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Use and Dosing

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Treatment of acutely decompensated congestive heart failure

Reconstitution: Reconstitute 1.5 mg vial by adding 5 mL of a preservative-free diluent (e.g., 5% dextrose and 0.2 or 0.45% sodium chloride, 0.9% sodium chloride) taken from a prefilled 250-mL infusion bag. The final contents of the vial are then added back to the original 250-mL infusion bag for dilution, to yield a final nesiritide concentration of approximately 6 mcg/mL

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[Outline]

Indications

Contraindications

Black Box Warnings

Dosing Adjustment

Renal Dose Adjustment

Hepatic Dose Adjustment

Warnings/Precautions

Cautions: Use cautiously in

Pregnancy/Breast Feeding

Pregnancy Category:C

Breastfeeding: It is not known whether nesiritide is excreted in breast milk. Manufacturer advises caution

Adverse Reactions

Clinical Pharmacology

Brands and Availability

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US Trade Name(s)

US Availability

Natrecor

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Canadian Trade Name(s)

Canadian Availability

Natrecor

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UK Trade Name(s)

UK Availability

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Australian Trade Name(s)

Australian Availability


[Outline]

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Classification

Cardiovascular

Vasodilators
Other