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Drug Details

Atimos Modulite 12 micrograms inhaler

• Drug Class Description
  Adrenergics, inhalants; selective ?2-adrenoreceptor agonists - ATC code: R03A C13
• Generic Name
  formoterol fumarate dihydrate
• Presentation
  Pressurised inhalation solution
• Description
  Each metered dose contains 12 micrograms of formoterol fumarate dihydrate. This corresponds to a delivered dose of 10.1 micrograms.
• Indications
  

  For the long-term symptomatic treatment of persistent, moderate to severe asthma in patients requiring regular bronchodilator therapy in combination with long-term anti-inflammatory therapy (inhaled and / or oral glucocorticoids).

  Glucocorticoid therapy should be continued on a regular basis.

  Atimos is indicated for the relief of broncho-obstructive symptoms in patients with chronic obstructive pulmonary disease (COPD).

   

   

   

• Adult Dosage
  

  The dosage depends on the type and severity of disease.

  The following dosages are recommended for adults, including elderly patients, and adolescents aged 12 years and above:

  Asthma

  Adults and adolescents aged 12 years and above:

  Usually one actuation in the morning and evening (24 micrograms of formoterol fumarate dihydrate per day). In severe cases, up to a maximum of two actuations in the morning and evening (48 micrograms of formoterol fumarate dihydrate per day).

  The maximum daily dose is 4 actuations (48 micrograms of formoterol fumarate dihydrate).

  Chronic Obstructive Pulmonary Disease (COPD)

  Adults (aged 18 years and above)

  The usual dose is one actuation twice daily (one in the morning and one in the evening, 24 micrograms formoterol fumarate dihydrate per day).

  The daily dose for regular use should not exceed 2 inhalations. If required, additional inhalations above those prescribed for regular therapy may be used for relief of symptoms, up to a maximum total daily dose of 4 inhalations (regular plus required). More than 2 inhalations should not be taken on any single occasion.

  Patients should not use the inhaler beyond three months from the date of dispensing by the pharmacist.

  Although Atimos Modulite has a rapid onset of action, long-acting inhaled bronchodilators should be used for maintenance bronchodilator therapy.

  Atimos Modulite is not intended to relieve acute asthma attacks.

  In the event of an acute attack, a short-acting β₂-agonist should be used.

  Patients should be advised not to stop or change their steroid therapy when Atimos Modulite is introduced.

  If the symptoms persist or worsen, or if the recommended dose of Atimos Modulite fails to control symptoms (maintain effective relief), this is usually an indication of a worsening of the underlying condition.

  Renal or hepatic impairment

  There is no theoretical reason to suggest that Atimos Modulite dosage requires adjustment in patients with renal or hepatic impairment, however, no clinical data have been generated to support its use in these groups.

  Instructions for Use

  To ensure proper administration of the drug, the patient should be shown how to use the inhaler by a physician or other health professional.

  Before the first use of the inhaler and after 3 days or more of non-use one actuation should be discharged in the air in order to ensure a faultless function. As far as possible patients should stand or sit in an upright position when discharging the inhaler.

  1. Remove the protecting cap from the mouthpiece.

  2. Breathe out as deeply as possible.

  3. Hold the canister vertically with its body upwards and put the mouthpiece between well-closed lips.

  4. Deeply inspire through the mouth and, at the same time, press on the upper part of the inhaler to actuate the puff.

  5. Hold breath as long as possible without any effort and, finally, remove the inhaler from the mouth.

  Should a further puff be inhaled, the inhaler should be kept in a vertical position for about half minute, then steps 2 to 5 repeated.

  After use, the mouthpiece should be closed with the protecting cap.

  IMPORTANT: Steps 2 to 4 should not be performed too quickly.

  Should a part of gas be sprayed from the upper part of the inhaler or from the mouth side, operations should be performed again starting from step 2.

  For patients with weak hand-grip it could be easier to hold the inhaler with both hands. Therefore, the upper part of the inhaler is held with both index fingers and its lower part is held with both thumbs.

  The use of a spacer device with the inhaler is usually recommended for patients who have difficulty in coordinating inhalation with actuation, however, no clinical data are available for Atimos Modulite with spacers.

• Child Dosage
  

  Asthma

  Children younger than 12 years of age:

  The safety and efficacy of Atimos Modulite in children younger than 12 years of age has not been established yet, therefore Atimos Modulite should not be used in children.

   

• Elderly Dosage
  

   

   

• Contra Indications
  

  Known hypersensitivity to the active substance or to any of the excipients.

• Special Precautions
  

  Atimos Modulite should not be used (and is not sufficient) as the first treatment for asthma.

  Although Atimos may be introduced as add-on therapy when inhaled corticosteroids do not provide adequate control of asthma symptoms, patients should not be initiated on Atimos during an acute severe asthma exacerbation, or if they have significantly worsening or acutely deteriorating asthma.

  Serious asthma-related adverse events and exacerbations may occur during treatment with Atimos. Patients should be asked to continue treatment but to seek medical advice if asthma symptoms remain uncontrolled or worsen after initiation of Atimos.

  Atimos Modulite should be used strictly in accordance with the dosage recommendations. Once asthma symptoms are controlled, consideration may be given to gradually reducing the dose of Atimos. Regular review of patients as treatment is stepped down is important. The lowest effective dose of Atimos should be used.

  A sudden and progressive deterioration of the asthmatic disorder can be life-threatening and requires immediate medical intervention. Considerably exceeding the prescribed individual doses or the total daily dose can be hazardous due to the effects on the heart (cardiac arrhythmia, rise in blood pressure), in combination with changes in the salt concentrations in body fluids (electrolyte shifts), and must therefore be avoided.

