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Review: could Methadone hydrochloride cause Heart rate decreased?

Summary: Heart rate decreased is reported only by a few people who take Methadone hydrochloride.

We study 2,080 people who have side effects while taking Methadone hydrochloride from FDA and social media. Among them, 3 have Heart rate decreased. Find out below who they are, when they have Heart rate decreased and more.

You are not alone: join a mobile support group for people who take Methadone hydrochloride and have Heart rate decreased >>>

 

 

 

 

Methadone hydrochloride

Methadone hydrochloride has active ingredients of methadone hydrochloride. It is often used in pain. (latest outcomes from 2,842 Methadone hydrochloride users)

Heart rate decreased

Heart rate decreased has been reported by people with high blood pressure, multiple sclerosis, pain, depression, osteoporosis. (latest reports from 11,761 Heart rate decreased patients)

On Dec, 31, 2014: 2,078 people reported to have side effects when taking Methadone hydrochloride. Among them, 3 people (0.14%) have Heart Rate Decreased.

Trend of Heart rate decreased in Methadone hydrochloride reports

Time on Methadone hydrochloride when people have Heart rate decreased * :

n/a

Age of people who have Heart rate decreased when taking Methadone hydrochloride * :

0-12-910-1920-2930-3940-4950-5960+
Heart rate decreased0.00%0.00%0.00%0.00%0.00%33.33%66.67%0.00%

Severity of Heart rate decreased when taking Methadone hydrochloride ** :

n/a

How people recovered from Heart rate decreased ** :

n/a

Top conditions involved for these people * :

  1. Atrial flutter (1 people, 33.33%)
  2. Hiv infection (1 people, 33.33%)
  3. Anxiety (1 people, 33.33%)
  4. Drug dependence (1 people, 33.33%)
  5. Sleep disorder (1 people, 33.33%)

Top co-used drugs for these people * :

  1. Aspirin (1 people, 33.33%)
  2. Seroquel xr (1 people, 33.33%)
  3. Flecainide acetate (1 people, 33.33%)
  4. Coumadin (1 people, 33.33%)
  5. Digoxin (1 people, 33.33%)

* 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 Heart Rate Decreased while taking Methadone Hydrochloride?

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- support group for people who take Methadone hydrochloride and have Heart Rate Decreased
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- support group for people who have Heart Rate Decreased

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Can you answer these questions (Ask a question):

  • Can long-term methadone use cause or increase the risk of colon cancer?
    I had a two-level spinal fusion at L4-S1 in 2000 after being injuried at work in Sept. 24, 1997. I lost everything after...the unjury, ability to do my job, my wife and family (couldn't take the strain) my home, my sense of self and purpose, direction and belonging...credit rating and ability to pay my bills.
    After a long period of waiting to settle my workmens' comp. case, I returned home, from the Bat Area back to Arizona to take of my mother with a yet un dianosed case of moderate dementia.
    Then, in 2011 I had a 2nd surgery to relieve spinal stenosis btwn. L2-L4, just above the fusion site.
    I've been taking methadone since early 2004, a little over ten years, now. I've had high blood pressure since my injury.

    Now, I waiting to be scheduled for a colonoscopy, with my father having had polyps and the way I've been feeling..drained, tired all the time, and stomach pains ( in addition to my chronic low back pain), I...
    find myself wondering if there is any relationtionship between the methadone and other meds and cancer?
  • Can methadone cause my aynurism to burst?
    A doctor is lowering my dose of Methadone I take for severe back pain due to my aneurysm because he said the Methadone could cause a stroke w/my aneurysm. Has anyone else heard of this? Thank you!!!
  • I am prescribed methadone and lamictal. at my peak, i nod a little. is this normal? (2 answers)
    I began taking Methadone during my pregnancy per Drs order. I was only on Vicodine, Ambien, Seraquil and Lexapro and stopped immediately after the positive pregnancy result. I have never experienced the nod before. I hate it. Am I the only 1? I'm only on 55mgs of Methadone and 25mgs of Lamictal.
  • Treatment for a dvt in person with lung cancer
    Have contracted a large painful DVT in groin thru calf. Hospicis doctor will only administer Aspirin 325 mg. what I have researched does this not address dissolving clot. Hospicis doctor told me the tumor lung cancer was more likely to bleed with treatment to dissolve clot. She was negative and said the lung cancer was going to cause death anyway so she wouldn't treat large painful DVT because it may cause bleeding, i.e. more harm.



