- Approval Id
- 5e4f173d8fb8d9b5
- Drug Approval Emc Name
- Eudemine 50mg Tablets
- Drug Name
- Eudemine 50mg Tablets
- Company Name
- RPH Pharmaceuticals AB
- Company Address
- Box 603, 101 32 Stockholm, Sweden
- Company Website
- //www.recipharm.com
- Company Telephone
- +44 (0)845 023 0467
- Company Medical Info Direct Line
- +44 207 862 1716
- Company Medical Info Email
- safety@elc-group.com
- Company Customer Care Direct Line
- +44(0)845 023 0467
- Company Stock Availability
- +44(0)845 023 0467
- Atc Code
- V03AH01
- Legal Category
- Prescription only medicine
- Authorisation Holder
- RPH Pharmaceuticals AB
Box 603
101 32 Stockholm
Sweden
- Authorisation Number
- PL 36301/0021
- Authorisation Date
- 17 December 1992 / 17 December 1997
- Instruction Authorisation Holder
- RPH Pharmaceuticals AB
Box 603
101 32 Stockholm
Sweden
- Instruction Authorisation Number
- PL 36301/0021
- Instruction Authorisation Date
- 17 December 1992 / 17 December 1997
- Instruction Composition
- Each tablet contains 50mg diazoxide
\*\*Excipient (s) with known effect\*\*
Each tablet contains 37.0 mg lactose monohydrate and 46.640 mg sucrose
For full list of excipients, see section 6.1
- Instruction Dosage Form
- White to off white, round, biconvex, sugar coated tablet.
- Instruction Clinical Particulars
- 4.1 Therapeutic indications
Eudemine tablets are used in the treatment of intractable hypoglycaemia.
Diazoxide also causes salt and water retention.
\*\*Hypoglycaemia\*\*: Diaoxide administered orally is indicated for the treatment of intractable hypoglycaemia with severe symptoms from a variety of causes including: idiopathic hypoglycaemia in infancy, leucine-sensitive or unclassified; functional islet cell tumours both malignant and benign if inoperable, extra-pancreatic neoplasms producing hypoglycaemia; glycogen storage disease; hypoglycaemia of unknown origin.4.2 Posology and method of administration
\*\*Posology\*\*
Hypoglycaemia:
In hypoglycaemia, the dosage schedule of Eudemine tablets is determined according to the clinical needs and the response of the individual patient. For both adults and children a starting oral dose of 5mg/kg body weight divided into 2 or 3 equal doses per 24 hours will establish the patient's response and thereafter the dose can be increased until the symptoms and blood glucose level respond satisfactorily. Regular determinations of the blood glucose in the initial days of treatment are essential. The usual maintenance dose is 3 - 8mg/kg/day given in two or three divided doses.
In adults with benign or malignant islet-cell tumours producing large quantities of insulin, high dosages of up to 1,000mg per day have been used.
In children with leucine-sensitive hypoglycaemia, a dosage range of 15- 20mg/kg/day is suggested.
\*Renal impairment\*
Reduced doses may be required in patients with impaired renal function.
\*\*Method of administration\*\*
Oral use4.3 Contraindications
Hypersensitivity to the active substance, other thiazides, or to any of the excipients listed in section 6.1
In the treatment of hypoglycaemia, Eudemine is contraindicated in all cases which are amenable to surgery or other specific therapy.4.4 Special warnings and precautions for use
In the treatment of hypoglycaemia it is necessary that the blood pressure be monitored regularly.
Retention of sodium and water is likely to necessitate therapy with an oral diuretic such as frusemide or ethacrynic acid. The dosage of either of the diuretics mentioned may be up to 1g daily. It must be appreciated that if diuretics are employed then both the hypotensive and hyperglycaemic activities of diazoxide will be potentiated and it is likely that the dosage of diazoxide will require adjustment downwards. In patients with severe renal failure it is desirable to maintain, with diuretic therapy, urinary volumes in excess of 1 litre daily. Hypokalaemia should be avoided by adequate potassium replacement.
