Tolterodine Tartrate 2mg Film Coated Tablets
Out of date information, search anotherSUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
Tolterodine tartrate 2mg Film-coated Tablets
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each film-coated tablet contains tolterodine tartrate 2 mg corresponding to 1.37 mg tolterodine.
For the full list of excipients, see section 6.1.
3 PHARMACEUTICAL FORM
Film-coated tablets
Tolterodine tartrate 2 mg: White, round, biconvex, 5.5mm film-coated tablets marked with “T2” on one side.
4 CLINICAL PARTICULARS
4.1 Therapeutic indications
Symptomatic treatment of urge incontinence and/or increased urinary frequency and urgency as may occur in patients with overactive bladder syndrome.
4.2 Posology and method of administration Posology
Adults (including elderly):
The recommended dose is 2 mg twice daily except in patients with impaired liver function or severely impaired renal function (GFR<30 ml/min) for whom the recommended dose is 1 mg twice daily (see section 4.4). In case of troublesome side effects the dose may be reduced from 2 mg to 1 mg twice daily.
The effect of treatment should be re-evaluated after 2-3 months (see section 5.1).
Paediatric patients:
Tolterodine is not recommended for use in children due to a lack on insufficient data on efficacy (see section 5.1).
Method of administration:
The tablets are for oral use and should be swallowed whole.
4.3 Contraindications
Tolterodine is contraindicated in patients with
- Urinary retention
- Uncontrolled narrow angle glaucoma
- Myasthenia gravis
- Hypersensitivity to the active substance or to any of the excipients listed in section 6.1
- Severe ulcerative colitis
- Toxic megacolon
4.4 Special warnings and precautions for use
Tolterodine shall be used with caution in patients with
- Significant bladder outlet obstruction at risk of urinary retention
- Gastrointestinal obstructive disorders, e.g. pyloric stenosis
- Renal impairement (see section 4.2)
- Hepatic disease (see section 4.2 and 5.2)
- Autonomic neuropathy
- Hiatus hernia
- Risk for decreased gastrointestinal motility
Multiple oral total daily doses of immediate release 4 mg (therapeutic) and 8 mg (supratherapeutic) tolterodine have been shown to prolong the QTc interval (see section 5.1).
The clinical relevance of these findings is unclear and will depend on individual patient risk factors and susceptibilities present. Tolterodine should be used with caution in patients with risk factors for QT-prolongation including:
- Congenital or documented acquired QT prolongation
- Electrolyte disturbances such as hypokalaemia, hypomagnesaemia and hypocalcaemia
- Bradycardia
- Relevant pre-existing cardiac diseases (i.e. cardiomyopathy, myocardial ischaemia, arrhythmia, congestive heart failure)
- Concomitant administration of drugs known to prolong QT-interval including Class IA (e.g. quinidine, procainamide) and Class III (e.g. amiodarone, sotalol) antiarrhythmics.
This especially holds true when taking potent CYP3A4 inhibitors (see section 5.1). Concomitant treatment with potent CYP3A4 inhibitors should be avoided (see section 4.5).
As with all treatments for symptoms of urgency and urge incontinence, organic reasons for urge and frequency should be considered before treatment.
4.5 Interaction with other medicinal products and other forms of interaction
Concomitant systemic medication with potent CYP3A4 inhibitors such as macrolide antibiotics (e.g. erythromycin and claritromycin), antifungal agents (e.g. ketoconazole and itraconazole) and antiproteases is not recommended due to increased serum concentrations of tolterodine in poor CYP2D6 metabolisers with (subsequent) risk of overdosage (see section 4.4).
Concomitant medication with other drugs that possess antimuscarinic properties may result in more pronounced therapeutic effect and side-effects. Conversely, the therapeutic effect of tolterodine may be reduced by concomitant administration of muscarinic cholinergic receptor agonists.
The effect of prokinetics like metoclopramide and cisapride may be decreased by tolterodine.
