Salbutamol
Salbutamol WZF belongs to a group of medicines called beta-adrenergic agonists. It causes relaxation of the bronchial muscles and airways.
Salbutamol WZF is used:
Salbutamol WZF is indicated for use in adults and children aged 6 years and older.
Before starting treatment with Salbutamol WZF, the patient should discuss it with their doctor or pharmacist.
When using high doses of salbutamol, caution should be exercised. If side effects occur, discontinue the medicine and consult a doctor.
The patient should inform their doctor or pharmacist about all medicines they are currently taking or have recently taken, as well as any medicines they plan to take.
In the event of a planned surgical procedure with general anesthesia, the doctor should discontinue Salbutamol WZF 6 hours before the procedure, if possible, to protect the patient from side effects (e.g., irregular heartbeat).
If the patient is pregnant or breastfeeding, or thinks they may be pregnant, or plans to have a child, they should consult their doctor before taking this medicine.
The medicine can inhibit uterine contractions and may make delivery more difficult.
The doctor may recommend using Salbutamol WZF during pregnancy only if the benefits to the mother outweigh the potential risks to the fetus.
Salbutamol is likely to pass into breast milk. If the medicine is necessary, the patient should stop breastfeeding.
There is no data on the effect of salbutamol on driving or operating machinery.
If the patient has previously been diagnosed with intolerance to certain sugars, they should consult their doctor before taking the medicine.
This medicine should always be taken as directed by the doctor. If there are any doubts, the patient should consult their doctor or pharmacist.
Usually, the following doses are used:
Adults and children over 12 years old
Initial dose: 2 mg to 4 mg, up to three to four times a day.
If necessary, the initial dose can be repeated, but at least 6 hours should be allowed between doses. If the effect of these doses is insufficient, they can be gradually increased, but the dose should not exceed 8 mg four times a day.
If side effects occur during dose increases, the medicine should be discontinued.
Single doses greater than 4 mg should only be used if there is no response to lower doses.
Elderly patients and those with increased sensitivity to this medicine or similar medicines:
Initial dose: 2 mg up to four times a day.
If the effect is insufficient, the doctor may increase the dose to 8 mg three to four times a day.
The maximum daily dose of Salbutamol WZF is 32 mg.
Children aged 6 to 12 years
Initial dose: 2 mg up to three to four times a day. If necessary, the initial dose can be repeated, but at least 6 hours should be allowed between doses.
If the effect is insufficient, the dose can be gradually increased, but it should not exceed 6 mg four times a day (24 mg). If side effects occur during dose increases, the medicine should be discontinued.
After taking a higher dose than recommended, the following may occur: chest pain, convulsions, increased or decreased blood pressure, rapid or irregular heartbeat, nervousness, headache, dizziness, tremors, dry mouth, nausea, and insomnia. The patient should stop taking the medicine and consult their doctor immediately.
If it has been less than an hour since taking the medicine, the doctor may perform gastric lavage. If necessary, the doctor will provide appropriate treatment.
The patient should not take a double dose to make up for a missed dose.
If the patient has any further doubts about taking this medicine, they should consult their doctor or pharmacist.
Like all medicines, Salbutamol WZF can cause side effects, although not everybody gets them.
If the patient experiences the first symptoms of hypersensitivity (e.g., facial swelling, lip swelling, tongue swelling, throat swelling, causing difficulty breathing or swallowing, bronchospasm, acute circulatory failure), they should contact their doctor immediately. Such symptoms are very rare.
Very common (more than 1 in 10 people):
Common (less than 1 in 10 people):
Uncommon (less than 1 in 100 people):
Rare (less than 1 in 1,000 people):
Very rare (less than 1 in 10,000 people):
Chest pain (related to heart disease such as angina) may occur in some people. If such symptoms occur, the patient should not stop taking the medicine abruptly but should consult their doctor as soon as possible.
Frequency not known (frequency cannot be estimated from the available data):
If the patient experiences any side effects, including any side effects not listed in this leaflet, they should inform their doctor, pharmacist, or nurse. Side effects can be reported directly to the Department of Drug Safety Monitoring of the Office for Registration 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.
Reporting side effects will help gather more information on the safety of the medicine.
Store in a temperature below 25°C.
Store blisters in the outer packaging to protect from light.
Keep the medicine out of the sight and reach of children.
Do not use this medicine after the expiry date stated on the carton and blister after: EXP.
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/LOT means the batch number.
Medicines should not be disposed of via wastewater or household waste. The patient should ask their pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
Salbutamol WZF 2 mg is a white, round, flat tablet with a notch on one side and the letter "S" below it.
The packaging contains 30 tablets in 2 blisters of 15 tablets each, placed in a cardboard box.
Salbutamol WZF 4 mg is a white, round, flat tablet with a notch and the number "4" above it and the letter "S" below it.
The packaging contains 25 tablets in 1 blister, placed in a cardboard box.
Zakłady Farmaceutyczne POLPHARMA S.A.
ul. Pelplińska 19, 83-200 Starogard Gdański
phone: +48 22 364 61 01
Zakłady Farmaceutyczne POLPHARMA S.A.
Production Plant in Nowa Dęba
ul. Metalowca 2, 39-460 Nowa Dęba
Date of the last update of the leaflet:December 2024
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