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       Ask question       Write review       Answered/ Unanswered       Reviews       WellConnected

Review: could Suboxone cause Bone and joint pain (Joint pain)?





Summary: Bone and joint pain is found among people who take Suboxone, especially for people who are female, 50-59 old, have been taking the drug for 1 - 6 months, also take medication Percocet, and have Drug dependence.

We study 7,235 people who have side effects while taking Suboxone from FDA and social media. Among them, 149 have Bone and joint pain. Find out below who they are, when they have Bone and joint pain and more.

You are not alone: join a mobile support group for people who take Suboxone and have Bone and joint pain >>>

Suboxone

Suboxone has active ingredients of buprenorphine hydrochloride; naloxone hydrochloride. It is often used in opiate withdrawal. (latest outcomes from Suboxone 8,267 users)

Bone and joint pain

Bone and joint pain has been reported by people with rheumatoid arthritis, osteoporosis, high blood pressure, high blood cholesterol, multiple sclerosis.(latest reports from Bone and joint pain 117,673 patients)

On Nov, 28, 2014: 7,235 people reported to have side effects when taking Suboxone. Among them, 149 people (2.06%) have Bone And Joint Pain.

Trend of Bone and joint pain in Suboxone reports

Time on Suboxone when people have Bone and joint pain * :

< 1 month1 - 6 months6 - 12 months1 - 2 years2 - 5 years5 - 10 years10+ years
Bone and joint pain14.29%42.86%30.95%4.76%7.14%0.00%0.00%

Gender of people who have Bone and joint pain when taking Suboxone * :

FemaleMale
Bone and joint pain75.00%25.00%

Age of people who have Bone and joint pain when taking Suboxone * :

0-12-910-1920-2930-3940-4950-5960+
Bone and joint pain0.00%0.00%0.00%4.66%22.28%23.32%26.94%22.80%

Severity of Bone and joint pain when taking Suboxone ** :

leastmoderateseveremost severe
Bone and joint pain0.00%25.00%50.00%25.00%

How people recovered from Bone and joint pain ** :

while on the drugafter off the drugnot yet
Bone and joint pain0.00%33.33%66.67%

Top conditions involved for these people * :

  1. Drug dependence (76 people, 51.01%)
  2. Pain (30 people, 20.13%)
  3. Anxiety (20 people, 13.42%)
  4. Depression (18 people, 12.08%)
  5. Hypertension (16 people, 10.74%)

Top co-used drugs for these people * :

  1. Percocet (50 people, 33.56%)
  2. Wellbutrin (24 people, 16.11%)
  3. Prozac (23 people, 15.44%)
  4. Xanax (23 people, 15.44%)
  5. Dilaudid (22 people, 14.77%)

* 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.

Do you have Bone And Joint Pain while taking Suboxone?

You are not alone! Join a mobile support group:
- support group for people who take Suboxone and have Bone And Joint Pain
- support group for people who take Suboxone
- support group for people who have Bone And Joint Pain

Drugs in real world that are associated with:

Could your condition cause:

Can you answer these questions (Ask a question):

  • What is the possible explanation for arthralgia upon xolair medication for asthma? (1 answer)
    (Asked by a 20 year old woman who has Arthralgia, and takes Xolair)
    Female, 20 years old with severe asthma is being medicated with Xolair (Omalizumab) over the last six months. Although the patient is getting better she is suffering of severe arthralgia mainly in arms and legs. What is the possible explanation for arthralgia upon Xolair medication for asthma?
    Reply
  • What side effects from nuvigil and cymbalta creating seretonin syndrome? (2 answers)
    (Asked by a 53 year old woman who has Hot Red Skin On Face Neck And Back, and takes Suboxone , Nuvigil, Cymbalta)
    My dr thinks that all the drugs I'm on are causing sedition syndrome. But I have t seen where a symptom was red flushed skin?
    Reply
  • Does neurontin cause arthritis. after taking it for 3 months, i started ints.
    (Asked by a 56 year old woman who has Joint Pain, and takes Neurontin)
    After having sciatic pain for almost a year, a doctor prescribed Neurontin. I took it for 3 months until I started getting severe joint pain. I weened myself off of it a month ago and am still having severe joint pain. There has not been any other changes in my life except Neurontin. Does this go away eventually.
    Reply
  • Have been on suboxone strips almost a year. i have just recently since yesterday got sick i have strep throat and my throat is really hurting and i can't even speak today. can i still take my strips? (1 answer)
    (Asked by a 33 year old woman who has I Have Strep Throat And A Severe Sore Throat And Can't Speak Any, and takes Amoxicillin, Suboxone )
    I just wonder if it will be ok today to go ahead and use my suboxone strips or will it do more damage than good? It's never bothered my throat before but my throat is so bad right now that I don't know if it will hurt or help? I'm supposed to take 2 8mg strips a day? Help!!!!???
    Reply
  • Why are my medications making me look bloated (1 answer)
    (Asked by a 38 year old woman who has Bloating, and takes Effexor Xr, Suboxone)
    In 2008 I started the Suboxone Program. I Started on 16mg since then, I have been up and down on my doses. I was put on this drug as a result of my addiction to to over the counter opiates. I was also prescribed Seroquel, I stopped taking the Seroquel it wasn't helping me in anyway and I gained so much weight. In 2012 I was diagnosed with Bipolar and my psychiatrist put me on 300Mg Effexor, 20Mg Olanzipane and 1000Mg of Valpro. After 10 months I was able to stop taking the Valpro and Olanzipane. No matter how much weight I lose, I always appear so puffy and bloated in the face, especially under my eyes, they look like I haven't slept for weeks. I have very low self esteem as it is, this is making me feel miserable. I should also mention, that i got down 1MG of the Suboxone, after various stresses I went right back up to 18Mg. I have finally started to turn a corner and I am now reducing my dose at the right pace. It would make me feel so much better if I knew if even one more person was having this experience. Any feedback would be so appreciated. I send this with love from Australia :)
    Reply

