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Generated Narrative: Bundle TEST PURPOSES ONLY - trelegy
Language: en
Profile: Bundle - ePI
Final Document at 2022-02-16 13:28:17+0000 by Organization ACME industry for Bundle: identifier = http://ema.europa.eu/identifier#None; type = document; timestamp = 2023-06-27 10:09:22+0000
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identifier: http://ema.europa.eu/identifier
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domain: Human use
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Document Content
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Language: en
Profile: Composition (ePI)
identifier: http://ema.europa.eu/identifier
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status: Final
type: Package Leaflet
category: Raw
date: 2022-02-16 13:28:17+0000
author: Organization ACME industry
title: TEST PURPOSES ONLY - trelegy
Mode | Time |
Official | 2022-02-16 13:28:17+0000 |
Step-by-step instructions
What is in this leaflet
What Trelegy Ellipta is
Trelegy Ellipta contains three active substances called fluticasone furoate, umeclidinium bromide and vilanterol. Fluticasone furoate belongs to a group of medicines called corticosteroids, often simply called steroids. Umeclidinium bromide and vilanterol belong to a group of medicines called bronchodilators.
What Trelegy Ellipta is used for
Trelegy Ellipta is used to treat chronic obstructive pulmonary disease (COPD) in adults. COPD is a long- term condition characterised by breathing difficulties that slowly get worse.
In COPD the muscles around the airways tighten, making breathing difficult. This medicine widens these muscles in the lungs, reducing the swelling and irritation in the small air passages and making it easier for air to get in and out of the lungs. When used regularly, it can help to control your breathing difficulties and reduce the effects of COPD on your everyday life.
Trelegy Ellipta should be used every day and not only when you have breathing problems or other symptoms of COPD. It should not be used to relieve a sudden attack of breathlessness or wheezing. If you get this sort of attack you must use a quick-acting inhaler (such as salbutamol). If you do not have a quick-acting inhaler contact your doctor.
Do not use Trelegy Ellipta:
Warnings and precautions
Talk to your doctor before using Trelegy Ellipta
Check with your doctor if you think any of these may apply to you.
Immediate breathing difficulties If you get tightness of the chest, coughing, wheezing or breathlessness immediately after using your Trelegy Ellipta inhaler:
stop using this medicine and seek medical help immediately, as you may have a serious condition called paradoxical bronchospasm.
Eye problems during treatment with Trelegy Ellipta If you get eye pain or discomfort, temporary blurring of vision, visual halos or coloured images as well as red eyes during treatment with Trelegy Ellipta: stop using this medicine and seek medical help immediately. These may be signs of an acute attack of narrow-angle glaucoma.
Infection of the lung Because you are using this medicine for COPD, you may be at an increased risk of developing an infection of the lungs known as pneumonia. See section 4 Possible side effects for information on symptoms to look out for while you are using this medicine.
Tell your doctor as soon as possible if you develop any of these symptoms.
Children and adolescents Do not give this medicine to children or adolescents below the age of 18 years.
Other medicines and Trelegy Ellipta Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines. If you are not sure what your medicine contains talk to your doctor or pharmacist.
Some medicines may affect how this medicine works, or make it more likely to have side effects. These include:
Pregnancy and breast-feeding
If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor for advice before taking this medicine. Do not use this medicine if you are pregnant unless your doctor tells you that you can.
It is not known whether the ingredients of this medicine can pass into breast milk. If you are breast-feeding, you must check with your doctor before you use Trelegy Ellipta. Do not use this medicine if you are breast- feeding unless your doctor tells you that you can.
Driving and using machines
It is unlikely that this medicine will affect your ability to drive or use machines.
Trelegy Ellipta contains lactose
If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before using this medicine.
Always use this medicine exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure.
The recommended dose is one inhalation every day at the same time of day. You only need to inhale once a day because the effect of this medicine lasts for 24 hours.
Do not use more than your doctor tells you to use.
