Medication info
Sinil Talniflumate Tablet

Sinil Talniflumate Tablet

Prescription medicationTabletOral
Ingredient · strength
Talniflumate›370mg / 1 tablet
Manufacturer / importer
Sinil Pharmaceutical Co., Ltd.
Appearance
Pale yellow circular film-coated tablet
Packaging
30 tablets/bottle, 500 tablets/bottle
Approval status
Active

MFDS item code 199501941 · Notified 1995.08.19

Summary

Main use
Treatment of arthritis (including rheumatoid arthritis)
Who takes it
Adults
Adult dose
Administer talniflumate 370 mg orally 3 times daily. For severe cases, administer 740 mg per dose. The dose may be adjusted appropriately according to age and symptoms.

Ingredients

Manufacturer
Sinil Pharmaceutical Co., Ltd.

Efficacy & effects

Treatment of arthritis (including rheumatoid arthritis)

  • Rheumatoid arthritis
  • osteoarthritis
  • degenerative joint disease
View approved original text

Rheumatoid arthritis and osteoarthritis are representative joint diseases. Rheumatoid arthritis occurs due to an immune system disorder, causing inflammation and pain in the joints. Osteoarthritis is a degenerative joint disease that occurs from the wearing away of cartilage, mainly affecting the elderly. Treatment of these diseases can relieve joint pain and inflammation and reduce inconvenience in daily life. This medication is used in the treatment of rheumatoid arthritis and osteoarthritis.

How to take

Adult dose

Administer talniflumate 370 mg orally 3 times daily. For severe cases, administer 740 mg per dose. The dose may be adjusted appropriately according to age and symptoms.

Precautions

This medication should be consulted with a doctor or pharmacist if consumed by individuals who regularly drink more than three glasses of alcohol a day, as there is a risk of gastrointestinal bleeding. This medication may pose risks to the cardiovascular system, so those with heart diseases or risk factors should be especially cautious and seek immediate medical attention if cardiovascular symptoms appear. This medication could cause serious gastrointestinal issues such as gastrointestinal bleeding, ulcers, or perforation, so elderly patients or those with a history of gastrointestinal diseases should be particularly careful and should consult a healthcare professional immediately if gastrointestinal symptoms arise. Individuals with a history of peptic ulcers or who have had allergic reactions to this medication, as well as those hypersensitive to aspirin or other non-steroidal anti-inflammatory drugs (NSAIDs), should not take this medication. It is safer for individuals with severe impairment of liver, kidney, or heart function, as well as pregnant or breastfeeding women, to avoid this medication. Various side effects such as nausea, vomiting, diarrhea, skin rashes, asthma attacks, blood pressure changes may occasionally occur, so if any abnormal symptoms arise during use, notify a healthcare professional immediately. This medication should be taken in the shortest duration possible at the minimum dosage, and regular blood tests and liver and kidney function tests should be conducted with long-term use. Interactions may occur if taken with other anti-inflammatory pain relievers or specific medications, so it is essential to inform the healthcare professional of any other medications being taken. Women who could become pregnant should confirm their pregnancy status, and it is safer not to take this medication during pregnancy or breastfeeding. This medication should not be administered to children, especially those under 12 years of age, and caution should be exercised for the elderly as they are at higher risk for side effects. Store this medication in a safe place out of the reach of children, and it is advised not to transfer it to another container.

Side effects

  • Gastrointestinal hemorrhage
  • cardiovascular thrombotic reactions
  • myocardial infarction
  • stroke
  • nausea
  • vomiting
  • photosensitivity
  • asthma attacks
  • hypotension
  • general weakness
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  • hypersensitivity shock
  • diarrhea
  • abdominal bloating
  • constipation
  • dyspepsia
  • ulcerative stomatitis
  • abdominal pain
  • hematemesis
  • colitis
  • exacerbation of Crohn's disease
  • increased blood pressure
  • tachycardia
  • chest pain
  • arrhythmia
  • palpitations
  • congestive heart failure
  • edema
  • hypertension
  • heart failure
  • bullous reaction
  • Stevens-Johnson syndrome
  • Lyell syndrome
  • rash
  • urticaria
  • pruritus
  • purpura
  • dizziness
  • acute renal failure
  • interstitial nephritis
  • nephrotic syndrome
  • fluoride toxicity
  • abnormal liver tests
  • thrombocytopenia
  • exfoliative dermatitis
  • mucocutaneous syndrome
  • toxic epidermal necrolysis
  • anemia
  • anaphylactic-like reactions
  • bronchospasm
  • severe bronchospasm

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

Storage

This medication should be stored in a tightly sealed container to prevent air or moisture from entering, and it is recommended to keep it at room temperature, neither too hot nor too cold. This way, the effectiveness of the medication can be maintained for a longer period, preventing deterioration.

Appearance and packaging

Appearance

Pale yellow circular film-coated tablet

Package unit

30 tablets/bottle, 500 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.