Nesiritide Side Effects
Medically reviewed by Drugs.com. Last updated on Oct 12, 2024.
Applies to nesiritide: intravenous powder for injection.
Important warnings
This medicine can cause some serious health issues
You should not use this medicine if you have very low blood pressure, or if your heart cannot pump blood properly.
Get emergency medical help if you have signs of an allergic reaction: hives; difficult breathing; swelling of your face, lips, tongue, or throat.
Tell your caregivers at once if you have:
-
a light-headed feeling, like you might pass out; or
-
little or no urination.
Common side effects may include:
This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects.
For healthcare professionals
Applies to nesiritide: intravenous powder for injection.
General adverse events
The most frequently reported side effects were hypotension, headache, nausea, renal impairment, and back pain.[Ref]
Cardiovascular
- Very common (10% or more): Hypotension (12%)[Ref]
Renal
- Very common (10% or more): GFR decreased (up to 31.4%), serum creatinine increased (up to 28%)[Ref]
Nervous system
- Common (1% to 10%): Headache, dizziness[Ref]
Dermatologic
Musculoskeletal
- Common (1% to 10%): Back pain[Ref]
Metabolic
- Common (1% to 10%): Hypoglycemia[Ref]
Gastrointestinal
- Common (1% to 10%): Nausea[Ref]
Local
- Postmarketing reports: Infusion site extravasation[Ref]
Hypersensitivity
- Postmarketing reports: Hypersensitivity reaction[Ref]
References
1. (2022) "Product Information. Natrecor (nesiritide)." Scios Inc
More about nesiritide
- Check interactions
- Compare alternatives
- Dosage information
- During pregnancy
- Drug class: vasodilators
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Further information
Nesiritide side effects can vary depending on the individual. Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
Note: Medication side effects may be underreported. If you are experiencing side effects that are not listed, submit a report to the FDA by following this guide.