GELOPLASMA 3 Grams Solution for Infusion

Nchi: Ayalandi

Lugha: Kiingereza

Chanzo: HPRA (Health Products Regulatory Authority)

Nunua Sasa

Taarifa za kipeperushi Taarifa za kipeperushi (PIL)
01-02-2018
Tabia za bidhaa Tabia za bidhaa (SPC)
01-02-2018

Viambatanisho vya kazi:

MODIFIED LIQUID GELATINE, SODIUM CHLORIDE, MAGNESIUM CHLORIDE HEXAHYDRATE, POTASSIUM CHLORIDE, SODIUM LACTATE SOLUTION

Inapatikana kutoka:

Fresenius Kabi Limited

ATC kanuni:

B05AA

INN (Jina la Kimataifa):

MODIFIED LIQUID GELATINE, SODIUM CHLORIDE, MAGNESIUM CHLORIDE HEXAHYDRATE, POTASSIUM CHLORIDE, SODIUM LACTATE SOLUTION

Kipimo:

3 Grams

Dawa fomu:

Solution for Infusion

Dawa ya aina:

Product subject to prescription which may not be renewed (A)

Eneo la matibabu:

Blood substitutes and plasma protein fractions

Idhini hali ya:

Authorised

Idhini ya tarehe:

2007-04-20

Taarifa za kipeperushi

                                WHAT IS IN THIS LEAFLET
1. What GELOPLASMA, solution for infusion, is and what it is used for
2. What you need to know before you use GELOPLASMA, solution for
infusion
3. How to use GELOPLASMA, solution for infusion
4. Possible side effects
5. How to store GELOPLASMA, solution for infusion
6. Contents of the pack and other information
1. WHAT GELOPLASMA, SOLUTION FOR INFUSION, IS AND WHAT IT IS USED FOR
GELOPLASMA is a solution for intravenous infusion. It contains
gelatin, which belongs to
a group of medicines known as plasma volume expanders. Plasma volume
expanders
work by increasing the fluid in your blood stream, which helps keep
your blood stream and
therefore your blood pressure stable.
This medicine is an emergency treatment in case of low blood volume in
the following
situations:
• Haemorrhage
_(bleeding),_
dehydration,
capillary
leak
_(increased _
_microvascular _
_permeability),_
burns;
• severe vasodilatation _(widening of blood vessels)_ from
traumatic, surgical, septic or toxic
origin.
It is also used in the treatment of low blood volume associated with
hypotension _(low blood_
_pressure)_
in the context of severe vasodilatation related to the effects of
hypotensive
drugs, notably during anesthesia.
2. WHAT YOU NEED TO KNOW BEFORE YOU USE GELOPLASMA,SOLUTION FOR
INFUSION
DO NOT USE GELOPLASMA, SOLUTION FOR INFUSION:
• if you are allergic to gelatin or any of the other ingredients of
this medicine (listed in sec-
tion 6);
• if you are allergic to an allergen called
“galactose-α-1,3-galactose (alpha-Gal)” or to red
meat (mammal meat) and offal;
• if you have an excess of fluid in the body;
• if you have hyperkalaemia _(excess of potassium in the blood)_;
• if you have an high accumulation of alkaline substance (e.g.
bicarbonate, lactate) in your
blood and body fluid;
• if you are at the end of pregnancy (during labour/delivery): see
"Pregnancy, breast-
feeding and fertility" section.
WARNINGS AND PRECAUTIONS
Talk to your doctor, pharmacist or nurse before using GELOPLASMA,
solutio
                                
                                Soma hati kamili
                                
                            

Tabia za bidhaa

                                SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
Geloplasma, Solution for Infusion
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
* partially hydrolysed and succinylated
For the full list of excipients, see section 6.1.
Ionic formula
Sodium
=
150
mmol/l
Potassium
=
5
mmol/l
Magnesium
=
1.5 mmol/l
Chloride
=
100
mmol/l
Lactate
=
30
mmol/l
Total osmolality: 295 mOsm/kg
pH: 5.8 to 7.0
3 PHARMACEUTICAL FORM
Solution for infusion.
Clear and colourless to slightly yellowish solution.
4 CLINICAL PARTICULARS
4.1 THERAPEUTIC INDICATIONS
Emergency treatment of states of shock:
-
hypovolaemic shock resulting from : haemorrhage, dehydration,
capillary leak, burns;
-
vasoplegic shock of traumatic, surgical, septic or toxic origin.
Treatment of relative hypovolaemia associated with hypotension in the
context of vasoplegia related to the effects of
hypotensive drugs, notably during anesthesia.
4.2 POSOLOGY AND METHOD OF ADMINISTRATION
Posology
Dosage volume and rate of administration depend upon the individual
patient status, circumstances and response to
vascular replacement.
Modified liquid gelatin is given by IV infusion (drip infusion). The
infusion rate can be increased using a pump.
Modified liquid gelatin*
amount expressed as anhydrous gelatin
……………………………………....
3.0000 g
Sodium chloride
………………………………………………………………
0.5382 g
Magnesium chloride hexahydrated
…………………………………………...
0.0305 g
Potassium chloride
……………………………………………………………
0.0373 g
Sodium (S)-lactate solution
amount expressed as sodium lactate
………………………………………….
0.3360 g
per 100 ml of solution for infusion
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                                Soma hati kamili