Diarix Tablet (Furosemide)
Furosemide 40mg
Tablet · Prescription medication
Shinil Pharmaceutical Co., Ltd.
MFDS item code 197500450 · Notified 1975.03.13
This product's status changed to Expired on 2024.04.01. It may no longer be sold, so consult a doctor or pharmacist before taking it.
Treatment of edema (cardiac, renal, hepatic, etc.) and hypertension
This medication is used to treat hypertension and cardiac edema resulting from decreased heart function, renal edema caused by kidney disease, hepatic edema due to liver disease, and peripheral vascular edema. In injectable form, it is also effective for the treatment of acute pulmonary edema. It helps manage various forms of edema and hypertension, improving the patient's symptoms.
(Oral: tablets) Adults: Administer 20-80㎎ of furosemide orally once daily, continuously or every other day. If the effect is insufficient, increase the dose by 20-40㎎ every 6-8 hours and administer 1-2 times daily. In severe cases, up to 600㎎ per day may be administered. For hypertension, administer 80㎎ per day in 2 divided doses. If the effect is insufficient, administer in combination with another antihypertensive agent (e.g., reserpine). (Injection) Adults: Inject 20-40㎎ of furosemide intravenously or intramuscularly once daily. If the effect is insufficient, increase the dose by 20㎎ every 2 hours and inject 1-2 times daily.
(Oral: tablets) Children: Administer 2㎎ per ㎏ of body weight of this medicine. If the effect is insufficient, increase the dose by 1-2㎎ per ㎏ of body weight every 6-8 hours. (Injection) Children: Inject 1㎎ per ㎏ of body weight intravenously or intramuscularly. Increase the dose by 1㎎ per ㎏ of body weight every 2 hours and inject.
This medication is a powerful diuretic that expels water and salt from the body. Overdosage may lead to dehydration and electrolyte imbalance, requiring regular blood tests and dosage adjustments. Patients with allergies to this medication, severe dehydration, or severely impaired kidney function should not take it. Pregnant or breastfeeding women should also avoid this medication, and caution is warranted as serious side effects may occur when taken with certain medications. Patients with urinary retention, cardiovascular diseases, diabetes, liver disease, or kidney disease should use this medication carefully under strict medical observation. Regular monitoring of blood pressure, electrolyte levels, and kidney function is necessary during use, and immediate action should be taken if dehydration or electrolyte imbalances occur. Elderly patients are particularly at risk of dizziness and fainting due to low blood pressure and dehydration, so they should start at lower doses and be closely monitored. It is advisable to avoid hazardous activities such as work at heights or operating heavy machinery while taking this medication. This medication is best taken on an empty stomach, and consultation with a doctor is recommended if taken with certain other medications, as this may affect side effects or efficacy. In the case of overdose, immediate medical attention should be sought, and electrolyte and fluid status must be corrected. This medication should be stored out of reach of children and should not be transferred to other containers.
Hyponatremia, Hypochloremia, Hypokalemia, Hypocalcemia, Hypomagnesemia, Electrolyte disturbance, Metabolic alkalosis, Dehydration, Hypovolemia, Increased serum creatinine and urea, Increased serum cholesterol and triglycerides, Increased serum uric acid, Gout attacks, Impaired glucose tolerance, Pseudo-Bartter syndrome, Arrhythmia, Orthostatic hypotension, Thrombosis, Vasculitis, Acute urinary retention, Interstitial nephritis, Renal calcification, Kidney stones, Increased BUN and serum creatinine, Increased urine output, Increased urinary sodium and chloride, Renal failure, Thirst, Nausea, Vomiting, Diarrhea, Acute pancreatitis, Anorexia, Intrahepatic cholestasis, Increased liver transaminases, Jaundice, Visual disturbances, Hearing impairment, Tinnitus, Hearing loss, Itching, Urticaria, Rash, Blistering dermatitis, Erythema multiforme, Exfoliative dermatitis, Stevens-Johnson syndrome, Toxic epidermal necrolysis, Pemphigus-like lesions, Acute generalized pustular rash, Purpura, Photosensitivity reactions, Drug-induced rash (DRESS), Licheniform reactions, Anaphylaxis, Systemic lupus erythematosus exacerbation, Sensory disturbances, Hepatic encephalopathy, Decreased concentration, Reduced responsiveness, Confusion, Dizziness, Heaviness, Lightheadedness, Drowsiness, Weakness, Syncope, Loss of consciousness, Thrombocytopenia, Leukopenia, Neutropenia, Agranulocytosis, Eosinophilia, Anemia, Aplastic anemia, Hemolytic anemia, Blood hyperviscosity, Muscle cramps, Stiffness, Myasthenia, Increased risk of patent ductus arteriosus, Pain at the site of intramuscular injection, Fever, Weakness, Fatigue
Not everyone experiences these, and they can vary from person to person.
This medication may be sensitive to light; therefore, it should be stored in an opaque and airtight container to prevent degradation and maintain its effectiveness.
White round tablet
30 tablets/bottle, 250 tablets/bottle, 1000 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.