Review: could Morphine cause Difficulty breathing (Breathing difficulty)?
Summary: Difficulty breathing is found among people who take Morphine, especially for people who are female, 60+ old, have been taking the drug for < 1 month, also take medication Morphine sulfate, and have Pain.
We study 48,671 people who have side effects while taking Morphine from FDA and social media. Among them, 3,341 have Difficulty breathing. Find out below who they are, when they have Difficulty breathing and more.
You are not alone: join a mobile support group for people who take Morphine and have Difficulty breathing >>>
Morphine has active ingredients of morphine sulfate. It is often used in pain. (latest outcomes from 49,763 Morphine users)
Difficulty breathing has been reported by people with high blood pressure, asthma, rheumatoid arthritis, pain, chronic obstructive pulmonary disease. (latest reports from 165,443 Difficulty breathing patients)
On Jan, 30, 2015: 48,666 people reported to have side effects when taking Morphine. Among them, 2,819 people (5.79%) have Difficulty Breathing.
Time on Morphine when people have Difficulty breathing * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
|Difficulty breathing||71.96%||15.50%||5.54%||2.58%||3.32%||1.11%||0.00% |
Gender of people who have Difficulty breathing when taking Morphine * :
|Difficulty breathing||54.55%||45.45% |
Age of people who have Difficulty breathing when taking Morphine * :
|Difficulty breathing||0.14%||0.42%||1.62%||3.60%||7.91%||16.78%||28.75%||40.76% |
Severity of Difficulty breathing when taking Morphine ** :
|least||moderate||severe||most severe |
|Difficulty breathing||0.00%||66.67%||16.67%||16.67% |
How people recovered from Difficulty breathing ** :
|while on the drug||after off the drug||not yet |
|Difficulty breathing||0.00%||0.00%||100.00% |
Top conditions involved for these people * :
- Pain (592 people, 21.00%)
- Multiple myeloma (206 people, 7.31%)
- Metastases to bone (204 people, 7.24%)
- Hypertension (152 people, 5.39%)
- Breast cancer (129 people, 4.58%)
Top co-used drugs for these people * :
- Morphine sulfate (1,341 people, 47.57%)
- Zometa (812 people, 28.80%)
- Aspirin (616 people, 21.85%)
- Aredia (613 people, 21.75%)
- Lasix (529 people, 18.77%)
* 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.
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- Morphine and amenorrhea
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...
- Faslodex driven hell
I have metastatic breast cancer...which has spread to my bones. Needless to say...I'm not a happy camper. Faslodex was my oncologist’s drug of choice for me. I've been on it since July 28, 2014....My first month was loading dosage...and each month that has followed I receive two injections in my tush...250mg each...for a total of 500mg monthly. Tomorrow, Monday November 17, 2014, will be my third round...not including the month of loading. As per my PET scan one month ago...the Faslodex has not started working. From everything I have been told...and read...it takes four to even six rounds to start working...if in fact it works at all.....@%^&*@#...says it all...if ya know what I mean.
What has kicked in from Faslodex...are some horrific side effects......About a month ago...I started having a strange little cough...dry...most of the time.....At times the cough becomes uncontrollable for aprox 15 / 20 minutes...then calms. NOTHING works at relieving it...although I suck down water like it is my last drink on earth...and use a wonderful...soothing throat drop, Halls Breezers...Cool Berry...which eases me...even if it is only psychologically, it is magical. The cough has gotten considerably worse over time...and for those that don't know me...I am sure they think I smoke ten packs a day. My voice is also affected at times due to the cough. My breathing is horrific...and I can no longer walk for any length of time...or for more than a short distance.....Nor can I walk and talk without coughing...and or losing my breath. Stamina...this I have none of!!! And this past week...the shit hit the fan.....Joining the cough...are bone and joint pains...as well as muscle pain. When I called my doctor...@ Sloan Kettering...I spoke with the nurse...and she had not a damn clue as to what might help. As a matter of fact...she told me that she has never heard of any of the side effects that I am now having. WHAT'S WRONG WITH THIS PICTURE???? EVERYTHING!!! However...when I check reputable sites...I find not a few...but hundreds of other people with the same side effects.
From what I have read on all the sites...the only way "WE" are going to get help with issues like these...is by sharing with one another. Not one of the individuals that I speak of has had any positive help with their side effects from their doctors. Am I pissed off??? You bet I am. As for depression...that only comes in small doses for me.....like yesterday...when my body hurt me so badly...my cough was out of control...I had difficulty breathing...and I could not stand on my own two feet without holding on. That moment in time has passed...but for how long??? What will I be hit with next??? When???
- 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.
- 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.
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From this study (1 year ago):
Started Alimta and neurontin 4 days ago and started having increased shortness of breath with minimal exertion.
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