
Ask a doctor about a prescription for VIAFLO GLUCOSALINE POTASSIUM 4%, 0.18%, 0.15% SOLUTION FOR INFUSION
Package Leaflet: Information for the User
Viaflo Glucosalino Potásico 4%, 0.18%, 0.15%, Solution for Infusion
Active Substances: Glucose Monohydrate, Sodium Chloride, and Potassium Chloride
Read all of this leaflet carefully before you start using this medicine because it contains important information for you.
In this leaflet, Viaflo Glucosalino Potásico 4%, 0.18%, 0.15%, Solution for Infusion will be referred to as Viaflo Glucosalino Potásico.
Contents of the Package Leaflet:
Viaflo Glucosalino Potásico is a solution of glucose monohydrate, sodium chloride, and potassium chloride in water. Sodium chloride and potassium chloride are chemical substances (often referred to as "salts") that are found in the blood.
It is used to prevent and treat the following disorders:
inability to ingest food, which implies the need to obtain energy from another source
You will not be given Viaflo Glucosalino Potásicoin the following cases:
Your doctor should be especially careful when administering Viaflo Glucosalino Potásico to you
Viaflo Glucosalino Potásico is a hypertonic solution (concentrated). When it is administered, the solution will become hypotonic due to its low sodium content. Your doctor will take this into account when calculating the amount to be administered to you.
Warnings and Precautions
If you develop or have developed any of the following medical conditions, inform your doctor:
This may increase the risk of low sodium levels in the blood and may cause headache, nausea, seizures, lethargy, coma, brain inflammation, and death. Brain inflammation increases the risk of death and brain damage. People at higher risk of brain inflammation are:
If you develop any of these disorders, additional tests will be necessary to monitor your condition. Your doctor will take blood and urine samples to check the levels of chemical substances in the blood (plasma electrolytes). You will also have an electrocardiogram (ECG) performed.
It may be necessary to change your other medications.
Children
Viaflo Glucosalino Potásico should be administered with caution in children.
Newborns, especially premature and low-birth-weight babies, are at higher risk of developing high or low blood sugar levels (hypoglycemia or hyperglycemia) due to the infusion of glucose solutions. Low blood sugar levels in newborns can cause prolonged seizures, coma, and brain damage. High blood sugar levels have been associated with cerebral hemorrhage, late-onset bacterial and fungal infections, intestinal infection (necrotizing enterocolitis), eye problems (retinopathy of prematurity), lung problems (bronchopulmonary dysplasia), prolonged hospital stay, and death.
Children are at higher risk of having or developing low sodium levels in the blood (hyponatremia). Hyponatremia can cause headache, nausea, seizures, lethargy, coma, brain inflammation (cerebral edema), and death. Acute hyponatremic encephalopathy is a serious complication, especially in children.
Your doctor is aware of this and will closely monitor the amount of chemical substances such as sodium and chloride in your child's blood (plasma electrolytes).
Other Medicines and Viaflo Glucosalino Potásico
Tell your doctor or pharmacist if you are using or have recently used other medicines.
Other medicines that may affect or be affected by potassium chloride, sodium chloride, and glucose infusion include:
Some medicines act on the vasopressin hormone. These may include:
If you need a blood transfusion at the same time as the infusion, you will receive the blood in another vein.
Using Viaflo Glucosalino Potásico with Food and Drinks
You should ask your doctor what you can eat or drink.
Pregnancy, Breast-feeding, and Fertility
Consult your doctor or nurse before using this medicine.
If you are pregnant or breast-feeding, think you may be pregnant, or are planning to have a baby, consult your doctor or nurse before using this medicine.
If you are given Viaflo Glucosalino Potásico during labor, there is a small possibility that the glucose may affect the fetus, causing:
However, no relationship has been demonstrated between glucose infusion and the mentioned effects.
If another medicine is added to this infusion solution during pregnancy or breast-feeding, you should:
Driving and Using Machines
The infusion does not affect your ability to drive or use machines.
A doctor or nurse will give you the infusion. Your doctor will decide how much you need and when it will be given to you, depending on your age, weight, clinical and biological status (your state of health). This may also be influenced by other treatments you are receiving.
