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Naproxen and kidney insufficiency
I have kidney insufficiency (51%), aged 70. I also have rheumatoid arthritis in my feet and is very painful. Before I ask my doctor, is it advisable for me to take Naproxen and PPI's?
I have kidney insufficiency (51%), aged 70. I also have rheumatoid arthritis in my feet and is very painful. Before I ask my doctor, is it advisable for me to take Naproxen and PPI's?
jacartist
in
Lung Conditions Community Forum
2 years ago
Severe Flare up but no bleeding..
Hi, Is anybody else experiencing painful flare ups but no bleeding? If so, how are you managing? I'm currently on Naproxen 500mg twice a day, codeine 30mg twice a day, and am unable to leave my flat as I'm unable to walk due to the constant pain. I've been diagnosed with stage 4 endometriosis and just
Hi, Is anybody else experiencing painful flare ups but no bleeding? If so, how are you managing? I'm currently on Naproxen 500mg twice a day, codeine 30mg twice a day, and am unable to leave my flat as I'm unable to walk due to the constant pain. I've been diagnosed with stage 4 endometriosis and just
LaLuz
in
Endometriosis UK
2 years ago
Severe constant pelvic pain
I’m in so much pain and the doctors can’t seem to diagnose it. 5 weeks ago I had painful urination and I was given antibiotics. But a couple of weeks later it progressed to severe pelvic pain, I have lower abdominal aches, dark cloudy urine that smells strong. For the past 2 days I’ve been getting chills
I’m in so much pain and the doctors can’t seem to diagnose it. 5 weeks ago I had painful urination and I was given antibiotics. But a couple of weeks later it progressed to severe pelvic pain, I have lower abdominal aches, dark cloudy urine that smells strong. For the past 2 days I’ve been getting chills
Patience147
in
Pelvic Pain Support Network
2 years ago
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Severe pain but clear ultrasound?
Hi all, I was diagnosed with Endo via laparoscopy in 2018. Since then I've struggled to get care/treatment on the NHS so mostly self managing. A couple of weeks ago I woke up with a different, severe type of pelvic pain, so bad I thought it might be something different. Ended up in a&e - doctors suspected
Hi all, I was diagnosed with Endo via laparoscopy in 2018. Since then I've struggled to get care/treatment on the NHS so mostly self managing. A couple of weeks ago I woke up with a different, severe type of pelvic pain, so bad I thought it might be something different. Ended up in a&e - doctors suspected
Squirrel1991
in
Endometriosis UK
2 years ago
Are my expectations too high?
I was diagnosed 15 months ago. I was started on prednisolone then added methotrexate then sulfasalazine then abatacept. I am now taking all four plus co codamol and naproxen occasionally. I would have expected to be able to function but my hands are still very stiff and painful and am very fatigued.
I was diagnosed 15 months ago. I was started on prednisolone then added methotrexate then sulfasalazine then abatacept. I am now taking all four plus co codamol and naproxen occasionally. I would have expected to be able to function but my hands are still very stiff and painful and am very fatigued.
