How long does it take for meloxicam to work

Common Questions and Answers about How long does it take for meloxicam to work


I am unable personally to take the drug as it is a NSAID and unfortunately for me I am allergic to all nsaids. I hope others reply to your post. I know with all drugs there are side effects. I always review a drug or cream before I used it. I know my Rhumatologist gave me some rx cream but after I read the very fine print i realized it was also an nsaid. It would have been dangerous for me to apply it!!
My father in law is on Tramadol 50mg 3 times a day and it use to work for him and now it don't. I think his body is just use to it and it won't work anymore. I am trying to talk him into getting on a new pain med cause I really hate to see him in pain all the time (like me). I have alot of face pain due to some bad dentist working on me and didn't know what they was doing. So I get to live with the pain for the rest of my life.
With a mentor like Tony Dungy, I think Michael has a better than average chance of staying true to his word and working to help resolve some of the damage he has done. For those of you who don't know Coach Dungy, he was here in Indianapolis for many seasons coaching the Colts. During that time, there were very few cases of any kind of criminal or deviant behavior by any Colts player. Compare that to the Pacers (our NBA team) who routinely have 3 or 4 players arrested each year!
Now, I have researched a bit about the drug, checking the insert and also several websites, such as, and all of them say not to take the medication for longer then 5 consecutive days and that it is not indicated for the treatment of chronic pain. I am worried of the side effects and the specific warning of the 5 day maximum.
I do not know how it is for others, but for me I have never been able to get a Docter to give me more meds for my pain. I only take my cymbolta and busepar and balacet. And sometimes I feel as if im going mad. But my doc wont help me. So i go to the emergency room and they always help me.
My question is; does anyone have suggestions for something EFFECTIVE that I can take for long term, chronic pain w/out the old monkey showing up? I'm too old and much too tired to entertain that nasty little creep again but I am going to have to take something for pain until forever. As little Acetominophen as possible bc of the Hep C.
I do have a Valtrex prescription for backup, but rarely have to use it. I haven't used anything (needed to) for a long time, knock on wood. I've had sun exposure recenty and am not feeling well, so I decided to update my knowledge; research the amount of lysine I needed to take, etc, and found this site. I'm lucky enough to not have breakouts very often, but the flu-like symptoms can be quite disabling as well.
It's crazy how you've had so much come your way, and have had to fight through and overcome so much in your life, yet it is the pills and the addiction that finally takes you down. That just goes to show how serious, conniving, and over powering addiction is. IT can take the strongest people and break them down so far that they are willing to do almost anything to get out. It is sad, the way addiction tears threw people's lives and takes you down a path of darkness and despair.
It is a very painful disease and I've yet to find a pain med to help it. Including meloxicam and ibuprofen 800.. you can also do physical therapy. Like accupunture to help relieve some pain.. I hope this is useful. And please from my experience don't let it go.
I ended up finding a wonderful doctor. She is a very intelligent Romanian woman. They must have wonderful medical schools in Romania, because she was able to determine the cause of my undiagnosed joint pains, with 1 VISIT. She was so sweet and really cared. She made a promise to me that she would never waste my time or money, with unnecessary tests and visits. I thought that was really cool.
Which means the possibility does exist! I asked how I can be tested for it now. He said I need to confront my surgeon and ask him for a sample of the screws or pins inserted in my neck". He could then test me for the allergy. He also said that I would develop weakness, redness and warmth over the area that they were placed in. So, If any of you REALLY think that this allergy is a possibility then get a sample of the metal from your surgeon and take it to an allergist and get tested.
I had that prescribed to me when I had all 4 wisdom teeth removed and with TN it does nothing but make me pass out. Try some Tremidol (has to be prescribed) or Oxycodone. The burning sensation will not go away, but any other pain associated with it might be dissolved.
), so he gave it to me as a trial and told me just to discontinue if it didn't work for me. That doctor thought I had arthritis and fibromyalgia because my joints in my hands and ankles were swollen and prescribed Mobic for it but at the end I went to a rheumatologist and after a lot of blood tests he told me I didn't have arthritis nor fibromyalgia. They still don't know what I have.
Your doctor should be able to set up a realistic taper schedule for you. When taking opiates long term, it is always a good idea to take a 'drug holiday' to re-evaluate your true pain levels. Whatever decision you make, we will be here for you. Withdrawls can be hard, but they are doable. This site is full of wonderful, supportive people who can help you through it. I wish you nothing but the best of luck and hope that you can find some comfort.
