Package Leaflet: Information for the Patient
Jinarc 15 mg tablets
Jinarc 30 mg tablets
Jinarc 45 mg tablets
Jinarc 60 mg tablets
Jinarc 90 mg tablets
Tolvaptan
This medicine is subject to additional monitoring, which will allow for quick identification of new safety information. You can help by reporting any side effects you may get. The last section of this leaflet includes information on how to report side effects.
Read all of this leaflet carefully before you start taking this medicine, because it
contains important information for you.
Contents of the pack
Jinarc is a medicine used to treat a disease known as "autosomal dominant polycystic kidney disease" (ADPKD). This disease leads to the development of fluid-filled cysts in the kidneys, which can cause pressure on the surrounding tissues and reduce kidney function, potentially leading to kidney failure. Jinarc is used to treat ADPKD in adults with chronic kidney disease (CKD) stage 1 to 4 with signs of rapid disease progression.
The active substance in Jinarc is tolvaptan, which blocks the effect of vasopressin, a hormone involved in the formation of cysts in the kidneys of patients with ADPKD. By blocking the effect of vasopressin, Jinarc slows the development of kidney cysts in patients with ADPKD, reduces the symptoms of the disease, and increases urine production.
Do not take Jinarc:
Warnings and precautions
Consult your doctor before starting to take Jinarc:
Jinarc may cause your liver to not function properly. For this reason, please inform your doctor immediately if you experience signs that may indicate liver problems, such as:
During treatment with Jinarc, your doctor will ask you to have monthly blood tests to monitor changes in your liver function.
Drinking enough water
Jinarc causes water loss because it increases urine production. This water loss can lead to side effects such as dry mouth and thirst or even more serious side effects such as kidney problems (see section 4). Therefore, it is essential that you have access to water and can drink enough fluids when you feel thirsty. Before going to bed, you should drink one or two glasses of water, even if you do not feel thirsty, and also drink water after urinating at night. You should be particularly careful if you have a condition that reduces adequate fluid intake or if you are at higher risk of dehydration, for example, if you have vomiting or diarrhea. Due to the increased urine production, it is also essential to always have a bathroom nearby.
Children and adolescents
Jinarc has not been studied in children and adolescents (under 18 years) and, therefore, is not recommended for use in this population.
Other medicines and Jinarc
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines, including those obtained without a prescription.
In particular, inform your doctor if you are taking:
It may not be a problem to take these medicines at the same time as Jinarc. Your doctor will decide what is best for you.
Using Jinarc with drinks and alcohol
Do not drink grapefruit juice while taking Jinarc.
Pregnancy and breastfeeding
Do nottake this medicine if you are pregnant or breastfeeding.
Women of childbearing potential should use reliable contraceptive methods while being treated with this medicine.
If you are pregnant or breastfeeding, or 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
Some people may feel dizzy, weak, or tired after taking Jinarc. If you experience these effects, do not drive or use tools or machines.
Jinarc contains lactose.
If your doctor has told you that you have an intolerance to some sugars, consult them before taking this medicine.
Only specialized doctors in the treatment of ADPKD can prescribe Jinarc. Follow your doctor's instructions for taking this medicine exactly. If you are unsure, consult your doctor or pharmacist again.
Dose
The daily dose of Jinarc should be divided into two doses, one higher than the other. The higher dose should be taken in the morning when you get up, at least 30 minutes before breakfast, while the lower dose should be taken 8 hours later.
The dose combinations are:
45 mg + 15 mg
60 mg + 30 mg
90 mg + 30 mg
Normally, your treatment will start with a dose of 45 mg in the morning and 15 mg 8 hours later. Your doctor may gradually increase your dose up to a maximum combination of 90 mg in the morning and 30 mg 8 hours later. To determine the best dose for you, your doctor will regularly check how you tolerate the prescribed dose. You should always take the highest tolerable dose combination prescribed by your doctor.
If you are taking other medicines that may increase the effects of Jinarc, you may receive lower doses. In this case, your doctor may prescribe Jinarc tablets with 30 or 15 mg of tolvaptan, which you should take once a day in the morning.
Method of administration
Swallow the tablets whole with a glass of water.
The morning dose should be taken at least 30 minutes before breakfast. The second daily dose can be taken with or without food.