Concomitant treatment with fluoxetine (a potent CYP2D6 inhibitor) does not result in a clinically significant interaction since tolterodine and its CYP2D6-dependent metabolite, 5-hydroxymethyl tolterodine are equipotent.
Drug interaction studies have shown no interactions with warfarin or combined oral contraceptives (ethinyl estradiol/levonorgestrel).
A clinical study has indicated that tolterodine is not a metabolic inhibitor of CYP2D6, 2C19, 2C9, 3A4 or 1A2. Therefore an increase of plasma levels of drugs metabolised by these isoenzymes is not expected when dosed in combination with tolterodine.
4.6. Fertility, pregnancy and lactation
Pregnancy
There are no adequate data from the use of tolterodine in pregnant women.
Studies in animals have shown reproductive toxicity (see section 5.3). The potential risk for humans is unknown.
Consequently, tolterodine is not recommended during pregnancy.
Breastfeeding
No data concerning the excretion of tolterodine into human milk are available. Tolterodine should be avoided during lactation.
Fertility
No data from fertility studies are available.
4.7 Effects on ability to drive and use machines
Since this drug may cause accommodation disturbances and influence reaction time, the ability to drive and use machines may be negatively affected.
4.8. Undesirable effects
Due to the pharmacological effect of tolterodine it may cause mild to moderate antimuscarinic effects, like dryness of the mouth, dyspepsia and dry eyes.
Adverse reactions are listed below, by system organ class and by frequency. Frequencies are defined as: very common (>1/10) common (>1/100 to < 1/10), uncommon (>1/1,000 to < 1/100), rare (>1/10,000 to <1/1,000); very rare (< 1/10000) and not known (cannot be estimated from available data).
The table below reflects the data obtained with tolterodine in clinical trials and from post marketing experience. The most commonly reported adverse reaction was dry mouth, which occurred in 23.4 % of patients treated with tolterodine SR and in 7.7 % of placebo-treated patients.
Infections and infestations Common: Bronchitis, sinusitis
Immune system disorders
Uncommon: Hypersensitivity not otherwise specified
Not known: Anaphylactoid reactions
Psychiatric disorders Uncommon: Nervousness
Not known: Confusion, hallucinations, disorientation
Nervous system disorders
Common: Dizziness, somnolence, headaches
Uncommon: Paraesthesia, memory impairment
Eye disorders
Common: Dry eyes, abnormal vision (including abnormal accommodation)
Ear and labyrinth disorders Unommon: Vertigo
Cardiac disorders
Uncommon: Palpitations, cardiac failure, arrhythmia
Not known: Tachycardia,
Vascular disorders Not known: Flushing
Gastrointestinal disorders Very Common: Dry mouth
Common: Dyspepsia, constipation, abdominal pain, flatulence, diarrhoea
Not known: Gastroesophageal reflux, vomiting
Skin and subcutaneous tissue disorders Not known: Angioedema, dry skin
Renal and urinary disorders Common: Dysuria
Uncommon: Urinary retention
General disorders and administration site conditions Common: Fatigue, peripheral oedema
Uncommon: Chest pain,
Investigations
Common: Increased weight
Cases of aggravation of symptoms of dementia (e.g. confusion, disorientation, delusion) have been reported after tolterodine therapy was initiated in patients taking cholinesterase inhibitors for the treatment of dementia.
Paediatric population:
In two paediatric phase III randomised, placebo-controlled, double-blind studies conducted over 12 weeks where a total of 710 paediatric patients were recruited, the proportion of patients with urinary tract infections, diarrhoea and abnormal behaviour was higher in patients treated with tolterodine than placebo (urinary tract infection: tolterodine 6.8 %, placebo 3.6 %; diarrhoea: tolterodine 3.3 %, placebo 0.9 %; abnormal behaviour: tolterodine 1.6 %, placebo 0.4 %) (see section 5.1).
