Reliable Cefotaxime Sodium Injection 1g/10ml for Medical Use

Product Details
Customization: Available
Application: Internal Medicine
Usage Mode: For external use
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  • Reliable Cefotaxime Sodium Injection 1g/10ml for Medical Use
  • Reliable Cefotaxime Sodium Injection 1g/10ml for Medical Use
  • Reliable Cefotaxime Sodium Injection 1g/10ml for Medical Use
  • Reliable Cefotaxime Sodium Injection 1g/10ml for Medical Use
  • Reliable Cefotaxime Sodium Injection 1g/10ml for Medical Use
  • Reliable Cefotaxime Sodium Injection 1g/10ml for Medical Use
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Basic Info.

Model NO.
AMC13008-07
State
Liquid
Shape
Powder
Type
Organic Chemicals
Pharmaceutical Technology
Chemical Synthesis
Packing
1g/10ml, 10′s/Box, 100boxes/CTN
CTN Size
55*30*31.5cm
OEM/ODM
Support
Transport
Shipping
Transport Package
10′s/Box
Specification
1g/10ml
Trademark
Medipharm or OEM
Origin
China
HS Code
3004209099
Production Capacity
100000ctns/Month

Product Description

 
Reliable Cefotaxime Sodium Injection 1g/10ml for Medical Use
 
Cefotaxime Sodium for Injection
 
Name Cefotaxime Sodium for Injection
Specification 1g/10ml, 10's/box, 100boxes/ctn
Packing 55*30*31.5cm
Brand Medipharm or OEM
Transport Shipping

Indications:
It is suitable for pneumonia and other lower respiratory tract infection, urinary tract infection, meningitis, septicemia, abdominal infection, pelvic infection, skin soft tissue infection, reproductive tract infection, bone and joint infection caused by sensitive bacteria. Cefotaxime can be used as the drug of choice in children with meningitis.

Dosage and Administration:
For adults, 2 ~ 6g a day, divided into 2 ~ 3 times intravenous injection or intravenous drip; Severely infected people are 2 to 3g every 6 to 8 hours, and the maximum daily dose is not more than 12g. Treatment for uncomplicated Streptococcus pneumoniae pneumonia or acute urinary tract infection, 1g every 12 hours.
For newborns less than 7 days old, 50mg/kg every 12 hours, and for newborns greater than 7 days old, 50mg/kg every 8 hours. In patients with meningitis, the dose can be increased to 75mg/kg every 6 hours, all administered intravenously.
Patients with severe renal dysfunction should be appropriately reduced when using this product. When the serum creatinine value exceeds 424μmol/L(4.8mg) or the creatinine clearance is less than 20ml/, the maintenance dose of this product should be halved. When serum creatinine exceeds 751μmol/L(8.5mg), the maintenance amount is 1/4 of the normal amount. Hemodialysis patients need 0.5 ~ 2g a day. However, one dose should be added after dialysis.


Adverse reaction:
The incidence of adverse reactions is low, about 3% ~ 5%.
(1) There are rash and drug fever, phlebitis, diarrhea, nausea, vomiting, loss of appetite, etc.
(2) Mild elevation of alkaline phosphatase or serum aminotransferase, temporary elevation of blood urea nitrogen and creatinine.
(3) leukopenia, acidocytosis or thrombocytopenia were rare.
(4) Occasional headache, numbness, difficulty breathing, and facial flushing.
(5) Very few patients may develop mucosal candidiasis.


Note:
People allergic to cephalosporins and those with a history of penicillin anaphylactic shock or immediate reaction should not use this product.

Storage instructions:
Store below 25 degrees and protect from light. Keep out of reach of children.

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Reliable Cefotaxime Sodium Injection 1g/10ml for Medical Use
 
Reliable Cefotaxime Sodium Injection 1g/10ml for Medical Use
 
 
Reliable Cefotaxime Sodium Injection 1g/10ml for Medical Use
 
 
Reliable Cefotaxime Sodium Injection 1g/10ml for Medical Use
 
 
Reliable Cefotaxime Sodium Injection 1g/10ml for Medical Use
 

Reliable Cefotaxime Sodium Injection 1g/10ml for Medical Use

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