Products
The content of this site is intended for health care professionals only. A health care professional is a person authorised to prescribe and dispense human medical products (a physician, a pharmacist).
By ticking the box >I hereby confirm that I am a health care professional< you have confirmed to be a health care professional and you have understood the definition of a health care professional according to applicable legal regulations.
By clicking „Enter“ you acknowledge that the information on the following pages is intended exclusively for health care professionals and not for lay public, with all risks and consequences arising therefrom for lay public. These risks may result in misinterpretation, misjudgement of your own health condition or incorrect preference of a human medical product. You also acknowledge that you and your doctor decide together whether the treatment with a human medical product subject to prescription is appropriate for you and you should always consult your doctor or pharmacist whether the treatment with a human medical product subject to prescription is appropriate for you.
Irrigation solutions
Wound irrigation solutions are used to hydrate the wound, to remove debris and bacteria, to assist in visual inspection, to prevent infection, and to improve healing and cosmesis. Sterile irrigating solutions are sterile or nonpyrogenic isotonic solutions, made under sterile conditions. The container closure system consists of a plastic bag and tubing with two ports.
- Sodium chloride 0,9% IRRISOL 1000 ml, 2000 ml, 3000 ml, 5000 ml
- Ringer IRRISOL 1000 ml, 2000 ml, 3000 ml, 5000 ml
- AQUA IRRISOL 1000 ml, 2000 ml, 3000 ml, 5000 ml
In upcoming few months IMUNA PHARM will bring mentioned solutions with bigger volume (2000 ml, 5000 ml) in plastic bag with one port . We are working on Lactated Ringer’s Irrigation too. This solution is useful as an Irrigating fluid for body joints because it approximates the electrolyte composition of synovial fluid, and provides a transparent fluid medium with optical properties suitable for good visualization of the interior joint surface during endoscopic examination.
The content of this site is intended for health care professionals only. A health care professional is a person authorised to prescribe and dispense human medical products (a physician, a pharmacist).
By ticking the box >I hereby confirm that I am a health care professional< you have confirmed to be a health care professional and you have understood the definition of a health care professional according to applicable legal regulations.
By clicking „Enter“ you acknowledge that the information on the following pages is intended exclusively for health care professionals and not for lay public, with all risks and consequences arising therefrom for lay public. These risks may result in misinterpretation, misjudgement of your own health condition or incorrect preference of a human medical product. You also acknowledge that you and your doctor decide together whether the treatment with a human medical product subject to prescription is appropriate for you and you should always consult your doctor or pharmacist whether the treatment with a human medical product subject to prescription is appropriate for you.
Infusion solutions
- AQUA PRO INJEKCIONE IMUNA 100ML, 250ML, 500ML, 1000ML
- Sodium chloride 0,9% 100ML, 250ML, 500ML, 1000ML
- INFUSIO NATRII CHLORATI ISOTONICA 1/2 CUM GLUCOSO 5 IMUNA 100ML, 250ML, 500ML, 1000ML
- INFUSIO GLUCOSI 5 IMUNA 100ML, 250ML, 500ML
- INFUSIO GLUCOSI 10 IMUNA 100ML, 250ML, 500ML
- INFUSIO GLUCOSI 20 IMUNA 100ML, 250ML, 500ML
- INFUSIO GLUCOSI 40 IMUNA 100ML, 250ML, 500ML
- INFUSIO MANNITOLI 10 IMUNA 100ML, 250ML, 500ML
- INFUSIO MANNITOLI 20 IMUNA 100ML, 250ML, 500ML
- INFUSIO RINGERI IMUNA 100ML, 250ML, 500ML, 1000ML
- INFUSIO KALII CHLORATI CONCENTRATA IMUNA 100ML
The content of this site is intended for health care professionals only. A health care professional is a person authorised to prescribe and dispense human medical products (a physician, a pharmacist).
By ticking the box >I hereby confirm that I am a health care professional< you have confirmed to be a health care professional and you have understood the definition of a health care professional according to applicable legal regulations.
By clicking „Enter“ you acknowledge that the information on the following pages is intended exclusively for health care professionals and not for lay public, with all risks and consequences arising therefrom for lay public. These risks may result in misinterpretation, misjudgement of your own health condition or incorrect preference of a human medical product. You also acknowledge that you and your doctor decide together whether the treatment with a human medical product subject to prescription is appropriate for you and you should always consult your doctor or pharmacist whether the treatment with a human medical product subject to prescription is appropriate for you.
