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tllaes (@tllaes)

Is anyone using Rytary

Parkinson's Disease | Last Active: Jan 2 7:15pm | Replies (64)

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@hjscheib

Thanks for the Pan Foundation website. I will get in touch with them to find out if I can find some cost support for Rydary. I posted my costs in the previous response. I've been a PD patient now for exactly 6 years on August 15th. I have been taking carbidopa/levodopa, 25-100 mg tabs, 2 per dose, 3 times per day, coupled with Azilect (rasagilene,
mg, for "blocking" the development of the disease and reducing the PD symptoms; and venlafaxine, 225 mg, dose per .day

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Replies to "Thanks for the Pan Foundation website. I will get in touch with them to find out..."

Worst symptom is in the non-movement area – the nervousness & anxiety I almost consistently get (now) after the mid-day dose of 4 Rytary capsules. I can't determine if the anxiety/nervousness is a result of the diminishing effects of the venlafaxine or with too much of the Rydary building up.

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