Viewing nowPastel Tablet 20 mg (Famotidine)
Famotidine 20mg
Tablet · Prescription medication
Samchundang Pharm. Co., Ltd.

MFDS item code 202000476 · Approved 2020.01.29 · Insurance code 651205380
Improvement of gastric ulcers and gastric mucosal lesions
This medication is used in the treatment of peptic ulcers, including gastric and duodenal ulcers, anastomotic ulcers, and upper gastrointestinal bleeding. It is also effective for gastroesophageal reflux disease and Zollinger-Ellison syndrome. It helps to improve lesions such as erosion, bleeding, redness, and swelling of the gastric mucosa during acute exacerbations of acute and chronic gastritis. This medication contributes to relieving symptoms by protecting the gastric mucosa and reducing gastric acid secretion. It is used to restore the patient's gastrointestinal health and improve symptoms.
For gastric and duodenal ulcers, anastomotic ulcers, upper gastrointestinal bleeding, gastroesophageal reflux disease, Zollinger-Ellison syndrome: Famotidine 20 mg orally twice a day (after breakfast and dinner or at bedtime) or 40 mg once a day (at bedtime). For upper gastrointestinal bleeding, start treatment with an injectable form and switch to oral dosing thereafter. For acute gastritis and acute exacerbation of chronic gastritis: Famotidine 10 mg.
This drug should not be used by patients who are allergic to certain ingredients or have hereditary lactose metabolism disorders. Patients with renal or liver dysfunction, those with heart disease, and the elderly should use this drug with caution. Serious side effects such as allergic reactions, blood anomalies, severe skin conditions, liver dysfunction, muscle damage, cardiac rhythm abnormalities, changes in consciousness, and kidney issues may occur during use, necessitating careful observation. This medication dissolves in the mouth but is not absorbed through the mucosa, so it must be swallowed with water. Patients undergoing hemodialysis should be cautious, as the effectiveness of this medication may decrease when used with phosphate binders. Using this medication together with other specific drugs may reduce the effectiveness of this or other medications, so consulting a doctor or pharmacist is essential. Elderly patients may have decreased renal function, so the dosage should be adjusted or the dosing interval extended. Women who are pregnant or may become pregnant should only use this medication carefully when needed and should consider stopping breastfeeding if using it while nursing. Safety in children has not been fully established, so use should be avoided.
Shock, hypersensitivity (anaphylaxis, dyspnea, generalized flushing, angioedema, urticaria), pancytopenia, agranulocytosis, aplastic anemia, hemolytic anemia, thrombocytopenia, Stevens-Johnson syndrome, Lyell syndrome, liver dysfunction, jaundice, rhabdomyolysis, QT prolongation, ventricular tachycardia, ventricular fibrillation, altered consciousness, seizures, interstitial nephritis, acute renal failure, interstitial pneumonia, contraction failure.
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a tightly closed container to prevent air or moisture ingress. It is best to maintain the storage temperature between 1°C and 30°C.
White round film-coated tablets
30 tablets/bottle, 500 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.