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For bronchial asthma and certain allergic manifestations, e.g., angioedema, urticaria, serum sickness, anaphylactic shock, use epinephrine subcutaneously. The adult intravenous dose for hypersensitivity reactions or to relieve bronchospasm usually ranges from 0.1 to 0.25 mg injected slowly. Neonates may be given a dose of 0.01 mg per kg of body weight; for the infant 0.05 mg is an adequate initial dose and this may be repeated at 20 to 30 minute intervals in the management of asthma attacks.
Cardiac Resuscitation
Dosing Information
A dose of 0.5 mL (0.5 mg) diluted to 10 mL with sodium chloride injection can be administered intravenously or intracardially to restore myocardial contractility.
Intracardiac injection should only be administered by personnel well trained in the technique, if there has not been sufficient time to establish an intravenous route.
External cardiac massage should follow intracardial administration to permit the drug to enter coronary circulation. The drug should be used secondarily to unsuccessful attempts with physical or electromechanical methods.
Ophthalmologic Use
Dosing Information
Ophthalmologic use (for producing conjunctival decongestion, to control hemorrhage, produce mydriasis and reduce intraocular pressure) — use a concentration of 1:10,000 (0.1 mg/mL) to 1:1000 (1 mg/mL).
Regional Anesthesia
Dosing Information
A final concentration of 1:200,000 of epinephrine injection is recommended for infiltration injection, nerve block, caudal or other epidural blocks. From 0.3 to 0.4 mg of epinephrine (0.3 to 0.4 mL of 1:1000 solution) may be mixed with spinal anesthetic agents.
Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration.
Off-Label Use and Dosage (Adult)
Guideline-Supported Use
Acute Symptomatic Bradyarrhythmia
Developed by: ACC/AHA
Class of Recommendation: Class IIb
Strength of Evidence: Category B
If atropine is ineffective for the treatment of bradycardia with a pulse, then epinephrine or dopamine may be used, especially, with associated hypotension.[1]
There is limited information regarding FDA-Labeled Use of Epinephrine (injection) in pediatric patients.
Off-Label Use and Dosage (Pediatric)
Guideline-Supported Use
There is limited information regarding Off-Label Guideline-Supported Use of Epinephrine (injection) in pediatric patients.
Non–Guideline-Supported Use
Croup
Aerosolized levo-epinephrine (1:1000) is at least as effective as racemic epinephrine (2.25%) in the treatment of laryngotracheitis in children (6 months to 6 years of age) with moderate to severe croup.[5]
Wheezing
Subcutaneous epinephrine is effective in the treatment of acute wheezing in children less than 2 years of age.[6]
Contraindications
Epinephrine is contraindicated in patients with known hypersensitivity to sympathomimetic amines, in patients with angle closure glaucoma, and patients in shock (nonanaphylactic). It should not be used in patients anesthetized with agents such as cyclopropane or halothane as these may sensitize the heart to the arrhythmic action of sympathomimetic drugs.
Addition of epinephrine to local anesthetics for injection of certain areas (e.g., fingers, toes, ears, etc.) is contraindicated because of danger that vasoconstriction may result in sloughing of tissue.
Except as diluted for admixture with local anesthetics to reduce absorption and prolong action, epinephrine should not ordinarily be used in those cases where vasopressor drugs may be contraindicated, e.g., in thyrotoxicosis, diabetes, in obstetrics when maternal blood pressure is in excess of 130/80 and in hypertension and other cardiovascular disorders.
Epinephrine may induce potentially serious cardiac arrhythmias in patients not suffering from heart disease and in patients with organic heart disease or who are receiving drugs that sensitize the myocardium.
Parenterally administered epinephrine initially may produce constriction of renal blood vessels and decrease urine formation.
Epinephrine Injection, USP is subject to oxidation and should be protected against exposure to light and stored in light-resistant containers.
Epinephrine is the preferred treatment for serious allergic or other emergency situations even though this product contains sodium metabisulfite, a sulfite that may in other products cause allergic-type reactions including anaphylactic symptoms or life-threatening or less severe asthmatic episodes in certain susceptible persons. The alternatives to using epinephrine in a life-threatening situation may not be satisfactory. The presence of a sulfite in this product should not deter administration of the drug for treatment of serious allergic or other emergency situations.
Precautions
Do not use the Injection if its color is pinkish or darker than slightly yellow or if it contains a precipitate.
Do not administer unless solution is clear and container is intact. Discard unused portion.
Although epinephrine can produce ventricular fibrillation, its actions in restoring electrical activity in asystole and in enhancing defibrillation of the fibrillating ventricle are well documented. The drug, however, should be used with caution in patients with ventricular fibrillation.