Use Trelegy Ellipta regularly It is very important that you use Trelegy Ellipta every day, as instructed by your doctor. This will help to keep you free of symptoms throughout the day and night.
Trelegy Ellipta should not be used to relieve a sudden attack of breathlessness or wheezing. If you get this sort of attack you must use a quick-acting reliever inhaler (such as salbutamol).
How to use the inhaler See Step-by-step instructions at the end of this leaflet for full information.
Trelegy Ellipta is for inhalation use.
Once the tray is opened Trelegy Ellipta is ready to use.
If your symptoms do not improve
If your COPD symptoms (breathlessness, wheezing, cough) do not improve or get worse, or if you are using your quick-acting inhaler more often:
contact your doctor as soon as possible.
If you use more Trelegy Ellipta than you should
If you accidentally use too much of this medicine, contact your doctor or pharmacist for advice immediately as you may need medical attention. If possible, show them the inhaler, the package or this leaflet. You may notice that your heart is beating faster than usual, you feel shaky, you have visual disturbances, have a dry mouth, or have a headache.
If you forget to use Trelegy Ellipta
Do not inhale a double dose to make up for a forgotten dose. Just inhale your next dose at the usual time. If you become wheezy or breathless, use your quick-acting inhaler (such as salbutamol), then seek medical advice.
If you stop using Trelegy Ellipta
Use this medicine for as long as your doctor recommends. Do not stop unless your doctor advises you to, even if you feel better, as your symptoms may get worse.
If you have any further questions on the use of this medicine, ask your doctor, pharmacist or nurse.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Allergic reactions Allergic reactions to Trelegy Ellipta are rare (they may affect up to 1 in 1 000 people). If you have any of the following symptoms after taking Trelegy Ellipta, stop using it and tell your doctor immediately:
Immediate breathing difficulties If your breathing or wheezing gets worse straight after using this medicine, stop using it and get medical help immediately.
Pneumonia (infection of the lung) in COPD patients (common side effect) Tell your doctor if you have any of the following while using Trelegy Ellipta these could be symptoms of a lung infection:
Other side effects
Common (may affect up to 1 in 10 people)
Uncommon (may affect up to 1 in 100 people)
Rare (may affect up to 1 in 1 000 people)
Reporting of side effects
If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system listed in Appendix V. By reporting side effects you can help provide more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the carton, tray and inhaler after EXP .
The expiry date refers to the last day of that month.
Do not store above 30 C.
Keep the inhaler inside the sealed tray in order to protect from moisture and only remove immediately before first use. Once the tray is opened, the inhaler can be used for up to 6 weeks, starting from the date of opening the tray. Write the date the inhaler should be thrown away on the label in the space provided. The date should be added as soon as the inhaler has been removed from the tray.
If stored in a refrigerator, allow the inhaler to return to room temperature for at least one hour before use.
Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.
What Trelegy Ellipta contains
The active substances are fluticasone furoate, umeclidinium bromide and vilanterol.
Each single inhalation provides a delivered dose (the dose leaving the mouthpiece) of 92 micrograms of fluticasone furoate, 65 micrograms umeclidinium bromide equivalent to 55 micrograms umeclidinium and 22 micrograms of vilanterol (as trifenatate).
The other ingredients are lactose monohydrate (see section 2 under Trelegy Ellipta contains lactose ) and magnesium stearate.
What Trelegy Ellipta looks like and contents of the pack Trelegy Ellipta is an inhalation powder, pre-dispensed. The Ellipta inhaler consists of a light grey plastic body, a beige coloured mouthpiece cover and a dose counter. It is packaged in a foil laminate tray with a peelable foil lid. The tray contains a desiccant sachet, to reduce moisture in the packaging.
The active substances are present as a white powder in separate blister strips inside the inhaler.
Trelegy Ellipta is available in packs of 1 inhaler containing either 14 or 30 doses (14 or 30 day supply) and in multipacks containing 90 (3 inhalers of 30) doses (90 day supply). Not all pack sizes may be marketed.
