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FAMOTIDINE 20MG TABLETS

Active substance: FAMOTIDINE

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FAMOTIDINE 20 mg FILM COATED
TABLETS FAMOTIDINE 40 mg FILM
COATED TABLETS
 

Read all of this leaflet carefully before you start taking this medicine.
• Keep this leaflet. You may want to read it again.
• If you have further questions, please ask your doctor or pharmacist.
• This medicine has been prescribed for you personally. Do not give it to anyone else. It may harm
them, even if their symptoms are the same as yours.
YOUR MEDICINE
Each tablet contains either 20 mg or 40 mg of the active ingredient Famotidine. Each tablet also
contains microcrystalline cellulose, pregelatinised starch, talc, magnesium stearate, lactose
monohydrate, hydroxypropylmethylcellulose, titanium dioxide (E171) and triacetin. Both strengths of
tablets are white. The 20 mg tablets are marked 'FD 20' on one side and 'G' on the other and the
40 mg tablets are marked 'FD 40' on one side and 'G' on the other. Famotidine Tablets are available in
blister packs of 28 tablets. Your pharmacist will dispense the number of tablets prescribed by your
doctor.
Product Licence Holder: Generics [UK) Limited, Station Close, Potters Bar, Herts EN6 1TL.
Manufacturer: Genpharm Inc, 85 Advance Road, Etobicoke, Ontario, M8Z 2S6, Canada.
WHAT FAMOTIDINE IS AND WHAT IT IS USED FOR
Your medicine is in the form of a film coated tablet. It contains Famotidine, which belongs to a group
of medicines called histamine (H2) antagonists or anti-ulcer drugs. These anti-ulcer drugs control the
secretion of gastric acid in the stomach. Famotidine can prevent this acid secretion. Famotidine can be
used for the following conditions:
• To help treat non-cancerous gastric (stomach) ulcers and duodenal ulcers
• To help prevent relapse of duodenal ulcers
• To help treat Zollinger-Ellison Syndrome (with a condition caused by too much stomach acid)
• To help treat acid reflux (burning pain caused by stomach acid escaping back up the foodpipe) and
the symptoms of an inflamed foodpipe (oesophagitis)
BEFORE YOU TAKE FAMOTIDINE TABLETS
Do not take this medicine and tell your doctor if:
• you have taken Famotidine or a similar medicine before and suffered an allergic or unpleasant
reaction
• you are allergic to any of the tablet ingredients
• you are breastfeeding.
You must tell your doctor before taking Famotidine Tablets if:
• you are pregnant or intend to become pregnant
• you have kidney problems
• you are already taking any of the following medicines:
*Antifungal medicine eg. Itraconazole, Ketoconazole; take 2 hours before Famotidine dose
*Probenecid, to treat gout * antacids; take Famotidine dose one to two hours before antacid
* Sucralfate; do not take dose within two hours of Famotidine dose
* Atazanavir, used in the treatment of HIV.
Famotidine may hide the symptoms of other diseases. Your doctor may carry out tests to diagnose
your condition and/or exclude other diseases before you start taking Famotidine.
Patients with rare hereditary problems of galactose intolerance, Lapp lactase deficiency or glucosegalactose malabsorption
Pregnancy
If you are pregnant or planning to become pregnant, talk to your doctor first before taking this
medicine If you do get pregnant while taking Famotidine tablets you must tell the doctor
straightaway.

Breast Feeding
Famotidine can pass into breast milk. Talk to your doctor before taking if you are breast-feeding or
planning to breast feed

 
Driving and operating machines
Do not drive or operate machines if you feel dizzy or get a headache while taking Famotidine tablets.
 

 

HOW TO TAKE FAMOTIDINE TABLETS

 
Famotidine Tablets can be taken before or after food.

 
ADULTS (including the elderly)
Duodenal or non-cancerous stomach ulcers - The usual dose is 40 mg of Famotidine
taken at bedtime. In some cases treatment may last for up to 8 weeks.
To prevent relapse of duodenal ulcers - The usual dose is 20 mg of Famotidine at bedtime.
To treat Zollinger-Ellison Syndrome - The usual starting dose is 20 mg of Famotidine four times a
day. Your doctor may need to increase this dose further depending how well the ulcers are healing. If
you have already been taking a similar medicine or your symptoms are severe, your doctor may start
you on a higher dose of Famotidine.
To treat the symptoms of acid reflux - The usual dose is 20 mg of Famotidine twice
daily. Treatment usually lasts for 6 weeks, but if necessary, for 12 weeks.
To treat the symptoms of oesophagitis (inflammation of the foodpipe) - The usual dose is 40
mg of Famotidine twice daily. Treatment usually lasts for 6 weeks, but if necessary, for 12 weeks.
If you suffer from kidney disease, your doctor will prescribe a lower dose of Famotidine.

 
CHILDREN Famotidine Tablets should not be given to children.

 
If you forget to take your dose of Famotidine Tablets, unless it is almost time for your next dose,
take it as soon as you remember. Otherwise, if you miss a dose do not double the next dose, just
carry on as before. If you take too much of your medicine contact your doctor immediately.
POSSIBLE SIDE EFFECTS

 
Famotidine is generally well tolerated, but like all medicines, can cause unwanted effects in
some patients. The most common effects, affecting less than 1 in 10 people, are constipation,
diarrhoea headache and feeling dizzy.

 
STOP taking Famotidine and seek medical attention immediately if you notice any
of the following:


Allergic reactions including rash, itching or hives , shortness of breath, wheezing or trouble
breathing, and swelling of the face, hands, feet, mouth, throat or eyes.
yellowing of the skin or whites of the eyes, dark urine, pale stool; which may be signs
of liver problems..
A severe blistering rash in which the surface layers of the skin peel.(e.g. StevensJohnson syndrome or condition known as Toxic Epidermal Necrolysis(TEN)





Also fever with sore throat or mouth ulcers, unusual bruising or bleeding of the skin, severe
skin reactions, including severe blistering of the lips eyes and mouth, tightness in the chest,
shortness of breath and a cough, a lung infection (pneumonia) which may be severe, muscle
cramps, joint pain, .



Very rarely, patients given this type of medicine by injection, have experienced an irregular
heart beat

Uncommon side effects, affecting less than 1 in 100 people, include skin rash, dry mouth, feeling
unusually tired or weak, feeling or being sick, stomach upset, loss of appetite, changes in taste, wind,
loss of weight and feeling bloated.
Rare effect, seen in less than 1 in 1000 people include swollen breasts in men - but it is not certain this
effect is caused by Famotidine.

Very rare effects, seen in less than 1 in 10,000 people, include depression, confusion, feeling
disorientated, hallucinations, feeling anxious or agitated. Impotence or loss of libido, tingling or
numbness in the fingers and toes, fits, difficulty sleeping, drowsiness, a change in blood liver enzymes
or suffering from hair loss
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 the sideeffects directly via the Yellow Card
Scheme at www.mhra.gov.uk/yellowcard. By reporting side effects you can help provide more
information on safety of this medicine.
STORING FAMOTIDINE 20 mg & 40 mg TABLETS

 
Keep




Famotidine Tablets out of the reach and sight of children.
Do not store above 25°C. Store in the original package.
Do not take this medicine after the expiry date shown on the label.
On the label you will find the letters 'Exp' followed by some numbers. These numbers are the
date when the medicine is no longer fit for use.
 Do not use this medicine after this date.

 
Date of leaflet preparation:
Date of leaflet revision: March 2014

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Source: Medicines and Healthcare Products Regulatory Agency

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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