Solucam Injection (Piroxicam)

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. The 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 conducted. (Injection) Adults: Administer 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. The 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 conducted. The oral or suppository formulation of this medicine may be used concomitantly, but the total amount administered by both routes must not exceed the maximum recommended daily dose.

This medication may cause gastrointestinal bleeding in patients who regularly consume more than three alcoholic beverages a day, so consultation with a doctor or pharmacist is essential. This medication may affect the cardiovascular system and increase the risk of severe complications such as heart attacks or strokes; therefore, individuals with cardiovascular diseases or risk factors need to exercise additional caution. This medication can cause severe adverse reactions such as gastrointestinal bleeding, ulcers, and perforations, particularly in the elderly or those with a history of gastrointestinal diseases, so symptoms should be closely monitored during treatment. Severe allergic reactions may occur on the skin; if unusual skin symptoms such as rash or itching appear, discontinue use immediately. This medication contains benzyl alcohol, which may be hazardous to newborns or premature infants, so caution is required. Injectable forms in ampoules may carry a risk of glass fragments contamination, so they must be handled carefully; extra caution is necessary, especially for children and the elderly. It is safer not to use this medication for individuals with a history of gastric ulcers or bleeding, serious liver, kidney, or heart diseases, pregnant or nursing women, children, or the elderly (especially those over 80 years old). Periodic testing of gastric, cardiac, and renal functions should be conducted while taking this medication, and if any abnormal symptoms occur, consult a physician immediately. There may be drug interactions with other medications; therefore, inform your doctor or pharmacist about any other medications you are currently taking. Pregnant or nursing women should not take this medication, and special caution is necessary for children and the elderly. In case of overdose, symptoms such as vomiting, drowsiness, and abdominal pain may occur, so strict adherence to dosage is crucial, and seek medical response immediately if abnormalities appear.

Gastrointestinal bleeding, peptic ulcer, hematemesis, hematochezia, epigastric pain, discomfort in the upper abdomen, loss of appetite, nausea, vomiting, diarrhea, loose stools, stomatitis, dyspepsia, abdominal distention, constipation, glossitis, shock, drug reaction with eosinophilia and systemic symptoms (DRESS syndrome), Stevens-Johnson syndrome, Lyell's syndrome, photosensitivity reactions, nail dystrophy, abnormal nail growth, hair loss, bullous reaction, anemia, granulocytopenia, thrombocytopenia, aplastic anemia, bone marrow suppression, purpura, leukopenia, pancytopenia, eosinophilia, hypertension, congestive heart failure, acute heart disease, jaundice, hepatitis, elevated AST/ALT, elevated ALP, elevated LDH, acute renal failure, fluid retention, oliguria, hematuria, proteinuria, elevated BUN, elevated 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 face and hands, dry mouth, generalized fatigue, blurred vision, eye irritation, shoulder stiffness, fever, palpitations, shortness of breath

This medication is sensitive to light, so it should be stored in an opaque container. Additionally, it is important to keep it in a cool room temperature to maintain its effectiveness.

Appearance

Ampoule: Brown ampoule injection filled with a pale yellow liquid Pre-filled: A glass tube filled with pale yellow transparent liquid sealed at both ends with rubber stoppers (part of the pre-filled syringe system)

Package unit

1ml/ampoule x 50