  Concomitant conditions

  Atimos Modulite should only be used with caution and under strict conditions of indication in patients with third degree atrioventricular block, idiopathic subvalvular aortic stenosis, hypertrophic obstructive cardiomyopathy, QT-interval prolongation, eg. congenital or drug-induced (QTc > 0.44 seconds), thyrotoxicosis, severe heart disease, especially acute myocardial infarction, coronary heart disease, congestive heart failure, occlusive vascular diseases, especially arteriosclerosis, arterial hypertension and aneurysm, hyperthyreosis, refractory diabetes mellitus, phaeochromocytoma.

  Atimos Modulite may only be used with special precautions (eg. monitoring) in patients with tachycardic arrhythmia (accelerated and / or irregular heart beat). The inhalation of high doses of formoterol may cause a rise in blood sugar levels. This parameter should therefore be closely monitored in diabetics. If anaesthesia with halogenated anaesthetics is planned, it should be ensured that Atimos Modulite is not administered for at least 12 hours before the start of anaesthesia.

  Paradoxical bronchospasm

  As with every inhalation therapy, paradoxical bronchospasm can occur in rare cases. In such cases the medicinal product should be discontinued immediately and the therapeutic program should be modified by the physician.

  Hypokalaemia

  There is evidence that under formoterol therapy the decrease of blood potassium levels is higher than during treatment with short acting β₂-sympathomimetics (eg. salbutamol). Therefore potassium levels have to be regularly monitored particularly in patients with low basic potassium values or peculiar risks for decreased blood potassium levels. The monitoring should also be conducted if no decreased levels occurred under previous treatment with short acting β₂-sympathomimetics. Where applicable, potassium has to be substituted.

  The hypokalaemia may be particularly distinctive in patients with severe asthma receiving concomitant treatment with theophylline, glucocorticoids and/or diuretics. Due to decreased serum potassium levels the effect of digitalis containing medicinal products is enhanced.

  As the risk related to hypokalaemia is potentiated by hypoxia care should be taken in patients with acute severe asthma.

   

• Interactions
  

  Drugs such as quinidine, disopyramide, procainamide, phenothiazines, antihistamines and tricyclic antidepressants may be associated both with QT-interval prolongations and an increased risk of ventricular arrhythmia.

  Concomitant administration of other sympathomimetic agents may potentiate the undesirable effects of Atimos Modulite.

  The simultaneous use of formoterol and theophylline can result in mutual potentiation of effects, and there is also the likelihood of increased undesirable effects such as cardiac dysrhythmia. Compounds which themselves potentiate sympathomimetic effects, such as L-dopa, L-thyroxine, oxytocin or alcohol, can also affect cardiovascular regulation when taken at the same time as formoterol.

  Administration of Atimos Modulite to patients being treated with monoamine oxidase inhibitors or tricyclic antidepressants should be performed with caution, since the action of β₂-adrenergic stimulants on the cardiovascular system may be potentiated.

  Concomitant treatment with xanthine derivatives, steroids, or diuretics may potentiate a possible hypokalaemic effect of β₂-agonists. Hypokalaemia may increase susceptibility to cardiac arrhythmias in patients treated with digitalis.

  β-adrenergic blockers may weaken or antagonise the effect of Atimos Modulite. Therefore, Atimos Modulite should not be given together with β-adrenergic blockers (including eye drops) unless there are compelling reasons for their use.

   

• Adverse Drug Reactions
  

  The frequency of Adverse Reactions has been classified as follows:

  Common ( 1/100 < 1/10 )

  Uncommon ( 1/1,000 < 1/100 )

  Rare ( 1/10,000 < 1/1,000 )

  Very rare ( < 1/10,000 )

  Blood and lymphatic system disorders

  Very rare: thrombopenia

  Metabolism and nutrition disorders

  Uncommon: hypokalaemia, hyperglycaemia

  Psychiatric disorders

  Uncommon: restlessness

  Very rare: abnormal behaviour, sleep disorders, hallucinations

  Nervous system disorders

  Common: tremor, headache

  Uncommon: dizziness, dysgeusia

  CNS stimulating effects have been sporadically reported following inhalation of β₂- sympathomimetics, manifesting as hyperexcitability. These effects were mainly observed in children up to 12 years of age.

  Cardiac disorders

  Common: palpitations

  Uncommon: tachycardia, tachyarrhythmia

  Rare: ventricular extrasystoles, angina pectoris

  Very rare: atrial fibrillation

  Respiratory, Thoracic and Mediastinal Disorders

  Common: cough

  Uncommon: throat irritation

  Rare: bronchospasm paradoxical

  Very rare: dyspnoea, exacerbation of asthma

  Gastrointestinal disorders

  Uncommon: nausea

  Skin and Subcutaneous tissue disorders

  Uncommon: pruritus, rash, hyperhidrosis

  Rare: urticaria, angioedema

  Musculoskeletal and connective tissue disorders

  Uncommon: muscle cramps, myalgia

  Renal and urinary disorders

  Rare: Nephritis

  General disorders and administration site conditions

  Very rares: oedema peripheral

  Investigations

  Uncommon: blood insulin increased, free fatty acids increased, blood ketone body increased

  Rare: blood pressure increased, blood pressure decreased

  Tremor, nausea, dysgeusia, throat irritation, hyperhidrosis, restlessness, headache, dizziness and muscle cramps may resolve spontaneously within one to two weeks of continued treatment.