4.9 Overdose
The highest dose given to human volunteers of tolterodine L-tartrate is 12.8 mg as a single dose. The most severe adverse events observed were accommodation disturbances and micturition difficulties.
In the event of tolterodine overdose, treat with gastric lavage and give activated charcoal.
Treat symptoms as follows:
• Severe central anticholinergic effects (e.g. hallucinations, severe excitation): treat with physostigmine
• Convulsions or pronounced excitation: treat with benzodiazepines
• Respiratory insufficiency: treat with artificial respiration
• Tachycardia: treat with beta-blockers
• Urinary retention: treat with catheterization
• Mydriasis: treat with pilocarpine eye drops and/or place patient in dark room
An increase in QT interval was observed at a total daily dose of 8 mg immediate release tolterodine (twice the recommended daily dose of the immediate release formulation and equivalent to three times the peak exposure of the prolonged release capsule formulation) administered over four days. In the event of tolterodine overdose, standard supportive measures for managing QT prolongation should be adopted.
5 PHARMACOLOGICAL PROPERTIES
5.1 Pharmacodynamic properties
Pharmacotherapeutic group: Urinary antispasmodics, ATC code: G04B D07
Tolterodine is a competitive, specific muscarinic receptor antagonist with a selectivity for the urinary bladder over salivary glands in vivo. One of the tolterodine metabolites (5-hydroxymethyl derivative) exhibits a pharmacological profile similar to that of the parent compound. In extensive metabolisers this metabolite contributes significantly to the therapeutic effect (see section 5.2).
Effect of the treatment can be expected within 4 weeks.
Effect of treatment with Tolterodine 2 mg twice daily after 4 and 12 weeks, respectively, compared with placebo (pooled data). Absolute change and percentage change relative to baseline.
|
Variable |
4-week studies |
12-week studies | ||||
|
Tolterodine 2 mg b.i.d. |
Placebo |
Statistical significance vs. placebo |
Tolterodine 2 mg b.i.d. |
Placebo |
Statistical significance vs. placebo | |
|
Number of micturitions per 24 hours |
-1.6 (-14%) n=392 |
-0.9 (-8%) n=189 |
* |
-2.3 (-20%) n=354 |
-1.4 (-12%) n=176 |
** |
|
Number of incontinence episodes per 24 hours |
-1.3 (-38%) n=288 |
-1.0 (-26%) n=151 |
n.s. |
-1.6 (-47%) n=299 |
-1.1 (-32%) n=145 |
* |
|
Mean volume voided per micturition (ml) |
+25 (+17%) n=385 |
+12 (+8%) n=185 |
* * * |
+35 (+22%) n=354 |
+10 (+6%) n=176 |
*** |
|
Number of patients with no or minimal bladder problems after treatment (%) |
16% n=394 |
7% n=190 |
** |
19% n=356 |
15% n=177 |
n.s. |
n.s.=not significant; *=p<0.05; **= p<0.01; ***= p<0.001
The effect of tolterodine was evaluated in patients, examined with urodynamic assessment at baseline and, depending on the urodynamic result, they were allocated to a urodynamic positive (motor urgency) or a urodynamic negative (sensory urgency) group. Within each group, the patients were randomised to receive either tolterodine or placebo. The study could not provide convincing evidence that tolterodine had effects over placebo in patients with sensory urgency.
The clinical effects of tolterodine on QT interval were studied in ECGs obtained from over 600 treated patients, including the elderly and patients with pre-existing cardiovascular disease. The changes in QT intervals did not significantly differ between placebo and treatment groups.
