Medication info

Taniful Tablets (Tafinaplumate)

Prescription medicationTabletOralExpired
Ingredient · strength
Talniflumate›370mg / 1 tablet
Manufacturer / importer
AhnGuk New Pharm Co., Ltd.
Appearance
Yellow film-coated round tablets
Packaging
30 tablets/bottle, 100 tablets/bottle, 300 tablets/bottle, 500 tablets/bottle, 1000 tablets/bottle
Approval status
Expired

MFDS item code 201905457 · Approved 2019.07.31

This product's status changed to Expired on 2024.07.31. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

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

Ingredients

Manufacturer
AhnGuk New Pharm Co., Ltd.

Efficacy & effects

Treatment of arthritis (including rheumatoid arthritis)

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

This medication is used for the treatment of rheumatoid arthritis and osteoarthritis (degenerative arthritis).

How to take

Adult dose

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

Precautions

This medication should be discussed with a doctor or pharmacist before use by individuals who regularly consume more than three glasses of alcohol daily. There is a risk of gastrointestinal bleeding in individuals who frequently consume alcohol while taking this medication. This medication may increase the risk of cardiovascular diseases and can lead to serious cardiovascular problems such as myocardial infarction or stroke. Individuals with a history of cardiovascular diseases or risk factors should be especially cautious and closely monitor cardiovascular symptoms during treatment. This medication can cause serious gastrointestinal side effects such as gastrointestinal bleeding, ulcers, and perforations, with an increased risk in the elderly. Prolonged use may increase the likelihood of gastrointestinal adverse reactions, so gastrointestinal symptoms should be closely observed. Individuals with a history of peptic ulcers or an allergy to this medication or its components, as well as those with allergic reactions to aspirin or other non-steroidal anti-inflammatory drugs, should not take this medication. Additionally, patients with severe liver, kidney, or heart disorders, and pregnant or lactating women should avoid its use. Patients with slightly impaired liver or kidney function, those taking diuretics, and the elderly should use this medication with caution, and those with a history of allergies should also be careful. While taking this medication, gastrointestinal symptoms such as nausea, vomiting, diarrhea, and abdominal pain may occur, as well as hypersensitivity reactions like skin rashes, hives, and itching. Rarely, cardiovascular abnormalities, kidney function impairment, and central nervous system symptoms may occur, so if any unusual symptoms arise, immediate consultation with a healthcare professional is necessary. This medication should be used at the minimum effective dose for the shortest duration possible, and if used long-term, regular blood tests and assessments of liver and kidney function are required. Interactions may occur when taken with other anti-inflammatory analgesics, aspirin, diuretics, ACE inhibitors, anticoagulants, etc., so it is essential to inform healthcare personnel. During pregnancy, especially in the later stages, it should not be taken as it may harm the fetus, and lactating women should consider discontinuing breastfeeding during its use. Children under 12 years old should not take this medication, and the elderly should start at particularly low doses and be cautious of side effects. This medication should be kept out of reach of children and it is advisable not to transfer it to other containers.

Side effects

  • nausea
  • vomiting
  • photosensitivity
  • asthma attack
  • hypotension
  • general malaise
  • hypersensitivity shock
  • diarrhea
  • abdominal distension
  • constipation
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  • dyspepsia
  • ulcerative stomatitis
  • abdominal pain
  • hematemesis
  • colitis
  • exacerbation of Crohn's disease
  • gastrointestinal bleeding
  • peptic ulcer
  • perforation
  • hypertension
  • tachycardia
  • chest pain
  • arrhythmia
  • palpitations
  • congestive heart failure
  • edema
  • hypertension
  • heart failure
  • vesicular reaction
  • Stevens-Johnson syndrome
  • Lyell's syndrome
  • rash
  • urticaria
  • pruritus
  • purpura
  • chickenpox
  • dizziness
  • acute renal failure
  • interstitial nephritis
  • nephrotic syndrome
  • fluoride toxicity
  • abnormal liver tests
  • thrombocytopenia

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 infiltration, and the temperature should be kept between 1 and 30 degrees Celsius at room temperature for safe storage. This storage method helps maintain the medication's effectiveness and prevents deterioration.

Appearance and packaging

Appearance

Yellow film-coated round tablets

Package unit

30 tablets/bottle, 100 tablets/bottle, 300 tablets/bottle, 500 tablets/bottle, 1000 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.