Digoxin 0.0625mg tablets

• Keep this leaflet. You may need to read it again.
• If you have any further questions ask your doctor, pharmacist or nurse.
• This medicine has been prescribed for you only. 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 side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. See section 4.

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

• Are allergic to digoxin, other cardiac glycosides or any of the other ingredients of this medicine (listed in section 6).
• Have serious heart problems, such as those with the conduction of the electrical impulses in the heart, especially if you have a history of Stokes-Adams attacks (abrupt, short-lived loss of consciousness caused by a sudden change in heart rate or rhythm).
• Have an irregular heart-beat caused by cardiac glycoside intoxication or conditions such as Wolff-Parkinson-White syndrome.
• Have obstructive cardiomyopathy (enlargement of the heart muscle).

Talk to your doctor, pharmacist or nurse before using this medicine:

• If you are taking this medicine, your doctor may ask you to have regular blood tests to determine the amount of digoxin in the blood. This may be useful in the case of patients with kidney disorders.
• If you develop digoxin toxicity, this can lead to various forms of heart rhythm disturbances, some of which resemble the rhythm disturbances for which the product was prescribed.
• If you have abnormal heart rhythm (heart block) and you are taking this medicine, contact your doctor immediately if you feel one or more of the following symptoms: fainting, short-lasting loss of consciousness, dizziness or light-headedness, fatigue (tiredness), shortness of breath, chest pain, irregular heart-beat or confusion.
• If you have a sinoatrial disorder (a disorder in the conduction of electrical impulses in the heart such as Sick Sinus Syndrome), in some patients with a sinoatrial disorder this medicine can cause a slow and/or irregular heart-beat. Sometimes this will cause tiredness, weakness and dizziness and when your heartbeat is very slow you may faint.
• If you have recently suffered a heart attack.
• When heart failure occurs along with the collection of an abnormal protein in the heart tissue (cardiac amyloidosis), an alternative therapy may be prescribed by the doctor.
• If you have myocarditis (inflammation of the heart muscle) this may cause vasoconstriction (narrowing of the blood vessels) on rare occasions. Your doctor may prescribe you a different medicine.
• If you have Beri-beri disease (caused by a vitamin B1 deficiency).
• If you have constrictive pericarditis (inflammation of the sac which contains the heart).
• If you are taking diuretics (drugs which promote urine production and help reduce the amount of water in your body) with or without an ACE inhibitor (mainly used to treat high blood pressure), your doctor will prescribe a lower dose of digoxin. Do not stop taking digoxin without talking to your doctor.
• If you have a heart test called an ECG (electrocardiogram), tell the person doing the test that you are taking digoxin as it can affect the meaning of the results.
• If you have severe respiratory (lung) disease (as you may have an increased sensitivity to digoxin).
• If you have low levels of oxygen reaching certain parts of your body, low levels of potassium, abnormally low levels of magnesium or increased levels of calcium in your blood.
• If you have thyroid disease (such as an under-active or over-active thyroid) as you might require changes in the dose of this medicine.
• If you have malabsorption syndrome (you cannot absorb minerals from your food properly) or if you have ever had gastrointestinal reconstruction surgery.
• If you will receive electric shock treatment to correct an abnormal heart-beat.

Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines. Taking several medicines can sometimes have harmful consequences or lead to unwanted interactions.

Sensitivity to digoxin can be increased by medicines which lower the level of potassium in the blood. These include:

• diuretics,
• lithium salts (antidepressants),
• corticosteroid based products,
• carbenoxolone (a product which strengthens the gastric mucosa).

The following medicines increase the level of digoxin in the blood, which can increase the risk of toxicity:

• certain products which affect the heart: amiodarone, flecainide, prazosin, propafenone, quinidine,
• canagliflozin (used to treat of type 2 diabetes mellitus),
• certain antibiotics: erythromycin, clarithromycin, tetracycline, gentamicin, trimethoprim,
• daclatasvir (used in combination with other medications to treat hepatitis C),
• flibanserin (used to treat low sexual desire in women who have not gone through menopause),
• isavuconazole (used to treat fungal infections),
• itraconazole (used to treat fungal infections),
• ivacaftor (used to treat cystic fibrosis),
• spironolactone (a drug which increases the amount of urine you produce),
• alprazolam (a sedative which may be used to treat anxiety),
• indomethacin (used to treat inflammation),
• quinine (may be used to prevent malaria infection),
• propantheline (used to prevent muscle spasms),
• mirabegron (used to treat overactive bladder that causes a sudden urge to urinate resulting in involuntary loss of urine),
• nefazodone (an antidepressant),
• atorvastatin (lowers blood cholesterol),
• cyclosporine (an immunosuppressant often used to prevent transplant rejection),
• epoprostenol (used to treat pulmonary arterial hypertension),
• tolvaptan (used to treat low blood sodium levels),
• conivaptan (used to treat low blood sodium levels),
• carvedilol (used to treat mild to severe congestive heart failure and high blood pressure),
• ritonavir (used to treat HIV infection and AIDS),
• taleprevir (used to treat hepatitis C infection),
• dronedarone (used to treat irregular heart-beat),
• ranolazine (used to treat chest pain),
• simeprevir (used in combination with other medications to treat hepatitis C),
• telmisartan (used to treat high blood pressure),
• lapatinib (used to treat breast cancer),
• ticagrelor (used to prevent heart attack or stroke),
• verapamil (used to treat high blood pressure),
• felodipine (used to treat high blood pressure),
• tiapamil (used to treat chest pain),
• vandetanib (used to treat certain cancers of the thyroid gland),
• velpatasvir (used in combination with other medications to treat hepatitis C),
• P-glycoprotein inhibitors.
• Venetoclax (is used to treat patients with chronic lymphocytic leukaemia)
• Vemurafenib (used to treat adult patients with a type of cancer called melanoma)
• Proton pump inhibitors (PPIs) (used to relieve symptoms of acid reflux, or gastroesophageal reflux disease (GERD)

