Medication info

Teliphen Tablet (Talniflumate)

Prescription medicationTabletOralExpired
Ingredient · strength
Talniflumate›370mg / 1 tablet
Manufacturer / importer
Bivocorn Pharmaceutical Co., Ltd.
Appearance
Orange round film-coated tablet
Packaging
30 tablets/bottle, 500 tablets/bottle
Approval status
Expired

MFDS item code 200401242 · Notified 2004.04.29

This product's status changed to Expired on 2024.04.01. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

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

Ingredients

Manufacturer
Bivocorn Pharmaceutical Co., Ltd.

Efficacy & effects

Treatment of arthritis (e.g., rheumatoid arthritis)

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

This medication is used for rheumatoid arthritis and osteoarthritis, i.e., degenerative arthritis. Rheumatoid arthritis is a disease characterized by inflammation in the joints due to an immune system disorder, while osteoarthritis is associated with pain and functional decline due to degenerative changes in the joints. This drug helps reduce inflammation and alleviate pain, thereby improving joint movement. Therefore, it is effective in relieving discomfort caused by arthritis and enhancing the quality of daily life.

How to take

Adult dose

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

Precautions

This medication may cause gastric bleeding in individuals who regularly consume more than three servings of alcohol daily, so it should be taken only after consulting a physician or pharmacist. This medication can affect the cardiovascular system and may increase the risk of serious cardiovascular diseases, such as myocardial infarction or stroke, so individuals with cardiovascular diseases or risk factors should be cautious. Serious adverse reactions such as bleeding, ulceration, and perforation may occur in the gastrointestinal tract, particularly in the elderly, who may be at higher risk, necessitating close monitoring for gastrointestinal symptoms during treatment. Individuals with a history of peptic ulcers, allergies to this drug or its components, hypersensitivity to aspirin or other non-steroidal anti-inflammatory drugs, pregnant or breastfeeding women, and those with severe liver, kidney, or heart disorders should not take this medication. Individuals with mild to moderate liver, kidney, or heart disorders, the elderly, and those taking diuretics should use this medication cautiously. Those allergic to specific dye components should also be vigilant. During treatment, nausea, vomiting, diarrhea, abdominal pain, skin rashes, hives, and, rarely, serious skin reactions or respiratory symptoms may occur, so it is essential to consult a healthcare professional immediately if any adverse reactions arise. This medication should be used at the lowest effective dose and for the shortest duration possible, and regular blood tests and liver and kidney function tests are required for long-term use. It is advisable to avoid taking this medication with other non-steroidal anti-inflammatory drugs, and there may be interactions with specific blood pressure medications, diuretics, anticoagulants, lithium, and methotrexate, so consult healthcare professionals if co-administering. During pregnancy, especially in late stages, it may harm the fetus, so it should not be taken; if breastfeeding, it may transfer to breast milk, necessitating suspension of nursing or discontinuation of the drug. The use of this medication is not recommended for children under 12 years old, and the elderly should start with a lower dose and be vigilant for adverse reactions. This medication should be stored out of reach of children, and transferring it to other containers could compromise its quality, so caution is advised.

Side effects

  • Nausea
  • vomiting
  • phototoxicity
  • asthma attacks
  • systemic malaise due to hypotension
  • hypersensitivity shock
  • diarrhea
  • abdominal distension
  • constipation
  • dyspepsia
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  • ulcerative stomatitis
  • abdominal pain
  • hematemesis
  • colitis
  • exacerbation of Crohn’s disease
  • gastrointestinal bleeding
  • peptic ulcer
  • perforation
  • increased blood pressure
  • tachycardia
  • chest pain
  • arrhythmia
  • palpitations
  • hypotension
  • congestive heart failure
  • edema
  • hypertension
  • heart failure
  • vesicular reactions
  • Stevens-Johnson syndrome
  • Lyell syndrome
  • rash
  • hives
  • itching
  • purpura
  • 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 must be stored in a container that blocks light and is sealed to prevent air access. The storage temperature should be maintained between 1 to 30 degrees Celsius.

Appearance and packaging

Appearance

Orange round 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.