Epinephrine should be used cautiously in patients with hyperthyroidism, hypertension and cardiac arrhythmias. All vasopressors should be used cautiously in patients taking monoamine oxidase (MAO) inhibitors.
Adverse Reactions
Clinical Trials Experience
There is limited information regarding Clinical Trial Experience of Epinephrine (injection) in the drug label.
Postmarketing Experience
Transient and minor side effects of anxiety, headache, fear and palpitations occur only with systemic therapeutic doses, especially in hyperthyroid individuals. Adverse effects such as cardiac arrhythmias and excessive rise in blood pressure may occur with systemic therapeutic doses or with inadvertent overdosage. Other adverse reactions include cerebral hemorrhage, hemiplegia, subarachnoid hemorrhage, anginal pain in patients with angina pectoris, anxiety, restlessness, headache, tremor, weakness, dizziness, pallor and respiratory difficulty. Such reactions are unlikely when epinephrine is diluted to 1:200,000 for injection with local anesthetic agents.
Drug Interactions
Epinephrine should not be administered concomitantly with other sympathomimetic drugs (such as isoproterenol) because of possible additive effects and increased toxicity. Combined effects may induce serious cardiac arrhythmias. They may be administered alternately when the preceding effect of other such drugs has subsided.
Administration of epinephrine to patients receiving cyclopropane or halogenated hydrocarbon general anesthetics such as halothane which sensitize the myocardium, may induce cardiac arrhythmia. When encountered, such arrhythmias may respond to administration of a beta-adrenergic blocking drug. Epinephrine also should be used cautiously with other drugs (e.g., digitalis glycosides) that sensitize the myocardium to the actions of sympathomimetic agents.
Diuretic agents may decrease vascular response to pressor drugs such as epinephrine.
Epinephrine may antagonize the neuron blockade produced by guanethidine resulting in decreased antihypertensive effect and requiring increased dosage of the latter.
Animal reproduction studies have not been conducted with epinephrine. It is also not known whether epinephrine can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Epinephrine should be given to a pregnant woman only if clearly needed.
Australian Drug Evaluation Committee (ADEC) Pregnancy Category
There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of Epinephrine (injection) in women who are pregnant.
Labor and Delivery
Parenteral administration of epinephrine if used to support blood pressure during low or other spinal anesthesia for delivery can cause acceleration of fetal heart rate and should not be used in obstetrics when maternal blood pressure exceeds 130/80.
Nursing Mothers
There is no FDA guidance on the use of Epinephrine (injection) with respect to nursing mothers.
Pediatric Use
There is no FDA guidance on the use of Epinephrine (injection) with respect to pediatric patients.
Geriatic Use
There is no FDA guidance on the use of Epinephrine (injection) with respect to geriatric patients.
Gender
There is no FDA guidance on the use of Epinephrine (injection) with respect to specific gender populations.
Race
There is no FDA guidance on the use of Epinephrine (injection) with respect to specific racial populations.
Renal Impairment
There is no FDA guidance on the use of Epinephrine (injection) in patients with renal impairment.
Hepatic Impairment
There is no FDA guidance on the use of Epinephrine (injection) in patients with hepatic impairment.
Females of Reproductive Potential and Males
There is no FDA guidance on the use of Epinephrine (injection) in women of reproductive potentials and males.
Immunocompromised Patients
There is no FDA guidance one the use of Epinephrine (injection) in patients who are immunocompromised.
Administration and Monitoring
Administration
Intracardial
Intravenous
Subcutaneous
Monitoring
There is limited information regarding Monitoring of Epinephrine (injection) in the drug label.
IV Compatibility
There is limited information regarding IV Compatibility of Epinephrine (injection) in the drug label.
Overdosage
Acute Overdose
Signs and Symptoms
Erroneous administration of large doses of epinephrine may lead to precordial distress, vomiting, headache, dyspnea, as well as unusually elevated blood pressure.
Management
Toxic effects of overdosage can be counteracted by injection of an alpha-adrenergic blocker and a beta-adrenergic blocker. In the event of a sharp rise in blood pressure, rapid-acting vasodilators such as the nitrites, or alpha-adrenergic blocking agents can be given to counteract the marked pressor effect of large doses of epinephrine.
Chronic Overdose
There is limited information regarding Chronic Overdose of Epinephrine (injection) in the drug label.
