Sinemet : Is there anyone who is on or has... - Cure Parkinson's

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Sinemet

Annie81963 profile image
Annie81963
•8 Replies

Is there anyone who is on or has been on sinemet that can tell me about any side effects they may have had or are now experiencing. Thanks 😊

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Annie81963
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rustjudge profile image
rustjudge

I have endured constipation, nocturia, insomnia, dry mouth , and dyskinesias. I have reduced my sinemet intake and it has abated some of the aforementioned problems.

JSJ

Kachimom profile image
Kachimom in reply to rustjudge

For dry mouth I read that brushing your teeth and mouth wash help with that. I have tried both at different times and they do help.

Kachimom profile image
Kachimom

I have been on Sinimet for about a year now, after taking several other PD meds. Sinimet has done the most for me but the one side effect that really bothers me is Dyskenisia. I also feel that taking it with food helps to keep the Dyskinesa at bay. Extended release Sinimet works good for me. Along with the Sinimet, I take Amatidine.

paddyfields profile image
paddyfields in reply to Kachimom

Taking sinemet with food/protein will reduce the amount of available dopamine which might indicate you are on too high a dose of sinemet. Just a thought.

dewey098 profile image
dewey098 in reply to Kachimom

I agree with this advice. In terms of cause and effect, there appears to be a direct connection between taking (too much???) Sinemet and Dyskinesa.

Trenny profile image
Trenny

I have been on increasing doses of sinemet and have reached one three times a day, which I have to stay on for two or three weeks . If I don't have any side effects, or benefit, I then have to increase by half a tablet daily up to three times daily.

I have been feeling very tired in the evenings and could quite easily go to bed at 9pm or before. I do notice a dry mouth at night. I still sleep quite well, but get up several times and think there is a degree of urinary retention.

I am going to ask the consultant if I can have a long-acting form as I have difficulty remembering to take the afternoon dose at about 2pm. I take the third dose at about 6 or 7 pm.

Annie81963 profile image
Annie81963

Thank you everyone who responded. I've been on it for years and was wondering if anyone has any side effects.

dianegale profile image
dianegale

i have been on it for two years and it works great for my polymiositis. i am almost normal but the dowm side is that it wears off 3 and a . half to 4 hours and the next dose takes 20 mimutes to 1 and a half hours to take effect. when it is workingi stay busy but its hard at night time to stay busy . i find my mood effects it also

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