Famotidine 20 mg film-coated 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 Famotidine is and what it is used for
2. What you need to know before you take Famotidine
3. How to take Famotidine
4. Possible side effects
5. How to store Famotidine
6. Contents of the pack and other information

• you are allergic to famotidine, other H2−receptor antagonists or any of the other ingredients of this medicine (listed in section 6).

Talk to your doctor, pharmacist or nurse before taking Famotidine if:

• there is a possibility of a malignant growth (tumour) being present in your stomach.
• you have kidney problems.
• you have been taking a high dose of famotidine for a long time. Your doctor may monitor your blood count and liver function.

Tell your doctor, pharmacist or nurse if you are taking , have recently taken or might take any other medicines, including those obtained without prescription. This includes herbal medicines.

Medicines which may interact with famotidine:

• Famotidine may decrease the effect of posaconazole oral suspension (a drinkable medicine used to prevent and treat some fungal infections).
• Famotidine may decrease the effect of dasatinib, erlotinib, gefitinib, pazopanib (medicines used to treat cancer).
• Ketoconazole (should be administered 2 hours before famotidine) or itraconazole, used to treat fungal infections
• Probenecid , used to treat gout
• Antacids, for indigestion (famotidine should be administered 1-2 hours before taking an antacid)
• Sucralfate, used to treat and prevent the recurrence of ulcers (sucralfate should not be administered within 2 hours of taking famotidine)
• Calcium carbonate, when used as a medicine for high blood phosphate levels in patients on dialysis
• Atazanavir, used for treatment of HIV infection

If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor, pharmacist or nurse for advice before taking this medicine.

Pregnant

If you are pregnant or suspect you are pregnant, you should not take famotidine unless your doctor thinks the benefits outweigh the risks.

Breast-feeding

If you are breast−feeding, you should either stop taking famotidine or stop breast-feeding as it is excreted in breast milk.

Whilst taking famotidine you may feel dizzy or have a headache. If you develop these symptoms, you should not drive or operate machinery or do activities which require you to be alert and have quick reactions.

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

If you accidentally take too many tablets, contact your doctor or nearest hospital emergency department immediately for advice. Remember to take this leaflet or any remaining tablets with you.

Take it as soon as you remember, unless it is nearly time for your next dose. If you miss a dose, do not take a double dose to make up for a forgotten dose.

It is important that you keep taking Famotidine for as long as your doctor has told you to.

In case of long-standing ulcer disease, abrupt withdrawal after symptom relief should be avoided.

• Allergic reactions: swelling of the face throat or tongue, difficulty in breathing or dizziness (anaphylaxis)
• Difficulty in breathing or wheezing (bronchospasm)
• Severe blistering of the skin, mouth, eyes and genitals (Stevens Johnson syndrome, toxic epidermal necrolysis)
• Shortness of breath or dry cough due to inflammation of the lungs (interstitial pneumonia)
• Swelling of the deeper layers of the skin caused by a build-up of fluid (angioneurotic oedema)

Common side-effects (may affect up to 1 in 10 people):

• headache
• dizziness
• constipation
• diarrhoea

Uncommon side-effects (may affect up to 1 in 100 people):

• feeling and/or being sick (nausea/vomiting)
• abdominal pain
• excessive wind/feeling bloated (flatulence)
• tiredness (fatigue)
• dry mouth
• loss of appetite (anorexia)
• taste disorder
• severe itching (pruritus)
• rash
• skin rashes with the formation of wheals (urticaria)

Rare side-effects (may affect up to 1 in 1,000 people):

• an increase in liver enzymes in the blood (detected through blood tests)

Very rare side-effects (may affect less than 1 in 10,000 people):

• reduction in blood platelets, which increases risk of bleeding or bruising (thrombocytopenia)
• reduction in white blood cells (leukopenia, neutropenia),
• reduction in white blood cells which may make infections more likely (agranulocytosis)
• reduction in blood cells which can cause weakness, bruising or make infections more likely (pancytopenia)
• reversible psychic disturbances including:
  • hallucinations (seeing or hearing things that are not real)
  • disorientation
  • confusion
  • anxiety disorders
  • restlessness (agitation)
  • depression
  • disorders of sexual function (reduced libido)
  • difficulty in sleeping (insomnia)
• inability to maintain an erection (impotence)
• tingling or numbness in the hands or feet (paraesthesia)
• sleepiness or drowsiness (somnolence)
• fits (convulsions), epileptic seizures including grand mal seizures (particularly in patients with kidney problems)
• hair loss (alopecia)
• chest tightness
• muscle cramps
• joint pain (arthralgia)
• inflammation of liver (hepatitis)
• yellowing of the skin and whites of the eyes (jaundice)
• abnormal liver function tests
• worsening of existing liver disease
• abnormal heart rhythm where the heart beats too slowly (AV block)
• disrupted heart rhythm/irregular heartbeat (arrhythmias)
• heart rhythm condition that may cause a fast heartbeat (QT prolongation) (especially in patients with impaired kidney function)

• enlargement of breasts in men (gynaecomastia) (not known if caused by Famotidine)

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 http://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 famotidine.

Famotidine 20 mg film-coated tablets:

Each film-coated tablet contains 20 mg of famotidine.

Famotidine 40 mg film-coated tablets:

Each film-coated tablet contains 40 mg of famotidine.

The other ingredients are:

Tablet core: cellulose, microcrystalline (PH 101), maize starch, sodium starch glycolate, hydroxypropyl cellulose, cellulose, microcrystalline (PH 102) and magnesium stearate.

Tablet coat:

Famotidine 20 mg film-coated tablets:

Hydroxypropyl cellulose (E463), hypromellose (E464), titanium dioxide (E171) and iron oxide yellow (E172).

Famotidine 40 mg film-coated tablets:

Hydroxypropyl cellulose (E463), hypromellose (E464) and titanium dioxide (E171).

Famotidine 20 mg film-coated tablets:

Light yellow to yellow, round, approximately 6 mm in diameter, film coated tablets debossed with “11” on one side and plain on the other side.

Famotidine 40 mg film-coated tablets:

White, round, approximately 8 mm in diameter, film-coated tablets, debossed with “12” on one side and plain on the other side.

10, 20, 28, 30, 50, 56, 60, 90 or 100 film-coated tablets in blisters.

Not all pack sizes may be marketed.