Guest guest Posted February 5, 2012 Report Share Posted February 5, 2012 This is for M. I noticed your on the patch, I was on that too and it worked great but I couldn't figure out how to keep it on and take a shower. I too can drive with my pain medicine. with out my pain medicine heck no though, but my husband is afraid of me driving and scared of me getting pulled over but I have a clean record. any tips of how to keep the patch on for me would be great cause I am tempted to go back to that pain doctor cause he would give me the patch but I don't know how to keep it on during the summer. Thank you for all the advice in the world. in Az age 32 --- M. wrote: > > I am on Duragesic (3 100mg/hr patches every 48hrs; delivering 450mcg/hr) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 5, 2012 Report Share Posted February 5, 2012 My doctor gave me a constant supply of boxes that are filled with this material you put over bandages and etc. to keep them on. These things are so thin its like really fine fine plastic that is sticky. I can't remember the name. I can't get out of bed right now but I will post the name later. The doc also gave me an inhaler pump with steroids to spray straight onto my skin before I put the patch on so that the patch wouldn't eat up me skin > wrote: > any tips of how to keep the patch on for me would be great cause I am tempted to go back to that pain doctor cause he would give me the patch but I don't know how to keep it on during the summer. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 11, 2012 Report Share Posted February 11, 2012 TegaDerm or Askina Derm clear dressings (large versions of what they put over an IV in the hospital) work WONDERS. Most insurance will cover them. I get them delivered (for free) by National Rehab (nationalrehab dot com). One of the many reasons that I like them is because they work with almost every insurance company in the country. Sorry that it took so long for my to reply, my health has been VERY bad lately. Plus, I got kicked out of my pain management doctor's office for missing an appointment because my father in law (who was supposed to drive me there) fell a few hours before and ended up in the ER. Steve M in PA > wrote: > any tips of how to keep the patch on for me would be great Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 11, 2012 Report Share Posted February 11, 2012 where do you put your patch? that sucks that you got kicked outta your pain doctor. I have yet to get my blood and drug testing done plus see my primary care doctor again for a new pain doctor, damn me!! I can be so damn lazy and I guess it's just much easier to stay in bed in the cold. well my husband wants me to find a pain doctor that will give the methadone to me considering he said it's the only medicine that will make me do anything and he is probably right, i have a bad habit of forgetting stuff, he don't forget much. so if I was to go back to the patch, that's what works for you, where to you put your patch on?? Thanks in Az > M. wrote: > TegaDerm or Askina Derm clear dressings (large versions of what they > put over an IV in the hospital) work WONDERS. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 11, 2012 Report Share Posted February 11, 2012 rub some rubbing Alcohol let it dry then put it on > wrote: > any tips of how to keep the patch on for me would be great Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 11, 2012 Report Share Posted February 11, 2012 and i forgot i would put it on my left or right side of my chest > wrote: > any tips of how to keep the patch on for me would be great Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 12, 2012 Report Share Posted February 12, 2012 Try using ace bandage to keep in place. I use it to hold ice pack in place. Works well on knee and leg. Â Â Â Viv in C.T. > wrote: > any tips of how to keep the patch on for me would be great Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 13, 2012 Report Share Posted February 13, 2012 There are several approved locations, but I find that the best location (for me and for my wife) is on the upper arm, but sometimes I will put it on my lower arm when the skin on my upper arms needs a break. My wife used to put it on her upper back, but her shoulder blades cause too much motion which cause too many issues with patch adhesion. The MOST IMPORTANT factor in patch placement is how much that skin moves. Loose skin causes issues. Methadone is nice because it is cheap and affects the kappa opioid receptors as well as the mu-opioid receptors. The only reason it isn't my primary pain medication is that it has to be taken 3-4 times per day when used for pain. It has a very long half-life, but pain relief wears off after 6-12 hours (for most people). The other problem with methadone is that there is no extended release form. Also, the largest pill is 10mg, so if you take 100mg/day, that's ten pills and some people take more than 100mg PER DOSE (up to 40 pills per day). Methadone also requires an EKG before starting it and another every 6 months to monitor for prolonged QT syndrome. Some doctors will also want regular blood tests. Duragesic is nice because it needs changed only once every 2-3 days. Most insurance makes you start out with once every 72 hour dosing. Once my dose was increased from 12mcg/hr to 25mcg/hr I could feel a drastic reduction in pain relief and withdrawal symptoms 12 hours before each patch change, which continued until roughly 12 hours after each patch change (the medication goes from the patch to SubQ fat to blood, which take 12 hours). When I told my doctor about it wearing off 12 hours before each patch change, she wanted my to change it every 60 hours (2.5 days), until I reminded her that it takes twelve hours for a patch to kick in and then she switched me to 48 hour dosing. If you and your doctor decide that Duragesic is for you, you may want to keep an eye out for this, and if you have problems, immediately report them to your doctor. I have talked to (both verbally and online) dozens of people who have used Duragesic as well as a dozen or so doctors and pharmacists and not one of them has EVER even so much as heard of a patient doing well on 72 hour dosing, they