HOSPASOL 167 mmol/L SOLUTION FOR INFUSION
How to use HOSPASOL 167 mmol/L SOLUTION FOR INFUSION
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This page provides general information and does not replace a doctor’s consultation. Always consult a doctor before taking any medication. Seek urgent medical care if symptoms are severe.
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Introduction
PACKAGE LEAFLET: INFORMATION FOR THE USER
HOSPASOL®167 mmol/l Solution for infusion
Sodium bicarbonate
Read all of this leaflet carefully before you start using this medicine because it contains important information for you.
- Keep this leaflet, you may need to read it again.
- If you have any further questions, ask your doctor, pharmacist, or nurse.
- If you get any side effects, talk to your doctor, pharmacist, or nurse. This includes any possible side effects not listed in this leaflet. See section 4.
Contents of the pack:
- What Hospasol 167 mmol/l is and what it is used for
- What you need to know before you use Hospasol 167 mmol/l
- How to use Hospasol 167 mmol/l
- Possible side effects
- Storage of Hospasol 167 mmol/l
- Contents of the pack and other information
1. What Hospasol 167 mmol/l is and what it is used for
Hospasol 167 mmol/l is used in hospitals or special centers during dialysis sessions to correct the chemical imbalance of the blood caused by kidney failure.
It replaces the bicarbonate that the body loses during:
- Acetate-Free Biofiltration (AFB) or
- Continuous Venovenous Hemofiltration Free of Acetate (AFCVVHF).
It also helps to restore the body's bicarbonate levels, which are lost when the kidneys do not function properly (kidney failure).
2. What you need to know before you use Hospasol 167 mmol/l
Do not use Hospasol 167 mmol/l
If you are being treated with a dialysis method that uses a supplementary buffer.
Warnings and precautions
Consult your doctor, pharmacist, or nurse before starting treatment with Hospasol 167 mmol/l.
It is essential to monitor the concentration of salts (electrolytes) in the blood, as well as the body's acid-base balance. Therefore, the composition of the blood should be checked regularly.
Pay special attention to the following:
The pH value of the blood. In case of high pH (alkalosis), Hospasol 167 mmol/l should not be used.
The sodium level in the blood, if you have heart and/or kidney failure. An overdose of sodium can lead to fluid retention in the body (hypervolemia) and particularly in the lungs (pulmonary edema).
The blood vessels, as inflammation associated with thrombus formation (thrombophlebitis) can occur if the product is administered through a small peripheral vein.
The level of proteins, amino acids, and water-soluble vitamins in the blood, as significant losses can occur during dialysis.
Using Hospasol 167 mmol/l with other medicines
Tell your doctor, pharmacist, or nurse if you are using, have recently used, or might use any other medicines.
You must do this because the concentration in the blood of some of these medicines may decrease during treatment with Hospasol 167 mmol/l. Your doctor will decide if any of the medicines need to be changed.
Pregnancy, breastfeeding, and fertility
There are no adequate data on the use of Hospasol 167 mmol/l in pregnant or breastfeeding women.
If you are pregnant or breastfeeding, your doctor will decide whether you should undergo treatment with Hospasol 167 mmol/l.
Driving and using machines
Hospasol 167 mmol/l does not affect the ability to drive and use machines.
3. How to use Hospasol 167 mmol/l
Hospasol 167 mmol/l is a product used in hospitals or special centers with dialysis equipment. It should only be administered by medical professionals.
The volume of Hospasol 167 mmol/l and therefore the dose used will depend on the patient's condition. The doctor responsible for the treatment will determine the dose volume.
Do not useHospasol 167 mmol/l if the solution is cloudy or if the packaging is damaged. All seals must be intact.
If you use more Hospasol 167 mmol/l than you should
An overdose can lead to a concentration that is too low of potassium (hypokalemia) and/or glucose (hypoglycemia) in the blood. If an overdose occurs, the administration of Hospasol 167 mmol/l should be stopped immediately and dialysis should be performed. Continuous monitoring of blood gases should be carried out.
Your doctor will take the necessary corrective measures and adjust the dose.
If you have any further questions on the use of this medicine, ask your doctor, pharmacist, or nurse.
4. Possible side effects
Like all medicines, this medicine can cause side effects, although not everybody gets them.
There are some side effects that may be due to the hemodialysis process, for example:
- nausea
- vomiting
- muscle cramps
- high blood pressure (hypertension)
- chills
- fever
Reporting of side effects
If you experience any side effects, talk to your doctor, pharmacist, or nurse, even if it is possible side effects 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.
5. Storage of Hospasol 167 mmol/l
Keep this medicine out of the sight and reach of children.
