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Medicine overview

Indications of Adrin

Established / Emergency Indications

  • Anaphylaxis: Adrin is the first-line emergency treatment for severe allergic reactions (anaphylaxis) of any cause, including insect stings, foods, drugs, latex, or idiopathic anaphylaxis.
  • Cardiac arrest (ACLS): Adrin is used as part of Advanced Cardiovascular Life Support (ACLS) protocols for cardiac arrest, including asystole, pulseless electrical activity, and shock-refractory ventricular fibrillation/pulseless ventricular tachycardia.
  • Severe acute asthma/bronchospasm: Adrin may be used for severe, life-threatening bronchospasm or acute asthma exacerbation that has failed to respond adequately to inhaled bronchodilator (e.g., salbutamol) therapy.
  • Septic shock (adjunct): Adrin is used as an adjunct vasopressor to raise mean arterial blood pressure in adults with hypotension associated with septic shock that is inadequately responsive to first-line vasopressors and fluid resuscitation.

Combination / Adjunct Use

  • Local anesthetic additive: Adrin is combined with local anesthetics (e.g., lidocaine) to prolong the duration of local/regional anesthesia and reduce surgical-site bleeding through local vasoconstriction.
  • Croup: Nebulized racemic or L-Adrin is used in hospital settings for moderate-to-severe croup (laryngotracheobronchitis) to reduce airway edema.

Use of Adrin outside emergency settings (e.g., as a vasoconstrictor additive) should follow standard clinical protocols and physician guidance.

Composition

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.

Description

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.

Therapeutic Class

Sympathomimetic agent / Emergency anti-anaphylactic agent (Adrin)

Pharmacology

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.

  • Alpha-1 effects: Vasoconstriction of skin, mucosa, and splanchnic vasculature, which raises systemic vascular resistance and blood pressure, and reduces mucosal edema and angioedema in anaphylaxis.
  • Beta-1 effects: Increased heart rate (positive chronotropy) and myocardial contractility (positive inotropy), improving cardiac output during cardiac arrest and shock.
  • Beta-2 effects: Bronchodilation (relieving bronchospasm in anaphylaxis and severe asthma) and stabilization of mast cells, reducing further release of histamine and other inflammatory mediators.

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.

Dosage & Administration of Adrin

Anaphylaxis

PopulationDoseRoute
Adults and children ≥30 kg0.3-0.5 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 kg0.01 mg/kg (max single dose 0.3 mg), or per weight-banded auto-injector strengthIntramuscular, anterolateral thigh

Cardiac Arrest (ACLS)

RouteDose
Intravenous/intraosseous1 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

Severe Acute Asthma/Bronchospasm

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.

Septic Shock (Adjunct Vasopressor)

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.

As Additive to Local Anesthetics

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.

Administration of Adrin

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.

Interaction of Adrin

  • Non-selective beta-blockers (e.g., propranolol): Can blunt the beneficial beta-adrenergic effects of Adrin and lead to unopposed alpha-adrenergic stimulation, causing severe hypertension and reflex bradycardia; use with caution and be prepared to manage blood pressure.
  • Monoamine oxidase inhibitors (MAOIs) and tricyclic antidepressants: May potentiate the cardiovascular effects of Adrin, increasing the risk of severe hypertension and arrhythmias.
  • Other sympathomimetics: Concurrent use with other sympathomimetic agents (e.g., other vasopressors, decongestants) can have additive cardiovascular effects, including hypertension and arrhythmias.
  • Volatile anesthetics (e.g., halothane) and digoxin: May sensitize the myocardium to the arrhythmogenic effects of Adrin.
  • Alpha-blockers (e.g., phentolamine): Antagonize the vasoconstrictive alpha-effects of Adrin and may unmask its beta-2 vasodilatory effect, causing hypotension.

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.

Contraindications

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.

Side Effects of Adrin

Common, generally transient effects of Adrin used in emergencies include:

  • Anxiety, restlessness, or a feeling of fear
  • Tremor
  • Palpitations and rapid heart rate
  • Headache
  • Sweating and pallor
  • Dizziness
  • Nausea or vomiting

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 & Lactation

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.

Precautions & Warnings

  • Cardiac arrhythmias: Adrin can provoke or worsen cardiac arrhythmias, including ventricular fibrillation; use with caution in patients with known arrhythmias outside of cardiac arrest resuscitation.
  • Hypertension and cardiovascular disease: Adrin can cause marked increases in blood pressure and myocardial oxygen demand; use with caution in patients with hypertension, coronary artery disease, or arteriosclerosis, though this should not delay treatment of true anaphylaxis.
  • Hyperthyroidism: Adrin may exacerbate symptoms of hyperthyroidism.
  • Diabetes mellitus: Adrin can raise blood glucose levels; monitor glucose in diabetic patients receiving repeated doses.
  • Narrow-angle glaucoma: Caution is advised for non-emergency use, as Adrin may increase intraocular pressure.
  • Extremities and end-arterial circulation: Avoid injecting Adrin (particularly with local anesthetics) into the fingers, toes, nose, ears, or genitals because of the risk of vasoconstriction-related tissue ischemia.
  • Sulfite sensitivity: Some Adrin formulations contain sodium metabisulfite, which may cause allergic-type reactions in sulfite-sensitive individuals; this should not preclude emergency use in anaphylaxis.

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 Effects of Adrin

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.

Storage Conditions

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.

Use In Special Populations

  • Elderly: Adrin should be used with caution in elderly patients, who may have unrecognized cardiovascular disease and be more sensitive to hypertensive and arrhythmogenic effects; however, Adrin should not be withheld in a true anaphylaxis or cardiac arrest emergency.
  • Renal impairment: No specific dose adjustment is established; Adrin is used based on clinical response with monitoring.
  • Hepatic impairment: No specific dose adjustment is established, though patients may have altered catecholamine metabolism; use with clinical monitoring.
  • Cardiovascular disease: Use with caution outside of emergencies; see Precautions and Warnings.

Duration Of Treatment

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.

Drug Classes

Catecholamine; Sympathomimetic (alpha- and beta-adrenergic agonist); Vasopressor; Bronchodilator; Anti-anaphylactic agent (Adrenaline)

Mode Of Action

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.

Pregnancy

C

Pediatric Uses

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.

Frequently Asked Questions

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.

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