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Prednisone, Morphine Sulfate, Tramadol Hydrochloride, Sulfamethoxazole And Trimethoprim for a 42-year old woman





Summary: 2 female patients aged 42 (±5) who take the same drugs are studied.

This is a personalized study for a 42 year old female patient who has Bronchitis, Pain. The study is created by eHealthMe based on reports from FDA and social media.

What are the drugs

Prednisone has active ingredients of prednisone. It is often used in rheumatoid arthritis. (latest outcomes from Prednisone 150,015 users)

Morphine sulfate has active ingredients of morphine sulfate. It is often used in pain. (latest outcomes from Morphine sulfate 19,045 users)

Tramadol hydrochloride has active ingredients of tramadol hydrochloride. It is often used in pain. (latest outcomes from Tramadol hydrochloride 6,864 users)

Sulfamethoxazole and trimethoprim has active ingredients of sulfamethoxazole; trimethoprim. It is often used in urinary tract infection. (latest outcomes from Sulfamethoxazole and trimethoprim 5,752 users)

What are the conditions

Bronchitis (inflammation of the mucous membrane in the bronchial tubes) can be treated by Azithromycin, Prednisone, Zithromax, Levaquin, Avelox, Albuterol Sulfate. (latest reports from Bronchitis 35,081 patients)

Pain can be treated by Hydrocodone Bitartrate And Acetaminophen, Vicodin, Percocet, Tramadol Hydrochloride, Ibuprofen, Norco. (latest reports from Pain 291,941 patients)

On Nov, 26, 2014: 2 females aged 37 (±5) who take Prednisone, Morphine Sulfate, Tramadol Hydrochloride, Sulfamethoxazole And Trimethoprim are studied

Prednisone, Morphine Sulfate, Tramadol Hydrochloride, Sulfamethoxazole And Trimethoprim outcomes

Information of the patient in this study:

Age: 37

Gender: female

Conditions: Bronchitis, Pain

Drugs taking:
- Prednisone - 10MG (prednisone): used for < 1 month
- Morphine Sulfate - 30MG (morphine sulfate): used for 2 - 5 years
- Tramadol Hydrochloride - 50MG (tramadol hydrochloride): used for 1 - 2 years
- Sulfamethoxazole And Trimethoprim (sulfamethoxazole; trimethoprim): used for < 1 month

eHealthMe real world results:

Drug effectiveness over time :

n/a

Most common drug interactions over time * :

< 1 month1 - 6 months6 - 12 months1 - 2 years2 - 5 years5 - 10 years10+ yearsnot specified
n/an/an/an/an/an/an/aMyalgia (muscle pain)
Tardive Dyskinesia (a disorder that involves involuntary movements)
Eye Swelling
Arthralgia (joint pain)
Weight Bearing Difficulty (difficulty due to weight of thigh fat deposition)
Amnesia (deficit in memory caused by brain damage, disease, or psychological trauma)
Impaired Gastric Emptying
Spinal Osteoarthritis (joint cartilage loss in spine)
Abdominal Pain
Gingival Swelling (gums swelling)

* Some reports may have incomplete information.

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.

You can also:

You are not alone! Join a related mobile support group:
- support group for people who have Bronchitis
- support group for people who have Pain
- support group for people who take Morphine Sulfate
- support group for people who take Prednisone
- support group for people who take Sulfamethoxazole And Trimethoprim
- support group for people who take Tramadol Hydrochloride

Recent conversations of related support groups:

Can you answer these questions (Ask a question):

More questions for: Bronchitis, Pain, Sulfamethoxazole And Trimethoprim

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

  • My finger tendons broke on prednisone
    Twelve years ago I was put on prednisone for sudden hearing loss. The prednisone helped the hearing loss (for as long as I took the drug; hearing loss returned after I stopped the prednisone.) But I kept getting ruptured tendons in my fingers, which I had to splint to use. I couldn't figure out why in heck this was happening. My doctor(s) didn't have a clue. I suspected the ruptures might have to do with prednisone. Now I know they were caused by it. When I stopped the prednisone, the tendon-ruptures stopped, too. This should be Must Tell information for any doctor who prescribes this dangerous drug.
  • 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.
  • Prednisone rx 3,3,2,2,1,1 plan suicidal haunts all day
    I came home from the Hospitol with a 3,3,2,2,1,1 Rx.
    I took (3) and spent the rest of the day contenplating Suicide.
    The rest of the Rx went in the Toilet by 7:pm.
    I wonder how many this Killed.
  • Prednisone induced cushing's syndrome
    Prescribed Prednisone 20mg twice daily. Took for six weeks and developed weaken muscles and swollen face. Was hospitalized and informed I had severe Cushing's Syndrome. Host of problems included glucose over 400, inflammed pancreas, triglycerides over 4,000 and vision problems. Muscles were wasted and weak so fell several times. Had to regain strength and learn to walk again with physical therapy. Left with foggy thinking, fatigue, muscle myopathy and peripheral neuropathy. Also developed osteopenia. Afterwards was placed on hydrocortisone and Lyrica for pain. Later found liver damage.
  • 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.

More reviews for: Bronchitis, Pain, Sulfamethoxazole And Trimethoprim

Comments from related studies:

  • From this study (1 month ago):

  • peanuts on Mar, 31, 2010:

    my friend is suffering from rhumatory arthertis.and is currenty taking cocaine. oxy cotin,prestine, wellbutrim, predisone 10mg what side effects should she expect ?????

    Reply

    mtntexas on May, 11, 2013:

    Just ask John Belushi

    Reply

    2cents on Mar, 6, 2013:

    I'll second that!

    Reply

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NOTE: The study is based on active ingredients. Other drugs that have the same active ingredients are also considered.

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