Jaltop Tablet (Jaltoprofen)

Adult dose

For Jaltoprofen, take 80 mg orally three times a day. For a single dose, administer 80 to 160 mg orally.

This medication may increase the risk of gastrointestinal bleeding in individuals who regularly consume more than three alcoholic drinks per day. Therefore, consultation with a physician or pharmacist is essential. Nonsteroidal anti-inflammatory drugs (NSAIDs), including this medication, may increase the risk of serious cardiovascular issues such as cardiovascular disease, myocardial infarction, and stroke. Patients with cardiovascular disease or risk factors need to be particularly cautious and should closely monitor for cardiovascular symptoms while taking this medication. Additionally, this medication can cause serious adverse reactions involving the gastrointestinal tract, including gastrointestinal bleeding, ulcers, and perforation, and the risk may be higher in elderly patients or those who take it long-term. If symptoms of abdominal pain or bleeding appear, immediate consultation with healthcare personnel is necessary. Patients with a history of peptic ulcers, severe blood disorders, liver impairment, kidney impairment, or heart failure, as well as those who are hypersensitive to this medication, should not take it. Patients who have had allergic reactions to aspirin or other NSAIDs should also avoid taking it. This medication should be used cautiously in patients with a history of peptic ulcers, those with liver or kidney function issues, asthma patients, hypertensive patients, and elderly individuals, who may require monitoring during treatment and regular health check-ups for adverse reactions. During treatment, symptoms such as gastrointestinal discomfort, headache, dizziness, skin rashes, and shortness of breath may occur; if these occur, discontinue use immediately and consult a healthcare professional. The risk of adverse effects may increase when this medication is taken with other NSAIDs or specific medications, so it's important to inform the healthcare provider of any medications currently in use. It should not be taken during the late stages of pregnancy due to the risk of fetal vascular closure, and it should only be used cautiously in the early and mid-pregnancy under a physician's discretion at the lowest possible dose. Breastfeeding women should avoid taking this medication as it can pass into breast milk. Safety in pediatric patients has not been established, and the dosage and frequency may need to be adjusted in elderly patients due to decreased kidney function. This medication should be kept out of reach of children and not transferred to other containers to maintain quality.

Serious side effects

• Urticaria
• severe swelling (edema)
• chest tightness
• difficulty breathing
• cold sweat
• pallor
• gastrointestinal bleeding
• myocardial infarction
• stroke
• gastrointestinal or intestinal bleeding

Mild side effects

• Gastric discomfort
• stomach pain
• nausea
• upper abdominal pain
• stomatitis
• vomiting
• diarrhea
• abdominal pain
• feeling of fullness in the stomach
• heartburn

This medication should be stored in a tightly closed container to protect it from air and moisture. The storage temperature should be maintained at room temperature between 1 and 30 degrees Celsius.

Appearance

White round film-coated tablets

Package unit

30 tablets/bottle, 500 tablets/bottle