Diazoxide should be used with caution in patients with cardiac failure or impaired cardiac reserve in whom sodium and water retention may worsen or precipitate congestive heart failure. A direct effect on myocardium and cardiac function cannot be excluded.
Diazoxide should be used with care in patients with impaired cardiac or cerebral circulation and in patients with aortic coarctation, aortic stenosis, arteriovenous shunt, heart failure or other cardiovascular disorders in which an increase in cardiac output could be detrimental.
Diazoxide should be administered with caution to patients with hyperuricaemia or a history of gout, and it is advisable to monitor serum uric acid concentration.
Whenever Eudemine is given over a prolonged period regular haematological examinations are indicated to exclude changes in white blood cell and platelet counts.
Also in children there should be regular assessment of growth, bone and psychological maturation.
The very rapid, almost complete protein binding of diazoxide requires cautious dosage to be used in patients whose plasma proteins may be lower than normal.
This medicinal product contains lactose and sucrose. Patients with rare hereditary problems of galactose intolerance, fructose intolerance total lactase deficiency, sucrase-isomaltase insufficiency or glucose-galactose malabsorption should not take this medicine.4.5 Interaction with other medicinal products and other forms of interaction
Drugs potentiated by diazoxide therapy include: oral diuretics, antihypertensive agents and anticoagulants.
Phenytoin levels should be monitored as increased dosage may be needed if administered concurrently with diazoxide.
The risk of hyperglycaemia may be increased by concurrent administration of corticosteroids or oestrogen-progestogen combinations.4.6 Pregnancy and lactation
\*\*Pregnancy\*\*
Eudemine tablets are only to be used in pregnant women when the indicated condition is deemed to put the mother's life at risk.
Prolonged oral therapy with diazoxide during pregnancy has been reported to cause alopecia in the newborn.
\*\*Lactation\*\*
Eudemine tablets should not be given to nursing mothers as the safety of diazoxide during lactation has not been established.4.7 Effects on ability to drive and use machines
None known.4.8 Undesirable effects
With oral therapy, nausea is common in the first two or three weeks and may require relief with an anti-nauseant. Prolonged therapy has given rise to reports of hypertrichosis lanuginosa, anorexia and hyperuricaemia.
Extra-pyramidal side-effects have been reported with oral diazoxide. It was found that extra-pyramidal effects such as parkinsonian tremor, cogwheel rigidity and oculogyric crisis could be easily suppressed by intravenous injection of an antiparkinsonian drug such as procyclidine and that they could be prevented by maintenance therapy with such a drug given orally.
Other adverse effects of Eudemine tablets which have been reported are listed below.
\*\*Blood and lymphatic system disorders\*\*
Leucopenia, thrombocytopenia, decreased haemoglobin and / or haematocrit, eosinophilia, bleeding
\*\*Immune system disorders\*\*
Hypogammaglobulinaemia, hypersensitivity reactions such as rash, fever and leucopenia, decreased immunoglobulins (IgG) in infants,
\*\*Endocrine disorder\*\*
Hirsutism, galactorrhoea, pancreatitis, increased serum androgens
\*\*Metabolism and nutrition disorders\*\*
Hyperuricaemia (after prolonged therapy), hyperosmolar non-ketotic coma, inappropriate hyperglycaemia including ketoacidosis
\*\*Psychiatric disorders\*\*
Anorexia (after prolonged therapy), decreased libido
\*\*Nervous system disorders\*\*
Extra-pyramidal side-effects such as parkinsonian tremor, cogwheel rigidity and oculogyric crisis, headache, dizziness
\*\*Eye disorders\*\*
Blurred vision, transient cataracts, subconjunctival haemorrhage, ring scotoma, diplopia, lacrimation.
