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Mepacrine
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Mepacrine
I guess my question is does
mepacrine
only affect the colpur on yr face or it is all over. Im so fed up of trying things and then having to deall with something else it just gets me down any experiences would really help. Thank you x
I guess my question is does
mepacrine
only affect the colpur on yr face or it is all over. Im so fed up of trying things and then having to deall with something else it just gets me down any experiences would really help. Thank you x
Flows
in
LUPUS UK
2 months ago
Lupus sle treatment
Hey everyone I was diagnosis in may lasy year I'm on hydroxychlorquine 200mg twice a day steroids 15mg azathioprine 100 which has been incresed to 125 for 4 weeks and the 150 after that and 3 times a week I'm on
Mepacrine
for 3 months then that will become daily anyone else on
mepacrine
?
Hey everyone I was diagnosis in may lasy year I'm on hydroxychlorquine 200mg twice a day steroids 15mg azathioprine 100 which has been incresed to 125 for 4 weeks and the 150 after that and 3 times a week I'm on
Mepacrine
for 3 months then that will become daily anyone else on
mepacrine
?
Emz04
in
LUPUS UK
9 months ago
HAIR LOSS
Dermatologist said combination of long-term use of steroids, Rituximab,
Mepacrine
any one of these or combination. I know with medical issues over last 11 years I should not be worried about hair loss but it is really getting me down. Any words of wisdom
Dermatologist said combination of long-term use of steroids, Rituximab,
Mepacrine
any one of these or combination. I know with medical issues over last 11 years I should not be worried about hair loss but it is really getting me down. Any words of wisdom
Haired
in
LUPUS UK
4 months ago
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New meds
Yesterday was given
mepacrine
but its unlicensed and not used often. Im a bit freak out by this. Has anyone else had this medication or know anything about it. Any information would be appreciated. Thank you
Yesterday was given
mepacrine
but its unlicensed and not used often. Im a bit freak out by this. Has anyone else had this medication or know anything about it. Any information would be appreciated. Thank you
Flows
in
LUPUS UK
8 months ago
CARPEL TUNNEL
I am on 5mg maintenance Steroids/ Rituximab /
Mepacrine
for Lupus& Sjogrens. Any advice would be appreciated. X
I am on 5mg maintenance Steroids/ Rituximab /
Mepacrine
for Lupus& Sjogrens. Any advice would be appreciated. X
Haired
in
LUPUS UK
10 months ago
Mepacrine?? Alternative to Hydroxychoroquine
Also if any of you are on alternatives to Hydroxychoroquine like
Mepacrine
if so are you still on Hydroxychoroquine or are you on a combination of Mepa and another drug? These are what I need to find out if anyone has any issues or answers would be most grateful. Thank you kind ladies and men
Also if any of you are on alternatives to Hydroxychoroquine like
Mepacrine
if so are you still on Hydroxychoroquine or are you on a combination of Mepa and another drug? These are what I need to find out if anyone has any issues or answers would be most grateful. Thank you kind ladies and men
KnitSewPurl
in
LUPUS UK
10 months ago
Armpit swelling
I'm on hydroxychloroquine,
mepacrine
, Asprin, clopidogrel, Ikervis eye drops. I’ve never been offered A biopsy . anyone else had a similar experience? Any advice welcome Thanks
I'm on hydroxychloroquine,
mepacrine
, Asprin, clopidogrel, Ikervis eye drops. I’ve never been offered A biopsy . anyone else had a similar experience? Any advice welcome Thanks
bathouse
in
LUPUS UK
9 months ago
sacroilitis-advice please
Hello Currently on HCQ 400mg
Mepacrine
50mg Clopidogrel 75 Asprin 75 Ikervis eye drops having the most awful sacroilitis, steroids helped but off them now Anyone else suffered this and what treatment were you offered thank You
Hello Currently on HCQ 400mg
Mepacrine
50mg Clopidogrel 75 Asprin 75 Ikervis eye drops having the most awful sacroilitis, steroids helped but off them now Anyone else suffered this and what treatment were you offered thank You
bathouse
in
LUPUS UK
1 year ago
Lupus & Sjogrens with Rituximab Infusions
Also on 5mg maint steroids and
Mepacrine
also Helliocare photosensitivity tablets, blood pressure tablets, folic acid calcichew, Asprin.
Also on 5mg maint steroids and
Mepacrine
also Helliocare photosensitivity tablets, blood pressure tablets, folic acid calcichew, Asprin.
Haired
in
LUPUS UK
1 year ago
Is this GCA? My first post here.
I take methotrexate, mycophenolate mofetil, Hydroxychloroquine and
Mepacrine
, plus Amitriptyline and omeprazole. Please photos below. Thank you in advance. Wendy
I take methotrexate, mycophenolate mofetil, Hydroxychloroquine and
Mepacrine
, plus Amitriptyline and omeprazole. Please photos below. Thank you in advance. Wendy
Wendy39
in
PMRGCAuk
1 year ago
Lupus rash/spots spread to scalp.
