Summary of medicine characteristics - ZICLASEG 30 MG PROLONGED-RELEASE TABLETS
1 NAME OF THE MEDICINAL PRODUCT
Ziclaseg 30mg prolonged-release tablets.
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each tablet contains 30mg gliclazide.
For a full list of excipients, see section 6.1.
3 PHARMACEUTICAL FORM
Prolonged-release tablet.
White to off-white capsule shaped, biconvex tablet debossed with “30” on one side, and plain on the other side.
4 CLINICAL PARTICULARS
4.1 Therapeutic indications
Non insulin-dependent diabetes (type 2) in adults when dietary measures, physical exercise and weight loss alone are not sufficient to control blood glucose.
4.2 Posology and method of administration
Posology
Adults:
The daily dose may vary from 1 to 4 tablets per day i.e 30 – 120mg taken orally in a single intake at breakfast time.
It is recommended that the tablet(s) are swallowed whole without chewing.
If a dose is forgotten, there must be no increase in the dose taken the next day.
As with any hypoglycaemic agent, the dose should be adjusted according to the individual patients metabolic response (blood glucose, HbAlc).
Initial Dose:
The recommended starting dose is 30mg daily.
If blood glucose is effectively controlled, this dose may be used for maintenance treatment.
If blood glucose is not adequately controlled, the dose may be increase to 60, 90 or 120mg daily, in successive steps. The interval between each dose increment should be at least 1 month except in patients whose blood glucose has not reduced after two weeks of treatment. In such cases, the dose may be increased at the end of the second week of treatment.
The maximum recommended daily dose is 120mg.
Switching from Gliclazide 80mg tablets to Ziclaseg 30mg prolonged release tablets: 1 tablet of Gliclazide 80mg is comparable to 1 tablet of Ziclaseg 30mg prolonged release tablets. Consequently the switch can be performed provided a careful blood monitoring.
Switching from another oral antidiabetic agent to Ziclaseg 30mg prolonged release tablets:
Ziclaseg 30mg prolonged release tablets can be used to replace other oral antidiabetic agents.
The dosage and the half-life of the previous antidiabetic agent should be taken into account when switching to Ziclaseg 30mg prolonged release tablets.
A transitional period is not generally necessary. A starting dose of 30mg should be used and this should be adjusted to suit the patient’s blood glucose response, as described above.
When switching from a hypoglycaemic sulphonylurea with a prolonged half-life, a treatment free period of a few days may be necessary to avoid an additive effect of the two products, which might cause hypoglycaemia. The procedure described for initiating treatment should also be used when switching to treatment with Ziclaseg 30mg prolonged release tablets i.e a starting dose of 30mg/day followed by a step wise increase in dose, depending on the metabolic response.
Combination treatment with other antidiabetic agents:
Ziclaseg 30mg prolonged release tablets can be given in combination with biguanides, alpha glucosidase inhibitors or insulin.
In patients not adequately controlled with Ziclaseg 30mg prolonged release tablets, concomitant insulin therapy can be initiated under close medical supervision.
Special Populations
Elderly (over 65):
Ziclaseg 30mg prolonged release tablets should be prescribed using the same dosing regimen recommended for patients under 65 years of age.
In patients with renal impairment:
In patients with mild to moderate renal insufficiency the same dosing regimen can be used as in patients with normal renal function with careful patient monitoring. These data have been confirmed in clinical trials.
In patients at risk of hypoglycaemia:
undernourished or malnourished
severe or poorly compensated endocrine disorders (hypopituitarism, hypothyroidism, adrenocorticotrophic insufficiency)
withdrawal of prolonged and/or high dose corticosteroid therapy
severe vascular disease (severe coronary heart disease, severe carotid impairment, diffuse vascular disease)
It is recommended that the minimum daily starting dose of 30mg is used.
Paediatric Population
The safety and efficacy of Ziclaseg 30 mg prolonged release tablets in children and adolescents have not been established. No data are available.
4.3 Contraindications
The use of Ziclaseg is contraindicated in patients with:
Hypersensitivity to gliclazide or to any of the excipients listed in section 6.1, other sulphonyureas or sulphonamides.
