Crotalidae Polyvalent Immune Fab

Brand names: CroFab
Drug class: Antineoplastic Agents

Usage of Crotalidae Polyvalent Immune Fab

North American Crotaline Snakebite Envenomation

Treatment of envenomation following snakebites involving North American Crotalinae (pit vipers, Crotalinae, crotalines; formerly known as Crotalidae or crotalids). Designated an orphan drug by FDA for this use.

Crotalinae subfamily of venomous snakes includes rattlesnakes, copperheads, and cottonmouths or water moccasins.

May be effective in management of minimal, moderate, or severe envenomation involving Crotalus atrox (Western diamondback rattlesnake), C. adamanteus (Eastern diamondback rattlesnake), C. scutulatus (Mojave rattlesnake), Agkistrodon piscivorus (cottonmouth or water moccasin), and other North American crotalines.

Consultation with experts experienced in treating snakebites (e.g., regional certified poison control center at 800-222-1222) recommended to guide treatment decisions regarding individual patients.

Relate drugs

How to use Crotalidae Polyvalent Immune Fab

General

  • Initiate treatment as soon as possible after Crotalinae snakebite in patients with signs of progressive envenomation (e.g., worsening local injury, coagulation abnormality, other systemic signs of envenomation).
  • Has been effective in clinical studies when given within 6 hours of snakebite.
  • Monitor closely during and following administration.

    • Administration

    IV Administration

    Administer by IV infusion.

    Reconstitution and Dilution

    Must be reconstituted and diluted prior to administration.

    Reconstitute appropriate number of vials of lyophilized Crotalidae polyvalent immune Fab (ovine) by adding 18 mL of 0.9% sodium chloride injection to each vial; mix by continuously manually inverting vial at a rate of 1 or 2 inversions per second until no solid material is visible in vial. Avoid foaming; do not shake. Reconstituted solution should be opalescent.

    Combine contents of appropriate number of reconstituted vials and dilute total dose (total combined reconstituted vials) in 250 mL of 0.9% sodium chloride and gently swirl to mix. Because of concerns regarding fluid overload, consider lower volume of dilution fluid for children weighing <10 kg.

    Use reconstituted and diluted solution within 4 hours after reconstitution. (See Stability.)

    Rate of Administration

    Administer by IV infusion over 60 minutes.

    Start initial infusion using reduced rate of 25–50 mL/hour for first 10 minutes; observe patient closely for sensitivity or other reactions. If reduced rate well tolerated, give remaining initial infusion and subsequent infusions at rate of 250 mL/hour.

    Dosage

    Dosage expressed in terms of the number of vials.

    Base initial dose (number of vials), need for additional initial doses to achieve envenomation control, and number of subsequent doses required to sustain envenomation control on individual patient response.

    Age-related dosage adjustments not indicated.

    Pediatric Patients

    North American Crotaline Snakebite Envenomation Initial Dosage IV

    4–6 vials. Manufacturer states initial dose may vary from minimum of 4 vials to maximum of 12 vials based on clinical judgment and severity of envenomation. In those with life-threatening symptoms (e.g., shock, serious active bleeding), some experts state consider initial dose of 8–12 vials in consultation with experts experienced in treating crotaline snakebites.

    Monitor closely for up to 1 hour after completion of initial infusion; determine whether initial envenomation control achieved (i.e., local manifestations arrested and not progressing, systemic symptoms resolved, coagulation abnormalities normalized or trending towards normalization).

    If initial envenomation control not achieved, give additional 4- to 6-vial doses until envenomation is controlled.

    Maintenance Dosage IV

    After initial envenomation control established, give 2-vial doses every 6 hours for up to 18 hours to maintain response. Use of scheduled dosage regimen after initial control may provide best control of subsequent envenomation symptoms, especially coagulopathies, that may result from continued venom release from depot sites.

    After initial 18-hour scheduled maintenance dosage regimen, may give additional 2-vial doses if considered necessary based on patient’s clinical course. Optimum dosage schedule not established for these additional maintenance doses after 18-hour regimen.

