Pain Management :: DNA /genetic Test To Determine Medication?
Nov 12, 2014
Has anyone had a DNA test to determine the effectiveness of pain medication? I have chronic 24/7 migraines and take high doses of Dilaudid (16 mgs) every 3-4 hours. Even at this dosage the pain is only reduced to about a 6 on the pain scale. What were the findings from your test? Did it provide any useful information or was it a way for my pain management dr to pad his pockets? As it is I have to see him every 4 weeks and provide a urine sample every other month. After 4 years you would think he could rest assured that I am not taking more than prescribed. I'm just afraid he looks at me like a way to make more money. Any, I digress. Please let me know about the DNA testing.
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Is there a blood test that is done to determine if someone has Autoimmune disorder?
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I was recently tested negative for all STDs except herpes type 2 which I have had for years and so wasn't tested. I forgot to tell the doctor I am on Valtrex 500mg daily for suppressive antiviral treatment. Can this have an effect on the results of the tests for gonorrhea, chlamydia, syphilis, HIV, or hepatitis (hepatitis)?
Can I reply on the negative results or do I need retesting after coming off the herpes antiviral medication?
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I have been taking antidepressant for almost an year. I changed few brands, nothing was helpful for me.
Recently I learned that there is a genetic test for antidepressant. I wonder if I can order it by Internet. I live outside of US and here there is no chance to find one.
Do you know if it's possible to order genetic test kid by Internet?
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I've already wrote a post below but just wondering if anyone knows how long the genetic test takes. I had mine two weeks ago but have now been told it could be 4 - 6 weeks. My bloods came back showing that I am anemic so my doctor doubts I have HH anyway. I have all the symptons and now waiting to be referred to gastro for my third lot of investigation. I am thinking the doctors really are not clued up about this at the moment.
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I have been living with neuropathy pain for about 4 to5 years now. it seem as of lately that about 5 to 10 minutes after I take my pain medication that pain get strong for about 15-20 minutes and then the meds kick in and ease the pain. is this normal?
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I was switched from Nucynta 50mg to to Opana 5mg (OxyMorphone) by my Pain Mgt doctor and I have a total different experience. I don't know if they messed up or what, but here's the issue.
While I was on Nucynta, I would take it, and eventually feel the effects, i.e. the lightheadedness, the "high" feeling, and also the pain relief. The reason I was switched was that Nucynta gave me migraines. Bad enough where I got ill and had to run to bed with all lights off.
Onced I was switched to Opana 5mg, things were different. I took 3 last night, my very first dosage, and took the first. No effects, no pain relief, no "high" feeling, nothing. So, about a hour and fifteen minutes later, I took another one. Still nothing. So I wait again, same amount of time, took a third pill...... Nothing.
So, when I saw the doctor originally and was switched, I was told that Opana was an equivalent to the nucynta. So, if it's an equivalent, why did I go from 50mg to 5mg? I'm just curious. I know they are different drugs and probably manufacturers. Can anyone shed some light on this bizarre issue?
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I was in a car accident about a week ago and 4 days after the accident I started having pain on the left side of my ribs right under my breast when I take deep breathes, yawn, sneeze, ect. It a little swollen but doesn't hurt to touch. what could this be?
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Couple days ago I stepped out of bed and almost hit the floor as the excruciating pain shot through my calves. I have not exercised or done anything extreme. I have tried stretching and over-the-counter pain meds ..
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I have excruciating pain on my right side almost constantly and when I take a 1mg xanax, my pain goes away. Why is this? A Lot of people question this when I tell it but in all honesty it works. I wouldn't be telling it on here as telling it on here doesn't benefit me at all. I would just like to know why a xanax will stop my pain on my right side. Any ideas?
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I have asked to be removed from all pain medications as they were not helping at all and did not want to just keep increasing dosage. So my PM Dr. suggested i try Ativan or Diazepam before bed and also a muscle relaxant called Baclofen for spasms during the day (which i had been on in 2013) it did not work, but he insists on trying it over the Soma 350mg i had been on before the surgery.... any input
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I have been on 3 pills a day of norco 10/325, I want to slowly taper off. I need a plan that would be with no W/D's. I thought about starting a reduction of 1/2 a pill every week until I am free of the pills.
I also need to stop taking celexa, I am going to cut back 1/4 a week to iam off.
Will this work?
Or do I need to get suboxone and is that addicting.
Once off the pills, I don't know what I will do about my chronic pain.
