Solleton Tablet (Jaltoprofen)

Adult dose

The recommended dosage for Jaltoprofen is 80 mg taken orally three times a day. For single administration, 80-160 mg should be taken orally.

This medication should be consulted with a doctor or pharmacist if taken by individuals who regularly consume more than three alcoholic beverages per day, as it increases the risk of gastrointestinal bleeding. Patients with cardiovascular disease or risk factors may face an increased risk of cardiomyopathy, stroke, and other cardiovascular issues while taking this medication, so caution is required. This medication can cause serious issues, such as gastrointestinal bleeding, ulcers, and perforation, so elderly patients and those with a history of gastrointestinal diseases should be especially careful. Patients with peptic ulcers, serious blood disorders, severely impaired liver or kidney function, heart failure, or allergies to this medication or its components should not take it. Patients with a history of asthma, allergic reactions, sensitivity to aspirin, pregnant women in the late stages of pregnancy, nursing mothers, and those with certain genetic metabolic disorders should also avoid using this medication. While taking this medication, various side effects such as gastrointestinal disturbances, headache, dizziness, allergic reactions, blood disorders, and liver or kidney function abnormalities may occur, so immediate consultation with medical personnel is required if symptoms arise. Long-term use necessitates regular blood tests and liver and kidney function assessments, and if abnormal findings occur, the drug should be discontinued. This medication may interact with other non-steroidal anti-inflammatory drugs, ACE inhibitors, diuretics, anticoagulants, lithium, and methotrexate, necessitating caution when used together. During pregnancy, especially in the late stages, it should not be used due to potential risks to the fetus, and caution is advised in early or mid-pregnancy as well. Nursing mothers should avoid this medication as it can be transferred through breast milk. Elderly patients should be monitored for dosage adjustment due to possible increased drug concentration due to impaired kidney function. This medication should be kept out of the reach of children and should not be transferred to other containers.

Serious side effects

Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, gastrointestinal bleeding, peptic ulcers, hemorrhagic colitis, shock, symptoms resembling anaphylaxis, Stevens-Johnson syndrome, toxic epidermal necrolysis (Lyell's syndrome), decrease in red blood cells, decrease in hemoglobin, decrease in hematocrit, agranulocytosis, thrombocytopenia, hemolytic anemia, aplastic anemia, jaundice, acute kidney failure, nephrotic syndrome, hematuria, edema

Mild side effects

• Nausea
• stomach pain
• vomiting
• upper abdominal pain
• stomatitis
• dizziness
• diarrhea
• abdominal pain
• gastric discomfort
• vomiting

This medication should be stored in a sealed container to protect it from air and moisture. It is advisable to keep the storage temperature between 1 to 30 degrees Celsius.

Appearance

White film-coated tablet

Package unit

90 tablets/PTP (10 tablets/PTP x 9), 500 tablets/bottle