Apixaban
(a-pix-a-ban)Classification
Pharmacotherapeutic: Factor Xa inhibitor
Clinical: Anticoagulant
Eliquis
CATEGORY AND SCHEDULE
Pregnancy Risk Category: B
Do not confuse:
apixaban with
rivaroxaban, argatroban, or
dabigatran
General Information
Apixaban belongs to the factor Xa inhibitor group of anticoagulant group of drugs. They are effective for reducing the risk of stroke, systemic embolism in pts with nonvalvular atrial fibrillation. Prophylaxis of DVT following hip or knee replacement surgery, and also to treat DVT and PE and to reduce the risk of recurrent DVT/PE following initial therapy
Apixaban can cause severe reactions, such as: Increased risk for bleeding/hemorrhagic events. May cause serious, potentially fatal bleeding, accompanied by one or more of the following: a decrease in Hgb of 2 g/dL or more; a need for 2 or more units of packed RBCs; bleeding occurring at one of the following sites: intracranial, intraspinal, intraocular, pericardial, intra-articular, intramuscular with compartment syndrome, retroperitoneal. Serious reactions include jaundice, cholestasis, cytolytic hepatitis, Stevens-Johnson syndrome, hypersensitivity reaction, anaphylaxis
Action
Selectively blocks active site of factor Xa, a key factor in the intrinsic and extrinsic pathway of blood coagulation cascade
Therapeutic Effect
Inhibits clot-induced platelet aggregation, fibrin clot forma
Availability (Rx)
Tablets: 2.5 mg, 5 mg
Uses
Deep venous thrombosis(DVT)
after hip or knee replacement, to prevent
stroke and embolism in atrial fibrillation
(nonvalvular)
Unlabeled uses: Prevention of recurrent
stroke or TIA
Precautions
Pregnancy (B), Breastfeeding, dialysis,
hepatic/renal disease, labor, surgery, prosthetic heart valves
Black Box Warning: Abrupt discontinuation, epidural, spinal anesthesia, lumbar
puncture
• You have heart problems
• You have hepatic diseases
• You have kidney problems
• You are taking other medicines
Indications and Dosages
‣ To Treat deep vein thrombosis (DVT) and pulmonary embolism (PE)
PO
• Adults: 10 mg bid × 7 days, then 5 mg bid ≥6 mo, to reduce recurrence >6 mo 2.5 mg bid
‣ To reduce risk of recurrence of deep vein thrombosis and pulmonary embolism after completion of treatment for acute DVT or PE
PO
• Adults: 2.5 mg bid daily after at least 6 mo of treatment for DVT or PE
‣ To Treat DVT prophylaxis and PE prophylaxis in patients undergoing knee or hip replacement surgery
PO
• Adults: 2.5 mg twice daily beginning 12 to 24 hours after surgery and lasting
12 days for knee replacement and 35 days for hip replacement
‣ To Treat Stroke prophylaxis and systemic embolism prophylaxis
PO
• Adults: 5 mg bid; in those with any
2 of the following—age ≥80 yr, body
weight ≤60 kg, or serum creatinine ≥1.5
mg/dL—reduce the dose to 2.5 mg bid.
Also decrease the dose to 2.5 mg bid
(strong inhibitor of both CYP3A4 and Pglycoprotein)
‣ Dosage in Renal Impairment
PO
• DVT/PE/Reduce Risk Recurrent DVT, Postoperative: No adjustment
• Nonvalvular A-fib, HD:SCr < 1.5: No adjustment
• SCr 1.5 or greater, age older than 80 yrs, weight 60 kg or less: 2.5 mg 2 times/day
• Hemodialysis end-stage renal disease
maintained on hemodialysis, adult: 5 mg bid; reduce to 2.5 mg
bid if patient is ≥80 yr or ≤60 kg
‣ Dosage in Hepatic Impairment
• Mild Impairment: No dose adjustment
• Moderate Impairment: Use caution
• Severe Impairment: Not recommended
Pharmacokinetics
Readily absorbed after PO administration. Peak plasma concentration: 3–4 hrs.
Protein binding: 87%. Metabolized in liver. Excreted primarily in urine, feces.
