Medication info
Flumagen Tablets (Talniflumate)

Flumagen Tablets (Talniflumate)

Prescription medicationTabletOral
Ingredient · strength
Talniflumate›370mg / 1 tablet
Manufacturer / importer
Austin Pharmaceuticals Co., Ltd.
Appearance
Orange round film-coated tablet
Packaging
30 tablets/bottle, 500 tablets/bottle
Approval status
Active

MFDS item code 200501801 · Notified 2005.03.16 · Insurance code 654303190

Summary

Main use
Relief of arthritis (including osteoarthritis)
Who takes it
Adults
Adult dose
Administer talniflumate 370 mg orally 3 times daily. In severe cases, administer 740 mg per dose. Adjust the dose as appropriate according to age and symptoms.

Ingredients

Manufacturer
Austin Pharmaceuticals Co., Ltd.

Efficacy & effects

Relief of arthritis (including osteoarthritis)

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

Rheumatoid arthritis and osteoarthritis are representative joint diseases. Rheumatoid arthritis is a chronic inflammatory disease caused by a malfunction of the immune system, and osteoarthritis is a degenerative disease caused by the wear of joint cartilage. This medication is used to relieve the symptoms of these types of arthritis, reduce pain, and improve joint function.

How to take

Adult dose

Administer talniflumate 370 mg orally 3 times daily. In severe cases, administer 740 mg per dose. Adjust the dose as appropriate according to age and symptoms.

Precautions

People who regularly consume more than three glasses of alcohol per day must consult a doctor or pharmacist before taking this medication. Individuals who consume large amounts of alcohol are at a higher risk of gastrointestinal bleeding when taking this medication. This medication may affect the cardiovascular system and can cause serious thrombotic issues such as myocardial infarction or stroke, so individuals with cardiovascular diseases or risk factors should be particularly cautious. Any cardiovascular symptoms should be reported to healthcare providers immediately, and patients should be well informed about these symptoms and how to address them. This medication may cause serious gastrointestinal issues such as bleeding, ulceration, or perforation, and the risk is higher for elderly patients. If any gastrointestinal symptoms occur during use, immediate evaluation and treatment in a hospital is necessary. Individuals with a history of peptic ulcers, allergies to any ingredient in this medication, severe liver, kidney, or heart disease, or who are pregnant or breastfeeding should not take this medication. Caution should be exercised when using this medication in individuals with poor liver or kidney function, in elderly patients, and in those taking diuretics, as well as in patients with a history of allergies. Various side effects such as nausea, vomiting, diarrhea, abdominal pain, skin rash, hives, dizziness, etc., may occur, and if any unusual symptoms arise, immediate consultation with healthcare providers is necessary. Long-term use of this medication may affect liver and kidney function, so regular testing is required, and if any abnormal findings occur, the medication should be discontinued. Additionally, this medication may raise blood pressure or exacerbate existing hypertension, so patients who need blood pressure management should be cautious. Interactions may occur when this medication is taken alongside other anti-inflammatory pain relievers, anticoagulants, diuretics, lithium, methotrexate, etc., so it is essential to inform healthcare providers about all medications being taken. During pregnancy, particularly in the later stages, it may pose risks to the fetus, so women who are pregnant or may become pregnant should not take this medication. Women who are breastfeeding should also avoid taking this medication as it can affect the baby through breast milk, and they should either stop breastfeeding or avoid taking this medication. Children under 12 years of age should not use this medication, and elderly patients should use the minimum dosage carefully and pay special attention to side effects. This medication should be kept out of the reach of children and should not be transferred to another container for safety.

Side effects

  • Nausea
  • vomiting
  • photosensitivity
  • asthma attack
  • systemic fatigue 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
  • hypertension
  • tachycardia
  • chest pain
  • arrhythmia
  • palpitations
  • hypotension
  • congestive heart failure
  • edema
  • hypertension
  • heart failure
  • vesicular reaction
  • Stevens-Johnson syndrome
  • Lyell's syndrome
  • rash
  • urticaria
  • itching
  • purpura
  • dizziness
  • acute renal failure
  • interstitial nephritis
  • nephrotic syndrome
  • fluoride poisoning
  • 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 closed container to prevent exposure to air or moisture. It is also recommended to store it at room temperature between 1 degree and 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.