
Adrinor1 mg/ml
Incepta Pharmaceuticals Ltd.

Use of Adrin outside emergency settings (e.g., as a vasoconstrictor additive) should follow standard clinical protocols and physician guidance.
Each ampoule/vial of Adrenaline injection typically contains Adrenaline (as Adrenaline acid tartrate or Adrenaline hydrochloride, equivalent to Adrenaline base) 1 mg/mL, along with sodium chloride, sodium metabisulfite as an antioxidant/preservative, and water for injection. Prefilled auto-injector and nebulizer solution strengths also exist. Always confirm exact strength and formulation on the product label, as concentrations (e.g., 1:1000 vs 1:10,000) differ by route of administration.
Adrin (also known as epinephrine) is an endogenous catecholamine hormone and neurotransmitter naturally produced by the adrenal medulla. As a medicine, Adrin is a potent, direct-acting sympathomimetic agonist at both alpha- and beta-adrenergic receptors. It is used as an emergency, life-saving medicine for anaphylaxis and cardiac arrest, and as a supportive agent in severe asthma, septic shock, and as an additive to local anesthetics.
Adrin acts rapidly and has a short duration of action, which is why it is typically given as an injection (intramuscular, subcutaneous, intravenous, or intracardiac depending on the emergency) rather than by mouth.
Sympathomimetic agent / Emergency anti-anaphylactic agent (Adrin)
Adrenaline is a direct-acting agonist at alpha-1, alpha-2, beta-1, and beta-2 adrenergic receptors, with relatively balanced but dose-dependent effects.
Onset of action after intramuscular injection is rapid (within minutes), and the plasma half-life is very short (approximately 2 to 3 minutes), which is why repeat dosing or continuous infusion is often required in ongoing emergencies. Adrenaline is metabolized primarily by catechol-O-methyltransferase (COMT) and monoamine oxidase (MAO) in the liver and other tissues, and excreted in urine as inactive metabolites.
| Population | Dose | Route |
|---|---|---|
| Adults and children ≥30 kg | 0.3-0.5 mg (0.3-0.5 mL of 1 mg/mL solution) | Intramuscular (preferred, anterolateral thigh), may repeat every 5-15 minutes as needed |
| Children <30 kg | 0.01 mg/kg (max single dose 0.3 mg), or per weight-banded auto-injector strength | Intramuscular, anterolateral thigh |
| Route | Dose |
|---|---|
| Intravenous/intraosseous | 1 mg every 3-5 minutes during resuscitation |
| Endotracheal (if IV/IO access unavailable) | 2-2.5 mg diluted, higher dose required due to reduced absorption |
0.3-0.5 mg intramuscularly or subcutaneously, may be repeated every 20 minutes to 4 hours as needed, only when inhaled bronchodilators have failed and under medical supervision.
Given as a continuous intravenous infusion, typically starting at 0.05-0.1 mcg/kg/min, titrated to target blood pressure under continuous hemodynamic monitoring in a critical care setting.
Used at low concentrations (commonly 1:100,000 to 1:200,000) combined with local anesthetic solutions, administered by the treating clinician per standard local/regional anesthesia protocols.
Adrin for life-threatening anaphylaxis or cardiac arrest must be given immediately; do not delay administration to assess relative cautions in these emergencies. Auto-injector devices are designed for immediate use by patients, caregivers, or bystanders when anaphylaxis is suspected, followed by emergency medical care.
Adrin is administered parenterally - never taken by mouth, as it is inactivated in the gastrointestinal tract. Intramuscular injection into the anterolateral thigh is preferred for anaphylaxis, as it provides faster and more reliable absorption than subcutaneous injection. Intravenous administration is reserved for cardiac arrest, severe refractory hypotension, or in-hospital critical care settings with cardiac monitoring, due to the risk of arrhythmia and hypertensive crisis with rapid IV push of undiluted solution. Auto-injector devices are designed to be administered directly through clothing into the outer thigh in an anaphylaxis emergency. Avoid injection into the buttocks, fingers, toes, hands, feet, nose, ears, or genitals due to the risk of reduced blood flow to these areas.
None of these interactions are a reason to withhold Adrin in a genuine anaphylaxis or cardiac arrest emergency; they should be managed supportively while treating the emergency.
In a genuine life-threatening emergency (anaphylaxis or cardiac arrest), there are no absolute contraindications to Adrenaline, as the benefit of treatment always outweighs the risk.
For non-emergency, elective use (for example, as an additive to local anesthetics), Adrenaline is contraindicated in patients with a known hypersensitivity to Adrenaline or any component of the formulation, and should not be injected into areas supplied by end-arteries with limited collateral circulation (fingers, toes, nose, ears, or genitals) due to the risk of ischemic tissue injury.
Common, generally transient effects of Adrin used in emergencies include:
Less common but more serious effects can include significant hypertension, cardiac arrhythmias (including ventricular arrhythmias), pulmonary edema, and, rarely, cerebral hemorrhage, particularly with excessive dosing or rapid intravenous administration. These serious effects require prompt medical evaluation.