Type 1 diabetes
Diabetic pre-coma and coma, diabetic keto-acidosis
Severe renal or hepatic insufficiency – in these cases the use of insulin is recommended.
Treatment with miconazole (see section 4.5)
Lactation (see section 4.6)
4.4 Special warnings and precautions for use
Hypoglycaemia:
This treatment should be prescribed only if the patient is likely to have a regular food intake (including breakfast). It is important to have a regular carbohydrate intake due to the increased risk of hypoglycaemia if a meal is taken late, if an inadequate amount of food is consumed or if the food is low in carbohydrate. Hypoglycaemia is more likely to occur during low-calorie diets, following prolonged or strenuous exercise, alcohol intake or if a combination of hypoglycaemic agents is being used.
Hypoglycaemia may occur following administration of sulphonylureas (see Section 4.8). Some cases may be severe and prolonged. Hospitalisation may be necessary and glucose administration may need to be continued for several days.
Careful selection of patients, of the dose used, and clear patient directions are necessary to reduce the risk of hypoglycaemic episodes.
Factors which increase the risk of hypoglycaemia:
Patient refuses or (particularly in elderly subjects) is unable to co-operate
Malnutrition, irregular mealtimes, skipping meals, periods of fasting or dietary
changes.
Imbalance between physical exercise and carbohydrate intake
Renal insufficiency
Severe hepatic insufficiency
Overdose of Gliclazide 30mg prolonged release tablets
Certain endocrine disorders – thyroid disorders, hypopituitarism and adrenal
insufficiency.
Concomitant administration of certain other medicines (See section 4.5)
Renal and hepatic insufficiency:
The pharmacokinetics and/or pharmacodynamics of gliclazide may be altered in patients with hepatic insufficiency or severe renal failure. A hypoglycaemic episode occurring in these patients may be prolonged, so appropriate management should be initiated.
Patient information:
The risks of hypoglycaemia, together with its symptoms (see section 4.8), treatment, and conditions that predispose to its development, should be explained to the patient and to family members.
The patient should be informed of the importance of following dietary advice, of taking regular exercise, and of regular monitoring of blood glucose levels.
Poor blood glucose control:
Blood glucose control in a patient receiving antidiabetic treatment may be affected by any of the following: St. John’s Wort (Hypercium perforatum) preparations (see section 4.5), fever, trauma, infection or surgical intervention. In some cases, it may be necessary to administer insulin.
The hypoglycaemic efficacy of any oral antidiabetic agent, including gliclazide, is attenuated over time in many patients: this may be due to progression in the severity of the diabetes, or to a reduced response to treatment. This phenomenon is known as secondary failure which is distinct from primary failure, when an active substance is ineffective as first-line treatment. Adequate dose adjustment and dietary compliance should be considered before classifying the patient as secondary failure.
Dysglycaemia:
Disturbances in blood glucose, including hypoglycaemia and hyperglycaemia have been reported, in diabetic patients receiving concomitant treatment with fluoroquinolones, especially in elderly 5
patients. Indeed, careful monitoring of blood glucose is recommended in all patients receiving at the same time Gliclazide 30mg prolonged release tablets and a fluoroquinolone.
Laboratory tests: Measurement of glycated haemoglobin levels (or fasting venous plasma glucose) is recommended in assessing blood glucose control. Blood glucose self-monitoring may also be useful.
Haematological Effects:
Treatment of patients with G6PD-deficiency with sulphonylurea agents can lead to haemolytic anaemia. Since gliclazide belongs to the chemical class of sulphonylurea drugs, caution should be used in patients with G6PD-deficiency and a non-sulphonylurea alternative should be considered
4.5 Interaction with other medicinal products and other forms of interaction
The following products are likely to increase the risk of hypoglycaemia
Contra-indicated combination
Miconazole (systemic route, oromucosal gel): increases the hypoglycaemic effect
with possible onset of hypoglycaemic symptoms, or even coma.