IMMODIN®
Pharmacotherapeutic group:
Immunopreparations (ATC code: L03AX)
Characteristics:
IMMODIN® (lyophylised human leucocyte-derived dialysate) is a mixture of biologically active immunomodulating agents. Active substances in IMMODIN® affect proliferation and differentiation of different types of cells, i.e. maturation into functional stages. The drug is indicated in cellular immune disorders that have been demonstrated in children from 6 months of age, adolescents and adults.
For detailed information click here.
Pharmacotherapeutic group:
Immunopreparations
Characteristics:
IMMODIN® contains biologically active substances liable to normalise specific cell-mediated immunity of the recipient. IMMODIN® is indicated in cellular immune disorders that have been demonstrated in children from 6 months of age, adolescents and adults.
For detailed information click here.
The content of this site is intended for health care professionals only. A health care professional is a person authorised to prescribe and dispense human medical products (a physician, a pharmacist).
By ticking the box >I hereby confirm that I am a health care professional< you have confirmed to be a health care professional and you have understood the definition of a health care professional according to applicable legal regulations.
By clicking „Enter“ you acknowledge that the information on the following pages is intended exclusively for health care professionals and not for lay public, with all risks and consequences arising therefrom for lay public. These risks may result in misinterpretation, misjudgement of your own health condition or incorrect preference of a human medical product. You also acknowledge that you and your doctor decide together whether the treatment with a human medical product subject to prescription is appropriate for you and you should always consult your doctor or pharmacist whether the treatment with a human medical product subject to prescription is appropriate for you.
ALTEANA®
Pharmacotherapeutic group:
Immunopreparations, anti-tetanus vaccine (ATC code: J07AM01)
Characteristics
ALTEANA® is prepared from tetanus toxin that is inactivated by formaldehyde and subsequently purified while maintaining antigenicity. To increase the imunizing effect the anatoxin is adsorbed on a mineral carrier (aluminium hydroxide). The vaccine is intended for primary vaccination and booster vaccination against tetanus. It induces production of specific antibodies after intramuscular application and confers protection against tetanus infection.
For details click here
Pharmacotherapeutic group:
Immunopreparations, anti-tetanus vaccine
Characteristics
ALTEANA® is an anti-tetanus vaccine. It is intended for active immunisation against tetanus or post-traumatic prophylaxis in children and adults where proof of vaccination cannot be demonstrated or with incomplete vaccination against tetanus. Immunity develops shortly after the administration of the second dose and is boosted by the third dose; the immunity is maintained for approximately 10-15 years after revaccination.
For details click here.
The content of this site is intended for health care professionals only. A health care professional is a person authorised to prescribe and dispense human medical products (a physician, a pharmacist).
By ticking the box >I hereby confirm that I am a health care professional< you have confirmed to be a health care professional and you have understood the definition of a health care professional according to applicable legal regulations.
By clicking „Enter“ you acknowledge that the information on the following pages is intended exclusively for health care professionals and not for lay public, with all risks and consequences arising therefrom for lay public. These risks may result in misinterpretation, misjudgement of your own health condition or incorrect preference of a human medical product. You also acknowledge that you and your doctor decide together whether the treatment with a human medical product subject to prescription is appropriate for you and you should always consult your doctor or pharmacist whether the treatment with a human medical product subject to prescription is appropriate for you.
Flebogamma® DIF 100 mg/ml*
Pharmacotherapeutic group:
Immune sera and immunoglobulins: immunoglobulins, normal human, for intravascular administration (ATC code: J06BA02)
Characteristics
One ml contains 100 mg of normal human immunoglobulin obtained from human plasma pools (*donors from the Slovak Republic). It is indicated as substitution therapy in adults, children and adolescents (2-18 years of age): Primary immunodeficiency syndrome with reduced antibody production. Hypogammaglobulinaemia and recurrent bacterial infections in patients with chronic lymphocytic leukaemia who have previously failed prophylactic antibiotic therapy. Hypogamaglobulinaemia and recurrent bacterial infections in patients with multiple myeloma who have failed to respond to pneumococcal immunisation. Hypogammaglobulinaemia in HSCT patients (hematopoietic stem cell transplantation). Congenital AIDS with recurrent bacterial infections. Immunomodulation in adults, children and adolescents (2-18 years): Idiopatic thrombocytopenic purpura (ITP) in patients at high risk of bleeding or prior to surgery to correct the platelet count. Guillain-Barré syndrome. Kawasaki disease.