The effect of tolterodine on QT-prolongation was investigated further in 48 healthy male and female volunteers aged 18-55 years. Subjects were administered 2 mg BID and 4 mg BID tolterodine as the immediate release formulations. The results (Fridericia corrected) at peak tolterodine concentration (1 hour) showed mean QTc interval increases of 5.0 and 11.8 msec for tolterodine doses of 2 mg BID and 4 mg BID respectively and 19.3 msec for moxifloxacin (400 mg) which was used as an active, internal control. A pharmacokinetic/pharmacodynamic model estimated that QTc interval increases in poor metabolisers (devoid of CYP2D6) treated with tolterodine 2 mg BID are comparable to those observed in extensive metabolisers receiving 4 mg BID. At both doses of tolterodine, no subject, irrespective of their metabolic profile, exceeded 500 msec for absolute QTcF or 60 msec for change from baseline that are considered thresholds of particular concern. The 4 mg BID dose corresponds to a peak exposure (Cmax) of three times that obtained with the highest therapeutic dose of Protol SR capsules.
Paediatric population
Efficacy in the paediatric population has not been demonstrated. Two paediatric phase 3 randomised, placebo-controlled, double-blind 12 week studies were conducted using tolterodine extended release capsules. A total of 710 paediatric patients (486 on tolterodine and 224 on placebo) aged 5-10 years with urinary frequency and urge urinary incontinence were studied. No significant difference between the two groups was observed in either study with regard to change from baseline in total number of incontinence episodes/week (see section 4.8).
5.2 Pharmacokinetic properties
Pharmacokinetic characteristics specific for this formulation: Tolterodine is rapidly absorbed. Both tolterodine and the 5-hydroxymethyl metabolite reach maximal serum concentrations 1-3 hours after dose. The half-life for tolterodine given as the tablet is 2-3 hours in extensive and about 10 hours in poor metabolisers (devoid of CYP2D6). Steady state concentrations are reached within 2 days after administration of the tablets.
Food does not influence the exposure to the unbound tolterodine and the active 5-hydroxymethyl metabolite in extensive metabolisers, although the tolterodine levels increase when taken with food. Clinically relevant changes are likewise not expected in poor metabolisers.
Absorption: After oral administration tolterodine is subject to CYP2D6 catalysed first-pass metabolism in the liver, resulting in the formation of the 5-hydroxymethyl derivative, a major pharmacologically equipotent metabolite.
The absolute bioavailability of tolterodine is 17 % in extensive metabolisers, the majority of the patients, and 65% in poor metabolisers (devoid of CYP2D6).
Distribution: Tolterodine and the 5-hydroxymethyl metabolite bind primarily to orosomucoid. The unbound fractions are 3.7% and 36%, respectively. The volume of distribution of tolterodine is 113 l.
Elimination: Tolterodine is extensively metabolised by the liver following oral dosing. The primary metabolic route is mediated by the polymorphic enzyme CYP2D6 and leads to the formation of the 5-hydroxymethyl metabolite. Further metabolism leads to formation of the 5-carboxylic acid and N-dealkylated 5-carboxylic acid metabolites, which account for 51 % and 29 % of the metabolites recovered in the urine, respectively. A subset (about 7%) of the population is devoid of CYP2D6 activity. The identified pathway of metabolism for these individuals (poor metabolisers) is dealkylation via CYP3A4 to N-dealkylated tolterodine, which does not contribute to the clinical effect. The remainder of the population is referred to as extensive metabolisers. The systemic clearance of tolterodine in extensive metabolisers is about 30 l/h. In poor metabolisers the reduced clearance leads to significantly higher serum concentrations of tolterodine (about 7-fold) and negligible concentrations of the 5-hydroxymethyl metabolite are observed.
The 5-hydroxymethyl metabolite is pharmacologically active and equipotent with tolterodine. Because of the differences in the protein-binding characteristics of tolterodine and the 5-hydroxymethyl metabolite, the exposure (AUC) of unbound tolterodine in poor metabolisers is similar to the combined exposure of unbound tolterodine and the 5-hydroxymethyl metabolite in patients with CYP2D6 activity given the same dosage regimen. The safety, tolerability and clinical response are similar irrespective of phenotype.
