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Naproxen Sodium 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

Main ingredient: Naproxen sodium. Molecular formula: C14H13NaO3 Molecular weight: 252.25

Name Description Content CAS NO. Manufacturer
Naproxen sodiumIngredients

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

More
26159-34-2 33

Appearance

This product is 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, 2 tablets for the first time, 1 tablet each time thereafter, and once every 6-8 hours if necessary.

Adverse Reactions

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

Precautions

1 Pregnant women and lactating women are prohibited from using this product. 2 People with asthma, nasal polyposis syndrome, angioedema, and those who are allergic to aspirin or other antipyretic analgesics are prohibited from using this product. 3 Patients with peptic ulcers or a history of peptic ulcers are prohibited from using this product.

Special Population Medication

Precautions for children: The common dosage for children is 10mg/kg per day for anti-rheumatic, divided into 2 doses. Precautions for pregnancy and lactation: Forbidden. Precautions for the elderly: 1. For anti-rheumatic, 0.25g to 0.5g at a time, once in the morning and evening, or 0.25g in the morning and 0.5g at night. 2. For pain relief, 0.5g for the first time, 0.25g for each time thereafter, once every 6 to 8 hours if necessary. 3. For acute attack of gouty arthritis, 0.7g for the first time, 0.25g for each time thereafter, once every 8 hours until the acute attack stops.

Drug Interactions

1 Drinking alcohol or using 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 potassium and increase the blood concentration of potassium. 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 you are taking other medicines, please consult a doctor or pharmacist before using this product.

Storage

Keep in a light-proof, sealed and dry place

Packaging Specification

0.275g

Validity Period

36 months

Manufacturer

Tianjin Jinhong Shengli Pharmaceutical Co., Ltd.

  • Founded in:

    2002-11-12
  • Address:

    No. 3 Guanghai Road, Economic Development Zone, Jinghai District, Tianjin
  • Tax NO.:

    911202237440196368
  • Registered Funds:

    14 million yuan
  • Website:

  • Email:

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