    Can anyone tell me if use of warfarin or other blood thinners are less likely used in lung cancer patients? When admitted to Hospicis in Dec I was on Warfarin and continued use for several weeks until Hospicis stopped treatment.



    I'm considering leaving Hospicis and returning to my previous doctors. I am significantly improved now from Dec. My oxygen use was 5 lt when admitted to Hospicis and now almost never require oxygen use.
  • Is it safe to take methadone(52mg daily), metoprolol extended release(75mg daily) & xanax(1mg twice daily) (2 answers)
    I'm just wanting to know if its safe to take all 3. I've been on methadone for 7yrs and about a yr ago i started tapering and started at 130mg, but am now at 52mg. I've been on the Metoprolol(extended release) for about a yr now taking 50mg in AM, and 25mg in PM. I just started taking the Xanax about 3wks ago .5mg twice daily/as needed. Stopped taking birth control 3months ago, so wondering if some side effects are because of the birth control, and not the other meds. Thanks!

More questions for: Methadone hydrochloride, Heart rate decreased

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

  • Methadone and forgetting basic things.
    I have been in MMT (Methadone Maintenance Treatment) for around 7 1/2 years for chronic pain. I have gotten to where I forget things that I never would or did before and the longer in time the worse it has gotten I am currently looking at some different meds for treatment. The loss of memory is everything from childhood memories to what I did yesterday I may pay something and if I dont write it diwn I will forget it things I have known all my life I have forgotten. I can't say 100% it is from the MMT or not however I will sag I had no such problems before and I am at age 38 so I believe I am much too young to have severe memory loss that I am currently experiencing and whats scary is what if it never comes back and continues to decline?
  • 3 strong drugs together against neuropathic pain
    Neuropathic pain debuted when I was 24, now I'm 50. Received diagnosed with Ehler-Danlos syndrome (EDS), joint hypermobility type, when I was 35 years old. So it can take some time to get a diagnose. And as EDS-patient I do not belong to any clinic. Orthopedics says that EDS is not orthopedic, rheumatology says that EDS is not an autoimmune disease, GPs say that EDS is too difficult, and so on. Sooner or later we all end up at Psychiatry, even if we are not depressed.

    The first kind of pain I got when I was 24 came from low back, but I experienced as pelvic pain and leg pain. It was clearly a neuropathic pain, but it took years to find out. Later it was treated by a pain clinic with cortisone around the genitofemoral nerves (both sides). Since this treatment didn't result in lasting freedom from pain, the pain clinic started to give me RF (radio frequency) treatment. This made the pain disappeared after one year, and I was 80% free from it between 2002 and 2014, 12 years. The pain doctors said pain could return after 10 years.

    The other kind of neuropathic pain started 2003 with intense stomach pain. During 6 months I could hardly eat nothing due to nausea and vomiting. After this 6 months, stomach pain changed to almost unbearable pain in upper back.
    What happened 2003, and what all the doctors missed, was that the right lowest ribs slid up over the sternum. This rib dislocation is till there today, but now with a lot of cartilage formed around the rib where it is stuck in the lower end of the sternum. The dislocation is clearly visible on X-ray. This has greatly affected the thoracic spine. I have a scoliosis which I had not before 2003. And I still have severe pain in the thoracic spine.

    It was initially treated with morphine daily, and later with Durogesic (fentanyl), but this didn't help much. 2005 I was hospitalized because I had too much pain to take care of myself and my hygiene. After some months the doctors started to give me clonazepam because the muscles along the spine was in a chronic seizures. Clonazepam helped, but I could still have a lot of pain in two vertebrae in the thoracic spine. It felt as if someone drilled into the vertebrae without anesthesia. After a few months, doctors also prescribed me methadone. Then the pain disappeared almost completely. Since 2006, I have eaten clonazepam and methadone every day, and I need to sleep in an armchair to not get more pain because of moving during sleep.

    There are side effects. After 1,5 years with clonazepam and methadone I started to have panic attacks. Or rather one long panic attack which didn't stop before I got treatment with amitryptilin and pregabalin (Lyrica). These 2 medicines stopped the panic disorder completely after some hours, and the panic was then gone. Then I got side effects of these 2 medicines, amitryptilin & Lyrica, too. I gained a lot of weight (from 83 to 148 kg) and got much water (edema) in both my legs under the knees and in both feet. The feet could swallow to the double size. 2012 I stopped with amitryptilin and started to loose weight again (in Aug 2014 below 80 kg) and get less water in my legs. Today I eat as little medicines I can, but I have to take methadone, clonazepam and Lyrica every day, twice. If I try to take away one of these 3 medicines, I got pain problems at once. Lyrica is the most painful one to take away. In Sept-Dec 2013 I lowered Lyrica from 300 mg daily, to 150, then to 75 and finally 0 mg. The pain I had was extremely difficult to handle. It didn't help to take more methadone or anything else. I have checked on Internet and found that many people got pain from quitting with Lyrica. Most people start eating it again. So did I. But 2006 and 2007 it was enough to treat the pain with methadone and clonazepam, I got the Lyrica against anxiety not pain. But today I take Lyrica against pain.

