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

: ePI document Bundle for emend Package Leaflet for language en - XML Representation

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          <div xmlns="http://www.w3.org/1999/xhtml" xml:lang="en" lang="en"><a name="Composition_composition-en-e4e2fe5de212dd30e27726e0694aae72"> </a><p class="res-header-id"><b>Generated Narrative: Composition composition-en-e4e2fe5de212dd30e27726e0694aae72</b></p><a name="composition-en-e4e2fe5de212dd30e27726e0694aae72"> </a><a name="hccomposition-en-e4e2fe5de212dd30e27726e0694aae72"> </a><a name="composition-en-e4e2fe5de212dd30e27726e0694aae72-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/1/03/262/001</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 - emend</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 xmlns="http://www.w3.org/1999/xhtml"><p>What is in this leaflet</p><ol type="1"><li>What EMEND is and what it is used for</li><li>What you need to know before you take or give EMEND</li><li>How to take EMEND</li><li>Possible side effects</li><li>How to store EMEND</li><li>Contents of the pack and other information</li></ol></div>
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            <title value="1. What emend is and what it is used for"/>
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              <div xmlns="http://www.w3.org/1999/xhtml"><p>EMEND contains the active substance aprepitant and belongs to a group of medicines called "neurokinin 1 (NK1) receptor antagonists". The brain has a specific area that controls nausea and vomiting. EMEND works by blocking signals to that area, thereby reducing nausea and vomiting. EMEND capsules are used in adults and adolescents from the age of 12 years in combination with other medicines to prevent nausea and vomiting caused by chemotherapy (cancer treatment) that are strong and moderate triggers of nausea and vomiting (such as cisplatin, cyclophosphamide, doxorubicin or epirubicin).</p></div>
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            <title value="2. What you need to know before you take emend"/>
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              <div xmlns="http://www.w3.org/1999/xhtml"><p>Do not take EMEND</p><ul><li><p>if you or the child is allergic to aprepitant or any of the other ingredients of this medicine (listed in section 6).</p></li><li><p>with medicines containing pimozide (used to treat psychiatric illnesses), terfenadine and astemizole (used for hay fever and other allergic conditions), cisapride (used for treating digestive problems). Tell the doctor if you or the child is taking these medicines since the treatment must be modified before you or the child start taking EMEND. Warnings and precautions Talk to the doctor, pharmacist, or nurse before you take EMEND or give this medicine to the child. Before treatment with EMEND, tell the doctor if you or the child have liver disease because the liver is important in breaking down the medicine in the body. The doctor may therefore have to monitor the condition of your or the child s liver. Children and adolescents Do not give EMEND 80 mg and 125 mg capsules to children under 12 years of age, because the 80 mg and 125 mg capsules have not been studied in this population. Other medicines and EMEND EMEND can affect other medicines both during and after treatment with EMEND. There are some medicines that should not be taken with EMEND (such as pimozide, terfenadine, astemizole, and cisapride) or that require a dose adjustment (see also Do not take EMEND ). The effects of EMEND or other medicines might be influenced if you or the child take EMEND together with other medicines including those listed below. Please talk to the doctor or pharmacist if you or the child is taking any of the following medicines:</p></li><li><p>birth control medicines which can include birth control pills, skin patches, implants, and certain Intrauterine devices (IUDs) that release hormones may not work adequately when taken together with EMEND. Another or additional non-hormonal form of birth control should be used during treatment with EMEND and for up to 2 months after using EMEND,</p></li><li><p>cyclosporine, tacrolimus, sirolimus, everolimus (immunosuppressants),</p></li><li><p>alfentanil, fentanyl (used to treat pain),</p></li><li><p>quinidine (used to treat an irregular heart beat),</p></li><li><p>irinotecan, etoposide, vinorelbine, ifosfamide (medicines used to treat