


Ask a doctor about a prescription for Cetip
Cetirizine Dihydrochloride
This medicine should always be taken exactly as described in the package leaflet or as directed by a doctor, pharmacist, or nurse.
The active substance of Cetip is cetirizine dihydrochloride, which belongs to a group of medicines called antihistamines.
This medicine is used to treat adults and children aged 6 years and above with hay fever (seasonal allergic rhinitis), perennial allergic rhinitis (persistent allergic rhinitis), and urticaria (hives).
Cetip relieves the symptoms associated with these conditions, including itching, sneezing, runny or itchy nose, hives, and itchy or watery eyes.
If after 2 days there is no improvement or you feel worse, you should contact a doctor.
Before taking Cetip, tell your doctor, pharmacist, or nurse.
No interactions have been observed between alcohol (at a blood concentration of 0.5 mg/ml, corresponding to a blood alcohol level of about 0.5 per mille) and cetirizine used at the recommended dose. However, as with all antihistamines, it is recommended to avoid taking alcohol while taking this medicine.
Good oral hygiene is recommended during long-term treatment with this medicine, as there is an increased risk of tooth or gum infections.
as these may interact with Cetip.
Examples of medicines that may affect cetirizine include:
Food does not affect the absorption of cetirizine.
If you are pregnant, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.
Do not take this medicine if you are breastfeeding.
Before taking any medicine, consult your doctor or pharmacist.
A full list of excipients is provided in section 6.
Always take this medicine exactly as described in the package leaflet or as directed by your doctor, pharmacist, or nurse. If you are unsure, consult your doctor, pharmacist, or nurse.
Do not take more than one tablet per day. If after a few days there is no improvement, consult your doctor.
Recommended dose:
The tablet can be divided into equal doses.
Patients with liver or kidney impairment:the recommended dose is 5 mg (half a tablet) once daily. Consult your doctor before taking this medicine.
If you accidentally take too many tablets, contact your doctor or the nearest hospital emergency department immediately, even if you feel fine.
Drowsiness or dizziness may occur; do not drive or operate machinery.
Take this medicine in its original packaging to show the doctor what you have taken.
If you forget to take a tablet, take it as soon as you remember, provided that it is at least 24 hours before the next dose.
Do not take a double dose to make up for a forgotten dose.
If you have any further questions on the use of this product, ask your doctor, pharmacist, or nurse.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
The doctor will assess the severity of these symptoms and decide on any further necessary action.
During post-marketing experience, the following side effects have been reported.
The frequency of these side effects is defined as follows:
common (affects less than 1 in 10 people but more than 1 in 100 people),
uncommon (affects less than 1 in 100 people but more than 1 in 1,000 people),
rare (affects less than 1 in 1,000 people but more than 1 in 10,000 people),
very rare (affects less than 1 in 10,000 people).
There have also been reports of memory loss and (or) memory disturbances.
In very rare cases, suicidal thoughts have been reported. If you experience any of these side effects, stop taking the tablets and consult your doctor.
If you experience any side effects, including those not listed in the package leaflet, tell your doctor or pharmacist.
Side effects can be reported directly to the Department for Monitoring of Adverse Reactions to Medicinal Products, Urzad Rejestracji Produktow Leczniczych, Wyrobów Medycznych i Produktow 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, you can help provide more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date stated on the carton after EXP. The expiry date refers to the last day of that month.
No special precautions for storage are necessary.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
If you have previously been diagnosed with intolerance to some sugars, consult your doctor before taking this medicine.
Milapharm Sp. z o.o.
pl. Gen. Józefa Hallera 5/14A
03-464 Warsaw
Phone: (+48) 699 711 147
Medicofarma S.A.
ul. Tarnobrzeska 13
26-613 Radom
PharmaS d.o.o.
Industrijska cesta 5
44317 Potok, Popovača
Croatia
DE:
Cetirizine Dihydrochloride IPCA 10 mg Film-Coated Tablets
PL:
Cetip
PT:
Zarec 10 mg Film-Coated Tablets
The best alternatives with the same active ingredient and therapeutic effect.
Discuss dosage, side effects, interactions, contraindications, and prescription renewal for Cetip – subject to medical assessment and local rules.