Medication info

Megapudin Tablet 10mg (Lafutidine)

Prescription medicationTabletOralApproval withdrawn
Ingredient · strength
Lafutidine›10mg / 1 tablet
Manufacturer / importer
LNC Bio Co., Ltd.
Appearance
White round film-coated tablet
Packaging
30 tablets/bottle, 300 tablets/bottle
Approval status
Approval withdrawn

MFDS item code 202001514 · Approved 2020.03.04

This product's status changed to Approval withdrawn on 2024.09.04. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

Main use
Treatment and improvement of gastrointestinal disorders (ulcers, gastritis, etc.); preanesthetic medication; combination therapy for eradication
Who takes it
Adults
Adult dose
1. Short-term treatment of gastric ulcers: The usual dose is 10 mg of lafutidine orally twice daily, in the morning and at bedtime. In clinical trials with treatment for up to 8 weeks, most ulcers healed within 8 weeks, although the healing period may vary among patients. 2. Short-term treatment of duodenal ulcers: The usual dose is 10 mg of lafutidine orally twice daily, in the morning and at bedtime. In clinical trials with treatment for up to 6 weeks, most ulcers healed within 6 weeks, although the healing period may vary among patients. 3. Improvement of gastric mucosal lesions in acute and chronic gastritis: The usual dose is 10 mg of lafutidine orally once daily at bedtime. In clinical trials with treatment for up to 2 weeks, most lesions healed within 2 weeks, although the healing period may vary among patients. 4. Concomitant antibiotic therapy in patients with peptic ulcers infected with Helicobacter pylori: Administer lafutidine 20mg, clarithromycin 500mg, and amoxicillin 1000mg twice daily for 7 or 14 days. 5. Premedication for anesthesia: The usual dose is 10 mg of lafutidine per dose, administered orally twice (at bedtime on the day before surgery and 2 hours before anesthesia on the day of surgery). 6. Treatment of reflux esophagitis: Administer 10 mg of lafutidine per dose orally twice daily.

Ingredients

Manufacturer
LNC Bio Co., Ltd.

Efficacy & effects

Treatment and improvement of gastrointestinal disorders (ulcers, gastritis, etc.); preanesthetic medication; combination therapy for eradication

  • Gastric ulcers
  • duodenal ulcers
  • acute gastritis
  • chronic gastritis
  • gastric mucosal lesions
  • peptic ulcers
  • gastroesophageal reflux disease
View approved original text

This medication is used to treat gastric ulcers and duodenal ulcers. It also improves gastric mucosal damage caused by acute and chronic gastritis, and is used in combination with antibiotics for patients with peptic ulcers due to Helicobacter pylori infection. It is effective for the treatment of gastroesophageal reflux disease and is administered to patients before anesthesia to assist with necessary preparations. It is used to improve symptoms associated with various gastrointestinal disorders.

How to take

Adult dose

1. Short-term treatment of gastric ulcers: The usual dose is 10 mg of lafutidine orally twice daily, in the morning and at bedtime. In clinical trials with treatment for up to 8 weeks, most ulcers healed within 8 weeks, although the healing period may vary among patients. 2. Short-term treatment of duodenal ulcers: The usual dose is 10 mg of lafutidine orally twice daily, in the morning and at bedtime. In clinical trials with treatment for up to 6 weeks, most ulcers healed within 6 weeks, although the healing period may vary among patients. 3. Improvement of gastric mucosal lesions in acute and chronic gastritis: The usual dose is 10 mg of lafutidine orally once daily at bedtime. In clinical trials with treatment for up to 2 weeks, most lesions healed within 2 weeks, although the healing period may vary among patients. 4. Concomitant antibiotic therapy in patients with peptic ulcers infected with Helicobacter pylori: Administer lafutidine 20mg, clarithromycin 500mg, and amoxicillin 1000mg twice daily for 7 or 14 days. 5. Premedication for anesthesia: The usual dose is 10 mg of lafutidine per dose, administered orally twice (at bedtime on the day before surgery and 2 hours before anesthesia on the day of surgery). 6. Treatment of reflux esophagitis: Administer 10 mg of lafutidine per dose orally twice daily.