If you require a high volume or rapid infusion of Viaflo Glucosalino Potásico, your doctor will monitor your ECG (electrocardiogram).
It will usually be given to you through a plastic tube connected to a needle in a vein, almost always in your arm. However, your doctor may use another method to administer the medicine to you.
Before and during the infusion, your doctor will monitor:
If you have kidney failure, you will receive a lower dose.
If you are given too much Viaflo Glucosalino Potásico
If you are given too much Viaflo Glucosalino Potásico (overdose), the following symptoms may occur:
If you notice any of these symptoms, you should inform your doctor immediately. Your infusion will be stopped and you will be treated depending on the symptoms.
If a medicine has been added to Viaflo Glucosalino Potásico before the overdose, this medicine may also cause side effects. You should read the list of possible symptoms in the package leaflet of the added medicine.
If you stop the Viaflo Glucosalino Potásico infusion
Your doctor will decide when you should stop receiving this infusion
If you have any other questions about the use of this product, ask your doctor.
Like all medicines, Viaflo Glucosalino Potásico can cause side effects, although not everybody gets them.
Some of the possible side effects related to the method of administration are:
If a medicine has been added to the infusion solution, it may also cause side effects. These side effects will depend on the added medicine. You should read the list of possible symptoms in the package leaflet of the added medicine.
Reporting Side Effects
If you experience side effects, talk to your doctor or nurse, even if it is a side effect not listed in this leaflet
You can also report side effects directly through the Spanish Pharmacovigilance System for Human Use Medicines, https://www.notificaRAM.es. By reporting side effects, you can help provide more information on the safety of this medicine.
Viaflo Glucosalino Potásico does not require special storage conditions
Keep this medicine out of the sight and reach of children.
Do not use Viaflo Glucosalino Potásico after the expiration date stated on the bag after CAD. The expiration date is the last day of the month indicated.
Viaflo Glucosalino Potásico should not be administered if:
the container is damaged.
This leaflet does not contain all the information about this medicine. If you have any doubts, ask your doctor, pharmacist, or nurse.
Composition of Viaflo Glucosalino Potásico
The active ingredients are potassium chloride (1.5 g per liter), sodium chloride (1.8 g per liter), and glucose (40 g per liter, equivalent to glucose monohydrate 44 g).
The only excipient is water for injectable preparations.
Appearance of the Productand Container Content
Viaflo Glucosalino Potásico is a clear solution, free from visible particles. It is presented in polyolefin/polyamide plastic bags (Viaflo). Each bag is packaged in a sealed protective overbag.
The bag sizes are:
The bags are supplied in boxes, each containing the following quantities:
Only some package sizes may be marketed.
Marketing Authorization Holder
Baxter S.L.
Pouet de Camilo 2, 46394 Ribarroja del Turia (Valencia)
Manufacturer
Bieffe Medital SA
Ctra de Biescas-Senegüé, 22666 Sabiñánigo (Huesca), Spain
Date of Last Revision of this Leaflet: April 2018
Detailed and updated information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/
This information is intended only for healthcare professionals
Handling and Preparation
Use only if the solution is clear, without visible particles, and if the container is not damaged. Administer immediately after connecting the infusion equipment.
Do not remove the unit from the overbag until it is ready for use. The inner bag maintains the product's sterility.
Do not connect plastic containers in series. This type of use can produce gas embolisms due to residual air dragged from the primary container before the administration of the liquid contained in the secondary container is completed.
The pressurization of intravenous solutions in flexible plastic containers to increase flow rates can lead to a gas embolism if the residual air in the container is not fully evacuated before administration.
The use of an intravenous administration set with a ventilation filter in the open position could cause a gas embolism. This type of intravenous administration set with the ventilation filter in the open position should not be used with flexible plastic containers.
The solution must be administered with sterile equipment using an aseptic technique. The equipment must be primed with the solution to prevent air from entering the system.
Added medications can be introduced before or during infusion through the injection point.
Medications known or determined to be incompatible should not be used.
Before adding a medication, verify that it is soluble and/or stable in Viaflo Glucosalino Potásico 4%, 0.18%, 0.15% and that the pH range of the solution is adequate.
Consult the leaflet of the medication to be added and any other relevant literature.
