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Is anyone using Rytary?

Parkinson's Disease | Last Active: Aug 24 11:08am | Replies (102)

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@21amy

I was on Mirapex for 11 years. After 11 years I changed from my first neurologist PA to Mayo. They immediately stopped the Mirapex and started me on Sinimet. I get very nauseated from Sinimet so switched to Rytary about 2 months ago. I feel like I have less off time, less nausea and feel less fatigued. I still have more nausea than I would like. I take Lodosyn and Domperidone with each dose of Rytary to help with the nausea. Does anyone have any suggestions for nausea. I am taking 3 capsules 3 times a day of the Rytary. I am seeing my neurologist at Mayo today and am hoping to either increase my dose to 4 capsule 3 times a day or 3 capsules 4 times a day. I live in Minnesota and there is some type of community program in Minneapolis that makes it affordable. I pay $15/month. Other wise it was over $1000 a month. I have to call this center when I have 1 week supply left and then they over night send it to me. Mayo set this up for me.

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Replies to "I was on Mirapex for 11 years. After 11 years I changed from my first neurologist..."

Hello @21amy,

I see that you had an appointment with your neurologist in June. Was the doctor able to help you with the nausea or the changes you were wanting to the Rytary dosage?