Ibuprofen extended-release capsules
Function and Efficacy
This product can inhibit the synthesis of prostaglandins and has antipyretic, analgesic and anti-inflammatory effects.
Ingredients
Each tablet of this product contains 0.3g of ibuprofen, the main ingredient. The auxiliary materials are: sucrose, starch, stearic acid, povidone K30, and ethanol.
| Name | Description | Content | CAS NO. | Manufacturer |
|---|---|---|---|---|
| IbuprofenIngredients |
This product can inhibit the synthesis of prostaglandins and has antipyretic, analgesic and anti-inflammatory effects. More |
15687-27-1 | 54 | |
| SucroseExcipients |
This product can inhibit the synthesis of prostaglandins and has antipyretic, analgesic and anti-inflammatory effects. More |
57-50-1 | 71 | |
| StarchExcipients |
This product can inhibit the synthesis of prostaglandins and has antipyretic, analgesic and anti-inflammatory effects. More |
9005-25-8 | 77 | |
| Stearic acidExcipients |
This product can inhibit the synthesis of prostaglandins and has antipyretic, analgesic and anti-inflammatory effects. More |
57-11-4 | 26 | |
| EthanolExcipients |
This product can inhibit the synthesis of prostaglandins and has antipyretic, analgesic and anti-inflammatory effects. More |
64-17-5 | 89 |
Appearance
This product contains white spherical pellets, aluminum-plastic packaging
Indication
It is used to relieve mild to moderate pain such as headache, joint pain, migraine, toothache, muscle pain, neuralgia, and dysmenorrhea. It is also used for fever caused by the common cold or influenza.
Usage and Dosage
Oral. Adults, 1 capsule at a time, 2 times a day (once in the morning and once in the evening)
Adverse Reactions
1. A small number of patients may experience nausea, vomiting, abdominal pain, diarrhea, constipation, flatulence, burning sensation in the stomach or mild indigestion, gastrointestinal ulcers and bleeding, elevated transaminases, headache, dizziness, tinnitus, blurred vision, mental tension, drowsiness, lower limb edema or sudden weight gain. 2. Rare rash, urticaria, and itching. Extremely rare severe skin allergic reactions, exfoliative dermatitis, Stevens-Johnson syndrome, or bullous skin diseases such as erythema multiforme and epidermal necrolysis. 3. Rare allergic nephritis, cystitis, nephrotic syndrome, renal papillary necrosis or renal failure, especially during long-term use, which are usually accompanied by elevated serum urea levels and edema. Rare bronchospasm and asthma aggravation. 4. Patients with a history of intestinal diseases such as ulcerative colitis and Crohn's disease may have their condition aggravated. 5. Extremely rare hematopoietic disorders (anemia, leukopenia, thrombocytopenia, pancytopenia, agranulocytosis, initial symptoms are: fever, sore throat, superficial oral ulcers, flu-like symptoms, severe fatigue, unexplained bruises or bleeding) or liver disease, liver failure, hepatitis. 6. Extremely rare severe allergic reactions, symptoms include: edema of the face, lips, tongue and throat, dyspnea, tachycardia, hypotension (anaphylactic reaction, angioedema or shock). 7. Edema, hypertension, fluid retention and heart failure have been reported with treatment with nonsteroidal anti-inflammatory drugs. 8. In patients with autoimmune diseases (such as systemic lupus erythematosus, mixed connective tissue disease), there have been individual cases of symptoms of aseptic meningitis during ibuprofen treatment, such as stiff neck, headache, nausea, vomiting, fever or confusion. 9. Stop taking this medicine and consult your doctor immediately if you experience any of the following symptoms: Allergic reactions, such as rash and itching, sometimes with difficulty breathing or swelling of the lips, tongue, throat, or face; Rash, peeling, and mouth ulcers: worsening asthma; Stomach ulcers, vomiting blood or brown particles (like coffee grounds), or passing black tarry stools; Worsening of intestinal disease (ulcerative colitis or Crohn's disease): unexplained bruising or bleeding, fever, sore throat, mouth ulcers, extreme paleness or weakness; Meningitis (symptoms may include stiff neck, headache, nausea, vomiting, fever, or confusion; especially if you have an autoimmune disease (such as systemic lupus erythematosus, mixed connective tissue disease); Less or more urine than usual, cloudy urine, blood in the urine, or pain and/or swelling in your back (especially the legs): feeling short of breath or swelling in the legs and feet, chest pain, sudden weakness on one side, sudden slurred speech; Liver problems, such as jaundice, symptoms may include yellowing of the skin and whites of the eyes.
Precautions
1. Patients who are allergic to ibuprofen, excipients in this product, aspirin or other non-steroidal anti-inflammatory drugs are prohibited from using this product. 2. Pregnant and lactating women are prohibited from using this product. 3. Asthmatic patients who are allergic to aspirin are prohibited from using this product. 4. Patients with liver disease, kidney disease and heart disease are prohibited from using this product. 5. Patients who are taking other drugs containing ibuprofen or other non-steroidal anti-inflammatory drugs, including those taking drugs known to be specific cyclooxygenase-2 inhibitors, are prohibited from using this product. Unless recommended by a doctor. 6. Patients with a history of upper gastrointestinal bleeding or perforation related to the use of steroidal anti-inflammatory drugs are prohibited from using this product. 7. Patients with active or previous history of peptic ulcer, gastrointestinal bleeding or perforation are prohibited from using this product.
Special Population Medication
Precautions for children: Children must use under adult supervision. Precautions for pregnancy and lactation: Use with caution. Precautions for the elderly: Elderly patients are prone to adverse reactions due to decreased liver and kidney function, so they should be used with caution or in a reduced dosage.
Drug Interactions
1. When this product is used together with other antipyretic, analgesic and anti-inflammatory drugs, it may increase intestinal adverse reactions and may cause ulcers. 2. When this product is used together with anticoagulants such as heparin and dicoumarol, it may lead to prolonged prothrombin time and increased bleeding tendency. 3. When this product is used together with digoxin, methotrexate and oral hypoglycemic drugs, the blood concentration of these drugs can be increased, so it is not suitable to be used together. 4. When this product is used together with furosemide (furananilide), the latter's sodium excretion and hypoglycemic effect are reduced: when used together with antihypertensive drugs, the latter's antihypertensive effect is also reduced. 5. If used together with other drugs, drug interactions may occur. Please consult a doctor or pharmacist for details.
Storage
Seal and store (10-300).
Packaging Specification
0.3 g
Validity Period
36 months
Manufacturer
Zhuhai Rundu Pharmaceutical Co., Ltd.
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Founded in:
1999-12-30 -
Address:
No. 6, Airport North Road, Sanzao Town, Jinwan District, Zhuhai City -
Tax NO.:
91440400192520640G -
Registered Funds:
334.893286 million yuan -
Website:
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Email: