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 over 6 years of age.
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, and if side effects occur, the medicine should be discontinued and the doctor consulted.
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, 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 difficult. The doctor may recommend taking 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 some sugars, they should consult their doctor before taking the medicine.
This medicine should always be taken according to the doctor's recommendations. In case of doubts, consult a doctor or pharmacist. The following doses are usually taken: Adults and children over 12 years of age 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 a 6-hour interval should be maintained 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 taken if there is no response to lower doses. Elderly patients and those with hypersensitivity 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 between 6 and 12 years of age Initial dose: 2 mg up to three to four times a day. If necessary, the initial dose can be repeated, but at least a 6-hour interval should be maintained 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.
A double dose should not be taken 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 immediately consult their doctor. Such symptoms occur very rarely.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 diseases such as angina). If such symptoms occur, the patient should not suddenly stop taking the medicine but should consult their doctor as soon as possible. Frequency not known (frequency cannot be estimated from available data):
If any side effects occur, including any side effects not listed in this leaflet, the patient should inform their doctor, pharmacist, or nurse. Side effects can be reported directly to the Department of Medicinal Product Monitoring, Urząd Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych, Al. Jerozolimskie 181C, 02-222 Warsaw, Tel.: +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, more information can be collected on the safety of the medicine.
Store at a temperature below 25°C. Store blisters in the outer packaging to protect from light. The medicine should be stored out of the reach and sight 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 indicates the expiry date, and after the abbreviation Lot/LOT, it indicates 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 are white, round, flat tablets with a notch on one side and the letter "S" below it. The package contains 30 tablets in 2 blisters of 15 tablets each, placed in a cardboard box. Salbutamol WZF 4 mg are white, round, flat tablets with a notch on one side, the number "4" above it, and the letter "S" below it. The package contains 25 tablets in 1 blister, placed in a cardboard box.
Zakłady Farmaceutyczne POLPHARMA S.A., ul. Pelplińska 19, 83-200 Starogard Gdański, tel. +48 22 364 61 01
Zakłady Farmaceutyczne POLPHARMA S.A., Oddział Produkcyjny w Nowej Dębie, ul. Metalowca 2, 39-460 Nowa Dęba, Date of last revision of the leaflet:December 2024
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