Nifedipine

Nifedipine

DEA Class; Rx

Common Brand Names; Procardia, Procardia XL, Adalat CC, Nifedical XL, Adalat, Afeditab CR, Nifediac CC

  • Calcium Channel Blockers; 
  • Calcium Channel Blockers, Dihydropyridine
Oral calcium-channel blocker; prototype dihydropyridine with more prominent effects on vasodilation and coronary flow than diltiazem and verapamil; lacks effects on AV conduction; primarily used for angina, Prinzmetal’s angina, and HTN.

Indicated for the treatment of variant angina (Prinzmetal angina) and chronic stable angina.

For the treatment of hypertension.
For the treatment of proteinuria associated with diabetic nephropathy.
For the treatment of persistent singultus (hiccups).
For the inhibition of uterine contractions in premature labor.
For the treatment of achalasia.
For the treatment of high altitude pulmonary edema associated with altitude sickness.
For altitude sickness prophylaxis, specifically prevention of high altitude pulmonary edema.
For the treatment of anal fissures.
For the treatment of pulmonary hypertension.

Hypersensitivity to nifedipine or other calcium-channel blockers

Cardiogenic shock

Concomitant administration with strong CYP3A4 inducers (eg, rifampin, rifabutin, phenobarbital, phenytoin, carbamazepine, St John’s wort) significantly reduces nifedipine efficacy

Immediate release preparation (sublingually or orally) for urgent or emergent hypertension

Adverse effects differ between short-acting (conventional) and extended-release formulations, with the conventional preparations having more serious adverse drug reactions in some cases

  • Peripheral edema (10-30%)
  • Dizziness (23-27%)
  • Flushing (23-27%)
  • Headache (10-23%)
  • Heartburn (11%)
  • Nausea (11%)
  • Muscle cramps (8%)
  • Mood change (7%)
  • Nervousness (7%)
  • Cough (6%)
  • Dyspnea (6%)
  • Palpitations (6%)
  • Wheezing (6%)
  • Hypotension, transient (5%)
  • Urticaria (2%)
  • Pruritus (2%)
  • Constipation (<2%)
  • Chest pain (<2%)

Use with caution in (≤4 weeks) myocardial infarction (MI), congestive heart failure (CHF), advanced aortic stenosis, peripheral edema, symptomatic hypotension, unstable angina, concurrent use of beta blockers, hepatic or renal impairment, persistent progressive dermatologic reactions, exacerbation of angina (during initiation of treatment, after a dose increase, or after withdrawal of beta blocker)

Short-acting nifedipine may be less safe than other calcium-channel blockers in management of angina, hypertension, or acute MI

Use cautiously in combination with quinidine

Conventional (short-acting) form not indicated for hypertension

Use extended-release form with caution in severe GI stenosis; rare reports of GI obstructive symptoms in patients with known strictures or without history of GI obstruction in association with ingestion of long-acting nifedipine; bezoars can occur in very rare cases and may necessitate surgical intervention

Extended-release form contains lactose; thus, patients with rare hereditary problems of galactose intolerance, Lapp lactase deficiency, or glucose-galactose malabsorption should not take this medicine

Cirrhosis: Clearance reduced and systemic exposure increased

CYP3A inhibitors (eg, ketoconazole, fluconazole, itraconazole clarithromycin, erythromycin, grapefruit, nefazodone, saquinavir, indinavir, nelfinavir, ritonavir) may inhibit nifedipine metabolism and result in increased exposure when coadministered

Strong CYP3A inducers (eg, rifampin, rifabutin, phenobarbital, phenytoin, carbamazepine, and St John’s wort) may enhance nifedipine metabolism and result in decreased exposure when coadministered

Avoid use in heart failure due to lack of benefit, and/or worse outcomes with calcium channel blockers in general

Use with caution in patients with hypertrophic cardiomyopathy and outflow tract obstruction; reduction in afterload may worsen symptoms associated with this condition

Avoid use of immediate release formulation in the elderly; may cause hypotension and risk precipitating myocardial ischemia

Pregnancy category: C

Lactation: Drug is distributed into breast milk; manufacturer suggests discontinuing drug or refraining from nursing (however, American Academy of Pediatrics states that drug is safe for nursing)

Adults

90 mg/day PO for Procardia XL or 180 mg/day PO for immediate-release capsules for angina; 90 mg/day PO for most extended-release tabs and 120 mg/day PO for Procardia XL for hypertension.

Elderly

90 mg/day PO for Procardia XL or 180 mg/day PO for immediate-release capsules for angina; 90 mg/day PO for most extended-release tabs and 120 mg/day PO for Procardia XL for hypertension.

Adolescents

Safety and efficacy have not been established; however, up to 3 mg/kg/day PO (not to exceed 180 mg/day) for extended-release tablets has been used off-label for hypertension; 0.5 mg/kg/dose (not to exceed 10 mg/dose) has been used off-label for hypertensive urgency/emergency.

Children

Safety and efficacy have not been established; however, up to 3 mg/kg/day PO (not to exceed 180 mg/day) for extended-release tablets has been used off-label for hypertension; 0.5 mg/kg/dose (not to exceed 10 mg/dose) has been used off-label for hypertensive urgency/emergency.

Nifedipine

capsule

  • 10mg
  • 20mg

tablet, extended release

  • 30mg
  • 60mg
  • 90mg
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