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Plaquenil
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Feeling discouraged
So my Rheumy increased my
Plaquenil
200mg to twice daily along with Meloxicam 15mg and hydrocodone for pain. I think I'm feeling better since I'm not in constant pain.
So my Rheumy increased my
Plaquenil
200mg to twice daily along with Meloxicam 15mg and hydrocodone for pain. I think I'm feeling better since I'm not in constant pain.
Twinks80
in
NRAS
8 years ago
FED UP!! Can't tolerate any DMARD....Should I give them up??
I spoke to hospital pharmacy who said that
Plaquenil
were no longer being manufactured. I seem to be able to take the Zentiva brand for three days before the side effects hit me really hard so stop them for a week before I try again. Don't know what to do for the best.
I spoke to hospital pharmacy who said that
Plaquenil
were no longer being manufactured. I seem to be able to take the Zentiva brand for three days before the side effects hit me really hard so stop them for a week before I try again. Don't know what to do for the best.
ellilu58
in
NRAS
8 years ago
Same old, same old..........
So the story that
Plaquenil
has been discontinued does not apply to the drug itself but rather to the suppliers of the pharmacies. The fact that Doctors can still prescribe
Plaquenil
also shows that another story that the
Plaquenil
no longer has a NHS licence, is untrue.
So the story that
Plaquenil
has been discontinued does not apply to the drug itself but rather to the suppliers of the pharmacies. The fact that Doctors can still prescribe
Plaquenil
also shows that another story that the
Plaquenil
no longer has a NHS licence, is untrue.
Twdibwd
Volunteer
in
St Thomas Lupus Trust
8 years ago
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Diagnosed at 14 now turning 18
I do listen when it comes to taking my cell-cept and
plaquenil
and Enalapryl everyday and night. But when doctors tell me the best way to live my life is to stay inside from the sun, lay in bed and it to take it easy...I don't listen. Why? That's not living.
I do listen when it comes to taking my cell-cept and
plaquenil
and Enalapryl everyday and night. But when doctors tell me the best way to live my life is to stay inside from the sun, lay in bed and it to take it easy...I don't listen. Why? That's not living.
Kathleen1998
in
LUPUS UK
8 years ago
Onward, but with your love.
I am still on
Plaquenil
, and meloxicam. Meditation and prayer. No stress. A d doing all activities with ease. I am going to really need each and everyone of you, as i do get frightened, discouraged, and hopeless at times.Thank you, those of you who reached out to me. Much LoveLight.
I am still on
Plaquenil
, and meloxicam. Meditation and prayer. No stress. A d doing all activities with ease. I am going to really need each and everyone of you, as i do get frightened, discouraged, and hopeless at times.Thank you, those of you who reached out to me. Much LoveLight.
Casimir
in
LUPUS UK
8 years ago
Professor Graham Hughes' Monthly Blog August 2016
Aches & pains (Fibromyalgia) Balance Constipation Allergies Memory Course skin FATIGUE FATIGUE FATGUE _____________________________________________________________________ At its simplest, treat all three – thyroid for the lazy thyroid, with junior aspirin for the Hughes Syndrome, and quinine (
Plaquenil
Aches & pains (Fibromyalgia) Balance Constipation Allergies Memory Course skin FATIGUE FATIGUE FATGUE _____________________________________________________________________ At its simplest, treat all three – thyroid for the lazy thyroid, with junior aspirin for the Hughes Syndrome, and quinine (
Plaquenil
MaryF
Administrator
in
Hughes Syndrome APS Forum
8 years ago
Finally got a diagnosis of Antiphospholipid syndrome.
Ive got an urgent appointment back with my rheumatologist on Monday (never known an appointment be given so fast) and Dr Martlew has reccommrnded that I be started on
Plaquenil
for my exhaustion and joint pain. Im just hoping my Rheumatologist is not funny about it when I go on Monday.
Ive got an urgent appointment back with my rheumatologist on Monday (never known an appointment be given so fast) and Dr Martlew has reccommrnded that I be started on
Plaquenil
for my exhaustion and joint pain. Im just hoping my Rheumatologist is not funny about it when I go on Monday.
Billie-Jo79
in
Hughes Syndrome APS Forum
8 years ago
Seronegative rheumatoid arthritis
I am currently taking prednisone, methotrexate and
plaquenil
.
I am currently taking prednisone, methotrexate and
plaquenil
.
Jabmzmom
in
Cure Arthritis Community
8 years ago
Is this Pallindromic rheumatism?
I am on
Plaquenil
, with no problems but how much of the stiffness and ache I am having is from the OA I have in fingers, feet, and knees ?
I am on
Plaquenil
, with no problems but how much of the stiffness and ache I am having is from the OA I have in fingers, feet, and knees ?
HilaryWB
in
NRAS
8 years ago
Have you ever thought your meds increased your RA symptoms?
I get scared that maybe it's the
Plaquenil
because it only really started getting worse once I was diagnosed. So torn over what to do.
I get scared that maybe it's the
Plaquenil
because it only really started getting worse once I was diagnosed. So torn over what to do.