cancer),</p></li><li><p>medicines containing ergot alkaloid derivatives such as ergotamine and diergotamine (used for treating migraines),</p></li><li><p>warfarin, acenocoumarol (blood thinners; blood tests may be required),</p></li><li><p>rifampicin, clarithromycin, telithromycin (antibiotics used to treat infections),</p></li><li><p>phenytoin (a medicine used to treat seizures),</p></li><li><p>carbamazepine (used to treat depression and epilepsy),</p></li><li><p>midazolam, triazolam, phenobarbital (medicines used to produce calmness or help you sleep),</p></li><li><p>St. John s Wort (an herbal preparation used to treat depression),</p></li><li><p>protease inhibitors (used to treat HIV infections),</p></li><li><p>ketoconazole except shampoo (used to treat Cushing s syndrome - when the body produces an excess of cortisol),</p></li><li><p>itraconazole, voriconazole, posaconazole (antifungals),</p></li><li><p>nefazodone (used to treat depression),</p></li><li><p>corticosteroids (such as dexamethasone and methylprednisolone),</p></li><li><p>anti-anxiety medicines (such as alprazolam),</p></li><li><p>tolbutamide (a medicine used to treat diabetes). Tell the doctor or pharmacist if you or the child are taking, have recently taken, or might take any other medicines. Pregnancy and breast-feeding This medicine should not be used during pregnancy unless clearly necessary. If you or the child are pregnant or breast-feeding, may be pregnant or are planning to have a baby, ask the doctor for advice before taking this medicine. For information regarding birth control, see Other medicines and EMEND . It is not known whether EMEND is excreted in human milk; therefore, breast-feeding is not recommended during treatment with this medicine. It is important to tell the doctor if you or the child are breast-feeding or are planning to breast-feed before taking this medicine. Driving and using machines It should be taken into account that some people feel dizzy and sleepy after taking EMEND. If you or the child feels dizzy or sleepy, avoid driving, riding a bicycle or using machines or tools after taking this medicine (see Possible side effects ). EMEND contains sucrose EMEND capsules contain sucrose. If you or the child have been told by your doctor that you or the child have an intolerance to some sugars, contact the doctor before taking this medicine. EMEND contains sodium This medicine contains less than 1 mmol sodium (23 mg) per capsule, that is to say essentially sodium-free .</p></li></ul></div>
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              <div xmlns="http://www.w3.org/1999/xhtml"><p>Always take this medicine or give this medicine to the child exactly as the doctor, pharmacist or nurse has told you. You should check with the doctor, pharmacist or nurse if you are not sure. Always take EMEND together with other medicines, to prevent nausea and vomiting. After treatment with EMEND, the doctor may ask you or the child to continue taking other medicines including a corticosteroid (such as dexamethasone) and a 5HT3 antagonist (such as ondansetron) for preventing nausea and vomiting. Check with the doctor, pharmacist or nurse if you are not sure. The recommended oral dose of EMEND is: Day 1:</p><ul><li><p>one 125 mg capsule 1 hour before you start your chemotherapy session and Days 2 and 3:</p></li><li><p>one 80 mg capsule each day</p></li><li><p>If no chemotherapy is given, take EMEND in the morning.</p></li><li><p>If chemotherapy is given, take EMEND 1 hour before you start your chemotherapy session. EMEND can be taken with or without food. Swallow the capsule whole with some liquid. If you take more EMEND than you should Do not take more capsules than the doctor recommends. If you or the child has taken too many capsules, contact your doctor immediately. If you forget to take EMEND If you or the child has missed a dose, contact your doctor for advice. If you have any further questions on the use of this medicine, ask the doctor or pharmacist.</p></li></ul></div>
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            <title value="4. Possible side effects"/>
