Naproxen Enteric Coated Pellets Capsules
Function and Efficacy
This product is a non-steroidal anti-inflammatory analgesic that can inhibit the synthesis of prostaglandins and exert anti-inflammatory and analgesic effects.
Ingredients
Each tablet of this product contains 0.125 grams of naproxen, and the excipients are starch, microcrystalline cellulose, povidone K30, sodium carboxymethyl starch, and polyacrylic acid resin II.
| Name | Description | Content | CAS NO. | Manufacturer |
|---|---|---|---|---|
| NaproxenIngredients |
This product is a non-steroidal anti-inflammatory analgesic that can inhibit the synthesis of prostaglandins and exert anti-inflammatory and analgesic effects More |
22204-53-1 | 30 | |
| StarchExcipients |
This product is a non-steroidal anti-inflammatory analgesic that can inhibit the synthesis of prostaglandins and exert anti-inflammatory and analgesic effects. More |
9005-25-8 | 78 | |
| Microcrystalline celluloseExcipients |
This product is a non-steroidal anti-inflammatory analgesic that can inhibit the synthesis of prostaglandins and exert anti-inflammatory and analgesic effects. More |
9004-34-6 | 89 | |
| Sodium carboxyl methylstarchExcipients |
This product is a non-steroidal anti-inflammatory analgesic that can inhibit the synthesis of prostaglandins and exert anti-inflammatory and analgesic effects. More |
9063-38-1 | 46 |
Appearance
This product is a white-capped transparent corpus luteum capsule, and the contents are white or off-white enteric-coated micropellets.
Indication
Used to relieve mild to moderate pain such as joint pain, muscle pain, neuralgia, headache, toothache, and dysmenorrhea.
Usage and Dosage
Oral administration: Adults take 2 capsules at a time, 2-3 times a day.
Adverse Reactions
May cause nausea, vomiting, indigestion, constipation, stomach discomfort, dizziness, headache, drowsiness, tinnitus, shortness of breath, dyspnea, asthma, itchy skin, lower limb edema; may cause blurred vision or visual impairment, hearing loss, diarrhea, oral irritation or pain, palpitations, and sweating; may cause gastrointestinal bleeding, kidney damage, allergic rash, depression, muscle weakness, abnormal blood count, and liver damage.
Precautions
It is contraindicated for those who are allergic to this product. It is contraindicated for pregnant women and lactating women. It is contraindicated for those with asthma, nasal polyposis syndrome, neuroangioedema, and those who are allergic to aspirin or other antipyretic analgesics. It is contraindicated for patients with hemophilia or thrombocytopenia and active ulcer disease.
Special Population Medication
Precautions for children: Not yet clear. Precautions for pregnancy and lactation: Not yet clear. Precautions for the elderly: Not yet clear.
Drug Interactions
Drinking alcohol or using it with other anti-inflammatory analgesics can increase gastrointestinal adverse reactions and the risk of ulcer attacks. When used with anticoagulants such as heparin and dicoumarol, the bleeding time is prolonged, bleeding tendency may occur, and there is a possibility of gastrointestinal ulcers. This product can reduce the sodium excretion and antihypertensive effects of furosemide. This product can inhibit the excretion of potassium and increase the blood concentration of potassium. When used with probenecid, the blood concentration of this product increases, the half-life is prolonged, the efficacy is increased, but the adverse reactions also increase accordingly. If you are taking other medicines, please consult a doctor or pharmacist before using this product.
Storage
seal.
Packaging Specification
0.125g
Validity Period
Tentative 24 months
Manufacturer
Hangzhou Conba Pharmaceutical Co., Ltd.
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Founded in:
2000-03-27 -
Address:
No. 568, Binkang Road, Changhe Street, Binjiang District, Hangzhou City, Zhejiang Province -
Tax NO.:
91330108716159914E -
Registered Funds:
380 million yuan -
Website:
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Email: