Experiences with

Tildiem Retard

I am currently on, Ezetimibe 10mg x 1 Isosorbide mononitrate 60mg x 1 Famotadine 20mg x 1 Tildiem retard 90mg x 2 Aspirin 75mg x 1 Rosuvastatin 5mg x 1 Amlodipine 5mg x 1 I have just been told to stop the Amlodipine as I had awful side affects.

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.

We thought we would ask our surgery pharmacist for more tablets but she said can’t do as they might react with her heart medicine which is Tildiem Retard 180mg twice a day. Despite phone calls and emails to our Glos cardiologist there is no reply.

Is there anyone taking 100mg Flecainide twice daily and Tildiem 60 mg twice daily? If so, have you had any problems with this combination?

I have heart disease suffer from occasional angina (whenever I exert myself eg walk up a slope) and my heart consultant has prescribed Ranolazine (alongside my other meds eg Edoxaban , Tildiem and Candesarten). However the side effects of Ranolazine are horrendous, especially the dizziness so frankly

Bisoprolol makes me so tired. No energy, exhausted. Consultant has just changed me to Tildiem. Does anyone take this drug and what are SE please UPDATE cant tolerate it. Only taken 2 so far but nearly took myself to A&E last night. Felt so ill

I feel like I have been through the wringer the past several months. My movement disorder specialist switched me from Rytary 48.75/195 (2 capsules 6X daily) to CREXONT 87.5/350 (2 capsules 3X daily, in order to see if it gave me more ON time. I started it on a Wednesday and by Friday I was feeling

I was put on metoprolol tartrate 25mg twice a day. It was prescribed because in the doctor's exam room I had BP140/90. I gained a lot of weight and had severe edema in my legs. It was winter in Colorado. I wore winter boots but couldn't lace them up because my feet were so swollen. I wondered

MY wife was looking for an address. She rifled through my inbox and found two unopened letters. Both letters had been sent nearly a year ago. When I get letters I read them then tuck the letter back into the envelope--to save the address--and store them in my inbox. I must have put the letters

Hi! My HWP has been experiencing some strange symptoms. Recently his body temp dropped to 95.6 and his BP has 200/120. We were at a soccer field watching grandkids play, and he could barely keep himself upright to walk to the car. It was very scary. Cardiologist gave me ER BP meds which helped and

Everyone knows about placebo, that being told something will help you means you'll get better even if it's a sugar pill. But what about Nocebo, the opposite end of the spectrum? What if negative thoughts leads to a worsening condition? The docs ask regularly about my signs; How is my balance

Recently my Neurologist wrote me a prescription for Rytary, however it's not covered by my drug plan and was going to cost me $883.00 per month, so I cancelled it. I'm in my 10th year with the diagnosis and it's getting pretty difficult to minimize the off times with just the C/L IR. Any advice would

I’m looking for anyone that has successfully replaced all or part of their Rytary or C/L dose with Mucuna. I am currently taking 3 x 195mg Rytary 5x per day at 6am 10am 2pm 6pm and 2am. I have been experiencing a lot more Off times, often between 8am and 11am and then 3pm-5pm. About 2 weeks ago I started

Hi Doc, I gave the Rytary idea a go. To refresh, take 45 rytary at bedtime to hopefully give me a base to then add sinemet ir thru the day. It didn't go well. In fact, the rytary just made me feel awful in my head and gut so I aborted. I resumed the sinemet regiment of basically 1/2 and 3/4 doses

I’ve been using Rytary 145 mg with 1 25/100 , I take Em release first, then 2 hours later the Rytary, it would give me about two hours- 3 on time and then another 25/100 and then in 2 hours 145 Rytary. It was working pretty well and then I started getting to much dyskinesia, so I backed off a bit

I was diagnosed with PD 5 yrs ago last Nov. I was an active 79 yrs young. My symptoms were tremor in foot that eventually has spread to legs, hands, curling in toes. My Neuro started me on C/L 25/100 4x daily. I can't say I have ever felt any good on times or any help from it.. It's like my body

It seems like my symptoms are progressing at what I feel is an alarming rate. i have had a knee repacement 8/29/24. currently, i take Crexont.(seems to be a rytary look alike, a timed release capsule that reduced the amount of times I had to take meds ) from 5x/day with rytary to 3x/day with crexmont

I have had Parkinson’s for 25 years. Dr is considering the pump when approved by Medicare. No telling how long that will be. In the meantime I have been on Rytary 3 95s every 3 hours. I have just developed dystonia (very painful) in my upper shoulder and neck. Dr just gave me a steroid shot, didn’t seem

Here listed are the side effects that my wife had while taking Rytary for 10 days These are listed for most, if not all of the Park drugs fatigue - she was napping more than usual dizziness when standing confusion was increasing constipation sleep problems (insomnia) On the 10th day, she collalpsed

Has anyone tried Crexont? Supposed to be better than Rytary 🤔 My doctor has prescribed it for me but still awaiting insurance authorization. https://crexont.com/