More questions for: Suboxone, Bone and joint pain

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

  • Faslodex driven hell
    (Posted by a 60 year old woman who has Depression, Stamina, Breathing Difficulty, Muscle Pain, Bone And Joint Pain, Cough, and takes Faslodex)
    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???
  • Pacemaker experience
    (Posted by a 62 year old man who has Heart Rate Decreased, Sick Sinus Syndrome, and takes Suboxone)
    I had a pacemaker installed about 5 weeks ago. I went to the doctors because I was feeling fatigue, shortness of breath, I felt as if someone was holding my heart in their hand and I had some confusion and dizziness.

    To get to the point, after my first visit with my PCP I decided to go directly to emergency via 911 since my PCP was basically ignoring, or better put, had no sense of urgency regarding how I was feeling even though she knew my heart rate had dropped and was steady at 44 bpm, my normal rate 62 bpm.

    The night I was in observation at the hospital I dropped to 20 bpm, next day I had a pacemaker installed, had I not taken the initiative to call the hospital I don't know if I would have continued dropping until I was dead, I don't know enough about the science behind this to draw that conclusion but common sense tells me yes.

    I have explained this in another post but I cannot find it, not sure what I am doing wrong, so I am writing another post because I have more to add after a couple of weeks since my last post.

    The issue I have is I am still tired after more than a month after the installation of the pacemaker. I had the bpm (beats per minute) on my pacemaker increased from 60, the factory settings, to somewhere in the mid 60's.......so I thought. I went to the hospital twice to have my pacemaker "tweaked" but when I met with the cardiologist for my "one week" follow up, which took almost three weeks to see him due to his heavy schedule, he told me there were never any changes made to my pacemaker, I was still at 60 bpm. How could this be since I was told twice it had been increased? I had the wand on my chest and the nurse made the changes which were made due to my complaining about being exhausted still, the reason I went to the PCP in the first place five weeks ago.
    Was she playing mind games, thinking the power of suggestion would make me feel better? If so I am disgusted to think she would feel I was faking my feelings of exhaustion, what she did had absolutely no effect on how poorly I was feeling.

    To get to the point, I finally had my first meeting with the surgeon, he raised my bpm to 75 from 60, was going to go to 80 but changed his mind. The moment he made the change to 75 bpm from my original 60 he asked if I was feeling better, feeling better after 60 seconds of changing the bpm, how is that possible? I told him no, kind of too soon to tell. His reply was "it looks like we have done everything we can on our end, your heart was not significantly damaged, your pacemaker is working as it should, therefore there must be something else making you feel so poorly so I suggest you see an internal medicine specialist." My brain had a big WHAT sign flashing, I couldn't believe what he was saying, basically beat it and move on, I don't have the time to deal with you anymore. Lets see, the appointment lasted 25 minutes and he does not have the time to work with me anymore, sorry but that irritates the hell out of me.

    He was washing his hands of me, nothing else he could do so spend time and money finding out what the problem is with an internest, it is not my heart according to the cardiologist. The appointment ended and I left wondering how I was going to find out what is causing my issues.

    To my great fortune a nurse with 20 years experience teaching doctors and nurses how to use the pacemaker computer asked me to come into her office after my appointment with the cardiologist, she asked me this prior to seeing the doctor. Thank God she did as the doctor did not do a thorough job adjusting the pacemaker, she adjusted what the doctor had, tweaked the pacemaker a bit, had me walk for 10 minutes and come back to the office and did a bit more tweaking, I slowly started feeling a touch better. She asked me to come back in two weeks and she would see if the pacemaker needed to be tweaked a bit more. I was walking on air, still not close to my "normal", thrilled I was not just a number being tossed in the heap of unfixed people. I am feeling 70% better than how I felt prior to the doctor and her tweaking the pacemaker. Had she not been there that day and had the opportunity to do this I would be on a never ending search for what is making me feel so exhausted and!
    dizzy.