    Adults

    North American Crotaline Snakebite Envenomation Initial Dosage IV

    4–6 vials. Manufacturer states initial doses may vary from minimum of 4 vials to maximum of 12 vials based on clinical judgment and severity of envenomation. In those with life-threatening symptoms (e.g., shock, serious active bleeding), some experts state consider initial dose of 8–12 vials in consultation with experts experienced in treating crotaline snakebites.

    Monitor closely for up to 1 hour after completion of infusion; determine whether initial envenomation control is achieved (i.e., local manifestations arrested and not progressing, systemic symptoms resolved, coagulation abnormalities normalized or trending towards normalization).

    If initial envenomation control not achieved, give additional 4- to 6-vial doses until envenomation is controlled.

    Maintenance Dosage IV

    After initial envenomation control established, give 2-vial doses every 6 hours for up to 18 hours to maintain response. Use of scheduled dosage regimen after initial control may provide best control of subsequent envenomation symptoms, especially coagulopathies, that may result from continued venom release from depot sites.

    After initial 18-hour scheduled maintenance dosage regimen, may give additional 2-vial doses if considered necessary based on patient’s clinical course. Optimum dosage schedule not established for these additional maintenance doses after 18-hour regimen.

    Prescribing Limits

    Pediatric Patients

    North American Crotaline Snakebite Envenomation IV

    Maximum dose and maximum total dosage not known; total dosage of up to 18 vials used in clinical trials without toxic effects.

    Adults

    North American Crotaline Snakebite Envenomation IV

    Maximum dose and maximum total dosage not known; total dosage of up to 18 vials used in clinical trials without toxic effects.

    Special Populations

    No special population dosage recommendations.

    Warnings

    Contraindications

  • Known hypersensitivity to papaya or papain is a contraindication, unless benefits outweigh risks and appropriate drugs and equipment for management of anaphylactic reactions are readily available. (See Papain Hypersensitivity under Cautions.)

    • Warnings/Precautions

    Sensitivity Reactions

    Contains purified immunoglobulin fragments from blood of sheep immunized with snake venom. (See Actions.) Heterologous animal proteins can cause severe acute hypersensitivity reactions (anaphylaxis, anaphylactoid reactions), delayed hypersensitivity reactions (late serum reaction, serum sickness), or possible febrile responses to immune complexes formed by animal antibodies and neutralized venom components.

    Skin sensitivity testing not considered necessary and not recommended.

    Use caution if repeat course is indicated for a subsequent envenomation episode since patients may become sensitized to the antivenin.

    Anaphylaxis and Anaphylactoid Reactions

    Acute allergic reactions, including anaphylaxis and anaphylactoid reactions, may occur during or shortly after IV infusion of Crotalidae polyvalent immune Fab (ovine).

    Immediate hypersensitivity reactions, including hypotension, tongue swelling, chest discomfort, angioedema, bronchospasm, wheezing, tracheal edema, dyspnea, and/or lip swelling, reported in 0.1–6% of patients. Rarely, immediate hypersensitivity reaction appeared to be anaphylactoid reaction related to extremely rapid IV infusion rate (i.e., 640 mL/hour).

    Monitor closely for signs and symptoms of acute hypersensitivity (e.g., urticaria, pruritus, erythema, angioedema, bronchospasm with wheezing or cough, stridor, laryngeal edema, hypotension, tachycardia).

    If anaphylaxis or any severe hypersensitivity reaction occurs, immediately discontinue IV infusion and initiate appropriate therapy (e.g., epinephrine, corticosteroids, maintenance of adequate airway, oxygen, IV fluids, IV antihistamines, albuterol, maintenance of BP) as indicated.

    Delayed Hypersensitivity or Serum Reactions

    Delayed hypersensitivity or serum reactions may occur.

    Late serum reactions (rash, pruritus, urticaria, or serum sickness consisting of severe rash and pruritus) reported in 14% (6/42) of patients in initial clinical trials; in other studies, delayed hypersensitivity or serum sickness reported in 5–11% of patients.

    Most common signs and symptoms are rash and fever. Generally mild and respond to treatment with antihistamines and corticosteroids.

