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Generated Narrative: Bundle TEST PURPOSES ONLY - skyclarys
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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type: Medicinal Product
domain: Human use
status: active
legalStatusOfSupply: Medicinal product subject to medical prescription
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Document Content
Generated Narrative: Composition composition-en-3c1db916d2062445ec61cc58880ca8a2
Language: en
Profile: Composition (ePI)
identifier: http://ema.europa.eu/identifier
/EU/1/23/1786/001
status: Final
type: Package Leaflet
category: Raw
date: 2022-02-16 13:28:17+0000
author: Organization ACME industry
title: TEST PURPOSES ONLY - skyclarys
Mode | Time |
Official | 2022-02-16 13:28:17+0000 |
What is in this leaflet
What is Skyclarys? Skyclarys contains the active substance omaveloxolone, which activates a specific protein, Nrf2, in your body.
What is Skyclarys used for? Skyclarys is used to treat adults and adolescents who are at least 16 years of age who have Friedreich s ataxia, a neurodegenerative movement disorder. Friedreich s ataxia is a rare inherited disease that causes progressive damage to your nervous system and movement problems.
How does Skyclarys work? The protein called Nrf2 in your body has a key role in managing oxidative stress (a condition that can damage cells in your body) and has a protective role against neurodegenerative diseases. In patients with Friedreich s ataxia, Nrf2 activity is reduced. Skyclarys activates Nrf2 so it can manage oxidative stress.
In a clinical trial patients treated with Skyclarys scored better on tests of neurological function than patients who were treated with an inactive substance.
Do not take Skyclarys if you are allergic to omaveloxolone or any of the other ingredients of this medicine (listed in section 6).
Warnings and precautions
Talk to your doctor before taking Skyclarys:
Tell your doctor about all the medicines you are taking before you start Skyclarys.
Your doctor will check to see how well your liver is working and will check your cholesterol level before you start taking Skyclarys. Your doctor will also check your level of BNP (B-type natriuretic peptide, a blood test for heart problems) before you start taking Skyclarys.
Talk to your doctor while taking Skyclarys Contact your doctor immediately if you have sudden weight gain, swelling of legs, ankles, or feet, or shortness of breath, which may be signs or symptoms of heart problems while taking Skyclarys. Your doctor will decide on treatment and whether Skyclarys should be continued.
Your doctor will be checking blood tests while you are taking Skyclarys. This will include liver blood tests to see how your liver is working while taking Skyclarys. Your doctor will decide on whether to discontinue Skyclarys if liver problems develop. Other blood tests that your doctor will do will check cholesterol and BNP after you start Skyclarys.
Tell your doctor if you have weight loss with Skyclarys.
Children and adolescents Do not give Skyclarys to children and adolescents below the age of 16 years because it has not yet been studied in this group of patients.
Other medicines and Skyclarys Tell your doctor if you are taking, have recently taken, or might take any other medicines. This is because some medicines may affect the way Skyclarys works. Also, Skyclarys may affect the way some medicines work.
Certain medicines may increase the risk of side effects of Skyclarys by increasing the levels of Skyclarys in the blood. Some of these medicines include:
Certain medicines may reduce how well Skyclarys works by decreasing the amount of Skyclarys in the blood. Some of these medicines include:
Skyclarys may reduce how well some other medicines work by decreasing the amount of these medicines in the blood. Some of these medicines include:
Talk to your doctor if you are taking any medicines, particularly those mentioned above, as they may affect the way Skyclarys or other medicines work.
Skyclarys with food and drink Avoid eating grapefruit or grapefruit juice while taking Skyclarys.
Pregnancy You should not take Skyclarys if you are pregnant, think you may be pregnant, or are planning to have a baby. Tell your doctor immediately if you become pregnant while you are being treated with Skyclarys.
Birth Control Using Skyclarys can reduce the effectiveness of hormonal birth control. You should use a different method of birth control, such as a non-hormonal IUD (intrauterine device) or barrier contraceptives such as condoms. A reliable method of birth control should be used during Skyclarys treatment and for 28 days after stopping treatment with Skyclarys. Talk to your doctor about the most suitable birth control for you.
Breast-feeding Do not breast-feed your baby while you are being treated with Skyclarys. It is not known if this medicine passes into the breast milk.
Driving and using machines Some patients may feel tired after taking this medicine. If you feel tired after taking Skyclarys, avoid driving and using machines.
Skyclarys contains a negligible amount of sodium This medicine contains less than 1 mmol sodium (23 mg) per dose, that is to say essentially sodium free .
Always take this medicine exactly as your doctor has told you. Check with your doctor if you are not sure.
