Search
Search
About
Log in
Join
Experiences with
Tenoxicam
Posts
Communities
199 public posts
Filter results
NSAIDs Might Exacerbate or Suppress COVID-19 Depending on Timing, Mouse Study Suggests.
( NSAIDs = Nonsteroidal anti-inflammatory drugs, eg Aspirin, Ibuprofen, Paracetamol ) New research shows that non-steroidal anti-inflammatory drugs (NSAIDs) reduced both antibody and inflammatory responses to SARS-CoV-2 infection in mice. The study appears this week in the Journal of Virology, a publication
( NSAIDs = Nonsteroidal anti-inflammatory drugs, eg Aspirin, Ibuprofen, Paracetamol ) New research shows that non-steroidal anti-inflammatory drugs (NSAIDs) reduced both antibody and inflammatory responses to SARS-CoV-2 infection in mice. The study appears this week in the Journal of Virology, a publication
2greys
in
Lung Conditions Community Forum
4 years ago
Argh!!!
Hi all, I have undifferentiated connective tissue disease and I’m having an awful flare up (the worst since diagnosis 3 years ago) causing bladder issues and pain and I can barely shuffle from one room to the next - mostly in bed. I’m getting a blood test tomorrow. Any ideas on how I might be ‘fixed’
Hi all, I have undifferentiated connective tissue disease and I’m having an awful flare up (the worst since diagnosis 3 years ago) causing bladder issues and pain and I can barely shuffle from one room to the next - mostly in bed. I’m getting a blood test tomorrow. Any ideas on how I might be ‘fixed’
Oxfordjojo
in
LUPUS UK
4 years ago
Help with Lower Scrotum and Perineum Pain
Hi All, I wanted to document my experience in hopes of getting good insights and helping others with similar pathology. That is, throbbing pain and tightness in the lower scrotum, behind scrotum and perineum area. 3-4 weeks prior to 4/5/2020, I started feeling tightness around my scrotum area. I ignored
Hi All, I wanted to document my experience in hopes of getting good insights and helping others with similar pathology. That is, throbbing pain and tightness in the lower scrotum, behind scrotum and perineum area. 3-4 weeks prior to 4/5/2020, I started feeling tightness around my scrotum area. I ignored
pelvicpainquestions
in
Pelvic Pain Support Network
4 years ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
Early Morning Aching
Hello All You Lovely People! I have had PMR for over 3 years and am tapering, using DSNS method, down to 6 and a half from 7 mgs pred. I also have inflammatory arthritis for which I take Meloxicam (7 mgs daily). I also take 10mgs Amitriptyline supposedly to help me sleep but "may also help with your
Hello All You Lovely People! I have had PMR for over 3 years and am tapering, using DSNS method, down to 6 and a half from 7 mgs pred. I also have inflammatory arthritis for which I take Meloxicam (7 mgs daily). I also take 10mgs Amitriptyline supposedly to help me sleep but "may also help with your
Louisa1840
in
PMRGCAuk
4 years ago
Kidney transplants and meloxicam
My husband is 18 years post kidney transplant. Due to severe pain in “private” areas we went to the ER last night where they prescribed meloxicam. Does anyone have any knowledge on whether a kidney transplant patient can take meloxicam?
My husband is 18 years post kidney transplant. Due to severe pain in “private” areas we went to the ER last night where they prescribed meloxicam. Does anyone have any knowledge on whether a kidney transplant patient can take meloxicam?
CSCleary
in
Kidney Transplant
4 years ago
Good News! But what about the joints (ankles, knees, elbows)?
Happy Monday, everyone. My pilgrimage to Rochester, Minnesota went well, last week. 656 days post diagnosis my PSA is, again, dropping after a modest post-radiation flair--now down to 0.14 (from the low three digits in April of '18). I'm pleased with the trajectory but I don't think I'll make it to zero
Happy Monday, everyone. My pilgrimage to Rochester, Minnesota went well, last week. 656 days post diagnosis my PSA is, again, dropping after a modest post-radiation flair--now down to 0.14 (from the low three digits in April of '18). I'm pleased with the trajectory but I don't think I'll make it to zero
StePeteMN
in
Advanced Prostate Cancer
5 years ago
Duloxetine
Has anyone had any bad interactions using Duloxetine with other meds?? I started it 2 days ago and haven't slept in 2 days because of it. I take Meloxicam, Gabapentin, & Ropinirole. It made my nerves way worse than they were.
