Medication info
Claricin Tablet (Clarithromycin)

Claricin Tablet (Clarithromycin)

Prescription medicationTabletOral
Ingredient · strength
Clarithromycin›250mg / 1 tablet
Manufacturer / importer
Myungmoon Pharmaceutical Co., Ltd.
Appearance
Yellow oval film-coated tablets with a vanilla flavor
Packaging
30 tablets/bottle, 100 tablets/bottle
Approval status
Active

MFDS item code 200403215 · Notified 2004.02.18 · Insurance code 649802940

Summary

Main use
Treatment of infections (respiratory, skin, and mycobacterial infections) and eradication of Helicobacter pylori in duodenal ulcers
Who takes it
Adults · Children
Adult dose
○ Adults: The usual dose of clarithromycin is 250mg (potency) twice daily. For severe infections, the dose is 500mg (potency) twice daily. The usual treatment period is 7~14 days. In patients with renal impairment whose creatinine clearance is 30mL/min or less, the dose should be reduced by half. That is, 250mg (potency) once daily, or, for severe infections, 250mg (potency) twice daily. Do not administer this medicine to these patients for more than 14 days. ○ Mycobacterial infections: The dose of this medicine is 500mg (potency) twice daily. In this case, it must be administered in combination with other antimycobacterial agents such as ethambutol, clofazimine, and rifampin. ○ Eradication of Helicobacter pylori in patients with duodenal ulcers: Administer this medicine at 500mg (potency) three 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 at 500mg (potency) three times daily for 14 days (days 1~14), and administer omeprazole 40mg once daily for 28 days (days 1~28). ○ Children aged 12 years and older: same as adults
Child dose
For children under 12 years of age, use clarithromycin dry syrup.

Ingredients

Manufacturer
Myungmoon Pharmaceutical Co., Ltd.

Efficacy & effects

Treatment of infections (respiratory, skin, and mycobacterial infections) and eradication of Helicobacter pylori in duodenal ulcers

  • Bronchitis
  • pneumonia
  • pharyngitis
  • sinusitis
  • skin and skin structure infections
  • mycobacterial infections
  • duodenal ulcers
View approved original text

This drug is effective in treating infections caused by various bacteria. It is particularly used for lower respiratory tract infections such as bronchitis and pneumonia, as well as upper respiratory tract infections such as pharyngitis and sinusitis. It is also helpful in treating skin and skin structure infections, as well as mycobacterial infections caused by Mycobacterium avium and Mycobacterium intracellulare. In patients with duodenal ulcers, this drug is used to eliminate Helicobacter pylori. Because it is effective against various causative bacteria, it is widely used in the treatment of multiple bacterial infections. This drug effectively treats bacterial infections.

How to take

Adult dose

○ Adults: The usual dose of clarithromycin is 250mg (potency) twice daily. For severe infections, the dose is 500mg (potency) twice daily. The usual treatment period is 7~14 days. In patients with renal impairment whose creatinine clearance is 30mL/min or less, the dose should be reduced by half. That is, 250mg (potency) once daily, or, for severe infections, 250mg (potency) twice daily. Do not administer this medicine to these patients for more than 14 days. ○ Mycobacterial infections: The dose of this medicine is 500mg (potency) twice daily. In this case, it must be administered in combination with other antimycobacterial agents such as ethambutol, clofazimine, and rifampin. ○ Eradication of Helicobacter pylori in patients with duodenal ulcers: Administer this medicine at 500mg (potency) three 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 at 500mg (potency) three times daily for 14 days (days 1~14), and administer omeprazole 40mg once daily for 28 days (days 1~28). ○ Children aged 12 years and older: same as adults

Child dose

For children under 12 years of age, use clarithromycin dry syrup.

