Ccocks Plus Tablets

Adult dose

Adults: Take 1 tablet twice daily. This medicine may be taken with or without food. Take this medicine whole; do not crush or split it. ○ Patients with hepatic impairment This medicine is not recommended for initial treatment in patients with hepatic impairment who require a dose reduction (see Precautions for Use, 5. General Precautions)

Patients who regularly consume alcohol in amounts exceeding certain daily limits should consult a physician or pharmacist before taking this medication. There is a risk of gastric bleeding when taking this medication. This medication may increase the risk of cardiovascular disease; therefore, individuals with cardiovascular issues, such as heart attack or stroke, should exercise particular caution. It should be used at the lowest possible dose for the shortest duration. If cardiovascular symptoms occur, medical attention should be sought immediately. Additionally, this medication can cause serious issues such as ulcers, bleeding, and perforation in the gastrointestinal tract; individuals with a history of gastrointestinal diseases should take care before use. Elderly patients or those at high risk for gastrointestinal bleeding should be especially cautious and consult medical personnel immediately if gastrointestinal symptoms occur. This medication is not to be administered to individuals with specific allergic reactions, severe heart, liver, or kidney diseases, patients with active peptic ulcers or inflammatory bowel disease, or women who are pregnant or breastfeeding. Patients with liver or kidney dysfunction or those with asthma, high blood pressure, or heart failure should use this medication cautiously and require regular testing and monitoring during use. While taking this medication, side effects such as headaches, indigestion, skin rashes, and swelling may occur, and serious symptoms should be discussed with a physician immediately. This medication may interact with other drugs, so it is important to inform a physician or pharmacist if any other medications are being taken. Women who are pregnant or planning a pregnancy should consult a professional, as this medication may affect reproductive capacity. Elderly patients may have decreased kidney, liver, and heart function, necessitating special caution during use. Dizziness or drowsiness may occur while taking this medication, so it is advisable to avoid driving or operating machinery. Long-term use of this medication may require regular blood tests and monitoring of liver and kidney function. If any unusual findings arise, discontinuation of use is necessary. In case of overdose, symptoms such as lethargy, nausea, vomiting, and abdominal pain may appear, and appropriate medical treatment should be sought immediately. When storing, ensure the medication is out of reach of children and avoid transferring it to other containers.

Gastrointestinal hemorrhage, cardiovascular thromboembolic reaction, myocardial infarction, stroke, perforation of the upper and lower gastrointestinal tract, ulcer, bleeding, dyspepsia, nausea, upper abdominal pain, constipation, diarrhea, dry mouth, esophageal pain, stomatitis, acute pyelonephritis, facial edema, pain at the insertion site, peripheral edema, fever, pruritus, psoriasis, rash, skin swelling, elevation of alanine aminotransferase, elevation of aspartate aminotransferase, hypertension, increase in blood uric acid, elevation of gamma-glutamyltransferase, arthralgia, back pain, coccygodynia, flank pain, headache, carpal tunnel syndrome, lymphadenopathy, cholelithiasis, bronchitis, sinusitis, upper respiratory tract infection, urinary tract infection, pharyngitis, rhinitis, anemia, thrombocytopenia, hypersensitivity, insomnia, anxiety, confusion, dizziness, muscle tone increase, drowsiness, blurred vision, tinnitus, palpitations, congestive heart failure, arrhythmia, tachycardia, hypertension, flushing, cough, vomiting, abdominal pain, bloating, gastric ulcer, dental disease, duodenal ulcer, esophageal ulcer, intestinal perforation, pancreatitis, elevation of liver enzymes, itching, urticaria, petechiae, angioedema, alopecia, vesicular dermatitis, peripheral edema, influenza-like illness, injury, bursitis, contact dermatitis, injection site reaction, skin nodules, dysgeusia, albuminuria, cystitis, hematuria, dysuria, frequency of urination, nephrolithiasis, urinary incontinence, blurred vision, cataract, conjunctivitis, eye pain, glaucoma, ocular hemorrhage, retinal artery or vein occlusion, increase in serum creatinine, elevation of β2-microglobulin, increase in NAG, positive urine hematuria, positive urine protein, renal impairment, acute renal failure, interstitial nephritis, breast tenderness, menopausal symptoms, fibrocystic breast disease, thoracic neoplasm, chest pain, dysmenorrhea, menstrual disorders, vaginal bleeding, vulvitis, prostatic disorders, ovarian cysts, hearing loss, ear abnormalities, otalgia, hearing impairment, liver dysfunction, hepatitis, jaundice, liver failure, acute hepatitis, hepatic necrosis, increase in serum sodium, increase in serum potassium, increase in BUN, increase in CPK, diabetes mellitus, hypercholesterolemia, hyperglycemia, hypokalemia, hyperkalemia, increase in NPN, increase in creatinine, increase in alkaline phosphatase, weight gain, anorexia, increase in LDH, hypoglycemia, hyponatremia, bursitis, arthrosis, myalgia, cervical dystonia, synovitis, tendinitis, myositis, leg cramps, fractures, tendon rupture, pain in the back, muscle rigidity, decrease in hematocrit, increase in hemoglobin, epistaxis, thrombocytopenic purpura, agranulocytosis, aplastic anemia, pancytopenia, leukopenia, chest pain, sudden death, anaphylactic-like reaction, angioedema, anorexia, depression, nervous system hyperreactivity, drowsiness, fatal intracranial hemorrhage, hallucinations, worsening of epilepsy, bronchospasm, exacerbation of bronchospasm, dyspnea, laryngitis, pneumonia, epistaxis, speech disorder, vesicular dermatitis, dermatitis, nail disease, photosensitivity reaction, erythematous rash, papular rash, skin dryness, increased sweating, erythema multiforme, exfoliative dermatitis, Stevens-Johnson syndrome, toxic epidermal necrolysis, eczematous dermatitis, cholestasis, cholestatic hepatitis, jaundice, photosensitive reaction, Stevens-Johnson syndrome, erythema multiforme, toxic epidermal necrolysis, drug rash with eosinophilia and systemic symptoms, acute generalized exanthematous pustulosis, exfoliative dermatitis, acute renal failure, hyponatremia, tubular interstitial nephritis, nephrotic syndrome, focal segmental glomerulosclerosis, menstrual disorders, female infertility, chest pain, heartburn, dry mouth, nausea, diarrhea, weakness, hypertriglyceridemia, hypercholesterolemia, transaminitis, elevation of ALT, elevation of AST, itching, leukopenia, neutropenia, chest discomfort, blurred vision, epigastric discomfort, gastritis, gastrointestinal pain, gastroesophageal reflux disease, epigastric pain not related to food, insomnia

This medication can be sensitive to air or moisture, so it should be stored in a sealed container. Additionally, it is best to keep it at room temperature between 1 and 30 degrees Celsius. This helps to maintain the effectiveness of the medication for a longer period.

Appearance

Yellow rectangular film-coated tablets composed of two layers

Package unit

30 tablets/bottle, 300 tablets/bottle