If you take more Jinarc than you should
If you have taken more tablets than prescribed, drink plenty of water and contact your doctor or the nearest hospital immediately.Remember to take the package leaflet with you to show what you have taken. If you take the higher dose too late, you may need to go to the bathroom more frequently at night.
If you forget to take Jinarc
If you forget to take your medicine, take the dose as soon as you remember on the same day. If you have not taken the tablets for one day, take the normal dose the next day. Do nottake a double dose to make up for the missed individual doses.
If you stop taking Jinarc
If you stop taking Jinarc, your kidney cysts may grow as quickly as they did before you started treatment with this medicine. Therefore, you should only stop taking Jinarc if you experience side effects that require urgent medical attention (see section 4) or if your doctor tells you to do so.
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.
Serious side effects:
If you experience any of the following side effects, you may need urgent medical attention. Stop taking Jinarc and contact a doctor or go to the nearest hospital immediately if:
Jinarc may cause your liver to not function properly.
Tell your doctor if you experience symptoms of nausea, vomiting, fever, fatigue, loss of appetite, abdominal pain, dark urine, jaundice (yellowing of the skin or eyes), itching (pruritus) of the skin, or muscle and joint pain with fever.
Other side effects:
Very common: may affect more than 1 in 10 people
Common: may affect up to 1 in 10 people
Uncommon: may affect up to 1 in 100 people
Frequency not known: cannot be estimated from the available data
Reporting of side effects
If you experience 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 through 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 outer carton, blister pack, and on the blister strip after EXP. The expiry date refers to the last day of the month shown.
Store in the original package to protect from light and moisture.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help protect the environment.
Jinarc Composition
The active ingredient is tolvaptan.
Each 15 mg Jinarc tablet contains 15 mg of tolvaptan.
Each 30 mg Jinarc tablet contains 30 mg of tolvaptan.
Each 45 mg Jinarc tablet contains 45 mg of tolvaptan.
Each 60 mg Jinarc tablet contains 60 mg of tolvaptan.
Each 90 mg Jinarc tablet contains 90 mg of tolvaptan.
The other ingredients are lactose monohydrate (see section 2), cornstarch, microcrystalline cellulose, hydroxypropylcellulose, magnesium stearate, and aluminum lake of indigo carmine.
Appearance of Jinarc and Package Contents
The different doses of Jinarc tablets have different shapes and engravings:
15 mg tablet: blue, triangular, engraved with "OTSUKA" and "15" on one side.
30 mg tablet: blue, round, engraved with "OTSUKA" and "30" on one side.
45 mg tablet: blue, square, engraved with "OTSUKA" and "45" on one side.
60 mg tablet: blue, modified rectangle, engraved with "OTSUKA" and "60" on one side.
90 mg tablet: blue, pentagonal, engraved with "OTSUKA" and "90" on one side.
The medication is supplied with the following package sizes:
Jinarc 15 mg tablets: blisters with 7 or 28 tablets
Jinarc 30 mg tablets: blisters with 7 or 28 tablets
Jinarc 45 mg tablets + Jinarc 15 mg tablets: blisters with or without a carton box containing
14 (7 tablets of the highest dose + 7 tablets of the lowest dose),
28 (14 tablets of the highest dose + 14 tablets of the lowest dose) or
56 (28 tablets of the highest dose + 28 tablets of the lowest dose) tablets.
Jinarc 60 mg tablets + Jinarc 30 mg tablets: blisters with or without a carton box containing 14 (7 tablets of the highest dose + 7 tablets of the lowest dose),
28 (14 tablets of the highest dose + 14 tablets of the lowest dose) or
56 (28 tablets of the highest dose + 28 tablets of the lowest dose) tablets.
Jinarc 90 mg tablets + Jinarc 30 mg tablets: blisters with or without a carton box containing
14 (7 tablets of the highest dose + 7 tablets of the lowest dose),
28 (14 tablets of the highest dose + 14 tablets of the lowest dose) or
56 (28 tablets of the highest dose + 28 tablets of the lowest dose) tablets.
Only some package sizes may be marketed.
Marketing Authorization Holder
Otsuka Pharmaceutical Netherlands B.V.