    Beside weight gain and leg edema, clonazepam and Lyrica significantly affect the sexual desire. And Lyrica alone makes it almost impossible to ejaculate. All four drugs together (clonazepam, methadone, amitryptiline and Lyrica), make one forget all about sex life. You don't even miss it. When I stopped with amitryptiline and lowered Lyrica (still taking clonazepam and methadone), I could suddenly easily get erections again, feel desire, but not getting orgasms. This is quite difficult to deal with.

    The pain pattern is greatly affected, by pain and by the medicines. So is the mood. I get something which feels like heavy depression, especially if I take the medicines late that day. I should take a medicine like methadone 3 times a day, because the effects of the tablet lasts around 8 hours. But I take them every 12 hours, to have a low consumption in case doctors prescribe them too late (which happens, and then it's good to have a spouse going to the pharmacy buying them for you, because you have too much pain to go yourself).

    Since methadone is also used for treating heroine addicts, medical staff treat you with disrespect when they see that it says "methadone" in your health record. I need to show a certificate that says that I deal with chronic neuropathic pain, that I never have had problems with drug addiction, to get normal respect.

    I wanted to share this because I think I am alone in the world with these medicines in combination against neuropathic pain caused by hypermobile joints, joint dislocation and muscle spasms. After trying almost everything else, including surgery cutting nerves, methadone, clonazepam and Lyrica seems to be the only way to kill my pain. But it's a life where you always is questioned, because of the use of methadone. I can guarantee that everybody in the world should accept these medicines if they had experienced the unbearable pain I had in upper back before they started to give me clonazepam and methadone.
  • Pacemaker experience
    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.
  • Nexium improves my constipation
    Started taking Nexium 1 week ago and I noticed improvement with my chronic constipation.
  • Xanax bed wetting will it stop and do i wear diapers or die (1 response)
    I am on the very edge of crazy. So starting this is pushing ne way over. I'm 49 for crap sakes. I am so tired of the pain in my body and I am just tired, this is the last slap I can't anymore. Naturally alcohol I am sure is just about the end game along with cuts.
    Just want to bleed out and not hurt anymore and be so scared to leave my house or sleep. I just want to sleep forever.

More reviews for: Methadone hydrochloride, Heart rate decreased

Comments from related studies:

  • From this study (2 days ago):

  • I take a lot of medications other than Methadone as follows:
    1.Remeron (30 mg daily)
    2. Elavil (100 mg daily)
    3. Trazadone (300 mg daily)
    4. Cymbalta (120 mg daily)
    5. gabapentin (1600 mg daily)
    6. vistaril (75 mg daily)
    7. Vytorin (10/40 mg)
    8. synthroid (100 mg.)

    Reply

  • From this study (1 month ago):

  • Rosacea appeared after a few months on Methadone.

    Reply

  • From this study (2 months ago):

  • I have pain on the left side of my chest below the rib cage, but I can't seem to find it though when I push on that area, but when I move or cough can feel it there. It comes and goes, but always seems to be there. I drink coffee, and have just started using a morning egg white protein mix by Jay Robb the last few weeks, along with an energy supplement. It seems to be more pronounced now, and I am contemplating seeing a doctor. I figured I had pulled stomach muscles on that side as I know that can also make this type of pain. Pushing on it doesn't locate the pain. I have had this more than a year, but since it comes and goes figured it was an ulcer.
    Could it be a simple ulcer brought on by years (12) of methadone use? I use between 10 to 15mG/day which isn't a lot but I did use more when the pain was worse. I had been using up to 30mg/day about three years ago and started using less as the pain seemed better. I had surgery for a ruptured C5/C6 disk (no fused disk) in 2001 and that never got rid of all of the pain in arm/hand and left side of neck, though it did take care of the pain in between my shoulders. I took oxycontin for the first few years up to 60mG/day, and then started methadone treatment as it was cheaper, and the results were as good.

    Reply

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