Quran Injection 50 mg (Ranitidine Hydrochloride)
Ranitidine Hydrochloride 56mg
Prescription medication
Ildong Pharmaceutical Co., Ltd.
MFDS item code 198600224 · Notified 1986.04.04
This product's status changed to Approval withdrawn on 2024.07.30. It may no longer be sold, so consult a doctor or pharmacist before taking it.
Treatment of gastric and duodenal ulcers and gastroesophageal reflux disease.
This medication is effective in treating gastric and duodenal ulcers, Zollinger-Ellison syndrome, and gastroesophageal reflux disease. It is also used to prevent Mendelson's syndrome during preoperative anesthesia and helps treat ulcers that may arise post-surgery. Additionally, it is used to treat upper gastrointestinal bleeding due to acute stress ulcers and acute gastric mucosal lesions. This drug is effective in improving various gastrointestinal conditions.
As ranitidine, administer 50 mg intravenously or intramuscularly 3-4 times daily. For intravenous administration, dilute 50 mg in 20 mL of normal saline or dextrose solution and administer slowly over at least 2 minutes, or mix it in IV fluid and administer as a continuous intravenous drip at a rate of 25 mg/hr over 2 hours. For pre-anesthetic medication (to prevent Mendelson's syndrome), administer 50 mg intramuscularly or slowly intravenously over 1 minute 45-60 minutes before anesthesia onset.
Clinical studies for pediatric use have not been established.
This medication should be opened carefully as it comes in glass ampoules to prevent glass fragments from mixing in, especially with children and the elderly. It should not be used in patients with a history of allergic reactions to this drug or its components. In patients with impaired kidney function, the drug may remain in the body for an extended period, thus the dosage should be reduced or the dosing interval extended. Patients with poor liver function, a history of drug allergies, the elderly, and those with acute porphyria should use this medication with caution. While using this medication, severe allergic reactions, blood disorders, liver dysfunction, irregular heartbeats, gastrointestinal issues, or neurological symptoms may occur; if any unusual symptoms arise, discontinue use and seek medical attention immediately. It is vital to monitor the patient's condition regularly and perform blood tests, liver function tests, and kidney function tests during treatment. Elderly patients or those with chronic diseases may be at increased risk of pneumonia, so caution is warranted. If this medication is to be injected intravenously for more than five days, there is a possibility of elevated liver enzyme levels, so daily liver function tests are recommended. If oral administration is possible, it is advised to switch to oral medication as soon as feasible. This medication may interact with other drugs, so it is essential to inform the doctor or pharmacist if other medications are being taken, especially when used with anticoagulants, as there may be an increased risk of bleeding. Women who are pregnant or may become pregnant, as well as nursing women, should carefully weigh the risks and benefits of using this medication. The safety of this drug in children has not been adequately established, thus caution is advised. In cases of overdose, gastric emptying treatment should be received along with appropriate symptomatic treatment, and blood dialysis may be performed if necessary. When administrating the injection, pain or hardness at the injection site may occur, and there is a risk of irregular heartbeats; therefore, the injection should be administered slowly. This medication may mask the symptoms of stomach cancer, so patients with gastric ulcers or newly developed dyspepsia who are middle-aged or older should be checked for malignancy before use. Long-term use may affect eye health, so regular ophthalmological examinations are necessary.
Rash, fever, angioedema, hypotension, chest pain, vascular edema, granulocytopenia, elevated serum creatinine levels, leukopenia, thrombocytopenia, liver function impairment (increased AST, ALT, γ-GTP, ALP levels), bradycardia, atrioventricular block, tachycardia, vasculitis, constipation, nausea, vomiting, abdominal distension, abdominal pain, loss of appetite, diarrhea, dizziness, drowsiness, headache, heaviness in the head, insomnia, agitation, anxiety, confusional state, depression, hallucination.
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a cool place below 30 degrees Celsius, protected from light in a sealed container, to maintain its efficacy for a longer period.
A clear liquid that is colorless to light yellow in color, packaged in brown ampoules.
50 ampoules/box [(2 mL/ampoule)]
Even with the same ingredient, strength, dosage form and how it is taken can differ.
Ranitidine Hydrochloride 56mg
Prescription medication
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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.