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
Full name:
Authorised dose form:
Legal status of supply:
Domain:
Resource status:
Product classification:
Document Details
Generated Narrative: Bundle TEST PURPOSES ONLY - genvoya
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
Document Subject
Generated Narrative: MedicinalProductDefinition mp9e5179bf4e803289b510a39f498792d0
identifier: http://ema.europa.eu/identifier
/EU/1/15/1061/001
type: Medicinal Product
domain: Human use
status: active
legalStatusOfSupply: Medicinal product subject to medical prescription
name
productName: Genvoya 150 mg/150 mg/200 mg/10 mg film-coated tablets
type: Full name
part
part: nan
type: Invented name part
part
part: nan
type: Scientific name part
part
part: nan
type: Strength part
part
part: nan
type: Pharmaceutical dose form part
Usages
Country Jurisdiction Language EU EU en
Document Content
Generated Narrative: Composition composition-en-9e5179bf4e803289b510a39f498792d0
Language: en
Profile: Composition (ePI)
identifier: http://ema.europa.eu/identifier
/EU/1/15/1061/001
status: Final
type: Package Leaflet
category: Raw
date: 2022-02-16 13:28:17+0000
author: Organization ACME industry
title: TEST PURPOSES ONLY - genvoya
Mode | Time |
Official | 2022-02-16 13:28:17+0000 |
If Genvoya has been prescribed for your child, please note that all the information in this leaflet is addressed to your child (in this case please read your child instead of you ).
What is in this leaflet
Genvoya contains four active substances:
Genvoya is a single tablet for the treatment of human immunodeficiency virus 1 (HIV-1) infection in adults, adolescents and children 2 years of age and older, who weigh at least 14 kg.
Genvoya reduces the amount of HIV in your body. This will improve your immune system and reduce the risk of developing illnesses linked to HIV infection.
Do not take Genvoya
If you are allergic to elvitegravir, cobicistat, emtricitabine, tenofovir alafenamide or any of the other ingredients of this medicine (listed in section 6 of this leaflet).
If you are taking one of these medicines:
alfuzosin (used to treat an enlarged prostate gland)
dabigatran (used to prevent and treat blood clots)
amiodarone, quinidine (used to correct irregular heartbeats)
carbamazepine, phenobarbital, phenytoin (used to prevent seizures)
rifampicin (used to prevent and treat tuberculosis and other infections)
dihydroergotamine, ergometrine, ergotamine (used to treat migraine headache)
cisapride (used to relieve certain stomach problems)
St. John s wort (Hypericum perforatum, a herbal remedy used for depression and anxiety) or products that contain it
lomitapide, lovastatin, simvastatin (used to lower blood cholesterol)
lurasidone, pimozide (used to treat abnormal thoughts or feelings)
sildenafil (when used to treat pulmonary arterial hypertension a lung disease that makes breathing difficult)
orally administered midazolam, triazolam (used to help you sleep and/or relieve anxiety)
If any of these applies to you, do not take Genvoya and tell your doctor immediately.
Warnings and precautions
You must remain under the care of your doctor while taking Genvoya.
This medicine is not a cure for HIV infection. While taking Genvoya you may still develop infections or other illnesses associated with HIV infection.
Talk to your doctor before taking Genvoya:
If you have hepatitis B infection, liver problems may become worse after you stop taking Genvoya. It is important not to stop taking Genvoya without talking to your doctor: see section 3, Do not stop taking Genvoya.
While you are taking Genvoya
Once you start taking Genvoya, look out for:
Signs of inflammation or infection
Joint pain, stiffness or bone problems
If you notice any of these symptoms, tell your doctor immediately. For more information see section 4, Possible side effects.
There is a possibility that you may experience kidney problems when taking Genvoya over a long period of time (see Warnings and precautions).
Children and adolescents
Do not give this medicine to children under 2 years of age, or weighing less than 14 kg regardless of age. The use of Genvoya in children under 2 years of age, or weighing less than 14 kg has not yet been studied.