The following medicines may increase or have no effect on the levels of digoxin in the blood:

• nifedipine, diltiazem, angiotensin receptor blockers (ARBs) and ACE inhibitors (used to treat high blood pressure and congestive heart failure),
• non-steroidal anti-inflammatory drugs (NSAIDs) and cyclooxygenase-2 enzyme (COX-2) inhibitors (used to treat pain and inflammation).

If you have heart failure and are taking sennosides (increase the amount of stools you produce to help you have bowel movements) along with digoxin you may have a moderately increased risk of digoxin toxicity.

The following medicines reduce the level of digoxin in the blood:

• antacids (used to treat gastric acidity),
• some bulk-forming laxatives (increase the amount of stools you produce to help you have bowel movements),
• kaolin-pectin (used to treat diarrhoea),
• acarbose (used to treat some types of diabetes),
• certain antibiotics: neomycin, penicillamine, rifampicin,
• some cytostatic drugs (used as chemotherapy for cancer treatment),
• metoclopramide (a product for treating nausea and vomiting),
• sulfasalazine (a product to counteract inflammatory diseases of the intestine),
• adrenaline (used to treat severe allergic reactions),
• salbutamol (a product used to treat asthma),
• colestyramine (lowers blood cholesterol),
• phenytoin (used to treat epilepsy),
• St. John’s wort (Hypericum perforatum) (used to treat depression),
• bupropion (used to treat depression),
• P-glycoprotein inducers,
• supplemental enteral nutrition (being fed by a feeding tube).

If you are taking digoxin along with the following medicines you may have an increased risk of irregular heart rhythm:

• intravenous calcium,
• beta-blockers,
• sympathomimetics (used to treat heart attack and low blood pressure).

If you are taking digoxin and suxamethonium (used to help muscle relaxation and treat short-term paralysis), you may have an increased risk of high potassium levels in the blood.

This medicine may be taken on an empty stomach or with most meals. However, you should avoid taking Digoxin tablets with foods that are high in fibre, also known as 'dietary fibre', because the level of digoxin absorbed by the body can be reduced.

Pregnancy

Your doctor will prescribe this medicine with caution during pregnancy.

You may require a higher dose of this medicine if you are pregnant.

This medicine could be given to the mother to treat abnormally high heart rate and congestive heart failure in the unborn child.

Side effects of digoxin treatment affecting the mother may also affect the unborn child.

Breastfeeding

This medicine is excreted in breast milk, but in very small amounts. Therefore, this medicine can be used by women who are breast-feeding.

Fertility

There is no information available on the effect of digoxin on fertility.

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.

Since dizziness and blurred or yellow vision have been reported, you should exercise caution before driving a vehicle, using machinery or participating in dangerous activities.

Digoxin tablets contain lactose (a sugar). If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicinal product.

If you have taken too much of the Digoxin tablets or a child has taken the medicine by accident, contact your doctor, hospital or poison centre to evaluate the risks and get more information.

The main symptoms of digoxin toxicity are heart rhythm disturbances and gastrointestinal symptoms which may happen before heart rhythm disturbances. Gastrointestinal symptoms include loss of appetite, nausea and vomiting. Other symptoms of digoxin toxicity include dizziness, fatigue, a general feeling of being unwell and various neurological disturbances including visual disturbances (more yellow-green than usual). The neurological and visual symptoms may persist even after other signs of toxicity have been resolved. In chronic toxicity, non-heart related symptoms, such as weakness and a general feeling of being unwell, may be the main symptoms.

Do not take a double dose to make up for the forgotten dose.

Your doctor will tell you how long you should take digoxin. Do not stop your treatment early without consulting your doctor.

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 Yellow Card Scheme. Website: 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 medicine.

• The active ingredient is digoxin, each tablet contains 0.0625 mg (62.5 micrograms).
• The other ingredients are lactose monohydrate, maize starch, indigo carmine, modified maize starch, rice starch, povidone and magnesium stearate.

Within the carton is an amber glass bottle that contains 28,50,100 or 500 blue tablets, an amber glass bottle with child resistant closure that contains 56 blue tablets, or a blister pack of 30 or 90 blue tablets. A blue, round, biconvex tablet debossed "DO6" on the one side and plain on the other side

Not all pack sizes may be marketed.

Marketing Authorisation Holder:

Manufactured by:

PL 39699/0008