all required 48 hour dosing. When you start Duragesic, you need to be opioid tolerant (taking at least 30mg/day oxycodone, 60mg/day morphine, or equivalent) for the 25mcg/hr patches (or stronger). They came out with 12mcg/hr patches (which deliver 12.5 mcg/hr of fentanyl). My doctor had me on 30mg/day oxycodone and switched me to 12mcg/hr fentanyl, which caused me to go into withdrawal. Duragesic has worked well for me, but it is not for everyone. Both methadone and fentanyl can have life threatening side effects if doses are increased too rapidly. If you end up on Duragesic, I recommend that you go on the generic Mylan pacthes as they are matrix based (no reservoir) and slightly safer than the reservoir based Actavis patches. I have no experience with the new Sandoz patches, but they are matrix based. Sandoz patches are authorized generics, meaning they are manufactured by and identical to the name brand Duragesic patches (except they say fentanyl instead of Duragesic). Mylan will also provide Askina Derm free of charge (Sandoz doesn't). They will mail you a form you have to send back. They'll ask you to mail it, but you can email or fax it to get them faster and avoid the postage (just ask them for the email or fax to send it to). If anyone needs the email of the person at Mylan who handles this, I can look it up in my email. I like the Tegaderm better, so I order them. Plus, I am on the largest patches (100mcg/hr), which are too large for the AskinaDerm. They technically fit, but there isn't enough of a border for them to work. If you don't like one brand of fentanyl patch, just ask your pharmacist to order a different one and try it out. Same goes for the overlays. Steve M in PA This is not medical advice. Do not change, start, or discontinue any treatment without first discussing it with your doctor of other qualified healthcare professional. > wrote: > where do you put your patch? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 13, 2012 Report Share Posted February 13, 2012 An ACE bandage can cause the patch to overheat and deliver too much medication. I HIGHLY recommend that you do NOT use am ACE bandage over ANY transdermal patch, but if you device to do so, PLEASE use EXTENDED caution. An ACE bandage will also cause that skin to sweat, causing the adhesive to completely release. The adhesive in fentanyl patches is hydrophobic, meaning water (like sweat or saliva) causes it to release. That would also cause additional skin irritation. The monograph for fentanyl patches always says that you should NEVER cover the patch with anything except clear dressings. There are several reasons for this, including: • risk of altered absorption, including overdose • in the event of overdose, the EMT would not know that you are on it out what side your on, highly critical information. You can also use medical tape to create a border, but this doesn't work nearly as well. Steve M in PA, age 22 Married with 3 year old daughter Non-text portions of this message have been removed] Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 13, 2012 Report Share Posted February 13, 2012 Steve m I thought you had to wear the patches on places with a lot of body fat. Do they really stick to your arms? I have been wearing them on my belly as I sure have a lot of fat there! Becky Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 15, 2012 Report Share Posted February 15, 2012 The amount of body fat is not important. There are small amounts of body fat everywhere on your body, that's all you need. The patches actually worked better for me when I had mostly muscle in my arms and almost no body fat (before I got sick). Additional fat just means that the patches take longer to work and the skin will move more, which means that the patches [especially the larger ones] don't stick as well. The thickness of the skin is far more important than the amount of subcutaneous fat. According to page 8 of Mylan's " A Guide to proper Application and Use " , but the " belly " isn't one of the approved locations. This is the same with all brands, Mylan is just the first one that came to my mind. http://bit.ly/xCJH7O By the way, aren't the illustrations in this ridiculous? How many chronic pain patients do you know with that much muscle mass? Are they trying to make us feel worse? (And, it's not just Mylan, all of them do it). Duragesic Instructions (approved places- chest, back, flank, upper arm) http://bit.ly/AfuIRb Yes, they do stick on my arms fairly well (better than anywhere else), but I do use Tegaderm overlays to keep them on (I didn't need the overlays with the 12, 25, or 50 mcg patches, but I need overlays for the 75s and 100s). I hope this information helps. Steve M in PA I thought you had to wear the patches on places with a lot of body fat. Do they really stick to your arms? I have been wearing them on my belly as I sure have a lot of fat there! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 15, 2012 Report Share Posted February 15, 2012 Re: My arms are skinny but I change from one arm to the other every 48 hours. I am on the 100mcg patch and use the Mylan brand as it seems to stick much better. When I first started using them about years ago, I changed from each side and under the breast but I was nauseated which may have been because I was not used to them as I know longer have that problem. I had my second lower back surgery with ten years in between. I had fusion, plates and screws put in just above the previous ones which they removed. I had a glorious three weeks of being pain free but all of the pain is back. Since it has only been three months, I am praying that healing will still take place. I do have neuropathy in my feet that started about two years after my first surgery. I have had almost anything you could think of to try to find solutions before deciding on the second surgery. Wishing the best for everyone. Lois > Steve m > I thought you had to wear the patches on places with a lot of body fat. Do > they really stick to your arms? I have been wearing them on my belly as I > sure have a lot of fat there! > > Becky > > Quote Link to comment Share on other sites More sharing options...
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