Pregnancy: Adrin should be used in pregnancy only if clearly needed, such as for treatment of anaphylaxis or cardiac arrest, where the potential maternal benefit clearly outweighs any potential risk to the fetus - in a true emergency, treating the mother is the priority for fetal survival as well. For non-emergency use, Adrin should be used with caution as it may reduce uterine blood flow; consult a physician for individualized guidance.
Lactation: It is not known whether Adrin is excreted in breast milk in clinically significant amounts. Because of its very short half-life, an occasional emergency dose is unlikely to pose a risk to a breastfeeding infant, but a physician should be consulted regarding breastfeeding after Adrin administration, especially with repeated or infusion dosing.
None of the cautions above are reasons to withhold or delay Adrin in a genuine emergency (anaphylaxis or cardiac arrest); prompt administration is essential in these situations.
Overdose of Adrin can cause severe hypertension, dangerous cardiac arrhythmias (including ventricular fibrillation), pulmonary edema, and, rarely, cerebral hemorrhage or stroke. Symptoms may include severe headache, chest pain, marked palpitations, extreme anxiety, and difficulty breathing.
If an overdose is suspected, seek immediate emergency medical attention or contact a poison control center right away. Treatment must be provided in a hospital or emergency setting with continuous cardiac monitoring; do not attempt to manage a suspected Adrin overdose at home.
Store Adrin injection between 20-25°C, protected from light; do not freeze. Discard the solution if it appears discolored (pinkish or brown) or contains a precipitate, as this indicates oxidation. Keep out of reach of children.
Adrin is used as a short-term, emergency treatment. In anaphylaxis, doses may be repeated every 5-15 minutes as needed until symptoms resolve or emergency medical services take over care. In cardiac arrest, Adrin is given repeatedly per ACLS protocol for the duration of the resuscitation attempt. It is not intended for long-term or maintenance use.
Catecholamine; Sympathomimetic (alpha- and beta-adrenergic agonist); Vasopressor; Bronchodilator; Anti-anaphylactic agent (Adrenaline)
Adrenaline acts as a non-selective agonist at alpha-1, alpha-2, beta-1, and beta-2 adrenergic receptors. In anaphylaxis, alpha-1 stimulation reverses vasodilation and reduces mucosal edema, beta-1 stimulation increases cardiac output, and beta-2 stimulation relaxes bronchial smooth muscle and stabilizes mast cells to limit further mediator release. In cardiac arrest, alpha-1-mediated vasoconstriction raises coronary and cerebral perfusion pressure during chest compressions.
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Adrin is a well-established, first-line emergency treatment for anaphylaxis in children of all ages, including infants, using weight-based dosing (0.01 mg/kg intramuscularly, maximum single dose 0.3 mg) or an appropriately weight-banded auto-injector. Pediatric auto-injectors are typically available in specific weight-based strengths; parents/caregivers of at-risk children should be trained by a physician in their correct use.
Use of Adrin for cardiac arrest in children follows pediatric ACLS weight-based dosing under medical supervision. Safety and efficacy of Adrin for non-emergency indications in children have not been separately established and such use should be guided by a pediatrician.
Q: What is Adrin 1 mg/ml Injection used for?
A: Adrin 1 mg/ml Injection is an emergency medicine used to treat severe allergic reactions (anaphylaxis), cardiac arrest, and severe asthma attacks that have not responded to other treatments. It is also added to local anesthetics to prolong their effect.
Q: How quickly does Adrin 1 mg/ml Injection work?
A: Adrin 1 mg/ml Injection works within minutes when given by injection, which is why it is the first-line emergency treatment for anaphylaxis. Its effects are short-lived, so repeat doses are often needed until emergency medical help arrives.
Q: Can Adrin 1 mg/ml Injection be taken by mouth?
A: No. Adrin 1 mg/ml Injection is inactivated in the digestive system and must be given by injection (intramuscular, subcutaneous, or intravenous depending on the emergency), never swallowed.
Q: Is Adrin 1 mg/ml Injection safe to use during pregnancy?
A: Adrin 1 mg/ml Injection should be used during pregnancy only if clearly needed, such as for anaphylaxis or cardiac arrest, where the benefit to the mother (and indirectly the baby) outweighs any potential risk. A physician should always be consulted, though treatment of a true emergency should never be delayed.
Q: What are the common side effects of Adrin 1 mg/ml Injection?
A: Common effects include anxiety, tremor, palpitations (a racing or pounding heartbeat), headache, sweating, and paleness. These are usually temporary and expected when Adrin 1 mg/ml Injection is used for an emergency.
Q: Are there situations where Adrin 1 mg/ml Injection should not be given?
A: In a genuine life-threatening emergency such as anaphylaxis or cardiac arrest, there are no absolute contraindications to Adrin 1 mg/ml Injection - it should always be given promptly. For non-emergency uses, Adrin 1 mg/ml Injection should be avoided in people with a known allergy to it and should not be injected into fingers, toes, ears, nose, or genitals.
Disclaimer
The information provided is accurate to the best of our knowledge, but it does not replace professional medical advice. We cannot guarantee its completeness or accuracy, and the absence of specific information about a drug should not be taken as an endorsement. We are not responsible for any consequences arising from this information, so please consult a healthcare professional for any concerns or questions.