What is the difference between provigil and nuvigil

Common Questions and Answers about What is the difference between provigil and nuvigil

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Life as me and near me was unpleasant and unsafe. I have taken both Provigil and Nuvigil over the past three years. These are expensive meds but both do more to noticably improve my daily life than any other drug I take. I'd give up many other things to continue to afford either one. Initially I too took Provigil only on work days. I found that I was better able to function at work but guaranteed to drag through or sleep through my days off. THAT is not a fun plan!
Provigil is more expensive and I actually had more side effects with Provigil. Nuvigil is the 2nd generation of Provigil and the manufacturer has lowered the price to get everyone "switched" before the patent on Provigil expires in 2011. For me, the difference between Nuvigil and Provigil was amazing. Nuvigil gave me back my life. Provigil let me leave the house but I had trouble functioning. And since Provigil is "going away" it is tough to even get samples.
My neuro office no longer gets samples of Provigil because of the drug company switch to Nuvigil. That proved to be a good thing for me! For me there is a wonderful difference between Provigil and Nuvigil. Nuvigil starts to work faster, lasts longer, and really gives me mental energy that I haven't had in several years. The only down side for me is that Nuvigil has basically returned my energy and mental skills to normal. That is good.
it, I would just be a druggie pill popper. But they explained there is a difference between needing the drug and wanting it for a high/abuse etc. I learned to look at it that way. I have confidence that the surgery will eliminate most of the sleep disorders situation but until that route has been decided, I'm getting by. And this forum has been a huge help. Hope you all have a great weekend.
Plus, my issue is not 'sleepiness' (which is what Nuvigil and Provigil are indicated for) but rather sever muscle fatigue. I think that people with MS understand the difference between feeling 'sleepy' and feeling 'fatigued'. I have heard that Ritalin works well for fatigue for some pwMS, but have not tried it myself.
) and i don't want to get into Provigil/Nuvigil/dextroamphetamine, etc. i was just welcoming comments from the thyroid crowd here what a good ratio of levo to Cytomel may be for someone whose TSH is around 2.00 on 100 mcg levo right now and you still feel comatose? i know you are all not doctors out there, but your input is usually quite educated and your comments are valuable to me. thanks a lot. could i expect energy boosts from Cytomel?
The trick is to understand whatever illness you have and know what is normal for you. This is easier than it sounds. No two cases of MS are the same. Each case is different because in each person there is different nerve damage or inflammation. There are drugs for fatigue. Provigil, Nuvigil, and Adderall for examples.
Oh, I read that wrong. You DO know the difference. LOL ~ I'm a dork. What is the difference to you? I'm curious as I have different types of fatigue.
//www.medhelp.org/forums/neuro/archive/8896.html "Over the last year I have had some minimal numbness and tingling in the very tips of my fingers and toes and occasional fleeting stabbing pains in random places of my body. I have chronic HCV so I also have a lot of joint and muscle aches and pains. Over the last couple of weeks, I have started having frequent sharp stabbing pains in my hands and feet and in the last week an increase in the numbness.
There is adderall, provigil, and nuvigil. If you also have real gait problems you can be on Ampyra (which is not FDA approved for anything but gait) but helps some with fatigue.
This is when i long for my end of day fatigue to come back, this second type is 1000 times worse and there is nothing i can do but wait it out. It is only when the fatigue shifts a little that i can get working on all the other things that are happening to me, all the shaking, spasms, spasticity, language etc this years episode was bad, i needed the fatigue to reduce enough for me to re-learn how to walk and talk before it does i am dependent on others for everything.
The fatigue isn't gone, but I'm thinking more clearly and the fatigue is better with the Provigil and the other medicine to help me get a deeper sleep. MS and other brain diseases can cause sleep disorders including sleep apnea. I would highly recommend a visit to the sleep disorder clinic for the sleep study if your insurance pays the cost (highly costly).
Hey guys and dolls, Latest research has come out that basically shows that fatigue may precede a dx of MS and should be considered as a possible early sx of MS, i'm sure more research will follow. June 7, 2011 (Montreal, Quebec, Canada) — Fatigue is a solitary symptom in almost one third of patients who go on to develop multiple sclerosis (MS), sometimes years later, according to a study presented here at the annual meeting of the Consortium of Multiple Sclerosis Centers.
I did research Nuvigil and found that Provigil is basically the same and available as a generic. Any thoughts on that or any of the other meds? I've been getting better for the last few weeks (basically since the lumbar puncture--go figure) but slowly. I can work almost full-time again, though I'm exhausted when I get home and basically do nothing else. I don't want this to happen again! I guess no one does.
I'd be suspect if you have been more tired or sleepy for months and haven't gone into a relapse with additional symptoms. There is a difference between fatigue and tiredness and sleepiness. I don't claim to understand the nuances, but a neuro who specializes in sleep disorders and studies will. Remember Lulu, we need to be cautious about falling into the temptation to blame all our ills on the MiSery. I've been diagnosed with both sleep apnea and MS.
In the meantime, June is around the corner, and you'll get to the specialist to know for sure what is going on. Don't beat yourself up over not volunteering and doing the extras now. Taking that burden off yourself will relieve a lot of pressure. And, when you can do it - go.
They trust that the microbiologists who designed the tests and the interpretation know what they're doing. In the case of Lyme, this is a tragically wrong assumption.
It kinda reminds me of what being in a coma might feel like. Can anyone tell me what this is and is it possible not to be able to wake up from it, what ever "it" is?
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