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              <div xmlns="http://www.w3.org/1999/xhtml"><p>Like all medicines, this medicine can cause side effects, although not everybody gets them. Stop taking EMEND and see a doctor immediately if you or the child notice any of the following side effects, which may be serious, and for which you or the child may need urgent medical treatment:</p><ul><li><p>Hives, rash, itching, difficulty breathing or swallowing (frequency not known, cannot be estimated from the available data); these are signs of an allergic reaction. Other side effects that have been reported are listed below. Common side effects (may affect up to 1 in 10 people) are:</p></li><li><p>constipation, indigestion,</p></li><li><p>headache,</p></li><li><p>tiredness,</p></li><li><p>loss of appetite,</p></li><li><p>hiccups,</p></li><li><p>increased amount of liver enzymes in your blood. Uncommon side effects (may affect up to 1 in 100 people) are:</p></li><li><p>dizziness, sleepiness,</p></li><li><p>acne, rash,</p></li><li><p>anxiousness,</p></li><li><p>burping, nausea, vomiting, heartburn, stomach pain, dry mouth, passing wind,</p></li><li><p>increased painful or burning urination,</p></li><li><p>weakness, generally feeling unwell,</p></li><li><p>hot flush/reddening of the face or skin,</p></li><li><p>fast or irregular heartbeats,</p></li><li><p>fever with increased risk of infection, lowering of red blood cells. Rare side effects (may affect up to1 in 1,000 people) are:</p></li><li><p>difficulty thinking, lack of energy, taste disturbance,</p></li><li><p>sensitivity of the skin to sun, excessive sweating, oily skin, sores on skin, itching rash, Stevens-Johnson syndrome/toxic epidermal necrolysis (rare severe skin reaction),</p></li><li><p>euphoria (feeling of extreme happiness), disorientation,</p></li><li><p>bacterial infection, fungal infection,</p></li><li><p>severe constipation, stomach ulcer, inflammation of the small intestine and colon, sores in mouth, bloating,</p></li><li><p>frequent urination, passing more urine than normal, presence of sugar or blood in urine,</p></li><li><p>chest discomfort, swelling, change in the manner of walking,</p></li><li><p>cough, mucus in back of throat, throat irritation, sneezing, sore throat,</p></li><li><p>eye discharge and itching,</p></li><li><p>ringing in the ear,</p></li><li><p>muscle spasms, muscle weakness,</p></li><li><p>excessive thirst,</p></li><li><p>slow heartbeat, heart and blood vessel disease,</p></li><li><p>lowering of white blood cells, low sodium levels in the blood, weight loss. Reporting of side effects If you or the child gets 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></li></ul></div>
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              <div xmlns="http://www.w3.org/1999/xhtml"><p>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. Store in the original package in order to protect from moisture. Do not remove the capsule from its blister until you are ready to take it. 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.</p></div>
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            <title value="6. Contents of the pack and other information"/>
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              <div xmlns="http://www.w3.org/1999/xhtml"><p>What EMEND contains</p><ul><li><p>The active substance is aprepitant. Each 125 mg hard capsule contains 125 mg of aprepitant. Each 80 mg hard capsule contains 80 mg of aprepitant.</p></li><li><p>The other ingredients are sucrose, microcrystalline cellulose (E 460), hydroxypropylcellulose (E 463), sodium laurilsulfate, gelatin, titanium dioxide (E 171), shellac, potassium hydroxide, and black iron oxide (E 172); the 125 mg hard capsule also contains red iron oxide (E 172) and yellow iron oxide (E 172). What EMEND looks like and contents of the pack The 125 mg hard capsule is opaque with a white body and pink cap with 462 and 125 mg printed radially in black ink on the body. The 80 mg hard capsule is opaque with a white cap and body with 461 and 80 mg printed radially in black ink on the body. EMEND 125 mg and 80 mg hard capsules are supplied in the following pack sizes:</p></li><li><p>Aluminium blister containing one 80 mg capsule</p></li><li><p>2-day treatment pack containing two 80 mg capsules</p></li><li><p>5 Aluminium blisters each containing one 80 mg capsule</p></li><li><p>Aluminium blister containing one 125 mg capsule</p></li><li><p>5 Aluminium blisters each containing one 125 mg capsule</p></li><li><p>3-day treatment pack containing one 125 mg capsule and two 80 mg capsules Not all pack sizes may be marketed. Marketing Authorisation Holder and Manufacturer Merck Sharp &amp; Dohme B.V. Waarderweg 2031 BN Haarlem The Netherlands For any information about this medicine, please contact the local representative of