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My dr. did a CT scan on my left side to see if I had sciatica as I had a lot of symptoms of it. It showed minimum damage to the nerve. I was not told what to do next? Should I get a follow up with what kind of specialist? Would a MRI show more information then the CT scan?
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will i have withdraws after taking suboxone 3 weeks? they put me back on pain meds because i having surgery soon
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I went to my Pm yesterday and let him know that I wanted off the methadone. So since I had to see the NP because it was considered an emergency visit they decided they were going to put me on the patch where you wear it for three day then take it off. So I asked about the side effect and after hearing them something in me panic and snapped and I said forget I want off of everything. So as off right now I am coming off of the methadone. I decided that with the scare of my heart and the new neurological problems they only way to know is if I come off of the meds. I am still on the Topamax he did not want to take me off of that because I have been on it for over a year and never had a problem. SO I am hoping in with 2 months we will know if it was the meds causing the neurological problems or the something else.
What made me snap was I was telling him that I wanted something for the muscle because I was having a lot of spasms and tightness and off of the methadone and he totally ignored me and said well we are going to give you something a lot strong and this should work since the methadone has not been working. It was as if he was not listening to me. He said to me you are going to Cleveland clinic (CCF) to be treated for the muscle so the will figure it out soon, I said yes but I do not get medicine from them because I have a contract with you. I don't know why he would not give me a muscle relaxer but I feel better knowing that I am coming off of the medicine for a while I just hope I can handle the pain long enough to see of it is neurological or a side effect from the methadone....
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.I had a C5-C7 disc fusion done 5 years ago that alleviated all of the pain in my neck and shoulders. What I am left with is a severe case of peripheral neuropathy. My feet and legs are numb to the touch but hypersensitive when I walk so I cannot go very long distances without the tingling burning throbbing pain. This pain is heightened at night when I go to sleep thanks mostly to the 300mg of Lyrica twice daily. I had an EMG nerve conductivity test performed which of course indicated severe neuropathy.
Now I am going to a neurologist who says I have to put up with the pain. I am going back on Monday to my neurosurgeon to ask for a lower MRI (never done) and I wanted a referral to PM because the pain is out of hand on 600mg of Lyrica daily. I have been on Oxycodone before and hated it and I do not like the stigma attached to these drugs so I thought I would ask my doctors to consider Methadone. What does everyone think? I know Methadone has its own stigma but is long acting and something I NEED right now and probably for good as I have had this neuropathy for 5 years.
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I have suspected Piriformis Syndrome & SI Joint Dysfunction also causing sciatica, have also had some nerve pain in the back of my thigh, occasional calf cramps, foot cramps, and foot pain. Since my last Cortisol injection into my SI joint it has made everything horribly worse, I cannot sit now for very long without severe left foot pain that makes me feel nauseous it's so horrible. I have informed the consultant of this and am on a waiting list to go back and see him, this is the 2nd time the injections have caused me extra pain so have now lost faith in these and want to try alternatives.
My consultant previously wanted to put me on Amitriptyline but I have been on this before and was taken off it due to serious sedative side effects (even fell asleep eating in a restaurant) was on a small dose and still didn't improve with time. So I've read that Nortriptyline is an alternative with less side effects, can anyone advise if they have had less sedative side effects with this than Amitriptyline please?
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So I'm on 10 mg norco 4 x daily. I keep telling the doctor if I can take 5 a day because 4 isn't enough and I'm in a lot of pain. he doesn't even respond I'm frustrated. Should I ask for percocet 4 x daily.
Wouldn't I have to take 10mg percocet for it to be stronger then 10 mg norco since percocet 7.5 mg is equivalent to 1o mg norco
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I have a few questions about withdrawal I have been taking between 2-4 Norco 5/325 for the last year for pain and i'm ready to get off but im so scared to go through the withdrawls so i'm wondering ow bad it would be I have read so many stories on the internet but they are taking way more then me any advice would be great I want my life back......
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So told doctor about fentanyl issue and he said we could give Percocet a try again. Ni was getting nausea from it before. So I said ok, now have a script for 90 Percocet 7.5mg. Just had 60 Norco filled last Saturday hoping this won't be an issue at pharmacy. He said the Percocet will be more effective for pain. Also I have a box of unopened fentanyl patches. Can I return them to the pharmacy? I don't want to have pharmacy and my insurance think I'm stocking up on meds.
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i took norco for first time it made me feel jittery doesn't have the same ingredients as vicodin. maybe it was just my nerves?
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