EPIPEN- epinephrine injection
REMEDYREPACK INC.
----------
HIGHLIGHTS OF PRESCRIBING INFORMATIONThese highlights do not include all the information needed to use EPIPEN
® and EPIPEN Jr
® safely and effectively. See full prescribing information for EPIPEN and EPIPEN Jr.
EPIPEN ® (epinephrine injection), for intramuscular or subcutaneous use EPIPEN Jr ® (epinephrine injection), for intramuscular or subcutaneous use Initial U.S. Approval: 1939 INDICATIONS AND USAGEEpiPen and EpiPen Jr are non-selective alpha and beta-adrenergic receptor agonist indicated in the emergency treatment of allergic reactions (Type I) including anaphylaxis. ( 1) DOSAGE AND ADMINISTRATIONDOSAGE FORMS AND STRENGTHS
CONTRAINDICATIONSNone ( 4) WARNINGS AND PRECAUTIONS
ADVERSE REACTIONSAdverse reactions to epinephrine include anxiety, apprehensiveness, restlessness, tremor, weakness, dizziness, sweating, palpitations, pallor, nausea and vomiting, headache, and/or respiratory difficulties. ( 6) To report SUSPECTED ADVERSE REACTIONS, contact Mylan at 1-877-446-3679 (1-877-4-INFO-RX) or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. DRUG INTERACTIONS
USE IN SPECIFIC POPULATIONSSee 17 for PATIENT COUNSELING INFORMATION and FDA-approved patient labeling. Revised: 4/2023 |
EpiPen and EpiPen Jr are indicated in the emergency treatment of allergic reactions (Type I) including anaphylaxis to stinging insects (e.g., order Hymenoptera, which include bees, wasps, hornets, yellow jackets and fire ants) and biting insects (e.g., triatoma, mosquitoes), allergen immunotherapy, foods, drugs, diagnostic testing substances (e.g., radiocontrast media) and other allergens, as well as idiopathic anaphylaxis or exercise-induced anaphylaxis.
EpiPen and EpiPen Jr are intended for immediate administration in patients who are determined to be at increased risk for anaphylaxis, including individuals with a history of anaphylactic reactions.
Anaphylactic reactions may occur within minutes after exposure and consist of flushing, apprehension, syncope, tachycardia, thready or unobtainable pulse associated with a fall in blood pressure, convulsions, vomiting, diarrhea and abdominal cramps, involuntary voiding, wheezing, dyspnea due to laryngeal spasm, pruritus, rashes, urticaria or angioedema.
EpiPen and EpiPen Jr are intended for immediate administration as emergency supportive therapy only and are not a substitute for immediate medical care.
Discarding After Use:
The EpiPen and EpiPen Jr each contain 2 mL epinephrine solution. Approximately 1.7 mL remains in the auto-injector after activation, but is not available for future use, and should be discarded .
EpiPen and EpiPen Jr are intended for immediate administration as emergency supportive therapy and are not intended as a substitute for immediate medical care. In conjunction with the administration of epinephrine, the patient should seek immediate medical or hospital care. More than two sequential doses of epinephrine should only be administered under direct medical supervision [ see Indications and Usage (1), Dosage and Administration (2) and Patient Counseling Information (17)].
EpiPen and EpiPen Jr should only be injected into the anterolateral aspect of the thigh [ see Dosage and Administration (2) and Patient Counseling Information (17)].
Do not inject intravenously
Large doses or accidental intravenous injection of epinephrine may result in cerebral hemorrhage due to sharp rise in blood pressure. Rapidly acting vasodilators can counteract the marked pressor effects of epinephrine if there is such inadvertent administration.
Do not inject into buttock
Injection into the buttock may not provide effective treatment of anaphylaxis. Advise the patient to go immediately to the nearest emergency room for further treatment of anaphylaxis. Additionally, injection into the buttock has been associated with Clostridial infections (gas gangrene). Cleansing with alcohol does not kill bacterial spores, and therefore, does not lower this risk.
Do not inject into digits, hands or feet
Since epinephrine is a strong vasoconstrictor, accidental injection into the digits, hands or feet may result in loss of blood flow to the affected area. Advise the patient to go immediately to the nearest emergency room and to inform the healthcare provider in the emergency room of the location of the accidental injection. Treatment of such inadvertent administration should consist of vasodilation, in addition to further appropriate treatment of anaphylaxis [ see Adverse Reactions (6)].
Hold leg firmly during injection
Lacerations, bent needles, and embedded needles have been reported when EpiPen and EpiPen Jr have been injected into the thigh of young children who are uncooperative and kick or move during an injection. To minimize the risk of injection related injury when administering, hold the child’s leg firmly in place and limit movement prior to and during injection.
