Medicinal Product

Form and presentation of product administered

Route of administration

Indication for which the medicinal product may be administered

Dosage and conditions of administration

Place of administration

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Epinephrine (adrenaline) Injection

Epinephrine (adrenaline) injection presented as a pre-filled syringe or ampoule

Intramuscular or subcutaneous injection

Adults and Children: For the emergency treatment of anaphylactic shock

In accordance with the summary of product characteristics of the product administered and relevant national guidelines

Any place

Glucagon for injection

Glucagon hydrochloride for injection

Intramuscular or subcutaneous injection

Adults and children: For the emergency treatment of hypoglycaemia

In accordance with the summary of product characteristics of the product administered

Any place

Glyceryl trinitrate aerosol

Glyceryl trinitrate sublingual spray

Sublingual spray

Adults: For the emergency treatment of severe angina attack

In accordance with the summary of product characteristics of the product administered

Any place

Herpes zoster vaccine for injection

Live, attenuated, varicella-zoster virus powder and solvent for the suspension for injection

By intramuscular or subcutaneous injection

Prevention of zoster and zoster-related post-herpetic neuralgia

0.65ml for single administration in accordance with the summary of product characteristics of the product administered and Immunisation Guidelines for Ireland, as published and updated by the National Immunisation Advisory Committee of the Royal College of Physicians of Ireland

The premises of the retail pharmacy business in which the authorised person carries on professional practice

Influenza vaccine of a composition that has been approved for use in the European Union for the season in question

Influenza vaccine suspension for injection presented as a pre-filled syringe

By intramuscular injection only

Prevention of seasonal influenza

0.5ml or less for a single administration. In accordance with the summary of product characteristics of the product administered and Immunisation Guidelines for Ireland, as published and updated by the National Immunisation Advisory Committee of the Royal College of Physicians of Ireland. Only to be administered in connection with the carrying on of the registered retail pharmacy business in which the authorised person is employed or engaged.

Any suitable and appropriate place, having regard to public convenience and the need to protect the health and safety of the public and safely administer the product.

Influenza vaccine (live attenuated) nasal spray suspension of a composition that has been approved for use in the European Union for the season in question

Influenza vaccine nasal spray, suspension

By intranasal administration only

Prevention of seasonal influenza

Children and adolescents from 24 months: 0.2 ml (administered as 0.1 ml per nostril). For children who have not previously been vaccinated against seasonal influenza, a second dose should be given after an interval of at least 4 weeks. In accordance with the summary of product characteristics of the product administered and Immunisation Guidelines for Ireland, as published and updated by the National Immunisation Advisory Committee of the Royal College of Physicians of Ireland. Only to be administered in connection with the carrying on of the registered retail pharmacy business in which the authorised person is employed or engaged.

Any suitable and appropriate place, having regard to public convenience and the need to protect the health and safety of the public and safely administer the product.

Naloxone injection

Naloxone hydrochloride dihydrate 1mg/ml pre-filled injection

Intramuscular injection

Adults and children: Respiratory depression secondary to known or suspected narcotic overdose

In accordance with the summary of product characteristics of the product administered and relevant national guidelines

Any place

Naloxone Nasal Spray

Naloxone hydrochloride dihydrate 1.8 mg Nasal Spray Solution

Nasal administration

Adults and children: Respiratory depression secondary to known or suspected narcotic overdose

In accordance with the summary of product characteristics of the product administered or relevant national guidelines

Any place

Pneumococcal Polysaccharide Vaccine solution for injection

Pneumococcal Polysaccharide Vaccine solution for injection 25mcg/0.5ml in a pre-filled syringe or vial.

By intramuscular or subcutaneous injection

Active immunization against disease caused by the pneumococcal serotypes included in the vaccine

0.5ml for single administration, in accordance with the summary of product characteristics of the product administered and the specific timing of, and need for re-vaccination as determined by the Immunisation Guidelines for Ireland, as published and updated by the National Immunisation Advisory Committee of the Royal College of Physicians of Ireland

The premises of the retail pharmacy business in which the authorised person carries on professional practice

Salbutamol 100 mcg multi-dose inhaler

Salbutamol pressurised inhalation solution 100mcg multi-dose inhaler

Oral inhalation

Adults and children: For the emergency treatment of acute asthmatic attack

In accordance with the summary of product characteristics of the product administered or relevant national guidelines

Any place