Freeflex
SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
Potassium Chloride 0.15%, Sodium Chloride 0.9% IV Infusion BP, as Steriflex No. 12 or freeflex
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Polyfusor SD has the following composition:
|
Name |
Specification Reference |
%w/v |
|
Sodium Chloride for Injections |
EP |
0.9 |
|
Potassium Chloride |
EP |
0.15 |
3 PHARMACEUTICAL FORM
Intravenous fluid
4 CLINICAL PARTICULARS
4.1 Therapeutic indications
Potassium replacement therapy.
4.2 Posology and method of administration
Adults and Children
The volume and rate of infusion will depend upon the requirements of the individual patient and the judgement of the physician.
The rate of infusion should not exceed 10-20 mmols of potassium per hour. The total daily dosage of potassium should not exceed 200 mmols of potassium.
Children
The volume and rate of infusion will depend upon the requirements of the individual patient and the judgement of the physician.
Correspondingly reduced volumes and rates of infusion may be required.
Elderly
A reduced volume and rate of infusion may be necessary to avoid circulatory overload, particularly in patients with cardiac or renal insufficiency.
For intravenous infusion.
4.3 Contraindications
Addison’s disease, adrenal insufficiency, acute or chronic renal disease, oliguria, anuria and patients with hyperkalaemia.
4.4 Special warnings and precautions for use
Caution should be exercised in the volume and rate of infusion since fluid overload and hyperkalaemia may compromise cardiac function. Before administering potassium by the intravenous route a non-potassium containing hydrating solution should be administered to ensure adequate renal function.
The label states: Special care in renal failure rapid infusion may be harmful. Visible particles must not be used.
Contains 10 mmol Potassium (500 ml)
Contains 20 mmol Potassium (1000 ml)
4.5 Interaction with other medicinal products and other forms of interaction
Care should be exercised in the concurrent administration of potassium containing intravenous solutions and potassium sparing diuretics.
4.6 Pregnancy and lactation
The use of potassium containing solutions during pregnancy and lactation has not been assessed, but its use during these periods is not considered to constitute a hazard.
4.7 Effects on ability to drive and use machines
There is no effect on ability to drive and use machinery.
4.8 Undesirable effects
Adverse effects are usually due to hyperkalaemia and include listlessness, mental confusion, parasthesiae, weakness, hypertension, arrhythmias and sometimes cardiac arrest. Thrombosis of the selected vein may occasionally occur.
4.9 Overdose
Symptoms of overdosage include hypotension, cardiac arrhythmias, heart block and cardiac arrest. Treatment is to stop infusion immediately and if there is persistent acidosis, administer an intravenous infusion of sodium bicarbonate or sodium lactate. Hyperkalaemia may be reversed by the administration of calcium gluconate injection 10% with ECG monitoring.
5 PHARMACOLOGICAL PROPERTIES
5.1 Pharmacodynamic properties
Potassium chloride and sodium chloride provide essential ions to maintain the intracellular/extracellular milieu.
5.2 Pharmacokinetic properties
Not applicable
5.3 Preclinical safety data
N/A
PHARMACEUTICAL PARTICULARS
6.1 List of excipients
|
Name |
Specification Reference |
%w/v |
|
Water for Injections in bulk |
EP |
TO 100 |
|
Hydrochloric Acid |
EP |
QS |
|
Sodium Hydroxide |
BP |
QS |
6
6.2 Incompatibilities
Incompatibilities have been demonstrated in potassium containing intravenous infusions with for example; amikacin, amphotericin, benzyl-penicillin and dobutamine. Because of the nature if the plastic material of the steriflex bag (PVC) this solution should not be used as a vehicle for the administration of drugs which may be sorbed to the surface of the bag to varying and significant degrees.
6.3 Shelf life
24 months.
6.4 Special precautions for storage
Store at 2° to 25 °C
6.5 Nature and contents of container
The container is a flexible bag made of medical grade PVC.
a) A hermetically sealed polythene bag.
b) A rectangular pouch consisting of polyamide/polythene composite
c) Polyamide/Polyethylene-Propylene composite laminate welded to polypropylene ethylene propylene composite, plugged with a polycarbonate plug with either a bromobutyl (West 4481/45) or gum (West 7006/45) stopper.
Or
A flexible polyolefine bag sealed in a polyolefine overwrap.
6.6 Special precautions for disposal
Opening the overwrap:
Locate the corner tabs at the end of the bag. Grip the two tabs and pull the two halves of the overwrap apart, releasing the bag onto a clean surface.
Setting up the solution:
Position the roller clamp of the giving-set to just below the drip chamber and close. Hold the base of the giving set port firmly and grip the wings of the twist of tab. Twist to remove the protective cover.
Still holding the base of the giving-set port push the set spike fully into the port to ensure a leak proof connection.
Prime the set in accordance with the manufacturer’s instructions.
7 MARKETING AUTHORISATION HOLDER
Fresenius Kabi Limited
Cestrian Court
Eastgate Way
Manor Park
Runcorn
Cheshire
WA7 1NT
8 MARKETING AUTHORISATION NUMBER(S)
PL 08828/0065
9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE
AUTHORISATION
6th June 1989
DATE OF REVISION OF THE TEXT
April 1999