Aiprojen Clarithromycin Tablet 500mg

Adult dose

○ Adults: The usual dose of clarithromycin is 250mg (potency) twice daily. For severe infections, administer 500mg (potency) twice daily. The usual duration of treatment is 7～14 days. In patients with renal failure and creatinine clearance of 30mL/min or less, the dose should be reduced by half: 250mg (potency) once daily, or, for severe infections, 250mg (potency) twice daily. Do not administer for more than 14 days to these patients. ○ Mycobacterial infections: Administer 500mg (potency) twice daily as this medicine. In this case, it should be administered in combination with other antimycobacterial agents, such as ethambutol, clofazimine, or rifampin. ○ Eradication of Helicobacter pylori in patients with duodenal ulcer: Administer 500mg (potency) of this medicine 3 times daily in combination with omeprazole 40mg once daily for 14 days, followed by omeprazole 40mg once daily for 14 consecutive days. That is, administer clarithromycin 500mg (potency) 3 times daily for 14 days (days 1～14), and omeprazole 40mg once daily for 28 days (days 1～28).

Child dose

Children aged 12 years or older: Same as adults Children under 12 years: Use clarithromycin dry syrup.

This medication should not be administered to patients with allergies to certain components. Patients with hypersensitivity to clarithromycin or similar antibiotics should avoid using this drug. It is advisable for patients with heart rhythm problems, severe liver disease, or severe kidney function impairment to avoid this drug. Women who are pregnant or breastfeeding should also refrain from taking this medication. Care is needed as serious side effects may occur when taken in conjunction with other specific medications. This drug could affect liver and kidney function, so patients with related diseases should use it cautiously. During usage, various side effects such as allergic reactions or gastrointestinal disturbances, skin rashes may occur, and if any abnormal symptoms arise, immediate consultation with medical staff is necessary. Caution is advised as prolonged or high-dose usage may cause hearing damage or muscle abnormalities. To prevent antibiotic resistance, this drug should be taken in the correct dosage and duration as directed by a physician. Because there is a high possibility of interactions with other medications, all medications being taken should be disclosed to the medical staff. Women who may become pregnant should confirm their pregnancy status before taking this medication, and if pregnancy is confirmed during usage, they should immediately consult a doctor. Elderly patients and children require careful monitoring and dosage adjustments when administered. Dizziness or confusion may occur when driving or operating machinery, so caution is advised. In case of overdose, serious side effects may arise, therefore it is important to adhere to the prescribed dosage, and if any overdose happens, immediate medical attention should be sought. When storing, avoid direct sunlight and keep in a cool place; refrigeration is not recommended.

Shock, anaphylactic symptoms, dyspnea, convulsions, flushing, rash, itching, urticaria, skin flushing, angioedema, joint swelling, drug eruption, abdominal distension, nausea, vomiting, dyspepsia, abdominal pain, malaise, flatulence, diarrhea, oral mucosal erosion, upper abdominal pain, thirst, transient dental discoloration, pancreatitis, increased amylase, dysgeusia, anorexia, constipation, fecal discoloration, pseudomembranous colitis, hemorrhagic colitis, fever, cough, abnormal chest X-ray, eosinophilia, eosinophilic lung infiltrates, interstitial pneumonia, chronic bronchitis, acute maxillary sinusitis, eosinophilia, thrombocytopenia, pancytopenia, hemolytic anemia, leukopenia, agranulocytosis, dizziness, depression, loss of taste, loss of smell, anxiety, insomnia, nightmares, tinnitus, confusion, disorientation, hallucination, psychosis, depersonalization, convulsions, tremors, numbness, behavioral changes, manic behavior, Stevens-Johnson syndrome, toxic epidermal necrolysis, allergic purpura, drug rash (DRESS), jaundice, hepatocellular hepatitis, cholestatic hepatitis, increased liver enzymes, liver dysfunction, liver failure, fulminant hepatitis, elevated AST, elevated ALT, elevated γ-GTP, elevated LDH, elevated ALP, increased total bilirubin, anorexia, jaundice, dark urine, pruritus, abdominal tenderness, elevated serum creatinine, elevated BUN, interstitial nephritis, renal failure, rhabdomyolysis, myalgia, weakness, elevated CPK, elevated serum myoglobin, elevated urinary myoglobin, glossitis, stomatitis, oral candidiasis, QT prolongation, ventricular tachycardia, Torsades de pointes, malaise, headache, dysgeusia, hearing loss, paresthesia, arthralgia, myalgia, olfactory dysfunction, tinnitus, hearing impairment, hypoglycemia, tinnitus, hearing loss, vomiting, nausea, abdominal pain, purpuric rash, acute generalized exanthematous pustulosis, injection site phlebitis, injection site pain, injection site inflammation, fever, weakness, chest pain, chills, fatigue, abnormal albumin-globulin ratio, elevated serum alkaline phosphatase, elevated serum lactate dehydrogenase, increased INR, prolonged prothrombin time, abnormal urine color

This medication is sensitive to light and should be stored in a container that prevents light exposure. Additionally, to maintain the efficacy of the medication, it is recommended to store it at room temperature between 15 and 30 degrees Celsius.

Appearance

Yellow oval film-coated tablet

Package unit

30 tablets, 100 tablets