Do not store below 4°C
Do not use Hospasol 167 mmol/l after the expiry date which is stated on the label and on the carton. The expiry date is the last day of the month stated.
Hospasol 167 mmol/l can be disposed of with wastewater without harming the environment.
6. Contents of the pack and other information
Composition of HOSPASOL 167 mmol/l
The active substanceis:
1000 ml of solution contain: Sodium bicarbonate 14.0 g
Which corresponds to
Sodium, Na+ 167 mmol/l (167 mEq/l)
Bicarbonate, HCO3 167 mmol/l (167 mEq/l)
Theoretical osmolality: 334 mOsm/l
The other ingredientsare:
- Carbon dioxide (for pH adjustment)
- Water for injections
Appearance of the product Hospasol 167 mmol/l and pack contents
Hospasol 167 mmol/l comes in a single-compartment bag. The solution is clear and colorless.
Each bag contains a solution for infusion of 3000 ml or 5000 ml. The bag is wrapped in transparent film.
Each carton contains three bags of 3000 ml or two bags of 5000 ml and a leaflet.
Marketing authorisation holder
Vantive Belgium SRL
Boulevard d’Angleterre, 2
1420 Braine-l’Alleud
Belgium
Manufacturer
BIEFFE MEDITAL S.P.A.
Via Stelvio 94
23035 Sondalo (SO)
Italy
You can obtain more information about this medicine by contacting the local representative of the marketing authorisation holder:
Vantive Health, SL
C/ Pouet de Camilo, 2
46394 Ribarroja del Turia
Valencia
Spain
Date of last revision of this leaflet:
Detailed and up-to-date information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.es
This information is intended only for healthcare professionals:
HOSPASOL®167 mmol/l solution for infusion
It is essential to use a dialysis solution without a buffer (which does not contain acetate or bicarbonate). A dialysis solution with an appropriate composition for Acetate-Free Biofiltration should be selected.
It is essential to use a substitution fluid without a buffer (which does not contain acetate or bicarbonate). A substitution fluid with an appropriate composition for Continuous Venovenous Hemofiltration Free of Acetate should be selected.
Hospasol 167 mmol/l should be administered alone, without adding any other medicine, in particular, solutions that contain calcium or magnesium, as they could cause precipitation of calcium or magnesium carbonate.
Hospasol 167 mmol/l is injected into the venous return line or into the extracorporeal circuit before (pre-dilution) or after the hemofilter (post-dilution).
The doctor in charge must determine the volume, flow rate, and duration of dialysis.
The flow rates normally used for Acetate-Free Biofiltration are:
- Adults, adolescents, and elderly: 1500 to 2000 ml/hour
- Children: 30 to 40 ml/kg/hour
The flow rates used normally in Continuous Venovenous Hemofiltration Free of Acetate are:
- Adults, adolescents, and elderly: 85 to 530 ml/hour
- Children: 1.70 to 10.5 ml/kg/hour
INSTRUCTIONS FOR USE AND HANDLING
Hospasol 167 mmol/l is indicated for use only in dialysis machines specially designed for Acetate-Free Biofiltration (special hemodialysis technique) or for Continuous Venovenous Hemofiltration Free of Acetate.
Consult the instructions for use of the dialysis machine before starting treatment with Hospasol 167 mmol/l.
Do not remove from the packaging until ready to use.
Hospasol 167 mmol/l should only be used if the solution is clear, free of particles, and all seals are intact.
Aseptic techniques should be used throughout the administration process to the patient.
Before connecting and after removing the plug from the bag connector (the safety connector - safelink), disinfectant should be applied to the inside of it.
Before disconnecting, it is recommended to disinfect the external surfaces of the line connector and the safety connector (safelink).
The solution is for single use. Discard any unused remainder immediately.
From a microbiological point of view, once opened, the product should be used immediately. If not used immediately, the user will be responsible for the time and conditions of storage prior to use.
- Country of registration
- Dosage formINJECTABLE PERFUSION, 167 mmol/l (14 g/l)
- Prescription requiredYes
- Manufacturer
- This information is for reference only and does not constitute medical advice. Always consult a doctor before taking any medication. Oladoctor is not responsible for medical decisions based on this content.
- Alternatives to HOSPASOL 167 mmol/L SOLUTION FOR INFUSIONDosage form: HEMOFILTRATION, 2 mmol potassium/lActive substance: HemofiltratesManufacturer: Nikkiso BelgiumPrescription requiredDosage form: HEMOFILTRATION, 4 mmol potassium/lActive substance: HemofiltratesManufacturer: Nikkiso BelgiumPrescription requiredDosage form: HEMOFILTRATION, -Active substance: HemofiltratesManufacturer: Nikkiso BelgiumPrescription required
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