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Plaquenil
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Update and help
I am on warafin,
plaquenil
, alprazolan and recently ambien. The dr lowered my
plaquenil
and my lymph nodes started to swell then got what I think is a kidney infection and had blood in my urine. It seems if I get any infections my body go crazy.
I am on warafin,
plaquenil
, alprazolan and recently ambien. The dr lowered my
plaquenil
and my lymph nodes started to swell then got what I think is a kidney infection and had blood in my urine. It seems if I get any infections my body go crazy.
Scottc
in
Hughes Syndrome APS Forum
7 years ago
Newbie questions
My fatigue and joint pain is horrible, and although discouraged to not have a certain diagnoses, I'm happy to be starting the
plaquenil
in hopes of making the symptoms better. I have a few questions.... -has anyone had a similar situation?
My fatigue and joint pain is horrible, and although discouraged to not have a certain diagnoses, I'm happy to be starting the
plaquenil
in hopes of making the symptoms better. I have a few questions.... -has anyone had a similar situation?
Jodirae
in
LUPUS UK
7 years ago
Leg cramps and leg "jerks"
Am back on orencia,
plaquenil
, methotrexate, prednisone and diclofenac. I've had the RA for 40yrs. Anyone have an idea re: the leg cramps. Not able to sleep well at night or naptime. 😉
Am back on orencia,
plaquenil
, methotrexate, prednisone and diclofenac. I've had the RA for 40yrs. Anyone have an idea re: the leg cramps. Not able to sleep well at night or naptime. 😉
cageorge
in
NRAS
7 years ago
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Medication combination
Is it advisable to take meloxicam along with
Plaquenil
and methotrexate?
Is it advisable to take meloxicam along with
Plaquenil
and methotrexate?
determined4321
in
NRAS
7 years ago
Trying Fluoxetine(Prozac) for Raynauds
Getting muscle and joint pain, fatigue under control with Celebrex,
Plaquenil
, and low dose naltrexone. I also take a lot of vitamins and natural supplements. I tried taking a calcium channel blocker for my Raynauds, but it didn't help, and caused pretty significant edema in my feet and legs.
Getting muscle and joint pain, fatigue under control with Celebrex,
Plaquenil
, and low dose naltrexone. I also take a lot of vitamins and natural supplements. I tried taking a calcium channel blocker for my Raynauds, but it didn't help, and caused pretty significant edema in my feet and legs.
Boisecgm13
in
Scleroderma & Raynaud's UK (SRUK)
7 years ago
Cut back on Plaquenil?
Has anyone here ever been advised to cut back on
Plaquenil
dose because of low white blood count and low Neutrophil count? I saw a new Rheumy last week. He ran CBC. When these counts came back low (which the white count always does) he wanted me to cut my AM dose in half.
Has anyone here ever been advised to cut back on
Plaquenil
dose because of low white blood count and low Neutrophil count? I saw a new Rheumy last week. He ran CBC. When these counts came back low (which the white count always does) he wanted me to cut my AM dose in half.
mylafont
in
Hughes Syndrome APS Forum
7 years ago
How much to bump up?
I am currently taking
plaquenil
for 6 weeks in hopes that it will reduce inflammation and I will be able to then reduce to at least 10 slowly. I am finding that 12.5 is just not quite enough.
I am currently taking
plaquenil
for 6 weeks in hopes that it will reduce inflammation and I will be able to then reduce to at least 10 slowly. I am finding that 12.5 is just not quite enough.
bunnymom
in
PMRGCAuk
7 years ago
RA AND LOW MAGNESIUM?
I take: prednisone
plaquenil
sulfa
I take: prednisone
plaquenil
sulfa
Yittiebn
in
NRAS
7 years ago
Afraid might have to start biologics
I take
plaquenil
, prednisone and sulfasalazine for RA. Was on MTX with bad side effects so was switched to sulfa. Rheumy said that if no segnificant chance in 3 months we will start on biologics. My inflamation numbers are still high. No change. My Rheumy apointment is in 2 weeks.
I take
plaquenil
, prednisone and sulfasalazine for RA. Was on MTX with bad side effects so was switched to sulfa. Rheumy said that if no segnificant chance in 3 months we will start on biologics. My inflamation numbers are still high. No change. My Rheumy apointment is in 2 weeks.
Yittiebn
in
NRAS
7 years ago
Anyone else taking Sulfasalazine??
No
plaquenil
for me after all. He doesn't think it will be strong enough. So, sulfasalazine is being discussed with my hepatologist as I have PBC too. My hep emailed me that the sulfa RA drug would be OK to take. Probably start next week.
No
plaquenil
for me after all. He doesn't think it will be strong enough. So, sulfasalazine is being discussed with my hepatologist as I have PBC too. My hep emailed me that the sulfa RA drug would be OK to take. Probably start next week.
Ktltel
in
Cure Arthritis Community
7 years ago
Teeth problems and jaw bone exposed, please help!
