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European Commission Grants Intercept's Ocaliva® (obeticholic acid) Marketing Authorization
Last minute present before the Xmas :) http://ir.interceptpharma.com/releasedetail.cfm?ReleaseID=1004114
Last minute present before the Xmas :) http://ir.interceptpharma.com/releasedetail.cfm?ReleaseID=1004114
Betonarme
in
PBC Foundation
8 years ago
I am new here. Diagnosed with PBC in 2002 maybe starting Ocaliva soon.
She told me about a new medication called
Ocaliva
. I was wondering if anyone is taking this with some details. They say this could stop my itching and lower my numbers. Has anyone had any luck with this new medication? All help is appreciated.
She told me about a new medication called
Ocaliva
. I was wondering if anyone is taking this with some details. They say this could stop my itching and lower my numbers. Has anyone had any luck with this new medication? All help is appreciated.
Nicaganew
in
PBC Foundation
8 years ago
Is anyone on the new drug Ocaliva?
I went to my doctor today and he was very excited to tell me about this new drug
Ocaliva
for PBC that got FDA approved at the end of May and available since June. He wants my ALP numbers to go down more so I will be taking 2 URSO pills + 1
Ocaliva
5mg pill per day. I was taking 3 URSOs per day.
I went to my doctor today and he was very excited to tell me about this new drug
Ocaliva
for PBC that got FDA approved at the end of May and available since June. He wants my ALP numbers to go down more so I will be taking 2 URSO pills + 1
Ocaliva
5mg pill per day. I was taking 3 URSOs per day.
Pea1234
in
PBC Foundation
8 years ago
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OCA gets a green light from FDA
http://www.fiercebiotech.com/intercept-pharma-gets-accelerated-fda-ok-for-liver-drug-
ocaliva
http://www.fiercebiotech.com/intercept-pharma-gets-accelerated-fda-ok-for-liver-drug-
ocaliva
Betonarme
in
PBC Foundation
8 years ago
Things are looking up!
I posted on here a few days ago as my dad has pif and had declined dramatically over the last two weeks. He was admitted to hospital a week ago stuck in a cycle of coughing, shortness of breath and passing out. The hospital and his consultant were useless, he was discharged the following day and we
I posted on here a few days ago as my dad has pif and had declined dramatically over the last two weeks. He was admitted to hospital a week ago stuck in a cycle of coughing, shortness of breath and passing out. The hospital and his consultant were useless, he was discharged the following day and we
Saplam
in
Lung Conditions Community Forum
8 years ago
Slow letters to GPs
Why is it that consultants secretaries take so long to send letters to GPs? I know from experience that it does take a while usually about 3 weeks for the letters to be typed and forwarded to GPs but 5 weeks on and I am still waiting for my GP to get a letter from my Scleroderma specialist, to the extent
Why is it that consultants secretaries take so long to send letters to GPs? I know from experience that it does take a while usually about 3 weeks for the letters to be typed and forwarded to GPs but 5 weeks on and I am still waiting for my GP to get a letter from my Scleroderma specialist, to the extent
PaleIndian2
in
Scleroderma & Raynaud's UK (SRUK)
9 years ago
Question?
Has anyone on here suffered with really bad dry mouth no saliva especially at night, I was thinking of trying an artificial saliva spray are they any good? Any answers please would be appreciated thank you our should I book a doctor's appointment?
Has anyone on here suffered with really bad dry mouth no saliva especially at night, I was thinking of trying an artificial saliva spray are they any good? Any answers please would be appreciated thank you our should I book a doctor's appointment?
Silly-mummy
in
Lung Conditions Community Forum
9 years ago
Dry Mouth
I was diagnosed with Parkinsons about 8 years ago. I have recently started having a dry mouth resulting from a lack of saliva. This has caused me to have a very sore tongue, amongst other things. As this is a recent problem, I wonder if it is due to an addition to my medication. I have been prescribed
I was diagnosed with Parkinsons about 8 years ago. I have recently started having a dry mouth resulting from a lack of saliva. This has caused me to have a very sore tongue, amongst other things. As this is a recent problem, I wonder if it is due to an addition to my medication. I have been prescribed
Court
in
Cure Parkinson's
9 years ago
DLA unsuccessfull RANT!! :-(
I applied for DLA in March 2011, I had a 'no' reply in June 2011, it finally went to a tribunal hearing at end of October 2012!!! Which has been unsuccesful and have been informed I'm not emtitled on any level for care or mobility. I have arthritis, lupus, raynauds, fibromyalgia etc to name but a few
I applied for DLA in March 2011, I had a 'no' reply in June 2011, it finally went to a tribunal hearing at end of October 2012!!! Which has been unsuccesful and have been informed I'm not emtitled on any level for care or mobility. I have arthritis, lupus, raynauds, fibromyalgia etc to name but a few
heatherx
in
LUPUS UK
12 years ago
Sjogrens-just how dry can your mouth get?
I've long been diagnosed with Hughes and the man himself added mild Sjogrens a few years ago. At that time I was having dry eye problems and I have artificial tears for this. For quite some time now I've been having problems with a very dry mouth and throat which sometimes leads to great difficulty just
I've long been diagnosed with Hughes and the man himself added mild Sjogrens a few years ago. At that time I was having dry eye problems and I have artificial tears for this. For quite some time now I've been having problems with a very dry mouth and throat which sometimes leads to great difficulty just
tim47
in
Hughes Syndrome APS Forum
13 years ago
What are the treatment options for Sjögren's syndrome?
You may be referred to a number of different specialists when you are diagnosed with Sjögren's syndrome depending on the parts of your body that it affects. Rheumatologists (joint specialists) are the main doctors who have specialist knowledge of Sjögren's syndrome. This is because of the association
You may be referred to a number of different specialists when you are diagnosed with Sjögren's syndrome depending on the parts of your body that it affects. Rheumatologists (joint specialists) are the main doctors who have specialist knowledge of Sjögren's syndrome. This is because of the association
june_jdr
in
The Australian Sjögren's Syndrome Association
13 years ago
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