Viewing nowYoungpoong Famotidine Tablets
Famotidine 20mg
Prescription medication
Youngpoong Pharmaceutical Co., Ltd.

MFDS item code 198701520 · Notified 1987.04.16
Improvement of gastric ulcers and upper gastrointestinal bleeding (peptic ulcers, acute stress ulcers)
This medication is effective for peptic ulcer diseases such as gastric and duodenal ulcers, junctional ulcers, and upper gastrointestinal bleeding. It improves bleeding from acute stress ulcers or hemorrhagic gastritis and is also used in the treatment of gastroesophageal reflux disease and Zollinger-Ellison syndrome. Additionally, it helps improve gastric mucosal lesions (erosion, bleeding, redness, swelling) during acute exacerbations of acute gastritis and chronic gastritis. The injectable form is also used prior to anesthesia and is particularly effective for treating upper gastrointestinal bleeding. This drug alleviates various symptoms associated with gastrointestinal disorders and protects the gastric mucosa, improving digestive health.
Oral administration: 20 mg once, twice a day (after breakfast, after dinner, or at bedtime) or 40 mg once a day (at bedtime). Alternatively, 10 mg once, twice a day (after breakfast, after dinner, or at bedtime) or 20 mg once a day (at bedtime). Injectable form: Dissolve 20 mg in 20 ml of normal saline or dextrose solution and slowly administer intravenously twice a day (every 12 hours).
This medication should not be used in certain patients. Individuals allergic to this drug or similar drugs should not take it. Additionally, since it contains lactose, patients with genetic conditions that affect lactose digestion should avoid using this medication. Patients who should use this medication with caution include those with a history of drug allergies, patients with impaired kidney function, patients with heart diseases, patients with compromised liver function, and the elderly. In particular, patients with poor kidney function may need to reduce the dosage or extend the dosage interval due to the risk of increased drug concentration. This medication can cause various serious side effects. Rarely, shock or severe allergic reactions may occur, so if any unusual symptoms develop during use, the medication should be discontinued immediately and medical attention sought. Symptoms such as decreased blood cell count, anemia, or bleeding may require regular blood tests. Also, severe inflammatory reactions in the skin and mucosa, liver dysfunction, muscle breakdown, cardiac arrhythmias, loss of consciousness, nephritis, pneumonia, etc., may occur; thus, the medication should be discontinued if any abnormal symptoms arise. Common side effects may include skin rash, constipation, diarrhea, nausea, headache, drowsiness, dizziness, blood pressure changes, liver function abnormalities, neuropsychiatric symptoms, etc. If these symptoms are severe, the medication should be discontinued. During treatment, the therapeutic progress should be monitored closely, and if it proves ineffective, it is advisable to switch to other treatment methods. The tablets should dissolve in the mouth but should not be absorbed via the mucosa, so they must be swallowed with saliva or water. Patients undergoing hemodialysis should be cautious when taking this medication with phosphate binders, as it may affect calcium absorption. This medication can interact with other drugs. In particular, taking it with certain antifungals or some anticancer agents may reduce its effectiveness or conversely alter the concentration of other drugs, so it is essential to consult with a doctor or pharmacist. Elderly patients may be at risk of increased drug concentration due to decreased kidney function and should use it with caution, including dosage reduction or increased intervals. Women who are pregnant or may become pregnant should carefully consider the risks and benefits of taking this medication, as its safety during pregnancy has not been established. Additionally, this medication may pass into breast milk, so it is recommended that nursing mothers discontinue breastfeeding while on this medication. In children, the safety of this medication has not been sufficiently established, and experience with use is limited, so caution is necessary. This orally disintegrating tablet should be placed on the tongue and dissolved with saliva before swallowing and should not be taken lying down without water. Lastly, this medication may mask the symptoms of gastric cancer, so it should only be used after confirming that it is not gastric cancer.
Shock, hypersensitivity (anaphylaxis, dyspnea, generalized flushing, angioedema, urticaria), pancytopenia, agranulocytosis, aplastic anemia, hemolytic anemia, thrombocytopenia, Stevens-Johnson syndrome, Lyell's syndrome, liver dysfunction, jaundice, rhabdomyolysis, QT interval prolongation, ventricular tachycardia, ventricular fibrillation, altered consciousness, seizures, interstitial nephritis, acute renal failure, interstitial pneumonia, cardiac failure
Not everyone experiences these, and they can vary from person to person.
This medication should be stored at room temperature away from direct sunlight and must be kept in a tightly sealed container to prevent air or moisture ingress.
White round sugar-coated tablet
100 tablets/bottle, 500 tablets/bottle, 1000 tablets/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.
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For anything that needs medical judgment, consult a doctor or pharmacist.
This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.