eHealthMe - Personalized health information & community eHealthMe - Personalized health information & community

Personalized health information & community

  Tools   Community
All drugs: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
All conditions: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

Check symptoms       Compare drugs       Ask question       Write review       Answered/ Unanswered       Reviews

How effective is Oxycodone for Pain relief (Pain)?

Summary: 149 Oxycodone users have rated its effectiveness for Pain relief.

Overall ratings: 3.3/5
Long term ratings: 3.3/5

This is a review of how effective Oxycodone (oxycodone hydrochloride) is for Pain relief and for what kind of people. The study is created by eHealthMe and is updated continuously.

 

 

 

 

You are not alone: join a mobile support group for people who take Oxycodone for Pain relief >>>

What is Oxycodone

Oxycodone has active ingredients of oxycodone hydrochloride. It is often used in pain. (latest outcomes from 27,274 Oxycodone users)

Pain relief

Pain relief can be treated by Vicodin, Percocet, Tramadol Hydrochloride, Hydrocodone Bitartrate And Acetaminophen, Ibuprofen, Norco. (latest reports from 260,167 Pain Relief patients)

On Jan, 29, 2015: 149 people are studied for taking Oxycodone in Pain relief




Oxycodone effectiveness for Pain relief


Long term Oxycodone effectiveness for Pain relief

Oxycodone effectiveness for Pain relief (number of people):

not at allsomewhatmoderatehighvery high
Overall234505013
Long term
(1+ years)
11328258

Gender of people who take Oxycodone for Pain relief * :

FemaleMale
Pain relief48.32%51.68%

Age of people who take Oxycodone for Pain relief * :

0-12-910-1920-2930-3940-4950-5960+
Pain relief0.00%0.67%0.67%10.74%22.15%22.82%24.83%18.12%

Who find Oxycodone more effective for Pain relief?

Gender of people who find Oxycodone more effective * :

FemaleMale
Pain relief50.79%49.21%

Age of people who find Oxycodone more effective * :

0-12-910-1920-2930-3940-4950-5960+
Pain relief0.00%1.59%0.00%9.52%25.40%23.81%20.63%19.05%

* Approximation only. Some reports may have incomplete information.

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

What do you think? Post a comment.

Want to personalize this study to your gender and age? Start now.

Can you answer these questions (Ask a question):

  • What are safe alternatives to oxycontin? since moving to florida., no pharmacy stocks or can order it. suggestions?
    I've been on OxyContin for several years with pretty good results managing severe pain. Since moving south I'm finding that pharmacies cannot/will not carry it. Sent ex fr. Local md to mail order--one week later, still waiting.
    I'm desperate to find an effective alternative. Ideas?
  • I amwondering if i have myathesia gravis (1 answer)
    I am thinking that after a long bout of going nowhere with Drs. That I might have Myathesia Gravis. My Grandmother had it and I am thinking that my brother had it when he was born.He failed to thrive at first as he was unable to suck very well. He did make it though with a forced feeding of milk and bananas. He was sickly all his life though and recently died of cancer. I noticed that my eye is drooping on the left side. I have periods of extream fatigue, my left arm is tingly and I can't seem to feed myself without changing to my right hand. I have spinal stenosis and severe pain in my hip area but my right big toe seems to be tingly from time to time. I also have a swallow problem that causes me to choke or throw up the food or drink. Pills stay part way down a lot. My G.I. guy wants to strech my esophegus. I tend to eat soft foods and stay away from steak or anything chewy. I have congestive heart failure, sudden cardiac death, syncope all of which I greatfully managed to survive. I have fibromyalgia, and some nodules on my chest wall ( i forget what that is called) I have had 5 or 6 bouts with Costochrondritus which was way worse than actually having my heart stop. Costo hurts like a beech! I am frequently short of breath, exercize intolerant and have trouble holding my water.I have good dsys and bad days. Also my left hand and the base of my scalp goes all numb and tingly sometimes. There is also a terrible electric shock type feeling in my mid back area that makes me completely stop in my tracks and feel like I have been hit with a 350 lb pro football player. I have been hypokalimic after taking water pills (Ferosimide) i have taken prendisone for the Chosto and feel better immediatly, but I have mental reactions to too much Prendisone. I am very allergic to NSAID'S and pennicillian. Anyone got any ideas that the Drs have maybe not thought of... I would sure like to get better and go dance but the last time I danced I lasted 3 minutes before I had to fall into a chair.
  • How long does it take for pressure to return to normal if you quit taking norco?
    I stopped taking Norco as soon as I figured out that this might be the cause for my raised pressure. My doctor put me on drops and said I would have to stay on them for life. The drops burn and inflame my eye to the point of redness and pain. I went for a second opinion and tried another drop with the same result When I called both doctors back and told them about the Norco, neither think it is a problem. There is such a thing as too low pressure which can cause a detached retina. Since I had a detached retina in the other eye, I am worried about maybe lowering my pressure to low in my remaining good eye if I continue to take the drops. The P.A. said it is 'highly unlikely' my retina will detach. I would rather hear 'not possible' or quit the drops.
  • Do you have issues snoring from testosterone
    I was in an IED explosion in Afghanistan, had a TRAUMATIC BRAIN INJURY, 2005.JULY 28THlevels were extremely low. my V.A. doctor put me on testesterone 2011 BREAST CANCER, AUG 11TH 2012 HIT AND RUN ON MY MOTORCYCLE. DUE TO all the pain meds chemo, etcetera. MY testosterone. At first it was the best thing that had happened to me since I woke up in the hospital now I snore like a drunk Marined. and the culprit is the testosterone. I need to save my marriage and do something aboot this. any ideas what I can do
  • I'm interested in your study on anastrozole. i'm taking it and have so many side effects all in the form of pain. tylenol doesn't help and i can't take nsaids. i've only been on it for three months.
    I have bad knee pain, trouble walking, standing, due to pain. Stiff neck. Headache. I live in two story home and stairs are painful to climb. I care for my 97 year old mother and I'm extremely crabby with her. I also work (necessarily) for three hours a day but not every day. I've been on the Anastrozole for three months. Do I need to continue the Anastrozole? My score for how aggressive my breast cancer was came back a "three."