Other medicines and Genvoya
Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines. Genvoya may interact with other medicines. As a result, the amounts of Genvoya or other medicines in your blood may be affected. This may stop your medicines from working properly, or may make any side effects worse. In some cases, your doctor may need to adjust your dose or check your blood levels.
Medicines that must never be taken with Genvoya:
Medicines used in treating hepatitis B infection:
You should not take Genvoya with medicines containing:
tenofovir alafenamide
tenofovir disoproxil
lamivudine
adefovir dipivoxil
Tell your doctor if you are taking any of these medicines.
Other types of medicine: Talk to your doctor if you are taking:
mineral supplements, vitamins (including multivitamins), antacids and laxatives If you are taking medicines, oral supplements, antacids or laxatives containing minerals (such as magnesium, aluminium, calcium, iron, zinc), take them at least 4 hours before or at least 4 hours after Genvoya.
Tell your doctor if you are taking these or any other medicines. Do not stop your treatment without contacting your doctor.
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 or pharmacist for advice before taking this medicine.
Driving and using machines
Genvoya can cause dizziness. If you feel dizzy when taking Genvoya, do not drive or ride a bicycle and do not use any tools or machines.
Genvoya contains sodium
This medicine contains less than 1 mmol sodium (23 mg) per tablet, that is to say essentially sodium- free .
Genvoya contains lactose
If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicine.
If any of these applies to you, talk to your doctor before taking Genvoya.
Always take this medicine exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure.
There are two strengths of Genvoya tablets. Your doctor will prescribe the appropriate tablet for your age and weight.
The recommended dose is:
Adults, adolescents and children who weigh at least 25 kg: one tablet each day with food (one 150 mg/150 mg/200 mg/10 mg tablet)
Children 2 years of age and older, who weigh at least 14 kg but less than 25 kg: one tablet each day with food (one 90 mg/90 mg/120 mg/6 mg tablet)
Due to the bitter taste, it is recommended not to chew or crush the tablet.
If you have difficulty swallowing the tablet whole, you can split it in half. Take both halves of the tablet one after the other to get the full dose. Do not store the split tablet. The score line on the 90 mg/90 mg/120 mg/6 mg tablet is only there to help you break the tablet if your child has difficulty swallowing it whole.
Always take the dose recommended by your doctor. This is to make sure that your medicine is fully effective, and to reduce the risk of developing resistance to the treatment. Do not change the dose unless your doctor tells you to.
Do not take antacids or multivitamins at the same time as Genvoya. If you are taking medicines, oral supplements, antacids or laxatives containing minerals (such as magnesium, aluminium, calcium, iron, zinc), take them at least 4 hours before or at least 4 hours after Genvoya.
If you are on dialysis, take your daily dose of Genvoya following completion of dialysis.
If you take more Genvoya than you should
If you accidentally take more than the recommended dose of Genvoya you may be at increased risk of experiencing possible side effects with this medicine (see section 4, Possible side effects).
Contact your doctor or nearest emergency department immediately for advice. Keep the tablet bottle with you so that you can easily describe what you have taken.
If you forget to take Genvoya
It is important not to miss a dose of Genvoya.
If you do miss a dose:
If you vomit less than 1 hour after taking Genvoya, take another tablet with food.
Do not stop taking Genvoya
Do not stop taking Genvoya without talking to your doctor. Stopping Genvoya can seriously affect your response to future treatment. If Genvoya is stopped for any reason, speak to your doctor before you restart taking Genvoya tablets.
When your supply of Genvoya starts to run low, get more from your doctor or pharmacist. This is very important because the amount of virus may start to increase if the medicine is stopped for even a short time. The disease may then become harder to treat.
If you have both HIV infection and hepatitis B, it is especially important not to stop your Genvoya treatment without talking to your doctor first. You may require blood tests for several months after stopping treatment. In some patients with advanced liver disease or cirrhosis, stopping treatment is not recommended as this may lead to worsening of your hepatitis, which may be life-threatening.
