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Nitroprusside

Vasodilator — CARDIOVASCULAR SYSTEM

Also known as: nitroprussiat, nitroprusside sodium, nitroprusside sodium salt, sodium nitroferricyanide, sodium nitroprussiate, sodium nitroprusside, sodium nitroprusside hydrate, sodium nitrosylpentacyanoferrate

FDA approvedPMDA approvedATC C02DD01

Data last refreshed: (DrugCentral release 2024-11-01)

Key facts

Nitroprusside is a drug in the Vasodilator class catalogued in DrugCentral. It was first approved by the FDA in 1974. DrugCentral lists 2 molecular targets, including NPR1 and GUCY1B2|GUCY1A2|GUCY1A3|GUCY1B3. Recorded indications include Acute exacerbation of chronic congestive heart failure, Acute heart failure, Controlled Hypotension and Decompensated cardiac failure.

  • Drug class: Vasodilator.
  • Molecular targets: NPR1 and GUCY1B2|GUCY1A2|GUCY1A3|GUCY1B3 (2 listed in DrugCentral).
  • Indications: Acute exacerbation of chronic congestive heart failure, Acute heart failure, Controlled Hypotension, Decompensated cardiac failure and Hypertensive disorder and others.
  • ATC code: C02DD01 (Nitroferricyanide derivatives).

Indications & contraindications

Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).

Indications (7)

  • Acute exacerbation of chronic congestive heart failure
  • Acute heart failure
  • Controlled Hypotension
  • Decompensated cardiac failure
  • Hypertensive disorder
  • Hypertensive urgency
  • Malignant essential hypertension

Contraindications (14)

  • Acute cerebrovascular insufficiency
  • Acute nephropathy
  • Anemia
  • Benign intracranial hypertension
  • Chronic obstructive lung disease
  • Coarctation of aorta
  • Cobalamin deficiency
  • Disease of liver
  • Disorder of brain
  • Hyponatremia
  • Hypothyroidism
  • Hypovolemia
  • Leber's optic atrophy
  • Tobacco amblyopia

Mechanism & targets

Established pharmacologic classVasodilator

Molecular targets (2)

TargetGeneActionActivity
Atrial natriuretic peptide receptor 1NPR1unknown—
Soluble guanylate cyclaseGUCY1B2|GUCY1A2|GUCY1A3|GUCY1B3activator—

Regulatory approvals (2)

DateAgencyMarketed asApplicantOrphan
2021-08-25PMDA—MARUISHI PHARMACEUTICAL Co., Ltd
1974-05-10FDA—ROCHE

ATC classification

ATC codeTherapeutic hierarchy
C02DD01CARDIOVASCULAR SYSTEM › ANTIHYPERTENSIVES › ARTERIOLAR SMOOTH MUSCLE, AGENTS ACTING ON › Nitroferricyanide derivatives

Reported adverse-event signals

Strongest FDA FAERS disproportionality signals (log-likelihood ratio). A signal is a statistical association in spontaneous reports, not proof that the drug causes the event.

MedDRA termLLR
Fear96.4
Toxicity to various agents96.1
Renal failure92.2
Renal injury71.1
Anhedonia69.9
Unevaluable event63.5
Hypotension59.3
Blood cyanide increased58.2
Multiple organ dysfunction syndrome51.8
Emotional distress49.7

Chemical structure

Molecular formula—
Molecular weight—
CAS number—
InChIKey—
PubChem CID73415791

Frequently asked questions

Answers are generated from the structured data on this page, not written by hand.

What is Nitroprusside used for?

DrugCentral lists the following indications for Nitroprusside: Acute exacerbation of chronic congestive heart failure, Acute heart failure, Controlled Hypotension, Decompensated cardiac failure, Hypertensive disorder, Hypertensive urgency and Malignant essential hypertension.

How does Nitroprusside work?

Its molecular targets in DrugCentral include NPR1 and GUCY1B2|GUCY1A2|GUCY1A3|GUCY1B3 (activator).

When was Nitroprusside first approved?

Nitroprusside was first approved by the FDA in 1974.

What drug class does Nitroprusside belong to?

Nitroprusside is in the Vasodilator class.

Browse: all drugs starting with N · drug guides by category · protein targets A–Z.

Sources

How this page is built: methodology · editorial policy & corrections.

For research and educational use only — not medical advice. This page is compiled automatically from public databases. It is not written or reviewed by a clinician. Do not start, stop or change any treatment based on it; consult a qualified healthcare professional. Spotted an error? See our corrections policy or email hello@molforge.ai.

Quick facts

Status—
First approval1974-05-10
AgencyFDA
Targets2
Indications7
Formula—
DrugCentral ID4631
Interactive profile