\*\*Ear and labyrinth disorders\*\*
Tinnitus
\*\*Cardiac disorders\*\*
Cardiomegaly, cardiac failure, arrhythmias
\*\*Vascular disorders\*\*
Inappropriate hypotension
\*\*Respiratory, thoracic and mediastinal disorders\*\*
Dysponea, pulmonary hypertension
\*\*Gastrointestinal disorders\*\*
Nausea, vomiting, abdominal pain, diarrhoea, ileus, constipation, dysgeusia
\*\*Hepatobiliary disorders\*\*
Increased AST and alkaline phosphate
\*\*Skin and subcutaneous tissue disorders\*\*
Pruritis, dermatitis, lichenoid eruption
\*\*Musculoskeletal and connective tissue disorders\*\*
Musculoskeletal pain
\*\*Renal and urinary disorders\*\*
Azotemia, decreased creatinine clearance, reversible nephritic syndrome, haematuria and albuminuria.
\*\*Congenital, familial and genetic disorders\*\*
Hypertrichosis lanuginose (after prolonged therapy)
\*\*General disorders and administration site disorders\*\*
Voice changes and abnormal faces in children (on long term therapy), sodium retention, fluids retention.
\*\*\*\*Reporting of suspected adverse reactions\*\*\*\*
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via Yellow Card Scheme on the MHRA website (www.mhra.gov.uk/yellowcard) or search for MHRA yellow card in the Google Play or Apple app store.4.9 Overdose
Excessive dosage of diazoxide can result in hyperglycaemia. Severe hyperglycaemia may be corrected by giving insulin and less severe hyperglycaemia may respond to oral hypoglycaemics. Hypotension may be managed with intravenous fluids and in severe cases may require sympathomimetics.
- Instruction Pharmacology
- 5.1 Pharmacodynamic properties
Pharmacotherapeutic group: Drug for the treatment of hypoglycaemia. ATC Code: V03AH01.5.2 Pharmacokinetic properties
None stated.5.3 Preclinical safety data
None stated.
- Instruction Pharmaceutical Particulars
- 6.1 List of excipients
The tablet core consists of:
Lactose
Maize starch
Maize starch, pre-gelatinised
Magnesium stearate
Purified water
The tablet coating consists of:
Sugar (mineral water grade)
Gelatin coarse powder 200 bloom
Purified water
Opaglos AG-7350
Opaglos AG-7350 consists of:
Purified water
Carnauba wax (E903)
Beeswax, white (E901)
Polysorbate 20 (E432)
Sorbic acid (E200)6.2 Incompatibilities
Not applicable6.3 Shelf life
24 months6.4 Special precautions for storage
Store below 25°C6.5 Nature and contents of container
Plastic containers with tamper evident closure containing 100 tablets.6.6 Special precautions for disposal and other handling
No special requirements
Any unused medicinal product or waste material should be disposed of in accordance with local requirements.
- Instruction Content
- ## Composition
Each tablet contains 50mg diazoxide
\*\*Excipient (s) with known effect\*\*
Each tablet contains 37.0 mg lactose monohydrate and 46.640 mg sucrose
For full list of excipients, see section 6.1
## Pharmaceutical Form
White to off white, round, biconvex, sugar coated tablet.
## Clinical Particulars
4.1 Therapeutic indications
Eudemine tablets are used in the treatment of intractable hypoglycaemia.
Diazoxide also causes salt and water retention.
\*\*Hypoglycaemia\*\*: Diaoxide administered orally is indicated for the treatment of intractable hypoglycaemia with severe symptoms from a variety of causes including: idiopathic hypoglycaemia in infancy, leucine-sensitive or unclassified; functional islet cell tumours both malignant and benign if inoperable, extra-pancreatic neoplasms producing hypoglycaemia; glycogen storage disease; hypoglycaemia of unknown origin.4.2 Posology and method of administration
\*\*Posology\*\*
Hypoglycaemia:
In hypoglycaemia, the dosage schedule of Eudemine tablets is determined according to the clinical needs and the response of the individual patient. For both adults and children a starting oral dose of 5mg/kg body weight divided into 2 or 3 equal doses per 24 hours will establish the patient's response and thereafter the dose can be increased until the symptoms and blood glucose level respond satisfactorily. Regular determinations of the blood glucose in the initial days of treatment are essential. The usual maintenance dose is 3 - 8mg/kg/day given in two or three divided doses.
