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Treatment a Bust
Since I haven't seen much in the way of personal results using
Soriatane I thought I would give my experience.
I am a 44 year
old P sufferer, for over 20 years. I
have a significant amount of coverage on my legs, torso and elbows.
I have tried the usual range of medications, including a fair
amount of success using methotrexate.
Poor liver testing finally convinced me to try something else.
recommended by both my friend (a dermatologist) and my regular doctor.
I have tried reading testimonials about the efficacy but was (and
am still) surprised that there are so few, other than those I consider
related to the manufacturer.
tale starts about 12 weeks ago. My first two weeks were pure hell.
My skin dried and I flaked and itched insanely.
Moisturizers helped but the flaking was intense.
At 3 weeks I called my derm to explain the lack of results and my
acute discomfort (first time I
have ever needed to do that). In
fact, even though my lesions were thinning I was getting (for the first
time ever) a bad, bad guttate outbreak all over my torso (and I thought
the Soriatane was supposed to be prevent a worsening at the very least).
He explained that this was "normal" and that the medicine
takes 2-3 months for results. I
swallowed the words I was thinking of responding with and continued my
At this time
(with my derms approval) I decided to add my home, total body UV light to
my treatment. My results at 12
weeks were still disappointing so I went back to my derm and am now on the
eve of my first Enbrel injection. Wish
me luck since there aren't a whole lot of treatments to go to any more.
Bottom line on
the Soriatane: Didn't work
well. Thinned lesions (good).
Caused or exacerbated a guttate flare (bad).
Caused intense itching and flaking (bad).
Helped make me photo-sensitive, so Soriatane combined with UV
worked better (good). Overall
level of P is worse than before I started.
My results are comparable to UV treatment alone, but with the added
bonus of paying $400/month for the drug and not being able to donate blood
for three years. –Kurt
Ed’s Response: Thanks for this, Kurt. Your experiences are more-or-less described, from the manufacturer’s point of view, on this page —
What I don’t
know is if 12 weeks should be considered the “initial period,” during
which worsening is not uncommon, or should you be seeing
improvement if the drug is going to work for you?
tried Soriatane, but I’ve been through courses of both methotrexate and
cyclosporine, and with neither did I receive maximum benefit inside 12
weeks. Now, on Enbrel (a
so-called biologic), I’ve been
dosing for almost six months — three of those at twice
the normally-prescribed dose — and still haven’t seen any skin
For my own
sanity, I’ve learned to draw the line at 6 months (or, roughly, 24
weeks) with just about anything I try, unless it's specifically known to
been seeing more about using Soriatane in conjunction with other kinds of
therapy, including light therapy. I
guess that’s all right, but it does diminish one’s appreciation of the
promise of the drug. It
is especially disappointing if Soriatane, even in combination with a more
traditional therapy, still doesn’t do the trick.
this suggest to you that we’re still tap dancing around this disease?
It seems we haven’t been able to nail a thing.
P.S. Be sure to also read Soriatane Working After Juggling Dosage in this month's email.