Experiences with

Brufen Retard

Hi im 19 I'm now 3 days post op I had an ep study and catheter ablation.I had to spend 2hrs in recovery due to the fact I kept on stopping breathing, was foaming at mouth shaking and my blood pressure was extremly low, I had to spend 3hrs on oxygen due to the fact I kept stopping breathing. After I was

Have been on PAS page and Thyroid UK page for a few years but just thought I'd be greedy and join yourselves too. Have been having increasing levels of pain and discomfort for years but just told lose weight, take brufen. Last few years have been awful , eventually got a referral to Rheumatology. Bloods

Hi Fibro Family, I hope you are all coping these days. I have a few health conditions problems with my neck (spondylitis) knee damage (Chondromalacia ) and pain mainly in my lower back which makes me have to sit down after a few minutes, I feel it is like spasms. I am unable to get out now unless

hi Sue Hoping you’ll remember me. I’m Judith & live in uk I’m 74. my rls specialist In London increased my pregabalin by 100mg. I’m now on 200 mg am, 100 mg late afternoon & 200 mg b4 bedtime, so 500mg daily. I also take thyroxine, cocodamol if needed during the day. The Neurologist at the neurology

I have come off bisoprolol the last 3 weeks, but was put on a different tablet called Tildiem retard 90 mg twice a day.I had bad stomach and bowel pains that I didn't have before. I have Atrial fibrillation, very bad palpitations, and chest pain, these new tablets have improved my symptoms but not

I’m on 20mg of riveroxaban. I’m suffering with arthritis and ligament pain in back and hip. GP is referring me to orthopaedics but has suggested brufen gel. I asked if it was okay with riveroxaban and he said yes intermittently. Does anyone here on blood thinners use brufen gel?

Hoping for some advice. My wife has HCM and has had an ablation a few years ago. Her Afib seemed to calm down but recently it has increased dramatically. The ablation was carried out in London and appointments were not too difficult to obtain. We now live in Gloucestershire and it seems that getting

I think you should try amitriptyline and Cymbalta helps me ....90 mg Cymbalta and 25 mg amitriptyline.I also take tylex and Brufen at bad times. Very best of luck and good health Seastreak

currently after 1.5 years taking C/L, i am taking half pill every two hours. It wears off really fast with shortness of breath and bradykinesia, if I take one pill it gives me dyskinesia. A doctor in Mayo clinic switched me to rytary. It is expensive , do you think switching worth it?

I am interested in hearing from people who have tried the new drug Crexont. My neurologist wanted to me to try it and see if it would increase my on time. I am currently on Rytary. My concern is that one of the side effects is anxiety, although a low percentage is report this. >3%

I am interested in hearing from people who have tried the new drug Crexont. My neurologist wanted to me to try it and see if it would increase my on time. I am currently on Rytary. My concern is that one of the side effects is anxiety, although a low percentage is report this. >3%

Can anyone answer this question for me? I take Rytary Four to five times a day. It all works pretty good except my third dosage. I take 285 mg each dosage. The third dosage is at 1:00 and does not kick in. I have to take my 4th at 4;30 (a little early) and it kicks in fine. Maybe it’s food interference

I've posted several times this year about having a rough time getting meds to work well enough. In December '23, i started Rytary. Made me compulsive (i couldn't stop doing whatever i focused on, cleaning, crafting, etc.), and my already fragile sleep took a hit. Made me feel crazy! Lowering the initial

Male, living in CA. A report about my symptoms and how I learned to interpret them to avoid overdosing. When I was diagnosed I fairly soon switched to Rytary 245mgs. They would last about 5 hours and I was on 4/day which was good, along with 1 ongentys in the morning or evening. At bad times of stress

Rytary gives me terrible dyskinesia. I’ve tried backing down to a lower dose and it doesn’t work well. So the doc gave me amantadine for the dyskinesia and it gives me insomnia. Going crazy trying to dose. My spouse is having some walking issues and I had to take him for a MRI today. Under stress right

Good Morning: Having trouble when I go to the dentist. My teeth are breaking off easily. Just realized it’s probably due to poor nutrition.i lost right good amount of weight and with so many pills and even vitamins and lots of water I drink, not usually hungry. Suggestions to start improving this

I have never come across ‘punch drunk’ as a symptom of Pd, yet I do experience it and 2 posts in this group have recently mentioned it. Typically, if I miss or forget a dose (I take rytary 4x per day and 1 dose of Amantadine for dyskinesia, I suffer from many of the typical pd symptoms such as speech

https://finance.yahoo.com/news/amneal-receives-u-fda-approval-204500535.html Amneal Receives U.S. FDA Approval for IPX203 for Treatment of Parkinson’s Disease to Be Launched as CREXONT® (Carbidopa and Levodopa) Extended-Release Capsules Delivers more "Good On" time with less frequent dosing compared

I recently lowered my Rytary to help with dyskinesia. My feet are really hurting a Lot now, especially after being on them this morning. Should I go back on the higher dose?Trying to decide. What to do. Any advice? Could this be dystonia?

Ok, it does the manic then falling off a cliff thing to me. I'm only taking it now in the morning, but afternoon CR results in stacking and sleeplessness. I've lost weight. Dont want to exercise. Just walk a bit. Nervous system out of whack. I jump when someone speaks to me. Past five nights very little