Ipratropium bromide
Atrodil is a pressurized inhalation solution. The medicine contains ipratropium bromide, which belongs to a group of medicines called bronchodilators. Atrodil is indicated as a bronchodilator for the maintenance treatment of bronchospastic conditions in chronic obstructive pulmonary disease (COPD), including chronic bronchitis and emphysema, and in bronchial asthma.
Before starting to use Atrodil, discuss it with your doctor or pharmacist. Be particularly careful when using Atrodil:
Tell your doctor or pharmacist about all the medicines you are taking now or have taken recently, as well as any medicines you plan to take. Some medicines may interact with Atrodil. This may change the effect of Atrodil or other medicines. In particular, inform your doctor if you are taking any of the following medicines:
If you are pregnant or breastfeeding, think you may be pregnant, or plan to have a child, consult your doctor or pharmacist before using this medicine. The safety of using this medicine during pregnancy has not been established. Atrodil should only be used during pregnancy if your doctor considers it necessary. It is not known whether ipratropium bromide passes into breast milk. Therefore, Atrodil should only be used in breastfeeding women if your doctor considers it necessary.
No studies have been conducted on the effect of the medicine on the ability to drive and use machines. If you experience dizziness or vision disturbances (blurred vision, seeing a rainbow-colored ring around a light source) while using Atrodil, you should refrain from performing these activities.
The medicine contains small amounts of ethanol (alcohol), less than 100 mg per dose. One metered dose (puff) contains 8.42 mg of anhydrous ethanol.
This medicine should always be used as directed by your doctor. If you are unsure, consult your doctor or pharmacist. Your doctor will adjust the dosage to your individual needs. If not otherwise instructed, use the medicine as follows:
Adults and children over 6 years of age
2 puffs at each use, 4 times a day, but no more than 12 puffs per day. Do not exceed the recommended daily dose. If the treatment does not bring significant improvement or if your condition worsens, consult your doctor to establish a new treatment plan. In case of sudden or severely worsening shortness of breath (breathing difficulties), contact your doctor immediately. In children, Atrodil aerosol should only be used under adult supervision.
To achieve the best treatment results, it is essential to use the inhalation aerosol correctly, as described below. If you have any doubts after reading the instructions, consult your doctor, pharmacist, or nurse.
Remove the protective cap from the mouthpiece, see Figure 1.
Shake the inhaler.
Holding the inhaler, take a deep breath, and then immediately…
Place the mouthpiece in your mouth, holding it with your lips. After starting a slow, deep breath through your mouth, press the aerosol container firmly as shown below to release a dose of Atrodil. Then continue breathing in. See Figure 2.
Figure 2
Hold your breath for a few seconds, or as long as possible without discomfort, and then remove the mouthpiece from your mouth and breathe out.
If you need to take more than one dose, wait at least one minute and then shake the inhaler again and repeat steps 3, 4, and 5.
After use, put the protective cap back on the mouthpiece. The container is not transparent. Therefore, you cannot see if it is empty. The inhaler contains 200 doses. After they are used up, a small amount of solution may still be left in the container. However, you should replace the inhaler with a new one, as further use may not ensure the delivery of the correct dose of the medicine.
The inhaler mouthpiece should be washed at least once a week. It is essential to keep it clean to ensure that the medicine does not accumulate on the mouthpiece walls and block the inhaler's use. To wash the inhaler mouthpiece, first remove the protective cap and remove the medicine container from the inhaler. Rinse the mouthpiece with warm water until all visible impurities are removed - see Figure 3.
Figure 3
After washing, shake off the water and let the mouthpiece air dry. Do not useany drying devices. When the mouthpiece is dry, put the medicine container and protective cap back on the inhaler - see Figure 4.
Figure 4
The plastic mouthpiece is specially designed for use with the Atrodil inhalation aerosol to ensure the delivery of the correct dose of the medicine each time. The mouthpiece should never be used with any other inhalation aerosol, and vice versa, Atrodil inhalation aerosol should not be used with any other mouthpiece than the one provided with this medicine. Since the container is under pressure, do not use force to open it, and do not expose it to temperatures above 50°C. If using the inhaler is difficult for you, Atrodil should be used with the AeroChamber inhalation chamber in such situations. You should read the instructions for use of the AeroChamber inhalation chamber provided with the packaging to get detailed information on its proper use.
If you accidentally take a higher dose of the medicine than recommended, consult your doctor immediately. Mild symptoms of ipratropium bromide overdose may occur, such as dryness of the mucous membrane of the mouth, vision disturbances, and increased heart rate.
If you miss a dose, take it as soon as possible. However, if it is almost time for the next dose, skip the missed dose and take the next dose at the scheduled time. Do not take a double dose to make up for the missed dose. Then continue with your regular dosing schedule.
If you stop using Atrodil, breathing difficulties may recur or worsen. Therefore, you should use Atrodil for as long as your doctor recommends. If you have any further questions about using this medicine, consult your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Atrodil may cause the following symptoms:
Frequently(occurring in less than 1 in 10 patients):
Less frequently(occurring in less than 1 in 100 patients):
Rarely(occurring in less than 1 in 1,000 patients):
If you experience any side effects, including those not listed in this leaflet, tell your doctor or pharmacist. Side effects can be reported directly to the Department of Adverse Reaction Monitoring of Medicinal Products, Medical Devices, and Biocidal Products
Al. Jerozolimskie 181C
02-222 Warsaw
Phone: +48 22 49 21 301
Fax: +48 22 49 21 309
Website: https://smz.ezdrowie.gov.pl
Side effects can also be reported to the marketing authorization holder. By reporting side effects, you can help provide more information on the safety of this medicine.
Keep the medicine out of sight and reach of children. Protect from direct sunlight and do not freeze. Do not store above 30°C. Do not puncture or burn, even if the container appears to be empty. Do not use this medicine after the expiry date stated on the packaging. The expiry date refers to the last day of the month. The inscription on the packaging after the abbreviation EXP means the expiry date, and after the abbreviation Lot means the batch number. Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
Aluminum container with an FCP (fluorocarbon polymer) layer and a 50 µl metering valve with a PP mouthpiece and PP closure, in a cardboard box. Each container is filled with 10 ml of a colorless, clear solution, equivalent to approximately 200 doses.
Polpharma S.A.
Pelplińska 19, 83-200 Starogard Gdański
phone: +48 22 364 61 01
Polpharma S.A.
Pelplińska 19, 83-200 Starogard Gdański
Detailed instructions for using the Atrodil inhalation aerosol are available by scanning the following QR code with your smartphone. The same information is also available on the website: www.instrukcjeatrodil.pl
(QR code)
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LABORATORIO ALDO-UNIÓN S.L. | |
Baronesa de Maldá, No 73 | |
08950 Esplugues de Llobregat (Barcelona) | |
Spain |
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