Rytary for Parkinson's Disease User Reviews (Page 2)
Rytary has an average rating of 6.0 out of 10 from a total of 28 reviews for the treatment of Parkinson's Disease. 50% of reviewers reported a positive experience, while 36% reported a negative experience.
Reviews for Rytary
- shaking...
- Taken for 1 to 6 months
- November 30, 2020
"Was having uncontrollable shaking and muscles movement. Started on Rytary 95mg two times a day. Working great for me. Have reduced shaking and over all muscles movement by about 90%."
- DOLLIE
- Taken for 1 to 6 months
- December 23, 2019
"Rytary seems to work but I have morning nausea"
Frequently asked questions
- Is Rytary better than Sinemet?
- What is the difference between carbidopa, levodopa, and Rytary?
- How long does it take for Rytary to start working?
- How long does Rytary stay in your system?
Reviews may be edited to correct grammar/spelling or to remove inappropriate language and content. Reviews that appear to be created by parties with a vested interest are not published. This information is not intended to endorse any particular medication. While these reviews may be helpful, they are not a substitute for the expertise, knowledge, and judgement of healthcare professionals.
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- Drug class: dopaminergic antiparkinsonism agents
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"I was diagnosed with young-onset Parkinson's disease 4 years ago. I switched from carbidopa/levodopa after a few weeks. I'm on 61.25-245 mg four times a day, but it wears off after about 4.5 hours. I didn't know the side effects until my mom's doctor asked if she had compulsive behavior (she also has PD) on it. My dad immediately thought of me. I spent thousands compulsive shopping. I'm more than $20K in credit card debt (none before). Tried increasing the dose for tremors and pain, but got serious dyskinesia. I'm on amantadine too, and my legs have mottled spots all over, and I'm swollen everywhere. Vivid dreams and nightmares, sudden extreme fatigue. I'm not sure what's caused by the PD and what's the drugs to treat it. It does help with the overall symptoms of Parkinson's, but I still get Botox injections in my feet every three weeks for spasms."