HIGHLIGHT
Embolis 2.5/Embolis 5

Embolis 2.5/Embolis 5

apixaban

Manufacturer:

Zydus Healthcare

Distributor:

Zydus Healthcare
Concise Prescribing Info
Contents
Apixaban
Indications/Uses
Prevention of VTE in adults who have undergone elective hip or knee replacement surgery; stroke & systemic embolism in adults w/ non-valvular atrial fibrillation (NVAF), w/ ≥1 risk factors, eg, prior stroke or transient ischaemic attack (TIA); ≥75 yr; HTN; DM; symptomatic heart failure (NYHA Class ≥II). Treatment of DVT & pulmonary embolism (PE), & prevention of recurrent DVT & PE in adults.
Dosage/Direction for Use
Prevention of VTE (VTEp) in elective hip or knee replacement surgery 2.5 mg bid initiated 12-24 hr after surgery. Patient undergoing hip replacement surgery Duration of treatment: 32-38 days. Patient undergoing knee replacement surgery Duration of treatment: 10-14 days. Prevention of stroke & systemic embolism in patients w/ NVAF 5 mg bid. Severe renal impairment 2.5 mg bid. Patient w/ NVAF & at least 2 of the following characteristics: ≥80 yr, ≤60 kg, or serum creatinine ≥1.5 mg/dL 2.5 mg bid. DVT, PE 10 mg bid for the 1st 7 days followed by 5 mg bid. Prevention of recurrent DVT & PE 2.5 mg bid initiated following completion of 6 mth of treatment w/ apixaban 5 mg bid or w/ another anticoagulant. Patient undergoing cardioversion 5 mg bid for at least 2.5 days (5 single doses) before cardioversion to ensure adequate anticoagulation. If cardioversion is required before 5 doses of apixaban: 10 mg loading dose followed by 5 mg bid. Reduce to 5 mg loading dose followed by 2.5 mg bid if the patient meets criteria for dose reduction. Loading dose should be given at least 2 hr before cardioversion.
Administration
May be taken with or without food: Swallow w/ water. For patients w/ difficulty swallowing, crush tab & suspend in water/5% dextrose in water (D5W)/apple juice or mix w/ apple puree. Alternatively, crush tab & suspend in 60 mL water/D5W & administer immediately via nasogastric tube.
Contraindications
Hypersensitivity. Active clinically significant bleeding. Lesion or condition if considered a significant risk factor for major bleeding including current or recent GI ulceration, presence of malignant neoplasms at high risk of bleeding, recent brain or spinal injury, recent brain, spinal or ophth surgery, recent intracranial haemorrhage, known or suspected oesophageal varices, arteriovenous malformations, vascular aneurysms or major intraspinal or intracerebral vascular abnormalities. Concomitant treatment w/ any other anticoagulant agent eg, unfractionated heparin (UFH), LMWH (enoxaparin, dalteparin), heparin derivatives (fondaparinux), oral anticoagulants (warfarin, rivaroxaban, dabigatran) except under specific circumstances of switching anticoagulant therapy or when UFH is given at doses necessary to maintain an open central venous or arterial catheter. Hepatic disease associated w/ coagulopathy & clinically relevant bleeding risk.
Special Precautions
Conditions w/ increased risk of haemorrhage. Discontinue if severe haemorrhage occurs. Acute ischemic stroke. Not recommended in patients w/ prosthetic heart valves, w/ or w/o atrial fibrillation; history of thrombosis diagnosed w/ antiphospholipid syndrome; patients receiving concomitant systemic treatment w/ strong CYP3A4 & P-gp inhibitors (eg, azole-antimycotics) & HIV PIs (eg, ritonavir). Discontinue at least 48 hr prior to elective surgery or invasive procedures w/ a moderate or high risk of bleeding; at least 24 hr prior to elective surgery or invasive procedures w/ a low risk of bleeding. Temporary discontinuation; avoid lapses in therapy. Risk of developing spinal or epidural hematoma during spinal/epidural anesth or puncture which can result in long-term or permanent paralysis. Remove at least 5 hr prior to the 1st dose of apixaban indwelling epidural or intrathecal catheters. Not recommended as alternative to unfractionated heparin in patients w/ pulmonary embolism who are haemodynamically unstable or may receive thrombolysis or pulmonary embolectomy; patients undergoing hip fracture surgery. Patients w/ active cancer. Increased haemorrhagic risk in low body wt (<60 kg). Clotting tests [eg, prothrombin time (PT), INR & aPTT are affected]. Patients w/ rare hereditary problems of galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption should not take this medicinal product. Frequently monitor for signs & symptoms of neurological impairment (eg, numbness or weakness of the legs, bowel or bladder dysfunction). Concomitant use w/ other platelet aggregation inhibitors following surgery is not recommended; cSSRIs, SNRIs, or NSAIDs including ASA. Concomitant use w/ CYP3A4 & P-gp inducers & inhibitors. Severe renal impairment & mild or moderate hepatic impairment (Child Pugh A or B); elevated liver enzymes ALT/AST > 2x ULN or total bilirubin ≥ 1.5x ULN. Not recommended in patients w/ CrCl <15 mL/min or undergoing dialysis; severe hepatic impairment. Elderly. Childn & adolescent <18 yr. Not recommended during pregnancy. Lactation.
Adverse Reactions
Anaemia, haemorrhage, haematoma; epistaxis; nausea; GI & rectal haemorrhage, gingival bleeding; increased γ-glutamyltransferase; haematuria; contusion. Prevention of stroke & systemic embolism in adults w/ NVAF, w/ ≥1 risk factors (NVAF): Eye haemorrhage including conjunctival haemorrhage; hypotension. Treatment of DVT & PE, & prevention of recurrent DVT & PE (VTEt): Thrombocytopenia; mouth haemorrhage; increased ALT; skin rash; abnormal vag & urogenital haemorrhage.
Drug Interactions
Increased mean AUC & mean Cmax w/ ketoconazole (400 mg once daily). Decreased mean AUC & Cmax w/ rifampicin. Reduced plasma conc w/ other strong CYP3A4 & P-gp inducers (eg, phenytoin, carbamazepine, phenobarb or St. John's wort). Increased risk of bleeding w/ other anticoagulants, platelet aggregation inhibitors, SSRIs/SNRIs & NSAIDs including ASA. Additive effect on anti-factor Xa activity w/ enoxaparin. Concomitant use w/ medicinal products associated w/ serious bleeding [eg, thrombolytic agents, GPIIb/IIIa receptor antagonists, thienopyridines (eg, clopidogrel), dipyridamole, dextran & sulfinpyrazone] are not recommended. Reduced exposure w/ activated charcoal.
MIMS Class
Anticoagulants, Antiplatelets & Fibrinolytics (Thrombolytics)
ATC Classification
B01AF02 - apixaban ; Belongs to the class of direct factor Xa inhibitors. Used in the treatment of thrombosis.
Presentation/Packing
Form
Embolis 2.5 FC tab 2.5 mg
Packing/Price
30's
Form
Embolis 5 FC tab 5 mg
Packing/Price
30's
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