Hi everyone Hoping someone can please advise, brief summary of what's happened so far: -Diagnosed with lupus 2011 & started
plaquenil
. -This year had upper left gum infection, treated with antibiotics and then had the broken tooth causing the infection extracted.
Hi everyone Hoping someone can please advise, brief summary of what's happened so far: -Diagnosed with lupus 2011 & started
plaquenil
. -This year had upper left gum infection, treated with antibiotics and then had the broken tooth causing the infection extracted.
sitting-pretty
in
LUPUS UK
7 years ago
So fed up 😢
I'm so fed up with being so tired , every night I'm in bed for 8 and feel could go earlier, I've been on
plaquenil
and methotrexate 20mg injections with no difference, rheumatologist has recommended rituxamab infusions but feel I'm not so sure these look so severe I'm a bit scared to say the least has
I'm so fed up with being so tired , every night I'm in bed for 8 and feel could go earlier, I've been on
plaquenil
and methotrexate 20mg injections with no difference, rheumatologist has recommended rituxamab infusions but feel I'm not so sure these look so severe I'm a bit scared to say the least has
Harrisgran1
in
LUPUS UK
7 years ago
Medication allergies and lupus
The only reason I can take
plaquenil
and immuran is because I take prednisone also and I guess it helps with the allergic reaction. Thanks!!!!!!
The only reason I can take
plaquenil
and immuran is because I take prednisone also and I guess it helps with the allergic reaction. Thanks!!!!!!
Karynbrett
in
LUPUS UK
7 years ago
Ana positive but not clear about the diagnosis
They did prescribe naproxen and
plaquenil
( hydroxychloroquine). I've been having joint pain and other issues that's what originally sent me to rheumatologist. Confused and uncertain....kfrankie
They did prescribe naproxen and
plaquenil
( hydroxychloroquine). I've been having joint pain and other issues that's what originally sent me to rheumatologist. Confused and uncertain....kfrankie
Kfrankie
in
LUPUS UK
7 years ago
Anybody out there with lupus or shortens with vestibulitis/vulvadynia?
I've been on
plaquenil
now for 18 months with an improvement, although symptoms are exacerbated when I try to reduce my daily dose from 400mg to 300mg daily. By far my worst and most persistent symptom is vestibulitis that manifested with all the other symptoms a couple of years ago.
I've been on
plaquenil
now for 18 months with an improvement, although symptoms are exacerbated when I try to reduce my daily dose from 400mg to 300mg daily. By far my worst and most persistent symptom is vestibulitis that manifested with all the other symptoms a couple of years ago.
Belleo
in
LUPUS UK
7 years ago
How do you know if you APS specialist is actually that?
She increased the Warfarin to 3-4 and sent me for memory tests at Guys, and prescribed
Plaquenil
. I now see Dr Breen who is part of Prof Hunts team, who communicates with consultant in Home town and she is keeping me on the straight and narrow for Cerebral Aps.
She increased the Warfarin to 3-4 and sent me for memory tests at Guys, and prescribed
Plaquenil
. I now see Dr Breen who is part of Prof Hunts team, who communicates with consultant in Home town and she is keeping me on the straight and narrow for Cerebral Aps.
Peecue
in
Hughes Syndrome APS Forum
7 years ago
CRAPPY DISEASE !
Commenced methotrexate , worsening symptoms......
Plaquenil
was added .
Commenced methotrexate , worsening symptoms......
Plaquenil
was added .
Strayleaves
in
NRAS
7 years ago
Self love and acceptance
I was started initially on methotrexate, discontinued after three months, then
plaquenil
and sulfasalazine, which I am still currently on. I did try Arava but discontinued after 5 months. Right now I am in the process of getting prepared for biologics which I am hopeful.
I was started initially on methotrexate, discontinued after three months, then
plaquenil
and sulfasalazine, which I am still currently on. I did try Arava but discontinued after 5 months. Right now I am in the process of getting prepared for biologics which I am hopeful.
Dreamer1972
in
NRAS
7 years ago
Butterfly rash?
I'm on
plaquenil
400mg daily for the UCTD/FM. Thanks for your help 😊
I'm on
plaquenil
400mg daily for the UCTD/FM. Thanks for your help 😊
Leemaree44
in
LUPUS UK
7 years ago
LDN a strong anti-inflammatory??
I most probably will have to take
Plaquenil
. So, I will do that for the RA and LDN for the energy and "feel good" effect it gives me. Spoke with my doctor and many with RA take both. No drug interactions with them, or with the URSO either if you also have PBC like I do too.
I most probably will have to take
Plaquenil
. So, I will do that for the RA and LDN for the energy and "feel good" effect it gives me. Spoke with my doctor and many with RA take both. No drug interactions with them, or with the URSO either if you also have PBC like I do too.
Ktltel
in
LDN Research Trust
7 years ago
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