Granisetron Hydrochloride and Sodium Chloride Injection
Function and Efficacy
Pharmacological action: This product is a highly selective 5HT3 receptor antagonist, which has a good preventive and therapeutic effect on nausea and vomiting caused by radiotherapy, chemotherapy and surgery. Factors such as radiotherapy, chemotherapy and surgical operations can cause enterochromaffin cells to release 5HT, and 5HT can activate the 5HT3 receptors of the central nervous system or vagus nerve to cause vomiting reflex. The mechanism of this product in controlling nausea and vomiting is to antagonize the 5HT3 receptors in the central chemoreceptor area and peripheral vagus nerve endings, thereby inhibiting the occurrence of nausea and vomiting. This product has high selectivity and no side effects such as extrapyramidal reactions and excessive sedation. Toxicological studies Reproductive toxicity: When the subcutaneous dose of this product reaches 6 mg/kg/day (based on body surface area, it is 97 times the recommended dose for clinical intravenous administration),
Ingredients
Granisetron Hydrochloride
| Name | Description | Content | CAS NO. | Manufacturer |
|---|---|---|---|---|
| Granisetron HydrochlorideIngredients |
This product is a highly selective 5HT3 receptor antagonist, which has a good preventive and therapeutic effect on nausea and vomiting caused by radiotherapy, chemotherapy and surgery. It inhibits the occurrence of nausea and vomiting by antagonizing the 5HT3 receptors in the central chemoreceptor area and peripheral vagus nerve endings. This product has high selectivity and no side effects such as extrapyramidal reactions and excessive sedation. More |
107007-99-8 | 35 |
Appearance
This product is a colorless clear liquid.
Indication
Used for nausea and vomiting caused by radiotherapy and cytotoxic chemotherapy.
Usage and Dosage
This product is for intravenous drip. The recommended dose for adults is usually 3 mg, which is intravenously dripped 30 minutes before chemotherapy. Most patients only need to take the drug once, and the prevention effect on nausea and vomiting can last for more than 24 hours. If necessary, the drug can be given 1-2 times more, but the maximum daily dose should not exceed 9 mg. The infusion time should not be less than 15 minutes. The elderly and those with liver and kidney dysfunction do not need to adjust the dose.
Adverse Reactions
Common side effects include headache, fatigue, fever, constipation, and occasional transient asymptomatic increase in liver transaminases. These reactions are mild and can be recovered without special treatment.
Precautions
1. Patients with gastrointestinal obstruction are prohibited from using this product. 2. Patients who are allergic to this product are prohibited from using this product.
Drug Interactions
1 Granisetron is metabolized by the hepatic cytochrome P-450 drug metabolizing enzyme system. Inducing or inhibiting this enzyme can change the clearance rate and half-life of granisetron. 2 Granisetron itself does not induce or inhibit the cytochrome P-450 drug metabolizing enzyme system and can be used in combination with benzodiazepines, neuroleptics and anti-ulcer drugs.
Storage
Keep in a dark place and sealed. The validity period is tentatively set at two years.
Packaging Specification
100ml: Granisetron 3mg and sodium chloride 0.9g
Manufacturer
Jiangsu Embrace Sicence & Technology Development Co., Ltd.
-
Founded in:
2017-03-15 -
Address:
No. 29-2, Yingbin Avenue, Huai'an Economic and Technological Development Zone -
Tax NO.:
91320891MA1NK66M3L -
Registered Funds:
60 million yuan -
Email: