Review: could Morphine sulfate cause Insomnia?
Summary: Insomnia is found among people who take Morphine sulfate, especially for people who are female, 60+ old, have been taking the drug for < 1 month, also take medication Oxycontin, and have Pain.
We study 18,488 people who have side effects while taking Morphine sulfate from FDA and social media. Among them, 456 have Insomnia. Find out below who they are, when they have Insomnia and more.
You are not alone: join a mobile support group for people who take Morphine sulfate and have Insomnia >>>
Morphine sulfate has active ingredients of morphine sulfate. It is often used in pain. (latest outcomes from 19,049 Morphine sulfate users)
Insomnia (sleeplessness) has been reported by people with depression, quit smoking, pain, high blood pressure, stress and anxiety. (latest reports from 143,724 Insomnia patients)
On Jan, 29, 2015: 18,488 people reported to have side effects when taking Morphine sulfate. Among them, 456 people (2.47%) have Insomnia.
Time on Morphine sulfate when people have Insomnia * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
Gender of people who have Insomnia when taking Morphine sulfate * :
Age of people who have Insomnia when taking Morphine sulfate * :
Severity of Insomnia when taking Morphine sulfate ** :
|least||moderate||severe||most severe |
How people recovered from Insomnia ** :
|while on the drug||after off the drug||not yet |
Top conditions involved for these people * :
- Pain (199 people, 43.64%)
- Multiple myeloma (45 people, 9.87%)
- Insomnia (42 people, 9.21%)
- Hypertension (38 people, 8.33%)
- Anxiety (37 people, 8.11%)
Top co-used drugs for these people * :
- Oxycontin (118 people, 25.88%)
- Neurontin (112 people, 24.56%)
- Zometa (103 people, 22.59%)
- Ambien (100 people, 21.93%)
- Ativan (97 people, 21.27%)
* 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 Insomnia while taking Morphine Sulfate?
You are not alone! Join a mobile support group:
- support group for people who take Morphine sulfate and have Insomnia
- support group for people who take Morphine sulfate
- support group for people who have Insomnia
Recent conversations of related support groups:
- Support group for people who have Insomnia
Hi Everyone - I am desperate to talk to people who suffer like me. I have RLS and insomnia. I take Mirapex, Gabapenten, and have tried about 6 different kinds of sleeping pills and for the last 3 years I sleep about 3 to 4 hours a night. I can fall asleep but I cannot stay asleep. I am so sick of living like this. Nothing helps to keep me asleep. I go to bed at the same time every night (9) and around 1:00am, I wake up to go to the bathroom then the nightmare begins.... I cannot go back to sleep. I feel tired, depressed, alone and desperate for help. I have been to the Mayo Clinic twice and to numerous doctors and although they try, I can't get better. I exercise everyday for 1 - 1&1/2 hrs a day. I do not have any other health issues at all. This is a real big problem and a awful way to live. I just feel so alone and sad.
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More questions for: Morphine sulfate, Insomnia
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- Nardil side effects and my experience taking it
I have been on many SSRI AND SNRI medications that quickly became ineffective. Was told by a doctor friend that she had been on an MAOI inhibitor for many years with good results. After going thru a horrible withdrawal detox from the SNRI I had been on and then a period of no med at all I was started on Nardil, as I needed assistance from Pfizer, the many turner in affording the medicine. My friend was on Parnate, a different brand of an MAOI.
Within days, not weeks I felt the depression lifting. It was the most dramatic and fastest response I had ever had to any antidepressant .
Then the fainting started, falls with resulting broken ribs, bedridden and alone I lost over25 lbs in two weeks. I was of normal weight for my height. After I was able to function again, I noticed that my legs were very weak. We cut my dosage from 3 pills daily to 2. That seemed to have stopped the faint spells. However I still had/have low blood pressure that I monitor at home. My Systolic BP was usually in the 70's and 80's. One of the lowest was shocking to me. It was 52/27.
My son is a hospital RN and said they would never discharge a patient with Bp that low.
He was very worried about me as I live alone. I fainted twice after climbing the 13 stairs to my bedroom. The first fall was very bad as I was unconscious and my ribs were severely injured/fractured completely around the front and back and was in terrific pain. I took to my bed and did not seek medical attn. my last ambulance ride to the hospital a mile from my house cost $1000 and since I have no income or relatives/friends to call for help, I just lay in bed I awful pain that was woes when I tried to get out of bed. Thus I lost 25 lbs of muscle, since I had very little body fat.
It has been two months since that fall and still have one area of pain in the front left ribs and a swollen spleen. The doctor gave me no additional meds and just said to give my body more time to heal. So once again was changed to 2 pills daily instead of 3. The hypotension and fainting got better. But I am now left with very weak legs and fall easily and frequently. Guess I lost a lot of muscle mass with the weight loss. However after a lifetime of depression, Nardil works wonderfully for that which had been long-standing and severe for so many years. People noticed the change in me shortly after starting the Nardil. But I am stubborn about going off it despite all the side effects because it works so much better than any of the many others I had been put on over the years.
I am soon going to start doing leg exercises with ankle weights, starting with light weights are first and gradually increasing the weight as I hopefully rebuild my muscles and strength.
Also my vision has gotten blurry and I feel slightly retarded after the weeks in bed when I was breathing very shallowly due to the broken ribs and my brain was deprived of adequate oxygen.
Prior to all this I had an IQ of 140. If they tested me now, I know I would be way down from that. Also doing lung/breathing exercises to expand my lungs so I can take in more air with each breath.
So that is my story of Nardil, hypotension, and depression. I had to really suffer to remain on this med that worked so magically for me after so many failures. It meant that much to me to not be crippled by depression.
- Doxylamine succinate and severe restless legs and insomnia
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- 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: Morphine sulfate, Insomnia
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