For details click here
For more blood derivatives imported by Imuna Pharm a.s. to Slovakia in cooperation with Grifols click here(http://www.grifols.com/en/web/slovakia/products_and_services)
Pharmacotherapeutic group:
Immune sera and immunoglobulins: Immunoglobulins, normal human, for intravascular administration
Characteristics
Flebogamma DIF is a solution for infusion (dripping into vein). It contains an active substance human normal immunoglobulin (*prepared from plasma (the liquid part of blood) from Slovak donors). Flebogamma DIF is indicated for the treatment of patients who need to increase their blood antibody level to fight infections and other diseases.
The content of this site is intended for health care professionals only. A health care professional is a person authorised to prescribe and dispense human medical products (a physician, a pharmacist).
By ticking the box >I hereby confirm that I am a health care professional< you have confirmed to be a health care professional and you have understood the definition of a health care professional according to applicable legal regulations.
By clicking „Enter“ you acknowledge that the information on the following pages is intended exclusively for health care professionals and not for lay public, with all risks and consequences arising therefrom for lay public. These risks may result in misinterpretation, misjudgement of your own health condition or incorrect preference of a human medical product. You also acknowledge that you and your doctor decide together whether the treatment with a human medical product subject to prescription is appropriate for you and you should always consult your doctor or pharmacist whether the treatment with a human medical product subject to prescription is appropriate for you.
Flebogamma® DIF 50 mg/ml*
Pharmacotherapeutic group:
Immune sera and immunoglobulins: immunoglobulins, normal human, for intravascular administration (ATC code: J06BA02)
Characteristics
One ml contains 50 mg of normal human immunoglobulin obtained from human plasma pools (*donors from the Slovak Republic). It is indicated as substitution therapy in adults, children and adolescents (2-18 years of age): Primary immunodeficiency syndrome with reduced antibody production. Hypogammaglobulinaemia and recurrent bacterial infections in patients with chronic lymphocytic leukaemia who have previously failed prophylactic antibiotic therapy. Hypogamaglobulinaemia and recurrent bacterial infections in patients with multiple myeloma who have failed to respond to pneumococcal immunisation. Hypogammaglobulinaemia in HSCT patients (hematopoietic stem cell transplantation). Congenital AIDS with recurrent bacterial infections. Immunomodulation in adults, children and adolescents (2-18 years): Idiopatic thrombocytopenic purpura (ITP) in patients at high risk of bleeding or prior to surgery to correct the platelet count. Guillain-Barré syndrome. Kawasaki disease.
For details click here
For more blood derivatives imported by Imuna Pharm a.s. to Slovakia in cooperation with Grifols click here(http://www.grifols.com/en/web/slovakia/products_and_services)
Pharmacotherapeutic group:
Immune sera and immunoglobulins: Immunoglobulins, normal human, for intravascular administration
Characteristics
Flebogamma DIF is a solution for infusion (dripping into vein). It contains an active substance human normal immunoglobulin (*prepared from plasma (the liquid part of blood) from Slovak donors). Flebogamma DIF is indicated for the treatment of patients who need to increase their blood antibody level to fight infections and other diseases.
The content of this site is intended for health care professionals only. A health care professional is a person authorised to prescribe and dispense human medical products (a physician, a pharmacist).
By ticking the box >I hereby confirm that I am a health care professional< you have confirmed to be a health care professional and you have understood the definition of a health care professional according to applicable legal regulations.
By clicking „Enter“ you acknowledge that the information on the following pages is intended exclusively for health care professionals and not for lay public, with all risks and consequences arising therefrom for lay public. These risks may result in misinterpretation, misjudgement of your own health condition or incorrect preference of a human medical product. You also acknowledge that you and your doctor decide together whether the treatment with a human medical product subject to prescription is appropriate for you and you should always consult your doctor or pharmacist whether the treatment with a human medical product subject to prescription is appropriate for you.
