Product image of Kengrexal (Cangrelor Tetrasodium) supplied by GNH India

Kengrexal

Active Ingredient:
Cangrelor Tetrasodium
Origin:
EU

Kengrexal (Cangrelor Tetrasodium)

Cangrelor, the active ingredient in Kengrexal, is a P2Y12 receptor antagonist presented as an intravenous solution for intravenous use. It provides periprocedural antiplatelet therapy for patients undergoing percutaneous coronary intervention (PCI) and serves as an adjunct to anticoagulation in acute coronary syndrome patients undergoing PCI.

GNH India supplies Kengrexal as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Chiesi Farmaceutici S.P.A.

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Indications & Clinical Uses

Kengrexal is a P2Y12 receptor antagonist used in the management of coronary artery disease interventions.

  • Percutaneous coronary intervention (PCI): provides rapid, reversible platelet inhibition during the procedure to reduce thrombotic complications.
  • Acute coronary syndrome (ACS) undergoing PCI: serves as an adjunct to anticoagulation to lower the risk of procedural myocardial infarction.
  • Cardiac catheterization: ensures antiplatelet coverage during diagnostic and therapeutic catheter‑based procedures.

How It Works

  • Cangrelor binds reversibly to the platelet P2Y12 ADP receptor, blocking ADP‑induced activation of the GPIIb/IIIa complex and preventing platelet aggregation. This inhibition occurs rapidly after intravenous administration and is offset quickly as the drug is cleared, allowing precise control of antiplatelet effect during coronary interventions.

Side Effects

Kengrexal may cause a range of adverse reactions, most of which are related to its antiplatelet activity.

Common Side Effects

  • Bleeding: bruising, epistaxis, gastrointestinal hemorrhage.
  • Dyspnea: shortness of breath during infusion.
  • Infusion site reactions: pain, erythema, or phlebitis.

Serious or Rare Side Effects

  • Severe hemorrhage: intracranial or life‑threatening bleeding.
  • Thrombocytopenia: marked reduction in platelet count.
  • Anaphylaxis: acute allergic reaction with hypotension and airway compromise.
  • Cardiac arrest: rare but potentially fatal cardiac events.
  • Severe arrhythmias: ventricular tachycardia or fibrillation.

Precautions & Warnings

When using Kengrexal, clinicians should observe several safety measures.

  • Monitor bleeding: assess patients frequently for signs of hemorrhage.
  • Adjust for renal impairment: consider reduced clearance in patients with severe kidney dysfunction.
  • Avoid in active severe bleeding: contraindicated in patients with ongoing major bleeding.
  • Use caution with concomitant anticoagulants: increased risk of bleeding when combined with heparin, warfarin, or direct oral anticoagulants.
  • Discontinue before surgery: stop infusion at least one hour prior to invasive procedures.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Kengrexal can interact with other agents that affect hemostasis.

Major Interactions (Avoid)

  • Concurrent potent antiplatelet agents (e.g., clopidogrel, ticagrelor): may cause excessive bleeding.
  • Strong anticoagulants (e.g., unfractionated heparin, warfarin, direct oral anticoagulants): increase risk of severe hemorrhage.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): additive gastrointestinal bleeding risk.
  • Glycoprotein IIb/IIIa inhibitors: may enhance antiplatelet effect and bleeding.
  • Fibrinolytic therapy: combined use can lead to heightened hemorrhagic complications.

Frequently Asked Questions

Kengrexal is an intravenous antiplatelet medication indicated for periprocedural antiplatelet therapy in patients undergoing percutaneous coronary intervention (PCI) and as an adjunct to anticoagulation in acute coronary syndrome patients who are undergoing PCI.

Cangrelor acts by reversibly binding to the platelet P2Y12 ADP receptor, blocking ADP‑mediated activation of the GPIIb/IIIa complex and thereby preventing platelet aggregation. This rapid, short‑acting inhibition allows precise control of antiplatelet effect during coronary procedures.

The dosing regimen for Kengrexal is determined by the prescribing clinician based on the specific procedural context and patient characteristics. Typically, a loading bolus followed by a continuous intravenous infusion is used, but exact amounts and rates are set by the healthcare professional.

Safety of cangrelor in pregnancy and lactation has not been established. It should only be used when the potential benefit justifies the potential risk to the fetus or infant, and the decision should be made by the treating physician.

To order Kengrexal, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if needed) and necessary import documentation.

Kengrexal provides rapid, reversible platelet inhibition via intravenous administration, unlike oral P2Y12 inhibitors such as clopidogrel or ticagrelor which have slower onset and longer duration. This makes Kengrexal especially useful for short‑term, procedural antiplatelet needs where quick offset of effect is desired.

Kengrexal should be stored at 2‑8 °C in a refrigerator, protected from light. Do not freeze or shake the solution. Keep the container in its original packaging until use to maintain stability.

Kengrexal is given by intravenous infusion. A typical protocol involves an initial bolus dose followed by a continuous infusion over the duration of the coronary procedure, administered by qualified healthcare personnel under aseptic conditions.

The most serious risks include severe or life‑threatening bleeding, intracranial hemorrhage, thrombocytopenia, anaphylactic reactions, and rare cardiac events such as cardiac arrest or severe arrhythmias. Patients should be closely monitored for any signs of these complications.

Kengrexal is contraindicated in patients with active severe bleeding, a history of intracranial hemorrhage, known hypersensitivity to cangrelor or any component of the formulation, and in those for whom the risk of bleeding outweighs the anticipated benefit.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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