Review: could Suboxone cause Tardive dyskinesia?
Summary: Tardive dyskinesia is reported only by a few people who take Suboxone.
We study 7,235 people who have side effects while taking Suboxone from FDA and social media. Among them, 3 have Tardive dyskinesia. Find out below who they are, when they have Tardive dyskinesia and more.
You are not alone: join a mobile support group for people who take Suboxone and have Tardive dyskinesia >>>
Suboxone has active ingredients of buprenorphine hydrochloride; naloxone hydrochloride. It is often used in opiate withdrawal. (latest outcomes from Suboxone 8,267 users)
Tardive dyskinesia (a disorder that involves involuntary movements) has been reported by people with indigestion, abdominal distension, bipolar disorder, depression, gastrointestinal disorder.(latest reports from Tardive dyskinesia 23,204 patients)
On Nov, 28, 2014: 7,235 people reported to have side effects when taking Suboxone. Among them, 3 people (0.04%) have Tardive Dyskinesia.
Time on Suboxone when people have Tardive dyskinesia * :
Gender of people who have Tardive dyskinesia when taking Suboxone * :
|Tardive dyskinesia||33.33%||66.67% |
Age of people who have Tardive dyskinesia when taking Suboxone * :
|Tardive dyskinesia||0.00%||0.00%||0.00%||0.00%||50.00%||0.00%||50.00%||0.00% |
Severity of Tardive dyskinesia when taking Suboxone ** :
How people recovered from Tardive dyskinesia ** :
Top conditions involved for these people * :
- Gastrooesophageal reflux disease (1 people, 33.33%)
- Vomiting (1 people, 33.33%)
- Abdominal pain (1 people, 33.33%)
Top co-used drugs for these people * :
- Bactroban (2 people, 66.67%)
- Oxycodone hcl and acetaminophen (2 people, 66.67%)
- Diazepam (2 people, 66.67%)
- Protonix (2 people, 66.67%)
- Promethazine (2 people, 66.67%)
* Approximation only. Some reports may have incomplete information.
** Reports from social media are used.
Comments for this study:
laurenS (10 months ago):
I went through something very similar. I was in rehab and on a suboxon taper. I was completely off for about 2 days when all of a sudden I lost control over my tongue mucsels and by tongue began trashing and sticking out of my mouth uncontrollably. I also went to the er and they gave me 75 mg of benadryl and my symptoms lessened a lot. I also had uncontrolled twitching of my hands and feet. This symptoms started again as soon as the benadryl wore off, they also seemed to get worse the more anxiety i was under or more stressed i became. I went back on suboxon and i have not had another episode of what seems to be tardive dyskensia
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Jimmy gotti (10 months ago):
I was wondering if go I.g off suboxens will cause tardive dyoskinesia be cause I went a couple days of suboxens and I found myself at a hospital diagnose ,d with tardive dyoskinesia my jaw locked up and thrashing of the tounge and I was treated with 75 ml of benadryl three a iv and it went away within 1 minute it was so severe I'm scared to death of it coming on again , and I've been clean clean only taking suboxens can you give me answer???
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Do you have Tardive Dyskinesia while taking Suboxone?
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- support group for people who take Suboxone and have Tardive Dyskinesia
- support group for people who take Suboxone
- support group for people who have Tardive Dyskinesia
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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!
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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.
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