The excretion of radioactivity after administration of [14C]-tolterodine is about 77% in urine and 17% in faeces. Less than 1% of the dose is recovered as unchanged drug, and about 4% as the 5-hydroxymethyl metabolite. The carboxylated metabolite and the corresponding dealkylated metabolite account for about 51% and 29% of the urinary recovery, respectively.
The pharmacokinetics is linear in the therapeutic dosage range.
Specific patient groups
Impaired liver function
About 2-fold higher exposure of unbound tolterodine and the 5-hydroxymethyl metabolite is found in subjects with liver cirrhosis (see section 4.2 and 4.4).
Impaired renal function
The mean exposure of unbound tolterodine and its 5-hydroxymethyl metabolite is doubled in patients with severe renal impairment (inulin clearance GFR < 30 ml/min). The plasma levels of other metabolites were markedly (up to 12-fold) increased in these patients. The clinical relevance of the increased exposure of these metabolites is unknown. There is no data in mild to moderate renal impairment (see section 4.2 and 4.4).
Paediatric patients
The exposure of the active moiety per mg dose is similar in adults and adolescents. The mean exposure of the active moiety per mg dose is approximately two-fold higher in children between 5-10 years than in adults (see sections 4.2 and 5.1).
5.3 Preclinical safety data
In toxicity, genotoxicity, carcinogenicity and safety pharmacology studies no clinically relevant effects have been observed, except those related to the pharmacological effect of the drug.
Reproduction studies have been performed in mice and rabbits.
In mice, there was no effect of tolterodine on fertility or reproductive function. Tolterodine produced embryo death and malformations at plasma exposures (Cmax or AUC) 20 or 7 times higher than those seen in treated humans.
In rabbits, no malformative effect was seen, but the studies were conducted at 20 or 3 times higher plasma exposure (Cmax or AUC) than those expected in treated humans.
Tolterodine, as well as its active human metabolites prolong action potential duration (90% repolarisation) in canine purkinje fibres (14 - 75 times therapeutic levels) and block the K+-current in cloned human ether-a-go-go-related gene (hERG) channels (0,5 - 26,1 times therapeutic levels). In dogs prolongation of the QT interval has been observed after application of tolterodine and its human metabolites (3,1 - 61,0 times therapeutic levels). The clinical relevance of these findings is unknown.
6 PHARMACEUTICAL PARTICULARS
6.1 List of excipients
Tablet core:
Magnesium stearate Silica colloidal, anhydrous Sodium starch glycolate, type B Calcium hydrogen phosphate, dihydrate Cellulose, microcrystalline
Coating:
Silica colloidal, anhydrous Polyethylene glycol 400 Polyethylene glycol 8000 Hypromellose (E 464)
Hydroxypropyl cellulose (E 463)
Titanium dioxide (E 171)
6.2 Incompatibilities
Not applicable.
6.3 Shelf life
2 years.
6.4 Special precautions for storage
Store below 30°C.
6.5 Nature and contents of container
Aluminium/PVC/PVdC blister packs.
Tablet containers (HDPE) with a sealed cap (LDPE) and a desiccant (silica gel).
Pack sizes:
Blister packs: 4, 7, 10, 14, 20, 28, 30, 42, 50, 56, 60, 90, 100, 280, 500, 560 tablets
Tablet container: 4, 7, 10, 14, 20, 28, 30, 42, 50, 56, 60, 90, 100, 280, 500, 560 tablets
Not all pack sizes may be marketed.
6.6 Special precautions for disposal
No special requirements.
Any unused product or waste material should be disposed of in accordance with local requirements.
7 MARKETING AUTHORISATION HOLDER
Actavis Group PTC ehf.
Reykjavikurvegi 76-78 220 Hafnarfjordur Iceland
8 MARKETING AUTHORISATION NUMBER(S)
PL 30306/0412
9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
27/06/2012
10 DATE OF REVISION OF THE TEXT
17/12/2012