Mizollen 10 mg modified-release tablets
Mizolastine 10mg per tablet
Excipients with known effect:
Lactose monohydrate (125mg/tablet).
Hydrogenated castor oil (25mg/tablet).
Propylene glycol (0.45mg/tablet).
For the full list of excipients, see section 6.1
Oblong, white tablets with a scored line on one side and a mark "MZI 10" on the reverse side.
Mizolastine is a long-acting H1 -antihistamine indicated for the symptomatic relief of seasonal allergic rhinoconjunctivitis (hay fever), perennial allergic rhinoconjunctivitis and urticaria.
Adults, including the elderly, and children 12 years of age and over:
The recommended daily dose is one 10mg tablet.
- Hypersensitivity to the active substance or to any of the excipients listed in section 6.1.
- Concomitant administration with macrolide antibiotics or systemic imidazole antifungals.
- Significantly impaired hepatic function.
- Clinically significant cardiac disease or a history of symptomatic arrhythmias.
- Patients with known or suspected QT prolongation or with electrolyte imbalance, in particular hypokalaemia.
- Clinically significant bradycardia.
- Medicinal products known to prolong the QT interval, such as Class I and III anti-arrhythmics.
Mizolastine has a weak potential to prolong the QT interval in a few individuals. The degree of prolongation is modest and has not been associated with cardiac arrhythmias.
The elderly may be particularly susceptible to the sedative effects of mizolastine and the potential effects of the medicinal product on cardiac repolarisation.
Due to the presence of lactose, patients with rare hereditary problems of galactose intolerance, total lactase deficiency or glucose-galactose malabsorption should not take this medicine.
Mizolastine contains hydrogenated castor oil which can cause stomach upset and diarrhoea.
Although the bioavailability of mizolastine is high and the medicinal product is principally metabolised by glucuronidation, systemically administered ketoconazole and erythromycin moderately increase the plasma concentration of mizolastine and their concurrent use is contraindicated.
Concurrent use of other potent inhibitors or substrates of hepatic oxidation (cytochrome P450 3A4) with mizolastine should be approached with caution. These would include cimetidine, ciclosporin, and nifedipine.
Alcohol: In studies with mizolastine, no potentiation of the sedation and the alteration in performance caused by alcohol has been observed.
The safety of mizolastine for use in human pregnancy has not been established. The evaluation of experimental animal studies does not indicate direct or indirect harmful effects with respect to the development of the embryo or foetus, the course of gestation and peri- and post-natal development. However, as with all medicinal products, mizolastine should be avoided in pregnancy, particularly during the first trimester.
Mizolastine is excreted into breast milk, therefore its use by lactating women is not recommended.
Most patients taking mizolastine may drive or perform tasks requiring concentration. However, in order to identify sensitive people who have unusual reactions to medicinal products, it is advisable to check the individual response before driving or performing complicated tasks.
Common: dry mouth, diarrhoea, abdominal pain (including dyspepsia), nausea.
Not known: vomiting.
Central nervous system disorders and psychiatric disorders:
Common: drowsiness often transient, headache, dizziness.
Uncommon: anxiety and depression.
Uncommon: raised liver enzymes.
Very rare: low neutrophil count.
Body as a whole:
Common: asthenia often transient, increased appetite associated with weight gain.
Very rare: allergic reactions including anaphylaxis, angioedema, generalized rash/urticaria, pruritus and hypotension.
Uncommon: hypotension, tachycardia, palpitations.
Very rare: vasovagal attack.
Uncommon: arthralgia and myalgia.
Description of selected adverse reactions
There were reports of bronchospasm and aggravation of asthma but in view of the high frequency of asthma in the patient population being treated, a causal relationship remains uncertain.
Treatment with certain antihistamines has been associated with QT interval prolongation increasing the risk of serious cardiac arrhythmias in susceptible subjects.
Minor changes in blood sugar and electrolytes have been observed rarely. The clinical significance of these changes in otherwise healthy individuals remains unclear. Patients at risk (diabetics, those susceptible to electrolyte imbalance and cardiac arrhythmias) should be monitored periodically.
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 at: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.
In cases of overdose, general symptomatic surveillance with cardiac monitoring including QT interval and cardiac rhythm for at least 24 hours is recommended, along with standard measures to remove any unabsorbed medicinal product.
Studies in patients with renal insufficiency suggest that haemodialysis does not increase clearance of the medicinal product.
Antihistamines for systemic use (ATC code : R06AX25)
Mechanism of action
Mizolastine possesses antihistamine and antiallergic properties due to a specific and selective antagonism of peripheral histamine H1 receptors. It has also been shown to inhibit histamine release from mast cells (at 0.3 mg/kg orally) and the migration of neutrophils (at 3 mg/kg orally) in animal models of allergic reactions.
Clinical efficacy and safety
In man, histamine-induced wheal and flare studies have shown that mizolastine 10 mg is a rapid, potent (80 % inhibition after 4 hrs) and sustained (24hr) antihistamine. No tachyphylaxis occurred after long-term administration.
In both preclinical and clinical studies, no anticholinergic effect has been demonstrated.
Following oral administration mizolastine is rapidly absorbed. Peak plasma concentration is reached at a median time of 1.5 hours.
Bioavailability is 65% and linear kinetics have been demonstrated.
The mean elimination half-life is 13.0 hours with plasma protein binding of 98.4%.
In hepatic insufficiency the absorption of mizolastine is slower and the distribution phase longer, with a resulting moderate increase in AUC of 50%.
The principal metabolic pathway is glucuronidation of the parent compound. The cytochrome P450 3A4 enzyme system is involved in one of the additional metabolic pathways with formation of the hydroxylated metabolites of mizolastine. None of the identified metabolites contribute to the pharmacological activity of mizolastine.
An increase in mizolastine plasma levels, observed with systemic ketoconazole and erythromycin, led to concentrations equivalent to those obtained after a 15 to 20 mg dose of mizolastine alone.
In studies carried out in healthy volunteers, no clinically significant interaction has been recorded with food, warfarin, digoxin, theophylline, lorazepam, or diltiazem.
Pharmacological studies in several species have shown an effect on cardiac repolarisation at doses in excess of 10-20 times the therapeutic dose. In conscious dogs, mizolastine has shown pharmacological interactions with ketoconazole at the electrocardiographic level at 70 times the therapeutic dose.
Hydrogenated castor oil
Anhydrous colloidal silica
Titanium dioxide (E171)
3 years in Aluminium/ (oPA/Aluminium/PVC) blisters.
2 years in Aluminium/PVC blisters.
3 years in securitainers.
Store in the original package.
Aluminium/ (oPA/Aluminium/PVC) blisters: This medicinal product does not require any special temperature storage conditions.
Aluminium/PVC blisters and securitainers: Do not store above 25°C.
Aluminium/ (oPA/Aluminium/PVC) blisters : Packs of 4, 7, 10, 15, 20, 30, 50 or 100 tablets.
Aluminium/PVC blisters : Packs of 4, 7, 10, 15, 20, 30, 50 or 100 tablets.
Polypropylene tablet container with polyethylene caps : Packs of 4, 7, 10, 15, 20, 30, 50 or 100 tablets.
Not all pack sizes may be marketed.
Tablets should not be taken if they become discoloured.
Opella Healthcare UK Limited, trading as Sanofi
410 Thames Valley Park Drive
Date of first authorisation: 7 March 2003
Date of latest renewal: 21 November 2005