mirapex dosage for rls

I never realized what a good night's sleep felt like until Mirapex....I started out on a drug trial when this medication first was introduced; my dosage was .25mg. Now, 20 years later, I'm up to 1.5 mg per night, but still sleeping like a baby. The OTC "restless leg" drugs are helpful, but nothing works for RLS like Mirapex. If you are without prescription drug coverage or can't afford it, the manufacturer will supply your drugs if you qualify.

Yesterday my doctor prescribed me Mirapex Pramipexole Dihydrochloride tablets 0.125mg. I took two before bed and no RLS! I slept for 12 hours! BTW I'm down to one 10mg oxyneo and one 5mg oxtcocet. Staying like this for another day and than hitting ground zero tomorrow. Praying it won't be to bad, but with this new med for RLS I think I'm gong to be OK.

I also take Mirapex and it works well for me. I also have eaten bananas and that helps...google rls and see if you can find any other ideas.

s 0436, day 7 no vics and I did sleep about 6 hours, but I take 1mg klonopin every night for fibro and I take mirapex for RLS -- the vicodin also helps with RLS but the mirapex works better I promise...I get it in my legs, hips and arms and I just want to scream.......see if you can get some samples of that or requip bcuz even with insurance they are expensive. You can get through it - it will get better, oh, just remembered...mirapex.

I had tried all the usual medications for rls before taking the Ultram. I have tried requip, mirapex, sinamet, gabapentin, lyrica and a host of others. Ultram was the only one that worked well. For three and a half years I was free of the rls syptoms. Now though I am afraid I am going to experience not only increased rls symptoms but also the other withdrawl symptoms associated with quiting the Ultram. I am looking for responses from others that have been in this boat.

This has kept the RLS under control but about 7pm has sent me to sleep - most inconvenient for evening meetings! Today my specialist put me on Gabapentin - 100mg twice a day for one week, increasing by 100mg per dose per week up to 600mg in the sixth week. I have therefore stopped the Ropinerole. What I forget to ask is what time of day/night it is best to take the Gabapentin capsules. My RLS is (was) bad in the evenings & through the night.

Thank you Worried for the detailed information. I had no idea those extra receptor sites never went away!! I guess that's why the experts say that once you are an addict, you always will be. =( I understand the dangers of an addict messing around with dopamine. I just have such a tough time with the RLS. If it was only for four or five days, I could hang in there, but mine tends to last more like 14 or 15 days.

t know about the Monavie but what I take and is wonderful is Mirapex. I take it 3 times a day and have no restless legs unless I skip a dose or run out and then the RLS returns. I hope this has helped.

I was on mirapex for 3 years, my miracle drug, for my RLS during that period I develop a gambling addiction. I find out that this is a side of the mirapex.For the sake of my self and the loss od my my family I choose to get off of it.I It took me 2 trys to get off of them and have suceeded. I no long have the urge to gamble. ,Now I am on simumet for my RLS and it does not work like the mirapex , I wake up in the middle of the night and can't go to sleep.

I posted a couple of times , Mirapex is what my Mother takes for RLS. Someone else posted that they take it for RLS . Both having great success with it after many many yrs of drs. , meds and NO sleep.

However, when thinking of the future, I will have to admit I am more frightened of RLS which I have had since I was seven. I am taking Mirapex for relief of this torturous malady, but now I am afraid of the drug. I take .25mg four times a day. I have had episodes of going to sleep and dropping whatever it is I have in my hands. As of today, I am trying to cut down and take half a dose in the morning and at noon. The drug has made my life bearable.

I also take Mirapex for RLS and Parkinson's like syndrome...also called familiale tremors, which is hereditery. I take 1mg. at bedtime each night. The only side effect I have experienced is the dry, yucky tasting mouth in the morning, but brushing my teeth a couple of times usually takes care of the taste, and I keep something to drink on my nightstand every night. I have had great success with Mirapex, in fact I will not go without it...

Hi & Welcome, Just so I am clear..you went on a Methadone program to help come off of the pain meds, right? Now you went back on the pain pills to help with the Methadone withdrawal? I guess that is where i am confused. You did a very fast taper, although the dose was relatively low. No doubt you are suffering rls from the withdrawal (Methadone) which has a long half-life so 7 days is not a long time. I don't know if it effects you but Mirapex actually made my rls worse.