the Marketing Authorisation Holder. Belgique/Belgi /Belgien MSD Belgium T l/Tel: +32(0)<a href="mailto:27766dpoc_belux@merck.com">27766dpoc_belux@merck.com</a> Lietuva UAB Merck Sharp &amp; Dohme Tel. + 370 5278 02 <a href="mailto:msd_lietuva@merck.com">msd_lietuva@merck.com</a></p></li></ul><p>.: +359 2 819 <a href="mailto:3info-msdbg@merck.com">3info-msdbg@merck.com</a> Luxembourg/Luxemburg MSD Belgium T l/Tel: +32(0)<a href="mailto:27766dpoc_belux@merck.com">27766dpoc_belux@merck.com</a> esk republika Merck Sharp &amp; Dohme s.r.o. Tel: +420 233 010 <a href="mailto:dpoc_czechslovak@merck.com">dpoc_czechslovak@merck.com</a> Magyarorsz g MSD Pharma Hungary Kft. Tel.: +36 1 888 <a href="mailto:5hungary_msd@merck.com">5hungary_msd@merck.com</a> Danmark MSD Danmark ApS Tlf: + 45 4482 <a href="mailto:4dkmail@merck.com">4dkmail@merck.com</a> Malta Merck Sharp &amp; Dohme Cyprus Limited Tel: 8007 4433 (+356 99917558) <a href="mailto:malta_info@merck.com">malta_info@merck.com</a> Deutschland MSD Sharp &amp; Dohme GmbH Tel: 0800 673 673 673 (+49 (0) 89 4561 0) <a href="mailto:e-mail@msd.de">e-mail@msd.de</a> Nederland Merck Sharp &amp; Dohme B.V. Tel: 0800 9999 (+31 23 5153153) <a href="mailto:medicalinfo.nl@merck.com">medicalinfo.nl@merck.com</a> Eesti Merck Sharp &amp; Dohme O Tel.: +372 6144 <a href="mailto:msdeesti@merck.com">msdeesti@merck.com</a> Norge MSD (Norge) AS Tlf: +47 32 20 73 <a href="mailto:msdnorge@msd.no">msdnorge@msd.no</a> E MSD . . . . . : +30 210 98 97 <a href="mailto:dpoc_greece@merck.com">dpoc_greece@merck.com</a> sterreich Merck Sharp &amp; Dohme Ges.m.b.H. Tel: +43 (0) 1 26 <a href="mailto:dpoc_austria@merck.com">dpoc_austria@merck.com</a> Espa a Merck Sharp &amp; Dohme de Espa a, S.A. Tel: +34 91 321 06 <a href="mailto:msd_info@merck.com">msd_info@merck.com</a> Polska MSD Polska Sp. z o.o. Tel: +48 22 549 51 <a href="mailto:msdpolska@merck.com">msdpolska@merck.com</a> France MSD France T l: +33 (0) 1 80 46 40 Portugal Merck Sharp &amp; Dohme, Lda Tel: +351 21 <a href="mailto:4465inform_pt@merck.com">4465inform_pt@merck.com</a> Hrvatska Merck Sharp &amp; Dohme d.o.o. Tel: + 385 1 6611 <a href="mailto:croatia_info@merck.com">croatia_info@merck.com</a> Rom nia Merck Sharp &amp; Dohme Romania S.R.L. Tel: +40 21 529 29 <a href="mailto:msdromania@merck.com">msdromania@merck.com</a> Ireland Merck Sharp &amp; Dohme Ireland (Human Health) Limited Tel: +353 (0)1 <a href="mailto:2998medinfo_ireland@merck.com">2998medinfo_ireland@merck.com</a> Slovenija Merck Sharp &amp; Dohme, inovativna zdravila d.o.o. Tel: +386 1 5204 <a href="mailto:msd_slovenia@merck.com">msd_slovenia@merck.com</a> sland Vistor hf. Simi: +354 535 7Slovensk republika Merck Sharp &amp; Dohme, s. r. o. Tel: +421 2 <a href="mailto:58282dpoc_czechslovak@merck.com">58282dpoc_czechslovak@merck.com</a> talia MSD Italia S.r.l. Tel: 800 23 99 89 (+39 06 361911) <a href="mailto:medicalinformation.it@msd.com">medicalinformation.it@msd.com</a> Suomi/Finland MSD Finland Oy Puh/Tel: +358 (0)9 804 <a href="mailto:info@msd.fi">info@msd.fi</a></p><p>Merck Sharp &amp; Dohme Cyprus Limited .: 800 00 673 (+357 22866700) <a href="mailto:cyprus_info@merck.com">cyprus_info@merck.com</a> Sverige Merck Sharp &amp; Dohme (Sweden) AB Tel: +46 77 <a href="mailto:5700medicinskinfo@merck.com">5700medicinskinfo@merck.com</a> Latvija SIA Merck Sharp &amp; Dohme Latvija Tel: +371 <a href="mailto:67364msd_lv@merck.com">67364msd_lv@merck.com</a> United Kingdom (Northern Ireland) Merck Sharp &amp; Dohme Ireland (Human Health) Limited Tel: +353 (0)1 <a href="mailto:2998medinfoNI@msd.com">2998medinfoNI@msd.com</a> This leaflet was last revised in Other sources of information Detailed information on this medicine is available on the European Medicines Agency web site: <a href="http://www.ema.europa.eu">http://www.ema.europa.eu</a>. Package leaflet: Information for the user EMEND 125 mg powder for oral suspension aprepitant Read all of this leaflet carefully before you start using this medicine because it contains important information. This leaflet has been written for the parent or carer who will give this medicine to the child - please read this information carefully.</p><ul><li>Keep this leaflet. You may need to read it again.</li><li>If you have any further questions, ask the doctor, pharmacist, or nurse.</li><li>This medicine has been prescribed for the child only. Do not pass it on to others. It may harm them, even if their signs of illness are the same.</li><li>If the child gets any side effects, talk to the doctor, pharmacist, or nurse. This includes any possible side effects not listed in this leaflet. See section 4.</li></ul></div>