After addition, if there is a change in color and/or precipitates, insoluble complexes, or crystals appear, do not use the solution.
Mix the solution well when medications have been added.
Do not store solutions containing added medications.
For single use.
When medications are added, the tonicity should be checked before parenteral administration. A complete and careful aseptic mixture of any added medication is necessary. Solutions containing added medications should be used immediately after preparation, unless this has been carried out under controlled and validated aseptic conditions.
The addition of other medications or the use of an incorrect administration technique can cause the appearance of febrile reactions due to the possible introduction of pyrogens. In case of an adverse reaction, the infusion should be interrupted immediately.
Pediatric Population
In order to avoid a potentially fatal overdose during the infusion of intravenous solutions to newborns, special attention should be paid to the administration method. When using a syringe pump to administer liquids or medications intravenously to newborns, a solution bag should not be left connected to the syringe.
When using an infusion pump, all clamps on the intravenous administration set should be closed before removing the administration set from the pump or disconnecting the pump. This is required regardless of whether the administration set has an anti-free flow device.
The intravenous infusion device and administration set should be frequently monitored.
Discard after a single use.
Discard unused solution remains.
Do not reconnect partially used bags.
a- Remove the Viaflo bag from the protective overbag immediately before use.
b- Check for the absence of small leaks by squeezing the inner bag firmly. If leaks are detected, discard the solution, as it may not be sterile.
c- Check the transparency of the solution and the absence of foreign particles. Discard the solution if it is not transparent or contains foreign particles.
2- Preparation for Administration
Use sterile material for preparation and administration.
a- Hang the container by the handle
b- Remove the plastic protector from the outlet port at the bottom of the container.
c- Use an aseptic technique to prepare the infusion
d- Connect the administration set. Consult the instructions accompanying the set for connection, priming, and administration of the solution.
3- Techniques for Injecting Added Medication
Warning: Added medications may be incompatible (see section 5 "Incompatibilities of Added Medications" below)
To Add Medication Before Administration
a Disinfect the injection point
b Using a syringe with a 19G to 22G needle, puncture the resealable injection point and inject.
c Mix the medication and solution completely. For high-density medications, such as potassium chloride, gently tap the tubes while they are in a vertical position and mix.
Precaution: do not store bags with added medication.
To Add Medication During Administration
a Close the clamp on the administration set.
b Disinfect the injection point.
c Using a syringe with a 19G to 22G needle, puncture the resealable injection point and inject.
d Remove the container from the IV stand and/or turn it to put it in a vertical position.
e Empty both tubes by gently tapping them while the container is in a vertical position.
f Mix the solution and medication completely.
g Put the container back in the use position, reopen the clamp, and continue administration.
Before use, the physical and chemical stability of any medication added to the pH and Viaflo Glucosalino Potásico bag must be established. From a microbiological point of view, the diluted product should be used immediately unless the dilution has been carried out under controlled and validated aseptic conditions.
If it is not used immediately, the conditions and storage times used before its use are the responsibility of the user.
5- Incompatibilities of Added Medications
As with all parenteral solutions, before adding additional medications, their compatibility with the solution in the Viaflo container should be evaluated.
It is the responsibility of the physician to judge the incompatibility of the added medication to Viaflo Glucosalino Potásico by examining any change in color and/or precipitate, appearance of insoluble complexes, or crystals.
Consult the leaflet of the medication to be added.
Before adding a medication, verify that it is soluble and stable in water at the pH of Viaflo Glucosalino Potásico.
When compatible medication is added to this formulation, the solution should be administered immediately, unless the dilution has been carried out under controlled and validated aseptic conditions.
As a guide, the following medications are incompatible with Viaflo Glucosalino Potásico, although this list is not exhaustive:
Do not administer glucose simultaneously with whole blood through the same infusion equipment, as hemolysis and agglutination may occur.
Medications known to be incompatible should not be used.
The best alternatives with the same active ingredient and therapeutic effect.
Discuss dosage, side effects, interactions, contraindications, and prescription renewal for VIAFLO GLUCOSALINE POTASSIUM 4%, 0.18%, 0.15% SOLUTION FOR INFUSION – subject to medical assessment and local rules.