MEGLUMINE ANTIMONIATE, pentaval. antimony 81mg/ml, 5ml, amp

STD DINJMEGA4A-

Valid Article

Former Code(s): -X
The product is supplied (and stored) sterile, it must remain sterile until its use. Sterile = state of being free from all living microorganisms.
6.5.2 - Antileishmaniasis medicines
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.
P01CB01
Anatomical Therapeutic Chemical Classification according to WHOCC
The order of this product needs to be justified and is only acceptable under certain conditions.
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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MEGLUMINE antimoniate

Therapeutic Action

Indications

Cutaneous and mucocutaneous leishmaniasis

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Instructions for use

Follow the national or WHO protocol.

81 mg/ml pentavalent antimony is equivalent to 0.3 g/ml meglumine antimoniate.

The 5 ml ampoule contains 1.5 g of meglumine antimoniate.

Must be given as IM injection.

Precautions for Use

Contreindicated in patients with renal, cardiac or hepatic impairment.

Storage

  • Below 25ºC
  • After opening, use the product immediately.