Iranitidine Tablets (Ranitidine Hydrochloride)
Ranitidine Hydrochloride 168mg
Tablet · Prescription medication
Iworld Pharmaceutical Co., Ltd.
MFDS item code 201309682 · Approved 2013.10.11
This product's status changed to Expired on 2023.10.11. It may no longer be sold, so consult a doctor or pharmacist before taking it.
Improvement of gastric and duodenal ulcers and gastric mucosal lesions, relief of excess stomach acid
This medication is effective for various gastrointestinal disorders such as gastric and duodenal ulcers, Zollinger-Ellison syndrome, and gastroesophageal reflux disease. It is administered to prevent Mendelson's syndrome before surgery and helps in the treatment of ulcers after surgery. Additionally, it is used for gastric and duodenal ulcers caused by non-steroidal anti-inflammatory drugs (NSAIDs). It is also effective in improving gastric mucosal lesions associated with acute and chronic gastritis, acute exacerbation of gastric disorders, and upper gastrointestinal bleeding. In summary, this medication is used to improve various gastric-related diseases and symptoms.
For adults, the administration of ranitidine should be 150 mg per dose, taken twice daily, in the morning and at bedtime. 1) For gastric and duodenal ulcers: 150 mg once or twice daily or 300 mg once daily at bedtime; for duodenal ulcer patients, 300 mg may be administered twice daily. 2) For gastroesophageal reflux disease: 150 mg twice daily for 8 weeks or 300 mg once daily before bedtime.
For children aged 8 to 18 years, a single dose of 150 mg (2 mg per kg of body weight) may be administered up to twice a day.
This medication should not be used in patients who have had allergic reactions to this medication or its ingredients. It should not be administered to patients with a history of acute porphyria due to the risk of provoking seizures. Furthermore, patients who are genetically unable to break down lactose should not use this medication as it contains lactose. In patients with impaired kidney function, dosage should be reduced or the dosing interval should be increased as this medication may remain in the body for an extended period. Caution is also advised in patients with liver dysfunction. Patients with a history of drug allergies or elderly patients should be administered this medication carefully. Patients taking non-steroidal anti-inflammatory drugs may have an increased risk of gastrointestinal bleeding and should be monitored regularly. Gastric ulcer patients or those with new dyspeptic symptoms in middle age or older should verify malignancy status before use, as this medication may mask gastric cancer symptoms. Patients with Helicobacter pylori-associated gastric or duodenal ulcers should undergo eradication treatment simultaneously. This medication can rarely cause serious allergic reactions, blood abnormalities, liver dysfunction, cardiac rhythm issues, gastrointestinal symptoms, neurological disorders, and skin rashes. If any unusual symptoms occur, take the medication off immediately and consult a doctor. It is important to have regular blood, liver, and kidney function tests during treatment. Elderly patients or those with chronic diseases may be at increased risk of pneumococcal infections and should be cautious. Avoid driving or operating dangerous machinery if dizziness or drowsiness occurs after taking this medication. Be sure to inform your doctor or pharmacist of any other medications being taken due to potential drug interactions, especially with drugs that affect blood coagulation. This medication should be administered cautiously in pregnant or potentially pregnant women and nursing mothers only when necessary. Safety in children has not been fully established, so caution is necessary. This medication is primarily excreted via the kidneys, so elderly patients may require dosage adjustments due to decreased kidney function. Overdose is rarely associated with specific symptoms, but treatment may include vomiting or gastric lavage as appropriate. This medication should be stored out of the reach of children and should not be transferred to other containers. Long-term use may affect the eyes, so it is advisable to undergo ophthalmic examinations.
Shock (anaphylaxis), angioedema, bronchospasm, severe allergic reactions (urticaria, severe swelling), vascular edema, severe skin reactions (severe rash, blisters, skin peeling, pain in mucous membranes of the mouth/eyes), respiratory issues (difficulty breathing, asthma attacks, cough with fever accompanying respiratory issues), jaundice (yellowing of the skin or eyes, generalized lethargy), severe neurological symptoms (sudden and extremely severe headache)
Urticaria, rash, fever, hypotension, chest pain, abnormal blood tests (granulocytopenia, leukopenia, thrombocytopenia, eosinophilia), liver dysfunction (increased AST, ALT, γ-GTP, ALP levels), bradycardia, heart block, tachycardia, constipation, nausea, vomiting, abdominal bloating, abdominal pain, loss of appetite, diarrhea, dizziness, drowsiness, headache, heaviness, insomnia, agitation, anxiety, mental confusion, depression, hallucinations, blurred vision, involuntary movements
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a tightly sealed container that blocks light and in a dry place free from moisture. This storage method will help maintain the efficacy of the medication for a longer period.
White round film-coated tablet
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.