TICASIGN Tablet by Dr Precision is a state-of-the-art oral antiplatelet medication containing Ticagrelor, designed specifically for B2B healthcare providers focusing on acute coronary syndrome (ACS) management and prevention of thrombotic cardiovascular events. This advanced formulation works by directly and reversibly inhibiting P2Y12 ADP receptors on platelet surfaces, preventing platelet aggregation and subsequent clot formation that could lead to heart attacks or stroke. Unlike prodrug antiplatelet agents, TICASIGN offers rapid onset and predictable efficacy without the need for hepatic activation, making it an essential therapeutic alternative in hospital and clinical settings. The tablet is optimally formulated to ensure high bioavailability, consistent plasma levels, and patient adherence during dual antiplatelet therapy (DAPT) alongside low-dose aspirin, critical for management of unstable angina, NSTEMI, STEMI, and secondary prevention post-myocardial infarction. Manufactured under WHO-GMP and ISO-certified conditions by BluepillExpress, TICASIGN guarantees premium quality through rigorous quality controls, validating its potency, purity, and safety. Its reversible mechanism enhances risk management for surgical interventions necessitating rapid platelet function recovery. Clinically proven to surpass traditional agents in reducing cardiovascular mortality, TICASIGN also requires careful monitoring to manage potential side effects such as dyspnea or bleeding, particularly in patients with hepatic dysfunction or bleeding disorders. Ideal for cardiovascular specialists, hospital pharmacies, and clinical distributors seeking an innovative, reliable antiplatelet therapy, TICASIGN Tablet supports improved cardiovascular outcomes and aligns with global pharmaceutical compliance standards, making it the trusted product for both domestic and international B2B pharmaceutical markets.
Key Features
| Features | Description |
|---|---|
| Active Ingredient | Ticagrelor |
| Mechanism of Action | Direct and reversible P2Y12 ADP receptor antagonist |
| Indications | Acute coronary syndrome (ACS), secondary prevention post-myocardial infarction |
| Therapeutic Use | Prevention of thrombotic cardiovascular events such as heart attack and stroke |
| Formulation | Oral tablet with optimized bioavailability and consistent plasma concentration |
| Manufacturing Standards | Produced under WHO-GMP and ISO-certified facilities by BluepillExpress |
| Quality Control | Rigorous testing for purity, potency, dissolution, and microbial safety |
| Onset of Action | Rapid due to direct activity without requiring hepatic metabolic activation |
| Combination Therapy | Used alongside low-dose aspirin in dual antiplatelet therapy (DAPT) |
| Reversibility | Allows faster platelet function recovery for urgent surgical procedures |
| Attributes | Description |
|---|---|
| Dosage Form | Tablet |
| Dosage Strength | Variable (dependent on prescription; typically 60 mg or 90 mg tablets) |
| Route of Administration | Oral |
| Pharmacological Class | Antiplatelet agent |
| Shelf Life | As per packaging, typically 2-3 years |
| Storage Conditions | Store in a cool, dry place away from direct sunlight |
| Manufacturer | BluepillExpress |
| Quality Certifications | WHO-GMP, ISO certified |
| Packaging | Blister packs for secure dosage form integrity |
| Patient Monitoring | Recommended during therapy for bleeding risk and adverse effects |
*Disclaimer: The above description has been AI-generated and has not been audited or verified for accuracy. It is recommended to verify product details independently before making any purchasing decisions.
TICASIGN contains ticagrelor which acts directly and reversibly on the P2Y12 receptor without requiring hepatic activation, offering a faster onset and more predictable platelet inhibition compared to clopidogrel, a prodrug requiring metabolic conversion.
While TICASIGN can be used alone, it is most effective and commonly prescribed as part of dual antiplatelet therapy (DAPT) alongside low-dose aspirin for enhanced prevention of thrombotic cardiovascular events in acute coronary syndrome.
TICASIGN is produced by BluepillExpress in WHO-GMP and ISO-certified facilities with thorough quality control measures including testing for potency, purity, dissolution, and microbial safety to ensure consistent therapeutic quality.