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          <div xmlns="http://www.w3.org/1999/xhtml"><a name="MedicinalProductDefinition_mpe4e2fe5de212dd30e27726e0694aae72"> </a><p class="res-header-id"><b>Generated Narrative: MedicinalProductDefinition mpe4e2fe5de212dd30e27726e0694aae72</b></p><a name="mpe4e2fe5de212dd30e27726e0694aae72"> </a><a name="hcmpe4e2fe5de212dd30e27726e0694aae72"> </a><a name="mpe4e2fe5de212dd30e27726e0694aae72-en-US"> </a><p><b>identifier</b>: <code>http://ema.europa.eu/identifier</code>/EU/1/03/262/001</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>: EMEND 125 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>
        </text>
        <identifier>
          <system value="http://ema.europa.eu/identifier"/>
          <value value="EU/1/03/262/001"/>
        </identifier>
        <type>
          <coding>
            <system value="http://hl7.org/fhir/medicinal-product-type"/>
            <code value="MedicinalProduct"/>
            <display value="Medicinal Product"/>
          </coding>
        </type>
        <domain>
          <coding>
            <system value="http://hl7.org/fhir/medicinal-product-domain"/>
            <code value="Human"/>
            <display value="Human use"/>
          </coding>
        </domain>
        <status>
          <coding>
            <system value="http://hl7.org/fhir/publication-status"/>
            <code value="active"/>
            <display value="active"/>
          </coding>
        </status>
        <legalStatusOfSupply>
          <coding>
            <system value="https://spor.ema.europa.eu/rmswi"/>
            <code value="100000072084"/>
            <display
                     value="Medicinal product subject to medical prescription"/>
          </coding>
        </legalStatusOfSupply>
        <name>
          <productName value="EMEND 125 mg hard capsules"/>
          <type>
            <coding>
              <system value="https://spor.ema.europa.eu/lists/220000000000"/>
              <code value="220000000001"/>
              <display value="Full name"/>
            </coding>
          </type>
          <part>
            <part value="nan"/>
            <type>
              <coding>
                <system
                        value="https://spor.ema.europa.eu/lists/220000000000"/>
                <code value="220000000002"/>
                <display value="Invented name part"/>
              </coding>
            </type>
          </part>
          <part>
            <part value="nan"/>
            <type>
              <coding>
                <system
                        value="https://spor.ema.europa.eu/lists/220000000000"/>
                <code value="220000000003"/>
                <display value="Scientific name part"/>
              </coding>
            </type>
          </part>
          <part>
            <part value="nan"/>
            <type>
              <coding>
                <system
                        value="https://spor.ema.europa.eu/lists/220000000000"/>
                <code value="220000000004"/>
                <display value="Strength part"/>
              </coding>
            </type>
          </part>
          <part>
            <part value="nan"/>
            <type>
              <coding>
                <system
                        value="https://spor.ema.europa.eu/lists/220000000000"/>
                <code value="220000000005"/>
                <display value="Pharmaceutical dose form part"/>
              </coding>
            </type>
          </part>
          <usage>
            <country>
              <coding>
                <system value="urn:iso:std:iso:3166"/>
                <code value="EU"/>
                <display value="EU"/>
              </coding>
            </country>
            <jurisdiction>
              <coding>
                <system value="urn:iso:std:iso:3166"/>
                <code value="EU"/>
                <display value="EU"/>
              </coding>
            </jurisdiction>
            <language>
              <coding>
                <system value="urn:ietf:bcp:47"/>
                <code value="en"/>
                <display value="en"/>
              </coding>
            </language>
          </usage>
        </name>
      </MedicinalProductDefinition>
    </resource>
  </entry>
</Bundle>