


Ask a doctor about a prescription for Ketotifen Hasco
Ketotifen
Ketotifen HASCO, syrup is an antiallergic (antihistamine) medicine containing the active substance ketotifen. Its action involves inhibiting the release of allergic reaction mediators. It non-competitively blocks histamine H receptors, meaning that an increase in histamine concentration does not weaken the action of the medicine.
It inhibits the development of bronchial hyperreactivity, which manifests as a decrease in the frequency and severity of asthma attacks.
In the prevention of bronchial asthma, achieving full therapeutic effect may require treatment lasting several weeks.
Ketotifen HASCO is used in the prevention of bronchial asthma and in the symptomatic treatment of allergic rhinitis and allergic conjunctivitis (seasonal and perennial).
The medicine is not effective in interrupting a bronchial asthma attack.
Tell your doctor or pharmacist about all medicines you are taking, or have recently taken, and about medicines you plan to take.
Ketotifen may enhance the effect of medicines that depress the activity of the central nervous system (sedatives, hypnotics) and antihistamines (e.g. some antiallergic medicines).
Concomitant use with oral antidiabetic medicines may cause a decrease in the number of platelets (see section "When not to take Ketotifen HASCO").
Ketotifen HASCO may enhance the effect of alcohol, so do not drink alcohol while taking this medicine.
Take the medicine with a meal.
If you are pregnant or breastfeeding, think you may be pregnant or plan to have a child, consult your doctor or pharmacist before taking this medicine.
Ketotifen HASCO may be used during pregnancy only if absolutely necessary.
Due to the passage of ketotifen into breast milk, do not take Ketotifen HASCO if you are breastfeeding.
During the first few days of taking the medicine, reactions may be slowed down, so do not drive or operate machinery until you know how the medicine affects you.
If you have been diagnosed with intolerance to some sugars, consult your doctor before taking the medicine.
The medicine contains 2250 mg of sorbitol in 5 ml of syrup.
Sorbitol is a source of fructose. If you have been diagnosed with intolerance to some sugars or have been diagnosed with hereditary fructose intolerance, a rare genetic disorder in which the body does not break down fructose, consult your doctor before taking the medicine or giving it to your child.
Sorbitol may cause gastrointestinal discomfort and may have a mild laxative effect.
The medicine may cause allergic reactions (possible late reactions).
The medicine contains 100 mg of propylene glycol in 5 ml of syrup.
Sodium comes from the excipient disodium phosphate dodecahydrate. The medicine contains less than 1 mmol (23 mg) of sodium in 5 ml of syrup, which means the medicine is considered "sodium-free".
Always take this medicine exactly as your doctor has told you. If you are not sure, ask your doctor.
Take the medicine orally.
Recommended dose
Children from 7 months to 3 years of age – 0.25 ml of syrup (0.05 mg of ketotifen)/kg of body weight twice a day, in the morning and evening, with a meal.
Do not take more than 2.5 ml of syrup twice a day.
Children over 3 years of age and adults – 5 ml of syrup (1 mg of ketotifen) twice a day, in the morning and evening, with a meal. In patients sensitive to the sedative effect of ketotifen, the doctor may recommend gradual dose increase over the first week of treatment, starting with 2.5 ml of syrup (0.5 mg of ketotifen) twice a day, and then increasing the dose to the full therapeutic dose.
A measuring cup is attached to the packaging to measure the appropriate amount of syrup.
If you take more than the recommended dose, contact your doctor or pharmacist immediately.
The main symptoms of overdose are dizziness, excessive sedation and drowsiness, confusion and disorientation, rapid heartbeat, low blood pressure, circulatory and respiratory failure, coma, and especially in children, hyperactivity or seizures.
Apply symptomatic treatment. If the medicine was taken within the last hour, induce vomiting or perform gastric lavage. Activated charcoal may be beneficial. In case of excitement or seizures, short-acting barbiturates or benzodiazepines can be administered, in case of coma, controlled respiration and cardiovascular supportive therapy can be applied. If necessary, apply symptomatic treatment and monitor cardiovascular function.
Do not take a double dose to make up for a forgotten dose .
Sudden discontinuation of ketotifen may cause a relapse of asthma symptoms. If it is necessary to discontinue the medicine, do so gradually, over a period of 2 to 4 weeks, after consulting your doctor.
If you have any further questions about the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Frequent side effects(in 1 to 10 patients out of 100):
Uncommon side effects(in 1 to 10 patients out of 1000):
Rare side effects(in 1 to 10 patients out of 10,000):
Very rare side effects(in less than 1 patient out of 10,000):
Sedation, dry mouth, and dizziness may occur at the beginning of treatment, but usually disappear during further treatment.
If you experience any side effects, including any not listed in this leaflet, tell your doctor or pharmacist. Side effects can be reported directly to the Department of Monitoring of Adverse Reactions to Medicinal Products, Office for Registration of Medicinal Products, Medical Devices and Biocidal Products
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, you can help provide more information on the safety of this medicine.
Store in the original packaging, at a temperature not exceeding 25°C. 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 packaging. The expiry date refers to the last day of the month.
Do not throw away medicines via wastewater or household waste. Ask your pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
Bottle containing 100 ml of syrup, in a cardboard box.
Syrup with a strawberry flavor.
"PRZEDSIĘBIORSTWO PRODUKCJI FARMACEUTYCZNEJ HASCO-LEK" S.A.
51-131 Wrocław, ul. Żmigrodzka 242 E
Information about the medicine
tel.: + 48 22 742 00 22
e-mail: [email protected]
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Discuss dosage, side effects, interactions, contraindications, and prescription renewal for Ketotifen Hasco – subject to medical assessment and local rules.