Tolvaptan 90 mg + 30mg tablets

• Keep this leaflet. You may need to read it again.
• If you have any further questions, ask your doctor or pharmacist
• This medicine has been prescribed for you. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours.
• If you get any serious side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4.

1. What Tolvaptan is and what it is used for
2. What you need to know before you take Tolvaptan
3. How to take Tolvaptan
4. Possible side effects
5. How to store Tolvaptan
6. Contents of the pack and other information

• you are allergic to tolvaptan or any of the other ingredients of this medicine (listed in section 6) or if you are allergic to benzazepine or benzazepine derivatives (e.g. benazepril, conivaptan, fenoldopam mesylate or mirtazapine)
• you have been told that you have raised levels of liver enzymes in your blood which do not allow treatment with tolvaptan
• your kidneys do not work (no urine production)
• you have a condition which is associated with a very low blood volume (e.g. severe dehydration or bleeding)
• you have a condition which increases the sodium in your blood
• you do not realise when you are thirsty
• you are pregnant
• you are breastfeeding.

Talk to your doctor before taking Tolvaptan if you:

• suffer from liver disease.
• cannot drink enough water (see “drinking enough water” below) or have to restrict your fluid intake.
• have difficulties urinating (e.g. have an enlarged prostate).
• suffer from too high or too low blood sodium.
• had an allergic reaction in the past to benzazepine, tolvaptan or other benzazepine derivatives (e.g. benazepril, conivaptan, fenoldopam mesylate or mirtazapine), or to any of the other ingredients of this medicine (listed in section 6).
• have diabetes.
• have been told you have high levels of a chemical called uric acid in your blood (which may have caused attacks of gout).
• have advanced kidney disease.

This medicine may cause your liver to not work properly. Therefore, please inform your doctor immediately if you have signs that could indicate potential liver problems such as:

• nausea
• vomiting
• fever
• tiredness
• loss of appetite
• pain in the abdomen
• dark urine
• jaundice (yellowing of skin or eyes)
• itching of your skin
• flu-like syndrome (joint and muscle pain with fever)

During treatment with this medicine, your doctor will arrange monthly blood tests to check for changes in your liver function.

This medicine causes water loss because it increases your urine production. This water loss may result in side effects such as dry mouth and thirst or even more severe side effects like kidney problems (see section 4). It is therefore important that you have access to water and that you are able to drink sufficient amounts when you feel thirsty. Before bed-time you must drink 1 or 2 glasses of water even if you do not feel thirsty and you must also drink water after you urinate at night. Special care must be taken if you have a disease that reduces appropriate fluid intake or if you are at an increased risk of water loss e.g. in case of vomiting or diarrhoea. Due to the increased urine production, it is also important that you always have access to a toilet.

Do not give this medicine to children and adolescents (under age of 18 years) because it has not been studied in these age groups.

Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines, including medicines obtained without a prescription.

The following medicines may increase the effect of Tolvaptan:

• amprenavir, atazanavir, darunavir/ritonavir and fosamprenavir (used to treat HIV/AIDS),
• aprepitant (used to avoid nausea and vomiting in chemotherapy),
• crizotinib and imatinib (used to treat cancer),
• ketoconazole, fluconazole or itraconazole (used to treat fungal infections),
• macrolide antibiotics like erythromycin or clarithromycin,
• verapamil (used to treat heart diseases and high blood pressure),
• diltiazem (used to treat high blood pressure and chest pain).

The following medicines may lower the effect of Tolvaptan:

• phenytoin or carbamazepine (used to treat epilepsy),
• rifampicin, rifabutin or rifapentine (used to treat tuberculosis),
• St. John’s Wort (a traditional herbal medicinal product for the relief of slightly low mood and mild anxiety).

Tolvaptan may increase the effect of the following medicines:

• digoxin (used to treat irregular heart beat and heart failure),
• dabigatran (used to thin the blood),
• methotrexate (used to treat cancer, arthritis),
• ciprofloxacin (an antibiotic),
• sulfasalazine (used to treat inflammatory bowel disease or rheumatoid arthritis),
• metformin (used to treat diabetes).

Tolvaptan may lower the effect of the following medicines:

• vasopressin analogues such as desmopressin (used to increase blood clotting factors or to control urine output or bedwetting).

These medicines can affect or be affected by Tolvaptan:

• diuretics (used to influence the production of urine). Taken with tolvaptan these may increase the risk of side effects due to water loss or may cause kidney problems.
• diuretics or other medicines for the treatment of high blood pressure. Taken with tolvaptan these may increase the risk of low blood pressure when you stand up from sitting or lying down.
• medicines which increase the level of sodium in your blood or which contain large amounts of salt (e.g. tablets that dissolve in water and indigestion remedies). These may increase the effect of tolvaptan. There is a risk that this may lead to too much sodium in your blood.

It may still be alright for you to take these medicines and tolvaptan together. Your doctor will be able to decide what is suitable for you.

Do not drink grapefruit juice when taking this medicine.

Do not take this medicine if you are pregnant or breast-feeding.

Women of childbearing age must use reliable contraceptive measures during use of this medicine.

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.