Combinations which are not recommended
Phenylbutazone (systemic route): increases the hypoglycaemic effect of
sulphonylureas (displaces their binding to plasma proteins and/or reduces their elimination).
It is preferable to use a different anti-inflammatory agent, or else to warn the patient and emphasise the importance of self-monitoring. Where necessary, adjust the dose during and after treatment with the anti-inflammatory agent.
Alcohol: increases the hypoglycaemic reaction (by inhibiting compensatory
reactions) that can lead to the onset of hypoglycaemic coma.
Avoid alcohol or medicines containing alcohol.
Combinations requiring precautions for use
Potentiation of the blood glucose lowering effect and thus, in some instances, hypoglycaemia may occur when one of the following drugs is taken:
Other antidiabetic agents (insulins, acarbose, metformin, thiazolidinediones, dipeptidyl peptidase-4 inhibitors, GLP-1 receptor agonists), beta-blockers, fluconazole, angiotensin converting enzyme inhibitors (captopril, enalapril), H2-receptor antagonists, MAOIs, sulfonamides, clarithromycin and nonsteroidal anti-inflammatory agents.
The following products may cause an increase in blood glucose levels
Combination which is not recommended
Danazol: diabetogenic effect of danazol.
If the use of this active substance cannot be avoided, warn the patient and emphasise the importance of urine and blood glucose monitoring. It may be necessary to adjust the dose of the antidiabetic agent during and after treatment with danazol.
Combinations requiring precautions during use
Chlorpromazine (neuroleptic agent): high doses (>100 mg per day of
chlorpromazine) increase blood glucose levels (reduced insulin release).
6
Warn the patient and emphasise the importance of blood glucose monitoring. It may be necessary to adjust the dose of the antidiabetic active substance during and after treatment with the neuroleptic agent.
Glucocorticoids (systemic and local route: intra-articular, cutaneous and rectal
preparations) and tetracosactrin: increase in blood glucose levels with possible ketosis (reduced tolerance to carbohydrates due to glucocorticoids).
Warn the patient and emphasise the importance of blood glucose monitoring, particularly at the start of treatment. It may be necessary to adjust the dose of the antidiabetic active substance during and after treatment with glucocorticoids.
Ritodrine, salbutamol, terbutaline: (all intravenously): Increased blood glucose
levels due to beta-2 agonist effects.
Emphasise the importance of monitoring blood glucose levels. If necessary, switch to insulin.
Saint John’s Wort (Hypericum perforatum) preparations:
Gliclazide exposure is decreased by Saint John’s Wort-Hypericum perforatum. Emphasize the importance of blood glucose levels monitoring.
The following products may cause dysglycaemia
Combinations requiring precautions during use
Fluoroquinolones: in case of a concomitant use of Gliclazide 30mg prolonged
release tablets and a fluoroquinolone, the patient should be warned of the risk of dysglycaemia, and the importance of blood glucose monitoring should be emphasized.
Combination which must be taken into account
Anticoagulant therapy (Warfarin): Sulphonylureas may lead to potentiation of
anticoagulation during concurrent treatment.
Adjustment of the anticoagulant may be necessary.
4.6 Fertility, pregnancy and lactation
Pregnancy
There is no experience with the use of gliclazide during pregnancy in humans, even though there are few data with other sulphonylureas.
In animal studies, gliclazide is not teratogenic.
Control of diabetes should be obtained before the time of conception to reduce the risk of congenital abnormalities linked to uncontrolled diabetes.
Oral hypoglycaemic agents are not suitable, insulin is the drug of first choice for treatment of diabetes during pregnancy. It is recommended that oral hypoglycaemic therapy is changed to insulin before a pregnancy is attempted, or as soon as pregnancy is discovered.
Breast-feeding
It is not known whether gliclazide or its metabolites are excreted in breast milk. Given the risk of neonatal hypoglycaemia, the product is contra-indicated in breast-feeding mothers.
4.7 Effects on ability to drive and use machines
Ziclaseg 30 mg prolonged release tablet has no known influence on the ability to drive and use machines.
