Jaltofen Tablets (Jaltoprofen)
Zaltoprofen 80mg
Tablet · Prescription medication
HanPung Pharmaceutical Co., Ltd.
MFDS item code 201904549 · Approved 2019.07.04
This product's status changed to Expired on 2024.07.04. It may no longer be sold, so consult a doctor or pharmacist before taking it.
Anti-inflammatory and analgesic effects for chronic rheumatoid arthritis, osteoarthritis, etc.
This medication is used to alleviate inflammation and pain caused by various joint and muscle disorders such as chronic rheumatoid arthritis, osteoarthritis (degenerative arthritis), lumbago, periarthritis of the shoulder, and cervical radiculopathy. It also helps reduce inflammation and pain following surgery, trauma, and tooth extraction, assisting in the patient's recovery. It effectively improves inflammation and pain in various situations.
Jaltoprofen at a dose of 80 mg is administered orally three times a day. For single administration, 80 to 160 mg is taken orally.
This medication can increase the risk of stomach bleeding if taken by individuals who regularly consume more than three alcoholic beverages per day, so it is essential to consult a doctor or pharmacist. This medication may increase the risk of cardiovascular diseases and serious cardiovascular issues such as myocardial infarction or stroke, so patients with cardiovascular diseases or risk factors should exercise additional caution. During treatment with this medication, careful monitoring for changes in cardiovascular symptoms or signs is necessary, and if symptoms appear, medical personnel should be informed immediately. As a non-steroidal anti-inflammatory analgesic, this medication can cause serious gastrointestinal adverse reactions such as gastrointestinal bleeding, ulcers, and perforations, so patients with a history of gastrointestinal diseases or the elderly should be particularly cautious. The risk of gastrointestinal adverse reactions increases with long-term use, so if there are symptoms of gastrointestinal bleeding or discomfort during use, medical personnel should be consulted immediately. Patients with significant diseases such as peptic ulcers, severe blood disorders, liver dysfunction, renal failure, and heart failure should not take this medication, nor should it be administered to patients with hypersensitivity to the drug or allergies to aspirin and other non-steroidal anti-inflammatory drugs. Women in late pregnancy or breastfeeding, patients with inflammatory bowel disease, and those with genetic issues such as lactose intolerance should also not take this medication. Patients with a history of peptic ulcers, or issues with liver or kidney function, the elderly, and asthma patients should use this medication cautiously, and regular examinations are necessary for long-term use. This medication can cause a variety of side effects such as gastrointestinal disturbances, headaches, dizziness, allergic reactions, blood abnormalities, and liver and kidney function deviations, so if any unusual symptoms occur, it is essential to stop taking the medication and consult medical personnel. Interactions may occur when used in conjunction with other non-steroidal anti-inflammatory drugs, ACE inhibitors, aspirin, diuretics, lithium, methotrexate, anticoagulants, and antidiabetic agents, so it is vital to inform healthcare providers of any current medications being taken. During pregnancy, especially in the late stages, this medication should not be taken as it can affect the fetus; during the early and middle stages of pregnancy, it should only be taken in minimal doses when absolutely necessary. Breastfeeding mothers are advised to avoid this medication as it may be passed into breast milk. The safety of this medication in children has not been established, so special caution is required when administering it to children. The elderly may have decreased renal function, so dosage may need to be adjusted or the medication paused, and any changes in condition should be closely monitored during use. This medication should be stored in a safe place inaccessible to children, and it is recommended not to transfer it to another container.
Hives, severe swelling, chest tightness, difficulty breathing, cold sweats, paleness, severe allergic reactions, severe rash with high fever, blisters, peeling skin, pain in mucous membranes of mouth/eyes, severe skin adverse reactions, difficulty breathing, asthma attacks, respiratory abnormalities accompanied by cough and fever, jaundice, yellowing of the skin or eyes, extreme lethargy, liver abnormalities, sudden and severe headaches, thunderclap headache, seizures,.
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a tightly sealed container to avoid exposure to air or moisture, and it is recommended to keep it at room temperature between 1 and 30 degrees Celsius. Proper storage will help maintain the medication's efficacy and safety.
White round film-coated tablets
30 tablets/bottle, 500 tablets/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.
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For anything that needs medical judgment, consult a doctor or pharmacist.
This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.