Gravitate Health FHIR Implementation Guide
0.1.0 - CI Build
Gravitate Health FHIR Implementation Guide
0.1.0 - CI Build
Gravitate Health FHIR Implementation Guide, published by Gravitate Health Project. This guide is not an authorized publication; it is the continuous build for version 0.1.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/joofio/test-epi-composition/ and changes regularly. See the Directory of published versions
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"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\" xml:lang=\"en\" lang=\"en\"><a name=\"Composition_composition-en-f09921a712319be762e8c3e2baca4fd9\"> </a><p class=\"res-header-id\"><b>Generated Narrative: Composition composition-en-f09921a712319be762e8c3e2baca4fd9</b></p><a name=\"composition-en-f09921a712319be762e8c3e2baca4fd9\"> </a><a name=\"hccomposition-en-f09921a712319be762e8c3e2baca4fd9\"> </a><a name=\"composition-en-f09921a712319be762e8c3e2baca4fd9-en-US\"> </a><div style=\"display: inline-block; background-color: #d9e0e7; padding: 6px; margin: 4px; border: 1px solid #8da1b4; border-radius: 5px; line-height: 60%\"><p style=\"margin-bottom: 0px\">Language: en</p><p style=\"margin-bottom: 0px\">Profile: <a href=\"https://build.fhir.org/ig/HL7/emedicinal-product-info/StructureDefinition-Composition-uv-epi.html\">Composition (ePI)</a></p></div><p><b>identifier</b>: <code>http://ema.europa.eu/identifier</code>/EU/1/20/1460/001</p><p><b>status</b>: Final</p><p><b>type</b>: <span title=\"Codes:{https://spor.ema.europa.eu/rmswi/ 100000155538}\">Package Leaflet</span></p><p><b>category</b>: <span title=\"Codes:{http://hl7.eu/fhir/ig/gravitate-health/CodeSystem/epicategory-cs R}\">Raw</span></p><p><b>date</b>: 2022-02-16 13:28:17+0000</p><p><b>author</b>: <a href=\"Organization-mah-ema.html\">Organization ACME industry</a></p><p><b>title</b>: TEST PURPOSES ONLY - rozlytrek</p><h3>Attesters</h3><table class=\"grid\"><tr><td style=\"display: none\">-</td><td><b>Mode</b></td><td><b>Time</b></td></tr><tr><td style=\"display: none\">*</td><td><span title=\"Codes:{http://hl7.org/fhir/composition-attestation-mode official}\">Official</span></td><td>2022-02-16 13:28:17+0000</td></tr></table></div>"
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"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p>What is in this leaflet</p><ol type=\"1\"><li>What Rozlytrek is and what it is used for</li><li>What you need to know before you take Rozlytrek</li><li>How to take Rozlytrek</li><li>Possible side effects</li><li>How to store Rozlytrek</li><li>Contents of the pack and other information</li></ol></div>"
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"title" : "1. What rozlytrek is and what it is used for",
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"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p>What Rozlytrek is</p><p>Rozlytrek is a cancer medicine that contains the active substance entrectinib.</p><p>What Rozlytrek is used for</p><p>Rozlytrek is used to treat either:</p><ul><li>adults and children 12 years of age and older with solid tumour (cancer) in various parts of the body that is caused by a change in the neurotrophic tyrosine receptor kinase (NTRK) gene, or</li><li>adults with a type of lung cancer called non-small cell lung cancer (NSCLC) that is caused by a change in the ROS1 gene.</li></ul><p>NTRK gene fusion-positive solid tumour cancer</p><p>It is used when:</p><ul><li>a test has shown that your cancer cells have a change in genes called NTRK and has spread within the affected organ or to other organs in your body or if surgery to remove the cancer is likely to result in severe complications (see How Rozlytrek works below), and</li><li>you have not received treatment with medicines called NTRK inhibitors</li><li>other treatments have not worked or are not suitable for you.</li></ul><p>ROS1-positive non -small cell lung cancer (NSCLC)</p><p>It is used if your lung cancer:</p><ul><li>is ROS1-positive this means that your cancer cells have a change in a gene called ROS1<br/>(see How Rozlytrek works below),</li><li>is advanced for example, has spread to other parts of your body (metastatic), and</li><li>you have not received treatment with medicines called ROS1 inhibitors.</li></ul><p>How Rozlytrek works</p><p>Rozlytrek works by blocking the action of abnormal enzymes caused by a change in the NTRK or ROS1 genes that make them. The faulty enzymes encourage the cancer cells to grow.</p><p>Rozlytrek may slow down or stop the cancer growing. It may also help to shrink your cancer.</p></div>"
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"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p>Do not take Rozlytrek</p><ul><li>if you are allergic to entrectinib or any of the other ingredients of this medicine (listed in section 6). If you are not sure, talk to your doctor, pharmacist or nurse before taking Rozlytrek.</li></ul><p>Warnings and precautions</p><p>Talk to your doctor, pharmacist or nurse before taking Rozlytrek if:</p><ul><li>you have recently experienced memory loss, confusion, hallucinations, or mental status changes</li><li>you have a history of fractured bones, or conditions which may increase your risk of breaking bones, called osteoporosis or osteopaenia</li><li>you take medication to lower the levels of uric acid in your blood</li><li>you have heart failure (an inability for your heart to adequately pump blood to supply oxygen to the body) signs can include cough, shortness of breath, and swelling in your legs or arms</li><li>you have or had heart disorders or a heart conduction problem called prolonged QTc interval<br/>this is shown on an electro-cardiogram (ECG), or low levels of electrolytes (potassium, magnesium, calcium or phosphorus) in your blood</li><li>you have an inherited problem called galactose intolerance , congenital lactase deficiency or glucose-galactose malabsorption .</li></ul><p>Other medicines and Rozlytrek</p><p>Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines. This is because Rozlytrek can affect the way some other medicines work. Also, some other medicines can affect the way Rozlytrek works.</p><p>In particular, tell your doctor or pharmacist if you are taking any of the following medicines:</p><ul><li>medicines for fungal infections (anti-fungals) such as ketoconazole, itraconazole, voriconazole, posaconazole</li><li>medicines to treat Acquired Immune Deficiency Syndrome (AIDS)/Human immunodeficiency virus (HIV) infection such as ritonavir or saquinavir</li><li>a herbal medicine for depression St. John s Wort</li><li>medicines to stop seizures or fits (anti-epileptics) such as phenytoin, carbamazepine, or phenobarbital</li><li>medicines for tuberculosis such as rifampicin, rifabutin</li><li>medicines to treat solid cancers and blood cancer topotecan, lapatinib, mitoxantrone, apalutamide, methotrexate</li><li>a medicine for inflammation of joints or joint autoimmune disease (rheumatoid arthritis)<br/>methotrexate</li><li>a medicine for migraine-type headaches ergotamine</li><li>a medicine for relief of severe pain fentanyl</li><li>a medicine for mental illness (psychoses) or involuntary movements and sounds, also called Tourette Syndrome pimozide</li><li>a medicine for irregular heart rate quinidine</li><li>medicines to prevent formation of blood clots warfarin, dabigatran etexilate</li><li>medicines for gastric reflux (heartburn) cisapride, omeprazole</li><li>medicines to reduce blood cholesterol atorvastatin, pravastatin, rosuvastatin</li><li>medicines to suppress your body s immune system, or prevent the body from rejecting an organ transplant sirolimus, tacrolimus, cyclosporin,</li><li>medicines for depression paroxetine, fluvoxamine</li><li>medicines to reduce blood sugar levels repaglinide, tolbutamide</li><li>medicines for high blood pressure bosentan, felodipine, nifedipine, verapamil.</li></ul><p>If any of the above apply to you (or you are not sure), talk to your doctor or pharmacist before taking Rozlytrek.</p><p>Rozlytrek with food and drink</p><p>Do not drink grapefruit juice or eat grapefruit or Seville oranges during your treatment with Rozlytrek. It may increase the amount of the medicine in your blood to a harmful level.