Valsartan (Diovan)
Angiotensin II receptor blocker (ARB) that selectively blocks AT1 receptors. Used for hypertension, heart failure, and post-MI. Unlike ACE inhibitors, does not cause cough or angioedema (no effect on bradykinin). 25% oral bioavailability, unaffected by CYP metabolism, primarily eliminated unchanged in bile/feces. Available in combination with HCTZ, amlodipine, and sacubitril (Entresto for HF).
Projected serum levels — 80 mg, once daily
Maintenance schedule: 80 mg once daily (oral).
Modeled steady state after ~1 days: peak ≈ 15.3 mg, trough ≈ 1.6 mg body load. Population-based estimate over 15 days for a 80 mg dose at a 70 kg reference body mass — the interactive app scales curves to your doses, timing, and body mass.
Key facts
- Category
- ARB
- Route modeled
- Oral
- Model confidence
- inferred
- Half-life
- 6 h
- Common dose
- 80 mg
- Suggested maximum
- 320 mg/day
- Reference dose range
- 40–320 mg (single dose)
- Suggested cadence
- once daily
- Validated against
- 80 mg oral — Cmax 1.8 mg/L at 3 h
Documented interactions
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danger
Carbamazepine (Tegretol) + Valsartan (Diovan)
Carbamazepine (Tegretol) inducer of CYP2C9 predicted to change Valsartan (Diovan) AUC by ~0.40x
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danger
CBD (Cannabidiol) + Valsartan (Diovan)
CBD (Cannabidiol) reversible_inhibitor of CYP2C9 predicted to change Valsartan (Diovan) AUC by ~3.33x
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danger
Fluconazole + Valsartan (Diovan)
Fluconazole reversible_inhibitor of CYP2C9 predicted to change Valsartan (Diovan) AUC by ~3.33x
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danger
Fluvoxamine (Luvox) + Valsartan (Diovan)
Fluvoxamine (Luvox) reversible_inhibitor of CYP2C9 predicted to change Valsartan (Diovan) AUC by ~3.33x
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danger
Metronidazole (Flagyl) + Valsartan (Diovan)
Metronidazole (Flagyl) reversible_inhibitor of CYP2C9 predicted to change Valsartan (Diovan) AUC by ~3.33x
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danger
Milk Thistle (Silymarin / Silybin) + Valsartan (Diovan)
Milk Thistle (Silymarin / Silybin) reversible_inhibitor of CYP2C9 predicted to change Valsartan (Diovan) AUC by ~3.33x
Serum checks 27 modeled interaction pairings for valsartan (diovan) across your whole stack — absorption conflicts, enzyme inhibition, and nutrient depletion included.
Research behind this entry
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Valsartan, captopril, or both in myocardial infarction complicated by heart failure (VALIANT trial)
Landmark RCT (14,703 patients) demonstrating valsartan was as effective as captopril for reducing mortality after MI complicated by heart failure, establishing ARBs as valid ACE inhibitor alternatives.
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A randomized trial of valsartan in chronic heart failure (Val-HeFT)
Large RCT (5010 patients) showing valsartan added to standard HF therapy reduced composite morbidity/mortality by 13%, driven primarily by 24% reduction in heart failure hospitalizations.
2 published studies referenced in the app, each with a plain-language summary.