Has anyone had any bad interactions using Duloxetine with other meds?? I started it 2 days ago and haven't slept in 2 days because of it. I take Meloxicam, Gabapentin, & Ropinirole. It made my nerves way worse than they were.
KayKay90
in
Neuropathy Support
5 years ago
Leg cramps
Awake almost every nite with severe muscle cramps mainly right, sometime also left leg and foot. I do have sciatica nerve pain from a bone spur and a herniated disc and also spinal stenosis. Am 82 yr old woman. On no medications. Magnesium cream and pills dont help. Have slight kidney disease, stage
Awake almost every nite with severe muscle cramps mainly right, sometime also left leg and foot. I do have sciatica nerve pain from a bone spur and a herniated disc and also spinal stenosis. Am 82 yr old woman. On no medications. Magnesium cream and pills dont help. Have slight kidney disease, stage
Barbola
in
Pain Concern
5 years ago
Stuck and don't know where to go now
Hi everyone I recently (july) had nerve root block injections around S1. I had these first around 3years ago and they worked amazing and I felt great with no pain aftetwards. However, in around March this year I started to feel the pain coming back again. It was managed with Tramadol and Pregablin, which
Hi everyone I recently (july) had nerve root block injections around S1. I had these first around 3years ago and they worked amazing and I felt great with no pain aftetwards. However, in around March this year I started to feel the pain coming back again. It was managed with Tramadol and Pregablin, which
Leelee16661
in
Pain Concern
5 years ago
Resorting to private Rheumatologist
After several years of getting nowhere with my GP and his referral to NHS Rheumie (who disagree with Dr David Gotlieb in Cape Town who diagnosed me with Sero-Negative RA 16 years ago) I have now made an appt with a private consultant at a Nuffield Hosp. £180 for first consult, £90 each following consult
After several years of getting nowhere with my GP and his referral to NHS Rheumie (who disagree with Dr David Gotlieb in Cape Town who diagnosed me with Sero-Negative RA 16 years ago) I have now made an appt with a private consultant at a Nuffield Hosp. £180 for first consult, £90 each following consult
ZsaZsa22
in
NRAS
5 years ago
Need advice on RA not being diagnosed via NHS
My GPs are not helping me get a diagnosis of RA. I was diagnosed in Cape Town 16 years ago with sero negative post partum RA, but ten years ago moved back to Scotland, where the NHS RA Specialist said he couldn't find any markers. I am in so much pain as medication is now no longer being monitored
My GPs are not helping me get a diagnosis of RA. I was diagnosed in Cape Town 16 years ago with sero negative post partum RA, but ten years ago moved back to Scotland, where the NHS RA Specialist said he couldn't find any markers. I am in so much pain as medication is now no longer being monitored
ZsaZsa22
in
NRAS
5 years ago
Has anyone had this combo of bloodwork and symptoms?
I was dx'd with lupus in 1997 but have never had any kidney or liver or other organ involvement except possibly some CNS stuff. I have taken Plaquenil in the past, but for most of these years, I have just taken either Naproxen or Meloxicam to manage my inflammation. My CBC bloodwork always turns up with
I was dx'd with lupus in 1997 but have never had any kidney or liver or other organ involvement except possibly some CNS stuff. I have taken Plaquenil in the past, but for most of these years, I have just taken either Naproxen or Meloxicam to manage my inflammation. My CBC bloodwork always turns up with
lupette
in
LUPUS UK
5 years ago
Constant Burning/Stinging Inside Vagina/Urethra
Hello, I have been dealing with this issue for about 3 months now. I would like any insight on what you guys think this might be or what may help. The pain is so debilitating/scary that I have turned to God. I'll start by saying I've had these feelings/small episodes of this as a kid and teenager. I
Hello, I have been dealing with this issue for about 3 months now. I would like any insight on what you guys think this might be or what may help. The pain is so debilitating/scary that I have turned to God. I'll start by saying I've had these feelings/small episodes of this as a kid and teenager. I
cassie14
in
Pelvic Pain Support Network
5 years ago
Seronegative PMR
I have been diagnosed with PMR, but have none of the traditional markers; ESR 2 mm/hr (normal), and CRP 1.3 mg/L (normal). I've had it for 6 months and only received 100% relief after receiving 1 shot of corticosteriod in each shoulder 2months ago. I was on Meloxicam (anti-inflamatory) and Cyclobenzaprine
I have been diagnosed with PMR, but have none of the traditional markers; ESR 2 mm/hr (normal), and CRP 1.3 mg/L (normal). I've had it for 6 months and only received 100% relief after receiving 1 shot of corticosteriod in each shoulder 2months ago. I was on Meloxicam (anti-inflamatory) and Cyclobenzaprine
bmgtc
in
PMRGCAuk
5 years ago
Anemia
Just wondering if others have dealt with anemia while on Imbruvica. Terrible fatigue and joint pain set in about three weeks ago, just one week after a clear PET scan. My oncologist has stopped the Imbruvica for now and the Meloxicam I’d been on for the joint pain that is a result of the Imbruvica.
