Nimesulide Granules
Function and Efficacy
This product is a non-steroidal anti-inflammatory drug with anti-inflammatory, analgesic and antipyretic effects. Its mechanism of action is not yet fully understood, but it may be mainly related to the inhibition of prostaglandin synthesis, mediator release of leukocytes and oxidative reactions of polymorphonuclear leukocytes.
Ingredients
The main ingredient of this product is nimesulide, and its chemical name is: N-[4-nitro-2-phenoxyphenyl] methanesulfonamide.
| Name | Description | Content | CAS NO. | Manufacturer |
|---|---|---|---|---|
| NimesulideIngredients |
This product is a non-steroidal anti-inflammatory drug with anti-inflammatory, analgesic and antipyretic effects. Its mechanism of action is not yet fully understood, but it may be mainly related to the inhibition of prostaglandin synthesis, mediator release of leukocytes and oxidative reactions of polymorphonuclear leukocytes. More |
51803-78-2 | 14 |
Appearance
This product is light yellow granules.
Indication
This product is a non-steroidal anti-inflammatory drug and is only used when at least one other non-steroidal anti-inflammatory drug has failed. It can be used for the pain of chronic arthritis (such as osteoarthritis), pain after surgery and acute trauma, and symptomatic treatment of primary dysmenorrhea.
Usage and Dosage
Oral administration: 0.05-0.1g at a time, twice a day, after meals. The maximum single dose should not exceed 100mg, and the course of treatment should not exceed 15 days. It is recommended to use the minimum effective dose and the shortest course of treatment to reduce the occurrence of adverse drug reactions.
Adverse Reactions
This product has fewer side effects. Common side effects are heartburn, stomach pain and gastrointestinal disorders, but the symptoms are mild and short-lived, and rarely require interruption of treatment. In rare cases, patients develop allergic rashes after taking it. Even if the above symptoms do not occur when using nimesulide, it should be noted that this product, like other non-steroidal anti-inflammatory drugs, may cause dizziness, drowsiness, gastric ulcers or gastrointestinal bleeding and Stevens-Johnson syndrome.
Precautions
1. Patients who are allergic to this product, acetylsalicylic acid or other non-steroidal drugs are contraindicated. 2. Patients with active gastrointestinal bleeding or active peptic ulcer are contraindicated. 3. Patients with severe liver dysfunction and severe renal dysfunction (creatinine clearance rate 30 ml/min) are contraindicated.
Special Population Medication
Precautions for children: Only for children over 1 year old, the dosage is 5mg/kg body weight/day, divided into 2 to 3 doses, the maximum dose does not exceed 100mg, twice a day. For fever, the course of treatment does not exceed 3 days. For rheumatism, the course of treatment should be in accordance with the doctor's advice. Precautions for pregnancy and lactation: Like all new drugs, nimesulide is not recommended for use during pregnancy if it has not been confirmed through experiments whether nimesulide is toxic to the fetus. It is also not recommended to use this drug during lactation if it is not clear whether nimesulide can be excreted through breast milk. Precautions for the elderly: The dosage of medication for elderly patients should be strictly followed by the doctor's prescription, and the doctor can appropriately reduce the dosage according to the situation.
Drug Interactions
Due to the high plasma protein binding rate of this product, it may displace other protein-bound drugs. Furosemide affects the absorption of nimesulide, causing the AUC value of nimesulide to decrease by about 25%; fenofibrate, tolbutamide, and salicylic acid can displace nimesulide from plasma proteins, while furosemide, glibenclamide, and therapeutic doses of warfarin have no effect on the binding rate of nimesulide to proteins.
Storage
Seal and store in a dry place. The validity period is tentatively one year.
Packaging Specification
0.5 g: 50 mg
Validity Period
24 months