Some people may feel dizzy, weak or tired after being given Tolvaptan. If this happens to you, do not drive or use any tools or machines.

If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicine.

This medicine contains less than 1 mmol sodium (23 mg) per tablet, that is to say essentially ‘sodium-free’.

The daily amount of tolvaptan is split into two doses, one bigger than the other. The higher dose should be taken in the morning when you wake up, at least 30 minutes before the morning meal. The lower dose is taken 8 hours later.

The dose combinations are:

45 mg + 15 mg

60 mg + 30 mg

90 mg + 30 mg

Your treatment will normally 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 on waking and 30 mg after 8 hours. To find the best dose your doctor will regularly check how well you are tolerating a prescribed dose. You should always take the highest tolerable dose combination prescribed by your doctor.

If you take other medicines, which can increase the effects of tolvaptan you may receive lower doses. In this case your doctor may prescribe you tolvaptan tablets with 30 mg or 15 mg tolvaptan which have to be taken once a day in the morning.

Swallow the tablets without chewing, with a glass of water. The morning dose is to be taken at least 30 minutes before the morning meal.

The second daily dose can be taken with or without food.

If you have taken more tablets than your prescribed dose, drink plenty of water and contact your doctor or your local hospital immediately.

Remember to take the medicine pack with you so that it is clear what you have taken. If you take the higher dose very late in the day you may have to go to the toilet at night more frequently.

If you forget to take your medicine, you should take the dose as soon as you remember on the same day. If you do not take your tablets on one day, take your normal dose on the next day. DO NOT take a double dose to make up for forgotten individual doses.

If you stop taking this medicine your kidney cysts may grow as fast as they did before you started treatment with tolvaptan. Therefore, you should only stop taking this medicine if you notice side effects requiring urgent medical attention (see section 4) or if your doctor tells you to.

If you notice any of the following side effects, you may need urgent medical attention. Stop taking tolvaptan and immediately contact a doctor or go to the nearest hospital if you:

• find it difficult to urinate.
• experience swelling of the face, lips or tongue, itching, generalised rash, or severe wheezing or breathlessness (symptoms of an allergic reaction).

Tolvaptan may cause your liver not to work properly.

Consult your doctor if symptoms of nausea, vomiting, fever, tiredness, loss of appetite, pain in the abdomen, dark urine, jaundice (yellowing of skin or eyes), itching of your skin or joint and muscle pain with fever occur.

Very common (may affect more than 1 in 10 people)

• thirst (requiring excessive drinking of water)
• headache
• dizziness
• diarrhoea
• dry mouth
• increased need to urinate, to urinate at night, or to urinate more frequently
• fatigue

Common (may affect up to 1 in 10 people)

• dehydration
• high levels of sodium, uric acid and blood sugar
• decreased appetite
• taste changes
• gout
• difficulty sleeping
• fainting
• heart pounding
• shortness of breath
• belly pain
• full or bloated or uncomfortable feeling in the stomach
• constipation
• heartburn
• liver function abnormal
• dry skin
• rash
• itching
• hives
• joint pain
• muscle spasms
• muscle pain
• general weakness
• raised levels of liver enzymes in the blood
• weight loss
• weight gain

Uncommon (may affect up to 1 in 100 people)

• increase of bilirubin (a substance that can cause yellowing of skin or eyes) in the blood

Not known (frequency cannot be estimated from the available data)

• allergic reactions (see above)
• generalised rash
• acute liver failure (ALF)
• increased level of creatine phosphokinase (an enzyme that measures the muscle and heart function) in the blood

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 Yellow Card Scheme at: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.

By reporting side effects, you can help provide more information on the safety of this medicine.

• The active substance is Tolvaptan.
  Each Tolvaptan 15 mg tablet contains 15 mg tolvaptan.
  Each Tolvaptan 30 mg tablet contains 30 mg tolvaptan.
  Each Tolvaptan 45 mg tablet contains 45 mg tolvaptan.
  Each Tolvaptan 60 mg tablet contains 60 mg tolvaptan.
  Each Tolvaptan 90 mg tablet contains 90 mg tolvaptan.
• The other ingredients are lactose monohydrate, cellulose microcrystalline, croscarmellose sodium, povidone, magnesium stearate.

The different strengths of Tolvaptan tablets have different shapes and embossing:

Tolvaptan 15 mg tablets: White to off white, triangular, 6.1 x 5.7 mm tablets with marking “C6” debossed on one side.

Tolvaptan 30 mg tablets: White to off white, round 7.5 mm tablets with marking “C7” debossed on one side.

Tolvaptan 45 mg tablets: White to off white, square 8.5 x 8.5 mm tablets with marking “C8” debossed on one side.

Tolvaptan 60 mg tablets: White to off white, barrel, 11.3 x 7.0 mm tablets with marking “C9” debossed on one side.

Tolvaptan 90 mg tablets: White to off white, pentagonal, 11.3 x 11.5 mm tablets with marking “C10” debossed on one side.

Combined packs:

45 mg + 15 mg, 60 mg + 30 mg and 90 mg + 30 mg strengths:

56 tablets (28 tablets of each strength) in a carton

Not all pack sizes may be marketed.