Any benefits of Rytary over c/l? I’ve been having trouble with my c/l not working as fast or as long. She recommended maybe trying Rytary but from what I found on the net it’s pretty much c/l. Am I missing something?
Rytary?: Any benefits of Rytary over c/l... - Cure Parkinson's
Rytary?
Rytary is made from C/L. It contains three components: immediate release beads; two types of controlled release beads. This has the effect of lasting longer than normal C/L, but you lose some control. And, it costs much more.
Nope and I agree 100% with what John stated. . I’ve use Rytary for over a year. It actually works very well but like IR is greatly affected by protein intake, . It is extremely expensive!! I find a combination of IR and ER work best for me and it is affordable. ParkBear had an excellent thread on ER. (Generic is actually CR. Controlled Release )
Thank you for the kind words, and that discussion can be found here:
healthunlocked.com/cure-par...
Park bear, thank you so much for this. I am confused by one point though. You say, “ER CD-LD", which is actually Rytary and therefore not relevant to the discussion. ” Why is Rytary not relevant to the discussion? Perhaps a better question is, what is the difference between extended release and controlled release CD-LD? Thanks in advance.
In the context of my post Rytary was not relevant because the charts I posted were of Sinemet CR and its generic equivalent carbidopa levodopa ER versus Sinemet IR and its generic equivalent carbidopa levodopa IR. Impax labs is guilty of confusing the terminology by using “ER CD-LD" to refer to Rytary.
I've used Rytary for 6 years. I'm mostly broke and I live in the US. But because I'm monetarily challenged, there are 2 organizations who will pay for it. PAN Foundation and Kaiser Permanente (my insurance company). I've never had to pay anything for it. Kind of amazing.
What many fail to appreciate is that Rytary spreads the dose out so that it's less jarring on the poor old brain, theoretically resulting in less damage over the years and a longer "honeymoon". 6 years and it's still working fairly well. My dose has increased a bit, and I have to take one every 3 1/2 hours instead of 4 hours when I started, but I was in pretty poor shape before I started on Rytary. For 7 years before that, I was unable to take any PD meds; they all made me very ill. I got to experience PD up close. Not fun. But Rytary's helped me to last this long, and I'm still a lot better off than before I started taking it.
My story dittos JAS9’s. Upset stomach from C/L. 4 hrs. Between doses to 31/2.
I’m on my feet all day and often long days. So I can take 5 Rytary before the whistle blows. Less effective towards the end of the day accompanied by slow speech and tightness in my toe.
I’m keeping it together with the help of Rytary.
Been on Rytary for about one year It works much better than standard c/l for me. Keeps me on an even dose throughout the day. Prior to the Rytary I was on a study drug with similar results that worked even better but it isn’t on the market yet so my doctor prescribed the Rytary which he called the study drugs “great grandfather “. If you have wearing off problems you may like Rytary.
What's the name of the study drug? I think I may of heard of that study but I don't remember what it was called.
I've been on Rytary for 3 years and have positive things to say about the drug. I like the smoothed dosage delivery and I agree with JAS9 that maybe this means my body/brain will benefit from this. The big challenge is to not neutralize its effectiveness by eating protein. Sometimes it is challenging to do this, as the dosage is delivered over a large time window. I'm trying it with amantadine now as my normal 3x or 4x daily dosage of 195MG capsules is not working as well as in the past.
Avoiding the protein transport problem can be more of a challenge with Rytary, but I've learned something that has helped. Most people believe that they need more protein than they actually do. Here's a good video on the subject: youtu.be/7NW32vLq340
Now, it is true that PWP must be careful not to lose too much muscle mass so that we can better avoid or survive falls. This is also true for everyone over 65. Still, many believe they need more than they do, and there are risks in consuming too much protein (as mentioned in this video). How do you know how much protein you should take in? Follow the calculation in the video.
For example, my "ideal weight" is 145 lb, and following the video's calculation (145 * 0.4), I should get just 58 grams of protein a day. Because I have PD, I probably need 10% more, so make that 64 grams/day. Most people eating the Standard American Diet (SAD = fast food with a lot of highly processed sugars, oils, and fats) probably double that. You can calculate how much protein you're consuming by using the free and very excellent website cronometer.com/ So if you can safely reduce your protein intake, that should free up more of the transporter molecules that can get the L-dopa past the blood-brain barrier. I've seen a big difference when I do this.
Also, check out the many links to more excellent, related videos listed beneath this video (if viewed on Youtube.com).