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.

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 take Tildiem 500mg for AF and Hypertension .My BP had been creeping up so 6 weeks ago GP added in Losartan 25mg.Since then I have been aware of my heartbeat more, similar to when I started Diltiazem. My main worry is my resting heart rate has increased from 60 to 70.Has anyone else experienced an

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/

I'm 41 Yrs old, spouse, family man, with 3 children. To begin, at a young age, 22 yrs ago I was diagnosed with Parkinson's and given Sinement, carbidopa/ levodopa. Struggled through the years, but was able to maintain, had my girl, had 3 beautiful children, ran my business, bought our home, invested

Hello, I’m experiencing awful symptoms that are often intense and disturbing. It’s as if someone has flipped a switch, and I’m suddenly having unregulated breathing, heat waves in my entire body that feel like I am in an oven, dry as dust nasal passages, extreme weakness and fatigue which makes me feel

I haven't had success with the typical meds for PD If fact - the NeuPro patch and the Rytary made her worse So based on what I am learning from this community, I SHOULD try the following 1 NAC 2 B1 - high does thiamine 3 Lithium 4 Ambroxol 5 Mucuna Pruriens Questions - - Are there those that

My name is Phil. My wife Janet is 87 and has recently been diagnosed with atypical Parkinsons. We tried meds - NeuPro and Rytary BUT - because of the bad side effects (at least bad for Janet who weighs 86 lbs) - we have stopped both now The biggest issue is balance - - and falling backwards - breaking

I just returned from a conference (in the US) where the reps from Amneal said Crexont was priced significantly lower than Rytary which surprised me. They said it was done so that it would be more easily covered in Medicare Part D plans. I'm wondering if it is to get people on it and used to it

I am always super careful about not eating for at least an hour after taking my Rytary C/L ER, but if my digestive system is the least bit sluggish (I usually take Miralax daily, due to sporadic constipation), then I will have 2-3 days of rarely feeling “on”; I will do well to feel anywhere close to

I am always super careful about not eating for at least an hour after taking my Rytary C/L ER, but if my digestive system is the least bit sluggish (I usually take Miralax daily, due to sporadic constipation), then I will have 2-3 days of rarely feeling “on”; I will do well to feel anywhere close to

I hope others have experienced this and I am not the only one. I was diagnosed with PD in 2015. The past 6 months have been hell. I now experience irregular, rapid breathing about 30 to 45 minutes before I take my next dose of Rytary. I also basically “bottom out”, meaning I feel like I have no energy

for sleeping through the night I take two 25 mg quetiapine and three 36.5/145 rytary. For anxiety I take one .25 mg clonazapam 3x a day. I have been on this regimen for quite a few years now, and it has been very helpful. The quetiapam /rytary helps me fall asleep and get back to sleep if I wake