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How effective is Hydromorphone hydrochloride for Fibromyalgia?

Summary: 9 Hydromorphone hydrochloride users have rated its effectiveness for Fibromyalgia.

Overall ratings: 3.1/5
Long term ratings: 3.2/5

This is a review of how effective Hydromorphone hydrochloride (hydromorphone hydrochloride) is for Fibromyalgia and for what kind of people. The study is created by eHealthMe and is updated continuously.

 

 

 

 

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What is Hydromorphone hydrochloride

Hydromorphone hydrochloride has active ingredients of hydromorphone hydrochloride. It is often used in pain. (latest outcomes from 1,301 Hydromorphone hydrochloride users)

Fibromyalgia

Fibromyalgia (a long-term condition which causes pain all over the body) can be treated by Lyrica, Cymbalta, Savella, Gabapentin, Amitriptyline Hydrochloride, Neurontin. (latest reports from 26,917 Fibromyalgia patients)

On Jan, 30, 2015: 9 people are studied for taking Hydromorphone hydrochloride in Fibromyalgia




Hydromorphone hydrochloride effectiveness for Fibromyalgia


Long term Hydromorphone hydrochloride effectiveness for Fibromyalgia

Hydromorphone hydrochloride effectiveness for Fibromyalgia (number of people):

not at allsomewhatmoderatehighvery high
Overall01620
Long term
(1+ years)
01220

Gender of people who take Hydromorphone hydrochloride for Fibromyalgia * :

FemaleMale
Fibromyalgia100.00%0.00%

Age of people who take Hydromorphone hydrochloride for Fibromyalgia * :

0-12-910-1920-2930-3940-4950-5960+
Fibromyalgia0.00%0.00%0.00%0.00%0.00%22.22%55.56%22.22%

Who find Hydromorphone hydrochloride more effective for Fibromyalgia?

Gender of people who find Hydromorphone hydrochloride more effective * :

FemaleMale
Fibromyalgia100.00%0.00%

Age of people who find Hydromorphone hydrochloride more effective * :

0-12-910-1920-2930-3940-4950-5960+
Fibromyalgia0.00%0.00%0.00%0.00%0.00%0.00%0.00%100.00%

* Approximation only. Some reports may have incomplete information.

Find out which drug is more effective in real world to treat:

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Can you answer these questions (Ask a question):

  • Does humira cause excessive sweating?
    Having psoriaticarthritis,fibromyalgia,psoriais,restless leg syndrome,roseacea and high blood pressure means complex health issues and a complex list of medication to go with it. Iam suffering extreme sweating,flushing and now a tickled cough. Now it could be due to going through the change (menopause) but that started a year ago and although I was getting the flushes and sweating,it was nothing like it is now! To me,it seems the excessive sweating started roughly a month after taking Humira. Having so many health issues I'm in tune with any changes and note and monitor them. I started Humira 10 months ago now. My Psoriasis has cleared completely so I'm really pleased. Usually,there's a trade off and you end up with something else! Could the issues I have be down to a single drug on the list,or a combination?
  • Radiation and hydrmororphone
    Just wondering did anyone have side effects while going through radiation. I've been through " whole brain" 10x. This time so far it should run 5x over 3 tumors/cysts that developed over a handful of months. I'm just hoping not to lose all my hair lol!
  • I need to know psychological problems drug infusion dilaudid therapy? (1 answer)
    I have recently stolen some things from a loved ones house while residing there and hid the very valuable items and have no memory of it or where I hid the items that haven't been found,which resulted in my having to leave and been told never to return....I am devastated.... I loved those people I would have never done such a thing but it was all in my possession...only I could have done this, there was no one else in the home and all doors and windows were locked... but I have absolutely no memory of it...has anyone else had these experiences...yes I have done similar things but not to this degree...this almost resulted in my incarceration has anyone else had similar episodes???
  • Could fibromyalgia be caused from a gram negative infection 37 years ago?
    I have fibromyalgia and chronic fatigue that after being relatively stable is now becoming unmanag. I am trying to trace background my medical history to possibly find a cause for these syndroms.
  • Can xanax use cause female hair loss?
    I am losing a lot of hair. It started about two months ago, and I went to dermatologist who ordered some medication for two weeks. It stopped. I have been using Victoza for almost a year and take Xanax daily long term. Can either of these drugs cause my hair loss?? It's back now, and full speed. At this rate, I'll be bold in two weeks more. I'm desperate, but my doctors think if the Victoza is causing it, it will regenerate once I stop, which I'm in the process of doing. However, if there is a chance Xanax is causing it, I need to know to find an alternative drug for my nerves. Any help??

