Recommended Topic Related To:

Rattlesnake Antivenin

"Dec. 26, 2012 -- More than 4,000 preventable mistakes occur in surgery every year at a cost of more than $1.3 billion in medical malpractice payouts, according a new study.

How preventable? Well, researchers call them "never events" because"...

Rattlesnake Antivenin

WARNINGS

There have been isolated reports of cardiac arrest and death associated with Antivenin use.

Patients sensitive to Antivenin or horse serum may develop anaphylaxis, therefore, it is essential that prior to intravenous (IV) or intramuscular (IM) Antivenin administration a proper skin test be performed, interpreted, and therapy modified if indicated.

PRECAUTIONS

General

Constant attendance and observation of the patient for untoward reactions are mandatory when Antivenin is administered.

Should any systemic reaction occur, administration should be discontinued immediately and appropriate treatment initiated. Those responsible for administration and/or monitoring administration of Antivenin should be familiar with current recommendations for treatment of severe, immediate, systemic reactions (anaphylaxis) associated with use of heterologous sera.

Therapy with beta-adrenergic blockers, including cardioselective agents, has been associated with an increased severity of acute anaphylaxis (See DRUG INTERACTIONS).

Before administration of any product prepared from horse serum, appropriate measures must be taken in an effort to detect the presence of dangerous sensitivity: (1) A careful review of the patient's history, including any report of (a) asthma, hay fever, urticaria, or other allergic manifestations; (b) allergic reactions upon exposure to horses; and (c) prior injections of horse serum. (2) A suitable test for detection of sensitivity. A skin test should be performed in every patient prior to administration, regardless of clinical history.

Skin test – Inject intradermally 0.02 to 0.03 mL of a 1:10 dilution of Normal Horse Serum or Antivenin. A control test on the opposite extremity, using Sodium Chloride Injection, USP, facilitates interpretation. Use of larger amounts for the skin-test dose increases the likelihood of false-positive reactions, and in the exquisitely sensitive patient, increases the risk of a systemic reaction from the skin-test dose. A 10% rate of false negative skin test reactions has been reported.14 A 1:100 or greater dilution should be used for preliminary skin testing if the history suggests sensitivity. A positive reaction to a skin test occurs within five to thirty minutes and is manifested by a wheal with or without pseudopodia and surrounding erythema. In general, the shorter the interval between injection and the beginning of the skin reaction, the greater the sensitivity.

If the history is negative for allergy and the result of a skin test is negative, proceed with administration of Antivenin as outlined below. If the history is positive and a skin test is strongly positive, administration may be dangerous, especially if the positive sensitivity test is accompanied by systemic allergic manifestations. In such instances, the risk of administering Antivenin must be weighed against the risk of withholding it, keeping in mind that severe envenomation can be fatal. (See last paragraph of this section.)

A negative allergic history and absence of reaction to a properly applied skin test do not rule out the possibility of an immediate reaction. Also, a negative skin test has no bearing on whether or not delayed serum reactions (serum sickness) will occur after administration of the full dose.

If the history is negative, and the skin test is mildly or questionably positive, administer as follows to reduce the risk of a severe immediate systemic reaction: (a) Prepare, in separate sterile vials or syringes, 1:100 and 1:10 dilutions of Antivenin. (b) Allow at least 15 minutes between injections and proceed with the next dose if no reaction follows the previous dose. (c) Inject subcutaneously, using a tuberculin-type syringe, 0.1, 0.2, and 0.5 mL of the 1:100 dilution at 15-minute intervals; repeat with the 1:10 dilution, and finally undiluted Antivenin. (d) If a systemic reaction occurs after any injection, place a tourniquet proximal to the site of injections and administer an appropriate dose of epinephrine, 1:1000, proximal to the tourniquet or into another extremity. Wait at least 30 minutes before injecting another dose. The amount of the next dose should be the same as the last that did not evoke a reaction. (e) If no reaction occurs after 0.5 mL of undiluted Antivenin has been administered, switch to the intramuscular route and continue doubling the dose at 15-minute intervals until the entire dose has been injected intramuscularly or proceed to the intravenous route as described below under DOSAGE AND ADMINISTRATION.

Obviously, if the just-described schedule is used, 3 to 5 or more hours would be required to administer the initial dose suggested for a moderate or severe envenomation, and time is an important factor in neutralization of venom in a critically ill patient. Wingert and Wainschel4 have described a procedure based on the experience of their group which they have used in some severely envenomated patients who have positive sensitivity tests: 50 to 100 mg of diphenhydramine hydrochloride is given intravenously, followed by slow intravenous infusion of diluted Antivenin for 15 to 20 minutes while carefully observing the patient for symptoms and signs of anaphylaxis; if anaphylaxis does not occur, Antivenin is continued, maintaining close observation of the patient. Patients who require Antivenin but develop signs of impending anaphylaxis in spite of this or the procedure described earlier present a difficult problem, and consultation should be sought.

REFERENCES

4. RUSSELL, F.: Venomous bites and stings: Poisonous snakes. In The Merck Manual of Diagnosis and Therapy, pp. 2450-2456, 14th Ed., 1982.

14. JURKOVICH, G. et al: Complications of Crotalidae Antivenin therapy. The J. of Trauma 28:7, 1988.

Last reviewed on RxList: 10/2/2008
This monograph has been modified to include the generic and brand name in many instances.

A A A

Report Problems to the Food and Drug Administration

 

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.


Women's Health

Find out what women really need.

advertisement
advertisement
Use Pill Finder Find it Now See Interactions

Pill Identifier on RxList

  • quick, easy,
    pill identification

Find a Local Pharmacy

  • including 24 hour, pharmacies

Interaction Checker

  • Check potential drug interactions
Search the Medical Dictionary for Health Definitions & Medical Abbreviations