Tell your doctor immediately about new or unusual symptoms after you stop treatment, particularly symptoms you associate with hepatitis B infection.
If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Possible serious side effects: tell a doctor immediately
Any signs of inflammation or infection. In some patients with advanced HIV infection (AIDS) and a history of opportunistic infections (infections that occur in people with a weak immune system), signs and symptoms of inflammation from previous infections may occur soon after anti-HIV treatment is started. It is thought that these symptoms are due to an improvement in the body s immune response, enabling the body to fight infections that may have been present with no obvious symptoms.
Autoimmune disorders, when the immune system attacks healthy body tissue, may also occur after you start taking medicines for HIV infection. Autoimmune disorders may occur many months after the start of treatment. Look out for any symptoms of infection or other symptoms such as:
muscle weakness
weakness beginning in the hands and feet and moving up towards the trunk of the body
palpitations, tremor or hyperactivity.
If you notice the side effects described above, tell your doctor immediately.
Very common side effects (may affect more than 1 in 10 people)
Common side effects (may affect up to 1 in 10 people)
Uncommon side effects (may affect up to 1 in 100 people)
low red blood cell count (anaemia)
suicidal thoughts and suicide attempt (in patients who have had depression or mental health problems before), depression
problems with digestion resulting in discomfort after meals (dyspepsia)
swelling of the face, lips, tongue or throat (angioedema)
itching (pruritus)
hives (urticaria)
If any of the side effects get serious tell your doctor.
Other effects that may be seen during HIV treatment
The frequency of the following side effects is not known (frequency cannot be estimated from the available data).
During HIV therapy there may be an increase in weight and in levels of blood lipids and glucose. This is partly linked to restored health and life style, and in the case of blood lipids sometimes to the HIV medicines themselves. Your doctor will test for these changes.
Reporting of side effects If you get any side effects, talk to your doctor or pharmacist. 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 and bottle after {EXP}.
The expiry date refers to the last day of that month. Store in the original package in order to protect from moisture. Keep the bottle tightly closed.
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 Genvoya contains
The active substances are elvitegravir, cobicistat, emtricitabine and tenofovir alafenamide.
The other ingredients are
Tablet core: Lactose (as monohydrate), microcrystalline cellulose (E460), croscarmellose sodium, hydroxypropyl cellulose (E463), silicon dioxide (E551), sodium lauryl sulfate, magnesium stearate.
Film-coating: Polyvinyl alcohol (E1203), titanium dioxide (E171), polyethylene glycol (E1521), talc (E553b), iron oxide yellow (E172), indigo carmine aluminium lake (E132 - 150 mg/150 mg/200 mg/10 mg tablet only), iron oxide black (E172 - 90 mg/90 mg/120 mg/6 mg tablet only).
What Genvoya looks like and contents of the pack
Genvoya 150 mg/150 mg/200 mg/10 mg film-coated tablets are green, capsule-shaped tablets, debossed on one side with GSI and the number 510 on the other side of the tablet.
Genvoya 90 mg/90 mg/120 mg/6 mg film-coated tablets are green, capsule-shaped tablets, debossed on one side with GSI and scored on the other side of the tablet.
Genvoya comes in bottles of 30 tablets (with a silica gel desiccant that must be kept in the bottle to help protect your tablets). The silica gel desiccant is contained in a separate sachet or canister and should not be swallowed.
The following pack sizes are available: outer cartons containing 1 bottle of 30 film-coated tablets and outer cartons containing 90 (3 bottles of 30) film-coated tablets. Not all pack sizes may be marketed.
