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Review: could Ms contin cause Sleep - too much (Sleep Disorder)?

Summary: Sleep - too much is found among people who take Ms contin, especially for people who are male, 60+ old, have been taking the drug for 1 - 2 years, also take medication Oxycontin, and have Pain.

We study 8,076 people who have side effects while taking Ms contin from FDA and social media. Among them, 92 have Sleep - too much. Find out below who they are, when they have Sleep - too much and more.

You are not alone: join a mobile support group for people who take Ms contin and have Sleep - too much >>>

 

 

 

 

Ms contin

Ms contin has active ingredients of morphine sulfate. It is often used in pain. (latest outcomes from 8,255 Ms contin users)

Sleep - too much

Sleep - too much has been reported by people with depression, quit smoking, osteoporosis, pain, high blood pressure. (latest reports from 39,945 Sleep - too much patients)

On Jan, 26, 2015: 8,076 people reported to have side effects when taking Ms contin. Among them, 92 people (1.14%) have Sleep - Too Much.

Trend of Sleep - too much in Ms contin reports

Time on Ms contin when people have Sleep - too much * :

< 1 month1 - 6 months6 - 12 months1 - 2 years2 - 5 years5 - 10 years10+ years
Sleep - too much0.00%12.50%0.00%75.00%12.50%0.00%0.00%

Gender of people who have Sleep - too much when taking Ms contin * :

FemaleMale
Sleep - too much46.94%53.06%

Age of people who have Sleep - too much when taking Ms contin * :

0-12-910-1920-2930-3940-4950-5960+
Sleep - too much0.00%0.00%0.00%6.45%3.23%27.96%18.28%44.09%

Severity of Sleep - too much when taking Ms contin ** :

n/a

How people recovered from Sleep - too much ** :

n/a

Top conditions involved for these people * :

  1. Pain (62 people, 67.39%)
  2. Multiple myeloma (39 people, 42.39%)
  3. Migraine (13 people, 14.13%)
  4. Neoplasm malignant (12 people, 13.04%)
  5. Breast cancer (12 people, 13.04%)

Top co-used drugs for these people * :

  1. Oxycontin (57 people, 61.96%)
  2. Aredia (52 people, 56.52%)
  3. Zometa (52 people, 56.52%)
  4. Zoloft (49 people, 53.26%)
  5. Neurontin (47 people, 51.09%)

* Approximation only. Some reports may have incomplete information.

** Reports from social media are used.

How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.

Do you have Sleep - Too Much while taking Ms Contin?

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Drugs in real world that are associated with:

Could your condition cause:

Can you answer these questions (Ask a question):

