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Brand names: IVABRADINE, Corlanor
12.2 Pharmacodynamics Ivabradine tablets causes a dose-dependent reduction in heart rate. The size of the effect is dependent on the baseline heart rate (i.e., greater heart rate reduction occurs in subjects with higher baseline heart rate). At recommended doses, heart rate reduction is approximately 10 bpm at rest and during exercise. Analysis of heart rate reduction vs. dose indicates a plateau effect at doses > 20 mg twice daily. In a study of subjects with preexisting conduction system disea
Contraindications
11 documented side effects by frequency
10 Reddit threads analysed for IVABRADINE
Overall Sentiment
Slightly positive
Comparison Threads
0
Avg Post Score
218 upvotes
Most discussed side effects in community
TLDR, this post summarizes my key findings about Long Covid causes after 16 months of research; and $50k invested into tests & treatments… and breaks down my protocol of the most effective approach to healing. **My journey:** Over the past 16 months, I completely shut down my 7-figure business t
For context, I'm a 28 year old male. Dealing with long covid for 14 months now. Previously I was an athlete, training 1-2 hours in the gym every day + running 5k per day sprints. My main symptom has been **severe SOB (shortness of breath)**, so my daily 5k runs (which brought me so much joy) has bee
**NAD** but I am very keen to get to the bottom of why 10 months after getting covid in March 2020, I'm still occasionally experiencing heart palpitations. This post is specifically about heart palpitations, and not every other symptom; there are MANY mysteries about Long Covid, and since many of us
***Disclaimer:*** *I’m just a person trying to figure out how to live my best life with POTS, and hoping what I think I’ve learned for myself and my own situation can help other people figure out POTS and what is best for their own situations. I know how to read research, due to my academic training
Symptoms started at 13 for me, I was diagnosed with ADHD at 21, POTS at 22, heds at 23. Starting at 18 they gave me every mental health medicine imaginable, none worked. The ADHD medicines also failed one after the next. Eventually I was able to tolerate a small dose of vyvanse. Once my dysautonomia
TL;DR: After years of long Covid with dysautonomia-like symptoms, I am now hiking, cycling, working, and living a pretty much normal life. I would not say I am 100% - my energy is still not quite what it was, and I get some pain here and there, but my quality of life is pretty good. Key improvement
As the title suggests, I just want to share my amazingly positive experience on ivabradine. I have inappropriate sinus tachycardia + dysautonomia (generalised). After 2.5 years of being dismissed with 'anxiety' I finally found a cardiologist who put his ego aside and truly listened to me. My heart r
I developed POTS over the past year and a half, got my DX in February and immediately started treating it. It was always mild, I spent most of the day laying but I could easily get up, walk and even do things outside sometimes, all without fainting. I mostly had tachycardia and chronic fatigue. Now
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Dosage Forms
Tablet
Route
Oral