Precautions

This drug should not be administered to patients with certain medications or diseases. For example, individuals allergic to the components of this drug or similar antibiotics should not use this medication. Additionally, patients with cardiac arrhythmias or severe liver and kidney diseases should be cautious. It is also advisable for pregnant or breastfeeding women to avoid this drug. While using this medication, serious allergic reactions or gastrointestinal disturbances, liver function abnormalities may rarely occur, so symptoms should be closely monitored. If symptoms such as shortness of breath, rash, severe abdominal pain, or jaundice appear, immediate consultation with a physician is required. This drug can interact with multiple medications, so if you are taking other drugs, you must inform your doctor or pharmacist. Be especially cautious when using it with cardiac-related medications, certain antibiotics, hypoglycemics, anticoagulants, etc. Moreover, since this drug is excreted through the liver and kidneys, patients with compromised liver or kidney function may require dosage adjustments. Careful monitoring should also be carried out when administering it to children or the elderly. Finally, during the period of taking this drug, one should be wary of dizziness or confusion when driving or operating machinery.

Side effects

Shock, anaphylactic symptoms, shortness of breath, convulsions, redness, rash, itching, hives, skin redness, angioedema, joint swelling, drug rash, abdominal distension, nausea, vomiting, dyspepsia, abdominal pain, malaise, flatulence, diarrhea, oral erosion, upper abdominal pain, thirst, transient tooth discoloration, pancreatitis, increased amylase, dysgeusia, appetite loss, constipation, discoloration of stool, pseudomembranous colitis, hemorrhagic colitis, fever, cough, abnormal chest X-ray, eosinophilia, eosinophilic lung infiltration, 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, hallucinations, psychosis, depersonalization, convulsions, tremors, numbness, behavior changes, manic behavior, Stevens-Johnson syndrome, toxic epidermal necrolysis, allergic purpura, drug rash, jaundice, hepatocellular hepatitis, cholestatic hepatitis, increased liver enzyme levels, liver dysfunction, liver failure, fulminant hepatitis, elevated AST, elevated ALT, elevated γ-GTP, elevated LDH, elevated ALP, increased total bilirubin, appetite loss, dark-colored urine, itching, abdominal tenderness, elevated serum creatinine, elevated BUN, interstitial nephritis, kidney failure, rhabdomyolysis, glossitis, stomatitis, oral candidiasis, QT prolongation, ventricular tachycardia, Torsades de pointes, lethargy, headache, dysgeusia, hearing loss, paresthesia, arthralgia, myalgia, olfactory disturbance, tinnitus, hearing impairment, hypoglycemia, tinnitus, hearing loss, vomiting, purpuric rash, acute generalized exanthematous pustulosis, leukopenia, neutropenia, thrombocytosis, agranulocytosis, thrombocytopenia, anaphylactic reaction, angioedema, decreased appetite, insomnia, neuroirritability, loud noises, psychotic disorders, confusion state, abnormal dreams, dysgeusia, headache, loss of consciousness, movement disorder, non-vertiginous dizziness, drowsiness, tremors, convulsions, loss of taste, dysosmia, loss of smell, vestibular dizziness, hearing impairment, hearing loss, cardiac arrest, atrial fibrillation, ECG QT prolongation, extrasystole, palpitations, vasodilation, asthma, epistaxis, pulmonary embolism, diarrhea, vomiting, dyspepsia, nausea, abdominal pain, esophagitis, gastroesophageal reflux disease, gastritis, rectal pain, stomatitis, glossitis, abdominal distension, constipation, thirst, belching, bloating, acute pancreatitis, tongue discoloration, tooth discoloration, abnormal liver function tests, cholestasis, hepatitis, elevated alanine aminotransferase, elevated aspartate aminotransferase, elevated gamma-glutamyl transferase, liver failure, hepatocellular jaundice, rash, sweating, vesicular dermatitis, itching, hives, papulopustular rash, acne, Henoch-Schönlein purpura, muscle spasms, musculoskeletal rigidity, myalgia, rhabdomyolysis, myopathy, elevated serum creatinine, elevated blood urea nitrogen, kidney failure, nephritis, injection site phlebitis, injection site pain, injection site inflammation, lethargy, fever, weakness, chest pain, chills, fatigue, abnormal albumin-globulin ratio, increased serum alkaline phosphatase, elevated serum lactate dehydrogenase, increased international normalized ratio, prolonged prothrombin time, urine color abnormality

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

Storage

This drug should be stored in a tightly sealed container to prevent air or moisture from entering. It is best to store it at room temperature between 1 degree and 30 degrees.

Appearance and packaging

Appearance

Yellow oval film-coated tablets with a vanilla flavor

Package unit

30 tablets/bottle, 100 tablets/bottle

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.