Rare cases of serious skin and soft tissue infections, including necrotizing fasciitis and myonecrosis caused by Clostridia (gas gangrene), have been reported at the injection site following epinephrine injection for anaphylaxis. Clostridium spores can be present on the skin and introduced into the deep tissue with subcutaneous or intramuscular injection. While cleansing with alcohol may reduce presence of bacteria on the skin, alcohol cleansing does not kill Clostridium spores. To decrease the risk of Clostridium infection, do not inject EpiPen into the buttock [see Warnings and Precautions (5.2)]. Advise patients to seek medical care if they develop signs or symptoms of infection, such as persistent redness, warmth, swelling, or tenderness, at the epinephrine injection site.
The presence of a sulfite in this product should not deter administration of the drug for treatment of serious allergic or other emergency situations even if the patient is sulfite-sensitive.
Epinephrine is the preferred treatment for serious allergic reactions 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.
Some patients may be at greater risk for developing adverse reactions after epinephrine administration. Despite these concerns, it should be recognized that the presence of these conditions is not a contraindication to epinephrine administration in an acute, life-threatening situation. Therefore, patients with these conditions, and/or any other person who might be in a position to administer EpiPen or EpiPen Jr to a patient experiencing anaphylaxis should be carefully instructed in regard to the circumstances under which epinephrine should be used.
Patients with Heart Disease
Epinephrine should be administered with caution to patients who have heart disease, including patients with cardiac arrhythmias, coronary artery or organic heart disease, or hypertension . In such patients, or in patients who are on drugs that may sensitize the heart to arrhythmias , epinephrine may precipitate or aggravate angina pectoris as well as produce ventricular arrhythmias [ see Drug Interactions (7) and Adverse Reactions (6)].
Other Patients and Diseases
Epinephrine should be administered with caution to patients with hyperthyroidism, diabetes, elderly individuals, and pregnant women. Patients with Parkinson’s disease may notice a temporary worsening of symptoms.
Due to the lack of randomized, controlled clinical trials of epinephrine for the treatment of anaphylaxis, the true incidence of adverse reactions associated with the systemic use of epinephrine is difficult to determine. Adverse reactions reported in observational trials, case reports, and studies are listed below.
Common adverse reactions to systemically administered epinephrine include anxiety; apprehensiveness; restlessness; tremor; weakness; dizziness; sweating; palpitations; pallor; nausea and vomiting; headache; and/or respiratory difficulties. These symptoms occur in some persons receiving therapeutic doses of epinephrine, but are more likely to occur in patients with hypertension or hyperthyroidism [ see Warnings and Precautions (5.5)].
Cardiovascular Reactions
Reactions from Accidental Injection and/or Improper Technique
Skin and Soft Tissue Infections
Cardiac Glycosides, Diuretics, and Anti-arrhythmics
Patients who receive epinephrine while concomitantly taking cardiac glycosides, diuretics, or anti-arrhythmics should be observed carefully for the development of cardiac arrhythmias [see Warnings and Precautions (5.5)] .
Antidepressants, Monoamine Oxidase Inhibitors, Levothyroxine, and Antihistamines
The effects of epinephrine may be potentiated by tricyclic antidepressants, monoamine oxidase inhibitors, levothyroxine sodium, and certain antihistamines, notably chlorpheniramine, tripelennamine, and diphenhydramine.
Beta-Adrenergic Blockers
The cardiostimulating and bronchodilating effects of epinephrine are antagonized by beta- adrenergic blocking drugs, such as propranolol.
Alpha-Adrenergic Blockers
The vasoconstricting and hypertensive effects of epinephrine are antagonized by alpha- adrenergic blocking drugs, such as phentolamine.
Ergot Alkaloids
Ergot alkaloids may also reverse the pressor effects of epinephrine.
There are no adequate and well controlled studies of the acute effect of epinephrine in pregnant women. In animal reproductive studies, epinephrine administered by the subcutaneous route to rabbits, mice, and hamsters during the period of organogenesis was teratogenic at doses 7 times and higher than the maximum recommended human intramuscular and subcutaneous dose on a mg/m 2 basis. Epinephrine is the first-line medication of choice for the treatment of anaphylaxis during pregnancy in humans. Epinephrine should be used for treatment of anaphylaxis during pregnancy in the same manner as it is used in non-pregnant patients.
In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2 to 4% and 15 to 20%, respectively.
During pregnancy, anaphylaxis can be catastrophic and can lead to hypoxic-ischemic encephalopathy and permanent central nervous system damage or death in the mother and, more commonly, in the fetus or neonate. The prevalence of anaphylaxis occurring during pregnancy is reported to be approximately 3 cases per 100,000 deliveries.
