Booting Earth Optimization System
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Valsartan (ARB)
Treatment for Hypertensive heart disease
Typical Dosage: 40mg - 320mg daily
Effectiveness
87%
Safety Score
70%
Clinical Trials
2
Participants
500K
Comparative Safety Scale(Higher is safer)
Cyanide☠️
Meth💀
Cigarettes🚬
Chemo☢️
Alcohol🍺
Morphine💊
Antibiotics💉
Tylenol💊
Exercise🏃
Water💧
70
DangerousModerateSafe
Treatment Details
Dosage Range
40mg - 320mg daily
Time to Effect
2-4 weeks for full BP effect, months for cardiac remodeling
Treatment Duration
lifetime
Evidence Quality
HIGHNumber Needed to Treat (NNT)
18(Treat 18 patients to see 1 additional successful outcome)
Number Needed to Harm (NNH)
40(Treat 40 patients to see 1 additional serious adverse event)
Confidence Score
93%confidence in effectiveness data
Health Economics
Annual Cost of Care
Drug Cost:$100
Monitoring:$300
Side Effect Mgmt:$75
Total Annual:$475
Cost-Effectiveness Analysis
Cost-Effectiveness Rating
EXCELLENTICER
$25,000/QALY
QALYs Gained
2.4
Outcome-Based Costs
Cost per Responder
$659.72
Comparison vs Lisinopril (ACE Inhibitor)
Cost Difference
+$70/year
More expensive
QALY Difference
+0.05 QALYs
Better outcomes
Dominance
No dominance
Valsartan (ARB) Outcomes
for Hypertensive heart disease
Efficacy Outcomes
Overall Effectiveness
+87%
Response Rate
+72%
Common Side Effects
Dizziness
+5%
Hyperkalemia
+4%
Angioedema
+0.1%
Sources:
WARNING: LIMITED TRIALS AVAILABLE
You can search for trials, but you probably can't join any because the 1% Treaty hasn't passed yet. Most trials are severely limited by lack of funding and bureaucratic barriers. Help change this!
Active Clinical Trials
1 active trial recruiting for Valsartan (ARB) in Hypertensive heart disease
Effect of Sacubitril/Valsartan on Cardiac Function in Hypertensive Patients Stratified by BMI: A Real World Study
NCT05498675RECRUITING
180 participants
OBSERVATIONAL
Beijing, China
Started: Sep 1, 2021
Completed Clinical Trials
1 completed trial for Valsartan (ARB) in Hypertensive heart disease
Comparison of Valsartan With Amlodipine in Hypertensive Patients With Glucose Intolerance
NCT00129233COMPLETEDPHASE4
1.15K participants
INTERVENTIONAL
Nagoya, Japan
Started: Oct 1, 2004