CEFTRIAXONE sodium, eq. 250mg base, powd, vial+ lidocaine IM

STD DINJCEFL2V-

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.
J01DD04
Anatomical Therapeutic Chemical Classification according to WHOCC
Thermosensitive codes are defined for storage and transportation temperature requirements of the products.
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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CEFTRIAXONE + lidocaine (IM)

Therapeutic Action

Third-generation cephalosporin antibacterial

Indications

Severe bacterial infections (meningitis, pneumonia, typhoid fever, shigellosis, leptospirosis, tick-borne relapsing fevers, pyelonephritis, neurosyphilis, etc.)

Cervicitis, urethritis and conjunctivitis due to Neisseria gonorrhoeae, chancroid

Instructions for use

Reconstitute the powder vial with the solvent containing lidocaine.

The reconstituted solution with the solvent containing lidocaine must be given as IM injection only. Never administer by IV route or infusion.

The 250 mg dosage is intended for paediatric use.

Precautions for Use

Do not confuse with ceftriaxone alone given as slow IV injection or infusion.

Storage

  • Below 25ºC - Protect from sunlight
  • After reconstitution, use the solution immediately.