Management of anaphylaxis during pregnancy is similar to management in the general population. Epinephrine is the first line-medication of choice for treatment of anaphylaxis; it should be used in the same manner in pregnant and non-pregnant patients. In conjunction with the administration of epinephrine, the patient should seek immediate medical or hospital care.
In an embryofetal development study with rabbits dosed during the period of organogenesis, epinephrine was shown to be teratogenic (including gastroschisis and embryonic lethality) at doses approximately 40 times the maximum recommended intramuscular or subcutaneous dose (on a mg/m 2 basis at a maternal subcutaneous dose of 1.2 mg/kg/day for two to three days).
In an embryofetal development study with mice dosed during the period of organogenesis, epinephrine was shown to be teratogenic (including embryonic lethality) at doses approximately 8 times the maximum recommended intramuscular or subcutaneous dose (on a mg/m 2 basis at maternal subcutaneous dose of 1 mg/kg/day for 10 days). These effects were not seen in mice at approximately 4 times the maximum recommended daily intramuscular or subcutaneous dose (on a mg/m 2 basis at a subcutaneous maternal dose of 0.5 mg/kg/day for 10 days).
In an embryofetal development study with hamsters dosed during the period of organogenesis from gestation days 7 to 10, epinephrine was shown to be teratogenic at doses approximately 7 times the maximum recommended intramuscular or subcutaneous dose (on a mg/m 2 basis at a maternal subcutaneous dose of 0.5 mg/kg/day).
There is no information on the presence of epinephrine in human milk, the effects on breastfed infants, or the effects on milk production. Epinephrine is the first line-medication of choice for treatment of anaphylaxis; it should be used in the same manner in breastfeeding and non-breastfeeding patients.
EpiPen or EpiPen Jr may be administered to pediatric patients at a dosage appropriate to body weight [ see Dosage and Administration (2.1)] . Clinical experience with the use of epinephrine suggests that the adverse reactions seen in children are similar in nature and extent to those both expected and reported in adults. Since the doses of epinephrine delivered from EpiPen and EpiPen Jr are fixed, consider using other forms of injectable epinephrine if doses lower than 0.15 mg are deemed necessary.
Clinical studies for the treatment of anaphylaxis have not been performed in subjects aged 65 and over to determine whether they respond differently from younger subjects. However, other reported clinical experience with use of epinephrine for the treatment of anaphylaxis has identified that geriatric patients may be particularly sensitive to the effects of epinephrine. Therefore, EpiPen should be administered with caution in elderly individuals, who may be at greater risk for developing adverse reactions after epinephrine administration [ see Warnings and Precautions (5.5), Overdosage (10)].
Overdosage of epinephrine may produce extremely elevated arterial pressure, which may result in cerebrovascular hemorrhage, particularly in elderly patients. Overdosage may also result in pulmonary edema because of peripheral vascular constriction together with cardiac stimulation. Treatment consists of rapidly acting vasodilators or alpha-adrenergic blocking drugs and/or respiratory support.
Epinephrine overdosage can also cause transient bradycardia followed by tachycardia, and these may be accompanied by potentially fatal cardiac arrhythmias. Premature ventricular contractions may appear within one minute after injection and may be followed by multifocal ventricular tachycardia (prefibrillation rhythm). Subsidence of the ventricular effects may be followed by atrial tachycardia and occasionally by atrioventricular block. Treatment of arrhythmias consists of administration of a beta-adrenergic blocking drug such as propranolol.
Overdosage sometimes results in extreme pallor and coldness of the skin, metabolic acidosis, and kidney failure. Suitable corrective measures must be taken in such situations.
EpiPen (epinephrine injection, USP) 0.3 mg and EpiPen Jr (epinephrine injection, USP) 0.15 mg are single-dose auto-injectors and combination products containing drug and device components.
Each EpiPen Auto-Injector, 0.3 mg delivers a single dose of 0.3 mg epinephrine from epinephrine injection, USP 0.3 mg/0.3 mL in a sterile solution.
Each EpiPen Jr Auto-Injector, 0.15 mg delivers a single dose of 0.15 mg epinephrine from epinephrine injection, USP 0.15 mg/0.3 mL in a sterile solution.
Each 0.3 mL in the EpiPen Auto-Injector contains 0.3 mg epinephrine, 1.8 mg sodium chloride, 0.5 mg sodium metabisulfite, hydrochloric acid to adjust pH, and Water for Injection. The pH range is 2.2-5.0.
Each 0.3 mL in the EpiPen Jr Auto-Injector contains 0.15 mg epinephrine, 1.8 mg sodium chloride, 0.5 mg sodium metabisulfite, hydrochloric acid to adjust pH, and Water for Injection. The pH range is 2.2-5.0.