Marketing Authorisation Holder
GlaxoSmithKline Trading Services Limited 12 Riverwalk Citywest Business Campus Dublin Ireland
Manufacturer
Glaxo Wellcome Production Zone Industrielle No.2 23 Rue Lavoisier
27000 Evreux
France
For any information about this medicine, please contact the local representative of the Marketing Authorisation Holder:
Belgi /Belgique/Belgien GlaxoSmithKline Pharmaceuticals s.a./n.v. T l/Tel: + 32 (0) 10 85 52 Lietuva UAB BERLIN-CHEMIE MENARINI BALTIC
Tel: + 370 52 691 lt@berlin-chemie.com
Luxembourg/Luxemburg GlaxoSmithKline Pharmaceuticals s.a./n.v. Belgique/Belgien T l/Tel: + 32 (0) 10 85 52 esk republika GlaxoSmithKline, s.r.o. Tel: + 420 222 001 cz.info@gsk.com
Magyarorsz g Berlin-Chemie/A. Menarini Kft. Tel.: + 36 23501bc-hu@berlin-chemie.com
Danmark GlaxoSmithKline Pharma A/S Tlf: + 45 36 35 91 dk-info@gsk.com
Malta GlaxoSmithKline Trading Services Limited Tel: + 356 80065Deutschland GlaxoSmithKline GmbH & Co. KG Tel.: + 49 (0)89 36044 8produkt.info@gsk.com
Nederland GlaxoSmithKline BV Tel: + 31 (0)33 2081Eesti O Berlin-Chemie Menarini Eesti Tel: + 372 667 5ee@berlin-chemie.com
Norge GlaxoSmithKline AS Tlf: + 47 22 70 20
Menarini Hellas A.E. : + 30 210 83161 11- sterreich GlaxoSmithKline Pharma GmbH Tel: + 43 (0)1 97075 0 at.info@gsk.com
Espa a GlaxoSmithKline, S.A. Tel: + 34 900 202 es-ci@gsk.com
Polska GSK Services Sp. z o.o. Tel.: + 48 (0)22 576 9France Laboratoire GlaxoSmithKline T l: + 33 (0)1 39 17 84 diam@gsk.com
Portugal GlaxoSmithKline Produtos Farmac uticos, Lda. Tel: + 351 21 412 95 FI.PT@gsk.com
Hrvatska Berlin-Chemie Menarini Hrvatska d.o.o. Tel: + 385 1 4821 office-croatia@berlin-chemie.com
Rom nia GlaxoSmithKline Trading Services Limited
Tel: + 40 800672Ireland GlaxoSmithKline (Ireland) Limited Tel: + 353 (0)1 4955Slovenija Berlin-Chemie / A. Menarini Distribution Ljubljana d.o.o. Tel: + 386 (0)1 300 2slovenia@berlin-chemie.com
sland Vistor hf. S mi: +354 535 7Slovensk republika Berlin-Chemie / A. Menarini Distribution Slovakia s.r.o. Tel: + 421 2 544 30 slovakia@berlin-chemie.com
Italia GlaxoSmithKline S.p.A. Tel: + 39 (0)45 7741 Suomi/Finland GlaxoSmithKline Oy Puh/Tel: + 358 (0)10 30 30
GlaxoSmithKline Trading Services Limited : + 357 80070Sverige GlaxoSmithKline AB Tel: + 46 (0)8 638 93 info.produkt@gsk.com
Latvija SIA Berlin-Chemie/Menarini Baltic Tel: + 371 67103lv@berlin-chemie.com
United Kingdom (Northern Ireland) GlaxoSmithKline Trading Services Limited Tel: + 44 (0)800 221customercontactuk@gsk.com
This leaflet was last revised in .
Other sources of information
Detailed information on this medicine is available on the European Medicines Agency web site:
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