CARBOTOX
tbl 20×320 mg (blis.PVC/Al)
Pharmacotherapeutic group:
Digestives, adsorbents, acids (ATC code: A07BA51)
Characterisitics
Indications: Carbotox tablets are intended for the treatment of adult and adolescent population and children from 3 years of age. Without consulting a doctor adults including pregnant and breastfeeding women and adolescents can use the medicinal product on a short-term basis (maximum 2 days) in acute diarrhoea caused by food poisoning and irritable bowel syndrome. Children under 3 years of age should only use the drug based on doctor’s recommendation. The same applies for adults suffering from ulcerative colitis, gastritis and excessive food degradation in the bowel; they should only the product as recommended by their physician. The product is also used in diagnostic investigation of the gall bladder and bile ducts.
Method of administration
The usual dose is 2-4 tablets 3-4 times daily. A maximum single dose of 4-5 tablets cn be given to children from 3 years of age. Tablets should be swallowed whole with a small amount of water. A suspension should be made by disintegrating tablets in a small amount of liquid (water or unsweetened tea) for children.
The drug is not subject to medical prescription.
For details click here
tablets
(Carbo activatus, Natrii thiosulfas)
WHAT CARBOTOX IS AND WHAT IT IS USED FOR?
Carbotox belongs to the group of drugs containing activated charcoal that absorbs gases and toxic substances from the digestive tract. It contains sodium thiosulphate, a neutralizing agent for some poisons, with a mild laxative effect.
Carbotox is intended for the treatment of adults, adolescents and children from 3 yearso of age. Without consulting a doctor, adults including pregnant and breastfeeding women and adolescents can use the medicinal product on a short-term basis (maximum 2 days) in acute diarrhoea caused by food poisoning and irritable bowel syndrome.
The product is also used in diagnostic investigation of the gall bladder and bile ducts.
The drug is not intended for children under 3 years of age. Children from 3 years of age can use the drug only based upon doctor’s recommendation.
For details click here.
The content of this site is intended for health care professionals only. A health care professional is a person authorised to prescribe and dispense human medical products (a physician, a pharmacist).
By ticking the box >I hereby confirm that I am a health care professional< you have confirmed to be a health care professional and you have understood the definition of a health care professional according to applicable legal regulations.
By clicking „Enter“ you acknowledge that the information on the following pages is intended exclusively for health care professionals and not for lay public, with all risks and consequences arising therefrom for lay public. These risks may result in misinterpretation, misjudgement of your own health condition or incorrect preference of a human medical product. You also acknowledge that you and your doctor decide together whether the treatment with a human medical product subject to prescription is appropriate for you and you should always consult your doctor or pharmacist whether the treatment with a human medical product subject to prescription is appropriate for you.
CARBOSORB
plv por 1×25 g (bag PE)
Pharmacotherapeutic group:
Digestives, adsorbents, acids (ATC code: A07BA51)
Characterisitics
Indications: Carbosorb powder is intended for the treatment of adult and adolescent population and children from 3 years of age. Without consultin g a doctor, adults including pregnant and breastfeeding women and adolescents can use the medicinal product on a short-term basis (maximum 2 days) in acute diarrhoea caused by food poisoning, mild viral and bacterial intestinal infections, irritable bowel syndrome and acute poisoning with toxic agents. Children under 3 years of age should only use the drug based upon doctor’s recommendation. The same applies for adults suffering from ulcerative colitis, gastritis and excessive food degradation in the bowel as well as diarrhoea associated with a variety of underlying conditions (such as diabetes), they should only use the product as recommended by their physician. The product is also used in diagnostic investigation of the gall bladder and bile ducts.
Method of administration
The usual dose is 1-2 table spoons 3-4x daily. The powder should be dissolved in a necessary amount of liquid (water, unsweetened tea).
The drug is not subject to medical prescription.
For details click here
Oral powder
(Carbo activatus)
WHAT CARBOSORB IS AND WHAT IT IS USED FOR?
Carbosorb belongs to the group of drugs containing activated charcoal that absorbs gases and toxic substances from the digestive tract.
Carbosorb oral powder is intended for the treatment of adults, adolescents and children from 3 years of age. Without consulting a doctor, adults including pregnant and breastfeeding women and adolescents can use the medicinal product on a short-term basis (maximum 2 days) in acute diarrhoea caused by food poisoning, mild viral and bacterial intestinal infections, irritable bowel syndrome, and acute intoxications.
The drug is not intended for children under 3 years of age. Children from 3 years of age can use the drug only based upon doctor’s recommendation.