Epinephrine is a sympathomimetic catecholamine. Chemically, epinephrine is (-)-3,4- Dihydroxy-α-[(methylamino)methyl]benzyl alcohol with the following structure:
Epinephrine solution deteriorates rapidly on exposure to air or light, turning pink from oxidation to adrenochrome and brown from the formation of melanin. Replace EpiPen and EpiPen Jr if the epinephrine solution appears discolored (pinkish or brown color), cloudy, or contains particles.
Thoroughly review the patient instructions and operation of EpiPen or EpiPen Jr with patients and caregivers prior to use [ see Patient Counseling Information (17)].
Through its action on alpha-adrenergic receptors, epinephrine lessens the vasodilation and increased vascular permeability that occurs during anaphylaxis, which can lead to loss of intravascular fluid volume and hypotension.
Through its action on beta-adrenergic receptors, epinephrine causes bronchial smooth muscle relaxation and helps alleviate bronchospasm, wheezing and dyspnea that may occur during anaphylaxis.
Epinephrine also alleviates pruritus, urticaria, and angioedema and may relieve gastrointestinal and genitourinary symptoms associated with anaphylaxis because of its relaxer effects on the smooth muscle of the stomach, intestine, uterus and urinary bladder.
When given subcutaneously or intramuscularly, epinephrine has a rapid onset and short duration of action.
Long-term studies to evaluate the carcinogenic potential of epinephrine have not been conducted.
Epinephrine and other catecholamines have been shown to have mutagenic potential in vitro. Epinephrine was positive in the Salmonella bacterial reverse mutation assay, positive in the mouse lymphoma assay, and negative in the in vivo micronucleus assay. Epinephrine is an oxidative mutagen based on the E. coli WP2 Mutoxitest bacterial reverse mutation assay. This should not prevent the use of epinephrine where indicated [see Indications and Usage (1)].
The potential for epinephrine to impair reproductive performance has not been evaluated, but epinephrine has been shown to decrease implantation in female rabbits dosed subcutaneously with 1.2 mg/kg/day (40-fold the highest human intramuscular or subcutaneous daily dose) during gestation days 3 to 9.
EpiPen 2-Pak (epinephrine) injection is supplied with 2 single-dose pre-filled auto-injectors and 1 auto-injector trainer device: 0.3 mg/0.3 mL
NDC: 70518-1224-00
PACKAGING: 2 in 1 CARTON, 1 in 1 CONTAINER, 0.3 mL in 1 SYRINGE GLASS, TYPE 2
Storage and Handling
Protect from light. Epinephrine is light sensitive and should be stored in the carrier tube provided to protect it from light.
Store at 20°C to 25°C (68°F to 77°F); excursions permitted to 15°C to 30°C (59°F to 86°F) [See USP Controlled Room Temperature].
Do not refrigerate.
Before using, check to make sure the solution in the auto-injector is clear and colorless.
Replace the auto-injector if the solution is discolored (pinkish or brown color), cloudy, or contains particle.
Properly dispose all used, unwanted or expired EpiPen and EpiPen Jr auto-injectors.
Store at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature].
Repackaged and Distributed By:
Remedy Repack, Inc.
625 Kolter Dr. Suite #4 Indiana, PA 1-724-465-8762
See FDA-Approved Patient Labeling ( Patient Information and Instructions for Use)
A healthcare provider should review the patient instructions and operation of EpiPen and EpiPen Jr in detail, with the patient or caregiver.
Epinephrine is essential for the treatment of anaphylaxis. Patients who are at risk of or with a history of severe allergic reactions (anaphylaxis) to insect stings or bites, foods, drugs, and other allergens, as well as idiopathic and exercise-induced anaphylaxis, should be carefully instructed about the circumstances under which epinephrine should be used.
Administration
Instruct patients and/or caregivers in the appropriate use of EpiPen and EpiPen Jr. EpiPen should be injected into the middle of the outer thigh (through clothing, if necessary). Each device is a single-use injection. Advise patients to seek immediate medical care in conjunction with administration of EpiPen.
Instruct caregivers to hold the leg of young children firmly in place and limit movement prior to and during injection. Lacerations, bent needles, and embedded needles have been reported when EpiPen and EpiPen Jr have been injected into the thigh of young children who are uncooperative and kick or move during an injection [ see Warnings and Precautions (5.2)].
Instruct patients and/or caregivers to throw away the blue safety release immediately after using EpiPen and EpiPen Jr. This small part may pose a choking hazard for children.