Precautions

This medication should not be used in patients who are allergic to any component of this product. This medication contains lactose, so it should not be taken by patients with a genetic condition that prevents lactose digestion. Patients who have had a hypersensitivity to medications, those with compromised liver or kidney function, patients undergoing dialysis, and the elderly should use this medication with particular caution. This medication can rarely cause severe allergic reactions; if symptoms such as paleness, low blood pressure, or difficulty breathing develop, usage should be stopped immediately and medical attention sought. Liver function may deteriorate or jaundice symptoms may appear, so liver health should be monitored regularly, and if abnormalities are found, medication should be stopped and treatment initiated. There can be a decrease in the number of white blood cells or platelets in the blood; if symptoms such as sore throat, fatigue, or fever occur, consult a physician immediately. Rarely, severe side effects such as skin rash, convulsions, or cardiac rhythm disturbances have been reported, so caution is warranted. Common side effects may include constipation, diarrhea, headache, insomnia, dizziness, abdominal pain, and loss of appetite. Gastrointestinal symptoms may especially occur in patients with gastric ulcers or gastroesophageal reflux disease, so monitoring is essential. While taking this medication, there is a potential for concealed malignancies, so if symptoms such as weight loss, recurrent vomiting, or hematemesis occur, testing should be performed. Elderly patients may have diminished physical function, so medication dosages and intervals should be adjusted carefully. Dialysis patients may experience increased drug concentrations in the blood, so should start at a lower dose and proceed cautiously. Pregnant women should only use this medication when the benefit outweighs the risk under a physician's judgment, and nursing women are advised not to take this medication as it may be excreted in breast milk. This medication has not been established as safe for children, so its use is not recommended. This medication should be kept out of reach of children and stored in its original container to maintain the quality and safety of the drug.

Side effects

  • Shock
  • anaphylactic symptoms
  • facial pallor
  • hypotension
  • generalized rash
  • dyspnea
  • liver dysfunction
  • jaundice
  • agranulocytosis
  • pharyngitis
Show 79 more
  • generalized malaise
  • fever
  • thrombocytopenia
  • pancytopenia
  • aplastic anemia
  • seizures
  • interstitial nephritis
  • Stevens-Johnson syndrome
  • Riel syndrome
  • rhabdomyolysis
  • heart block
  • heart failure
  • constipation
  • diarrhea
  • hard stools
  • nausea
  • vomiting
  • abdominal bloating
  • anorexia
  • headache
  • insomnia
  • drowsiness
  • reversible confusional state
  • hallucinations
  • consciousness disturbance
  • dizziness
  • heat sensation
  • facial flushing
  • leukocytosis
  • eosinophilia
  • leukopenia
  • erythrocytopenia
  • reduced hematocrit
  • elevated ALT
  • elevated AST
  • elevated Al-P
  • elevated γ-GTP
  • elevated T-Bil
  • elevated LDH
  • elevated TTT
  • abnormal urine protein
  • elevated BUN
  • increased serum uric acid
  • elevated Cl
  • delayed maturation
  • elevated Na
  • reduced K
  • gynecomastia
  • edema
  • malaise
  • glossitis
  • headache
  • urticaria
  • skin rash
  • abdominal pain
  • dyspepsia
  • enteritis
  • gastric ulcer
  • erosive gastritis
  • duodenitis
  • bloating
  • nasopharyngitis
  • upper respiratory infection
  • bronchopneumonia
  • tinea
  • cough
  • oral-pharyngeal pain
  • oral-pharyngeal discomfort
  • wet cough
  • fatigue
  • chest pain
  • limb pain
  • joint pain
  • neck pain
  • itching
  • acne
  • contusion
  • insomnia
  • non-alcoholic steatohepatitis

Not everyone experiences these, and they can vary from person to person.

Storage

This medication should be stored in a tightly sealed container to protect it from air and moisture. It is advisable to maintain storage temperatures between 1 degree and 30 degrees Celsius.

Appearance and packaging

Appearance

White round film-coated tablet

Package unit

30 tablets/bottle, 300 tablets/bottle

Same-ingredient medicines

Even with the same ingredient, strength, dosage form and how it is taken can differ.

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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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.