Adults suffering from ulcerative colitis, gastritis and excessive food degradation in the bowel as well as diarrhoea associated with a variety of underlying conditions (such as diabetes) can use the product only upon doctor’s recommendation.
The product is also used in diagnostic investigation of the gall bladder and bile ducts.
The drug is not intended for children under 3 years of age. Children from 3 years of age can use the drug only upon doctor’s recommendation.
Adults suffering from ulcerative colitis, gastritis and excessive food degradation in the bowel as well as acute intoxications can use the product only upon doctor’s recommendation
For details click here.
The content of this site is intended for health care professionals only. A health care professional is a person authorised to prescribe and dispense human medical products (a physician, a pharmacist).
By ticking the box >I hereby confirm that I am a health care professional< you have confirmed to be a health care professional and you have understood the definition of a health care professional according to applicable legal regulations.
By clicking „Enter“ you acknowledge that the information on the following pages is intended exclusively for health care professionals and not for lay public, with all risks and consequences arising therefrom for lay public. These risks may result in misinterpretation, misjudgement of your own health condition or incorrect preference of a human medical product. You also acknowledge that you and your doctor decide together whether the treatment with a human medical product subject to prescription is appropriate for you and you should always consult your doctor or pharmacist whether the treatment with a human medical product subject to prescription is appropriate for you.
CARBOSORB
tbl 20×320 mg (blis.PVC/Al)
Pharmacotherapeutic group:
Digestives, adsorbents, acids (ATC code: A07BA51)
Characterisitics
Indications: Carbosorb tablets are intended for the treatment of adult and adolescent population and children from 3 years of age. Without consulting a doctor, adults and adolescents including pregnant and breastfeeding women can use the medicinal product on a short-term basis (maximum 2 days) in acute diarrhoea caused by food poisoning, mild viral and bacterial intestinal infections and irritable bowel syndrome. Children under 3 years of age should only use the drug based upon doctor’s recommendation. The same applies for adults suffering from ulcerative colitis, gastritis and excessive food degradation in the bowel as well as diarrhoea associated with a variety of underlying conditions (such as diabetes); they should only use the product as recommended by their physician. The product is also used in diagnostic investigation of the gall bladder and bile ducts.
Method of administration
The usual dose is 2-4 tablets 3-4 times daily (a single dose of 10-12 tablets can be given in diarrhoea or intoxication). A maximum single dose of 4-5 tablets can be given to children from 3 years of age. Tablets should be swallowed whole with a small amount of water. A suspension can be made by disintegrating tablets in a small amount of liquid (water or unsweetened tea) for children.
The drug is not subject to medical prescription.
For details click here
tablet
(Carbo activatus)
WHAT CARBOSORB IS AND WHAT IT IS USED FOR?
Carbosorb belongs to the group of drugs containing activated charcoal that absorbs gases and toxic substances from the digestive tract.
Carbosorb is intended for the treatment of adults, adolescents and children from 3 years oof age. Without consulting a doctor, adults including pregnant and breastfeeding women and adolescents can use the medicinal product on a short-term basis (maximum 2 days) in acute diarrhoea caused by food poisoning, mild viral and bacterial intestinal infections and irritable bowel syndrome; in acute intoxications after consulting the doctor.
The drug is not intended for children under 3 years of age. Children from 3 years of age can use the drug only based upon doctor’s recommendation.
Adults suffering from ulcerative colitis, gastritis and excessive food degradation in the bowel as well as diarrhoea associated with a variety of underlying conditions (such as diabetes) can use the product only upon doctor’s recommendation.
The product is also used in diagnostic investigation of the gall bladder and bile ducts.
For details click here.
The content of this site is intended for health care professionals only. A health care professional is a person authorised to prescribe and dispense human medical products (a physician, a pharmacist).
By ticking the box >I hereby confirm that I am a health care professional< you have confirmed to be a health care professional and you have understood the definition of a health care professional according to applicable legal regulations.
By clicking „Enter“ you acknowledge that the information on the following pages is intended exclusively for health care professionals and not for lay public, with all risks and consequences arising therefrom for lay public. These risks may result in misinterpretation, misjudgement of your own health condition or incorrect preference of a human medical product. You also acknowledge that you and your doctor decide together whether the treatment with a human medical product subject to prescription is appropriate for you and you should always consult your doctor or pharmacist whether the treatment with a human medical product subject to prescription is appropriate for you.
