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MODIFIED FLUID GELATIN/POLYGELIN,500ml,semi-rigid bt,PVCfree

https://unicat.msf.org/cat/product/11565
NST DINFPLAS1SRF5

Forbidden Article

Former Code(s): DINFPLAS152
The product is supplied (and stored) sterile, it must remain sterile until its use. Sterile = state of being free from all living microorganisms.
11.3 - Plasma substitutes
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.
B05AA06
Anatomical Therapeutic Chemical Classification according to WHOCC
1525
Thermosensitive codes are defined for storage and transportation temperature requirements of the products.
SC subscriptions: included in supply or field tools
OC subscriptions: included in supply or field order tools (e.g. UniField)
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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MODIFIED FLUID GELATIN / POLYGELIN

Non-standard item - FORBIDDEN -

Therapeutic Action

Plasma volume expander, colloid

Indications

No indications for MSF settings and contexts

Not included in MSF protocols

Colloid volume expanders are associated with severe adverse effects including allergic reactions (anaphylactic shock), acute kidney injury, colloid-induced coagulopathy, and increased risk of bleeding.

Synthetic colloids should not be used and do not replace blood products. They have no value in the management of haemorrhage and are potentially harmful.

Instructions for use

Prefer the solutions of dextrose 5%/ ringer lactate and/or dextrose 10%/ sodium chloride 0.18%.

Modified fluid gelatin has been removed from all the kits.

Contact your anaesthesia/intensive care advisor for more details.