I am on 6 monthly Rituximab Infusions,
Mepacrine
, Dermovate Cream, and maintenance Steroids 5 mg per day. Enjoy your Bank Holiday. X
I am on 6 monthly Rituximab Infusions,
Mepacrine
, Dermovate Cream, and maintenance Steroids 5 mg per day. Enjoy your Bank Holiday. X
Haired
in
LUPUS UK
1 year ago
APS Symptoms
I’m newly diagnosed as Type 2 diabetic (through steroid use) and have meds for that for the autoimmune diseases I take Steroids 10mg,
Mepacrine
, Apixaban, asprin, Azathioprine and DF118 (Dihydrocodine), when needed paracetamol/morphine. I can’t have HCQ or Gabba or Amatryptalines.
I’m newly diagnosed as Type 2 diabetic (through steroid use) and have meds for that for the autoimmune diseases I take Steroids 10mg,
Mepacrine
, Apixaban, asprin, Azathioprine and DF118 (Dihydrocodine), when needed paracetamol/morphine. I can’t have HCQ or Gabba or Amatryptalines.
WendyWoo50
in
Hughes Syndrome APS Forum
11 months ago
5 weeks on recovering from Covid-19
Once the paramedics left they went to my GP surgery which is on the road I live on and came back to say that I must stop taking
Mepacrine
and Hydroxychloroquine and other medicine for my Mixed Connective Tissue Disease and Lupus. I can only restart taking them once I felt better.
Once the paramedics left they went to my GP surgery which is on the road I live on and came back to say that I must stop taking
Mepacrine
and Hydroxychloroquine and other medicine for my Mixed Connective Tissue Disease and Lupus. I can only restart taking them once I felt better.
Ironmytherapy
in
LUPUS UK
3 years ago
Mepacrine
Does anyone take
mepacrine
? I have been prescribed this after having really bad constant headaches on hydroxychloroquine. How do you find it? Xx
Does anyone take
mepacrine
? I have been prescribed this after having really bad constant headaches on hydroxychloroquine. How do you find it? Xx
Aurali
in
LUPUS UK
3 years ago
Help with discoid lupus
Then I wasn’t getting better with it therefore i was put on
Mepacrine
. I had an adverse reaction and y whole body flared up with a itchy rash and blistered hands and feet like they had been in a fire . I’m now tying the quinorac again but still struggling .
Then I wasn’t getting better with it therefore i was put on
Mepacrine
. I had an adverse reaction and y whole body flared up with a itchy rash and blistered hands and feet like they had been in a fire . I’m now tying the quinorac again but still struggling .
Racingmurphy-1985
in
LUPUS UK
3 years ago
Mepacrine for Lupus Joint Pain?
I’ve just been given a prescription for
mepacrine
to add to my drug cocktail of hydroxycloriquine, mycophenolate, prednisolone and flecainide. The goal is to get a joint pain flare under control. Anyone have any success with this?
I’ve just been given a prescription for
mepacrine
to add to my drug cocktail of hydroxycloriquine, mycophenolate, prednisolone and flecainide. The goal is to get a joint pain flare under control. Anyone have any success with this?
ShannonB
in
LUPUS UK
3 years ago
RITUXIMAB INFUSION FOR LUPUS AND SJOGRENS
I was taken off medications including
Mepacrine
which really helped Sjogrens . Although brain fog, breathlessness has improved ( I felt Methotexrate increases symptons) my skin lupus symptoms/ flare up is getting worse and Sjogrens symptoms.
I was taken off medications including
Mepacrine
which really helped Sjogrens . Although brain fog, breathlessness has improved ( I felt Methotexrate increases symptons) my skin lupus symptoms/ flare up is getting worse and Sjogrens symptoms.
Haired
in
LUPUS UK
4 years ago
RITUXAN ANY ADVICE/ COMMENTS ON SIDE EFFECTS
Taken off Imuran and
Mepacrine
. Due to see consultant tomorrow to discuss RITUXAN as Lupus and Sjogrens symptoms getting worse . Any advice. Many thanks.
Taken off Imuran and
Mepacrine
. Due to see consultant tomorrow to discuss RITUXAN as Lupus and Sjogrens symptoms getting worse . Any advice. Many thanks.
Haired
in
LUPUS UK
4 years ago
Does anyone have Discoid Lupus that has caused permanent scarring and alopecia?
I am on Hydroxychloroquine and just been put back on
Mepacrine
too. I have also been told to use Dermovate cream on the lesions.
I am on Hydroxychloroquine and just been put back on
Mepacrine
too. I have also been told to use Dermovate cream on the lesions.
Purpleowl12
in
LUPUS UK
4 years ago
Sjogrens Syndrome
I am on
Mepacrine
for over 2 yrs now with no problems. Really helped fatigue. have skin Lupus On Methotexrate 8 months. Monday I woke up with numb arm from elbow down and very unsteady when tried to walk . As I had a stroke in Jan thought it was happening again.
I am on
Mepacrine
for over 2 yrs now with no problems. Really helped fatigue. have skin Lupus On Methotexrate 8 months. Monday I woke up with numb arm from elbow down and very unsteady when tried to walk . As I had a stroke in Jan thought it was happening again.
Haired
in
LUPUS UK
4 years ago
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