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IRON SUCROSE

FDA-approved approved Small molecule ✓ Verified May 2026 Quality 5/100

IRON SUCROSE is a Parenteral Iron Replacement [EPC] drug. It is currently FDA-approved (first approved 2000).

Iron sucrose is a small molecule supplement used to treat conditions such as iron deficiency, anemia, and anemia of chronic kidney disease. It is studied in clinical trials for the treatment of kidney disease and kidney failure.

At a glance

Generic nameIRON SUCROSE
Drug classParenteral Iron Replacement [EPC]
ModalitySmall molecule
PhaseFDA-approved
First approval2000

Approved indications

No approved indications tracked.

Common side effects

Serious adverse events

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

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Frequently asked questions about IRON SUCROSE

What is IRON SUCROSE?

IRON SUCROSE is a Parenteral Iron Replacement [EPC] drug.

What drug class is IRON SUCROSE in?

IRON SUCROSE belongs to the Parenteral Iron Replacement [EPC] class. See all Parenteral Iron Replacement [EPC] drugs at /class/parenteral-iron-replacement-epc.

When was IRON SUCROSE approved?

IRON SUCROSE was first approved on 2000.

What development phase is IRON SUCROSE in?

IRON SUCROSE is FDA-approved (marketed).

What are the side effects of IRON SUCROSE?

Common side effects of IRON SUCROSE include Headache, Respiratory tract viral infection, Peritonitis, Vomiting, Pyrexia, Dizziness. Serious adverse events: Anaphylactic-type reactions, Angioedema, Convulsions, Shock.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing