Fosteris indicated in the regular treatment of asthma where use of a combination product (inhaled corticosteroid and long-acting beta2-agonist) is appropriate: -patients not adequately controlled with inhaled corticosteroids and 'as needed' inhaled short-acting beta2-agonist or-patients already adequately controlled on both inhaled corticosteroids and long-acting beta2-agonists. Note: Foster is not appropriate for treatment of acute asthma attacks.

Fosteris for inhalation use.

Fosteris not intended for the initial management of asthma. The dosage of the components of Foster is individual and should be adjusted to the severity of the disease. This should be considered not only when treatment with combination products is initiated but also when the dose is adjusted. If an individual patient should require a combination of doses other than those available in the combination inhaler, appropriate doses of beta-2-agonists and/or corticosteroids by individual inhalers should be prescribed.Beclometasone dipropionate in Fosteris characterised by an extrafine particle size distribution which results in a more potent effect than formulations of beclometasone dipropionate with a non-extrafine particle size distribution (100 micrograms of beclometasone dipropionate extrafine in Foster are equivalent to 250 micrograms of beclometasone dipropionate in a non-extrafineformulation). Therefore the total daily dose of beclometasone dipropionate administered inFoster should be lower than the total daily dose of beclometasone dipropionate administered in anon-extrafine beclometasone dipropionate formulation.This should be taken into consideration when a patient is transferred from beclometasone dipropionate non-extrafine formulations to Foster; the dose of beclometasone dipropionate should be lower and will need to be adjusted to the individual needsof patients.

Dose recommendations for adults 18 years and above: One or two inhalations twice daily. The maximum daily dose is 4 inhalations daily.Dose recommendations for children and adolescents under 18 years:There is no experience with Fosterin children andadolescents under 18 years of age. Therefore Foster is not recommended for children and adolescents under 18 years until further data become available.

Patients should be regularly reassessed by a doctor, so that the dosage of Fosterremains optimaland is only changed on medical advice.The dose should be titrated to the lowest dose at which effective control of symptoms is maintained. When control of symptoms is maintained with the lowest recommended dosage, then the next step could include a test of inhaled corticosteroid alone. Patients should be advised to take Fosterevery day even when asymptomatic.Special patient groups: There is no need to adjust the dose in elderly patients. There are no data available for use of Fosterin patients with hepatic or renal impairment (see section 5.2). Instructions for useTo ensure proper administration of the drug, the patient should be shown how to use the inhaler correctly by a physician or other health professional. Correct use of the pressurised metereddose inhaler is essential in order that treatment is successful. The patient should be advised to read the Patient Information Leaflet carefully and follow the instructions for use as given in the Leaflet.

Before using the inhaler for the first time or if the inhaler has not been used for 14 days or more, one actuation should be released into the air in order to ensure that the inhaler is working properly. Wheneverpossible patients shouldstand or sit in an upright position when inhalingfrom their inhaler.The steps below should be followed:1. Remove the protectivecap from the mouthpieceand check that the mouthpiece is clean and free from dust and dirt or any other foreign objects.2. Breathe out as slowly and deeply as possible.3. Hold the canister vertically with its body upwards and put the lips around the mouthpiece.Do not bite the mouthpiece4. At the same time, breathe in slowly and deeply through the mouth. After starting to breathein, press down on the top of the inhaler to release one puff.5. Hold the breath for as long as possible and, finally, remove the inhaler from the mouth and breathe out slowly. Do not breath out into the inhaler.Should a further puff beneeded, keep the inhaler in a vertical position for about half a minuteandrepeat steps 2 to 5.After use, close with protectivecap.IMPORTANT: do not perform steps 2 to 5 too quickly.If mist appears following inhalation, either from the inhaler or from the sides of the mouth, the procedure should be repeatedfrom step 2.For patients with weak hands it maybe easier to hold the inhaler with both hands. Thereforethe index fingers should be placed on the top of the inhaler canister and both thumbs on the base of the inhaler.

Patients should rinse their mouth or gargle with water or brush the teethafter inhaling (see section 4.4).Cleaning Patients should be advised to read the Patient Information Leaflet carefully for cleaning instructions.For the regular cleaning of the inhaler, patients should remove the cap from themouthpiece and wipe the outside and inside of the mouthpiece with a dry cloth. They should not use water or other liquids to clean the mouthpiece.There are no clinical data available on the use of Fosterwith a spacer, therefore the recommended posologyrefers to the inhalation of the medicinal product without a spacer (with a standard actuator).

Fostermust not be used with any spacing device; if a spacing device is required the patients should have their treatment changed to either an alternative pressurised metered dose inhaler with a named spacing device or an inhalation powder.

Fostershould be used with caution (which may include monitoring)in patients with cardiac arrhythmias, especiallythird degree atrioventricular blockand tachyarrhythmias(accelerated and/or irregular heart beat), idiopathic subvalvular aortic stenosis, hypertrophic obstructive cardiomyopathy, severe heart disease, particularlyacute myocardial infarction, ischaemicheart disease, congestive heart failure, occlusive vascular diseases, particularlyarteriosclerosis, arterial hypertension and aneurysm.Caution should also be observed when treating patients with known or suspected prolongation of the QTc interval, eithercongenital or drug induced (QTc > 0.44 seconds). Formoterol itself may induce prolongation of the QTc interval.Caution is also required when Foster is used by patients with thyrotoxicosis, diabetes mellitus, phaeochromocytoma and untreated hypokalaemia.Potentially serious hypokalaemia may result from beta2-agonist therapy. Particular caution is advised in severe asthma as this effect may be potentiated by hypoxia. Hypokalaemia may also be potentiated by concomitant treatment with other drugs which can induce hypokalaemia, such as xanthine derivatives, steroids and diuretics (see Section 4.5). Caution is also recommended in unstable asthma when a number of “rescue” bronchodilators may be used.It is recommended that serum potassium levels are monitored in such situations.

The inhalation of formoterol may cause a rise in blood glucoselevels. Thereforeblood glucose should be closely monitored in patients with diabetes. If anaesthesia with halogenated anaesthetics is planned, it should be ensured that Fosteris not administered for at least 12 hours before the start of anaesthesiaas there is a risk of cardiac arrhythmias. As with all inhaled medication containing corticosteroids, FOSTER should be administered with caution in patients with active or quiescent pulmonary tuberculosis, fungal and viral infections in the airways.It is recommended that treatment with FOSTER should not be stoppedabruptly.

If patients find the treatment ineffective medical attention must be sought. Increasing use of rescue bronchodilators indicates a worsening of the underlying condition and warrants a reassessment of the asthma therapy. Sudden and progressive deterioration in control of asthma is potentially life threatening and the patient should undergo urgent medical assessment.Consideration should be given to the need for increase treatmentwith corticosteroids, either inhaled or oral therapy, or antibiotic treatment if an infection is suspected.Patients should not be initiated on Foster during an exacerbation, or if they have significantly worsening or acutely deteriorating asthma. Serious asthma-related adverse events and exacerbations may occur during treatment with Foster. Patients should be asked to continue treatment but to seek medical advice if asthma symptoms remain uncontrolled or worsen after initiation on Foster.As with other inhalation therapy paradoxical bronchospasm may occur withan immediate increase in wheezing and shortness of breathafter dosing. This should be treated immediately with a fast-acting inhaled bronchodilator. Fostershould be discontinued immediately, the patient assessed and alternative therapy instituted if necessary. Foster should not be used as the first treatment for asthma.For treatment of acute asthma attacks patients should be advised to have their short-acting bronchodilator available at all times.

Patients should be reminded to take Fosterdaily as prescribed even when asymptomatic. Once asthma symptoms are controlled, consideration may be given to gradually reducing the dose of Foster. Regular review of patients as treatment is stepped down is important. The lowest effective dose of Fostershould be used (see section 4.2).Systemic effects may occur with any inhaled corticosteroid, particularly at high doses prescribed for long periods. These effects are much less likely to occur with inhaled than with oral corticosteroids. Possible systemic effects include: Cushing's syndrome, Cushingoid features, adrenal suppression, growth retardation in children and adolescents, decrease in bone mineral density, cataract and glaucoma. Therefore, it is important that the patient is reviewed regularly, and the dose of inhaled corticosteroid is reduced to the lowest dose at which effective control of asthma is maintained.Prolonged treatment of patients with high doses of inhaled corticosteroids may result in adrenal suppression and acute adrenal crisis. Childrenaged less than 16 years taking/inhaling higher than recommended doses of beclometasone dipropionate may be at particular risk. Situations which could potentially trigger acute adrenal crisis, include trauma, surgery, infection or any rapid reduction in dosage. Presenting symptoms are typically vague and may include anorexia, abdominal pain, weight loss, tiredness, headache, nausea, vomiting, hypotension, decreased level of consciousness, hypoglycaemia, and seizures. Additional systemic corticosteroid covershould be considered during periods of stress or elective surgery. Care should be taken when transferring patients to Fostertherapy, particularly if there is any reason to suppose that adrenal function is impaired from previous systemic steroid therapy.

Patients transferring from oral to inhaled corticosteroids may remain at risk of impaired adrenal reserve for a considerable time. Patients who have required high dose emergency corticosteroid therapy in the past or have received prolonged treatment with or high doses of inhaled corticosteroids may also be at risk. This possibility of residual impairment should always be borne in mind in emergency and elective situations likely to produce stress, and appropriate corticosteroid treatment must be considered. The extent of the adrenal impairment may require specialist advice before elective procedures. Patients should be advised that Foster contains a small amount of ethanol (approximately 7 mg per actuation); however at normal doses the amount of ethanol is negligible and doesnot pose a risk to patients. Patients should be advised to rinse the mouth or gargle with water or brush the teethafter inhaling the prescribed dose to minimise the risk of oropharyngeal candida infection.

Pharmacokinetic interactionsBeclometasone dipropionate undergoes a very rapid metabolism via esterase enzymes without involvement of cytochrome P450 system.

Pharmacodynamic interactionsBeta-blockers (including eye drops) should be avoided in asthmatic patients. If beta-blockers are administered for compelling reasons, the effect of formoterol will be reduced or abolished.On the other hand, concomitant use of other beta-adrenergic drugs can have potentially additiveeffects, therefore caution is required whentheophylline or other beta-adrenerigic drugs are prescribed concomitantly with formoterol. Concomitant treatment with quinidine, disopyramide, procainamide, phenothiazines, antihistamines, monoamine oxidase inhibitors and tricyclic antidepressants can prolong the QTc-interval and increase the risk of ventricular arrhythmias. In addition L-dopa, L-thyroxine, oxytocin and alcohol can impair cardiac tolerance towards beta2-sympathomimetics. Concomitant treatment with monoamine oxidase inhibitors including agents with similar properties such as furazolidone and procarbazine may precipitate hypertensive reactions. There is an elevated risk of arrhythmias in patients receiving concomitant anaesthesia with halogenated hydrocarbons. Concomitant treatment with xanthine derivatives, steroids, or diuretics may potentiate a possible hypokalaemic effect of beta2-agonists (see section 4.4.).Hypokalaemia may increase the disposition towards arrhythmias in patients who are treated with digitalis glycosides. Foster contains a small amount of ethanol. There is a theoretical potential for interaction in particularly sensitive patients taking disulfiram or metronidazole

There is no experience with or evidence of safety of propellant HFA-134a in human pregnancy or lactation. However studies of the effect of HFA-134a on reproductive function and embryofetal development in animals have revealed no clinically relevant adverse effects.Pregnancy There are no relevant clinical data on the use of Fosterin pregnant women. Animal studies using beclometasone dipropionate and formoterol combination showed evidence of toxicity to reproduction after high systemic exposure (see 5.3 Preclinical safety data). Because of the tocolytic actions of beta2-sympathomimetic agents particular care should be exercised in the run up to delivery.Formoterol should not be recommended for use during pregnancy and particularly at the end of pregnancy or during labour unless there is no other (safer) established alternative. Foster should only be used during pregnancy if the expected benefits outweigh the potential risks.LactationThere are no relevant clinical data on the use of Foster in lactation in humans.Although no data from animal experiments are available, it is reasonable to assume that beclometasone dipropionate is secreted in milk, like other corticosteroids. While it is not known whether formoterol passes into human breast milk, it has been detected in the milk of lactating animals. Administration of Foster to women who are breast-feeding should only be considered if the expected benefits outweigh the potential risks.

Fosteris unlikely to have any effect on the ability to drive and operate machinery.

As Fostercontains beclometasone dipropionate and formoterol fumarate dihydrate, the type and severity of adverse reactions associated with each of the compounds may beexpected. There is no incidence of additional adverse events following concurrent administration of the two compounds. Undesirable effects which have been associated with beclometasone dipropionate and formoterol administered as a fixed combination (Foster) and as single agents are given below, listed by system organ class. Frequencies are defined as: very common (1/10),common (1/100 and <1/10),uncommon (1/1,000 and <1/100), rare (1/10,000 < 1/1,000) and very rare (≤1/10,000).Common and uncommonADRs were derived from clinical trial data. The incidence on placebo was not taken into account.

System Organ ClassAdverse ReactionFrequencyInfections and PharyngitisCommon

nfestationsInfluenza, oral fungal infection, pharyngeal and oesophagealcandidiasis, vaginal candidiasis, gastroenteritis, sinusitisUncommonBlood and the lymphatic system disordersGranulocytopeniaUncommonThrombocytopeniaVery rare Immune system disordersDermatitis allergicUncommonHypersensitivity reactions, including erythema, lips, face, eyeand pharyngeal oedemaVeryrare Endocrine disordersAdrenal suppressionVery rare Metabolism and nutrition disordersHypokalaemia, hyperglycaemiaUncommon

Psychiatric disordersRestlessnessUncommonAbnormal behaviour, sleep disorder, hallucination Very rare Nervous system disordersHeadacheCommonTremor, dizziness, UncommonEye disordersGlaucoma, cataractVery rare Ear and labyrinth disordersOtosalpingitisUncommonCardiac disordersPalpitations, electrocardiogram QT corrected interval prolonged, electrocardiogram change, tachycardia, tachyarrhythmiaUncommonVentricular extrasystoles, angina pectorisRare

Atrial fibrillationVery rare Vascular disordersHyperaemia, flushing UncommonRespiratory,thoracic and mediastinal disordersDysphoniaCommonRhinitis, cough, productive cough, throat irritation, asthmatic crisisUncommonBronchospasm paradoxicalRareDyspnoea, exacerbation of asthmaVery rare Gastrointestinal disordersDiarrhoea, dry mouth, dyspepsia, dysphagia, burning sensation of the lips, nausea, dysgeusiaUncommonSkin and subcutaneous tissue disordersPruritus, rash, hyperhidrosisUncommonUrticaria, angioneurotic oedemaRareMusculoskeletal, connective tissue and bone disordersMuscle spasms, myalgiaUncommonGrowth retardation in children and adolescentsVery rareRenal and urinary disordersNephritisRareGeneral disorders and administration site conditionsOedema peripheralVery rare InvestigationsC-reactive proteinincreased, platelet count increased, free fatty acids increased, blood insulin increased, blood ketone body increasedUncommonBlood pressure increased, blood pressure decreasedRare

