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Naproxen extended-release tablets

Function and Efficacy

This product is a non-steroidal anti-inflammatory drug that can inhibit the synthesis of prostaglandins and exert anti-inflammatory and analgesic effects.

Ingredients

Naproxen (C14H14O3)

Name Description Content CAS NO. Manufacturer
NaproxenIngredients

This product is a non-steroidal anti-inflammatory drug that can inhibit the synthesis of prostaglandins and exert anti-inflammatory and analgesic effects

More
22204-53-1 30

Appearance

This product is white or off-white tablets

Indication

Used to relieve mild to moderate pain such as joint pain, neuralgia, muscle pain, migraine, headache, dysmenorrhea, and toothache.

Usage and Dosage

Oral administration. Adults take 1 tablet once a day.

Adverse Reactions

1. Nausea, vomiting, indigestion, constipation, stomach discomfort, dizziness, headache, drowsiness, tinnitus, shortness of breath, dyspnea, asthma, itchy skin, lower limb edema. 2. Blurred vision or visual impairment, hearing loss, diarrhea, oral irritation or pain, palpitations, and sweating. 3. Gastrointestinal bleeding, kidney damage, allergic rash, depression, muscle weakness, abnormal blood count, and liver damage are occasionally seen.

Precautions

1 Pregnant women and lactating women are prohibited from using this product. 2 People with asthma, nasal polyposis syndrome, neuroangioedema, and those who are allergic to aspirin or other antipyretic analgesics are prohibited from using this product. 3 People with active gastric or duodenal ulcers are prohibited from using this product.

Special Population Medication

Precautions for children: Not for use in children under 2 years old. Precautions for pregnancy and lactation: Not for use in pregnant and lactating women. Precautions for the elderly: Use with caution in the elderly.

Drug Interactions

1 Drinking alcohol or taking it with other anti-inflammatory analgesics can increase gastrointestinal adverse reactions and the risk of ulcer attacks. 2 When used with anticoagulants such as heparin and dicoumarol, the bleeding time is prolonged, bleeding tendency may occur, and there is a possibility of causing gastrointestinal ulcers. 3 This product can reduce the sodium excretion and antihypertensive effects of furosemide. 4 This product can inhibit the excretion of lithium and increase the blood lithium concentration. 5 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. 6 If used with other drugs at the same time, drug interactions may occur. Please consult a doctor or pharmacist for details.

Storage

Sealed and light-proof.

Packaging Specification

0.25g

Validity Period

Tentative 2 years

Manufacturer

Di'ao Group Chengdu Pharmaceutical Co., Ltd.

  • Founded in:

    1997-07-31
  • Address:

    No. 518, Herui Road, Chengdu Hi-tech Zone
  • Tax NO.:

    91510100201913965Q
  • Registered Funds:

    71.01 million yuan
  • Website:

  • Email:

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