Medication info
Resel Coated Tablet

Resel Coated Tablet

Prescription medicationTabletOral
Ingredient · strength
Celecoxib›100mg / 1 tabletAngelica Gigas Root·Chaenomelis Fructus·Saposhnikovia Root·Dipsaci Radix·Acanthopanax Root Bark·Achyranthes Root·Clematidis Radix·Cinnamon Bark·Gentianae Macrophyllae Radix·Cnidium Rhizome·Gastrodia Rhizome·Safflower 25% Ethanol Soft Extract (3.5→1)›405.4mg / 1 tablet
Manufacturer / importer
Aliko Pharmaceutical Co., Ltd.
Appearance
Yellow oblong film-coated tablet consisting of two layers
Packaging
30 tablets/bottle, 300 tablets/bottle
Approval status
Active

MFDS item code 202302400 · Approved 2023.08.10 · Insurance code 656005480

Summary

Main use
Relief of symptoms of osteoarthritis (degenerative arthritis)
Who takes it
Adults
Adult dose
Adults: Take 1 tablet twice daily. This medicine may be taken with or without food. Take this medicine whole; do not crush or split it. ○ Patients with hepatic impairment This medicine is not recommended for initial treatment in patients with hepatic impairment who require a dose reduction (see Precautions for Use, 5. General Precautions)

Ingredients

Manufacturer
Aliko Pharmaceutical Co., Ltd.

Efficacy & effects

Relief of symptoms of osteoarthritis (degenerative arthritis)

  • Symptoms and signs of osteoarthritis and degenerative joint disease
View approved original text

Osteoarthritis is a condition that is mainly accompanied by joint pain, stiffness, and limited movement. This medication helps to relieve these symptoms. Patients can use it to reduce joint pain and discomfort, and to improve joint function. This will make daily movements more comfortable and enhance the quality of life. This medication is used to relieve the symptoms of osteoarthritis.

How to take

Adult dose

Adults: Take 1 tablet twice daily. This medicine may be taken with or without food. Take this medicine whole; do not crush or split it. ○ Patients with hepatic impairment This medicine is not recommended for initial treatment in patients with hepatic impairment who require a dose reduction (see Precautions for Use, 5. General Precautions)

Precautions

This medication should be discussed with a doctor or pharmacist before use by individuals who consume more than three standard drinks daily. This medication may increase the risk of cardiovascular thromboembolic events, so it should only be used at the lowest effective dose for the shortest duration, and immediate consultation with healthcare professionals is required if cardiovascular symptoms occur. There is a risk of gastrointestinal bleeding, ulcers, and perforations, so particular caution is needed in patients with a history of gastrointestinal disease or the elderly, and immediate treatment is necessary if gastrointestinal bleeding symptoms appear. Patients with hypersensitivity to this medication or with a history of allergy to specific drugs, as well as those with severe cardiovascular, liver, or kidney disease, or active peptic ulcers, should not use it. Caution is also required for patients with impaired liver or kidney function, asthma, heart failure, hypertension, edema, those on diuretics, and the elderly, with regular monitoring necessary. Patients taking this medication should undergo regular testing, including liver function, kidney function, and blood tests, to monitor for abnormal signs. Pregnant women or women of childbearing potential, as well as nursing mothers, should not take this medication, and those planning to become pregnant should consult a specialist. This medication may interact with other drugs, so it is essential to inform healthcare providers of any other medications being taken, particularly with antihypertensives, anticoagulants, diuretics, and antidepressants. Dizziness or drowsiness may occur during treatment, so driving or operating machinery should be avoided. This medication may cause severe skin reactions; thus, if symptoms such as skin rash, mucosal lesions, fever, or itching occur, discontinue use and consult a healthcare provider immediately. Overdose may result in weakness, nausea, vomiting, abdominal pain, and immediate medical attention is required. This medication must be kept out of reach of children and should not be transferred to another container.

Side effects

Gastrointestinal bleeding, cardiovascular thrombotic events, myocardial infarction, stroke, perforations of the upper and lower gastrointestinal tract, ulcers, bleeding, dyspepsia, nausea, upper abdominal pain, constipation, diarrhea, dry mouth, esophageal pain, stomatitis, COVID-19, acute pyelonephritis, facial edema, pain at the insertion site, peripheral edema, fever, pruritus, psoriasis, rash, skin swelling, increased alanine aminotransferase, increased aspartate aminotransferase, hypertension, elevated blood uric acid, increased gamma-glutamyl transferase, arthralgia, lumbar pain, coccygodynia, flank pain, headache, carpal tunnel syndrome, lymphadenopathy, cholelithiasis, palpitations, congestive heart failure, arrhythmia, tachycardia, hypertension, flushing, cough, vomiting, abdominal pain, bloating, gastric ulcer, dental disease, duodenal ulcer, esophageal ulcer, bowel perforation, pancreatitis, elevated liver enzymes, itching, urticaria, angioedema, alopecia, bullous dermatitis, peripheral edema, facial edema, influenza-like illness, damage, insomnia, anxiety, confusion, dizziness, muscle hypertonia, drowsiness, blurred vision, tinnitus, congestive heart failure, arrhythmia, tachycardia, flushing, pulmonary embolism, interstitial pneumonia, gastrointestinal hemorrhage, hepatitis, liver failure, fulminant hepatitis, liver necrosis, phototoxic reaction, Stevens-Johnson syndrome, erythema multiforme, toxic epidermal necrolysis, drug eruption with eosinophilia and systemic symptoms, acute generalized pustular eruption, exfoliative dermatitis, acute renal failure, hyponatremia, tubular interstitial nephritis, nephrotic syndrome, microscopic lesion glomerulonephritis, menstrual disorders, female infertility, chest pain, heartburn, dry mouth, nausea, diarrhea, weakness, hypertriglyceridemia, hypercholesterolemia, transaminitis, increased ALT, increased AST, itching, leukopenia, neutropenia, chest discomfort, headache, upper respiratory infection, blurry vision, gastritis, gastroesophageal reflux, edema, anorexia, nausea, vomiting, diarrhea

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

Storage

This medication should be stored in a tightly closed container to prevent exposure to air and moisture, ideally at a temperature between 1 to 30 degrees Celsius. Proper storage will maintain the effectiveness of the medication and prevent degradation.

Appearance and packaging

Appearance

Yellow oblong film-coated tablet consisting of two layers

Package unit

30 tablets/bottle, 300 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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For anything that needs medical judgment, consult a doctor or pharmacist.

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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.