What is the recommended dose of nifedipine (calcium channel blocker) for hypertension?

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Recommended Nifedipine Dosing for Hypertension

For hypertension treatment, nifedipine extended-release tablets should be administered at an initial dose of 30 mg once daily, with titration over 7-14 days to a usual maintenance dose of 30-60 mg once daily, not exceeding 90 mg daily. 1

Dosing Guidelines

  • Nifedipine extended-release tablets should be administered orally once daily on an empty stomach 1
  • Tablets should be swallowed whole, not bitten or divided as this would disrupt the extended-release mechanism 1
  • Initial starting dose should be 30 mg once daily 1, 2
  • Titration should proceed over a 7-14 day period based on therapeutic efficacy and safety 1
  • The usual maintenance dose range is 30-60 mg once daily 1, 2
  • Doses above 90 mg daily are not recommended for hypertension 1
  • If discontinuation is necessary, dosage should be decreased gradually under physician supervision 1

Formulation Considerations

  • Extended-release formulations (GITS - Gastrointestinal Therapeutic System) are preferred over immediate-release formulations for hypertension 2, 3
  • Immediate-release nifedipine (10-30 mg three times daily, maximum 90 mg/day) should not be used without concomitant beta-blockade due to risk of adverse cardiovascular events 4
  • The extended-release formulation provides sustained blood concentrations over 24 hours, improving adherence and reducing side effects 3

Efficacy and Dose Response

  • In clinical trials, 74.5% of patients achieved blood pressure control with 30 mg once daily, while 25.5% required titration to 60 mg 3
  • At week 20 of treatment, mean systolic/diastolic blood pressure decreased from 160.1/97.4 mmHg at baseline to 141.5/84.8 mmHg in the 30-mg group and 146.6/88.8 mmHg in the 60-mg group 3
  • Response to nifedipine is independent of age and type of previous antihypertensive therapy 3
  • Some patients with well-controlled hypertension on nifedipine GITS 30 mg may be able to switch to 20 mg once daily with continued efficacy 5

Side Effects and Monitoring

  • The three most common adverse events are headache (12.2%), peripheral edema (8.1%), and dizziness (2.9%) 3
  • Side effects are generally dose-related and associated with vasodilatory action 2
  • The frequency of adverse events is typically highest in the first 3 weeks of treatment and decreases subsequently 3
  • Co-administration with grapefruit juice should be avoided 1

Special Considerations

  • Nifedipine is a dihydropyridine calcium channel blocker that primarily causes peripheral arterial dilation with minimal effects on AV or sinus node 2
  • For patients with resistant hypertension, dihydropyridine CCBs like amlodipine and nifedipine extended-release are among the most studied agents 6
  • Some data suggest that long-acting formulations of nifedipine may have slightly greater antihypertensive actions than amlodipine but are associated with more edema 6
  • Nifedipine may be particularly useful for patients with relative bradycardia 4

Common Pitfalls

  • Using immediate-release formulations without beta-blockade can lead to reflex tachycardia and increased cardiovascular risk 4
  • Failing to administer the extended-release tablet whole (biting or dividing) disrupts the controlled-release mechanism 1
  • Not allowing sufficient time for dose titration (should be 7-14 days) 1
  • Exceeding the maximum recommended dose of 90 mg daily for hypertension 1
  • Not monitoring for peripheral edema, which is a common dose-limiting side effect 3

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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