I was dx almost 3 years ago now after one year Madopar was added to my mix of meds, I started on 3 tablets daily at 62.5mg and now I am on 10 per day at 62.5. How your dosage is worked out is by your weight. I was basically put on weight then you can take more pills or consider surgery as it is the pills which have made me loose over 2.5 stone since dx then I really don't have to many options I have to take the Madopar in conjunction with 3 other parkey meds but no one persons PD is the same as anothers.The Madopar is a excellent drug but it really depends on how you body reacts to it.I have found taking Entacapone actually improves how the Madopar work and lengthens to life of it. If things don't improve it may well be worth asking if you can try the Entacapone as well and don't wait and suffer in silence ring your PD dr's sec and tell them you are not having much luck. I am sure when ever I call my hospital next to my name on their PC probably says pain in the butt but I could not care less. We all deserve the best care and I am not backwards at coming forwards.
Entacapone is used too lengthen the effective dose of madopar or sinemet, sometimes its a combination dose of sinemet/entacapone called stalevo, Ideally you need a dose of madopar/sinemet first as entacapone on its own does Nothing. 1 in 10 dont tolerate it.
Hi Trev because it was used in conjuction with another drug can't say i really noticed much at all It we last Nov after a med review I was took of type then went from 6 MADOPAR up to 10 my max being 12.
Now they are my main drug without them and the others I use i would be wheelchair bound by now. I am only 50 and i refuse to let PD win.
Regatds BB.
I only found this out myself about a month ago from a friend at first, checked it with PD specialist because my meds have made me loose weight I was told straight put weight on and you can take more pills as we need fat reserved to distrutbute the drug effectively. With some drs unless you ask they seem to not like to give us info. BB x
Well I have been on Madopar for almost 5 weeks and shown little improvement (walking) but my arm/hand still the same.
Is it possible the meds will work when the dosage is increased as am still on the low starting dose?
Am just waiting on my letter from the PD nurse my referal has been sent to them by my neuro then I can discuss my dosage as next neuro appointment us in 11 weeks.
Also I read there's a small percentage of people with PD that don't respond very well to levodopa is this true?