Medication info
Philogen Tablet (Piroxicam)

Philogen Tablet (Piroxicam)

Prescription medicationTablet
Ingredient · strength
Piroxicam›20mg / 1 tablet
Manufacturer / importer
(Ltd.) Genupharma
Appearance
Light blue round tablet
Packaging
30 tablets/bottle, 300 tablets/bottle
Approval status
Active

MFDS item code 198700667 · Notified 1987.07.13 · Insurance code 698000110

Summary

Main use
Relief of joint disorders (e.g., rheumatoid arthritis) and chronic musculoskeletal pain (e.g., back pain)
Who uses it
Adults
Adult dosage
(Oral) Adults: Administer piroxicam 20 mg orally once daily. The maximum recommended daily dose is 20 mg of piroxicam. To reduce the risk of adverse reactions, use the minimum effective dose for the shortest duration possible. Therapeutic effect and tolerability should be reviewed within 14 days after starting this medicine. If continued treatment is considered necessary, more frequent reviews should be performed. (Injection) Adults: Administer piroxicam 20 mg by intramuscular injection once daily. The maximum recommended daily dose is 20 mg of piroxicam. To reduce the risk of adverse reactions, use the minimum effective dose for the shortest duration possible. Therapeutic effect and tolerability should be reviewed within 14 days after starting this medicine. If continued treatment is considered necessary, more frequent reviews should be performed. The oral or suppository formulation of this medicine may be used concomitantly; however, the total daily dose administered by both routes must not exceed the maximum recommended daily dose.

Ingredients

Manufacturer
(Ltd.) Genupharma

Efficacy & effects

Relief of joint disorders (e.g., rheumatoid arthritis) and chronic musculoskeletal pain (e.g., back pain)

  • Rheumatoid arthritis
  • osteoarthritis
  • ankylosing spondylitis
  • low back pain
  • shoulder periarthritis
  • frozen shoulder syndrome
View approved original text

This medication is used when other non-steroidal anti-inflammatory drugs have not been effective enough. It is primarily applied to chronic inflammatory diseases such as rheumatoid arthritis, osteoarthritis, and ankylosing spondylitis. It is also used for chronic musculoskeletal pain such as lower back pain, periarthritis of the shoulder, and adhesive capsulitis. It is administered only in these cases to relieve symptoms.

Dosage and Administration

Adult dosage

(Oral) Adults: Administer piroxicam 20 mg orally once daily. The maximum recommended daily dose is 20 mg of piroxicam. To reduce the risk of adverse reactions, use the minimum effective dose for the shortest duration possible. Therapeutic effect and tolerability should be reviewed within 14 days after starting this medicine. If continued treatment is considered necessary, more frequent reviews should be performed. (Injection) Adults: Administer piroxicam 20 mg by intramuscular injection once daily. The maximum recommended daily dose is 20 mg of piroxicam. To reduce the risk of adverse reactions, use the minimum effective dose for the shortest duration possible. Therapeutic effect and tolerability should be reviewed within 14 days after starting this medicine. If continued treatment is considered necessary, more frequent reviews should be performed. The oral or suppository formulation of this medicine may be used concomitantly; however, the total daily dose administered by both routes must not exceed the maximum recommended daily dose.

Precautions

This medication should be discussed with a doctor or pharmacist if the patient regularly consumes more than three drinks of alcohol per day, as there is a risk of gastrointestinal bleeding when taken with alcohol. This medication can affect the cardiovascular system and may lead to serious problems such as heart attacks or strokes. Those with cardiovascular diseases or risk factors should be particularly cautious and report any symptoms immediately. This medication may cause serious issues such as gastrointestinal bleeding, ulcers, or perforations, so elderly patients or those with a history of gastrointestinal diseases should use it cautiously. If gastrointestinal-related symptoms occur, the medication should be stopped immediately, and treatment should be sought. Severe skin rashes or allergic reactions may occur. If any skin abnormalities are observed within one month of starting treatment, the medication should be stopped immediately. Patients with gastrointestinal ulcers, bleeding, severe liver or kidney diseases, heart failure, hypertension, a history of drug allergies, those who are pregnant or breastfeeding, and individuals over 80 years of age should not take this medication. Patients with peptic ulcers or asthma, hypertension, or abnormal liver or kidney function should use this medication with caution and may require monitoring by a physician. This medication may cause side effects such as dyspepsia, nausea, vomiting, diarrhea, skin rashes, dizziness, and headaches. In severe cases, it should be discontinued immediately, and medical attention should be sought. Taking this medication with other non-steroidal anti-inflammatory drugs or certain medications may increase the risk of side effects, so it is crucial to inform healthcare providers of any current medications. It should not be used in late pregnancy, as it may pose a risk to the fetus, and it is also advisable not to take it while breastfeeding. Safety in children has not been established, and it should not be used in this population. Elderly patients have a higher risk of side effects and should take the minimum dosage with caution, reporting any unusual reactions immediately. In case of overdose, symptoms such as drowsiness, nausea, vomiting, and gastrointestinal bleeding may occur. Appropriate treatment should be received according to a doctor's instructions.

Side effects

Gastrointestinal bleeding, peptic ulcer, hematemesis, hematochesia, epigastric pain, upper abdominal discomfort, appetite loss, nausea, vomiting, diarrhea, loose stools, stomatitis, dyspepsia, abdominal distension, constipation, glossitis, shock, drug reaction with eosinophilia and systemic symptoms (DRESS syndrome), Stevens-Johnson syndrome, Lyell's syndrome (toxic epidermal necrolysis), photosensitivity reactions, onycholysis, abnormal nail growth, hair loss, bullous reactions, anemia, agranulocytosis, thrombocytopenia, aplastic anemia, bone marrow suppression, purpura, leukopenia, pancytopenia, eosinophilia, hypertension, congestive heart failure, acute cardiac disease, jaundice, hepatitis, elevated AST/ALT, elevated ALP, elevated LDH, acute kidney failure, fluid retention, oliguria, hematuria, urinary protein, elevated BUN, elevated serum creatinine, hyperkalemia, rash, pruritus, bronchospasm, urticaria, angioedema, vasculitis, serum sickness, drowsiness, dizziness, headache, tinnitus, paresthesia, depression, irritability, hallucinations, mood changes, mental confusion, allergic edema of the face and hands, dry mouth, general malaise, blurred vision, eye irritation, shoulder stiffness, fever, palpitations, dyspnea

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

Storage

This medication should be stored in a sealed container to prevent air or moisture from entering. It is also advisable to keep it away from direct sunlight and at a normal room temperature.

Appearance and packaging

Appearance

Light blue round 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.

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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.