Complete patient information, including dosage, directions for proper administration and precautions can be found inside each EpiPen or EpiPen Jr carton. A printed label on the surface of EpiPen shows instructions for use and a diagram depicting the injection process.
Training
Instruct patients and/or caregivers to use and practice with the Trainer to familiarize themselves with the use of EpiPen in an allergic emergency. The Trainer may be used multiple times. A Trainer device is provided in 2-Pak cartons.
Instruct patients and/or caregivers to immediately place the blue safety release back on the Trainer and reset it after practicing. This small part may pose a choking hazard for children.
Adverse Reactions
Epinephrine may produce symptoms and signs that include an increase in heart rate, the sensation of a more forceful heartbeat, palpitations, sweating, nausea and vomiting, difficulty breathing, pallor, dizziness, weakness or shakiness, headache, apprehension, nervousness, or anxiety. These signs and symptoms usually subside rapidly, especially with rest, quiet and recumbency. Patients with hypertension or hyperthyroidism may develop more severe or persistent effects, and patients with coronary artery disease could experience angina. Patients with diabetes may develop increased blood glucose levels following epinephrine administration. Patients with Parkinson’s disease may notice a temporary worsening of symptoms [ see Warnings and Precautions (5.5)] .
Accidental Injection
Advise patients to seek immediate medical care in the case of accidental injection. Since epinephrine is a strong vasoconstrictor when injected into the digits, hands, or feet, treatment should be directed at vasodilatation if there is such an accidental injection to these areas [ see Warnings and Precautions (5.2)].
Serious Infections at the Injection Site
Rare cases of serious skin and soft tissue infections, including necrotizing fasciitis and myonecrosis caused by Clostridia (gas gangrene), have been reported at the injection site following epinephrine injection for anaphylaxis. Advise patients to seek medical care if they develop signs or symptoms of infection, such as persistent redness, warmth, swelling, or tenderness, at the epinephrine injection site [ see Warnings and Precautions (5.3)].
Storage and Handling
Instruct patients to inspect the epinephrine solution visually through the clear window of the auto-injector periodically. Replace EpiPen and EpiPen Jr if the epinephrine solution appears discolored (pinkish or brown color), cloudy, or contains particles. Epinephrine is light sensitive and should be stored in the carrier tube provided to protect it from light. The carrier tube is not waterproof. Instruct patients that EpiPen and EpiPen Jr must be used or properly disposed once the blue safety release is removed or after use [ see Storage and Handling (16.2)].
Advise patients and caregivers to give used EpiPen and EpiPen Jr auto-injectors to their healthcare provider for inspection and proper disposal.
Advise patients and caregivers to promptly dispose of medicines that are no longer needed. Dispose of expired, unwanted, or unused EpiPen and EpiPen Jr auto-injectors in an FDA-cleared sharps container. Instruct patients not to dispose EpiPen or EpiPen Jr in their household trash. Instruct patients that if they do not have a FDA-cleared sharps disposal container, they may use a household container that is made of a heavy-duty plastic, can be closed with a tight-fitting and puncture-resistant lid without sharps being able to come out, upright and stable during use, leak-resistant, and properly labeled to warn of hazardous waste inside the container. Inform patients that they can visit the FDA website for additional information on disposal of unused medicines.
Complete patient information, including dosage, directions for proper administration and precautions can be found inside each EpiPen Auto-Injector carton.
Repackaged By / Distributed By: RemedyRepack Inc.
625 Kolter Drive, Indiana, PA 15701
(724) 465-8762
EPIPEN
® [/epeepen/]
(epinephrine injection, USP) Auto-Injector 0.3 mg
EpiPen
® = one dose of 0.3 mg epinephrine, USP 0.3 mg/0.3 mL
EPIPEN JR
® [/epeepen/ /joonyer/]
(epinephrine injection, USP) Auto-Injector 0.15 mg
EpiPen Jr
® = one dose of 0.15 mg epinephrine, USP 0.15 mg/0.3 mL
For allergic emergencies (anaphylaxis)
PATIENT INFORMATION
Read this Patient Information leaflet carefully before using the EpiPen ® or EpiPen Jr ® auto-injector and each time you get a refill. There may be new information. Anyone who may be able to administer the EpiPen or EpiPen Jr auto-injector should know how to use it before you have an allergic emergency.
This information does not take the place of talking with your healthcare provider about your medical condition or your treatment.
What is the most important information I should know about EpiPen and EpiPen Jr?
Symptoms of anaphylaxis may include:
What are EpiPen and EpiPen Jr auto-injectors?
What should I tell my healthcare provider before using EpiPen or EpiPen Jr?