Bone density decreasedVery rare

As with other inhalation therapy, paradoxical bronchospasm may occur (see 4.4 'Special Warnings and Precautions for Use').Among the observed adverse reactions those typically associated with formoterol are: hypokalaemia, headache, tremor, palpitations, cough,muscle spasmsand prolongation of QTc interval. Adverse reactions typically associated with the administration of beclometasone dipropionate are: oral fungal infections, oral candidiasis, dysphonia, throat irritation. Dysphonia and candidiasis may be relieved by gargling or rinsing the mouth with water or brushing the teethafter using the product. Symptomatic candidiasis can be treated with topical anti-fungal therapy whilst continuing the treatment with Foster.Systemic effects ofinhaled corticosteroids (e.g. beclometasonedipropionate) may occur particularly when administered at high doses prescribed for prolonged periods, these may include adrenal suppression, decrease in bone mineral density, growth retardation in children and adolescents, cataract and glaucoma (see also4.4).Hypersensitivity reactions including rash, urticaria pruritus, erhythema and oedema of the eyes, face, lips and throat may also occur.To report any side effect(s):The National Pharmacovigilance and Drug Safety Center (NPC)Fax +966-11-205-7662Call NPC at +966-11-2038222, Exts 2317-2356-2353-2354-2334-2340Tool Free Phone: 8002490000E-mail: npc.drug@sfda.gov.saWebsite: www.sfda.gov.sa/npc

Inhaled doses of Fosterup to twelve cumulative actuations (total beclometasone dipropionate1200 micrograms, Formoterol 72 micrograms) have been studied in asthmatic patients. The cumulative treatments did not cause abnormal effect on vital signs and neither serious nor severe adverse events were observed. Excessive doses of formoterol may leadto effects that are typical of beta2-adrenergic agonists: nausea, vomiting, headache, tremor, somnolence, palpitations, tachycardia, ventricular arrhythmias, prolongation of QTc interval, metabolic acidosis, hypokalaemia, hyperglycaemia. In case of overdose of formoterol, supportive and symptomatic treatment is indicated. Serious cases should be hospitalised. Use of cardioselective beta-adrenergic blockers may be considered, but only subject to extreme caution since the use of beta-adrenergic blocker medication may provoke bronchospasm.Serum potassium should be monitored.Acute inhalation of beclometasone dipropionate doses in excess of those recommended may lead to temporary suppression of adrenal function. This does not need emergency action as adrenal function is recovers in a few days, as verified by plasma cortisol measurements. In these patients treatment should be continued at a dose sufficient to control asthma.Chronic overdose of inhaled beclometasone dipropionate: risk of adrenal suppression(seesection 4.4.). Monitoring of adrenal reserve may be necessary. Treatment should be continued at a dose sufficient to control asthma

Pharmacotherapeutic group: Adrenergics and other drugs for obstructive airway diseases. ATC-code: R03 AK07.Mechanisms of action and pharmacodynamic effectsFostercontains beclometasone dipropionate and formoterol, which have different modes of action. In common with other inhaled corticosteroids and beta2-agonists combinations, additive effects are seen in terms of reduction of asthma exacerbations.Beclometasone dipropionateBeclometasone dipropionate given by inhalation at recommended doses has a glucocorticoid antiinflammatory action within the lungs, resulting in reduced symptoms and exacerbations of asthma with less adverse effects than when corticosteroids are administered systemically. Formoterol Formoterol is a selective beta2-adrenergic agonist that produces relaxation of bronchial smooth muscle in patients with reversible airways obstruction. The bronchodilating effect sets in rapidly, within 1-3 minutes after inhalation, and has a duration of 12 hours after a single dose. FOSTER In clinical trials in adults, the addition of formoterol to beclometasone dipropionate improved asthma symptoms and lung function and reduced exacerbations. In a 24-week study the effect on lung function of Fosterwas at least equal to that of the free combination of beclomeasone dipropionate and formoterol, and exceeded that of beclometasone dipropionate alone.