More questions for: Oxycodone, Pain relief

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

  • Mensis cycle and oxycontin
    I have severe back injuries. When I lived in another state, I was put on oxycontin and immediately my menstrual cycle (period] stopped for 1 year. When I moved to another state, I stopped taking this drug and my period returned normal. I eventually had to go back on this drug, (oxycontin) and since this time, 2 years now, I again have not had a period since beginning. If you are on this drug and are worried about your period stopping, fear not, it is a normal side effect. Hope this helps. ..
  • Which issue has caused my periodontitis, my fibromyalgia or spinal stenosis? (2 responses)
    At the age of 38 yrs old, I was diagnosed with Fibromyalgia and Spinal Stenosis. Obviously I had both of the disease for some years, and was struggling with the pain and symptoms for some time before I finally got checked, went through years being told they didn't find anything, told I had Herniated disks in My back only. Now with all the findings, there are 7 Herniated disks from My neck to My lower back.
    Also since 2010, I was diagnosed with Periodontitis and have been losing all of My teeth in the top of My mouth.
    I am 44 yrs old now, have been on disability for the last 4 years. I am down to 6 teeth in the top of My mouth, since having 1 removed just last week. They are telling Me that 3 more need to come out, and I am trying not to sink into total depression, especially since these are now My front teeth. I have a appointment today for a Denture Exam.

    I started researching today to see if this Periodontitis is related to either My Spinal Stenosis or My Fibromyalgia. Especially since I once again looked up the definition for Periodontitis. Which States;

    **Periodontal Disease and Bone Health. Periodontitis is a chronic infection that affects the gums and the bones that support the teeth. Bacteria and the body's own immune system break down the bone and connective tissue that hold teeth in place.

    Of course with My disease of Spinal Stenosis and the bone loss as well as the nerve narrowing, I thought the breaking down of the bone in the gums might have a connection. Research didnt find any linking.

    Now with Fibromyalgia, research showed 6 out of 17 thousand that they found. LOL Wow.. Well I guess I am "Number 7". Lucky Me! But it does make more sense now that looking at the definition. It is a Chronic infection (which Fibromyalia does create these) that effects the gums and bones. Bacteria and The Body's own Immune System break down the bone and connective tissue that hold the teeth. Which with Fibromyalgia, our Immune System is always all kinds of "Crazy"!

    Oh course you can not have any of these diseases, or any other health issues and wind up with Periodontitis. It happens. But I know from lots of reading, researching and living with Fibromyalgia, that it is "Very Possible"!

