GNH USA

Europe — EMA

Lacrat

GNH USA supplies Lacrat (Ticagrelor), a P2Y12 receptor antagonist for acute coronary syndrome and myocardial infarction. Request a quote for global supply.

Ticagrelor

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What is Ticagrelor?

Ticagrelor, the active ingredient in Lacrat, is a P2Y12 receptor antagonist presented as an oral tablet for oral use. It is prescribed to reduce thrombotic cardiovascular events in patients with acute coronary syndrome or myocardial infarction. The medication works by inhibiting platelet aggregation, thereby lowering the risk of clot formation that can lead to heart attacks or strokes.

GNH USA supplies Lacrat as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide with a focus on quality assurance and regulatory compliance.

What is Ticagrelor used for?

Ticagrelor is used in antiplatelet therapy to manage conditions associated with platelet‑driven thrombosis. - Acute coronary syndrome: reduces the risk of cardiovascular death, myocardial infarction and stroke. - Myocardial infarction: prevents recurrent ischemic events after an acute heart attack. - Prevention of thrombotic cardiovascular events: lowers the incidence of clot‑related complications in high‑risk patients.

What are the side effects of Ticagrelor?

Ticagrelor may be associated with a range of adverse reactions, varying from mild to severe.

Common Side Effects: - Dyspnea: shortness of breath, often occurring early in therapy. - Headache: mild to moderate intensity. - Nausea: occasional gastrointestinal upset. - Diarrhea: loose stools without severe dehydration.

Serious or Rare Side Effects: - Bleeding: including intracranial hemorrhage or gastrointestinal bleeding. - Bradyarrhythmia: significant slowing of heart rate. - Hepatotoxicity: elevated liver enzymes indicating liver injury. - Severe allergic reaction: rash, angioedema, or anaphylaxis.

What precautions apply to Ticagrelor?

When prescribing ticagrelor, clinicians should consider several precautionary measures to ensure patient safety. - Assess bleeding risk: evaluate history of hemorrhage, recent surgery, or anticoagulant use. - Monitor renal function: dose adjustment may be needed in severe impairment. - Review concomitant antiplatelet or anticoagulant therapy: avoid excessive anticoagulation. - Caution in patients with a history of asthma or chronic obstructive pulmonary disease: dyspnea may be exacerbated. - Pregnancy and lactation: use only if potential benefit justifies potential risk, as safety data are limited. - Store at below 25°C: keep in the original container, protect from moisture and light.

What does Ticagrelor interact with?

Ticagrelor can interact with other medicines, altering its antiplatelet efficacy or increasing adverse event risk.

Major Interactions (Avoid): - Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase ticagrelor plasma levels and bleeding risk. - Strong CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce efficacy, increasing thrombotic risk.

Moderate Interactions (Monitor Closely): - Anticoagulants (e.g., warfarin, direct oral anticoagulants): enhanced anticoagulant effect, monitor coagulation parameters. - NSAIDs or aspirin: additive bleeding risk, assess gastrointestinal protection. - Statins metabolized by CYP3A4 (e.g., simvastatin): may increase statin exposure, monitor for myopathy. - P-glycoprotein inhibitors (e.g., verapamil): may modestly raise ticagrelor concentrations.

Frequently asked questions

What is Lacrat used for?+
Lacrat contains ticagrelor, an antiplatelet agent indicated to reduce the risk of cardiovascular death, myocardial infarction and stroke in patients with acute coronary syndrome or a history of myocardial infarction. It is also used to prevent thrombotic events in high‑risk cardiovascular patients.
How does ticagrelor work?+
Ticagrelor reversibly blocks the platelet P2Y12 ADP receptor, preventing ADP‑mediated activation of the G_i protein pathway. This stops the conformational change of the glycoprotein IIb/IIIa receptor, reducing fibrinogen binding and platelet aggregation, thereby inhibiting clot formation.
What is the usual dose of Lacrat?+
The prescribed dose of Lacrat is determined by the treating physician based on the patient’s clinical condition, renal function and concomitant therapies. Dosage regimens are individualized and should follow the prescriber’s instructions and local labeling.
Is Lacrat safe during pregnancy or breastfeeding?+
Safety data for ticagrelor in pregnancy and lactation are limited. It should be used only if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.
How do I order Lacrat from GNH USA?+
To request Lacrat, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.
How does Lacrat compare with other antiplatelet drugs?+
Compared with clopidogrel, ticagrelor provides more rapid and consistent platelet inhibition because it does not require metabolic activation. It also offers reversible binding, allowing platelet function to recover sooner after discontinuation, but may have a higher incidence of dyspnea.
What are the storage and handling requirements for Lacrat?+
Lacrat should be stored at temperatures below 25 °C, in its original packaging, protected from moisture and light. Keep the product out of reach of children and avoid exposing it to excessive heat or humidity.
How is Lacrat administered?+
Lacrat is taken orally, usually as a tablet swallowed whole with water. It is typically taken with or without food, as directed by the prescribing clinician. Patients should follow the exact schedule provided by their healthcare professional.
What are the most serious risks associated with Lacrat?+
The most serious risks include major bleeding events such as intracranial hemorrhage, gastrointestinal bleeding, and severe allergic reactions. Patients should be monitored for signs of excessive bleeding and any sudden respiratory symptoms like dyspnea.
Who should not use Lacrat?+
Lacrat is contraindicated in patients with active pathological bleeding, a history of intracranial hemorrhage, severe hepatic impairment, or known hypersensitivity to ticagrelor or any of its excipients. Caution is also advised for patients on strong CYP3A4 inhibitors.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Ticagrelor
Route
Oral Use
Manufacturer
Medochemie Ltd.
Origin
EU

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