The systemic exposure to the active substances beclometasone dipropionate and formoterol in the fixed combination Fosterhave been compared to the single components.In a pharmacokinetic study conducted in healthy subjects treated with a single dose of Foster fixed combination (4 puffs of 100/6 micrograms) or a single dose of beclometasone dipropionate CFC (4 puffs of 250 micrograms) and Formoterol HFA (4 puffs of 6 micrograms), the AUC of beclometasone dipropionatemain active metabolite (beclometasone-17-monopropionate), and its maximal plasma concentration were, respectively, 35% and 19% lower withthe fixed combination, than with non-extrafine beclometasone dipropionate CFC formulation, in contrast,the rate of absorption was more rapid (0.5 vs 2h)with the fixed combination compared to non-extrafine beclometasone dipropionate CFC alone. For formoterol, maximal plasma concentration was similar after administration of the fixed or the extemporary combination and the systemic exposure was slightly higher after administration of Fosterthan with the extemporary combination. There was no evidence of pharmacokinetic or pharmacodynamic (systemic) interactions between beclometasone dipropionateand formoterol. Beclometasone dipropionate Beclometasone dipropionateis a pro-drug with weak glucocorticoid receptor binding affinity that is hydrolysed via esterase enzymes to an active metabolite beclometasone-17-monopropionate which has a morepotent topical anti-inflammatory activity compared with the pro-drug beclometasone dipropionate.Absorption distributionand metabolismInhaled beclometasone dipropionateis rapidly absorbed through the lungs; prior to absorption there is extensive conversion to its active metabolitebeclometasone-17-monopropionate via esterase enzymes that are found in most tissues. The systemic availability of beclometasone-17-monopropionatearises from lung (36%) and from gastrointestinal absorption of the swallowed dose. The bioavailability of swallowed beclometasone dipropionateis negligible however, pre-systemic conversion to beclometasone-17-monopropionateresults in 41%of the dose being absorbedas the active metabolite.There is an approximately linear increase in systemic exposure with increasing inhaled dose. The absolute bioavailability following inhalation is approximately 2% and 62% of the nominal dose for unchanged beclometasone dipropionate and beclometasone-17-monopropionaterespectively.Following intravenous dosing, the disposition of beclometasone dipropionateand its active metaboliteare characterised by high plasma clearance (150 and 120L/h respectively), with a small volume of distribution at steady state for beclometasone dipropionate(20L) and larger tissue distribution for its active metabolite (424L).Plasma protein binding is moderately high.

ExcretionFaecal excretion is the major route of beclometasone dipropionate elimination mainly as polar metabolites. The renal excretion of beclometasone dipropionateand its metabolites is negligible. The terminal elimination half-lives are 0.5 h and 2.7 h for beclometasone dipropionateand beclometasone-17-monopropionate respectively. Special populationsAs beclometasone dipropionateundergoes a veryrapid metabolism via esterase enzymes present in intestinal fluid, serum, lungs and liver, to originate the more polar productsbeclometasone-21-monopropionate, beclometasone-17-monopropionate,and beclometasonehepatic impairment is not expected to modify the pharmacokinetics and safety profile ofbeclometasone dipropionate.The pharmacokinetics of beclometasone dipropionatein patients with renal impairment has not been studied. As beclometasone dipropionateor its metabolites were not traced in the urine, an increase in systemic exposure is not envisaged in patients with renal impairment. FormoterolAbsorption and distributionFollowing inhalation, formoterol is absorbed both from the lung and from the gastrointestinal tract. The fraction of an inhaled dose that is swallowed after administration with an metered dose inhaler (MDI)may ranges between 60% and90%,At least 65% of the fraction that is swallowed is absorbed from the gastrointestinal tract.Peak plasma concentrations of unchanged drug occur within 0.5 to 1 hours after oral administration. Plasma protein binding of formoterol is 61-64% with 34% bound to albumin. There was no saturation of binding in the concentration range attained with therapeutic doses.The elimination half-life determined after oral administration is 2-3 hours. Absorption of formoterol is linear following inhalation of 12 to 96 μg of formoterol fumarate.MetabolismFormoterol is widely metabolised and the prominent pathway involves direct conjugation at the phenolic hydroxyl group. Glucuronide acid conjugate is inactive. The second major pathway involves O-demethylation followed by conjugation at the phenolic 2’-hydroxyl group. Cytochrome P450 isoenzymes CYP2D6, CYP2C19 and CYP2C9 are involved in the O-demethylation of formoterol. Liver appears to be the primary site of metabolism. Formoterol does not inhibit CYP450 enzymes at therapeutically relevant concentrations.ExcretionThe cumulative urinary excretion of formoterol after single inhalation from a dry powder inhalerincreased linearly in the 12 – 96 μg dose range. On average, 8% and 25% of the dose was excreted as unchanged and total formoterol, respectively. Based on plasma concentrations measured following inhalation of a single 120 μg dose by 12 healthy subjects, the mean terminal elimination half-life was determined to be 10 hours. The (R,R)- and (S,S)-enantiomers represented about 40% and 60% of unchanged drug excreted in the urine, respectively. The relative proportion of the two enantiomers remained constant over the dose range studied and there was no evidence of relative accumulation of one enantiomer over the other after repeated dosing.

