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Plaquenil
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Plaquenil v Hydroxychloroquine
Hi I am about to start on Hydroxychloroquine but I know there has been some controversy about the generic brand versus
Plaquenil
, the latter being much better at being tolerated.
Hi I am about to start on Hydroxychloroquine but I know there has been some controversy about the generic brand versus
Plaquenil
, the latter being much better at being tolerated.
CalebJacob
in
LUPUS UK
7 years ago
Biologics?
So I have now stopped that and take Meloxicam which I have always done and started
Plaquenil
. I am not in much pain apart from my knees and shoulders. I am not keen to take these new drugs, what experience has anyone had? it would be helpful to know. Many thanks Brenda.
So I have now stopped that and take Meloxicam which I have always done and started
Plaquenil
. I am not in much pain apart from my knees and shoulders. I am not keen to take these new drugs, what experience has anyone had? it would be helpful to know. Many thanks Brenda.
Brede
in
NRAS
7 years ago
Need help !
Hi, I'mat rheumatologist clinoc right now and she just prescribed me
Plaquenil
. She didn't gave me any diagnosis. It's based on my ANA 1:160 and C3 complement 89 (normal 90-180), and i have mild pain at my fingers joints. I just need to know is it ok to take paquenil or to take another opinion.
Hi, I'mat rheumatologist clinoc right now and she just prescribed me
Plaquenil
. She didn't gave me any diagnosis. It's based on my ANA 1:160 and C3 complement 89 (normal 90-180), and i have mild pain at my fingers joints. I just need to know is it ok to take paquenil or to take another opinion.
Dinasamir
in
LUPUS UK
7 years ago
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Plaquenil - Hydroxychloroquine
Hi all, my mum has suffered with arthritis for sometime now. Just getting over a night replacement at 53 - it was quite traumatic for her as the drs couldn't manage her pain right after the operation. Her other knee is now giving her lots of trouble and she has already said that she would sooner give
Hi all, my mum has suffered with arthritis for sometime now. Just getting over a night replacement at 53 - it was quite traumatic for her as the drs couldn't manage her pain right after the operation. Her other knee is now giving her lots of trouble and she has already said that she would sooner give
Oliversmum
in
Arthritis Action
7 years ago
Remicade
I am also on Methotrexate and
Plaquenil
. I figured every infusion my pain would get better, not worse. Just wondering other people's experiences with Remicade. Thank you
I am also on Methotrexate and
Plaquenil
. I figured every infusion my pain would get better, not worse. Just wondering other people's experiences with Remicade. Thank you
lovekittys
in
NRAS
7 years ago
ACCEPTANCE
I began
Plaquenil
in January, and found this blog while researching night-time itching of face and head. Thank you for the Wisdom and experience I find written in your posts. I don't feel so alone now. Let me in return, share a bit of my own wisdom .....
I began
Plaquenil
in January, and found this blog while researching night-time itching of face and head. Thank you for the Wisdom and experience I find written in your posts. I don't feel so alone now. Let me in return, share a bit of my own wisdom .....
Cmtcummins
in
LUPUS UK
7 years ago
Update from my last post... 1 slightly positive Ana and 2 negative ones, no symptoms... NO Lupus!
The second opinion was from a rheumatologist who put me on
plaquenil
even though the test came back negative, and I did not show any signs of inflammation.
The second opinion was from a rheumatologist who put me on
plaquenil
even though the test came back negative, and I did not show any signs of inflammation.
guis
in
LUPUS UK
7 years ago
Inflammatory mystery
They then said if that doesn't work take
plaquenil
(Antu Rheumatic drug) which causes SENSITIVITY TO SUNLIGHT! which I already am and the rheumatologist doesn't quite have the time (always running late) and I feel like I'm always rushed out the door. Could this still be a lupus thing?
They then said if that doesn't work take
plaquenil
(Antu Rheumatic drug) which causes SENSITIVITY TO SUNLIGHT! which I already am and the rheumatologist doesn't quite have the time (always running late) and I feel like I'm always rushed out the door. Could this still be a lupus thing?
lizd121
in
LUPUS UK
7 years ago
Here We Go...
Went to a new rheumatologist who gave sle as the primary illness (with possible ra and sjogren's as secondary) and was taken off of everything and put on
Plaquenil
. It took about five months of the medication plus high doses of anti-inflammatories and then it all went away (well, mostly all of it).
Went to a new rheumatologist who gave sle as the primary illness (with possible ra and sjogren's as secondary) and was taken off of everything and put on
Plaquenil
. It took about five months of the medication plus high doses of anti-inflammatories and then it all went away (well, mostly all of it).
yellowflowers
in
LUPUS UK
7 years ago
HAD IT!
