Medication info

Gadin Injection (Ranitidine Hydrochloride)

Prescription medicationInjections경구 · 근육 · 정맥Expired
Ingredient · strength
Ranitidine Hydrochloride›56mg / 1 ampoule
Manufacturer / importer
유니메드제약(주)
Appearance
An ampoule containing a light yellow transparent solution
Packaging
50 ampoules
Approval status
Expired

MFDS item code 199102954 · Notified 1991.11.08

This product's status changed to Expired on 2025.04.01. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

Main use
Treatment of gastrointestinal diseases such as gastric and duodenal ulcers and gastroesophageal reflux.
Who uses it
Adults
Adult dosage
As ranitidine, administer 50mg intravenously or intramuscularly 3-4 times a day. For intravenous administration, dilute this medication 50mg in 20ml of normal saline or dextrose solution and administer slowly for at least 2 minutes or mix it in infusion and deliver it at a rate of 25mg/hr over 2 hours. In the case of pre-anesthesia dosing, administer 50mg intramuscularly or slowly intravenously over 1 minute, 45-60 minutes before anesthetic induction.

Ingredients

Manufacturer
유니메드제약(주)

Efficacy & effects

Treatment of gastrointestinal diseases such as gastric and duodenal ulcers and gastroesophageal reflux.

  • Gastric ulcer
  • duodenal ulcer
  • Zollinger-Ellison syndrome
  • gastroesophageal reflux disease
  • Mendelson's syndrome
  • post-operative ulcers
  • upper gastrointestinal bleeding
  • peptic ulcer
  • acute stress ulcer
  • acute gastric mucosal lesions
View approved original text

This medication is effective in treating gastrointestinal diseases such as gastric and duodenal ulcers, Zollinger-Ellison syndrome, and gastroesophageal reflux disease. It is also administered to prevent Mendelson's syndrome before anesthesia and is used for ulcer treatment after surgery. Additionally, it helps in the treatment of upper gastrointestinal bleeding, acute stress ulcers, and acute gastric mucosal lesions. It acts safely and effectively on various gastrointestinal-related diseases, improving patients' symptoms.

Dosage and Administration

Adult dosage

As ranitidine, administer 50mg intravenously or intramuscularly 3-4 times a day. For intravenous administration, dilute this medication 50mg in 20ml of normal saline or dextrose solution and administer slowly for at least 2 minutes or mix it in infusion and deliver it at a rate of 25mg/hr over 2 hours. In the case of pre-anesthesia dosing, administer 50mg intramuscularly or slowly intravenously over 1 minute, 45-60 minutes before anesthetic induction.

Precautions

This medication should not be administered to patients with hypersensitivity to its components. Patients with impaired renal function may experience prolonged retention of this medication in the body, which can increase the risk of side effects; therefore, use caution by reducing the dosage or extending the administration interval. Caution is also needed for patients with impaired liver function, those with a history of drug hypersensitivity, and elderly patients. Patients with a rare history of acute porphyria should not use this medication. This medication may rarely cause serious allergic reactions, Blood abnormalities, liver dysfunction, cardiac problems, gastrointestinal symptoms, neurological anomalies, skin rashes, etc. If any abnormal symptoms occur, discontinue administration immediately and inform a healthcare provider. During treatment, regular blood tests, liver function tests, and renal function tests should be performed to monitor for abnormalities. Elderly patients or those with chronic pulmonary diseases, diabetes, or weakened immune systems should be cautious as they may have an increased risk of pneumonia. If high doses of this medication are administered intravenously for more than 5 days, liver enzyme levels may rise, and daily liver function tests are recommended. If oral administration is possible, it is advisable to switch to an oral form; this medication should only be used when oral administration is difficult. This medication may interact with other drugs, necessitating dosage adjustment or discontinuation of concomitant medications; therefore, it's essential to inform healthcare providers of any medications currently being taken. Pregnant women or those who might become pregnant and nursing mothers should only use this medication cautiously if necessary. The safety of this medication in pediatric patients has not been adequately established, so caution is advised for use. This medication may affect the results of certain clinical tests; thus, it is important to inform healthcare professionals during testing. In the event of overdose, emergency measures such as inducing vomiting or gastric lavage may be necessary, and in severe cases, blood dialysis may be required. Administration via injection may cause pain or induration at the injection site, and in patients at risk of abnormal heart rate, the infusion should be done slowly. This medication can mask symptoms of stomach cancer; therefore, gastric ulcer patients or those experiencing new or worsening dyspeptic symptoms in middle age should have malignancy ruled out before administration. Regular eye examinations are recommended to check eye health during long-term administration.

Side effects and when to seek care immediately

Serious side effects

  • Urticaria
  • angioedema
  • fever
  • bronchospasm
  • hypotension
  • chest pain
  • vascular edema
  • anaphylactic shock
  • jaundice
  • hepatitis
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  • altered consciousness
  • seizures
  • myoclonus
  • generalized weakness
  • skin or mucosal hemorrhage
  • fever
  • acute porphyric attacks
  • rhabdomyolysis
  • Stevens-Johnson syndrome
  • Lyell syndrome
  • aplastic anemia
  • heart block
  • acute interstitial nephritis.

Mild side effects

Granulocytopenia, increased serum creatinine, leukopenia, thrombocytopenia, bone marrow suppression, aplastic anemia, hypoplastic anemia, agranulocytosis, pancytopenia, autoimmune hemolytic anemia, eosinophilia, transient and reversible liver dysfunction (elevated AST, ALT, γ-GTP, ALP levels), bradycardia, heart block, tachycardia, vasculitis, cardiac arrest, constipation, nausea, vomiting, abdominal bloating, abdominal pain, loss of appetite,

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

Storage

This medication should be stored in a sealed container to protect it from air and light. It is advisable to keep it at room temperature and avoid direct sunlight. Proper storage helps maintain the medication's efficacy.

Appearance and packaging

Appearance

An ampoule containing a light yellow transparent solution

Package unit

50 ampoules

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.

Questions about this medicine

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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.