Guangdong Jiabo Pharmaceutical Propofo L Injection Emulsion for Anaesthesia (10ml: 200mg)

Product Details
Customization: Available
Function: Anesthetic and Adjuvant, Nervous System Drugs, Drug Treatment of Mental Disorder, Central Nervous System Agents
Certification: GMP
Manufacturer/Factory, Trading Company

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  • Guangdong Jiabo Pharmaceutical Propofo L Injection Emulsion for Anaesthesia (10ml: 200mg)
  • Guangdong Jiabo Pharmaceutical Propofo L Injection Emulsion for Anaesthesia (10ml: 200mg)
  • Guangdong Jiabo Pharmaceutical Propofo L Injection Emulsion for Anaesthesia (10ml: 200mg)
  • Guangdong Jiabo Pharmaceutical Propofo L Injection Emulsion for Anaesthesia (10ml: 200mg)
  • Guangdong Jiabo Pharmaceutical Propofo L Injection Emulsion for Anaesthesia (10ml: 200mg)
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Basic Info.

Model NO.
10ml: 200mg
Grade Standard
Medicine Grade
Type
Biological Products
State
Liquid
Volatile
Volatile
Application
Internal Medicine
Usage Mode
for External Use
Suitable for
Elderly, Children, Adult
Shape
IV
Pharmaceutical Technology
Chemical Synthesis
Transport Package
Carton
Specification
10ml: 200mg
Origin
Qingyuan, Guangdong, China
HS Code
3004909099

Product Description

  This information is only for medical or pharmacy professionals to read.                                               

                                                    
 Package insert of Propofo l Injectable Emulsion

    Please read the package insert carefully and use the product according to the guidance of physicians


Drug Name Generic name: propofo l injectable emulsion
Used name propofo l injection
Brand name: Di shi ning
English name: propofo  injectable emulsion
Chinese spell: Bingbofen Ruzhuangzhusheye
Strength :10ml:200mg
Description: The product is a white, uniform, and lacteal liquid.

Dosage and Administration:

The product is only used in the hospital or outpatient treatment room with well-found equipment, and must be used by the doctors trained in anesthesia and intensive care.
Continually monitor the breath and circulatory function (e.g. electrocardiogram, oxyhemoglobin saturation) of patients, and facilities for maintenance of a patent airway, providing artificial ventilation and other instituting resuscitation must be immediately available.
The product should not be administered by person involved in the conduct of the surgical/diagnostic procedure during the sedation of surgery and diagnostic procedure.
According to patient responses and premedication, the administration should be individualized. In general, the product anesthesia is supplemented with analgesic agents.

Intravenous administration :

The product can be used by infusion when it is undiluted. The repeated injection method should not be used when maintaining the anesthesia.
While infusing undiluted product, advice to use dropper, droplet counter, injection pump, volumetric infusion pump and other equipment in order to control the infusion rate.
Shake well before use Only just use the product with uniformity liquid and undamaged container .
Before use, wipe the neck of ampoule or the surface of rubber with alcohol swab or by spraying alcohol in order to clean. After use, the unused product should be discarded.
The product is a lipid emulsion free from preservative, which facilitate the quick growth of microorganism. After opening ampoule or small vial, immediately transfer the product into the sterile syringes or administration device, and the administration should commence promptly.
Keep that the product and the infusion system is sterile during the infusion. Use the three links or three-way valves to administer medications nearby the indwelling needle when simultaneously combining with other medications or liquids.
The product is not allowed to mix with other solutions to conduct the infusion and injection. But 5% glucose solution, 0.9% NaCl solution, 0.18% NaCl solution and 4% glucose solution are allowed to be administered nearby the indwelling needle with appropriate infusion apparatus.
It is not allowed to administrate the product with microorganism filter.
The product and infusion container containing the product is only used once and by one patient. The rest of the product should be discarded after using.

Attentions :
As with other general intravenous anesthetic, the product should be carefully administered to patients with the impaired heart, long, kidney and liver, hypovolemia or critically weakness. The clearance rate of propofo l depends on blood flow volume, the concurrent use of medications may reduce the clearance rate, whose may decrease cardiac output.
For patients with cardiovascular or respiratory insufficiency, and hypovolemia, perform the correct before using the product.
Confirm whether the patients receive the therapy of anti-epileptic, before implement the anesthesia on epileptic patients. Although the study found the product was effective in the aspect of treatment for status epilepticus, it may add the risk of epileptic seizure in the context of administering the product to epileptic patients.
Unless the special attention is paid to patients under the strictness monitoring, the product can be administered to the patients with severe heart failure and other severe myocardial diseases.

Storage: Preserve in a tightly container at 2~25ºC, do not freeze.
Package: vials, 5 PCS/box or 200 vials/carton
Expiry date: 24 months
Manufacturer Manufacturer name: Guangdong Jiabo Pharmaceutical Co., Ltd.
Manufacturing address: Bio-Pharmaceutical Park, High &New Technology industries development Zone, Qingyuan City, Guangdong Province  Website: jiabopharm.en.made-in-china.com

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