More questions for: Hydromorphone hydrochloride, Fibromyalgia

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

  • Severe leg/foot/ankle swelling from doxycycline
    Was given five-day course of doxycycline for sinusitis and laryngitis. By end of third day had ankle edema (never had before), then MASSIVE leg/foot/ankle edema by fourth day Discontinued on fifth day after research revealed side effect of doxycycline. Took almost a week for swelling to go comletely away. Also felt completely exhausted and seemed to make the coughing and laryngitis much worse also.
  • 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.
  • Not a great experience
    I was on norvasc for two months and had to go off because of severe swelling of feet and legs. Also rapid heart beat and very profuse sweating. it was horrible. It also raised my blood pressure. after going off BP dropped by @least 10 points both diastolic and systolic.
  • Sepsis hallucinations misdiagnosed
    I was admitted to the hospital at 10 p.m., with a total bowel blockage caused by scar-tissue adhesions. I had first gone to the ER at 3 a.m. that morning, but the ER doc misdiagnosed my condition as constipation. I was in extreme pain and also too weak to tell my husband when he first came home that I needed to return to the ER. By the time I returned, I became violently nauseated, and vomited repeatedly. Then a gastro-nasal tube was forced down my nose and into my stomach. I began hallucinating at approximately 5 p.m. the following day. I did not realize I was hallucinating, and thought my experiences were real. Some were quite coherent, such as believing there was a book sitting on table at home with a photo on the front showing a sculpture in white marble of a woman's hands holding the Bible, with barbed wire wrapped around her hands. I thought the sculpture had won the Nobel prize, and the book was the biography of the sculptor, whose mother had gone to extraordinary lengths to keep him safe from the Nazis. Some may actually have occurred during dreams, and were wildly improbable, but I don't recall ever going to sleep. At one point, I thought I was at a rest stop on the NJ turnpike, and saw the Nobel-winning sculptor there, working on a wood sculpture. The sculptor turned out to be the maintenance man on the hospital floor. I pulled out the naso-gastral tube three times, but was unaware that I had done so, although I do remember believing that I was buried beneath peat moss and feeling suffocated as I clawed my way out. I also thought I was at a party being given by a law firm which had sold its building to a school for gifted children, but I (also a lawyer) had been deposited there by my nurse and her boyfriend, who were supposed to have taken me to the OR. Some scenes from a book I had been reading made their way into my delusions, which were so real to me that I actually called some of the people involved later on and asked if the events had really happened. The hallucinations began before surgery and continued afterward. When I awoke from anesthesia, I thought the hospital staff was painting the doors to my upstairs bathroom, a project I'd been involved with before the blockage struck. I asked them how they knew what colors to use. They thought I was joking, and confirmed that they had gotten the colors right. Finally a neurologist was summoned, and I told her I was on the passenger ramp at La Guardia airport (instead of in a hospital in NC), and that I'd been born in Havana, Cuba (instead of Baltimore, MD.) I believed myself to be a member of the ruling party in Cuba (pre-Castro) and during an outdoor ceremony, an earthquake had struck, causing ancient monuments to come tumbling down. Later, I was bobbing in harbor waters near a huge ocean liner, with plastic bottles and other detritus floating by. The foregoing are only a small sample of the multitude of hallucinations. Occasionally, I was only an observer of astonishing events, but usually I was a participant. I recognized my husband and friends, but told them about many of these events, believing they had happened. The neurologist diagnosed clonazepam withdrawal. My other doctors later said this was unlikely, as I took clonazepam in small amounts on an erratic schedule, and was not dependent on the drug, although my prescription called for 3 mg. daily. Physician friends said my symptoms were more likely the result of sepsis. I did contract a urinary-tract infection from the catheter, and was being given antibiotics. Additionally, the nature of my underlying condition, and the delay in diagnosis and treatment, may have contributed to the sepsis. Hallucinations occur in only a very small percentage of sepsis sufferers, and in only a small percentage of those withdrawing suddenly from clonazepam. However, I do fit the profile of those who do experience hallucinations with sepsis, being female and aged 62 at the time of this description. After the three-day period, I returned to normal, although believing that my hallucinations had been real persisted for some days afterward. I recovered quickly from the surgery, although the pain persisted for a while, and I was walking easily (dragging my IV with me) through the hospital halls. This was the ONLY symptom I had. Not all the hallucinations were unpleasant -- in fact, they were highly interesting -- but they were incredibly complex. I still remember all the details, better than I remember what actually happened yesterday. Except for the urinary-tract infection, I had no other adverse effects from hospitalization -- no fever, chills, nausea, sweating, headaches, trembling or anything of that kind. The bowel blockage and the surgery were of course not fun, but in a way the hallucinations were fascinating. My own feeling, and that of the doctors who know me and my medical issues, is that my experiences were caused by sepsis, not clonazepam withdrawal, and the antibiotics I was given are probably what saved me.
  • So sleepy with savella
    I am just finishing the starter pack of Savella and I am so sleepy I can't hold my head up. My pain and other Fibromyalgia symptoms are tremendously better but I am sleeping like crazy. Hopefully I can have both doses at night and this will help. I am so glad to not be in pain but I need to be awake also. I am going to talk to my doctor about perhaps another medication to help curb the sleepiness. I can't use caffeine or stimulants due to anxiety but need something to take this sleepiness away.

More reviews for: Hydromorphone hydrochloride, Fibromyalgia

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  • I have been taking the same dosage for over a year but continue to get nauseated on a regular basis. At least once every 3-4 weeks I feel like I am overdosing, extremely itchy, headach, can not stay awake feel like I am going to pass out and extreme nausea up to 30 hours. Gravol suppositories help a bit and I sleep for 2 days even without the gravol. I have even decreased my dose to no avail. First stared about 3 1/2 years ago when I was taking Oxycontin. Doctors cannot find a reason for it. I feel like it is getting stored in my body and when it reaches a certain level I get the over dose feeling and it really scares me. I put my meds out each night for the next day so I dont have to guess if I have taken them so it' not like I made a mistake and took to much. I take 1 6mg long acting at night 2 in the morning and 1 4mg short acting at 5pm for breakthrough pain. I am still always in pain now that I have slowly decreased over the last 8 months but it scares me to much to continually go through this.

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