How much will Amlodipine (calcium channel blocker) lower blood pressure from baseline?

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Last updated: December 13, 2025View editorial policy

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Blood Pressure Reduction with Amlodipine

Amlodipine lowers blood pressure by approximately 12-13 mmHg systolic and 6-7 mmHg diastolic from baseline in patients with mild to moderate hypertension when measured 24 hours after dosing. 1

Evidence from FDA-Approved Labeling

The most definitive data comes from the FDA drug label, which synthesized 15 double-blind, placebo-controlled trials involving 800 patients on amlodipine:

  • Supine position: 13/7 mmHg reduction (systolic/diastolic) 1
  • Standing position: 12/6 mmHg reduction (systolic/diastolic) 1
  • These reductions were placebo-corrected and measured at 24 hours post-dose, demonstrating sustained efficacy throughout the dosing interval 1

Dose-Response Relationship

The magnitude of blood pressure reduction is dose-dependent within the therapeutic range:

  • 2.5 mg dose: Minimum effective dose, produces modest reductions 2
  • 5 mg dose: Standard starting dose, achieves approximately 11-13/9-10 mmHg reduction 3, 4
  • 10 mg dose: Maximum dose, provides the greatest blood pressure lowering effect 1, 2

After 4 weeks of treatment, medium-dose (2.5-5 mg) and high-dose (5-10 mg) groups showed significant reductions compared to placebo, while low-dose groups (1.25-2.5 mg) showed less consistent effects 2

Baseline Blood Pressure Impact

The magnitude of reduction correlates directly with baseline blood pressure elevation 1:

  • Patients with moderate hypertension (diastolic 105-114 mmHg) experienced approximately 50% greater response than those with mild hypertension (diastolic 90-104 mmHg) 1
  • Normotensive subjects experienced minimal changes (+1/-2 mmHg) 1

Time Course of Effect

The blood pressure lowering effect follows a predictable pattern:

  • Single dose: Blood pressure decreases gradually over 4-8 hours, with peak effect at 6-12 hours post-dose 1, 5
  • Chronic dosing: Steady-state is reached after 7-8 days of consecutive daily dosing 1
  • 24-hour control: Maintenance of effect throughout the dosing interval with little peak-to-trough variation (20-25% fluctuation) 5, 6

Clinical Trial Data Supporting These Estimates

A well-controlled study using continuous intra-arterial monitoring demonstrated:

  • Daytime blood pressure: Reduced from 165/103 to 147/89 mmHg (18/14 mmHg reduction) 6
  • Nighttime blood pressure: Reduced from 137/79 to 121/69 mmHg (16/10 mmHg reduction) 6
  • The normal circadian pattern was preserved 6

A comparative trial with 188 patients showed amlodipine (mean dose 8.8 mg) produced:

  • Supine: -12.8/-10.1 mmHg reduction 4
  • Standing: -11.5/-9.8 mmHg reduction 4

Special Populations

Black patients: Calcium channel blockers like amlodipine are particularly effective, showing greater blood pressure reduction compared to ACE inhibitors or ARBs in this population 7, 8

Elderly patients: The effect on systolic pressure is greater in older patients, likely due to higher baseline systolic pressures 1

Diabetic patients: Similar efficacy to non-diabetic patients, with equivalent blood pressure reductions 7

Important Clinical Considerations

  • Heart rate remains unchanged with amlodipine therapy (mean change +0.3 bpm in angina patients, no significant change in hypertensive patients) 1, 6
  • The gradual onset of action prevents reflex tachycardia 5
  • Discontinuation results in slow return to baseline over 7-10 days without rebound hypertension 5
  • Most patients require 2 or more antihypertensive medications to achieve target blood pressure <130/80 mmHg 7, 8

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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