Hulio 40 mg/0.8 ml solution for injection | Patient Info | Gerard Laboratories

Home
Medicines
Hulio 40 mg/0.8 ml solution for injection

Name:
Hulio 40 mg/0.8 ml solution for injection
Company:
Gerard Laboratories
Active Ingredients:
adalimumab
Legal Category:
Product subject to restricted prescription (C)

Patient Information Leaflet Patient Information Leaflet last updated on medicines.ie: 22/03/21

Summary of Product Characteristics last updated on medicines.ie: 4/1/2021

This medicinal product is subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions. See section 4.8 for how to report adverse reactions.

Click on this link to Download PDF directly

Company Products

Medicine Name	Active Ingredients
Medicine Name Abacavir/Lamivudine Mylan 600 mg/300 mg film-coated tablets	Active Ingredients Abacavir hydrochloride, Lamivudine
Medicine Name Agerdex 1mg Film Coated Tablets	Active Ingredients Anastrozole
Medicine Name Agomelatine Mylan 25 mg film-coated tablets	Active Ingredients Agomelatine
Medicine Name Amisulpride 50mg & 200mg Tablets	Active Ingredients Amisulpride
Medicine Name Amlodipine Mylan 5mg & 10mg Tablets	Active Ingredients Amlodipine besilate
Medicine Name Amlodipine/Valsartan Mylan 5mg/80mg, 5mg/160mg, 10mg/160mg film-coated tablets	Active Ingredients Amlodipine besilate, Valsartan
Medicine Name Areloger 7.5mg & 15mg Tablets	Active Ingredients Meloxicam
Medicine Name Aripil 5mg & 10mg Film-coated Tablets	Active Ingredients Donepezil Hydrochloride
Medicine Name Atazanavir Mylan 300 mg hard capsules	Active Ingredients Atazanavir sulfate
Medicine Name Atenetic 50/12.5mg & 100/25mg Film - coated Tablets	Active Ingredients Atenolol, Chlortalidone
Medicine Name Atorvastatin Mylan 10 mg, 20 mg, 40 mg & 80 mg film-coated tablets	Active Ingredients Atorvastatin calcium trihydrate
Medicine Name Atovaquone/Proguanil Hydrochloride 250 mg/100 mg film-coated tablets	Active Ingredients Atovaquone, Proguanil Hydrochloride
Medicine Name Azacitidine Mylan 25 mg/mL powder for suspension for injection	Active Ingredients azacitidine
Medicine Name Azromax 250mg Film-coated tablets	Active Ingredients Azithromycin monohydrate
Medicine Name Baclopar Tablets 10 mg	Active Ingredients Baclofen
Medicine Name Bisoprolol Mylan	Active Ingredients Bisoprolol Fumarate
Medicine Name Brabio 20mg/ml solution for injection, pre-filled syringe	Active Ingredients Glatiramer Acetate
Medicine Name Brabio 40mg/ml solution for injection, pre-filled syringe	Active Ingredients Glatiramer Acetate
Medicine Name Cifloxager 250 mg Film-coated Tablets	Active Ingredients Ciprofloxacin hydrochloride
Medicine Name Cifloxager 500 mg Film-coated Tablets	Active Ingredients Ciprofloxacin hydrochloride
Medicine Name Ciprager 10mg & 20mg Film Coated Tablets	Active Ingredients citalopram hydrobromide
Medicine Name Ciprager 40mg Film Coated Tablets	Active Ingredients citalopram hydrobromide
Medicine Name Ciprofloxacin Mylan 2mg/1ml solution for infusion	Active Ingredients Ciprofloxacin
Medicine Name Clopidogrel Mylan 75 mg film-coated tablets	Active Ingredients clopidogrel hydrochloride
Medicine Name Darunavir Mylan 800 mg film-coated tablets	Active Ingredients darunavir ethanolate

Items Per Page :

1 - 0 of 116 items.Total: Infinity pages

When a pharmaceutical company changes any document, a new version is published on medicines.ie. For each version, we show the dates it was published on medicines.ie and the reasons for change.

Updated on 22 March 2021 PIL

Reasons for updating

Change to section 6 - manufacturer
Change to section 6 - date of revision

Updated on 4 January 2021 SPC

Reasons for updating

Change to section 2 - Qualitative and quantitative composition
Change to section 4.2 - Posology and method of administration
Change to section 4.4 - Special warnings and precautions for use
Change to section 4.5 - Interaction with other medicinal products and other forms of interaction
Change to section 4.8 - Undesirable effects
Change to section 5.1 - Pharmacodynamic properties
Change to section 5.2 - Pharmacokinetic properties
Change to section 10 - Date of revision of the text

Legal category: Product subject to restricted prescription (C)

Updated on 4 January 2021 PIL

Reasons for updating

Change to Section 1 - what the product is
Change to section 1 - what the product is used for
Change to section 2 - what you need to know - warnings and precautions
Change to section 2 - use in children and adolescents
Change to section 2 - interactions with other medicines, food or drink
Change to section 2 - pregnancy, breast feeding and fertility
Change to section 2 - driving and using machines
Change to section 3 - use in children/adolescents
Change to section 4 - possible side effects
Change to section 6 - what the product contains
Change to section 6 - date of revision

Updated on 23 October 2020 SPC

Reasons for updating

Change to section 4.8 - Undesirable effects
Change to Section 4.8 – Undesirable effects - how to report a side effect
Change to section 10 - Date of revision of the text

Legal category: Product subject to restricted prescription (C)

Updated on 23 October 2020 PIL

Reasons for updating

Change to section 4 - possible side effects
Change to section 4 - how to report a side effect
Change to section 6 - date of revision

Updated on 10 April 2020 PIL

Reasons for updating

Change to section 4 - how to report a side effect

Updated on 6 March 2020 SPC

Reasons for updating

Change to section 5.1 - Pharmacodynamic properties
Change to section 10 - Date of revision of the text

Legal category: Product subject to restricted prescription (C)

Updated on 29 October 2019 PIL

Reasons for updating

Change to section 6 - marketing authorisation holder
Change to section 6 - date of revision

Updated on 13 August 2019 PIL

Reasons for updating

New PIL for new product

Updated on 13 August 2019 SPC

Reasons for updating

New SPC for new product

Legal category: Product subject to restricted prescription (C)