</p><p>Pregnancy, breast-feeding and fertility</p><p>Women and contraception</p><p>You should not become pregnant while taking this medicine because it could harm the baby. If you are able to become pregnant, you must use highly effective contraception while on treatment and for at least 5 weeks after stopping treatment.</p><p>It is not known if Rozlytrek can reduce the effect of birth control medicines (pills or implanted hormonal contraceptives). You should use another reliable method of birth control such as a barrier method (e.g. condom) so you do not become pregnant while you are taking Rozlytrek and for 5 weeks after you stop treatment.</p><p>Talk to your doctor about the right methods of contraception for you and your partner.</p><p>Men and contraception</p><p>Your female partner should not become pregnant while you are taking this medicine because it could harm the baby. If your female partner is able to become pregnant, you must use highly effective contraception while on treatment and for at least 3 months after stopping treatment. Talk to your doctor about the right methods of contraception for you and your partner.</p><p>Pregnancy</p><ul><li>Do not take Rozlytrek if you are pregnant. This is because it may harm your baby.</li><li>If you become pregnant when taking the medicine or during the 5 weeks after taking your last dose, tell your doctor straight away.</li></ul><p>Breast-feeding</p><p>Do not breast-feed while taking this medicine. This is because it is not known if Rozlytrek can pass over into breast milk and could therefore harm your baby. Driving and using machines</p><p>Rozlytrek may affect your ability to drive or use machines. Rozlytrek may cause you to:</p><ul><li>have blurred vision</li><li>feel dizzy</li><li>pass out (lose consciousness)</li><li>feel tired</li><li>have changes in your mental status, feel confused or see things that are not there (hallucinations). If this happens, you should not drive, use a bicycle, or operate heavy machinery until your symptoms resolve. Talk to your doctor or pharmacist about whether it is okay for you to drive or use machines.</li></ul><p>Rozlytrek contains:</p><ul><li>lactose (a type of sugar). If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicine.</li><li>sunset yellow FCF (E110) in 200 mg hard capsules only. This is a colouring agent, which may cause allergic reactions.</li></ul></div>"
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"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p>Always take this medicine exactly as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are not sure.</p><p>How much to take</p><p>Adults</p><ul><li>The recommended dose is 3 capsules of 200 mg once a day (total amount 600 mg).</li><li>If you feel unwell, sometimes your doctor may lower your dose, stop treatment for a short time or stop treatment completely.</li></ul><p>Children</p><ul><li>Rozlytrek can be used in children 12 years of age and older.</li><li>Your doctor will work out the correct dose to use this will depend on the height and weight of the child.</li></ul><p>How to take</p><p>Take Rozlytrek by mouth with or without food. Swallow each capsule whole. Do not open or dissolve the capsules since the contents of the capsule are very bitter.</p><p>If you vomit after taking Rozlytrek</p><p>If you vomit immediately after taking a dose of Rozlytrek, take another dose.</p><p>If you take more Rozlytrek than you should</p><p>If you take more Rozlytrek than you should, talk to a doctor or go to hospital straight away. Take the medicine pack and this leaflet with you.</p><p>If you forget to take Rozlytrek</p><ul><li>If your next dose is more than 12 hours later, take the missed dose as soon as you remember.</li><li>If there are less than 12 hours until your next dose, do not take the missed dose. Then take your next dose at the usual time.</li><li>Do not take a double dose to make up for a missed dose.</li></ul><p>If you stop taking Rozlytrek</p><p>Do not stop taking this medicine without talking to your doctor first. It is important to take Rozlytrek every day for as long as your doctor prescribes it for you.</p><p>If you have any further questions on the use of this medicine, ask your doctor, pharmacist or nurse.</p></div>"
