Medication info
Oksopen Tablet (Sodium Loxoprofen Hydrate)

Oksopen Tablet (Sodium Loxoprofen Hydrate)

Prescription medicationTablet경구
Ingredient · strength
Loxoprofen Sodium Hydrate›68.1mg / 1 tablet
Manufacturer / importer
오스틴제약(주)
Appearance
White to yellowish round tablets
Packaging
30 tablets/bottle, 300 tablets/bottle
Approval status
Active

MFDS item code 200402096 · Notified 2004.11.05 · Insurance code 654302150

Summary

Main use
Treatment of inflammation and pain in rheumatoid arthritis and osteoarthritis (degenerative arthritis), etc.
Who takes it
Adults
Adult dose
1. For indications 1, 2: ○ Adults: Administer sodium loxoprofen (anhydrous) 60 mg orally three times a day. For single dose treatment, administer 60-120 mg orally. 2. For indication 3: ○ Adults: Administer sodium loxoprofen (anhydrous) 60 mg orally. In principle, it can be administered twice a day, with a maximum daily dose of 180 mg. It is preferred to avoid taking on an empty stomach.

Ingredients

Manufacturer
오스틴제약(주)

Efficacy & effects

Treatment of inflammation and pain in rheumatoid arthritis and osteoarthritis (degenerative arthritis), etc.

  • Chronic rheumatoid arthritis
  • osteoarthritis
  • low back pain
  • adhesive capsulitis
  • carpal tunnel syndrome
  • postoperative pain
  • post-traumatic pain
  • pain after tooth extraction
  • acute upper respiratory infections
  • acute bronchitis
View approved original text

This medication exhibits anti-inflammatory and analgesic effects for joint diseases such as chronic rheumatoid arthritis and osteoarthritis, alleviating pain. It is also effective for pain due to inflammation from low back pain, adhesive capsulitis, and carpal tunnel syndrome. It reduces inflammation and pain after surgery, trauma, and tooth extraction, thus alleviating patient discomfort. It provides antipyretic and analgesic effects when dealing with acute upper respiratory infections, especially when accompanied by acute bronchitis, improving symptoms. This drug is used to relieve various inflammation-related pains and fever.

How to take

Adult dose

1. For indications 1, 2: ○ Adults: Administer sodium loxoprofen (anhydrous) 60 mg orally three times a day. For single dose treatment, administer 60-120 mg orally. 2. For indication 3: ○ Adults: Administer sodium loxoprofen (anhydrous) 60 mg orally. In principle, it can be administered twice a day, with a maximum daily dose of 180 mg. It is preferred to avoid taking on an empty stomach.

Precautions

People who regularly consume more than three drinks a day should consult a doctor or pharmacist before taking this medication. This is because the risk of gastrointestinal bleeding may increase when taking this drug. This drug can affect the cardiovascular system and may increase the risk of myocardial infarction and stroke. Those with cardiovascular diseases or risk factors should be particularly cautious, and both doctors and patients should carefully monitor for symptoms. This drug can cause serious gastrointestinal disorders such as gastrointestinal bleeding, ulcers, and perforation. Elderly individuals or those with a history of gastrointestinal disease should be more cautious, and if symptoms of gastrointestinal bleeding occur during administration, immediate treatment is necessary. Patients with a history of peptic ulcer, severe blood disorders, liver dysfunction, kidney impairment, heart failure, or who are allergic to any component in this medication should not use it. Additionally, individuals who have had allergic reactions to aspirin or other non-steroidal anti-inflammatory drugs (NSAIDs), as well as pregnant women in late pregnancy or breastfeeding mothers, should not take this medication. Caution and doctor's instructions are necessary when administering this drug to those with a history of peptic ulcers, blood disorders, liver dysfunction, kidney impairment, hypertension, heart failure, elderly individuals, etc. This drug can produce allergic reactions such as rash, itching, and hives, so consumption should be stopped if such symptoms occur. In severe cases, symptoms of shock or anaphylaxis may appear, so caution is required. Gastrointestinal issues may include abdominal pain, nausea, vomiting, diarrhea, and gastrointestinal bleeding, and medical staff should be notified immediately if any of these symptoms occur. This drug can cause central nervous system symptoms such as drowsiness, dizziness, and headaches, so care must be taken when driving or operating machinery. Liver dysfunction or kidney impairment may occur, so regular check-ups are necessary during long-term use, and administration should cease immediately if any abnormalities are detected. This medication may interact with other NSAIDs or specific medications, so notify your doctor of any other medications being taken. During pregnancy, especially in the later stages, this medication should not be taken as it may affect the fetus, and women who are potentially pregnant should exercise caution in its use. It is also safer to avoid this drug while breastfeeding. Safety in children has not been established, so it is advisable not to administer this medication to children. Elderly patients have an increased risk of adverse reactions when taking this drug, so careful management is required. Finally, this medication should be stored out of reach of children, and transferring it to another container can lead to degradation of quality or accidents, so care should be taken.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (edema), tightness in the chest, difficulty breathing, shock, anaphylactic-like reactions, peptic ulcers, perforation, hematemesis, melena, blood in stool, shock, liver dysfunction (including jaundice), fulminant hepatitis, acute renal failure, interstitial nephritis, interstitial pneumonia, asthma attacks, Stevens-Johnson syndrome (skin and mucosal syndrome), toxic epidermal necrolysis (Lyell syndrome), erythema multiforme, acute generalized exanthematous pustulosis, aseptic meningitis

Mild side effects

  • Occasionally
  • rash
  • itching
  • fever
  • abdominal pain
  • discomfort in the upper abdomen
  • loss of appetite
  • nausea
  • vomiting
  • diarrhea
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  • constipation
  • a sensation of chest warmth
  • indigestion
  • stomatitis
  • thirst
  • abdominal bloating
  • drowsiness
  • numbness
  • dizziness
  • headaches
  • anemia
  • hemolytic anemia
  • leukopenia
  • thrombocytopenia
  • eosinophilia
  • edema
  • chest pain
  • anxiety
  • fatigue
  • palpitations
  • hematuria
  • proteinuria
  • fever
  • resolution
  • abnormal chest X-ray findings
  • eosinophilia
  • edema.

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

Storage

This drug should be stored in a tightly sealed container to protect it from air and moisture. The recommended storage temperature is between 1°C and 30°C at room temperature. This helps to maintain the drug's efficacy.

Appearance and packaging

Appearance

White to yellowish round tablets

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.