Viewing nowLansoton LFDT Tablet 15 mg (Lansoprazole)
Lansoprazole 15mg
Orally disintegrating Tablet · Prescription medication
Takeda Pharmaceuticals Korea Co., Ltd.

MFDS item code 200510973 · Approved 2005.04.19 · Insurance code 696300120
Effectively treats duodenal ulcers and gastric ulcers (active, NSAID-induced) and eradicates Helicobacter pylori, treats gastroesophageal reflux disease and erosive esophagitis, and suppresses hypersecretion.
This medication is used for the short-term treatment of active duodenal ulcers and active benign gastric ulcers. It also helps eradicate Helicobacter pylori to prevent recurrence of duodenal ulcers. After treatment, it can be used for maintenance therapy to prevent recurrence of duodenal ulcers. It is effective in treating gastric ulcers caused by nonsteroidal anti-inflammatory drugs and reducing the risk of occurrence. It is also used for the short-term treatment of symptoms related to gastroesophageal reflux disease and erosive esophagitis, and for pathological hypersecretion states such as Zollinger-Ellison syndrome. It is widely used for various gastrointestinal diseases.
This medication should be taken before meals, placed on the tongue to dissolve with saliva or taken with water. It should not be chewed or crushed. 1. Short-term treatment of active duodenal ulcer: 15 mg of lansoprazole taken orally once daily for 4 weeks. 2. Short-term treatment of active benign gastric ulcer: 30 mg of lansoprazole taken orally once daily for 8 weeks. 3. Eradication of Helicobacter pylori to prevent recurrence of duodenal ulcer.
Children and adolescents aged 12 to 17: 1. Short-term treatment of symptoms related to non-erosive gastroesophageal reflux disease: 15 mg once daily for 8 weeks. 2. Short-term treatment of erosive esophagitis: 30 mg once daily for 8 weeks.
This drug contains the artificial sweetener aspartame and should not be taken by patients with the hereditary condition phenylketonuria. Patients with allergies to this drug or its components, or with hypersensitivity reactions to penicillin-type or macrolide antibiotics, should not use this medication. Pregnant women and patients with genetic issues such as lactose intolerance or galactose intolerance should avoid taking it. Patients with a history of drug allergies or reduced liver function, the elderly, breastfeeding women, and children should use this drug with caution. The drug may cause severe allergic reactions, blood abnormalities, liver dysfunction, or skin rashes; if symptoms occur, consult medical personnel immediately. Mild side effects such as headaches, diarrhea, abdominal pain, nausea, and vomiting have also been reported; symptoms should be carefully monitored. Long-term use may lead to vitamin B12 deficiency, hypomagnesemia, and increased fracture risk, necessitating regular check-ups. If gastric ulcers or malignant tumors are suspected, it should be used only after a proper diagnosis, and if side effects occur during treatment, the drug should be discontinued, and appropriate measures taken. There are many interactions with other drugs, so patients taking antibiotics, antivirals, anticoagulants, immunosuppressants, etc., should inform their doctor or pharmacist. Pregnant or breastfeeding women should not take this medication; if unavoidable, consult a specialist before making a decision. Children and elderly patients need dosage adjustments and careful observation; in case of overdose, seek medical attention immediately. Store this medication out of children's reach, and do not transfer it to another container for safety.
Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, generalized rash, facial swelling, difficulty breathing, shock, pancytopenia, agranulocytosis, hemolytic anemia, neutropenia, thrombocytopenia, anemia, jaundice, acute interstitial nephritis, toxic epidermal necrolysis (Lyell syndrome), mucocutaneous syndrome (Stevens-Johnson syndrome), DRESS syndrome, interstitial pneumonia, interstitial nephritis, acute renal failure, membranous colitis.
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 exposure, ideally at room temperature between 1 and 30 degrees Celsius. This helps maintain the drug's effectiveness.
The drug is a white to yellowish-white tablet with red to brown spots.
100 tablets (10 tablets/PTP x 10), 98 tablets (7 tablets/PTP x 14)
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.