Aminocaproic Acid

DEA Class; Rx

Common Brand Names; Amicar

  • Antifibrinolytic Agents

Oral and parenteral inhibitor of fibrinolysis
Used for enhancing hemostasis when fibrinolysis contributes to bleeding
Associated with potential risk for clotting or thrombosis.

Indicated for the treatment of hemorrhage caused by hyperfibrinolysis.

For dental bleeding in patients with hemophilia A.
For intracranial rebleeding prophylaxis after recent aneurysmal subarachnoid hemorrhage.
For the treatment of hemorrhagic cystitis† induced by cyclophosphamide therapy, radiation therapy, or interstitial cystitis.
For the prevention of secondary ocular hemorrhage in patients with traumatic hyphema.
For angioedema prophylaxis in patients with hereditary angioedema.
For surgical bleeding prophylaxis in cardiac surgery.
For the treatment of symptomatic intracranial bleeding occurring within 24 hours after administration of IV alteplase for treatment of acute ischemic stroke.

In presence of DIC without concomitant heparin

Evidence of active intravascular clotting process

Confusion

Vision decrease

Vomiting

Headache

Convulsions

Malaise

Muscle weakness

Dizziness

Tinnitus

Nausea

Bradycardia

Thrombosis

Edema

Hypotension

Stroke

Syncope

Intracranial hypertension

Peripheral ischemia

Pulmonary embolism

Dyspnea

Congestion

Diarrhea

Abdominal pain

Leukopenia

Agranulocytosis

Coagulation disorder

Dry ejaculation

Injection site reactions (pain/necrosis)

Myopathy

Pruritus

Rash

Renal failure

Anaphylaxis

Use cautioni in renal/cardiac/hepatic impairment

Risk of myopathy

In patients with upper urinary tract bleeding, therapy has been known to cause intrarenal obstruction in form of glomerular capillary thrombosis or clots in renal pelvis and ureters; for this reason, drug should not be used in hematuria of upper urinary tract origin, unless possible benefits outweigh risks

Avoid rapid IV administration

Therapy inhibits both action of plasminogen activators and to a lesser degree, plasmin activity; drug should not be administered without a definite diagnosis and/or laboratory finding indicative of hyperfibrinolysis (hyperplasminemia)

Preservative benzyl alcohol linked to fatal “Gasping Syndrome” in premature neonates

Skeletal muscle weakness with necrosis of muscle fibers reported following prolonged administration (rare); Clinical presentation may range from mild myalgias with weakness and fatigue to severe proximal myopathy with rhabdomyolysis, myoglobinuria, and acute renal failure; muscle enzymes, especially creatine phosphokinase (CPK) are elevated; monitor CPK levels in patients on long-term therapy; stop therapy if rise in CPK noted; resolution follows discontinuation of therapy; however, syndrome may recur if therapy restarted

Inhibition of fibrinolysis may theoretically result in clotting or thrombosis; there is no definite evidence that therapy has been responsible for few reported cases of intravascular clotting which followed treatment; rather, it appears that intravascular clotting was most likely due to patient’s preexisting clinical condition, eg, the presence of DIC; it has been postulated that extravascular clots formed in vivo may not undergo spontaneous Iysis as do normal clots

Therapy should not be administered with Factor IX Complex concentrates or Anti-Inhibitor Coagulant concentrates, as risk of thrombosis may increase

Reports have appeared in literature of increased incidence of certain neurological deficits,j including hydrocephalus, cerebral ischemia, or cerebral vasospasm associated with use of antifibrinolytic agents in treatment of subarachnoid hemorrhage (SAH); all of these events have also been described as part of the natural course of SAH, or as a consequence of diagnostic procedures such as angiography; drug relatedness remains unclear

Pregnancy Category: C

Lactation: Not known whether excreted in breast milk, use caution

Adults

30 g/day IV or PO; 36 g/day IV or PO has been used off-label in subarachnoid hemorrhage.

Elderly

30 g/day IV or PO; 36 g/day IV or PO has been used off-label in subarachnoid hemorrhage.

Adolescents

Safety and efficacy have not been established.

Children

Safety and efficacy have not been established.

 

Aminocaproic Acid

injectable solution

  • 250mg/mL

syrup

  • 1.25g/5mL

tablet

  • 500mg
  • 1,000mg

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