Review: could Morphine cause Memory impairment (Memory loss)?
Summary: Memory impairment is found among people who take Morphine, especially for people who are female, 50-59 old, have been taking the drug for < 1 month, also take medication Morphine sulfate, and have Pain.
We study 48,649 people who have side effects while taking Morphine from FDA and social media. Among them, 761 have Memory impairment. Find out below who they are, when they have Memory impairment and more.
You are not alone: join a mobile support group for people who take Morphine and have Memory impairment >>>
Morphine has active ingredients of morphine sulfate. It is often used in pain. (latest outcomes from Morphine 49,746 users)
Memory Impairment has been reported by people with multiple sclerosis, depression, high blood pressure, pain, high blood cholesterol.(latest reports from Memory Impairment 62,109 patients)
On Nov, 29, 2014: 48,649 people reported to have side effects when taking Morphine. Among them, 761 people (1.56%) have Memory Impairment.
Time on Morphine when people have Memory impairment * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
|Memory impairment||45.59%||10.29%||13.24%||7.35%||16.18%||7.35%||0.00% |
Gender of people who have Memory impairment when taking Morphine * :
|Memory impairment||64.67%||35.33% |
Age of people who have Memory impairment when taking Morphine * :
|Memory impairment||0.00%||0.00%||1.18%||4.72%||13.89%||21.49%||29.88%||28.83% |
Severity of Memory impairment when taking Morphine ** :
|least||moderate||severe||most severe |
|Memory impairment||12.50%||75.00%||6.25%||6.25% |
How people recovered from Memory impairment ** :
|while on the drug||after off the drug||not yet |
|Memory impairment||10.00%||0.00%||90.00% |
Top conditions involved for these people * :
- Pain (243 people, 31.93%)
- Breast cancer (40 people, 5.26%)
- Metastases to bone (39 people, 5.12%)
- Depression (38 people, 4.99%)
- Hepatitis c (36 people, 4.73%)
Top co-used drugs for these people * :
- Morphine sulfate (373 people, 49.01%)
- Xanax (159 people, 20.89%)
- Neurontin (147 people, 19.32%)
- Oxycontin (146 people, 19.19%)
- Zometa (133 people, 17.48%)
* 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 Memory Impairment while taking Morphine?
You are not alone! Join a mobile support group:
- support group for people who take Morphine and have Memory Impairment
- support group for people who take Morphine
- support group for people who have Memory Impairment
Drugs in real world that are associated with:
Could your condition cause:
Can you answer these questions (Ask a question):
- Is vomiting all liquids common while taking morphine
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.
- Why would i get copd since i never smoked?
I have several autoimmune disorders, I was shocked to get the COPD diagnosis since I have never smoked but I had second hand smoke first 23 years of my life.
My doctor said my Autoimmune Hepatitis and Primary Biliary Cholingitis set me up for COPD.
- Anyone taking amitza for the relief of constipation associated with taking morphinefor chronic pain? if so, does atmotza provide adequate relief of this type of constipation?
I am just trying to get effective relief of my extreme constipation that has just recently began following my doctor prescribing morphine for relief of my chronic pain. I am hoping that the medicine Amitza is going to have an Osmotic affect on my constipation. I am very thankful for any helpful responses to this post.
P.S. I am currently taking 60 mg of Morphine Sulfate (taken once daily)
- Does loss of taste from morphine come back ?
I was given morphine 3 months ago and have loss my ability to taste ever since.
More questions for: Morphine, Memory impairment
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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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- Higher than a kite, and dumber than one of those saying i can no longer remember!
I told my shrink I didn't want to try anymore antidepressants... that they make me crazy-stupid(pristiq), crazy-nympho(wellbutrin), or crazy-sloth(lexapro). I have complex ptsd, did, and gad. I really don't want to take anything... I just want to work out, eat right, and try to put myself back on track. It seems like every time I try these pills I get pushed off course. Anyways here's my experience with pristiq. Day1) dilation ofpupils was noticed with in a few hours, it started to feel like I was on sshrooms....I'd look in the mirror and feel so much love...just stand there staring. I slept better than I did in months. Day 2) Sadly though, when I woke up I couldn't climax, it was like I was numb. My pupils were still dilated and I still felt an out pouring of love and admiration while looking at myself. I tried hard not to fixate and get ready for work. I noticed that my tummy wasn't bloated anymore, I hadn't felt this much releaf in months. As I took my daily 50mg I reassured myself that it was ok not to climax in favor of all the good things I'm feeling now. Pristiq didn't interfere with my routine other than climaxing. Day 3) I awoke well rested with a happy tummy and it didn't bother me a bit not to climax, I jumped out of bed and started my day with vigor. The moment I took my dose and left the house is the last thing I remember! From what I wrote in my calendar, the notes I took, and my phone history I can piece together the things I did for 7 more days!!! I went to work, but my coworker was on holidays so it was just me alone in the office, I have no family or friends in this country (I moved to get away from a bad situation, hence cptsd) anyways I had no interaction. The only thing that brought me out was probably that I stopped taking the medication on day7 (According to the amount of medication left)....it's taken 14 more days to get out of the pristiq fog. During that time I've experienced nightly vivid dreams/ nightmares, extreme sweating and high body temperature, my stomach discomfort fluctuates but I can control it through diet, I'm able to climax again though it takes time, my pupils returned to normal a few days after I returned to myself...I seem to have memory impairment.
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I stopped taking the chantix and the headaches gradually came back but it took me awhile to make this correlation. Once I did, I started taking the chantix again. it started working immediately... taking the migraines and neck pain away again! Now, I can take 1/2 of a pill every other day and that seems to keep the migraines away! There are side effects and I don't know if it would work for everyone but it sure worked for me!
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