Experiences with

Etodolac

I have Alendronic acid weekly, folic acid weekly, Calcichew daily and I am also on Gabapentin, Etodolac and Atorvastatin daily. Unfortunately I had COVID in March 2020 and I was in ICU on a ventilator.

Ok. Been putting off writing because it's going to be long. Rheumy still hasn't gotten back to me on CT scan done July 6. Hips screaming. Shoulders tolerable. Why has she not? She is only in the clinic 1 day/week now. Next appt. She set for me is Oct. 3! This from their nursing line who advised me to

After transplant I experienced multiple sinus infections that I never had before due to be immune suppresion and more recently due to new poor levels of air quality due to climate change, those are becoming more frequent with eye infection as well. My question concerning eye infections. Has anyone had

Hello, I have been suffering from symptoms over the last few weeks and I am struggling to get any progress with hospitals. I am 26 years old and I have never had any issues with headaches in my life. As a bit of background I have probably just had the most stressful year of my life and one of my aunties

Also taking 600mg Etodolac(Lodine) K2 90mcg, Gopo (rosehip +vit C), Magnesium glycinate 200, Acidopholus Extra 10, 1 daily, selenium 200mcg. Turmeric 400mg x 3 daily.

I take that because I also take a high dose ante inflammatory Etodolac (600mg!) I thought Ranitidine had been banned in the USA bust my consultant suggested I try it ! Also, what do other people take to protect their stomach? She’s also going to prescribe a spray for me to help my dry mouth.

I have discovered that my lodine (etodolac) anti inflammatory is responsible for some of the tiredness. I have been on it 10 years for my arthritis and have always known that it causes tiredness and fuzzy head but never to the extent I have now.

That and the usual folic acid and etodolac. All going well, however my skin is so dry and I keep getting lots of spots particularly on my face and shoulders and hairline. I am 54 so not an adolescent lol! Also not menopause as I had a total hysterectomy 10 years ago!

PROSTATE CANCER A five year journey trying for the best quality of life Our experience .. Jozef was diagnosed with multiple METS to the bones in June 2013 PSA 100 PSA doubling every month if we did not add anything He died July 2018 His red cell and platelets count were crashing

Currently trying etodolac, tried various NSAIDs, diclofinic, naproxen, ibrofen, etoricoxib, celecoxib also gabapentin, pregagablin (these are ones I remember!) either with no help or reactions to or made un fit to drive.

Is this a common, 'normal' thing to experience with anxiety? I have been very, very tired, sleeping at least 10 hours a night, waking up tired, wanting to sleep all day, and experiencing light headedness off and on if I'm not laying down. This has been going on for about 4 days. I find that if I get

I'm having Dr. patient relationship problems. I have been diagnoses with Small fiber polyneuropathy without Autonomic neuro. 2nd Fibromyalgia . I also have DDD in my lumbar. I'm 35 with 3 kids and have become unable to work. My last visit with my primary left me confused, anxieties, and mad. I had told

I was on Etodolac but didn't notice any improvement, so onto Arconia. Just be interesting to hear what others have noticed with it. MJ

My current medications are: Etodolac 600mg daily, Folic acid 5mg weekly, Hydrochloroquine 200mg x 2 daily, Levothyroxine 100mcg daily, Methotrexate 2.5mg x 5 weekly, Omeprazole 20mg daily, Reletrans patches 10mcg/hour weekly, Vensir XL 225mg daily. So do I feel any better with these medicines?

Taking pregabalin or gabapentin alongside amitriptyline as well as changing naproxen to etodolac 800mg. He also prescribed capsicum cream for my bone pain in my upper legs as well as getting me an appointment with the nurse to show me how to use the TENS machine that they will provide.

I'm not sure it's related...I'm on mtx leflunomide folic acid hydroxychloroquine prednisone etodolac . Occasionally I have this horrid Shap wrap around the chest pain.

I take Etodolac (anti-inflammatory) 300mg twice a day to help the pain in my joints, I have discoid lupus, but my GP thinks I may have SLE as I have many of the symptoms. I had an X-ray on Monday for my shoulder as this pain had been going on for sometime!

I have taken Etodolac and methocarbonol for months but they don't help.The orthopedic doctor said this is just part of having Parkinson deal with it.. I think patient with any chronic illness should have the right to the same kind of pain relief as any other patient.

I'm currently take omeprazole to prevent ulcers forming, sulpha salazine, hydroxy, and etodolac.

My doctor put me on Etodolac 600mg which helps a lot.In December I experienced pain at the base of my toes and in my ankle on my right foot.