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ASTHALIN is a brand name for Albuterol (also known as Salbutamol). The medicine, its uses, side effects and dosage are the same regardless of brand.
Used for: Asthalin Inhaler is indicated in adults, adolescents and children aged 4 to 11 years. For babies and children under 4 years of age, see section 4.2 and 5.1. Asthalin Inhaler provides short-acting (4 to 6 hour) bronchodilation with fast onset (within 5 minutes) in reversible airways obstruction. It is particularly…
Verbatim from this product's MHRA label. Tap a section to expand.
Posology Adults For the relief of acute asthma symptoms including bronchospasm, wheezing, shortness of breath and attacks of acute dyspnoea, or the reversible component of airways obstruction, one inhalation (100 micrograms) may be administered as a single starting dose.
This may be increased to two inhalations if necessary. To prevent allergen or exercise induced symptoms, two inhalations should be taken 10- 15 minutes before challenge. For chronic therapy, two inhalations up to four times a day. Paediatric population Relief of acute bronchospasm The usual dosage for children under the age of 12 years: one inhalation (100 micrograms).
The dose may be increased to two inhalations if required.
Children aged 12 years and over:
Dose as per adult population. Prevention of allergen or exercise-induced bronchospasm The usual dosage for children under the age of 12 years: one inhalation (100 micrograms) before challenge or exertion. The dose may be increased to two inhalations if required.
Children aged 12 years and over:
Dose as per adult population Chronic therapy The usual dosage for children under the age of 12 years: up to two inhalations 4 times daily.
Children aged 12 years and over:
Dose as per adult population Elderly No special dosage recommendations are made for older patients. For all patients, the maximum recommended dose should not exceed 8 inhalations in 24 hours. Each repetitive dosing, inhalations should not usually be repeated more often than every 4 hours.
4). Asthalin Inhaler cannot be used with any spacing device at this time. If a patient needs a spacing device an alternative product, which can be used with such a device, will need to be prescribed instead of Asthalin Inhaler. Instructions for use 1.
The mouthpiece cover should be removed and the patient should check inside and outside to make sure that the mouthpiece is clean and that there is no dust, dirt or foreign objects. If it needs cleaning the instructions for cleaning outlined below should be followed.
If the inhaler gets very cold, patients should be instructed to take the metal canister out of the plastic actuator and warm it in their hands for a few minutes before use. Patients should never use anything else to warm it up. The inhaler should be shaken prior to use.
Adverse events are listed below by system organ class and frequency. Frequencies are defined as: very common (≥1/10), common (≥1/100 to <1/10), uncommon (≥1/1000 to <1/100), rare (≥1/10,000 to <1/1000), very rare (<1/10,000) including isolated reports and not known (cannot be estimated from the available data).
Very common and common events were generally determined from clinical trial data. Rare, very rare and unknown events were generally determined from spontaneous data.
Immune system disorders Very rare:
Hypersensitivity reactions including angioedema, urticaria, bronchospasm, hypotension and collapse.
Metabolism and nutrition disorders Rare:
Hypokalaemia (especially in combination with xanthine derivatives, corticosteroids and diuretics) increased serum lactate levels and acidosis lactic. 4) Vascular disorders Rare: Peripheral vasodilatation.
Respiratory, thoracic and mediastinal disorders Uncommon:
Throat irritation Very rare: Paradoxical bronchospasm (with an immediate increase in wheezing after dosing). (As with other inhalation therapy, paradoxical bronchospasm may occur immediately after dosing. If this occurs, salbutamol should be discontinued immediately and, if needed, an alternative therapy instituted).
Gastrointestinal disorders Uncommon:
Mouth irritation Rare: nausea, vomiting, dry mouth, sore mouth.
Skin and subcutaneous tissue disorders Very rare:
Pruritus Musculoskeletal and connective tissue disorders Uncommon: Myalgia, muscle cramps 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.
Patients should be instructed in the proper use of the inhaler and their technique checked, to ensure that aerosol actuation is synchronised with inspiration of breath for the optimum delivery of the active substance to the lungs. Patients should be warned that they may experience a different taste upon inhalation compared to their previous inhaler.
The management of asthma should normally follow a stepwise programme, and the patient’s response should be monitored clinically and by lung function tests. , inhaled corticosteroids) should be advised to continue taking their anti-inflammatory medication even when symptoms decrease, and they do not require Asthalin Inhaler Increasing use of short-acting bronchodilators, in particular ß2-agonists to control symptoms, indicates deterioration of asthma control and patients should be warned to seek medical advice as soon as possible.
Under these conditions, the patient’s therapy plan should be reassessed. Patients with persistent asthma should receive optimal anti-inflammatory basic therapy with corticosteroids. Sudden and progressive deterioration in asthma control is potentially life threatening and consideration should be given to increasing or starting oral and/or inhaler corticosteroid therapy.
In patients considered at risk, daily peak flow monitoring may be instituted. Overuse of short-acting beta-agonists may mask the progression of the underlying disease and contribute to deteriorating asthma control, leading to an increased risk of severe asthma exacerbations and mortality.
