Medication info
Trimed tablet (Talniflumate)

Trimed tablet (Talniflumate)

Prescription medicationTabletOral
Ingredient · strength
Talniflumate›370mg / 1 tablet
Manufacturer / importer
Kips Biopharma Co., Ltd.
Appearance
Orange round film-coated tablet
Packaging
30 tablets/bottle, 300 tablets/bottle
Approval status
Active

MFDS item code 200404864 · Notified 2004.11.15 · Insurance code 693200150

Summary

Main use
Treatment of arthritis (including 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. Adjust the dose appropriately according to age and symptoms.

Ingredients

Manufacturer
Kips Biopharma Co., Ltd.

Efficacy & effects

Treatment of arthritis (including rheumatoid arthritis)

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

Rheumatoid arthritis and osteoarthritis (degenerative arthritis) are diseases that cause inflammation and pain in the joints. Rheumatoid arthritis is an autoimmune disease that causes inflammation and deformity of the joints, while osteoarthritis is a degenerative disease caused by the wear and tear of joint cartilage. This medication is used to alleviate the pain and inflammation associated with these types of arthritis and to improve joint function.

How to take

Adult dose

Administer 370 mg of talniflumate orally 3 times daily. For severe cases, administer 740 mg per dose. Adjust the dose appropriately according to age and symptoms.

Precautions

This medication may cause gastrointestinal bleeding in individuals who regularly consume three or more glasses of alcohol daily, so it is essential to consult a doctor or pharmacist. This medication can affect the cardiovascular system and may increase the risk of serious heart problems such as myocardial infarction or stroke, so patients with cardiovascular diseases or risk factors should exercise extra caution. This medication may cause serious gastrointestinal issues such as gastrointestinal bleeding, ulcers, or perforations; therefore, elderly patients or those with a history of gastrointestinal diseases are at higher risk and should be cautious. Patients with peptic ulcers or hypersensitivity to this medication, patients allergic to aspirin, pregnant and nursing women, and those with severe liver, kidney, or heart disorders should not take this medication. Patients with mildly reduced liver or kidney function, elderly patients, those taking diuretics, or patients allergic to certain dye components should use this medication with caution. This medication can cause various side effects, including digestive symptoms such as nausea, vomiting, diarrhea, abdominal pain, and, rarely, skin rash, allergic reactions, dizziness, and kidney issues; therefore, if any unusual symptoms occur, immediate consultation with medical professionals is necessary. This medication should be used at the lowest effective dose for the shortest duration possible; if used for long periods, regular blood tests and liver and kidney function assessments should be conducted. It is advisable not to take this medication with other nonsteroidal anti-inflammatory drugs, and caution is needed when combined with certain antihypertensive medications, diuretics, lithium, methotrexate, or anticoagulants due to potential interactions. Particularly in late pregnancy, this medication can be harmful to the fetus and should not be used; nursing mothers should consider ceasing breastfeeding or discontinuing the medication as it may pass into breast milk. This medication should not be used in children under 12 years of age, and seniors should take it with caution at the minimum dose due to a higher likelihood of side effects. This medication should be stored out of reach of children, and transferring it to other containers is not advisable for quality maintenance.

Side effects

  • Gastrointestinal bleeding
  • cardiovascular thrombotic reactions
  • myocardial infarction
  • stroke
  • nausea
  • vomiting
  • photosensitivity
  • asthma attacks
  • systemic malaise due to hypotension
  • hypersensitivity shock
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  • diarrhea
  • abdominal distension
  • constipation
  • indigestion
  • ulcerative stomatitis
  • abdominal pain
  • hematemesis
  • colitis
  • exacerbation of Crohn's disease
  • hypertension
  • tachycardia
  • chest pain
  • arrhythmia
  • palpitations
  • hypotension
  • congestive heart failure
  • edema
  • hypertension
  • heart failure
  • vesicular reactions
  • Stevens-Johnson syndrome
  • Reye's syndrome
  • rash
  • urticaria
  • pruritus
  • purpura
  • dizziness
  • acute renal failure
  • interstitial nephritis
  • nephrotic syndrome
  • fluoride toxicity
  • abnormal liver function tests
  • thrombocytopenia abnormality

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

Storage

This medication should be stored in a tightly sealed container to protect it from air and moisture exposure. Additionally, it is best to store the medication at room temperature between 1 and 30 degrees Celsius. Avoid extremely hot or cold places, and keep it in a cool place away from direct sunlight.

Appearance and packaging

Appearance

Orange round film-coated tablet

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.