  • 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.
  • I take klonopin and diltiazem (calcium channel blocker blood pressure medicine) and am concerned about side effects. my accupuncturist recommends the ashwagandha. anyone have any issues with this?
    I take these prescription medications but have been going to an accupuncturist since 2012. I have trouble sleeping at night without my clonazepam and take naps during the day and am having trouble losing weight. She thinks that my adrenal glands may be fatigued and told me to try something called Adrenal Response which contains Sensoril Ashwagandha. When I looked up Ashwaganda it said that it could interact with the Clonazepam or Klonopin and also with High blood pressure medication. I am a little concerned. I mentioned this to her and she said they both are metabolized by the liver and it should be ok to take it, just to take it an hour or more after I take the Clonazepam. Has anyone had any issues with interactions with their prescribed meds while taking Ashwagandha? I don't want to have to monitor my blood pressure because my blood pressure medication works good for me. Any help would be appreciated because I want to try it but I am a little scared too. Thanks, Crystal
  • Is osteoarthrisis caused by drinking alcohol
    Chronic pain in spine, right hip, right hand, swollen joints in both hands, swollen knees.
  • Is vomiting all liquids common while taking morphine (1 answer)
    I Recently started taking 6mg of Hydro-Morphine per day for pain. Every time i take the drug i vomit up any liquids I drink. i fell just fine without anything in my stomach but as soon as i eat or drink I instantly become nauseated and vomit everything. It is hard not to drink because the drug is making me very thirsty. So i try to drink and my body rejects it over and over again.. this goes on for hours (3-5)because i am sooo thirsty that I can not stop drinking.
  • Can mrsa cause chronic intestinal pseudo obstruction?
    I had a small bowel obstruction caused by adhesions from an appendectomy carried out 20yrs previously and had grumbling pain ever since but been labelled a malingerer by my family GP until one day at work when I started with terrible tummy ache and sickness like I'd never known, fetching up bile with force. I hated going to hospital after yrs of being called a moaner but after a day of rolling round in pain, temperature of 103 an dehydration, my Mammy insisted we go and I was seen straight away - to my shock I was in theatre within 3hrs with a serious obstruction.
    I never really recovered... The obstruction returned after 2 days and a portion of necrotic bowel was removed, then further fever and cellulitis then MRSA and deaths door.... Isolation in high dependency (intensive care) wound break down, ventilated and all related issues that come with that - chest infection, pneumonia, bed sores. Total time in hospital 8 months. Negative pressure dressing on laparotomy wound, colostomy, picc, 4 rounds of vancomycin, minor flirt with heart failure (just water related) an eventually everything healed. Had a large incisional hernia to repair and some corrective work to the horrific scarring but then the neuropathy started plus problems eating, spewing up after any solid food, more than a few forks, diarrhoea and sickness or constipation nausea and pain driving me mad, tried all manner of drugs, nerve blocks, physio, floating tank, acupuncture, opiates, non opiates, spinal cord stimulation, an now a consultant just had a 'eureka' moment and said were you treated with vancomycin when you had MRSA? If so I'm pretty sure you have chronic intestinal pseudo obstruction and is 90% sure but wants to take a muscle biopsy to be certain. I've had so much surgery and bad news in the last 10yrs I'm terrified of germs, hospital acquired bugs and anaesthetics, is there any other way? Or can I have this test done awake - conscious sedation? I had it before during spinal cord surgery so I know what's involved and it's better than GA as I know what's going on, who is doing what to me etc...
    Does anyone with a medical background know about this ailment/disease? Does it sound feasible that MRSA or it's treatment could have caused this? I was surgically debrided up to every other day when the vac pac/negative pressure machine and dressings were changed and the doctors told me I lost a great deal of tissue and had a lot of nerve damage due to the infection.
    Any patient perspectives on this illness would also be very much valued in helping me make a decision, moving forward. If all this is going to accomplish is to attach a label to the pain but not actually change anything, after fighting it for 10yrs now, avoiding hospital as much as I can, I really can't see the point of exploratory surgerys and biopsys now when it is known that I have this propensity towards adhesions and a new wound means a potentially new adhesion growth site.
    If it helps, the appendectomy happened when I was 10yrs old, the MRSA when I was 30 and I am now 40.
    Beat Wishes.

More questions for: Ms contin, Sleep - too much

You may be interested at these reviews (Write a review):

  • 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.