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"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p>Like all medicines, this medicine can cause side effects, although not everybody gets them. The following side effects may happen with this medicine.</p><p>Serious side effects</p><p>Tell your doctor straight away if you notice any of the following after having taken Rozlytrek. Your doctor may lower your dose, stop your treatment for a short time or stop your treatment completely:</p><ul><li>you have cough, shortness of breath, and swelling in your legs or arms (fluid retention). These can be signs of heart problems</li><li>you feel confused, have changes in mood, memory problems or hallucinations (see things that are not there)</li><li>you feel dizzy or light-headed, or feel your heart beating irregularly or fast, as this may be a sign of an abnormal heart rhythm</li><li>you notice any joint pain, bone pain, deformities or changes in your ability to move, as this may be a sign of fractures</li><li>you have kidney problems or arthritis, as this may be the result of high uric acid levels in your blood.</li></ul><p>Other side effects</p><p>Tell your doctor, pharmacist or nurse if you notice any of the following side effects:</p><p>Very common: may affect more than 1 in 10 people:</p><ul><li>feeling tired</li><li>constipation</li><li>changes in taste</li><li>feeling unsteady or dizzy</li><li>swelling</li><li>diarrhoea</li><li>feeling sick</li><li>abnormal sense of touch which feels like itching, tingling or burning sensation</li><li>lack of enough red blood cells (anaemia)</li><li>shortness of breath</li><li>weight gain</li><li>increased blood level of creatinine (a substance normally eliminated by the kidneys into the urine)</li><li>vomiting</li><li>cough</li><li>fever</li><li>muscle pain</li><li>pain including back pain, neck pain, musculoskeletal pain, pain in limbs</li><li>stomach or joint pain</li><li>any bone pain, deformities or changes in your ability to move (bone fractures)</li><li>headache</li><li>low blood pressure</li><li>increased blood levels of certain liver enzymes (AST/ALT)</li><li>abnormal unpleasant sensation in your arms or legs</li><li>loss of muscle coordination, being unsteady when walking</li><li>disturbance in normal sleep patterns</li><li>lung infection</li><li>urinary tract infection</li><li>muscle weakness</li><li>decreased appetite</li><li>blurred vision</li><li>rash</li><li>decreased number of a type of white blood cell called neutrophils</li><li>inability to empty your bladder completely</li><li>difficulty swallowing.</li></ul><p>Common: may affect up to 1 in 10 people:</p><ul><li>mood disorders</li><li>dehydration</li><li>fluid in your lungs</li><li>fainting</li><li>increased sensitivity of the skin to sunlight</li></ul><p>Uncommon: may affect less than 1 in 100 people:</p><ul><li>changes in certain chemicals in your blood caused by rapid breakdown of tumour cells, which may cause damage to organs, including the kidneys, heart, and liver.</li></ul><p>Tell your doctor, pharmacist or nurse if you notice any of the side effects above.</p><p>Reporting of side effects</p><p>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.</p></div>"
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"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><ul><li>Keep this medicine out of the sight and reach of children.</li><li>Do not use this medicine after the expiry date which is stated on the carton and the bottle after EXP. The expiry date refers to the last day of that month.</li><li>Store in the original package and keep the bottle tightly closed in order to protect from moisture.</li><li>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.</li></ul></div>"
