Ibuprofen Tablet
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Ibuprofen Tablet
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Product Details
Class A
Ibuprofen Tablet Instructions
Please read the instructions carefully and use as directed or purchase and use under the guidance of a pharmacist.
[Drug Name]
Generic name: Ibuprofen Tablets
English name: Ibuprofen Tablets
Pinyin: Buluofen Pian
[Ingredients]
Each tablet contains the active ingredient ibuprofen 0.1 g. Excipients include: pregelatinized starch, microcrystalline cellulose, low-substituted hydroxypropyl cellulose, hydroxypropyl methylcellulose, polysorbate 80, magnesium stearate, talc, silicon dioxide, sodium carboxymethyl starch.
[Properties]
This product is a sugar-coated tablet, appearing white after the coating is removed.
[Category of Action]
This product is an over-the-counter (OTC) antipyretic and analgesic medication.
[Indications]
For the relief of mild to moderate pain such as headache, arthralgia, migraine, toothache, myalgia, neuralgia, and dysmenorrhea. Also indicated for fever caused by common cold or influenza.
[Specification] 0.1 g
[Usage And Dosage]
Oral administration. For children aged 12 years and above and adults, take 2 tablets per dose. If pain or fever persists, repeat the dose after 4–6 hours, with a maximum of 4 doses within 24 hours. The dosage for children is listed in the table below:
Age (years) Weight (kg) Dose (tablets) Frequency
1-3 10-15 1/2 If the pain or fever persists,
the interval can be extended.
4-6 16-21 1 Repeat administration every 4–6 hours, 24
7-9 22-27 1.5 hours not exceeding 4 times.
10-12 28-32 2
[Untoward Effect]
1. A minority of patients may experience nausea, vomiting, gastric burning sensation, or mild dyspepsia, gastrointestinal ulcers and bleeding, elevated transaminase levels, headache, dizziness, tinnitus, blurred vision, nervousness, drowsiness, lower limb edema, or sudden weight gain.
2. Rare rashes, allergic nephritis, cystitis, nephrotic syndrome, renal papillary necrosis or renal failure, bronchospasm.
[Taboo]
1. Contraindicated in patients with hypersensitivity to other nonsteroidal anti-inflammatory drugs (NSAIDs).
2. Contraindicated in pregnant and lactating women.
3. Contraindicated in asthma patients with aspirin allergy.
[Matters Need Attention]
1. This product is a symptomatic treatment medication and should not be used for prolonged or excessive duration. For analgesia, the usage period should not exceed 5 days; for antipyresis, it should not exceed 3 days. If symptoms persist, consult a physician or pharmacist.
2. Use in children under 1 years of age should be guided by a physician.
3. Concomitant use of other medications containing antipyretic and analgesic agents (e.g., certain compound cold medicines) is contraindicated.
4. Alcohol or alcoholic beverages must not be consumed during the administration of this product.
5. Patients with the following conditions should use with caution: those aged over 60 years, bronchial asthma, hepatic or renal insufficiency, or coagulation disorders or platelet dysfunction (e.g., hemophilia).
6. The following conditions require physician-guided use: history of peptic ulcer, gastrointestinal bleeding, cardiac insufficiency, and hypertension.
7. In case of overdose or severe adverse reactions, seek immediate medical attention.
8. Contraindicated in patients with known hypersensitivity to this product. Use with caution in individuals with allergic predisposition.
9. Do not use if the product exhibits altered physical properties.
10. Keep this product out of reach of children.
11.Children must use under adult supervision.
12. If you are taking other medications, consult a physician or pharmacist before using this product.
13. Discontinue the medication and consult a physician if gastrointestinal bleeding or ulceration, chest pain, shortness of breath, weakness, or slurred speech occurs.
14. Discontinue use and consult a physician if rash or allergic reactions occur during the first use of this product.
[Drug Interaction]
1. Concomitant use of this product with other antipyretic, analgesic, or anti-inflammatory drugs may increase the risk of gastrointestinal adverse reactions and may lead to ulceration.
2. Concurrent use of this product with anticoagulants such as heparin or dicoumarol may prolong prothrombin time and increase the risk of bleeding.
3. Concomitant use of this product with digoxin, methotrexate, or oral hypoglycemic agents may increase the plasma concentrations of these drugs, and co-administration is not recommended.
4. When co-administered with furosemide (furosemide), the latter's natriuretic and antihypertensive effects are diminished; when used concomitantly with antihypertensive agents, the antihypertensive efficacy of the latter is also reduced.
5. Drug interactions may occur when used concomitantly with other medications. For details, please consult your physician or pharmacist.
[Pharmacological Effects]
This product inhibits the synthesis of prostaglandins, exhibiting antipyretic, analgesic, and anti-inflammatory effects.
Store in a tightly sealed container.
[Package]
Oral solid dosage form, packaged in high-density polyethylene (HDPE) bottles, 100 tablets/bottle.
[Validity]
36 months
[Implementation Standard]
China Pharmacopoeia 2020 Edition Part II
[Approval Number]
National Drug Approval Number H41023406
[Revision Date of Instruction]
December 30,2020
[Marketing Authorization Holder/Manufacturer]
Company Name: Henan Zhongjie Pharmaceutical Co., Ltd.
Registered address: South Railway Station, Xinxiang City, Henan Province
Production address: South Railway Station, Xinxiang City, Henan Province
Postal Code: 453003
Phone Number: +86-373-5071333
Fax: +86-373-5071222
Website: http://www.xxzjyy.com.cn
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