    Good luck.
    Glenn.
  • Had nms in 2005, will trileptal increase chance of recurrence?
    In 2005 I had NMS, which was not detected by my drs for 4 months. I'd been on Lexapro & Seroquel for 2 yrs, but was weaned from Lexapro & placed on Lamictal 3/05. Began getting low-grade fevers, which I was told were not caused by the Lamictal. I quit taking it anyway, fevers (along with uncontrollable shivering) continued & got higher. By 5/05 my temps were reaching 105 deg F. Husband said I became combative, refused to go to hospital. Early June/05 he came home to find me wrapped in blankets, with a temp over 105 F. He tried to place me in a tub of cold water, said I was rigid & screamed when he tried to move me. I was in the tub, speaking "in tongues" (his description, I have no memory of this). He called 911, took me to hospital. I woke, no idea where I was or why. After a lumbar puncture & 2 days in ICU I went home. The fevers continued...2 weeks later he came home to find me wrapped in sheets, towels, blankets, with the heat on full (it was in the 90's outside) he called ambulance again. I awoke to find myself under an ice blanket with nurses pushing large vials of dantrolene into both arms, several liters. Another LP, a stint in ICU...this time they told me it was NMS. The dr who dxd me said he was surprised I was alive, & not a vegetable, as my temp had peaked at 109 deg F. I suffered brain damage; short-term memory loss, brain can't control my body temp, my blood pressure went up. An arteriogram showed completely healthy heart & arteries, no plaque at all. I lost all body fat as well as some muscle mass. The fevers continued even after stopping the Seroquel. I visited my PCP for a checkup in 9/05, temp was normal. I started shuddering, my temp went up a full degree every 5 minutes. PCP admitted me to ER, my heart rate was over 272 B/M; they stopped my heart 3 times to "reset" it, which didn't work. I spent 3 days in hospital. Several months later my P doc tried me on Lamictal alone; I got Stevens-Johnson syndrome. I stopped the drug as soon as the signs appeared. I've been untreated, except for Neurontin & Primidone, until my manic episodes became unlivable. 3 weeks ago I went 8 days with no sleep, became psychotic. My P doc gave me Trileptal, which has evened my moods, but I've been getting low-grade fevers (highest was 103.6). Would having had NMS in the past make me more prone to falling to it again with the Trileptal? It's the only new med I've taken in over a year.
  • Androgel for secondary hypogonadism
    Severe swelling in legs, ankles and feet after being on my feet for more than one hour. Pain in calves and ankles. Feels like they're being squeezed or compressed. Pain dissipates after laying down for a few hours. Swelling never completely dissipates. Always some swelling in ankles.
  • Melatonin and diarrhea
    I have had difficulty sleeping most of my life. Difficulty going to sleep and waking up multiple times during the night were a usual pattern for me. Testing for sleep apnea did not show a positive result. A friend said to try Melatonin that for him it worked fine. I tried it and the diarrhea started almost immediately. Within days it was full blown water diarrhea. For fear of dehydration I stopped using Melatonin before two weeks time. And the hoped for results of helping my sleep problems were not solved with the Melatonin.
  • Michael my son died as a result of kolopin & ambien (6 responses)
    My beautiful son to whom I depended upon took his Life by suicide on July 16, 2013. He had been struggling with a sleep disorder. It seemed to begin in his last year of high school 2010. Mike was very strong in mind and in body. He became a certified personal trainer. He encouraged everyone around him and all of his clients. How can someone so strong be so weak?
    He had been heavily medicated by a sleep doctor, for years this doctor gave him different medicines and he began to show other heath impairments..I could not see so many things that are very clear to me now, I never saw the effect the drugs had on him. he was growing more tired and withdrawn. He knew so much about medicines that I thought he knew what was happening he and I both trusted the doctors. With each new problem that occurred there was always a new drug to try and along with it a new set of side effects. A new doctor was added to his care and this doctor right away gave an RX for Kolopin. He was already taking Ambien and the two dont seem to play well together. Mean while he was growing sicker and sicker. We constantly were going for this test or that test, never once did the sleep doctor ever think that the drugs being given were the cause of all of his distress.
    At one point he was unable to keep food down and was throwing up every day. More test that always revealed the same result. No problem found. The visits to the sleep doctor were the same as well his condition was worsening and chronic. and yet never once did the sleep doctor ever give the drugs a second thought. The known side effects for both of these drugs were suicide for ages between 16 to 22. Until his death I never read about any of the products he was on.
    On July 16, 2013 the day began with Mike not sleeping, he seemed angry, exhausted. he was getting ready to help us out at our office. Once there it seemed like nothing went his way and at one point got into argument with his dad, told me he hated him and decided to go into his office to talk to him. He began to cry, I had to leave for an appointment and I waved to him through a window. I could see him crying. He got up and just left our office. Later we would find that he called his pastor, his cousins and a friend all did not reply. One girl friend of his did, she told him to meet her for drinks he told her what happened and he needed to save money and needed to be at his training job shortly. Within a 15 minute span wrote us a suicide letter, drove off and shot himself. a few minutes after he did a passer bye called 911. They took him to the hospital. The police came to our office to inform us we need to get to the hospital. The shock of all shock.... He passed away 1:04 am on the 17 of July. I never thought I could be so lost and broken as I am. I miss you so much Michael!

More reviews for: Ms contin, Sleep - too much

Comments from related studies:

  • From this study (1 year ago):

  • want to find out of all my pain is a condition as well as my promary condition of back surgery and back pain

    Reply

  • From this study (6 years ago):

  • I just added Morphine Sulphate ER to list of other medications and just want to know possible interaction effects

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