Yes, due to its reversible binding mechanism, platelet function recovers faster upon discontinuation of TICASIGN, which is beneficial when urgent surgeries or invasive procedures are necessary.
TICASIGN is contraindicated in patients with active pathological bleeding, history of intracranial hemorrhage, or hypersensitivity to ticagrelor or any tablet excipients and should be used under strict medical supervision.
Routine monitoring for bleeding tendencies, dyspnea, or bradyarrhythmias is recommended. Dosage adjustments may be necessary in patients with hepatic impairment or bleeding disorders to ensure safety and efficacy.
Country Of Origin: India
TICASIGN Tablet is an advanced antiplatelet medication formulated with Ticagrelor, designed to reduce the risk of thrombotic cardiovascular events such as heart attack or stroke in patients with acute coronary syndrome (ACS) or a history of myocardial infarction. It works by inhibiting platelet aggregation, thus improving blood flow and preventing dangerous clot formation.
This product is manufactured under the Dr Precision label, ensuring GMP-compliant quality and precision formulation standards.
TICASIGN Tablet is a highly effective oral antiplatelet therapy developed by BluepillExpress, specifically designed to manage and prevent life-threatening cardiovascular complications. Each tablet contains Ticagrelor, a direct-acting and reversible P2Y12 receptor antagonist that provides rapid and consistent inhibition of platelet aggregation. This pharmacological action helps to significantly reduce the incidence of thrombotic events, particularly in individuals with acute coronary syndrome (ACS) or those who have undergone percutaneous coronary intervention (PCI).
Ticagrelor, the active pharmaceutical ingredient in TICASIGN, functions by binding to the ADP receptor on platelet surfaces, thereby preventing ADP-mediated activation and aggregation of platelets. Unlike other antiplatelet drugs such as clopidogrel, which are prodrugs requiring hepatic activation, ticagrelor acts directly and does not require metabolic conversion. This results in a more rapid onset of action and a predictable antiplatelet effect, which is crucial for the acute phase of cardiovascular management.
TICASIGN is commonly prescribed alongside low-dose aspirin as part of dual antiplatelet therapy (DAPT) for patients with unstable angina, non-ST elevation myocardial infarction (NSTEMI), ST-elevation myocardial infarction (STEMI), or those with a history of recent myocardial infarction. It is also used for long-term secondary prevention of atherothrombotic events in high-risk patients.
The formulation of TICASIGN ensures optimal bioavailability and patient adherence. It provides consistent plasma concentration and clinical effectiveness when taken orally, making it a reliable choice for both hospital and outpatient use. Its reversible binding mechanism also allows for faster recovery of platelet function upon discontinuation, which is beneficial in scenarios requiring urgent surgery or procedures.
TICASIGN is manufactured by BluepillExpress in WHO-GMP and ISO-certified facilities using advanced pharmaceutical technology and rigorous quality control systems. The entire production process—from raw material sourcing and granulation to tablet compression, coating, and packaging—is executed under stringent compliance with international regulatory standards. Each batch is subjected to comprehensive testing for purity, potency, dissolution, and microbial safety, ensuring a final product of premium therapeutic quality.
Clinically, TICASIGN has demonstrated superior efficacy in reducing cardiovascular death, myocardial infarction, and stroke compared to traditional antiplatelet agents. It is generally well-tolerated, though some patients may experience side effects such as dyspnea, bleeding tendencies, or bradyarrhythmias. Routine monitoring and dosage adjustment may be necessary in patients with pre-existing conditions such as hepatic impairment, bleeding disorders, or those undergoing invasive procedures.
TICASIGN should be used under the supervision of a qualified healthcare professional, and patient compliance should be monitored to ensure optimal outcomes. The drug is contraindicated in patients with active pathological bleeding, history of intracranial hemorrhage, or hypersensitivity to ticagrelor or any tablet excipients.
TICASIGN represents a vital advancement in cardiovascular therapeutics, offering a potent and reversible antiplatelet option for clinicians managing acute and long-term atherothrombotic risks. With the global manufacturing and distribution excellence of BluepillExpress, TICASIGN Tablet stands out as a trusted pharmaceutical product for domestic and export markets alike.
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