The actions of epinephrine resemble the effects of stimulation of adrenergic nerves. To a variable degree it acts on both alpha and beta receptor sites of sympathetic effector cells. Its most prominent actions are on the beta receptors of the heart, vascular and other smooth muscle. When given by rapid intravenous injection, it produces a rapid rise in blood pressure, mainly systolic, by (1) direct stimulation of cardiac muscle which increases the strength of ventricular contraction, (2) increasing the heart rate and (3) constriction of the arterioles in the skin, mucosa and splanchnic areas of the circulation.
When given by slow intravenous injection epinephrine usually produces only a moderate rise in systolic and a fall in diastolic pressure. Although some increase in pulse pressure occurs, there is usually no great elevation in mean blood pressure. Accordingly, the compensatory reflex mechanisms that come into play with a pronounced increase in blood pressure do not antagonize the direct cardiac actions of epinephrine as much as with catecholamines that have a predominant action on alpha receptors.
Total peripheral resistance decreases by action of epinephrine on beta receptors of the skeletal muscle vasculature and blood flow is thereby enhanced. Usually this vasodilator effect of the drug on the circulation predominates so that the modest rise in systolic pressure which follows slow injection or absorption is mainly the result of direct cardiac stimulation and increase in cardiac output. In some instances peripheral resistance is not altered or may even rise owing to a greater ratio of alpha to beta activity in different vascular areas.
Epinephrine relaxes the smooth muscles of the bronchi and iris and is a physiologic antagonist of histamine. The drug also produces an increase in blood sugar and glycogenolysis in the liver.
Intravenous injection produces an immediate and intensified response. Following intravenous injection epinephrine disappears rapidly from the blood stream.
Structure
Epinephrine Injection, USP 1:1000 is a sterile, nonpyrogenic solution. Each mL contains epinephrine 1 mg; sodium chloride 9 mg; sodium metabisulfite 0.9 mg added. May contain hydrochloric acid for pH adjustment.
The solution contains no bacteriostat or antimicrobial agent. It is administered by the following routes: intravenous, intracardiac (left ventricular chamber), via endotracheal tube into the bronchial tree, subcutaneous or intramuscular.
Epinephrine, USP is a sympathomimetic (adrenergic) agent designated chemically as 4-[1-hydroxy-2 (methylamino) ethyl]-1,2 benzenediol, a white, microcrystalline powder. It has the following structural formula:
Sodium Chloride, USP is chemically designated NaCl, a white, crystalline compound freely soluble in water.
Pharmacodynamics
There is limited information regarding Pharmacodynamics of Epinephrine (injection) in the drug label.
Pharmacokinetics
Epinephrine is rapidly inactivated in the body and is degraded by enzymes in the liver and other tissues.
The large portion of injection doses is excreted in the urine as inactivated compounds. The remainder is excreted in the urine as unchanged or conjugated compounds.
Nonclinical Toxicology
There is limited information regarding Nonclinical Toxicology of Epinephrine (injection) in the drug label.
Clinical Studies
There is limited information regarding Clinical Studies of Epinephrine (injection) in the drug label.
How Supplied
Epinephrine Injection, USP 1:1000 (1 mg/mL) is supplied in a 1 mL ampul single-dose container (NDC 0409-7241-25).
Store at 20 to 25°C (68 to 77°F). [See USP Controlled Room Temperature.]
Protect from light.
Storage
There is limited information regarding Epinephrine (injection) Storage in the drug label.
Images
Drug Images
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↑Hirao, M. (1988-06). "Endoscopic resection of early gastric cancer and other tumors with local injection of hypertonic saline-epinephrine". Gastrointestinal Endoscopy. 34 (3): 264–269. ISSN0016-5107. PMID3391382. Unknown parameter |coauthors= ignored (help); Check date values in: |date= (help)
↑Folwaczny, C. (1997-01). "Influence of prophylactic local administration of epinephrine on bleeding complications after polypectomy". Endoscopy. 29 (1): 31–33. doi:10.1055/s-2007-1004058. ISSN0013-726X. PMID9083734. Unknown parameter |coauthors= ignored (help); Check date values in: |date= (help)
↑Waisman, Y. (1992-02). "Prospective randomized double-blind study comparing L-epinephrine and racemic epinephrine aerosols in the treatment of laryngotracheitis (croup)". Pediatrics. 89 (2): 302–306. ISSN0031-4005. PMID1734400. Unknown parameter |coauthors= ignored (help); Check date values in: |date= (help)
↑Lowell, D. I. (1987-06). "Wheezing in infants: the response to epinephrine". Pediatrics. 79 (6): 939–945. ISSN0031-4005. PMID3295741. Unknown parameter |coauthors= ignored (help); Check date values in: |date= (help)
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