In adults with benign or malignant islet-cell tumours producing large quantities of insulin, high dosages of up to 1,000mg per day have been used.
In children with leucine-sensitive hypoglycaemia, a dosage range of 15- 20mg/kg/day is suggested.
\*Renal impairment\*
Reduced doses may be required in patients with impaired renal function.
\*\*Method of administration\*\*
Oral use4.3 Contraindications
Hypersensitivity to the active substance, other thiazides, or to any of the excipients listed in section 6.1
In the treatment of hypoglycaemia, Eudemine is contraindicated in all cases which are amenable to surgery or other specific therapy.4.4 Special warnings and precautions for use
In the treatment of hypoglycaemia it is necessary that the blood pressure be monitored regularly.
Retention of sodium and water is likely to necessitate therapy with an oral diuretic such as frusemide or ethacrynic acid. The dosage of either of the diuretics mentioned may be up to 1g daily. It must be appreciated that if diuretics are employed then both the hypotensive and hyperglycaemic activities of diazoxide will be potentiated and it is likely that the dosage of diazoxide will require adjustment downwards. In patients with severe renal failure it is desirable to maintain, with diuretic therapy, urinary volumes in excess of 1 litre daily. Hypokalaemia should be avoided by adequate potassium replacement.
Diazoxide should be used with caution in patients with cardiac failure or impaired cardiac reserve in whom sodium and water retention may worsen or precipitate congestive heart failure. A direct effect on myocardium and cardiac function cannot be excluded.
Diazoxide should be used with care in patients with impaired cardiac or cerebral circulation and in patients with aortic coarctation, aortic stenosis, arteriovenous shunt, heart failure or other cardiovascular disorders in which an increase in cardiac output could be detrimental.
Diazoxide should be administered with caution to patients with hyperuricaemia or a history of gout, and it is advisable to monitor serum uric acid concentration.
Whenever Eudemine is given over a prolonged period regular haematological examinations are indicated to exclude changes in white blood cell and platelet counts.
Also in children there should be regular assessment of growth, bone and psychological maturation.
The very rapid, almost complete protein binding of diazoxide requires cautious dosage to be used in patients whose plasma proteins may be lower than normal.
This medicinal product contains lactose and sucrose. Patients with rare hereditary problems of galactose intolerance, fructose intolerance total lactase deficiency, sucrase-isomaltase insufficiency or glucose-galactose malabsorption should not take this medicine.4.5 Interaction with other medicinal products and other forms of interaction
Drugs potentiated by diazoxide therapy include: oral diuretics, antihypertensive agents and anticoagulants.
Phenytoin levels should be monitored as increased dosage may be needed if administered concurrently with diazoxide.
The risk of hyperglycaemia may be increased by concurrent administration of corticosteroids or oestrogen-progestogen combinations.4.6 Pregnancy and lactation
\*\*Pregnancy\*\*
Eudemine tablets are only to be used in pregnant women when the indicated condition is deemed to put the mother's life at risk.
Prolonged oral therapy with diazoxide during pregnancy has been reported to cause alopecia in the newborn.
\*\*Lactation\*\*
Eudemine tablets should not be given to nursing mothers as the safety of diazoxide during lactation has not been established.4.7 Effects on ability to drive and use machines
None known.4.8 Undesirable effects
With oral therapy, nausea is common in the first two or three weeks and may require relief with an anti-nauseant. Prolonged therapy has given rise to reports of hypertrichosis lanuginosa, anorexia and hyperuricaemia.
Extra-pyramidal side-effects have been reported with oral diazoxide. It was found that extra-pyramidal effects such as parkinsonian tremor, cogwheel rigidity and oculogyric crisis could be easily suppressed by intravenous injection of an antiparkinsonian drug such as procyclidine and that they could be prevented by maintenance therapy with such a drug given orally.
Other adverse effects of Eudemine tablets which have been reported are listed below.
