Treatment Effectiveness
User reported effectiveness ratings Propranolol for various conditions.
Conditions | Major Improvement | Moderate Improvement | Much Worse | No Effect | Worse | Responses |
---|---|---|---|---|---|---|
Heart Murmur | 0 | 0 | 0 | 0 | 0 | 0 |
Hypertension | 20% | 40% | 10% | 30% | 0% | 10 |
Mitral Valve Prolapse | 25% | 34% | 13% | 25% | 3% | 76 |
PTSD | 17% | 22% | 0% | 44% | 17% | 18 |
Side Effects
User-reported side effects of Propranolol
Side Effect | Percent of Reports Propranolol |
---|---|
Diarrhea | 6% |
Chest Pain | 100% |
Constipation | 11% |
Chest Pain/heart Attack | 100% |
Complement Fixation | 0% |
Decreased Sex Drive | 21% |
Did Not Relieve Pain | 100% |
Difficulty Sleeping | 27% |
Disassociative Episodes | 3% |
Dissociation | 6% |
Dizziness or Lightheadedness | 44% |
Double Vision | 100% |
Excessive Tiredness | 44% |
Hallucinations | 4% |
Increased Head Pain | 13% |
Increased Sexual Pleasure | 0% |
Rapid Heartbeat | 10% |
Rash | 3% |
Supposed to Be for Imitrex - Heart Palpitations | 5% |
Upset Stomach | 15% |
Very Low Pulse | 36% |
Vomiting | 6% |
Weepiness | 11% |
K Side Effect | 1% |
Outcomes
Below is the degree of change seen after Propranolol is higher than average.

Outcomes Label
Outcomes
of
Below is the change in the listed outcome after
is higher than average.
(Math.abs(a['change']) < Math.abs(b['change'])) ? 1 : -1)"
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Propranolol Info
Property | Value |
---|---|
Variable Name | Propranolol |
Aggregation Method | SUM |
Analysis Performed At | 2020-05-05 |
Duration of Action | 21 days |
Filling Value | 0 |
Minimum Allowed Value | 0 count |
Number of Aggregate Predictors | 0 |
Number of Aggregate Outcomes | 0 |
Number of Measurements | 0 |
Number of Measurements (including those generated by tagged, joined, or child variables) | 0 |
Public | true |
Onset Delay | 30 minutes |
Unit | Count |
User Variables | 0 |
Variable Category | Treatments |
Variable ID | 94941 |