Marketing Authorisation Holder Gilead Sciences Ireland UC Carrigtohill County Cork, T45 DPIreland
Manufacturer Gilead Sciences Ireland UC IDA Business & Technology Park Carrigtohill County Cork Ireland For any information about this medicine, please contact the local representative of the Marketing Authorisation Holder:
Belgi /Belgique/Belgien Gilead Sciences Belgium SRL-BV T l/Tel: + 32 (0) 24 01 35 Lietuva Gilead Sciences Poland Sp. z o.o. Tel: + 48 22 262 8
Gilead Sciences Ireland UC .: + 353 (0) 1 686 1Luxembourg/Luxemburg Gilead Sciences Belgium SRL-BV T l/Tel: + 32 (0) 24 01 35 esk republika Gilead Sciences s.r.o. Tel: + 420 910 871 Magyarorsz g Gilead Sciences Ireland UC Tel.: + 353 (0) 1 686 1Danmark Gilead Sciences Sweden AB Tlf: + 46 (0) 8 5057 1Malta Gilead Sciences Ireland UC Tel: + 353 (0) 1 686 1Deutschland Gilead Sciences GmbH Tel: + 49 (0) 89 899890-0
Nederland Gilead Sciences Netherlands B.V. Tel: + 31 (0) 20 718 36 Eesti Gilead Sciences Poland Sp. z o.o. Tel: + 48 22 262 8Norge Gilead Sciences Sweden AB Tlf: + 46 (0) 8 5057 1
Gilead Sciences . . : + 30 210 8930 sterreich Gilead Sciences GesmbH Tel: + 43 1 260 Espa a Gilead Sciences, S.L. Tel: + 34 91 378 98 Polska Gilead Sciences Poland Sp. z o.o. Tel.: + 48 22 262 8France Gilead Sciences T l: + 33 (0) 1 46 09 41 Portugal Gilead Sciences, Lda. Tel: + 351 21 7928Hrvatska Gilead Sciences Ireland UC Tel: + 353 (0) 1 686 1Rom nia Gilead Sciences (GSR) S.R.L. Tel: + 40 31 631 18 Ireland Gilead Sciences Ireland UC Tel: + 353 (0) 214 825 Slovenija Gilead Sciences Ireland UC Tel: + 353 (0) 1 686 1 sland Gilead Sciences Sweden AB S mi: + 46 (0) 8 5057 1Slovensk republika Gilead Sciences Slovakia s.r.o. Tel: + 421 232 121 Italia Gilead Sciences S.r.l. Tel: + 39 02 439Suomi/Finland Gilead Sciences Sweden AB Puh/Tel: + 46 (0) 8 5057 1
Gilead Sciences . . : + 30 210 8930 Sverige Gilead Sciences Sweden AB Tel: + 46 (0) 8 5057 1Latvija Gilead Sciences Poland Sp. z o.o. Tel: + 48 22 262 8United Kingdom (Northern Ireland) Gilead Sciences Ireland UC
Tel: + 44 (0) 8000 113 This leaflet was last revised in
Detailed information on this medicine is available on the European Medicines Agency web site:
Entry 1 - fullUrl = Composition/composition-en-9e5179bf4e803289b510a39f498792d0
Resource Composition:
Generated Narrative: Composition composition-en-9e5179bf4e803289b510a39f498792d0
Language: en
Profile: Composition (ePI)
identifier:
http://ema.europa.eu/identifier
/EU/1/15/1061/001status: Final
type: Package Leaflet
category: Raw
date: 2022-02-16 13:28:17+0000
author: Organization ACME industry
title: TEST PURPOSES ONLY - genvoya
Attesters
Mode Time Official 2022-02-16 13:28:17+0000
Entry 2 - fullUrl = MedicinalProductDefinition/mp9e5179bf4e803289b510a39f498792d0
Resource MedicinalProductDefinition:
Generated Narrative: MedicinalProductDefinition mp9e5179bf4e803289b510a39f498792d0
identifier:
http://ema.europa.eu/identifier
/EU/1/15/1061/001type: Medicinal Product
domain: Human use
status: active
legalStatusOfSupply: Medicinal product subject to medical prescription
name
productName: Genvoya 150 mg/150 mg/200 mg/10 mg film-coated tablets
type: Full name
part
part: nan
type: Invented name part
part
part: nan
type: Scientific name part
part
part: nan
type: Strength part
part
part: nan
type: Pharmaceutical dose form part
Usages
Country Jurisdiction Language EU EU en