Phoenix Rising supports the Millions Missing global day of protest
Phoenix Rising is delighted to support the demands being made in the ME/CFS community’s first-ever global day of protest …
Discuss the article on the Forums.

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

Discussion in 'Problems Standing: Orthostatic Intolerance; POTS' started by Jesse2233, Dec 28, 2017.

?

How has ivabradine affected you?

  1. Significant improvement

    0 vote(s)
    0.0%
  2. Minor improvement

    3 vote(s)
    11.1%
  3. No change

    2 vote(s)
    7.4%
  4. Minor worsening

    3 vote(s)
    11.1%
  5. Major worsening

    0 vote(s)
    0.0%
  6. I have not tried ivabradine

    19 vote(s)
    70.4%
  1. manasi12

    manasi12

    Messages:
    85
    Likes:
    174
    @Gingergrrl ..
    Absolutely no problem. I can totally understand your situation.
    Meanwhile if u don't mind me asking did you ever have plaquenil ?
     
  2. Gingergrrl

    Gingergrrl Senior Member

    Messages:
    11,931
    Likes:
    34,990
    USA
    I have never taken Plaquenil but I know many people on PR have and could probably give you good feedback.
     
    manasi12 likes this.
  3. Chelby

    Chelby

    Messages:
    57
    Likes:
    87
    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.
     
    manasi12 likes this.

See more popular forum discussions.

Share This Page