Gonplex Capsule 2mg (Pomalidomide)

Adult dose

Before administering this medicine, consider the potential risks and benefits of this medicine and other alternative treatments. Cardiovascular risk increases with higher doses and longer exposure to this medicine; therefore, administer it for the shortest possible duration. Efficacy beyond 6 weeks and the safety of long-term administration beyond 6 months have not been established. Adverse reactions such as hypertension, angina, and edema may occur during treatment with this medicine. Therefore, during treatment, the need to continue therapy based on symptom relief and the response to treatment should be reassessed regularly at least once a month. The recommended dose is 2mg once daily, taken after a meal. Do not exceed a daily dose of 2mg. If there is no therapeutic benefit at the recommended dose, discontinue this medicine and consider an appropriate alternative treatment. Do not administer this medicine because there is no experience with its use.

This medication may increase the risk of gastrointestinal bleeding in individuals who regularly consume more than three drinks per day, so it must be discussed with a doctor or pharmacist. This medication can affect the cardiovascular system and may increase the risk of severe thrombotic reactions such as myocardial infarction or stroke. Therefore, it should be used for the shortest duration at the lowest effective dose possible, and any cardiovascular symptoms should be reported to healthcare professionals immediately. This medication can cause serious gastrointestinal issues such as gastrointestinal bleeding, ulcers, and perforation, so individuals with a history of gastrointestinal disease or the elderly should be especially cautious, and any symptoms of gastrointestinal bleeding (such as epigastric pain, black stools, or hematemesis) should be treated immediately. Individuals who are allergic to this medication or have certain conditions (e.g., uncontrolled hypertension, liver or kidney impairment, active gastric ulcer, congestive heart failure, pregnant women, etc.) should not take this medication. Asthma, heart failure, hypertension, edema, the elderly, and those with a history of peptic ulcers need to exercise special caution when taking this medication and must do so under medical supervision. During treatment, abnormal reactions such as upper abdominal pain, indigestion, headache, elevated blood pressure, shortness of breath, or skin rash may occur; patients should inform healthcare professionals if symptoms persist or worsen. This medication can affect liver and kidney functions, so regular blood tests and liver and kidney function tests are necessary, and if the test results show abnormalities, use should be discontinued. This medication can interact with other drugs, so anyone taking medications metabolized by the liver or antihypertensives, diuretics, anticoagulants, lithium, and methotrexate must consult a doctor. Women who are pregnant or may become pregnant and those who are breastfeeding should not take this medication. If pregnancy is confirmed during treatment, it should be stopped immediately. The safety and efficacy of this medication have not been established in children or adolescents under 18, so it is recommended not to use it in this population. The elderly may have decreased renal, liver, and cardiac function, so special care and monitoring are necessary when taking this medication. This medication may cause dizziness or drowsiness, so it is safe to avoid driving or operating machinery. This medication must be used according to the approved dosage and administration, kept out of reach of children, and should not be stored in other containers.

Gastrointestinal bleeding, serious cardiovascular thrombotic reactions, myocardial infarction, stroke, upper abdominal pain, indigestion, nasopharyngitis, pneumonia, dermatitis, bronchitis, soft tissue inflammation, boil, herpes zoster, influenza, syphilis, urinary tract infection, onychomycosis, colorectal polyp, anemia, skin papilloma, eosinophilia, hypersensitivity reaction, chemical allergy, diabetes, hypercholesterolemia, hyperkalemia, depressed mood, major depressive disorder, headache, insomnia, paresthesia, conscious depressive state, dizziness, drowsiness, lethargy, Alzheimer's type dementia, tremor, eye swelling, eyelid edema, blepharitis, blepharospasm, dry eyes, keratitis, macular hole, ear discomfort, positional vertigo, palpitations, angina, atrioventricular block, myocardial ischemia, hypertension, arrhythmia, high blood pressure, facial flushing, abnormal blood pressure, cough, dyspnea, asthma, rhinorrhea, oropharyngeal pain, productive cough, rhinitis, allergic rhinitis, upper abdominal pain, diarrhea, nausea, abdominal pain, vomiting, gastrointestinal motility disorder, irritable bowel syndrome, stool discoloration, food poisoning, gastric ulcer, gingivitis, dental disorder, dry mouth, enteritis, upper abdominal discomfort, gastritis, abdominal discomfort, lower abdominal pain, aphthous stomatitis, constipation, gastroesophageal reflux disease, colorectal polyp, esophagitis, hyperbilirubinemia, facial swelling, urticaria, erythema, neurodermatitis, itching, generalized itching, dry eczema, arthralgia, back pain, flat feet, joint swelling, neck pain, limb pain, plantar fasciitis, musculoskeletal pain, intervertebral disc herniation, muscle cramps, frequent urination, chronic kidney failure, microalbuminuria, urinary stones, breast pain, chest discomfort, facial edema, swelling, peripheral edema, fatigue, generalized edema, influenza-like illness, weight gain, asthenia, thirst, bruise, abrasion, laceration, traffic accident, spinal compression fracture, chills, fever, insect bite, concussion, ligament rupture, sprain, wound, wrist fracture,热感, drug overdose, neutrophilia, decreased unsaturated iron binding capacity, prolonged prothrombin time, decreased hemoglobin, increased alanine aminotransferase, increased aspartate aminotransferase, increased creatine kinase, increased serum creatinine, stroke, sensory anomalies, sensory reduction, rash, drug rash, skin erosion, tachycardia, conjunctival injection, gastrointestinal disorder, abdominal distension, decreased appetite, daydreaming, dysuria, lethargy, drowsiness, nausea, vomiting, upper abdominal pain, hypertension, acute renal failure, respiratory depression, coma

This medication should be stored in a tightly sealed container to prevent exposure to air and moisture. The storage temperature should be maintained at room temperature between 1°C and 30°C. This will help to safely preserve the effectiveness of the medication over time.

Appearance

A hard capsule with a white to pale yellow powder inside, with a white shell.

Package unit

30 capsules/bottle, 100 capsules/bottle