    There is a moral to this which I will let you draw your own conclusion. In my mind it is trust God will intervene, he certainly did when the nurse asked me to see her after the appointment with the surgeon. The reason I feel this way is because she was there and is only there on Fridays, the day I had my appointment. I never would have gone back again after my meeting with the doctor and I would have been spending needless hours and money looking through the wrong box for what ales me. Now it is obvious it was my pacemaker settings, my heart rate was set too low and the pacemaker was not fine tuned properly with the proper slope and other settings.

    Don't let these doctors do what mine tried doing with me, be aggressive and insist on more adjustments if you have issues similar to mine.

    AS I sit here I am still tired, I could easily take a nap but I am better than I was yesterday, significantly.

    Best of luck to all. Your comments will be very much appreciated.
  • Cymbalta caused joint pain
    (Posted by a 50 year old man who has Pain - Joints, and takes Cymbalta)
    I had taken Cymbalta for about 1.5 years and after taking it for a few months, I started having widespread joint pain. The joint pain has gotten worse and is becoming debilitating. Joint pain in the literature as a side affect of the drug but the joint pain seems to be permanent! I have not taken Cymbalta in a couple years but the joint pain has remained. I have had blood tests and my doctor says the tests show it is not arthritis.
  • Yawning after taking sub
    (Posted by a 55 year old man who has Watery Eyes, Runny Nose, Yawning, and takes Suboxone)
    Within a few minutes after I take my Suboxone film I seem to get intense yawning event along with runny nose & watery eyes lasting 5-15 mins. Sometimes I can make it subside by drinking a lot of water if I am in a place I can get it. I have been on Sub for approx 5 yrs. & have only noticed this side effect during the past 1 yr or so. It doesn't seem to matter if I take 1/2 or a whole film, (4mg or 8mg.)
    While this isn't life shattering it can be quite annoying if I am out in public, at work, etc. The yawning gets so intense at times I feel like my jaw will unhinge & can't control it at all.
    It seems paradoxical to me. Previously taking Sub would stop any typical opiate withdrawal symptoms such a yawing & runny nose & eyes. Now it actually causes this effect. I don't get any other feelings of going into withdrawal. Just those I mentioned. Could it be a reaction to the naloxone?
  • Xylitol caused joint pain
    (Posted by a 1 year old girl who has Joint Pain, and takes Xylitol )
    For over a year I was chewing nicotine gum with xylitol. During that period I developed worsening joint pain to the stage where I was diagnosed with fybromyalgia (there was no other explanation for the pain). The chemist changed the brand of 2mg gum and I instantly felt better chewing it. After a week of feeling great I investigated what was missing in the new gum ( which was much less sweet) and it was xylitol. If I chew two or three pieces with it I begin to ache ( as an experiment done once)
    I wanted to share this for ianyone else out there chewing gum and experiencing chronic pain. And yes, I know it should have got off the nicotine by now!

More reviews for: Suboxone, Bone and joint pain

Comments from related drug studies (Check your drugs):

  • After 3-4 days of taking adderall or any stimulants I start to get pimple like sores on my scalp, nose,eyes,mouth,face and vaginal area puss comes out of mi eyes and vaginal area. It seems like every hair follicle or cut becomes clogged and filled with puss. It burns when I use the restroom. My ey ...
    Reply
  • Was on sulfasalazine but made me unwell...changed to methotrexate but stopped because of blood results. Have raised blood sugar from steroids. Frequent urinary tract infections and self catheterisation. Retinal haemorrhage ( blots and dots) just discovered by optician with severe dry eyes
    Reply
  • the joint pain isn't as bad as the swelling!!! its been random & moves from joint to joint...my hands & fingers more severe...ive never had these symptoms before!! my doctor has run RA panels, MS panels etc...waiting on results!! started me on Mobic.....absolutely cant tell ive taken anything...no s ...
    Reply
  • I have always had brilliant naturally white teeth and since I started taking suboxone for pain management in lieu of methadone and hydrocodone my teeth are now grey/beige! I am really upset because the medication seems to work well. I am thinking it is because it dissolves in my mouth and I do not s ...
    Reply
  • I had surgery 5 weeks ago. Was on Norco before surgery and then after surgery. After surgery I developed terrible joint pain in fingers, knees, and terrible pain in bottom of feet. Difficult to walk
    Reply

More related studies for: Suboxone, Bone and joint pain

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

 
© 2014 eHealthMe.com. All rights reserved. Use of this site constitutes acceptance of eHealthMe.com's terms of service and privacy policy.