Medication info
Talumet Tablets (Talniflumate)

Talumet Tablets (Talniflumate)

Prescription medicationTabletOral
Ingredient · strength
Talniflumate›370mg / 1 tablet
Manufacturer / importer
Taegeuk Pharmaceutical Co., Ltd.
Appearance
Orange round film-coated tablets
Packaging
30 tablets/bottle, 500 tablets/bottle, 1000 tablets/bottle
Approval status
Active

MFDS item code 199400837 · Notified 1994.10.14 · Insurance code 644801920

Summary

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

Ingredients

Manufacturer
Taegeuk Pharmaceutical Co., Ltd.

Efficacy & effects

Treatment of arthritis (rheumatoid arthritis, etc.)

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

This medication is used for rheumatoid arthritis and osteoarthritis, i.e., degenerative arthritis.

How to take

Adult dose

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

Precautions

Before taking this medication, individuals who regularly consume more than three glasses of alcohol daily must consult a doctor or pharmacist. Excessive alcohol consumption while taking this medication can lead to serious side effects like gastrointestinal bleeding. This medication may increase the risk of cardiovascular diseases, so patients with heart conditions or risk factors must exercise caution. If cardiovascular symptoms arise, seek medical attention immediately, and patients should be aware of these symptoms. Additionally, this medication can cause severe issues like gastrointestinal bleeding, ulcers, and perforation, so elderly patients or those with a history of gastrointestinal disorders should use it cautiously. If any gastrointestinal adverse effects occur, consult medical personnel immediately, and in some cases, stopping the medication may be necessary. Individuals with a history of peptic ulcers or allergies to the components of this medication, or those with asthma or aspirin allergies, should not take this medication. Patients with severely impaired heart, liver, or kidney function should also avoid using this medication. Women who are pregnant or may become pregnant, as well as nursing mothers, should not take this medication. Patients with mild to moderate liver, kidney, or heart dysfunction should use this medication with caution, and elderly patients should also be monitored closely. In case of hypersensitivity reactions, symptoms like nausea, vomiting, skin rashes, or asthma attacks may occur; if any of these symptoms appear, discontinue use immediately and consult medical personnel. This medication can cause various side effects, including increased blood pressure, heart problems, skin reactions, and kidney damage, so inform medical personnel immediately upon symptom occurrence. Regular blood tests and liver and kidney function evaluations are necessary with prolonged use, and appropriate measures should be taken if any abnormalities are found. This medication can mask symptoms of infection; therefore, when an infection is suspected, it should be used with caution in conjunction with appropriate antibiotics. It is advisable not to take this medication with other anti-inflammatory analgesics, and since it may interact with specific drugs, be sure to inform your physician of any medications being taken. In late pregnancy, it may pose risks to the fetus, so women who are pregnant or planning to become pregnant should avoid its use. While nursing, this medication can be transmitted to breast milk and may cause side effects in the infant; therefore, consult a doctor before taking it if you are breastfeeding. Children under 12 years of age should not take this medication, and elderly patients should use the minimum effective dose cautiously. Store this medication out of reach of children and do not transfer it to other containers to ensure safety.

Side effects

  • Nausea
  • vomiting
  • photosensitivity
  • asthma attack
  • systemic malaise due to hypotension
  • hypersensitivity shock
  • diarrhea
  • abdominal distension
  • constipation
  • dyspepsia
Show 32 more
  • 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
  • Riel syndrome
  • rash
  • urticaria
  • pruritus
  • purpura
  • dizziness
  • acute renal failure
  • interstitial nephritis
  • nephrotic syndrome
  • fluoride toxicity
  • abnormal liver function 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 avoid contact with air and at a safe temperature between 1 degree and 30 degrees Celsius. Storing it this way helps maintain the medication's effectiveness and prevent degradation.

Appearance and packaging

Appearance

Orange round film-coated tablets

Package unit

30 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

No questions yet.

For anything that needs medical judgment, consult a doctor or pharmacist.

Related searches

Search tags

Suggested searches

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.