CEFOTAXIME sodium, eq. 500mg base, vial

STD DINJCEFO5V-

Valid Article

The product is supplied (and stored) sterile, it must remain sterile until its use. Sterile = state of being free from all living microorganisms.
Article is intended to be used with children (<12 years) ONLY.
6.2.2 - Watch group antibiotics
Classification of the medicines in groups and subgroups according to their therapeutic use. The classification used by MSF is based on the WHO Model List of Essential Medicines.
J01DD01
Anatomical Therapeutic Chemical Classification according to WHOCC
Thermosensitive codes are defined for storage and transportation temperature requirements of the products.
The product is part of at least one Kit. A kit is a collection of products (medical and/or logistic) that are needed for a certain intervention in emergency. The choice and quantity of the articles reflects the MSF protocols for this specific situation. The use of Kits allows to start an intervention without a detailed evaluation.
OC subscriptions: included in supply or field order tools (e.g. UniField)
SC subscriptions: included in supply or field tools
OC validations: approved for procurement and use by an OC for international or local orders specifying context and activity in Medical Standard Lists (MSL)

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CEFOTAXIME

Therapeutic Action

Third generation cephalosporin antibacterial

Indications

In hospitalised neonates:

Bacterial meningitis, in combination with another antibacterial

Urinary infection

Pneumonia

Gonococcal conjunctivitis

Instructions for use

  • IM or slow IV injection (3 to 5 minutes): reconstitute the powder vial with 2 ml water for injection.
  • IV infusion (20 to 60 minutes): reconstitute the powder vial in 0.9% NaCl or 5% dextrose.

For pneumonia in neonates, prefer ampicillin + gentamicin.

For gonococcal conjunctivitis in neonates, use cefotaxime only if ceftriaxone is not available or contraindicated.

Storage

Below 25°C - Protect from sunlight