Herikerbergweg 292
1101 CT, Amsterdam
Netherlands
Manufacturer
AndersonBrecon (UK) Limited
Units 2-7, Wye Valley Business Park, Brecon Road, Hay-on-Wye
Hereford - HR3 5PG
United Kingdom
Almac Pharma Services Ltd.
Almac House, 20 Seagoe Industrial Estate
Craigavon - BT63 5QD
United Kingdom
Almac Pharma Service (Ireland) Limited
Finnabair Industrial Estate, Dundalk,
Co. Louth - A91 P9KD
Ireland
Millmount Healthcare Limited
Block-7, City North Business Campus, Stamullen, Co.
Meath, K32 YD60
Ireland
You can request more information about this medication by contacting the local representative of the marketing authorization holder:
Belgium Otsuka Pharmaceutical Netherlands B.V. Tel: +31 (0) 20 85 46 555 | Lithuania Otsuka Pharmaceutical Netherlands B.V. Tel: +31 (0) 20 85 46 555 |
Bulgaria Otsuka Pharmaceutical Netherlands B.V. Tel: +31 (0) 20 85 46 555 | Luxembourg Otsuka Pharmaceutical Netherlands B.V. Tel: +31 (0) 20 85 46 555 |
Czech Republic Otsuka Pharmaceutical Netherlands B.V. Tel: +31 (0) 20 85 46 555 | Hungary Otsuka Pharmaceutical Netherlands B.V. Tel: +31 (0) 20 85 46 555 |
Denmark Otsuka Pharma Scandinavia AB Tel: +46 854 528 660 | Malta Otsuka Pharmaceutical Netherlands B.V. Tel: +31 (0) 20 85 46 555 |
Germany Otsuka Pharma GmbH Tel: +49 691 700 860 | Netherlands Otsuka Pharmaceutical Netherlands B.V. Tel: +31 (0) 20 85 46 555 |
Estonia Otsuka Pharmaceutical Netherlands B.V. Tel: +31 (0) 20 85 46 555 | Norway Otsuka Pharma Scandinavia AB Tel: +46 854 528 660 |
Greece Otsuka Pharmaceutical Netherlands B.V. Tel: +31 (0) 20 85 46 555 | Austria Otsuka Pharmaceutical Netherlands B.V. Tel: +31 (0) 20 85 46 555 |
Spain Otsuka Pharmaceutical S.A. Tel: +34 93 208 1020 | Poland Otsuka Pharmaceutical Netherlands B.V. Tel: +31 (0) 20 85 46 555 |
France Otsuka Pharmaceutical France SAS Tel: +33 147 080 000 | Portugal Otsuka Pharmaceutical Netherlands B.V. Tel: +31 (0) 20 85 46 555 |
Croatia Otsuka Pharmaceutical Netherlands B.V. Tel: +31 (0) 20 85 46 555 | Romania Otsuka Pharmaceutical Netherlands B.V. Tel: +31 (0) 20 85 46 555 |
Ireland Otsuka Pharmaceutical Netherlands B.V. Tel: +31 (0) 20 85 46 555 | Slovenia Otsuka Pharmaceutical Netherlands B.V. Tel: +31 (0) 20 85 46 555 |
Iceland Otsuka Pharma Scandinavia AB Tel: +46 854 528 660 | Slovakia Otsuka Pharmaceutical Netherlands B.V. Tel: +31 (0) 20 85 46 555 |
Italy Otsuka Pharmaceutical Italy S.r.l. Tel: +39 02 00 63 27 10 | Finland Otsuka Pharma Scandinavia AB Tel: +46 854 528 660 |
Cyprus Otsuka Pharmaceutical Netherlands B.V. Tel: +31 (0) 20 85 46 555 | Sweden Otsuka Pharma Scandinavia AB Tel: +46 854 528 660 |
Latvia Otsuka Pharmaceutical Netherlands B.V. Tel: +31 (0) 20 85 46 555 | United Kingdom Otsuka Pharmaceuticals (UK) Ltd. Tel: +44 (0)203 747 5300 |
Date of the last revision of this prospectus: MM/YYYY.
Other sources of information
Detailed information about this medication is available on the website of the European Medicines Agency: http://www.ema.europa.eu/.