    Monitor for signs and symptoms of delayed hypersensitivity reactions or serum sickness (e.g., rash, fever, myalgia, arthralgia) for up to 2–3 weeks; initiate appropriate treatment if necessary.

    Papain Hypersensitivity

    Traces of papain or inactivated papain residues may be present in the Crotalidae polyvalent immune Fab (ovine); papain is used in manufacturing process.

    Individuals allergic to papain, chymopapain, other papaya extracts, or the pineapple enzyme bromelain may be at risk of hypersensitivity reaction to the antivenin. Patients allergic to dust mites or latex may also be allergic to papain. (See Contraindications under Cautions.)

    Coagulopathy

    Coagulopathic effects, such as thrombocytopenia (platelet counts <150,000/mm3), hypofibrinogenemia (fibrinogen concentrations <150 mg/dL), and prolonged PT and PTT, are common in many snakebite victims (especially those with severe envenomation) and occur because snake venom can activate or inhibit activity of various coagulation factors and interfere with blood coagulation cascade.

    Recurrent coagulopathy, characterized by thrombocytopenia, hypofibrinogenemia, and prolonged PT, can occur 2–7 days or longer after successful initial envenomation control and may persist for 1–2 weeks or longer.

    Recurrent coagulation abnormalities reported in 7–32% of patients treated with Crotalidae polyvalent immune Fab (ovine). Reported in clinical studies only in patients who experienced coagulation abnormalities during initial hospitalization, but can initially appear at any time before, during, or after treatment.

    Clinical importance of recurrent coagulopathy and most appropriate strategies for prevention or management unknown. Optimum dosage schedule of the antivenin to prevent recurrent coagulopathy not determined. Because the antivenin may be cleared from circulation while crotaline venoms continue to be released from depot sites, repeated antivenin doses may be necessary to prevent and/or treat recurrence of venom effects. (See Dosage under Dosage and Administration.)

    Monitor for signs and symptoms of recurrent coagulopathy for up to 1 week or longer; carefully assess need for retreatment with the antivenin and use of any type of anticoagulant or antiplatelet drug. Some clinicians suggest that follow-up in patients treated with antivenin should include platelet counts, fibrinogen concentrations, hemoglobin, and PT at 2–3 days and 5–7 days after administration of antivenin and as clinically indicated. Avoid use of any drug that may decrease platelet function or prolong PT or PTT.

    Consider other causes of persistent coagulation abnormalities, including cancer, collagen disease, CHF, diarrhea, elevated temperature, hepatic disorders, hyperthyroidism, poor nutritional state, steatorrhea, and vitamin K deficiency.

    Infusion Reactions

    Monitor closely during IV infusion. Based on experience with antibody therapies, infusion reactions (fever, low back pain, wheezing, nausea) may be related to infusion rate and can be controlled by decreasing rate. (See Rate of Administration under Dosage and Administration.)

    Specific Populations

    Pregnancy

    Use during pregnancy only if clearly needed.

    Not known whether Crotalidae polyvalent immune Fab (ovine) can cause fetal harm if administered to a pregnant woman or whether it can affect reproduction capacity. No animal reproduction studies conducted.

    Lactation

    Not known whether distributed into milk.

    Use with caution in nursing women.

    Pediatric Use

    Efficacy and safety in pediatric patients similar to that in adults. Data from postmarketing retrospective study indicate 32% (78/247) of patients were ≤16 years of age (median age: 8.5 years). Has been used in children as young as 14 months of age without unusual adverse effects.

    Age-related dosage adjustments not indicated since venom dose following snakebite is expected to be similar in children and adults. To avoid fluid overload, fluid volume used to dilute the antivenin may need to be adjusted in children weighing <10 kg. (See Reconstitution and Dilution under Dosage and Administration.)

    Geriatric Use

    Efficacy and safety in geriatric patients appears comparable to that in overall patient population. Data from postmarketing retrospective study indicate 5% (13/247) of patients were >65 years of age (median age: 72 years).

    Common Adverse Effects

    Urticaria, rash, pruritus, nausea, coagulation disorder, back pain.

    What other drugs will affect Crotalidae Polyvalent Immune Fab

    No formal drug interaction studies.

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