Medication info
Naxen Soft Capsules (Naproxen)

Naxen Soft Capsules (Naproxen)

OTC medicationSoft capsule경구
Ingredient · strength
Naproxen›250mg / 1 capsule
Manufacturer / importer
신일제약(주)
Appearance
Green translucent oblong soft capsule containing light yellow to pale green contents
Packaging
10 capsules (10 capsules/PTP x 1)
Approval status
Active

MFDS item code 201306491 · Notified 2013.03.28

Summary

Main use
Improvement of arthritis such as rheumatoid arthritis and osteoarthritis
Who takes it
Adults
Adult dose
1. Rheumatoid arthritis, osteoarthritis, ankylosing spondylitis: Take 250–500 mg (1–2 tablets) of Naproxen orally, twice a day (every 12 hours). 2. Acute gout: Take a loading dose of 750 mg (3 tablets), and then take 250 mg (1 tablet) orally every 8 hours until the attack subsides. 3. Skeletal muscle disorders, postoperative pain, pain after tooth extraction, dysmenorrhea, tendonitis, bursitis: Take a loading dose of 500 mg of Naproxen orally.

Ingredients

Manufacturer
신일제약(주)

Efficacy & effects

Improvement of arthritis such as rheumatoid arthritis and osteoarthritis

  • Rheumatoid arthritis
  • osteoarthritis
  • ankylosing spondylitis
  • tendonitis
  • acute gout
  • dysmenorrhea
  • bursitis
  • skeletal muscle disorders
  • sprains
  • bruises
  • trauma
  • low back pain
View approved original text

This medication is used for various conditions including rheumatoid arthritis, osteoarthritis, ankylosing spondylitis, tendonitis, acute gout, and dysmenorrhea. It is also effective for bursitis, muscle strains and bruises, lower back pain, postoperative pain, migraines, and pain after tooth extraction. This medicine helps alleviate pain and inflammation associated with these conditions, thus improving the daily lives of patients. It is widely used for various problems related to joints and muscles, making it suitable for treating various types of pain. This medication is utilized for patients' recovery and pain relief.

How to take

Adult dose

1. Rheumatoid arthritis, osteoarthritis, ankylosing spondylitis: Take 250–500 mg (1–2 tablets) of Naproxen orally, twice a day (every 12 hours). 2. Acute gout: Take a loading dose of 750 mg (3 tablets), and then take 250 mg (1 tablet) orally every 8 hours until the attack subsides. 3. Skeletal muscle disorders, postoperative pain, pain after tooth extraction, dysmenorrhea, tendonitis, bursitis: Take a loading dose of 500 mg of Naproxen orally.

Precautions

Patients who regularly consume more than three drinks a day must consult with a physician or pharmacist before taking this medication. Regular drinkers of alcohol may have an increased risk of gastric bleeding while on this medication. This drug may have effects on the cardiovascular system, so patients with a history of heart disease or vascular issues should take special care. If cardiovascular symptoms appear, they must inform medical personnel immediately, regardless of whether they have a history of cardiovascular diseases. This medication may cause gastrointestinal burden, and serious issues such as gastric bleeding, ulcers, or perforations may occur, so patients must pay attention to gastric symptoms while taking it. Especially, elderly patients or those with a history of gastrointestinal disorders are at greater risk with this medication, requiring careful observation. Patients with peptic ulcers, severe blood disorders, liver impairment, very weak cardiac function, severely decreased renal function, and severe hypertension should not take this medication. Patients allergic to this drug or non-steroidal anti-inflammatory pain relievers, or have a history of hypersensitivity such as asthma, rhinitis, or urticaria, should avoid taking it. This medication may harm the fetus in the later stages of pregnancy, so it should not be used during that time. Nursing mothers are advised against using this medication as it may transfer to breast milk and cause side effects in infants. It is preferable not to use this medication in children under 2 years of age as its safety has not been established. Elderly patients have a higher risk of side effects such as gastric bleeding when taking this medication, so it should be used cautiously at the minimum dosage. When taking this medication for an extended time, periodic blood tests, liver function tests, and kidney function tests should be performed to monitor for abnormalities. Co-administration with other non-steroidal anti-inflammatory drugs may increase the risk of side effects, so such combinations should be avoided. When co-administering with specific drugs, interactions may occur, so consultation with a physician or pharmacist is necessary before taking. If severe headaches, rashes, difficulty breathing, signs of gastric bleeding, jaundice, or symptoms indicating decreased renal function occur during use, the medication should be discontinued immediately and medical consultation sought. Overdose may lead to symptoms such as drowsiness, nausea, and vomiting, necessitating immediate emergency treatment. This medication should be stored out of reach of children and care should be taken not to transfer it to another container, as this may alter its quality.

Side effects and when to seek care immediately

Serious side effects

Urticaria, severe swelling (edema), cold sweats, difficulty in breathing, respiratory distress, asthma episodes, hematemesis, gastric bleeding, peptic ulcers, perforation, blood disorders (agranulocytosis, leukopenia, thrombocytopenia, etc.), jaundice, hepatitis, renal impairment, hematuria, hyperkalemia, interstitial nephritis, nephrotic syndrome, renal failure, aseptic meningitis, severe headaches, confusion, Stevens-Johnson syndrome, epidermal necrolysis, anaphylactic reaction, eosinophilia, and

Mild side effects

  • Nausea
  • stomach pain
  • abdominal pain
  • vomiting
  • loss of appetite
  • dyspepsia
  • heartburn
  • diarrhea
  • constipation
  • stomatitis
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  • abdominal bloating
  • black stools
  • thirst
  • rash
  • itching
  • headache
  • drowsiness
  • cognitive dysfunction
  • dizziness
  • numbness in extremities
  • decreased libido
  • fatigue
  • depression
  • abnormal dreams
  • loss of concentration
  • disorientation
  • insomnia
  • muscle pain
  • muscle weakness
  • tinnitus
  • hearing impairment
  • visual impairment
  • palpitations
  • myasthenia
  • menstrual disorders
  • chills
  • fever

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

Interactions

Drug interactions

Do not take this medication with other non-steroidal anti-inflammatory drugs and Naproxen derivatives. Phenytoin-type anticonvulsants, sulfonamides, sulfonylurea blood glucose-lowering agents, propranolol and other beta-blockers, ACE inhibitors (such as captopril), loop diuretics and thiazide diuretics, probenecid, aspirin, lithium, methotrexate, coumarin anticoagulants (such as warfarin), zidovudine, fluoroquinolone antibiotics (such as enoxacin)

Storage

This medication should be stored in a tightly closed container to protect it from air and moisture. The storage temperature should be maintained at room temperature between 1 and 30 degrees Celsius.

Appearance and packaging

Appearance

Green translucent oblong soft capsule containing light yellow to pale green contents

Package unit

10 capsules (10 capsules/PTP x 1)

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.