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    Created in 2008, Phoenix Rising is the largest and oldest forum dedicated to furthering the understanding of and finding treatments for complex chronic illnesses such as chronic fatigue syndrome (ME/CFS), fibromyalgia (FM), long COVID, postural orthostatic tachycardia syndrome (POTS), mast cell activation syndrome (MCAS), and allied diseases.

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Ivabradine / Corlanor - 80% Response Rate in POTS Patients (Nov / 2017 Study) + Poll

How has ivabradine affected you?

  • Significant improvement

    Votes: 0 0.0%
  • Minor improvement

    Votes: 4 13.8%
  • No change

    Votes: 2 6.9%
  • Minor worsening

    Votes: 3 10.3%
  • Major worsening

    Votes: 0 0.0%
  • I have not tried ivabradine

    Votes: 20 69.0%

  • Total voters
    29
Messages
88
Ivabradine has to be the only drug I've taken where I have noticed literally nothing. It was like I took a pill of air.

Dr Chris O'C suggested retrying it though anyway. For now I am happy doing metroprolol & midorine.