However, patients should be made aware of the symptoms of hypoglycaemia and should be careful if driving or operating machinery, especially at the beginning of treatment.
4.8 Undesirable effects
Based on the experience with gliclazide, the following undesirable effects have been reported.
Hypoglycaemia
As for other sulfonylureas, treatment with Gliclazide 30mg prolonged release tablets can cause hypoglycaemia, if mealtimes are irregular and, in particular, if meals are skipped. Possible symptoms of hypoglycaemia are: headache, intense hunger, nausea, vomiting, lassitude, sleep disorders, agitation, aggression, poor concentration, reduced awareness and slowed reactions, depression, confusion, visual and speech disorders, aphasia, tremor, paresis, sensory disorders, dizziness, feeling of powerlessness, loss of self-control, delirium, convulsions, shallow respiration, bradycardia, drowsiness and loss of consciousness, possibly resulting in coma and lethal outcome.
In addition, signs of adrenergic counter-regulation may be observed: sweating, clammy skin, anxiety, tachycardia, hypertension, palpitations, angina pectoris and cardiac arrhythmia. Usually, symptoms disappear after intake of carbohydrates (sugar). However, artificial sweeteners have no effect. Experience with other sulfonylureas shows that hypoglycaemia can recur even when measures prove effective initially.
If a hypoglycaemic episode is severe or prolonged, and even if it is temporarily controlled by intake of sugar, immediate medical treatment or even hospitalisation are required. Gastrointestinal disturbances, including abdominal pain, nausea, vomiting dyspepsia, diarrhoea, and constipation have been reported: if these should occur they can be avoided or minimised if gliclazide is taken with breakfast.
The following undesirable effects have been more rarely reported:
Skin and subcutaneous tissue disorders: rash, pruritus, urticaria, angioedema,
erythema, maculopapular rashes, bullous reactions (such as Stevens-Johnson syndrome and toxic epidermal necrolysis)
Blood and lymphatic system disorders: Changes in haematology are rare. They may
include anaemia, leucopenia, thrombocytopenia, granulocytopenia. These are in general reversible upon discontinuation of medication.
Hepato-biliary disorders: raised hepatic enzyme levels (AST, ALT, alkaline
phosphatase), hepatitis (isolated reports). Discontinue treatment if cholestatic jaundice appears. These symptoms usually disappear after discontinuation of treatment.
Eye disorders
Transient visual disturbances may occur especially on initiation of treatment, due to changes in blood glucose levels.
Class attribution effects:
As for other sulfonylureas, the following adverse events have been observed: 8 cases of erythrocytopenia, agranulocytosis, haemolytic anaemia, pancytopenia, allergic vasculitis, hyponatremia, elevated liver enzyme levels and even impairment of liver function (e.g. with cholestasis and jaundice) and hepatitis which regressed after withdrawal of the sulfonylurea or led to life-threatening liver failure in isolated cases.
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 the Yellow Card Scheme Website: www.mhra.gov.uk/yellowcard.
4.9 Overdose
6 PHARMACEUTICAL PARTICULARS
6.1 List of excipients
Ziclaseg 30mg film coated tablets also contains:
Calcium hydrogen phosphate dihydrate, Povidone K30, Hypromellose and Magnesium stearate.
6.2 Incompatibilities
Not applicable.
6.3 Shelf life
2 years.
6.4 Special precautions for storage
Do not store above 25oC.
6.5 Nature and contents of container
Ziclaseg 30mg prolonged release tablets are packaged in clear PVC/aluminium blisters or clear PVC/Aclar foil blisters placed into cardboard boxes containing 10, 20, 28, 30, 56, 60, 90 and 120 tablets.
Not all pack sizes may be marketed.
6.6 Special precautions for disposal
6.6 Special precautions for disposalNo special requirements.
7 MARKETING AUTHORISATION HOLDER
Lupin Healthcare (UK) Limited
The Urban Building, 2nd floor
3–9 Albert Street, Slough, Berkshire
SL1 2BE, United Kingdom
8 MARKETING AUTHORISATION NUMBER(S)
PL 35507/0084
9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
19/01/2012