Version: Sample instructions for over-the-counter drugs published by the State Food and Drug Administration in 2007
Note: The instructions for Naproxen Sodium Tablets were issued by the State Food and Drug Administration on January 31, 2007 The "Notice on Publishing Sample Inserts for Over-the-Counter Drugs" No. 54 [2007] of the State Food and Drug Administration was released.
Drug name
Generic name: Naproxen sodium tablets
Trade name:
English name:
Chinese Pinyin:
Ingredients
Properties
Category of action
This product is an over-the-counter analgesic drug.
Indications
Used to relieve mild to moderate pain, such as joint pain, neuralgia, muscle pain, migraine, headache, dysmenorrhea, and toothache.
Specifications
Each tablet is 0.275g (equivalent to 0.25g of naproxen)
Dosage and usage
Orally administered. Adults, 2 tablets for the first time, 1 tablet every 68 hours if necessary.
Adverse reactions
1. Nausea, vomiting, indigestion, constipation, stomach discomfort, dizziness, headache, drowsiness, tinnitus, shortness of breath, difficulty breathing, asthma, skin itching, Edema of lower limbs.
2. Visible blurred vision or visual impairment, hearing loss, diarrhea, oral cavity pain or pain, palpitation, and excessive sweating.
3. Occasionally, gastrointestinal bleeding, kidney damage, allergic rash, mental depression, muscle weakness, abnormal blood count, and liver function damage may occur.
Taboos
1. Pregnant and lactating women are prohibited from taking this product.
2. It is prohibited for those with asthma, nasal polyposis syndrome, angioedema, and those allergic to aspirin or other antipyretic and analgesics.
3. It is contraindicated in patients with peptic tract ulcers or a history of peptic tract ulcers.
Precautions
1. This product is a symptomatic treatment drug and should not be used for a long time or in large quantities. It should not be used for pain relief for more than 5 days. If the symptoms are not relieved, please consult a physician or pharmacist.
2. Use with caution in patients with the following conditions: over 60 years old, bronchial asthma, liver and kidney insufficiency, coagulation mechanism or platelet dysfunction (such as hemophilia).
3. Patients with the following conditions should use it under the guidance of a physician: those with a history of peptic ulcer, gastrointestinal bleeding, cardiac insufficiency, and high blood pressure.
4. Please consult your physician or pharmacist regarding dosage for children.
5. Do not take other medicines containing antipyretic and analgesics (such as some compound anti-cold medicines) at the same time.
6. Do not drink alcohol or drinks containing alcohol while taking this product.
7. In case of overdose or serious adverse reactions, seek medical attention immediately.
8. People who are allergic to this product should not use it, and people with allergies should use it with caution.
9. It is prohibited to use this product when its properties change.
10. Please keep this product out of the reach of children.
11. Children must use it under adult supervision.
12. If you are using other drugs, please consult your physician or pharmacist before using this product.
13. If gastrointestinal bleeding or ulcers, chest pain, shortness of breath, weakness, slurred speech, etc. occur, the drug should be discontinued and a physician should be consulted.
14. If you experience rash or allergic symptoms when using this product for the first time, you should stop taking it and consult a physician.
Drug interactions
1. Drinking alcohol or using it with other anti-inflammatory analgesics can increase gastrointestinal adverse reactions and risk ulcers.
2. Used together with anticoagulants such as heparin and dicoumarol, the bleeding time may be prolonged, bleeding tendencies may occur, and may lead to 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 together with probenecid, the blood concentration of this product will increase, the half-life will be extended, and the efficacy will increase, but the adverse reactions will also increase accordingly.
6. Drug interactions may occur if used together with other drugs. Please consult a physician or pharmacist for details.
Pharmacological effects
This product is a non-steroidal anti-inflammatory drug that inhibits the synthesis of prostaglandins and exerts anti-inflammatory and analgesic effects.
Storage
Packaging
Validity period
Implementation standards
Approval number
Instruction Revision Date
Manufacturer
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