Michelle63
in
Cure Arthritis Community
8 years ago
Pbc and ra
Hello😊 I have had Pbc since October 2014 and I also have ra .which has gotten to the point of me being disabled, my rheumatologist wanted to put me on embrel but my insurance won't pay for it so she is starting me on
plaquenil
. Is there anybody taking this medication?
Hello😊 I have had Pbc since October 2014 and I also have ra .which has gotten to the point of me being disabled, my rheumatologist wanted to put me on embrel but my insurance won't pay for it so she is starting me on
plaquenil
. Is there anybody taking this medication?
Tracella
in
PBC Foundation
8 years ago
New to RA and this. Site
I am on
plaquenil
and gabopentin. My reuhmy wants to put me om methotrexate. I don't think this med is right for me. I don't do well with nausea and vomiting. Can you give me some ideas for meds that work almost the same way as methotrexate.
I am on
plaquenil
and gabopentin. My reuhmy wants to put me om methotrexate. I don't think this med is right for me. I don't do well with nausea and vomiting. Can you give me some ideas for meds that work almost the same way as methotrexate.
Penny66
in
Cure Arthritis Community
8 years ago
I AM NOT SERONEGATIVE!
They did put me back on
plaquenil
, which had worked very well for me when I was younger, even though I was ANA negative at the time, and later on a low dose of prednisone, both of which have been a help. Earlier, when I had told my neurologist that I thought I had APS, he said, “take aspirin.”
They did put me back on
plaquenil
, which had worked very well for me when I was younger, even though I was ANA negative at the time, and later on a low dose of prednisone, both of which have been a help. Earlier, when I had told my neurologist that I thought I had APS, he said, “take aspirin.”
AnnNY
in
Hughes Syndrome APS Forum
8 years ago
When will it ever get better?
🙁 I'm also on week 2 of the
Plaquenil
200mg daily and Meloxicam 15mg.
🙁 I'm also on week 2 of the
Plaquenil
200mg daily and Meloxicam 15mg.
Twinks80
in
NRAS
8 years ago
Interviews and RA disclosure.
Just taken me nearly a year to get sorted on
Plaquenil
, and it seems to be holding some of the 'nasties' at bay. My concern is say, I do an initial interview and wait until they call me back and then mention I have a touch of arthritis?
Just taken me nearly a year to get sorted on
Plaquenil
, and it seems to be holding some of the 'nasties' at bay. My concern is say, I do an initial interview and wait until they call me back and then mention I have a touch of arthritis?
cyprusmum
in
NRAS
8 years ago
Professor Graham Hughes Monthly Blog June 2016
Patient: A rheumatologist started me on
Plaquenil
– which has been fantastic. One tablet a day usually keeps both the fatigue and joint pains at bay. If I am going through a flare, my GP advises me to double the
Plaquenil
for a week or 2.
Patient: A rheumatologist started me on
Plaquenil
– which has been fantastic. One tablet a day usually keeps both the fatigue and joint pains at bay. If I am going through a flare, my GP advises me to double the
Plaquenil
for a week or 2.
MaryF
Administrator
in
Hughes Syndrome APS Forum
8 years ago
Seronegative rheumatoid arthritis with Sjögren
My name is Rachel and I was just diagnosed in February 2016, and started on
Plaquenil
right away, but after 4 months and no change my doctor switched me to methotrexate, and after one month my CRP inflammation was starting to go down :).
My name is Rachel and I was just diagnosed in February 2016, and started on
Plaquenil
right away, but after 4 months and no change my doctor switched me to methotrexate, and after one month my CRP inflammation was starting to go down :).
gabbyholbach
in
Cure Arthritis Community
8 years ago
Lupus SLE also Lupus anticoagulant
Was put on
plaquenil
and steroid and the methetrexate. But I was taken off them because my neutrophils had improved until methetrexate was introduced. I was also given co codomol, calcium + Vit D, Vit D.
Was put on
plaquenil
and steroid and the methetrexate. But I was taken off them because my neutrophils had improved until methetrexate was introduced. I was also given co codomol, calcium + Vit D, Vit D.
mona1163
in
Hughes Syndrome APS Forum
8 years ago
I finally got the call from my Rheumy with my results.
For now she has started me on Hydroxychloroquine (
Plaquenil
) once daily and Vit D 50,000 iu for a low Vit D level. Has anyone had any luck with the
Plaquenil
? I always get nervous starting new medicines. -Teresa ❤️
For now she has started me on Hydroxychloroquine (
Plaquenil
) once daily and Vit D 50,000 iu for a low Vit D level. Has anyone had any luck with the
Plaquenil
? I always get nervous starting new medicines. -Teresa ❤️
Twinks80
in
Cure Arthritis Community
8 years ago
I finally got the call from my Rheumy with my results.
For now she has started me on Hydroxychloroquine (
Plaquenil
) once daily and Vit D 50,000 iu for a low Vit D level. Has anyone had any luck with the
Plaquenil
? I always get nervous starting new medicines. -Teresa ❤️
For now she has started me on Hydroxychloroquine (
Plaquenil
) once daily and Vit D 50,000 iu for a low Vit D level. Has anyone had any luck with the
Plaquenil
? I always get nervous starting new medicines. -Teresa ❤️
Twinks80
in
NRAS
8 years ago
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