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Antipsychotics and levodopa are the only compounds as
far as i know that are known to cause dyskinesia.
Antipsychotics, also called neuroleptics, cause what
are called tardive dyskinesias (TDs), and levodopa
causes the various types of levodopa-induced
dyskinesias (LIDs).

The main difference between tardive and l-dopa induced
dyskinesias is that the former is “potentially”
irreversible (presumably the more developed they are
the less likely they are to go away even if treatment
is stopped) and the latter is not considered permanent
because they stop if treatment is stopped.

But honestly - short of having DBS, does anyone ever
go off l-dopa? As long as one has no choice but to
remain on l-dopa, dyskinesias are, practically
speaking, permanent. So, from that perspective they
can be said to be comparable.

i wanted to provide some sense of how disabling each
type dyskinesia is capable of becoming, and with what
frequency, but i could not find any studies/abstracts
comparing the two.

However, there is one way in which the two are
quantifiably different - LIDs are a *much* bigger risk
than TDs - with, according to one study, the 7 year
risk of developing TDs being 35% (on an old
neuroleptic - there are newer ones that are less
likely to cause TDs), while according to another study
the 10 year risk is just 11.4% - vs. the 5-year risk
of developing LIDs being anywhere from 50-100%,
depending on one’s age and which study one cites.

And yet, in spite of a much bigger risk of LIDs, a
mere 47 words are devoted to dyskinesias in the
Sinemet labeling (in one section, one is instructed to
call one's physician if one starts experiencing
involuntary movements or nausea), whereas Navane, and
old neuroleptic, devotes 535 in three different
sections to TDs, including the first paragraph in the
“WARNING” section, and Zybrexa, a new neuroleptic,
devotes 365.

i would like to know why that is.


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