Before you use your EpiPen or EpiPen Jr auto-injector, tell your healthcare provider about all your medical conditions. Your healthcare provider may give you more instructions about when and how to use EpiPen or EpiPen Jr if you have the following:
You may also receive more instructions if you:
Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins and herbal supplements. Tell your healthcare provider about all of your known allergies.
Especially tell your healthcare provider if you take certain asthma medicines.
EpiPen or EpiPen Jr and other medicines may affect each other, causing side effects. EpiPen or EpiPen Jr may affect the way other medicines work. Other medicines may affect how EpiPen or EpiPen Jr works.
Know the medicines you take. Keep a list of all your medicines, including over-the-counter medicines, vitamins and herbal supplements to show your healthcare provider and pharmacist when you get a new medicine.
Use your EpiPen or EpiPen Jr auto-injector for treatment of anaphylaxis as prescribed by your healthcare provider, regardless of your medical conditions or the medicines you take.
How should I use the EpiPen or EpiPen Jr auto-injector?
What are the possible side effects of EpiPen or EpiPen Jr?
EpiPen and EpiPen Jr may cause serious side effects.
Common side effects of EpiPen and EpiPen Jr include:
These side effects may go away with rest. Tell your healthcare provider if you have any side effect that bothers you or that does not go away.
These are not all the possible side effects of EpiPen or EpiPen Jr. For more information, ask your healthcare provider or pharmacist.
Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
How should I store EpiPen or EpiPen Jr auto-injectors?
Disposing of an Expired, Unused or Used EpiPen or EpiPen Jr Auto-Injector
Your EpiPen or EpiPen Jr auto-injector has an expiration date. Replace the pack of auto-injectors before the expiration date. Throw away (dispose of) expired, unwanted, or unused EpiPen and EpiPen Jr auto-injectors in an FDA-cleared sharps disposal container right away after use. Do not throw away the EpiPen or EpiPen Jr in your household trash. If you do not have an FDA-cleared sharps disposal container, you may use a household container that is:
When your sharps disposal container is almost full, you will need to follow your community guidelines for the right way to dispose of your sharps disposal container. There may be state or local laws about how you should throw away used needles and syringes. For more information about safe sharps disposal, and for specific information about sharps disposal in the state that you live in, go to the FDA’s website at: http://www.fda.gov/safesharpsdisposal
Visit the FDA’s website (https://www.fda.gov/drugs/safe-disposal-medicines/disposal-unused-medicines-what-you-should-know) for more information about how to throw away unused, unwanted or expired medicines.
After using your EpiPen or EpiPen Jr auto-injector in an allergic emergency, get emergency medical help right away. Take your used EpiPen or EpiPen Jr auto-injector with you to give to your healthcare provider for disposal.
General information about the safe and effective use of EpiPen and EpiPen Jr auto-injectors.
Medicines are sometimes prescribed for purposes other than those listed in a Patient Information leaflet. Do not use the EpiPen or EpiPen Jr auto-injector for a condition for which it was not prescribed. Do not give your EpiPen or EpiPen Jr auto-injector to other people.
This Patient Information leaflet summarizes the most important information about the EpiPen and EpiPen Jr auto-injectors. If you would like more information, talk to your healthcare provider. You can ask your pharmacist or healthcare provider for information about EpiPen and EpiPen Jr auto-injectors that is written for health professionals.
What are the ingredients in EpiPen and EpiPen Jr?
Active Ingredients: epinephrine
Inactive Ingredients: sodium chloride, sodium metabisulfite, hydrochloric acid, and water
Important Information
Incorrect Use |
Correct Use and Important Reminders |
Storage outside the protective case or storage of the EpiPen or EpiPen Jr auto-injector in extreme cold or heat. |
Always keep your EpiPen or EpiPen Jr stored in the protective case and at room temperature. Keep protective case in the outer carton to protect from light. Wrong storage may stop the EpiPen or EpiPen Jr from working. If the device has been in extreme cold or heat, the EpiPen or EpiPen Jr should be replaced. |
Failing to remove the auto-injector from the protective case before use. |
The EpiPen or EpiPen Jr auto-injector must be removed from the protective case it comes in before use. |
Failing to remove the blue safety top before use. |
Remove the blue safety top before use. EpiPen or EpiPen Jr will not activate with the blue safety top in place. |
Activating the auto-injector upside down which will cause an injection into the hand. |
The needle exits from the orange end of the EpiPen and EpiPen Jr auto-injector, which should be in contact with the outer thigh (upper leg) at a 90˚angle (perpendicular) to the thigh before and during activation. The orange needle end will extend to cover the needle after activation. If you can still see the needle, do not try to reuse the auto-injector. |
Failing to apply enough force to activate the EpiPen or EpiPen Jr auto-injector. |
EpiPen and EpiPen Jr should be administered by swinging and pushing the auto-injector firmly against the outer thigh. EpiPen and EpiPen Jr auto-injectors make a distinct pop sound when pushed against the thigh. The pop sound signals that the injection has started. The correct dose has been administered if the orange needle end is extended and the window is blocked. |
Administering at an injection site other than the outer thigh. |
Administer EpiPen or EpiPen Jr in the outer thigh only. |
Failing to hold the auto-injector in place for a full 3 seconds. |
Hold the EpiPen or EpiPen Jr auto-injector in place for a full 3 seconds following activation (count slowly 1, 2, 3). |
For more information and video instructions on the use of EpiPen and EpiPen Jr auto-injectors, go to www.epipen.com or call 1-800-395-3376.