    I would sure like to know what others with these 2 diseases are experiencing.
    Have a Blessed Day.
  • I take ambien and morphine to help me sleep at night
    I have had insomnia for 40 years. It began with menopause. At that time I was healthy and very active, I played tennis three times a week, I was a mother and a housewife and a teacher. When the insomnia began I had no pain. I'm 82 now and I have had continuous all over body pain for 5 years. No one has been able to diagnose my disease, they all just say it's arthritis or scoliosis or stenosis. I recently had an all over body scan but that still didn't help diagnose me nor help doctors make a diagnosis (I have been to every kind of doctor there is available to me here in Rancho Bernardo, Ca. For six months I have taken both Ambien and morphine just before going to bed. I have had no problems with that combination and the do allow me about 7 happy pain free hours of sleep at night.
  • Who cares about the patient? (1 response)
    I can't believe I'm still alive but quality of life is greatly diminished and no one cares. Not one doctor cares about how this one dr. prescribed all these drugs over a period of 5 years and I lost everything. I flat-lined sept 18, 2005 and was told by dr there in er that I would live 1-5 years and I had just lost my job as letter-carrier of over 17 years and my daughter was killed in dec of 2000, which I will always feel great responsibility because I knew I should have called her, it would have saved her life as she was killed in the firdale village apt fire and she didn't live there, she lived with me she was only 20 years old. So this crappy dr steven a creelman of seattle just kept throwing pills at me, telling me there was nothing wrong with any of the pills just me. I feared dr's and still do, I know they are just people and most people are good and caring but a lot are not. The Celebrex started after I was hit by a truck on the job in march of 2000. I will admit it relieved some pain but I had side affects immediately, within days to weeks. I was told by the crappy dr to shut up and take them as he originally told me they were not anti-inflamatorys but a new drug that did not upset stomach but they did. I felt trapped because it was an L&I and I didn't want to lose my job and so healthy and strong figured w/PT and rest I could overcome the accident pain which was lower back and neck well I couldn't sleep from pain and stomach but I couldn't tell crappy dr it would do no good. My daughter was killed Christmas night and that's a very hard one. I went back to work because my job was most of my life and I had friends at work. I continued to have more problems from Celebrex and I thought my stomach was on fire, it was blood clots that broke lose and I had to have an operation on my small instestine and what was worse is creelman, the crappy dr, when he told me it was an emergency umbililical hernia I told him I was going to get papers from owcp DOL as I would be off work at least 6 weeks. He said NO!!!!!!!!!! He closed the door and told me no, no I won't say it's from Celebrex when He really did know it was. I had an endoscopy 6 months later and that specialist said no more Celebrex. After that operation I just never felt good again I was swelling up my legs etc and fatique all kinds of not feeling good things and I was pissed at the crappy dr who by the said to me that no other dr would diagnose any different or believe me. So, it was in July of 04 and I was so sick I just went in there andhe was on vaction so another dr ran a bunch of blood tests for hiv which I told her was impossible and lupus and a few other things but no one there looked at any of the drugs except the pain medication which ironically was one of the only ones that didn't contribute to dvt & PE. when creelman got back I was still so sick I had left work and said I would be back in 2 weeks after I had some PT and rest. I couldn't sleep. That's when he prescribed REMERON. It was for sleep which it did help but I gained 50 lbs and within a couple months acquired tonsillitis, bhroinchitis, pneumonia, Phlebitis and a dvt which instead of referring me to a specialist he just presibed me an anti-inflammatory and another anti-depressant plus all the drugs He gave tons of samples which were never in noted in my files. I think he should have to pay me MONEY!! I have none since I have no job and I feel so terrible I wish I could just have my job back. And my Daughter but my health has been a Hematologist and injectable blood thinners. I hate the state of wash medical care about doctors but not the patients and I have no money to sue and it has been my experience not to mention crappy doctor SO WHO DO THE PATIENTS THAT ARE BADLY AFFECTED BY CRAPPY DCTORS GO TO? Oh I also couldn't be in the class-action suit because I didn't flat-line from heart attack. REALLY?
  • Are fm and premature menopause linked (2 responses)
    I was diagnosed with Fibromyalgia at 17. I coped really well with it until I tragically lost my sister, met and married my husband and had a child all in one year. The trauma and also overload of emotions including PND seemed to ramp up all my symptoms. I do not work, I am a SAHM to 3. I rest as often as possible and have learned a new kind of way to live my life and priorities as best possible with my good and bad days. I only medicate with pain medication on my worst days. The others I just breathe through it :-)

    After seeing an endocrinologist for what I thought was a thyroid issue, I was surprised and must admit upset to find my bloods revealed premature menopause. Im only 32.

    I have wondered if there is a link and how many Fibro suffers have or are going through menopause at a young age. Anytime a link is established somewhere I hold out hope it will lead to a cure. The key maybe in the connection and collection of symptoms. So Im happy to add my name to any study or statistic in regards to this new diagnosis.

    However I like many others may have gone through prem menopause even if we didn't have FM. You just don't know :-)

More reviews for: Oxycodone, Pain relief

Comments from related studies:

  • From this study (1 day ago):

  • Also have numbness in my fingers Started taking Losartan and adderall about the same time

    Reply

  • From this study (4 months ago):

  • Bad migraines and spitting up blood

    Reply

  • From this study (9 months ago):

  • Resulted in full removal of the colon

    Reply

Post a new comment    OR    Read more comments

NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT considered.

WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.

DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only, and has not been supported by scientific studies or clinical trials unless otherwise stated. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.

You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).

If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.

   

About - Terms of service - Privacy policy - Press - Testimonials - Contact us

 
© 2015 eHealthMe.com. All rights reserved. Use of this site constitutes acceptance of eHealthMe.com's terms of service and privacy policy.