Trade Names:Kalbitor- Injection, solution 10 mg/mL
Directly inhibits plasma kallikrein and blocks the conversion of high molecular weight kininogen to bradykinin, which is thought to relieve symptoms of localized swelling, inflammation, and pain in hereditary angioedema.
C max is 586 ng /mL. T max is 2 to 3 h. Mean AUC is 3,017 ng•h/mL.
Vd is 26.4 L.
Plasma Cl is 153 mL/min. Elimination half-life is 2 h. Renal elimination in the urine has been demonstrated.
Pharmacokinetic data are not available.Hepatic Function Impairment
Pharmacokinetic data are not available.Elderly
Age was not found to significantly affect exposure.Gender
Gender was not found to significantly affect exposure.
Treatment of acute attacks of hereditary angioedema.
Subcutaneous 30 mg in three 10 mg injections. An additional 30 mg may be administered within a 24-h period if the attack persists.
Store at 36° to 46°F. Store vials removed from refrigeration below 86°F and use within 14 days or return to refrigeration until use. Protect from light.
None well documented.
None well documented.
Headache (16%); fatigue (12%).
Nausea (13%); diarrhea (11%); vomiting (6%); upper abdominal pain (5%).
Injection-site reactions, including erythema, irritation, local bruising, pain, pruritus, and urticaria (7%).
Upper respiratory tract infections (8%).
Anaphylaxis has been reported after administration. Ensure that ecallantide is only administered by a health care provider with appropriate medical support to manage anaphylaxis and hereditary angioedema. Be aware of the similarities between hypersensitivity reactions and hereditary angioedema and monitor patients closely. Do not administer to patients with known hypersensitivity to ecallantide.
Observe patients for an appropriate period of time after administration, taking into account the time to onset of anaphylaxis seen in clinical trials.
Category C .
Safety and efficacy not established in children younger than 16 yr of age.
In general, exercise caution in dose selection, usually starting at the low end of the dosing range, reflecting greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy.
Severe hypersensitivity reactions, including anaphylaxis, have occurred. These reactions occurred within the first hour after dosing.
Patients have developed antibodies to ecallantide; long-term effects are unknown.
Overdosage has not been reported.
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