Psycho-Babble Medication | about biological treatments | Framed
This thread | Show all | Post follow-up | Start new thread | List of forums | Search | FAQ

Re: Selegeline Patch - Update?

Posted by Deborah14 on October 31, 2000, at 20:48:03

In reply to Re: Selegeline Patch - Update? » Deborah14, posted by chdurie2 on October 28, 2000, at 17:20:54

> > Caroline
I spoke yesterday with Mike Pass at Family Pharmacy in Sarasota, Florida and Steve at College Pharmacy in Boulder, Colorado about the selegeline gel. If ever I came away from two phone calls totally confused - it was yesterday. Mike, at Family, has made the selegeline gel before with the piracetam/hydergine. He also said that he could make it without the piracetam/hydergine although I do not believe he ever has. When I said I wanted the selegeline alone I felt that he was pushing the P/H combination, probably to make the drug more expensive. He couldn't give me a good explanation on what P/H does and why it is mixed with the selegeline. Could you explain what piracetam/hydergine is and why your p-doc prescribed it for you.
Mike said that without first speaking with my p-doc he estimates that I probably should start with the equivalent dose to one quarter of the amount I take orally. However, to tell you the truth, I felt uneasy about the conversation - as if he wasn't being totally upfront and truthful with me. I had to pry out information about possible allergic reactions to the bases that the gels were made from. He also said there was less adverse side effects from the gels than the pills but he really didn't or couldn't explain why.
I next spoke with Wellness Pharmacy in Alabama and they were very forthright about never having made a selegeline compound and were not comfortable doing it.
I finally spoke with, I believe it was, Steve at College Pharmacy and he also said that he had never made a selegeline gel. He told me that he did not think that it would have fewer side effects than the pills and explained to me why. I believe he said that only 19% of selegeline pills are metabolized on the first pass through the liver and that was a small amount and that a gel would pass the equivalent amount through too. He also said that I would need much higher amounts of the gels to get the equivalent effect as from the pills with the same adverse side effects. At this point, I don't know who to believe since organic chemistry is totally new to me. However, after reading the abstracts on the comparisons between the patch and the selegeline pills, I don't understand how College Pharmacy could be correct. The studies seems to indicate that the transdermal patch is more effective than the equivalent dose of the selegeline orally. I went back and even found an early study discussing the application of the selegeline directly to the skin of dogs (or maybe it was rats, who knows.) If the patch works, I don't understand why a gel won't work if the selegeline is mixed with an "effective" sterile base that enables it to be absorbed evenly into the skin without irritation, allergic reaction, and evaporation. Of course, it goes without saying in my mind that it appears that the transdermal delivery system has to be more efficacious; however under the Pharmacy Preservation Act of 1997, the FDA will not permit compounding pharmacists to formulate or make transdermal patch delivery systems for pharmaceuticals (inhalers are not permitted either).
I recounted all this information and gave the Medline abstracts I printed out to my p-doc today and he is more encouraging about trying the gel than I am at this point. Since I've been informed that the patch will not be commercially available for at least a year and I believe that a year is way overly optimistic for FDA approval, my pdoc is more than willing to try the gel since he knows that the selegeline works well for me. He first wants to speak with his psychopharmacy guru on the subject (who is "the" guru in the area) before jumping into purchasing the gel but he does not think , at this point, that it will hurt me and he is trying to find a way to up the dosage without increasing the side effects.
As I mentioned before, I have been on selegeline for over eight years as an AD. 30 mgs a day in the morning is the lowest amount I can take for it to be effective when my depression is under control. However, when my depression goes out of control, so to speak, I need to take 50 mgs a day. The adverse side effects at 30 mgs include an inability to fall sleep and sleep through the night uniterrupted, which is counteracted effectively by other medications at bedtime. The selegeline has to be taken in the morning otherwise, the adverse side effect on sleep is even more pronounced at 30 mgs. For example, I took the selegeline yesterday afternoon because I had to refill my prescription and even with my nightly meds, I was waking up every hour on the hour. By the way, Steve at College said that I should try the herb Triptophane to sleep. Also a 30 mgs, I have total lost my bowel function and have to take Miralax nightly to counteract the constipation. It works. The third side effect is very low libido.
However, if I increase the selegeline to 40 or 50 mgs I can' t sleep through the night no matter what I take to counteract this side effect. I can't fall asleep for hours and if I do I get maybe two or three hours of sleep, which is interrupted hourly. I'm up by 4 AM wide awake. The Miralax stops working at the increased dose of selegeline and I not only lose my libido entirely, I cannot respond. Its like the switch has been cut to my brain.
As a result, I keep ending back at 30 mgs a day when I really should be taking 50 mgs. My pdoc has even suggested alternating days between 30 and 40, or 40 and 50 but as soon as I go over the threshold of 30, the adverse effects become intolerable - immediately.
My p-doc may be less concerned about the hypertensive side effects of the selegeline than yours because I have been on it so long without any ill effects of that sort and I am allergic to all the foods one isn't supposed to eat - I don't eat cheese or any of the "forbidden" foods ever anyway. Also, he monitors my meds very strictly and I see him more than once a week.
On the one hand, I am very lucky because selegeline is the only AD to date that works, at all, for me. On the otherhand, it could work better. Each of us has our own unique brain chemistrys and backgrounds that makes our psychopharm treatment different. I don't want you to think that selegeline is a panacea in and of itself for me because it isn't, I take additional meds too for my other issues. However, because of my medical privacy beliefs - I am almost a "fanatic" in this area, I believe that it is not in my best interest nor anyone elses to discuss their private medical information on the Internet. The little I have revealed is a lot for me and goes against every thing I believe in. However, I believe that what I am gaining and giving by participating and trusting the people on this website is more than any identifiable information that may be revealed or invasion of my medical privacy that may occur.
P.S. I found the article you mentioned on Medline along with a slew of others that I bookmarked and printed out for my p-doc. Thanks for the help.


Share
Tweet  

Thread

 

Post a new follow-up

Your message only Include above post


Notify the administrators

They will then review this post with the posting guidelines in mind.

To contact them about something other than this post, please use this form instead.

 

Start a new thread

 
Google
dr-bob.org www
Search options and examples
[amazon] for
in

This thread | Show all | Post follow-up | Start new thread | FAQ
Psycho-Babble Medication | Framed

poster:Deborah14 thread:46818
URL: http://www.dr-bob.org/babble/20001022/msgs/47863.html