Oscardoggy
in
NRAS
3 years ago
LETROZOLE
Hi this is my first post 10 months ago when I just turned 60 I went for a routine mammogram and got a call back! Well it was like an outer body experience could not believe it was happening to me . So after 3 hours of mammograms, ultrasounds and biopsies they confirmed I had breast cancer! I had a 2cm
Hi this is my first post 10 months ago when I just turned 60 I went for a routine mammogram and got a call back! Well it was like an outer body experience could not believe it was happening to me . So after 3 hours of mammograms, ultrasounds and biopsies they confirmed I had breast cancer! I had a 2cm
Bunny286
in
My Breast Cancer Community
3 years ago
Help with lack of sleep 💤
Hi all hope you’re having a reasonable day? I’m quite new on here & newly diagnosed with fibromyalgia. I also have had osteoarthritis for many years. I take Naproxen as & when for pain but at the moment I can’t sleep. I use This Works pillow spray & wear compression socks. My Consultant & GP want me
Hi all hope you’re having a reasonable day? I’m quite new on here & newly diagnosed with fibromyalgia. I also have had osteoarthritis for many years. I take Naproxen as & when for pain but at the moment I can’t sleep. I use This Works pillow spray & wear compression socks. My Consultant & GP want me
Booksgranny
in
Fibromyalgia Action UK
3 years ago
Alternative to naproxen
Alternative to naproxen Hi I’ve been taking naproxen for some years now for RA, but I also have CKD ( chronic kidney disease). After going for my six monthly checkup with the RA specialist, she has suggested I stop naproxen and switch to co-codamol, which I reluctant to do. Has any one been in the
Alternative to naproxen Hi I’ve been taking naproxen for some years now for RA, but I also have CKD ( chronic kidney disease). After going for my six monthly checkup with the RA specialist, she has suggested I stop naproxen and switch to co-codamol, which I reluctant to do. Has any one been in the
Chris_O
in
NRAS
3 years ago
Problems getting prescriptions for naproxen and omeprazole
I have Rheumatoid Arthritis and I take hydroxy, methotrexate and abatacept Last week I requested some more naproxen. I don't take a lot if it these days since I started with abatacept so it was a year or more since my last prescription request. I was told 'there is a 3 star interaction with methotrexate
I have Rheumatoid Arthritis and I take hydroxy, methotrexate and abatacept Last week I requested some more naproxen. I don't take a lot if it these days since I started with abatacept so it was a year or more since my last prescription request. I was told 'there is a 3 star interaction with methotrexate
JenniferW
in
NRAS
3 years ago
Ankylosing spondylitis? What happens next?
6 years ago I was given diagnosis of Lupus after decade of pain and illness. I started taking Hydroxychloroquine which helped a little. I still take max dose. Not seen consultant since 2019. Finally agreed to see me face to face next week. I live with huge amount of pain, stiffness and inflammation.
6 years ago I was given diagnosis of Lupus after decade of pain and illness. I started taking Hydroxychloroquine which helped a little. I still take max dose. Not seen consultant since 2019. Finally agreed to see me face to face next week. I live with huge amount of pain, stiffness and inflammation.
Beau2016
in
NRAS
3 years ago
Non drowsy pain medication?
Hi all, I have endo between uterus and bowel, my left ovary is stuck to my pelvis and bowel and I have adeno as well. I've only tried ibuprofen, paracetemol, naproxen, codeine and co-codamol (over the counter strength) for pain relief and co-codamol works best to take the edge off. Unfortunately it
Hi all, I have endo between uterus and bowel, my left ovary is stuck to my pelvis and bowel and I have adeno as well. I've only tried ibuprofen, paracetemol, naproxen, codeine and co-codamol (over the counter strength) for pain relief and co-codamol works best to take the edge off. Unfortunately it
Kricam78
in
Endometriosis UK
3 years ago
What is the best pain relief for osteoarthritis?
Hi guys... I have had OA for a few years now and it's just getting progressively worse. I am also very overweight which doesn't help and have been battling with my weight all my life and I'm still trying everyday!!! The pain everyday is just chronic and has really taken a toll on my mental health as
Hi guys... I have had OA for a few years now and it's just getting progressively worse. I am also very overweight which doesn't help and have been battling with my weight all my life and I'm still trying everyday!!! The pain everyday is just chronic and has really taken a toll on my mental health as
fluffy10
in
Osteoarthritis Action
3 years ago
Questions and update
Hi all, I just have a couple questions: 1.When you get a steroid shot in a joint, is it normal to experience the joint being swollen a little while later and then the next day? Like almost solid swollen? And maybe something like feeling warm in the eyes? 2. Do you ever forget to write symptoms down
Hi all, I just have a couple questions: 1.When you get a steroid shot in a joint, is it normal to experience the joint being swollen a little while later and then the next day? Like almost solid swollen? And maybe something like feeling warm in the eyes? 2. Do you ever forget to write symptoms down
JennaShi
in
LUPUS UK
3 years ago
PMR return? flare or ?