INSTRUCTIONS FOR USE
EPIPEN
® [/epeepen/]
(epinephrine injection, USP) Auto-Injector 0.3 mg
EpiPen
® = one dose of 0.3 mg epinephrine,
USP 0.3 mg/0.3 mL
for intramuscular and subcutaneous use
EPIPEN JR
® [/epeepen/ /joonyer/]
(epinephrine injection, USP) Auto-Injector 0.15 mg
EpiPen Jr
® = one dose of 0.15 mg epinephrine,
USP 0.15 mg/0.3 mL
for intramuscular and subcutaneous use
This Instructions for Use contains information on how to administer the EpiPen and EpiPen Jr auto-injector.
Important Information You Need to Know Before Administering the EpiPen and EpiPen Jr Auto-Injector
Checking the Blue Safety Top
When receiving an EpiPen or EpiPen Jr auto-injector and before you need to use the EpiPen or EpiPen Jr auto-injector, do the following:
Preparing to Inject EpiPen or EpiPen Jr
Note the following while preparing to inject EpiPen or EpiPen Jr:
Make sure the EpiPen or EpiPen Jr auto-injector has not been used. If an EpiPen or EpiPen Jr auto-injector has been used:
Preparing to Inject a Child
Medicine Color:
|
Figure H. Medicine Viewing Window
Do not use the medicine if it is discolored (pinkish or brown color) or if the medicine has particles floating in it. Throw it away (dispose of) and use a new EpiPen or EpiPen Jr auto-injector (see the section “ Disposing of an Expired, Unused or Used EpiPen or EpiPen Jr Auto-Injector” on the Patient Information side of this leaflet).
Injecting EpiPen or EpiPen Jr
Step 1 Slide the EpiPen or EpiPen Jr auto-injector out of the case (Figure I)
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Step 2 Pull off the blue safety top (Figure J)
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Note: Do not twist or bend the blue safety top. Failure to pull out the blue safety top correctly (straight up and away) can cause accidental activation. Note: To avoid an accidental injection, never put your thumb, fingers or hand over the orange needle end. If an accidental injection happens, get emergency medical help right away. |
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Step 3 Inject the medicine by self (Figure K) or caregiver (Figure L) administration Place the orange needle end against the outer thigh, through clothing if needed. Push down firmly and hold in place for 3 seconds. Note: EpiPen and EpiPen Jr auto-injectors make a distinct pop sound when pushed against the thigh. This is normal and means that the EpiPen or EpiPen Jr auto-injector is working. After the pop, continue to press the EpiPen or EpiPen Jr auto-injector down firmly on the outer thigh for 3 seconds to make sure that the medicine is given. | |
Step 4 Check if used (Figure M) Lift the auto-injector straight out from the thigh. The orange needle end will extend to cover the needle. If the needle is visible, do not reuse it. Use a new auto-injector. Throw away the blue safety top. | |
Step 5 Get emergency medical help
After injecting EpiPen or EpiPen Jr, get emergency medical help right away. You can use a second EpiPen or EpiPen Jr auto-injector if symptoms continue or come back.
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Storing EpiPen and EpiPen Jr Auto-Injectors
Store the EpiPen and EpiPen Jr auto-injectors at room temperature between 68˚ F to 77˚ F (20˚ C to 25˚ C).
Keep protective case in the outer carton to protect from light. When exposed to air or light, the medicine in the EpiPen and EpiPen Jr auto-injector changes rapidly to a pinkish or brown color and should not be used.
Disposing of EpiPen and EpiPen Jr Auto-Injectors
After using your EpiPen or EpiPen Jr auto-injector, get emergency medical help right away. Take your used auto-injector with you to give to your healthcare provider for disposal.
Important: The blue safety top is a small part that may become a choking hazard for children. Throw away the blue safety top immediately after using the EpiPen or EpiPen Jr auto-injector.
Your EpiPen or EpiPen Jr auto-injector has an expiration date. Replace it before the expiration date.