CARBOCIT
tbl 20×320 mg (blis.PVC/Al)
Pharmacotherapeutic group:
Digestives, adsorbents, acids (ATC code: A07BA51)
Characterisitics
Indications: Carbocit tablets are intended for the treatment of adult and adolescent population and children from 3 years of age. Without consulting a doctor, adults and adolescents can use the medicinal product on a short-term basis (maximum 2 days) in acute diarrhoea caused by food poisoning, in mild viral and bacterial intestinal infections, and irritable bowel syndrome. Children under 3 years of age should only use the product based upon doctor’s recommendation. The same applies for adults suffering from ulcerative colitis, gastritis and excessive food degradation in the bowel as well as diarrhoea associated with a variety of underlying conditions (such as diabetes); they should only use the product as recommended by their physician.
Method of administration
The usual dose is 2-4 tablets 3-4 times daily (a single dose of 4-5 tablets can be given in diarrhoea). Tablets should be swallowed whole with a small amount of water (a suspension should be made by disintegrating tablets in a small amount of water or unsweetened tea for children). The drug is not subject to medical prescription.
For details click here
tablet
(Carbo activatus, Bismuthi subgallas, Acidum citricum monohydricum)
WHAT CARBOCIT IS AND WHAT IT IS USED FOR?
Carbocit belongs to the group of drugs containing activated charcoal that absorbs gases and toxic substances from the digestive tract. The bismuth compound has a local disinfectant and astringent effect in the digestive tract. Citric acid replaces proton deficiency resulting from insufficient excretion through gastric mucosa.
Carbocit is intended for the treatment of adults, adolescents and children from 3 yearso of age. Without consulting a doctor, adults and adolescents can use the medicinal product on a short-term basis (maximum 2 days) in acute diarrhoea caused by food poisoning, in mild viral and bacterial intestinal infections, and irritable bowel syndrome.
The drug is not intended for children under 3 years of age. Children from 3 years of age should only use the product based upon doctor’s recommendation.
Adults suffering from ulcerative colitis, gastritis and excessive food degradation in the bowel as well as diarrhoea associated with a variety of underlying conditions (such as diabetes) should only use the product as recommended by their physician.
For details click here.
The content of this site is intended for health care professionals only. A health care professional is a person authorised to prescribe and dispense human medical products (a physician, a pharmacist).
By ticking the box >I hereby confirm that I am a health care professional< you have confirmed to be a health care professional and you have understood the definition of a health care professional according to applicable legal regulations.
By clicking „Enter“ you acknowledge that the information on the following pages is intended exclusively for health care professionals and not for lay public, with all risks and consequences arising therefrom for lay public. These risks may result in misinterpretation, misjudgement of your own health condition or incorrect preference of a human medical product. You also acknowledge that you and your doctor decide together whether the treatment with a human medical product subject to prescription is appropriate for you and you should always consult your doctor or pharmacist whether the treatment with a human medical product subject to prescription is appropriate for you.
Human Albumin Grifols® 20%*
Pharmacotherapeutic group:
Blood substitutes and plasma proteins, albumin (ATC code: B05AA01)
Characteristics
Human Albumin Grifols 20% is a solution that contains 200 g/l of protein of which at least 95% is human albumin (*donors from the Slovak Republic). It is indicated for the restoration and maintainance of circulating blood volume where volume deficiency has been demonstrated and the use of colloid is appropriate. The choice of albumin rather than an artificial colloid will depend on the clinical situation of the individual patient, based on official recommendation.
For more blood derivatives imported by Imuna Pharm a.s. to Slovakia in cooperation with Grifols click here (http://www.grifols.com/en/web/slovakia/products_and_services)
Pharmacotherapeutic group:
Blood substitutes, plasma proteins, albumin.
Charakteristika
Human Albumin Grifols 20% is a solution for intravenous administration. The solution contains proteins isolated from human blood plasma (the liquid part of blood). The content of plasma proteins is 200 g per 1 litre in each vial of which at least 95% is human albumin.
This product belongs to the group of medicines called blood substitutes and plasma protein fractions.
For more blood derivatives imported by Imuna Pharm a.s. to Slovakia in cooperation with Grifols click here (http://www.grifols.com/en/web/slovakia/products_and_services)
The content of this site is intended for health care professionals only. A health care professional is a person authorised to prescribe and dispense human medical products (a physician, a pharmacist).