, daytime symptoms, night-time awakening, and activity limitation due to asthma) for proper treatment adjustment as these patients are at risk for overuse of salbutamol. The patient should be advised to seek medical advice if a previously effective dose ceases to be effective for at least three hours, and/or their asthma seems to be worsening.
The dosage or frequency of administration should only be increased on medical advice. Patients requiring long-term management with salbutamol device should be kept under regular surveillance. Salbutamol should be administered cautiously to patients with thyrotoxicosis, coronary insufficiency, hypertrophic obstructive cardiomyopathy, arterial hypertension, tachyarrhythmias, in concomitant use of cardiac glycosides or diabetes mellitus.
1. v. formulations of salbutamol are contraindicated for use in arresting uncomplicated premature labour and threatened abortion.
Not medical advice. Always read the patient information leaflet and follow your prescriber or pharmacist.
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2. The inhaler should be held upright with the thumb on the base, below the mouthpiece. Patients should breathe out as far as is comfortable and then. 3. Immediately place the mouthpiece in the mouth between the teeth, and close their lips around it.
Patients should be instructed to be careful not to bite the mouthpiece. 4. Breathe in slowly. Just after starting to breathe in through the mouth, patients should press down on the top of the inhaler to release a spray, while still breathing in steadily and deeply.
5. Patients should hold their breath, remove the inhaler from the mouth, and take their finger from the top of the inhaler. Patients should continue holding their breath for about 10 seconds, or as long as is comfortable, prior to breathing out slowly.
Patients should be instructed not to rush stages 3, 4 and 5. It is important that patients breathe in as slowly as possible just before using the inhaler. Patients should be instructed to try practising in front of a mirror for the first few times.
If patients see mist or spray coming from the inhaler or the sides of the mouth, they should start again from stage 2. 6. If patients are to take another spray, they should keep the inhaler upright, and wait about half a minute before repeating steps 2 to 5.
7. Once patients have finished using the inhaler, they should be instructed to always replace the mouthpiece cover to keep out dust and fluff and should make sure to replace the cover firmly and snap it into position. People with weak hands may find it easier to operate the inhaler with both hands, by putting both forefingers on the top of the inhaler, and both thumbs on the bottom below the mouthpiece.
For detailed instructions for use, the patient should be referred to the Patient Information Leaflet included in each pack, with specific reference to the pictograms which accompany the instructions for use. The inhaler should be cleaned at least once a week as described below, as it can become blocked, which will affect the way in which the inhaler works and will affect the amount of salbutamol which is inhaled.
1. First remove the metal can from the plastic actuator and take off the mouthpiece cover. 2. Rinse the plastic actuator, mouthpiece and mouthpiece cover in tap water; DO NOT place the metal can into water or clean the can using water.
Make sure the water runs through the actuator from both ends to ensure that the actuator orifice is clear and not blocked. 3. The plastic components (actuator and mouthpiece cover) should be placed in a warm place to dry thoroughly before re-assembling the inhaler.
Avoid drying near direct or excessive heat. The patient should follow the cleaning instructions described in the Patient Information Leaflet carefully in order to ensure that the inhaler continues to work properly. At first use of a new inhaler, or after a period when the inhaler has not been used (7 days or more), the inhaler should be shaken well and two sprays should be discharged prior to use, to prime the inhaler.
Method of Administration:
For inhalation use.
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Potentially serious hypokalaemia has been reported in patients taking β2 agonist therapy mainly from parenteral and nebulised administration. Particular caution is advised in acute severe asthma as this effect may be potentiated by concomitant treatment with xanthine derivatives, steroids, diuretics, long-term laxatives and by hypoxia.
Extra care should therefore be taken if β2-agonist are used in these groups of patients and it is recommended that serum potassium levels should be monitored in such situations. Care should be taken when treating acute asthma attacks or exacerbation of severe asthma as increased serum lactate levels, and rarely, lactic acidosis have been reported after high doses of salbutamol have been used in emergency situations.
9). Unwanted stimulation of cardiac adrenoceptors can occur in patients taking β2 agonist therapy. Cardiovascular effects may be seen with sympathomimetic drugs, including salbutamol. There is some evidence from post-marketing data and published literature of rare occurrences of myocardial ischaemia associated with ß-agonists.
g. ischaemic heart disease, arrhythmias or severe heart failure) who are receiving salbutamol should be warned to seek medical advice if they experience chest pain or other symptoms of worsening heart disease. Attention should be paid to assessment of symptoms such as dyspnoea and chest pain, as they may be either respiratory or cardiac in origin.
As with other inhalation therapy, the potential for paradoxical bronchospasm should be considered. If this occurs, the salbutamol should be discontinued immediately and an alternative presentation or a different fast acting inhaled bronchodilator given.
Solutions which are not of neutral pH may rarely cause paradoxical bronchospam in some patients. Salbutamol and non-selective ß-antagonists such as propranolol should not usually be prescribed together. In common with other ß-agonists, salbutamol can induce reversible metabolic changes such as increased blood glucose levels.
Patients with diabetes may be unable to compensate for the increase in blood glucose and the development of ketoacidosis has been reported. Concurrent administration of glucocorticoids can exaggerate this effect. Severe exacerbations of asthma must be treated in the normal way.