Apixer-2.5 Tablet
Apixaban 2.5 mg Tablets — Direct Oral Anticoagulant (DOAC) Therapy
| Composition | Apixaban 2.5 mg |
|---|---|
| Dosage Form | Tablet |
| Pack Type | Alu-Alu Blister |
| Pack Size | 10 x 10 Tablets |
| MRP | ₹ 2200 |
| Therapy | Neurology + Cardiac + Diabetic + G.P. — Direct Oral Anticoagulant (Factor Xa Inhibitor) |
| Storage | Store below 30 °C in a dry place, protected from light and moisture. |
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About Apixer-2.5 Tablet
Apixer-2.5 Tablet contains Apixaban 2.5 mg, a direct oral anticoagulant (DOAC) that selectively inhibits Factor Xa in the coagulation cascade. The 2.5 mg twice-daily strength is used for venous thromboembolism (VTE) prophylaxis after hip or knee replacement surgery, for extended VTE prevention, and for AF stroke prophylaxis in selected high-risk elderly patients meeting dose-reduction criteria.
DOACs have largely replaced warfarin in modern anticoagulation practice because of fixed dosing, no routine monitoring, fewer food and drug interactions, and a more favourable bleeding profile — particularly lower intracranial haemorrhage risk. Apixaban specifically has the lowest major bleeding rate among the DOAC class in head-to-head trials.
Apixer-2.5 is manufactured by Trumac Healthcare under WHO-GMP conditions and is available for monopoly-based PCD pharma franchise and third-party manufacturing — a high-margin cardiology SKU with growing prescription demand.
Indications
- Prophylaxis of VTE after hip or knee replacement surgery
- Extended VTE prophylaxis (after initial 6 months of treatment)
- Stroke and systemic embolism prevention in non-valvular AF (dose-reduction criteria: age ≥80, weight ≤60 kg, creatinine ≥1.5 mg/dL — any two of these)
- Secondary prevention of recurrent VTE
Mechanism of Action
Apixaban is a highly selective, reversible direct inhibitor of free and clot-bound coagulation Factor Xa. By inhibiting Factor Xa, Apixaban prevents the conversion of prothrombin to thrombin, suppresses fibrin formation, and reduces thrombus growth and propagation — without directly affecting platelet aggregation.
Dosage & Administration
VTE prophylaxis after hip/knee replacement: 2.5 mg twice daily for 12–35 days. Stroke prevention in AF (dose-reduction criteria met): 2.5 mg twice daily. Extended VTE prevention: 2.5 mg twice daily. Swallow with or without food.
Side Effects
Bleeding (most common: epistaxis, GI bleeding, haematuria, easy bruising). Anaemia, nausea. Rare: major bleeding, intracranial haemorrhage, hypersensitivity reactions. Compared with warfarin: lower intracranial bleeding rate.
Contraindications & Precautions
Active clinically significant bleeding. Hepatic disease with coagulopathy. Concomitant strong CYP3A4 + P-gp inhibitors (ketoconazole, ritonavir) or inducers (rifampicin). Pregnancy and breastfeeding. Prosthetic heart valves. Recent intracranial/spinal surgery. Severe renal impairment (CrCl < 15 mL/min).
Storage
Store below 30 °C in a dry place, protected from light and moisture.
Apixer-2.5 Tablet is available for monopoly-based PCD pharma franchise across India and for third-party manufacturing under your brand. WHO-GMP certified, with full visual-aid and promotional support. Become a Trumac franchise partner →
Frequently Asked Questions
What is Apixer-2.5 Tablet used for?
Apixer-2.5 Tablet contains Apixaban 2.5 mg and is used for VTE prophylaxis after hip/knee replacement, extended VTE prevention, and stroke prevention in atrial fibrillation in patients meeting dose-reduction criteria.
Do I need blood tests while on Apixaban?
Routine coagulation monitoring (INR) is not required with Apixaban — that is one of the main advantages over warfarin. Renal function should be checked periodically.
Is Apixer-2.5 available for PCD pharma franchise?
Yes, Trumac Healthcare offers Apixer-2.5 Tablet on monopoly-based PCD pharma franchise and for third-party manufacturing — a high-margin cardiology SKU.
How should Apixer-2.5 Tablet be stored?
Store below 30 °C in a dry place, away from direct sunlight and moisture.
Is Apixer-2.5 WHO-GMP certified?
Yes, Apixer-2.5 Tablet is manufactured in WHO-GMP and DCGI-compliant facilities.
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