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"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p>What Rozlytrek contains</p><p>The active substance is entrectinib. Rozlytrek 100 mg: each capsule contains 100 mg entrectinib Rozlytrek 200 mg: each capsule contains 200 mg entrectinib</p><p>The other ingredients are:</p><ul><li>Capsule content: tartaric acid, lactose (see section 2 Rozlytrek contains lactose ), hypromellose, crospovidone, microcrystalline cellulose, colloidal anhydrous silica, magnesium stearate.</li><li>Capsule shell: hypromellose, titanium dioxide (E171), yellow iron oxide (E172; for Rozlytrek 100 mg capsule), sunset yellow FCF (E110; for Rozlytrek 200 mg capsule). See section 2 Rozlytrek contains sunset yellow FCF (E110) .</li><li>Printing ink: shellac, propylene glycol, indigo carmine aluminium lake (E132).</li></ul><p>What Rozlytrek looks like and contents of the pack</p><p>Rozlytrek 100 mg hard capsules are opaque yellow with ENT 100 imprinted in blue on the body.</p><p>Rozlytrek 200 mg hard capsules are opaque orange with ENT 200 imprinted in blue on the body.</p><p>The capsules are provided in bottles containing either:</p><ul><li>30 hard capsules of Rozlytrek 100 mg, or</li><li>90 hard capsules of Rozlytrek 200 mg.</li></ul><p>Marketing Authorisation Holder</p><p>Roche Registration GmbH Emil-Barell-Strasse 1 79639 Grenzach-Wyhlen Germany</p><p>Manufacturer</p><p>Roche Pharma AG Emil-Barell-Strasse 1 79639 Grenzach-Wyhlen Germany</p><p>For any information about this medicine, please contact the local representative of the Marketing Authorisation Holder:</p><p>Belgi /Belgique/Belgien N.V. Roche S.A.<br/>T l/Tel: +32 (0) 2 525 82 Lietuva UAB Roche Lietuva<br/>Tel: +370 5 2546</p><p>: +359 2 818 44 Luxembourg/Luxemburg (Voir/siehe Belgique/Belgien) esk republika Roche s. r. O.<br/>Tel: +420 - 2 20382Magyarorsz g Roche (Magyarorsz g) Kft.<br/>Tel: +36 - 1 279 4Danmark Roche Pharmaceuticals A/S<br/>Tlf: +45 - 36 39 99 Malta (See Ireland)</p><p>Deutschland Roche Pharma AG<br/>Tel: +49 (0) 7624 Nederland Roche Nederland B.V.<br/>Tel: +31 (0) 348 438Eesti Roche Eesti O<br/>Tel: + 372 - 6 177 Norge Roche Norge AS<br/>Tlf: +47 - 22 78 90<br/>Roche (Hellas) A.E.<br/>: +30 210 61 66 sterreich Roche Austria GmbH<br/>Tel: +43 (0) 1 27Espa a Roche Farma S.A.<br/>Tel: +34 - 91 324 81 Polska Roche Polska Sp.z o.o.<br/>Tel: +48 - 22 345 18 France Roche<br/>T l: +33 (0) 1 47 61 40 Portugal Roche Farmac utica Qu mica, Lda<br/>Tel: +351 - 21 425 70 Hrvatska Roche d.o.o.<br/>Tel: +385 1 4722 Ireland Roche Products (Ireland) Ltd.<br/>Tel: +353 (0) 1 469 0Rom nia Roche Rom nia S.R.L.<br/>Tel: +40 21 206 47 Slovenija Roche farmacevtska dru ba d.o.o.<br/>Tel: +386 - 1 360 26 sland Roche Pharmaceuticals A/S<br/>c/o Icepharma hf<br/>S mi: +354 540 8Slovensk republika Roche Slovensko, s.r.o.<br/>Tel: +421 - 2 52638Italia Roche S.p.A.<br/>Tel: +39 - 039 2Suomi/Finland Roche Oy<br/>Puh/Tel: +358 (0) 10 554<br/>. . & .<br/>: +357 - 22 76 62 Sverige Roche AB<br/>Tel: +46 (0) 8 726 1Latvija Roche Latvija SIA<br/>Tel: +371 - 6 7039United Kingdom (Northern Ireland) Roche Products (Ireland) Ltd.<br/>Tel: +44 (0) 1707 366This leaflet was last revised in</p><p>This medicine has been given conditional approval . This means that there is more evidence to come about this medicine. The European Medicines Agency will review new information on this medicine at least every year and this leaflet will be updated as necessary.</p><p>Other sources of information</p><p>Detailed information on this medicine is available on the European Medicines Agency web site:</p></div>"
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"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><a name=\"MedicinalProductDefinition_mpf09921a712319be762e8c3e2baca4fd9\"> </a><p class=\"res-header-id\"><b>Generated Narrative: MedicinalProductDefinition mpf09921a712319be762e8c3e2baca4fd9</b></p><a name=\"mpf09921a712319be762e8c3e2baca4fd9\"> </a><a name=\"hcmpf09921a712319be762e8c3e2baca4fd9\"> </a><a name=\"mpf09921a712319be762e8c3e2baca4fd9-en-US\"> </a><p><b>identifier</b>: <code>http://ema.europa.eu/identifier</code>/EU/1/20/1460/001</p><p><b>type</b>: <span title=\"Codes:{http://hl7.org/fhir/medicinal-product-type MedicinalProduct}\">Medicinal