Just wondering if others have dealt with anemia while on Imbruvica. Terrible fatigue and joint pain set in about three weeks ago, just one week after a clear PET scan. My oncologist has stopped the Imbruvica for now and the Meloxicam I’d been on for the joint pain that is a result of the Imbruvica.
Survivor1951
in
CLL Support
5 years ago
Sciatica
Hi everyone....my PV jak2+ seems to be behaving itself at the moment, and want to thank everyone for their help with my recent mouth sores and advice on a mouth wash that is working brilliantly. 3 years ago I had sciatica, L5 disc, I had operation to rectify it, which worked well, I still get flair ups
Hi everyone....my PV jak2+ seems to be behaving itself at the moment, and want to thank everyone for their help with my recent mouth sores and advice on a mouth wash that is working brilliantly. 3 years ago I had sciatica, L5 disc, I had operation to rectify it, which worked well, I still get flair ups
Yvette49
in
Pain Concern
5 years ago
Inflammation v Diclofenac etc
For around ten years I have had AF (latest report said 74% of the time) and also chronic inflammatory joint and muscle pain; both have been satisfactorily controlled (AF by PM and Bisoprolol) (inflammation by Diclofenac) and I have functioned and worked fully (if a little slowly at times!) and painless
For around ten years I have had AF (latest report said 74% of the time) and also chronic inflammatory joint and muscle pain; both have been satisfactorily controlled (AF by PM and Bisoprolol) (inflammation by Diclofenac) and I have functioned and worked fully (if a little slowly at times!) and painless
quanglewangle
in
Atrial Fibrillation Support
5 years ago
Do you really have reflux do you have reoccurring yeast infections And are you taking an anti-inflammatory?
I have been reading all the post about gabapentin meloxicam and reflux. I hope my experience will help in someway years ago I was diagnosed with reflux after my third back surgery. I started having major problems with acid so they told me I had reflux. I tilted my bed got on Prilosec and did everything
I have been reading all the post about gabapentin meloxicam and reflux. I hope my experience will help in someway years ago I was diagnosed with reflux after my third back surgery. I started having major problems with acid so they told me I had reflux. I tilted my bed got on Prilosec and did everything
Aneato
in
LUPUS UK
6 years ago
Sulfau
I been taking sulfasalazine 500 mg about year or more now on top of muscle relaxants meloxicam 7.5 mg. Pain meds as needed xienty meds for years, pain cream, heat pads when episodes were so bad in an out ER. Blood pressure off the chain to low or to high. Just feeling so bad an trying to work part
I been taking sulfasalazine 500 mg about year or more now on top of muscle relaxants meloxicam 7.5 mg. Pain meds as needed xienty meds for years, pain cream, heat pads when episodes were so bad in an out ER. Blood pressure off the chain to low or to high. Just feeling so bad an trying to work part
Quee
in
NRAS
6 years ago
Two years in and now Meloxicam for pain
I haven't visited this site for a while and my journey with PMR as a companion has been fairly unremarkable for the past two years. I moved to Kent where my GP has been very supportive and allowed me to stay at 7.5/8 mg for almost a year, but a recent flare has left me struggling and he has prescribed
I haven't visited this site for a while and my journey with PMR as a companion has been fairly unremarkable for the past two years. I moved to Kent where my GP has been very supportive and allowed me to stay at 7.5/8 mg for almost a year, but a recent flare has left me struggling and he has prescribed
Zebedee44
in
PMRGCAuk
6 years ago
1
2
3
4
...
10
Next page
10
Filter results
Clear filters
Posted in
All communities
NRAS
73 results
LUPUS UK
28 results
Fibromyalgia Action UK
19 results
View top 10 communities
Sort by
Most Relevant
Newest