I completely agree and he had changed it to 1 1/2 every 5 hours, but the pain was coming on strong within about 2 1/2 to 3 hours, so he told me to try to take them closer together but back to one at a time. It seems like work ok this way, but when I've tried to cut out the somas because of the drowsiness, I seem to over compensate with the vicodins even though they both help completely different problems.
but my period pain got so made i ended up missing work for a week and for the ER doctor to not do anything but give me crappy pain meds. it continued to be like this for another two years. i still had no health insurance. i try my best to not call out of work and just ignored the pain again. one day i noticed i was having really bad low back pain and there was a bump there. my boyfriend and i, went to a chiropractor close by our apartment.
Ive taken it a few times but it never did anything for my pain but it might work for you so if he says to try it, it wont hurt....I hope your day is going well...Keep your head up your doing a wonderful job...Im thinking of you always....I havent been on hear much I have some health issues im dealing with going for a cardiac cath. tomorrow morning scared to death, they have to sedate me a little and I dont want anything in my body im gonna try and do it without.....
Sorry your hubby is unsympathetic about it. It is hard to get used to that's for sure. Your doctor should do tests to make sure it's not lupus, rheumatoid, or any other autoimmune distinguishable through blood work. That's what mine did, complete exam, and some x- rays. We've managed it well for quite some time, even though I do flare. It'll never be perfect but you do the best you can. Start exercising now, if you don't already, and it'll help you more than you think it will. Best wishes.
Hi Tramadol Warriors! Welcome to Part 53. This thread is full of helpful and kind people who want to help you get off this terrible drug. Please snuggle in and make yourself comfy. I know you can do it!
I sure do hope that it becomes FDA approved sooner than later. New medications for FM and CFS-ME take a long time to work their way through the system. It's very sad for those who suffer, and now with the recent discovery of the XMRV retrovirus, I hope new alternatives will become available to treat the infected people properly.
Do you have any other symptoms accompanying this inflammation/pain? It really sounds like it may just be something viral, but it could take awhile to get over it. I hope you feel better soon! If you see your doctor anytime soon, ask him/her what NSAID would be best for relieving the pain you're in and reducing the inflammation you're experiencing in particular areas.
Welcome Tramadol Warriors! We're all so glad to see you here. This is the place to be if you are trying to recover from Tramadol ... Please make yourself at home!
I was awake/conscious for most it and was even pleased when the docs were able to reproduce my symptoms! Unfortunately the recovery drug just didn't work therefore the confirmation of cardiac microvascular dysfunction. Emory, Mayo and U-FL,all researchers working on the same NIH study protocol for this dysfunction had not seen a case so severe. Needless to say a rough few days at Emory until they got my meds correct..............loads of IV nitro.
I have switched to Mobic (brand name for Meloxicam) NSAID. 15mg pill. Took first one last night. So far ok with Synthroid that I took an hour ago. Only thing is that not much pain relief ??? but I wonder if it "builds up" in my system .... I am hoping that it is going to work as taking it once a day is nice vs. 3X for the other one with side effects of dizziness/tired with the Synthroid. Being time-released is nice even dosing 24hrs long.
Over the years of recovery and reading about others, seeing others recover the main thing I have learned is that everyone's life is better without being a slave to Tramadol. You might be stuck and scared right now, but you can make the decision to get yourself off the hamster wheel of Tramadol dependency and even addiction. You don't have to live that way. There's lots of people here to help.
After Enbrel came along, my rheumatologist and I discussed it and decided to add it to the mtx to see if my flares would completely stop, and I'm happy to say that they have. No two people with RA respond the same way to the same meds, though. Mtx is a good medication on its own, and the good news is that it combines well with a number of newer medications so there's a good chance some combination will work for you.
Now I don't have to hide when I go pick it up or take them. But I plan on stopping mid dec. I think. I want to try to tapper, see if that works. Or else just stay home from work for a week and feel like crap.
If you ever start taking them as a recreational past time, or abuse them, then you will pay for it in the long run, cramps, headaches, depression, diarhia, vomiting, and more! What it all boils down to is, there is a reason they say to only take one every 6 to 8 hours AS NEEDED, for pain..... this is to help you from becoming dependant upon them, and also helps them do their job more efficiantly.
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