By ticking the box >I hereby confirm that I am a health care professional< you have confirmed to be a health care professional and you have understood the definition of a health care professional according to applicable legal regulations.
By clicking „Enter“ you acknowledge that the information on the following pages is intended exclusively for health care professionals and not for lay public, with all risks and consequences arising therefrom for lay public. These risks may result in misinterpretation, misjudgement of your own health condition or incorrect preference of a human medical product. You also acknowledge that you and your doctor decide together whether the treatment with a human medical product subject to prescription is appropriate for you and you should always consult your doctor or pharmacist whether the treatment with a human medical product subject to prescription is appropriate for you.
Human Albumin Grifols® 5%*
Pharmacotherapeutic group:
Blood substitutes and plasma proteins, albumin (ATC code: B05AA01)
Characteristics
Human Albumin Grifols 5% is a solution that contains 50 g/l of protein of which at least 95% is human albumin (*donors from the Slovak Republic). It is indicated for the restoration and maintainance of circulating blood volume where volume deficiency has been demonstrated and the use of colloid is appropriate. The choice of albumin rather than an artificial colloid will depend on the clinical situation of the individual patient, based on official recommendation.
For more blood derivatives imported by Imuna Pharm a.s. to Slovakia in cooperation with Grifols click here(http://www.grifols.com/en/web/slovakia/products_and_services)
Pharmacotherapeutic group:
Blood substitutes, plasma proteins, albumin.
Charakteristika
Human Albumin Grifols 5% is a solution for intravenous administration. The solution contains proteins isolated from human blood plasma (the liquid part of blood). The content of plasma proteins is 50 g per 1 litre in each vial of which at least 95% is human albumin.
This product belongs to the group of medicines called blood substitutes and plasma protein fractions.
For more blood derivatives imported by Imuna Pharm a.s. to Slovakia in cooperation with Grifols click here(http://www.grifols.com/en/web/slovakia/products_and_services)
The content of this site is intended for health care professionals only. A health care professional is a person authorised to prescribe and dispense human medical products (a physician, a pharmacist).
By ticking the box >I hereby confirm that I am a health care professional< you have confirmed to be a health care professional and you have understood the definition of a health care professional according to applicable legal regulations.
By clicking „Enter“ you acknowledge that the information on the following pages is intended exclusively for health care professionals and not for lay public, with all risks and consequences arising therefrom for lay public. These risks may result in misinterpretation, misjudgement of your own health condition or incorrect preference of a human medical product. You also acknowledge that you and your doctor decide together whether the treatment with a human medical product subject to prescription is appropriate for you and you should always consult your doctor or pharmacist whether the treatment with a human medical product subject to prescription is appropriate for you.
Fanhdi®
Pharmacotherapeutic group:
Antihaemorrhagic agent: blood coagulation factors, von Willebrand factor and coagulation factor VIII in combination. (ATC code: B02BD06)
Characteristics
Fanhdi® is a complex of human coagulation factor VIII and von Willebrand factor (*donors from the Slovak Republic). Fanhdi is indicated for the treatment and prophylaxis of bleeding in patients with haemophilia A (congenital factor VIII deficiency), for the prevention and treatment of bleeding in patients with von Willebrand disease (VWD) if treatment with desmopressin (DDAVP) is insufficient or contraindicated. This drug can be used for the treatment of acquired factor VIII deficiency.
For more blood derivatives imported by Imuna Pharm a.s. to Slovakia in cooperation with Grifols click here(http://www.grifols.com/en/web/slovakia/products_and_services)
Pharmacotherapeutic group:
Antihaemorrhagic agent: blood coagulation factor VIII: von Willebrand factor and blood coagulation factor VIII in combination.
Characteristics
Fanhdi® is a complex of human coagulation factor VIII and von Willebrand factor (*donors from the Slovak Republic). Fanhdi is indicated for the treatment and prophylaxis of bleeding in patients with haemophilia A (congenital factor VIII deficiency). Fanhdi is indicated for the treatment and prevention of bleeding in patients with von Willebrand disease (VWD), if treatment with desmopressin (DDAVP) is insufficient or contraindicated. This drug can be used for the treatment of acquired factor VIII deficiency.
