerve pain. At one point I was taking 400mg of morphine a day. By splitting up the doses I was able to get it down to 300mg a day. My periods stopped almost immediately, even when i was still taking small doses before I was even raised to 100+ mg a day.
Now I am taking (using) Fentanyl #75 patches plus Fentanyl #12 patches and they work great with no up-n-down from pills wearing off. I have been off morphine and using Fentanyl for almost one year now. I still don't get my period, though. They stopped when I was 43 and I don't miss them at all!! But when I read that there was no link between morphine and Amenorrhea I had to tell my tale...
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Prescribed to take 2 - 300 mg tablets of Clindamycin prior to dental procedure to to knee implant done a month and half before dental procedure. Took two pills one hour prior and immediate severe burning of throat, esophagous and stomach with constant nausea. Still have symptons - ie loss of voice, low grade nausea. have had multitude of tests - ie. EGD's, monometry, transesophageal (with transmitter to determine extent of now reflux) Have to eat small amounts of food at a time. Have lost 23 lbs. Affects my every day life - difficult to talk on phone, talking in groups - just limit my socialization. Could not work if I wanted to with voice. Throat is constantly sore.
- Prostatitis and prostate cancer acceleration due to anaesthetics
Caught Chlamydia in 1978. Interestingly, the partnered girl's sister worked in an aviary; and I found out later that Chlamydia originates from handling birdshit and birds are the carriers. Chlamydia was undiagnosed at the time, so it was listed under 'Non-specific urethritis'. Chlamydia wasn't named until about 8 years later. I was given tetracycline and told to stay off alcohol and sex. Yeah, really?
I was 24; highly sexed, and in night clubs and pubs most nights. I laid off the alcohol and after two weeks, I was good. The laying off sex, I understood, because of contamination of others (condoms were little used in 1978 in the singles arena); so I masturbated one night... and that caused me immense in my prostate, and pain and suffering for the rest of my life.
The ejaculation was extremely painful, and chronic prostatitis started. I was on and off medication for two years. I got light-sensitivity, which means in sunlight, I came out in burning rashes. I became allergic to tetracycline.
The message? Consultants are generally poor at communicating what not to do, and why not. Lay off sex he said. All he had to say was no sex, no masturbation; or you may suffer for the rest of your life. That would have done it.
No-one has been able to help me with this chronic prostatitis. In the early years it would come and go, but as the years have gone on, it has become more frequent, and now it is constant.
Four years ago I went in for major foot surgery, and flat-lined. I was in intensive care for 2 days, on a morphine drip for the pain.
When I awoke, I knew immediately I was suffering with my prostate. It was aching badly and I was urinating frequently. The nurses were amazed with how many 'bottles' I filled in such a short time.
For the next few months, I was in agony. I have tried every possible drug going, as well as prostate massage and the indignancy of a urethragram whilst female students were watching.
In November 2011 I went to see another consultant, who suggested a biopsy. I was diagnosed with prostate cancer. After much research, I now know that my diet and lifestyle, coupled with inflammation of the prostate with prostatitis, has caused prostate cancer. Yes, there is a direct relationship between prostatitis and prostate cancer.
I am now beating it, without drugs and without surgery. I have changed my diet to a vegan diet, no sugar, very little alcohol, and a lot of supplementation.
In December 2013, I went in for more foot surgery. I was unaware about the morphine at this time, so didn't consider it being a problem. I talk to the anaesthetist, who wanted me to have an epidural (injection in the spine to numb my lower body). At no point did he talk to me about my prostate history.
In recovery, I sensed a problem as soon as the anaesthetic began to wear off. It was like my prostate and testicles wanted to explode. I knew I was going to have problems. My intuition reminded me of three years ago with the morphine, so I asked the surgeon if he knew of these complications with morphine, but he didn't.
I spoke to the head of the post-operative ward and asked her if she had any experience of post-operative patients who suffered with prostatitis after surgery, and she confirmed she had. So here was a nurse who knew of the problems, but the surgeon and anaesthetist didn't. This is typical in the health service... the lack of sharing.
Not only did I suffer with the chronic prostatitis (and still am 11 month later) I was incontinent. It took 6 months of 4-times daily legal exercises to get back control of my bladder.
For me, morphine has a dire effect on my prostate.
Bear in mind that your prostate is designed to eliminate toxins, so it is flooded with morphine. I will do my best to ensure I check for morphine in any drugs or anaesthetics in future.
My first PSA level was 18, 3 ears ago. I brought it down to 13.5, then 10.4, 10.3, 10.9, 11.3, 14.3 and after the last surgery it spiked at 17.5. As a result, I have gone back to a stricter, greener raw diet to bring it down again.
Oh, and anther tip; you need to get your vitamin D3 blood count above 200n/mols (UK measure) to have any chance of not getting prostate cancer. Mine was 32 when I was diagnosed. Today it is over 200, from supplementation of 10000 ius a day. Minimum in the UK, recommended by scientists, is 75n/mols, and it's too low. OK if you have a great immune system, but not if you want to fight prostate cancer and prostatitis.
Black African males in the Northern US states and in Europe have twice as much risk, due to lack of sunlight. Sunlight on skin promotes vitamin D3, which is essential for the immune system and production of calcium.
Black African males need more sunlight to produce the same amount of vitamin D3 as a caucasian male. Also, any male who is bald and fat has a higher risk, so a Black African, obese bald male, has an extremely high risk of prostate cancer, unless they get their immune system in order.
The main way to fight all this, is on a clean, raw vegetable diet, pure water, no alcohol, sugar, processed or refined food, no meat, no dairy, no vegetable oil, no exceptions, and some breath-taking regular exercise. Just like we did 100 years ago. Go figure! Look at chronic disease studies of 100 years ago. 85% of all disease was from infection. Today 85% is from chronic disease.
Your prostate eliminates toxins, and today, we are overloading it. Remove the toxins (and the stress and anxiety) and things will improve. It's a hard road; but with it is you want to be healthier and live longer.
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More reviews for: Ms contin, Heartburn
Comments from related studies:
From this study (2 days ago):
had ptc /ih for 12 years. pyoderma onset dec 3rd 2014. horrible. over 65 blisters, bumps, papules, pustules, nodules all on my face. Had new derm accuse me of doing it deliberately to my face. horrific.
From this study (3 days ago):
No rapid heartbeat only chest pain all heart tests show no heart disease. After stopping aspirin developed burn in throat and indigestion.blood pressure always low.
From this study (4 days ago):
coolaero on Feb, 7, 2015:
there wont be side effect other that DEATH
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