He got mad that I followed the ER doc's order to stop
plaquenil
during a shingles outbreak. His response " Is he treating your autoimmune diseases too? Mayeb he should keep going. " The
plaquenil
was stealing my sight and I told him that.
He got mad that I followed the ER doc's order to stop
plaquenil
during a shingles outbreak. His response " Is he treating your autoimmune diseases too? Mayeb he should keep going. " The
plaquenil
was stealing my sight and I told him that.
Bahnmc
in
Cure Arthritis Community
7 years ago
Immunocompromised Health Care Worker with Lupus
I have been deemed 'in remission' but I am still on
Plaquenil
which has immunosuppressant effects so it is a bit of a concern for me working in health care where I am exposed to a higher risk of infection.
I have been deemed 'in remission' but I am still on
Plaquenil
which has immunosuppressant effects so it is a bit of a concern for me working in health care where I am exposed to a higher risk of infection.
elohcin
in
LUPUS UK
7 years ago
Hip pain in lupus. Yes or no?
I am on prednisone 5 mg a day, and
plaquenil
500 mg a day. When I had my last bad flare, I had pretty profound weakness and pain in my hips, ankles, feet, upper arms, and shoulders (profound shoulder weakness) as well as pain in my hands and fingers.
I am on prednisone 5 mg a day, and
plaquenil
500 mg a day. When I had my last bad flare, I had pretty profound weakness and pain in my hips, ankles, feet, upper arms, and shoulders (profound shoulder weakness) as well as pain in my hands and fingers.
nanleighh
in
LUPUS UK
7 years ago
Sulfasalazine
This week I started taking Sulfasalazine along with the
Plaquenil
which I've been taking this about 8months. Could anyone give me any insight on how you responded to similar treatment?
This week I started taking Sulfasalazine along with the
Plaquenil
which I've been taking this about 8months. Could anyone give me any insight on how you responded to similar treatment?
Twinks80
in
NRAS
7 years ago
New to forum..lupus sufferer ttc
I have come off mycophenolate but still on
plaquenil
and prednisone. Any tips? Thanks in advance :)
I have come off mycophenolate but still on
plaquenil
and prednisone. Any tips? Thanks in advance :)
Hidden
in
LUPUS UK
7 years ago
Wracked w pain all over at least once a month
I'm on
plaquenil
n warfarin. I was diagnosed 3 yrs ago after a stroke. I have a rheumatologist in NYC.where I live. She's a lupus specialist but Im thinking of going to see another specialist here because I think my APS has reached another level.
I'm on
plaquenil
n warfarin. I was diagnosed 3 yrs ago after a stroke. I have a rheumatologist in NYC.where I live. She's a lupus specialist but Im thinking of going to see another specialist here because I think my APS has reached another level.
loretta1106
in
Hughes Syndrome APS Forum
7 years ago
Hearing Loss ??
I have had Lupus for 17 years and have been taking
Plaquenil
all of that time. Recently I have been aware of hearing problems and after getting wax etc removed from ears I now have been given a diagnosis of moderate Sensorineural hearing loss in both ears.
I have had Lupus for 17 years and have been taking
Plaquenil
all of that time. Recently I have been aware of hearing problems and after getting wax etc removed from ears I now have been given a diagnosis of moderate Sensorineural hearing loss in both ears.
RuthRachel
in
LUPUS UK
7 years ago
APS and heart ablation
On
plaquenil
and aspirin. Today I was told I should undergo an ablation for SVT. Terrified! Has anyone had any experience with this procedure? Thanks.
On
plaquenil
and aspirin. Today I was told I should undergo an ablation for SVT. Terrified! Has anyone had any experience with this procedure? Thanks.
danapu
in
Hughes Syndrome APS Forum
7 years ago
Plaquenil
Is this the
plaquenil
you are talking about
Is this the
plaquenil
you are talking about
silemoran
in
Hughes Syndrome APS Forum
7 years ago
Relative success?!
It literally says 'we have discussed the possibility of an evolving auto immune disease' and recommends
plaquenil
200mg twice a day for 3 months and a follow up appointment in 8 weeks. That's it. Nothing else. Is this common?
It literally says 'we have discussed the possibility of an evolving auto immune disease' and recommends
plaquenil
200mg twice a day for 3 months and a follow up appointment in 8 weeks. That's it. Nothing else. Is this common?
DenverKUK
in
LUPUS UK
7 years ago
Still waiting for confirmed diagnosis
I know I will be on at least
plaquenil
to start (if bloods don't show anything). Does anyone know if this helps with hair loss or if there is anything I can ask the gp for? I'm not willing to lose my hair! Seriously frustrated...
I know I will be on at least
plaquenil
to start (if bloods don't show anything). Does anyone know if this helps with hair loss or if there is anything I can ask the gp for? I'm not willing to lose my hair! Seriously frustrated...
DenverKUK
in
LUPUS UK
7 years ago
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