Half-life: 12 hrs
Implementation
PO route
• Give without regard to meals
• If elective surgery or invasive procedures with moderate or high risk for bleeding, discontinue apixaban at least 24–48 hrs prior to procedure
Contraindications
Severe hypersensitivity to apixaban. Active pathologic bleeding
Cautions: Mild to moderate hepatic
impairment, severe renal impairment
(may increase bleeding risk). Avoid use
in pts with severe hepatic impairment,
prosthetic heart valve, significant rheumatic heart disease
Interactions
Individual drugs
• Antiplatelets, aspirin, fibrinolytics, heparin
NSAIDs (chronic use): Possibly increased
risk of bleeding
• Strong dual inducers of CYP3A4 and P-gp
such as carbamazepine, phenytoin, rifampin: Decreased effectiveness of
apixaban
strong dual inhibitors of CYP3A4 and P-gp
such as clarithromycin, itraconazole
Drug/laboratory tests
• PT, PTT, INR, coagulation
studies
Drugs/food
• Grapefruit products: may increase level/adverse effects
Herbal
• St. John’s wort may decrease level/effect• Flaxseed, garlic, ginger, ginkgo biloba, ginseng, omega-3 may increase risk of bleeding
Side effects
• CNS: Hemorrhagic stroke, syncope
• CV: Hypotension
• EENT: Epitaxis, gingival bleeding, ocular hemorrhage
• GI: Elevated bilirubin and liver enzymes, GI bleeding or hemorrhage,
fresh bleeding from rectum, hematemesis, melena, rectal hemorrhage
• GU: Hematuria, vaginal hemorrhage
• HEME: Excessive bleeding, including hemorrhage, hemorrhagic anemia,
thrombocytopenia
• SKIN: Ecchymosis, petechiae, rash
• MS: Muscle hemorrhage
• RESP: Hemoptysis
• Other: Anaphylaxis, angioedema, elevated alkaline phosphatase,
hematomas at injection sites
Nursing considerations
Baseline assessment
• Obtain baseline CBC• Question history of bleeding disorders, recent surgery, spinal punctures, intracranial hemorrhage, bleeding ulcers, open wounds, anemia, hepatic impairment
• Obtain full medication history including herbal products
Intervention/evaluation
• Periodically monitor CBC, stool for occult blood
• Be alert for complaints of abdominal/back pain, headache, confusion, weakness, vision change (may indicate hemorrhage)
• Question for increased menstrual bleeding/discharge
• Assess for any sign of bleeding: bleeding at surgical site, hematuria, blood in
stool, bleeding from gums, petechiae, ecchymosis
Equipment must be available for anaphylaxis
• Bleeding: bleeding may occur from
any body system; may be fatal if severe
• Neurologic status:
monitor for impairment, including numbness, paresthesia, weakness, confusion,
back pain, bowel/bladder impairment;
notify prescriber immediately
• Abrupt discontinuation: do not discontinue abruptly; if
bleeding occurs, consider using another
anticoagulant to prevent thromboembolic
events
• Epidural, spinal
anesthesia, lumbar puncture: avoid use
in these conditions, risk of hematoma and
permanent paralysis, may be increased
with use of other anticoagulants, thrombolytics, antiplatelets
• Hypersensitivity: rash, itching,
chills, fever; report to prescriber
• Beers: avoid in older adults; may
cause increased risk of bleeding, decreased creatinine clearance
Evaluation
Positive therapeutic result• Prevention/treatment of DVT
• Adequate anticoagulati
Patient/family teaching
• Instruct patient to Do not take/discontinue any medication except on advice from physician
• Tell patient unable to swallow whole tablets to crush tablet and mix with apple juice or water or
mix with applesauce and take immediately
• Tell patient not to stop taking apixaban without first consulting prescriber. If patient misses a
dose, instruct him to take it as soon as possible on the same day and resume the dosing schedule
the next day. Caution patient not to double dose to make up for the missed dose the day before.
• Report blood-tinged mucus from coughing, heavy menstrual bleeding,
headache, vision problems, weakness, abdominal pain, frequent bruising, bloody
urine or stool, joint pain or swelling
• Advise patient to report any unusual bleeding or bruising to the prescriber
• Inform patient that it
may take longer for her to stop bleeding and to take bleeding precautions, such as avoiding the
use of a razor and using a soft-bristle toothbrush
• Tell patient to alert all prescribers to use of apixaban therapy before any invasive procedure,
including dental work, is scheduled.
Advise female patient to notify prescriber immediately if pregnancy is suspected or known
• Avoid alcohol, aspirin, NSAIDs, herbal supplements, grapefruit products
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