After oral administration (40 to 80 μg), 6% to 10% of the dose was recovered in urine as unchanged drug in healthy subjects; up to 8% of the dose was recovered as the glucuronide.A total 67% of an oral dose of formoterol is excreted in urine (mainly as metabolites) and the remainder in the faeces. The renal clearance of formoterol is 150 ml/min.

Special populationsHepatic/Renal impairment: the pharmacokinetics of formoterol has not been studied in patients with hepatic or renal impairment.

The toxicity observed in animal studies with beclometasone dipropionate and formoterol, given in combination or separately, consisted mainly of effects associated with exaggerated pharmacological activity. They are related to the immuno-suppressive activityof beclometasone dipropionateand to the known cardiovascular effects of formoterol evident mainly in dogs. Neither increase in toxicity nor occurrence of unexpected findings were observedupon administration of the combination. Reproduction studies in rats showed dose-dependent effects. The combination was associated with reduced female fertility and embryofetal toxicity. High doses of corticosteroids to pregnant animals are known to cause abnormalities of fetal development including cleft palate and intra-uterine growth retardation, and it is likely that the effects seen with the beclometasone dipropionate/formoterol combination were due to beclometasone dipropionate. Theseeffects were noted only with high systemic exposure tothe active metabolite beclometasone-17-monoproprionate(200 fold the expected plasma levels in patients). Additionally, increased duration of gestation and parturition, an effect attributable to the known tocolytic effects of beta2-sympathomimetics, was seen in animal studies. These effects were noted when maternal plasma formoterol levels were below the levels expected in patients treated with Foster.Genotoxicity studies performed with a beclometasone dipropionate /formoterol combination do not indicate mutagenic potential. No carcinogenicity studies have been performed with the proposed combination. However animal data reported for the individual constituents do not suggest any potential risk of carcinogenicity in man.Preclinical data on the CFC free propellant HFA-134a reveal no special hazard for humans based on conventional studies of safety pharmacology, repeated dose toxicity, genotoxicity, carcinogenic potential and toxicity to reproduction.

Norflurane(HFA-134a)EthanolanhydrousHydrochloric acid

Not applicable.

Prior to dispensing to the patient:Store in a refrigerator (2-8°C) (for a maximum of 15 months).After dispensing:Do not store above 30°C (for a maximum of 2 months).The canister contains a pressurised liquid. Do not expose to temperatures higher than 50°C. Do not pierce the canister.

The inhalation solution is contained in a pressurised aluminium container sealed with a metering valve and fitted into a polypropyleneplastic actuatorwhich incorporates a mouthpiece and is provided witha plastic protective cap. Each pack contains:1 pressurised container which provides 120 actuations

For pharmacies:Enter the date of dispensing to the patient on the pack. Ensure that there is a period of at least 2 months between the date of dispensing and the expiry date printed on the pack.