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Ervin,

No I took it when it came out in August 1997 but when I got little benefit from
it I was switched to Requip about 6 months later.  I  now am taking 28 mg of
Requip per day and
may go as high as 35 mg to help me with episodes of painful dystonia until I
have my hoped - for  STN stimulator Surgery if all goes well in May.

Charlie.


ERVIN J MCCARTHY wrote:

> Hello Charlie.  I'm interested in your discussion on Mirapex.  I gather if
> you have been taking Mirapex since it came out, I would guess you have been
> taking it about two years.  Were there any beneficial effects during that
> period?  I have been taking Mirapex for about 2 1/2 months now and don't
> notice any good effects looking for it to relieve the tremor and fatigue.I
> am in the midst of trying to make a decision of whether to quit Mirapex.  I
> known I should look to my doctor's decision but I always entertain real
> experiences.  Thank you,
>
> [log in to unmask]
>
> -----Original Message-----
> From: Charles T. Meyer, M.D. <[log in to unmask]>
> To: [log in to unmask] <[log in to unmask]>
> Date: Friday, March 12, 1999 7:28 AM
> Subject: Re: Switching meds--info please?
>
> >HI Ann,
> >I  can comment more as a patient than as a physician.  Regarding the
> >switch from Mirapex to Requip,  I started Mirapex changing from Parlodel
> >during a hospitalization when Mirapex was first released.  My Neurologist
> >switched me calculating the equivalent dose of Mirapex rather than disable
> >me (even more) by phasing one down while increasing the other.  The Requip
> >was started after the Mirapex had reached beyond maximum dose without
> >substantial (increased) benefit. The requip was better (for me).  The
> >switch was while I was at home and was a sudden change giving me again
> >equivalent doses of Requip to the Mirapex.  As time has progressed either
> >the Requip has lost its effectiveness or my PD has gotten worse
> >(unfortunately I think it is the latter).  I currently am taking above the
> >recommended dose and after getting lab work I likely will be increasing
> >even more.   If you can put off the Sinemet that would make sense to me-
> >however if the Requip doesn't give you substantial reduction of symptoms-
> >to a level where your life can proceed reasonably normally-  I would not
> >hesitate to add the sinemet. Sinemet can give a response in a few days but
> >is usually titrated up slowly to give optimum effect.
> >
> >Good luck,
> >
> >Charlie
> >
> >serenityplus wrote:
> >
> >> Hi,
> >>
> >> I've been in the TEMPO study, which is a drug study for an MAO type B
> >> inhibitor, much like Selegiline. I've been on open label with the dose
> >> still blinded; also, I'm taking Mirapex, barely 1.5 mg/day (had some
> >> dose limiting side effects, like sleepiness, but no orthostatic
> >> hypotension.  I've haven't gotten a good response to Mirapex, and I
> >> feel, much as I would like to put off Sinemet (I'm 54, diag. a year
> >> ago, probably had it from about '89) that my symptoms are really
> >> getting in my way:  tremor is essential, not resting, so it's not a
> >> problem, but the inability to do much with my right hand, and dragging
> >> my right side is getting to be too much.
> >>
> >> I'm concerned that trying another agonist like Requip will take
> >> forever (My titration experience with Mirapex was VERY LONG) and may
> >> not do any more, and may cause problems for nothing.  I've read that
> >> it takes weeks or even months to get an adequate response from
> >> agonists.  I've taken Mirapex, albeit in small increasing doses, since
> >> last Sept. and it hasn't done much. I suppose the PD could be
> >> outpacing the therapy also.  Q:  Does Sinemet take long to show a
> >> response?  How tough is it to come off Mirapex (though maybe I
> >> shouldn't).  Any strategies coming to mind on handling starting
> >> generic carbadopa/levodopa with/without Mirapex?
> >>
> >> I would be grateful for any response.  Thanks!
> >>
> >> Ann
> >
> >--
> >***************************************************************************
> ***************
> >
> >Charles T. Meyer,  M.D.
> >Middleton (Madison), Wisconsin
> >[log in to unmask]
> >***************************************************************************
> ***************

--
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Charles T. Meyer,  M.D.
Middleton (Madison), Wisconsin
[log in to unmask]
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