GL Piroxicam Capsule 20 Milligrams

Adult dosage

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

Caution should be exercised if this medication is taken by individuals who regularly consume more than three alcoholic beverages per day, as it may cause gastrointestinal bleeding. Non-steroidal anti-inflammatory drugs like this one may increase the risk of cardiovascular issues such as heart attack and stroke, so those with cardiovascular diseases or risk factors should be particularly careful. Individuals who have a history of ulcers or gastrointestinal bleeding should consult with healthcare providers before taking this medication, as it may lead to serious gastrointestinal issues like bleeding, ulcers, and perforations. Elderly patients or those with a history of gastrointestinal diseases may experience gastrointestinal-related adverse reactions more frequently, so they should closely monitor for symptoms during treatment. This medication may cause serious skin reactions such as severe rashes, exfoliative dermatitis, and Stevens-Johnson syndrome, so discontinue use and notify healthcare providers immediately if any abnormal skin symptoms occur. It is safest for individuals with a history of gastrointestinal ulcers, bleeding, liver impairment, kidney impairment, heart failure, hypertension, blood abnormalities, or allergies not to take this medication. Additionally, this medication is not recommended for use during pregnancy or breastfeeding, or in patients aged 80 and older and in children. Regular blood tests, liver function tests, and kidney function tests should be performed during treatment to monitor for adverse reactions. The risk of side effects may increase if this medication is used in conjunction with other non-steroidal anti-inflammatory drugs, antiplatelet agents, anticoagulants, and certain antibiotics, so use in combination should always be discussed with healthcare providers. Symptoms such as nausea, vomiting, drowsiness, and gastrointestinal bleeding may occur in cases of overdose; therefore, adhere strictly to the dosage and seek medical attention immediately if any unusual symptoms arise. Keep this medication out of reach of children and do not transfer it to any other containers.

Peptic ulcer, hematemesis, hemorrhage, gastrointestinal bleeding, abdominal pain, discomfort in the upper abdomen, loss of appetite, nausea, vomiting, diarrhea, loose stools, stomatitis, dyspepsia, abdominal bloating, constipation, glossitis, shock, drug reaction with eosinophilia and systemic symptoms (DRESS syndrome), Stevens-Johnson syndrome, Lyell's syndrome, photosensitivity reaction, nail dystrophy, abnormal growth of toenails, hair loss, pustular reaction, anemia, granulocytopenia, thrombocytopenia, aplastic anemia, bone marrow suppression, purpura, leukopenia, pancytopenia, eosinophilia, hypertension, congestive heart failure, acute cardiac disease, jaundice, hepatitis, elevation of AST/ALT, elevation of ALP, elevation of LDH, acute renal failure, fluid retention, oliguria, hematuria, proteinuria, elevated BUN, increased serum creatinine, hyperkalemia, rash, pruritus, bronchospasm, urticaria, angioedema, vasculitis, serum sickness, drowsiness, dizziness, headache, tinnitus, numbness of hands and feet, depression, irritability, hallucinations, mood changes, mental confusion, allergic edema of the face and hands, dry mouth, general malaise, blurred vision, eye irritation, stiffness in shoulders, fever, palpitations, dyspnea

This medication should be stored in a tightly closed container to prevent air or moisture from entering. Proper storage will maintain the effectiveness of the medication and prevent degradation.

Appearance

A hard capsule containing white to light yellow contents with a white upper and lower shell.

Package unit

1000 capsules per bottle