But as you know what might work great for one patient might not work great for another. But maybe worth a try.

I'm on .25mg of Mirapex for RLS and am gaining weight. Has anyone else experienced this. Any idea as to why. Suggestions? Thanks!

RLS is now listed as a symptom and Mirapex as a treatment in the Pain Tracker. Thanks for the suggestion. Best, MedHelp Pain Tracker: http://www.medhelp.

Have any of you ever had issues falling asleep while on the mirapex? I find that once I do get to sleep it helps me stay asleep better. But for some reason the mirapex gives me anxiety and makes it harder for me to get to sleep. I spend up to 2 hours just trying to fall asleep. I even tried adding over the counter sleeping pills with it but still find it difficult to get to sleep.

Mirapex is amazing for RLS. Also yes a heating pad on your lower back does wonders. Your three days in. I'm twenty. The last three nights I haven't used mirapex or a heating pad. It's awesome! Stay strong. Just think, you really wanna go through everything again?

It's possible. Sleep deprivation causes a generalized nervous system excitability which can manifest in various muscle twitches and spasms. Mirapex (which is also used for Parkinson's) acts in your central nervous system to control your nervous system problems. Did you ever treat your sleep apnea? And if so, how was it treated?

My uncle just turned 60 years old and a doctor recently diagnosed him with RLS. But, the symptoms just don't seem to fit the typical pattern. For the past 9 - 12 months, he has had symptoms of "burning feet" and shaking of the lower extremties. The symptoms are worse during the day, but seem to get better when he lays in bed (symptoms alleviate during the night). He has seen several doctors who have ruled out: athlete's foot, diabetes, Parkinson's Disease ...

My prescriptions follow (N) for Neurologist pescribed, (GP) for General Physician, and (S) for Sleep Clinic. I am on 600 mg. of Neurontin 5xday (N), 1 mg. Mirapex 5xday (N), .5 mg. of Clonazepam 4xday (GP), 350 mg. of Soma (N), 65mg Darvon 3xday (N), Nexium (GP), Lasix (GP), K-dur (GP), lipitor (GP), lamictal (GP), wellbutrin (GP), naproxen (GP), and Nuvigil (S), and I think that's it. I see my neurologist on Tuesday.

OK, Is it possible that the Restless Leg Syndrome I was diagnosed with from a sleep study several years ago might have been an early symptom of my maybe possible MS? It recently occured to me that I list RLS as a neurological symptom on medical forms, and that as far as I know there is no real know cause for RLS. Low iron has aggravated it, but it wasn't low when I was tested for RLS.

yes it did work for me if its not working then I would go see your for something prescription for rls they have a few things now

Welcome, welcome welcome!! I am a long time sufferer of Restless Leg Syndrome, now called 'Restless Limb Syndrome,' since it's known to affect the arms AND the legs. I cannot take any of the dopamine medications to help with the RLS. RLS has now affected my arms as well as my legs. Sleeping escapes me on so many nights. I bite my arms in a useless effort to stop the creepy crawling sensations. I also was diagnosed with MS 14 years ago.

But waht i wanted to comment was something i read here from a poster about some meds for RLS... mirapex and requip... it seems they increase the dopamine levels with some side effects not to get overlooked by someone with addiction issues... The poster shared her experience with mirapex of getting addicted to gambling. It can happen. She even left a link of a documental made in Canada about this terrible effect of mirapex.

I HAVE RLS FOR MANY YEARS AND I AM ON 3MG REQUIP AND 1 MG KLONPIN, THAT HAS BEEN HELPING UP TO NOW. I DISCOVERED THAT MY THYROID IS VERY LOW. COULD THAT BE WHY MY RLS IS GETTING WORSE. I REALLY NEED SOME SLEEP!!! WHAT OTHER MEDS ARE HELPFUL. I REALLY HAVE ALOT OF PAIN IN MY LEGS ALSO. THANKS FOR AMY HELP.

Mirapex dosage for rls

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