Author Topic: Patient experiences of medications  (Read 22765 times)

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Offline $ilver

Re: Patient experiences of medications
« Reply #10 on: August 18, 2008, 08:35:11 AM »
Wow good info on there, my doctor told me nothing about my creams, been using dovobet WAYYYY to much acording to how its supposed to be used. I stopped using it a couple of weeks ago because I ran out and my p came back with a vengance.

Now I have found this forum and all its good info I feel realy let down by my GP.  :(

$ilver ;)

Offline Deeee

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Re: Patient experiences of medications
« Reply #11 on: September 27, 2008, 09:57:22 PM »
Thanks for that I have been on Cyclosporins for a month now and is brilliant  - just waiting for the new Tash to grow in.. I found out that it costs £24K for the NHS to keep someone on Cyclo for ten years which works out roughly at £50 a week... no wonder they make  your take that nasty MTX first which turns your brain to jelly!!..

Take care everyone... and remember it CANT KILL YOU!!

Dee
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Offline Liddy Cecelia

Re: Patient experiences of medications
« Reply #12 on: November 03, 2008, 11:51:28 AM »
Hi...

     patient experiences of and nurse perceptions of patient experiences of forced medication before, during and after forced medication; patient and nurse perceptions of alternatives to forced medication; and whether patients, according to patients and nurses, retrospectively approved of forced medication. Eleven patients and nurses were interviewed about a certain situation of forced medication. Data were analysed by content analysis. The findings demonstrate that forced medication evokes a number of patient experiences according to patients and nurses. These are related to the disease, the situation of being forcibly medicated and the drug. Patients mentioned several alternatives to the forced medication, whereas nurses mentioned no alternatives. A minority of the patients, and not as many patients as the nurses' thought, retrospectively approved of the use of forced medication. It can be concluded that patients and nurses do not share the same perceptions about what patients experience when forcibly medicated..........

Offline Talis

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Re: Patient experiences of medications
« Reply #13 on: November 03, 2008, 09:05:40 PM »
Not quite certain what point you are making here to be honest, can you clarify what you mean please?
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Offline AlanTyson

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Re: Patient experiences of medications
« Reply #14 on: November 10, 2008, 08:45:23 AM »
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....my doctor told me nothing about my creams, been using dovobet WAYYYY to much acording to how its supposed to be used...
This seems to be a common experience round here, sadly. Let's hope that slightly more enlightened modern medical education will gradually improve things. However, patients can do a lot...

(a) by asking questions, and preferably entering every consultation armed with a little list of questions not to forget to ask. I have found that in potentially stressful or intimidating meetings, I'll almost never get what I want or need unless I'm prepared, and armed with at least a scrap of paper with my 'agenda'; and...

(b) by reading carefully the 'patient information leaflet' that should be included inside every packet of medication. If it isn't there, ask for it.

As practically every professional is under pressure these days, and people are imperfect and usually rushed, those two steps would help interactions over medications a great deal.

(My daughter recently started her first doctor's job after qualification. I dearly hope she's managing to remember and practise the principles I know her to have been taught on how and how not to interact with patients.)

Offline the flakey 1

Re: Patient experiences of medications
« Reply #15 on: November 19, 2008, 05:10:39 PM »
Hi everyone, just found this site, at the moment i'm have UVB treatment, but when it comes to an end, after about 6 months my P comes back again. Has anyone got any advise for me on treatments to use, from their experiences, maybe something that will keep the flakes away a bit longer?

Offline dub07

Re: Patient experiences of medications
« Reply #16 on: November 19, 2008, 07:53:38 PM »
Very interesting. I'm on 50mg Enbrel twice a week at the moment, and noticed increased fatigue, but put it down to onset of winter. Seems common enough. Reassuring.

Thanks, Talis :)

Re: Patient experiences of medications
« Reply #17 on: December 06, 2008, 03:54:47 PM »
Hello I'm new here and suffer from what my Dermatalogist would call excema and his nurse calls psoriasis . I asked her how she knew the difference and her answer was of course can tell or experience well I think she could be right I know I have excema but while desperatly trying to battle an extremely ITCHY ELBOW with RUBBING ALCOHOL AND CALAMINE LOTION , I finally stopped in at the doctors and told him I have this itchy elbow which of course as many of you know almost plays with your sanity ITS SOOOO ITCHY , one look and the GP called it psoriasis and wrote a prescription for DOVOBERT OINTMENT ...well the releif was so dramaticly quick there may be no point to for me to visit a forum. 2 months of horrible itch and wearing calamine lotion 24 hours a day "gone" whew what a relief !

Offline allergic1

Re: Patient experiences of medications
« Reply #18 on: December 09, 2008, 04:58:38 PM »

Hi
Just wondering if anyone can share experiences of taking Acitretin.  I've been given this by my dermatologist because "injection therapy is too expensive".  I'm not very happy at taking yet another lot of tablets - the list of possible side effects is quite worrying.  Can anyone help?

Offline Cristina

Re: Patient experiences of medications
« Reply #19 on: December 10, 2008, 03:22:13 PM »
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Hi
Just wondering if anyone can share experiences of taking Acitretin.  I've been given this by my dermatologist because "injection therapy is too expensive".  I'm not very happy at taking yet another lot of tablets - the list of possible side effects is quite worrying.  Can anyone help?

Hello and welcome to PHO.  :)

I haven't used Acitretin, myself, but here is a link with member's experiences of using it....

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Hope it helps. x