The recommended dose is 150 mg (3 capsules) once per day.
Taking Skyclarys
Some medicines may cause side effects when taken at the same time as Skyclarys. If your doctor prescribes one of these medicines while you are taking Skyclarys, your doctor may reduce the dose of Skyclarys to prevent side effects when taking both drugs at the same time.
If you are sick after taking your usual dose, do not take replacement capsules. Take the capsules as usual the following day.
If you take more Skyclarys than you should If you take more Skyclarys than your doctor prescribed, talk to a doctor immediately. Take this leaflet with you.
If you forget to take Skyclarys If you miss a dose of Skyclarys, take the next dose as usual the following day. Do not take a double dose to make up for a forgotten dose.
If you stop taking Skyclarys Do not stop taking this medicine unless your doctor tells you. If you have any further questions on the use of this medicine, ask your doctor.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Some side effects with Skyclarys could be or could become serious
Talk to your doctor immediately if you have any of these side effects: Very common (may affect more than 1 in 10 people)
Based on your blood tests, your doctor may tell you that you have:
Other possible side effects of Skyclarys Very common (may affect more than 1 in 10 people)
Common (may affect up to 1 in 10 people)
Reporting of side effects If you get any side effects, talk to your doctor. 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 after EXP . The expiry date refers to the last day of that month.
This medicine does not require any special storage conditions.
If the capsule is opened and mixed with apple puree you must eat all the apple puree/medicine mixture immediately after making it. See section 3, Taking Skyclarys.
Do not use this medicine if you notice that the pack is damaged or shows signs of tampering.
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 Skyclarys contains
What Skyclarys looks like and contents of the pack Skyclarys 50 mg hard capsules are made of an opaque light green body imprinted with RTA 408 in white ink and a blue cap imprinted with 50 in white ink.
Skyclarys 50 mg is available in a pack containing 90 hard capsules and in a pack of 3 bottles, each containing 90 hard capsules.
Marketing Authorisation Holder Reata Ireland Limited Block A, George s Quay Plaza George s Quay Dublin 2 D02 E440 Ireland
Manufacturer Jenson R+ (Ireland) Limited Unit Daingean Hall N4 Axis Centre Longford N39 W6K0 Ireland
For any information about this medicine, please contact the local representative of the Marketing Authorisation Holder:
Belgi /Belgique/Belgien Biogen Belgium N.V./S.A. T l/Tel: +32 2 219 12 Lietuva Biogen Lithuania UAB Tel: +370 5 259 6
Te .: +359 2 962 12 Luxembourg/Luxemburg Biogen Belgium N.V./S.A. T l/Tel: +32 2 219 12 esk republika Biogen (Czech Republic) s.r.o. Tel: +420 255 706 Magyarorsz g Biogen Hungary Kft. Tel.: +36 (1) 899 9Danmark Biogen (Denmark) A/S Tlf: +45 77 41 57 Malta Pharma MT limited Tel: +356 213 37008/9
Deutschland Biogen GmbH Tel: +49 (0) 89 99 6Nederland Biogen Netherlands B.V. Tel: +31 20 542 2Eesti Biogen Estonia O
Tel: + 372 618 9Norge Biogen Norway AS Tlf: +47 23 40 01
Genesis Pharma SA : +30 210 8771 sterreich Biogen Austria GmbH Tel: +43 1 484 46 Espa a Biogen Spain SL Tel: +34 91 310 7Polska Biogen Poland Sp. z o.o. Tel.: +48 22 351 51 France Biogen France SAS T l: +33 (0)1 41 37 95 Portugal Biogen Portugal Tel.: +351 21 318 8Hrvatska Biogen Pharma d.o.o. Tel: +385 (0) 1 775 73 Rom nia Ewopharma AG Representative Office Tel: + 40 377 881 Ireland Biogen Idec (Ireland) Ltd. Tel: +353 (0)1 463 7Slovenija Biogen Pharma d.o.o. Tel.: +386 1 511 02 sland Icepharma hf S mi: +354 540 8Slovensk republika Biogen Slovakia s.r.o. Tel.: +421 2 323 340 Italia Biogen Italia s.r.l. Tel: +39 02 584 9Suomi/Finland Biogen Finland Oy Puh/Tel: +358 207 401
Genesis Pharma Cyprus Ltd : +357 22765Sverige Biogen Sweden AB Tel: +46 8 594 113 Latvija Biogen Latvia SIA Tel: + 371 68 688 United Kingdom (Northern Ireland) Biogen Idec (Ireland) Limited Tel: +44 (0) 1628 50 1This 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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date: 2022-02-16 13:28:17+0000
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