Product</span></p><p><b>domain</b>: <span title=\"Codes:{http://hl7.org/fhir/medicinal-product-domain Human}\">Human use</span></p><p><b>status</b>: <span title=\"Codes:{http://hl7.org/fhir/publication-status active}\">active</span></p><p><b>legalStatusOfSupply</b>: <span title=\"Codes:{https://spor.ema.europa.eu/rmswi 100000072084}\">Medicinal product subject to medical prescription</span></p><blockquote><p><b>name</b></p><p><b>productName</b>: Rozlytrek 100 mg hard capsules</p><p><b>type</b>: <span title=\"Codes:{https://spor.ema.europa.eu/lists/220000000000 220000000001}\">Full name</span></p><blockquote><p><b>part</b></p><p><b>part</b>: nan</p><p><b>type</b>: <span title=\"Codes:{https://spor.ema.europa.eu/lists/220000000000 220000000002}\">Invented name part</span></p></blockquote><blockquote><p><b>part</b></p><p><b>part</b>: nan</p><p><b>type</b>: <span title=\"Codes:{https://spor.ema.europa.eu/lists/220000000000 220000000003}\">Scientific name part</span></p></blockquote><blockquote><p><b>part</b></p><p><b>part</b>: nan</p><p><b>type</b>: <span title=\"Codes:{https://spor.ema.europa.eu/lists/220000000000 220000000004}\">Strength part</span></p></blockquote><blockquote><p><b>part</b></p><p><b>part</b>: nan</p><p><b>type</b>: <span title=\"Codes:{https://spor.ema.europa.eu/lists/220000000000 220000000005}\">Pharmaceutical dose form part</span></p></blockquote><h3>Usages</h3><table class=\"grid\"><tr><td style=\"display: none\">-</td><td><b>Country</b></td><td><b>Jurisdiction</b></td><td><b>Language</b></td></tr><tr><td style=\"display: none\">*</td><td><span title=\"Codes:{urn:iso:std:iso:3166 EU}\">EU</span></td><td><span title=\"Codes:{urn:iso:std:iso:3166 EU}\">EU</span></td><td><span title=\"Codes:{urn:ietf:bcp:47 en}\">en</span></td></tr></table></blockquote></div>"
},
"identifier" : [
{
"system" : "http://ema.europa.eu/identifier",
"value" : "EU/1/20/1460/001"
}
],
"type" : {
"coding" : [
{
"system" : "http://hl7.org/fhir/medicinal-product-type",
"code" : "MedicinalProduct",
"display" : "Medicinal Product"
}
]
},
"domain" : {
"coding" : [
{
"system" : "http://hl7.org/fhir/medicinal-product-domain",
"code" : "Human",
"display" : "Human use"
}
]
},
"status" : {
"coding" : [
{
"system" : "http://hl7.org/fhir/publication-status",
"code" : "active",
"display" : "active"
}
]
},
"legalStatusOfSupply" : {
"coding" : [
{
"system" : "https://spor.ema.europa.eu/rmswi",
"code" : "100000072084",
"display" : "Medicinal product subject to medical prescription"
}
]
},
"name" : [
{
"productName" : "Rozlytrek 100 mg hard capsules",
"type" : {
"coding" : [
{
"system" : "https://spor.ema.europa.eu/lists/220000000000",
"code" : "220000000001",
"display" : "Full name"
}
]
},
"part" : [
{
"part" : "nan",
"type" : {
"coding" : [
{
"system" : "https://spor.ema.europa.eu/lists/220000000000",
"code" : "220000000002",
"display" : "Invented name part"
}
]
}
},
{
"part" : "nan",
"type" : {
"coding" : [
{
"system" : "https://spor.ema.europa.eu/lists/220000000000",
"code" : "220000000003",
"display" : "Scientific name part"
}
]
}
},
{
"part" : "nan",
"type" : {
"coding" : [
{
"system" : "https://spor.ema.europa.eu/lists/220000000000",
"code" : "220000000004",
"display" : "Strength part"
}
]
}
},
{
"part" : "nan",
"type" : {
"coding" : [
{
"system" : "https://spor.ema.europa.eu/lists/220000000000",
"code" : "220000000005",
"display" : "Pharmaceutical dose form part"
}
]
}
}
],
"usage" : [
{
"country" : {
"coding" : [
{
"system" : "urn:iso:std:iso:3166",
"code" : "EU",
"display" : "EU"
}
]
},
"jurisdiction" : {
"coding" : [
{
"system" : "urn:iso:std:iso:3166",
"code" : "EU",
"display" : "EU"
}
]
},
"language" : {
"coding" : [
{
"system" : "urn:ietf:bcp:47",
"code" : "en",
"display" : "en"
}
]
}
}
]
}
]
}
}
]
}
IG © 2021+ Gravitate Health Project. Package hl7.eu.fhir.ghepi#0.1.0 based on FHIR 5.0.0. Generated 2024-10-14
Links: Table of Contents |
QA Report
The Gravitate Health project has received funding from the IMI 2 Joint Undertaking under grant agreement No 945334.
This joint undertaking receives support from the EU H2020 research and innovation programme and EFPIA.