\*\*Blood and lymphatic system disorders\*\*
Leucopenia, thrombocytopenia, decreased haemoglobin and / or haematocrit, eosinophilia, bleeding
\*\*Immune system disorders\*\*
Hypogammaglobulinaemia, hypersensitivity reactions such as rash, fever and leucopenia, decreased immunoglobulins (IgG) in infants,
\*\*Endocrine disorder\*\*
Hirsutism, galactorrhoea, pancreatitis, increased serum androgens
\*\*Metabolism and nutrition disorders\*\*
Hyperuricaemia (after prolonged therapy), hyperosmolar non-ketotic coma, inappropriate hyperglycaemia including ketoacidosis
\*\*Psychiatric disorders\*\*
Anorexia (after prolonged therapy), decreased libido
\*\*Nervous system disorders\*\*
Extra-pyramidal side-effects such as parkinsonian tremor, cogwheel rigidity and oculogyric crisis, headache, dizziness
\*\*Eye disorders\*\*
Blurred vision, transient cataracts, subconjunctival haemorrhage, ring scotoma, diplopia, lacrimation.
\*\*Ear and labyrinth disorders\*\*
Tinnitus
\*\*Cardiac disorders\*\*
Cardiomegaly, cardiac failure, arrhythmias
\*\*Vascular disorders\*\*
Inappropriate hypotension
\*\*Respiratory, thoracic and mediastinal disorders\*\*
Dysponea, pulmonary hypertension
\*\*Gastrointestinal disorders\*\*
Nausea, vomiting, abdominal pain, diarrhoea, ileus, constipation, dysgeusia
\*\*Hepatobiliary disorders\*\*
Increased AST and alkaline phosphate
\*\*Skin and subcutaneous tissue disorders\*\*
Pruritis, dermatitis, lichenoid eruption
\*\*Musculoskeletal and connective tissue disorders\*\*
Musculoskeletal pain
\*\*Renal and urinary disorders\*\*
Azotemia, decreased creatinine clearance, reversible nephritic syndrome, haematuria and albuminuria.
\*\*Congenital, familial and genetic disorders\*\*
Hypertrichosis lanuginose (after prolonged therapy)
\*\*General disorders and administration site disorders\*\*
Voice changes and abnormal faces in children (on long term therapy), sodium retention, fluids retention.
\*\*\*\*Reporting of suspected adverse reactions\*\*\*\*
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via Yellow Card Scheme on the MHRA website (www.mhra.gov.uk/yellowcard) or search for MHRA yellow card in the Google Play or Apple app store.4.9 Overdose
Excessive dosage of diazoxide can result in hyperglycaemia. Severe hyperglycaemia may be corrected by giving insulin and less severe hyperglycaemia may respond to oral hypoglycaemics. Hypotension may be managed with intravenous fluids and in severe cases may require sympathomimetics.
## Pharmacological Properties
5.1 Pharmacodynamic properties
Pharmacotherapeutic group: Drug for the treatment of hypoglycaemia. ATC Code: V03AH01.5.2 Pharmacokinetic properties
None stated.5.3 Preclinical safety data
None stated.
## Pharmaceutical Particulars
6.1 List of excipients
The tablet core consists of:
Lactose
Maize starch
Maize starch, pre-gelatinised
Magnesium stearate
Purified water
The tablet coating consists of:
Sugar (mineral water grade)
Gelatin coarse powder 200 bloom
Purified water
Opaglos AG-7350
Opaglos AG-7350 consists of:
Purified water
Carnauba wax (E903)
Beeswax, white (E901)
Polysorbate 20 (E432)
Sorbic acid (E200)6.2 Incompatibilities
Not applicable6.3 Shelf life
24 months6.4 Special precautions for storage
Store below 25°C6.5 Nature and contents of container
Plastic containers with tamper evident closure containing 100 tablets.6.6 Special precautions for disposal and other handling
No special requirements
Any unused medicinal product or waste material should be disposed of in accordance with local requirements.