Painful shoulder & arm. PMR return or Rotator cuff injury? Started to hurt mid Dec. Only in right side However both elbow joints sore when pressed Dr- 2 x so far. Bloods all normal. ( prev when I had PMR blood markers not raised much but in so much pain dr prescribed steroids- pain gone) Dr 2nd visit
Painful shoulder & arm. PMR return or Rotator cuff injury? Started to hurt mid Dec. Only in right side However both elbow joints sore when pressed Dr- 2 x so far. Bloods all normal. ( prev when I had PMR blood markers not raised much but in so much pain dr prescribed steroids- pain gone) Dr 2nd visit
suzieh
in
PMRGCAuk
3 years ago
Pain
Hi all any advice please I suffer really bad with pain in legs it’s so bad at night it keeps me awake. In the day it’s ok doesn’t really bother me. I take 30mg of amitriptoline every night and naproxen
Hi all any advice please I suffer really bad with pain in legs it’s so bad at night it keeps me awake. In the day it’s ok doesn’t really bother me. I take 30mg of amitriptoline every night and naproxen
Sammyd66
in
Fibromyalgia Action UK
3 years ago
Diagnosis
I am yet to get a fibromyalgia diagnosis as I still cannot get to speak to a doctor. I have been under a specialist for couple years for my shoulder pain and he did write to my doctor asking if blood tests could be carried out for arthritis which came back fine. After my latest appointment in December
I am yet to get a fibromyalgia diagnosis as I still cannot get to speak to a doctor. I have been under a specialist for couple years for my shoulder pain and he did write to my doctor asking if blood tests could be carried out for arthritis which came back fine. After my latest appointment in December
Pumperkins
in
Fibromyalgia Action UK
3 years ago
Update - Rheumy, methotrexate and Pred
So I got to talk to my Rheumy yesterday. She is very cross that the Rhemy nurse (not cross with me!) suggested going back up from 7mg to 12mg before Christmas (I had only got down to 7mg to have an MRI on my neck... I was not pain-free at this level). I explained that my neck, wrists and hands were making
So I got to talk to my Rheumy yesterday. She is very cross that the Rhemy nurse (not cross with me!) suggested going back up from 7mg to 12mg before Christmas (I had only got down to 7mg to have an MRI on my neck... I was not pain-free at this level). I explained that my neck, wrists and hands were making
Mamamia21
in
PMRGCAuk
3 years ago
Naproxem
Whilst suffering an attack of gout, I was prescribed Colchicine which I spoke about in a separate post Ive now suffered another attack and told the doctor I cant take the above drug as it spiked my tinnitus. So they have now prescribed Naproxen which to my mind is possibly just as bad. Anyone had experience
Whilst suffering an attack of gout, I was prescribed Colchicine which I spoke about in a separate post Ive now suffered another attack and told the doctor I cant take the above drug as it spiked my tinnitus. So they have now prescribed Naproxen which to my mind is possibly just as bad. Anyone had experience
Stravinsky1666
in
British Tinnitus Association
3 years ago
Neuropathic symptoms? In excruciating pain and not being taken seriously
Hello everyone, A bit of background: I have been on a very long waiting list with the NHS to see gynacology, I finally got seen in November and I was told my symptoms were suspected endometriosis and I was put on the waiting list for a laparoscopy. I'm still waiting and haven't heard anything 11 weeks
Hello everyone, A bit of background: I have been on a very long waiting list with the NHS to see gynacology, I finally got seen in November and I was told my symptoms were suspected endometriosis and I was put on the waiting list for a laparoscopy. I'm still waiting and haven't heard anything 11 weeks
Jaa64678
in
Endometriosis UK
3 years ago
Wait for appointment
My husband started with pain and swelling in his hands, awful fatigue and nausea about 2 months ago. GP did bloods and x ray, said no rheumatoid factor or inflammatory markers but referred him to rheumatology as an urgent referral as it’s having such an impact on his life and work. (And mine as I’m having
My husband started with pain and swelling in his hands, awful fatigue and nausea about 2 months ago. GP did bloods and x ray, said no rheumatoid factor or inflammatory markers but referred him to rheumatology as an urgent referral as it’s having such an impact on his life and work. (And mine as I’m having
Nuthatch
in
NRAS
3 years ago
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