For more information on how to throw away (dispose of) your expired EpiPen or EpiPen Jr auto-injector, see the section “ Disposing of an Expired, Unused or Used EpiPen or EpiPen Jr Auto-Injector” on the Patient Information side of this leaflet.
(epinephrine injection, USP) Auto-Injector 0.15 mg
EpiPen Jr
® = one dose of 0.15 mg epinephrine, USP 0.15 mg/0.3 mL
For more information about EpiPen or EpiPen Jr auto-injectors and proper use of the product, call Mylan at 1-877-446-3679 or visit www.epipen.com for an instructional video.
EpiPen Trainer Instructions for Use
In an emergency: Do not use the gray Trainer. Use your real yellow EpiPen® or real green EpiPen Jr® auto-injector.
Important Information
The EpiPen Trainer
Familiarize yourself with this gray Trainer. Practice until you are comfortable using it.
Your gray Trainer:
Caution: Know the difference between the Trainer and your real yellow EpiPen and real green EpiPen Jr Auto-Injector
Important differences between the Trainer and your real yellow EpiPen or real green EpiPen Jr auto-injector
Trainer (Gray) |
EpiPen (Yellow) |
EpiPen Jr (Green) |
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Contains medicine? |
No |
Yes |
Yes |
Has needle? |
No |
Yes |
Yes |
Comes in Protective Case? |
No |
Yes |
Yes |
Color of Label? |
Gray |
Yellow |
Green |
Has expiration date? |
No |
Yes |
Yes |
Can be reused? |
Yes |
No (use only one time) |
No (use only one time) |
Okay to remove and replace blue safety top? |
Yes |
No (remove just one time before use) |
No (remove just one time before use) |
Pressure needed to hold against thigh? |
Moderate |
Strong |
Strong |
Practice Instructions
Using the Trainer |
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Step 1 Pull off the blue safety top (Figure B) Grip the gray Trainer with one hand and with the orange end pointing down. Use the other hand to remove the blue safety top. Pull it straight up and away. Note: Do not twist or bend the blue safety top. Warning: Do not flip the blue safety top off using a thumb or by pulling it sideways or by bending and twisting the blue safety top. This may cause the real yellow EpiPen or real green EpiPen Jr auto-injector to accidentally activate. An EpiPen or EpiPen Jr auto-injector that has been activated by accident cannot be used for a patient in an emergency and must be replaced. | |
Step 2 Trainer injection simulation by self (Figure C) or caregiver (Figure D) administration Place the orange end against the outer thigh, over clothing if needed.
Note: The Trainer makes a distinct pop sound when pushed against the thigh. This is normal and means that the auto-injector is working. After the pop, continue to press the Trainer down firmly on the outer thigh for 3 seconds. | |
Step 3 Check if used (Figure E) Lift the Trainer straight out from the thigh. Inspect: The Trainer was activated correctly if the orange end is extended. If the orange end is not extended, repeat Step 1 and Step 2. | |
Step 4 Reset the Trainer (Figure F) Put the blue safety top back on the Trainer immediately. Place the orange end on a hard surface. Squeeze the sides of the orange end and push down on the Trainer with the other hand. Note: This resetting step should never be used with a real yellow EpiPen or real green EpiPen Jr auto-injector as this may result in injury. Never put your thumb, other fingers, or hand over the orange (needle) end of the real yellow EpiPen or real green EpiPen Jr auto-injector. |
Practice Session Information
In case of an allergic emergency, use the real yellow EpiPen or real green EpiPen Jr auto-injector and not the gray Trainer.
Follow instructions above. Repeat as often as needed until you are able to inject quickly and correctly. Regularly practice with the Trainer to make sure that you are able to use the real yellow EpiPen or real green EpiPen Jr auto-injector in an emergency situation.
Reread:
Train others who could help you in an emergency:
For more information about the EpiPen and EpiPen Jr auto-injector and the proper use of the products, go to www.epipen.com.
Repackaged and Distributed By:
Remedy Repack, Inc.
625 Kolter Dr. Suite #4 Indiana, PA 1-724-465-8762
DRUG: EPIPEN
GENERIC: epinephrine
DOSAGE: INJECTION
ADMINSTRATION: INTRAMUSCULAR
NDC: 70518-1224-0
PACKAGING: 0.3 mL in 1 SYRINGE
OUTER PACKAGING: 1 in 1 CONTAINER
OUTER PACKAGING: 2 in 1 CARTON
ACTIVE INGREDIENT(S):
INACTIVE INGREDIENT(S):
EPIPEN
epinephrine injection |
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Labeler - REMEDYREPACK INC. (829572556) |