Viewing nowFamogen Tablet (Famotidine)
Famotidine 20mg
Tablet · Prescription medication
Bivocons Pharmaceutical Co., Ltd.

MFDS item code 200401211 · Notified 2004.05.25 · Insurance code 658201570
Improvement of gastric ulcers and upper gastrointestinal bleeding, improvement of gastric mucosal lesions (erosions, bleeding, etc.)
This medication is effective in treating upper gastrointestinal bleeding caused by gastric and duodenal ulcers, anastomotic ulcers, peptic ulcers, acute stress ulcers, and hemorrhagic gastritis. It is also used for gastroesophageal reflux disease and Zollinger-Ellison syndrome. It aids in the improvement of gastric mucosal lesions such as erosions, bleeding, redness, and edema occurring during acute exacerbations of acute and chronic gastritis. This drug treats damage to the gastric mucosa, alleviates symptoms, and helps in patient recovery. Overall, it is used effectively to treat various ulcer and inflammatory diseases of the digestive tract.
For gastric and duodenal ulcers, anastomotic ulcers, upper gastrointestinal bleeding, gastroesophageal reflux disease, Zollinger-Ellison syndrome: Administer 20 mg orally twice a day (after breakfast, after dinner, or at bedtime) or 40 mg orally once a day (at bedtime). Usual treatment for upper gastrointestinal bleeding begins with an injection, and when oral administration becomes possible, it is switched to oral administration. For gastric mucosal lesions in acute gastritis and acute exacerbations of chronic gastritis
This medication should not be used by individuals allergic to its ingredients or other H2 receptor antagonists. Additionally, because it contains lactose, individuals with lactose intolerance or genetic lactose enzyme deficiency should not take this medication. Those who have had allergic reactions to drugs should be cautious when using this medication. Patients with poor kidney function may need to reduce the dosage or extend the interval between doses since the medication may remain in the body longer. Individuals with heart disease should use this medication with caution as cardiovascular side effects may occur. Those with weak liver function should use it carefully as symptoms may worsen. Elderly patients are at higher risk of impaired kidney function, which may lead to increased drug concentration, so caution is needed. During treatment, patients should monitor for signs of allergic reactions, blood abnormalities, skin rashes, liver dysfunction, muscle pain, heart rhythm disturbances, changes in consciousness, kidney issues, and pneumonia symptoms, and should immediately stop taking the medication and consult a doctor if any unusual symptoms occur. During treatment, regular checks should be made on symptoms and blood, liver, and kidney functions, and if ineffective, alternative treatment options may be considered. This medication dissolves in the mouth but is not absorbed through the oral mucosa, so it should be swallowed with water or saliva. Patients on dialysis taking this medication with phosphate binders may experience reduced effectiveness of the phosphate binders. There may be potential interactions with other drugs, so it is important to inform the doctor or pharmacist, especially when taking antifungal agents or certain chemotherapy drugs. Pregnant women or those who may become pregnant should take this medication only if the benefits outweigh the risks and breastfeeding women should discontinue breastfeeding as the drug may pass into breast milk. In children, the safety has not been fully established, so caution is necessary for use. This medication, in its oral dissolving form, can be placed on the tongue and taken after it dissolves in saliva, but should not be taken while lying down. Finally, this medication may hide symptoms of gastric cancer, so it is essential to confirm that it is not gastric cancer before use.
Shock, hypersensitivity (anaphylaxis, difficulty breathing, generalized flushing, angioedema, hives), 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, heart failure
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a tightly sealed container to prevent air and moisture penetration, and it is best stored at room temperature between 1 to 30 degrees Celsius. Storing it this way will help maintain the efficacy of the medication for a long time.
White round film-coated tablet
30 tablets/bottle, 300 tablets/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
Viewing nowFamotidine 20mg
Tablet · Prescription medication
Bivocons Pharmaceutical Co., Ltd.

Famotidine 20mg
Prescription medication
Dong-A ST Co., Ltd.

Famotidine 20mg
Tablet · Prescription medication
JW Pharmaceutical Corporation

Famotidine 20mg
Tablet · Prescription medication
(Stock Company) Ilhwa

Famotidine 20mg
Prescription medication
Youngpoong Pharmaceutical Co., Ltd.

Famotidine 20mg
Tablet · Prescription medication
Withus Pharmaceutical Co., Ltd.

Famotidine 20mg
Prescription medication
(Stock Company) Seoul Pharmaceutical

Famotidine 20mg
Tablet · Prescription medication
(Stock Company) Genupharm
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.
No questions yet.
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.