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# On 2024-Apr-28 aproximate price on "ZYRTEC TBL 10MG N30" in Riga city, Latvia is:
9.53€ 10.21$ 8.16£ 1101Rub 111.6SEK 41PLN 38.88₪
Maximum allowed state defined price ( from ZVA webpage) Euro:
* This table was compiled fully automatically, independently from any advertisers, transparently and without any modification relaying the open offers available on the mentioned dates.Only the distribution of over-the-counter remedies through the website is permitted in Latvia in accordance with national laws and regulations.
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ZYRTEC 10MG N10
Package leaflet: Information for the user
Zyrtec 10 mg film-coated tablets
Cetirizine dihydrochloride
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Always take this medicine exactly as described in this leaflet, or as your doctor or pharmacist have told you. - Keep this leaflet. You may need to read it again. - Ask your pharmacist if you need more information or advice. - If you get any side effects, talk to your doctor or pharmacist.This includes side effects not listed in this leaflet. See section 4. - You must talk to a doctor if you do not feel better or if you feel worse after 3 days.
What is in this leaflet:
1. What Zyrtec is and what it is used for 2. What you need to know before you take Zyrtec 3. How to take Zyrtec 4. Possible side effects 5. How to store Zyrtec 6. Content of the pack and further information
1. What Zyrtec is and what it is used for
Cetirizine dihydrochloride is the active ingredient of Zyrtec. Zyrtec is an antiallergic medication. In adults and children aged 6 years and above, Zyrtec 10 mg film-coated tablets are indicated - for the relief of nasal and ocular symptoms of seasonal and perennial allergic rhinitis. - for the relief of urticaria.
2. What you need to know before you take Zyrtec Do not take Zyrtec
- if you have a severe kidney disease (severe renal failure with creatinine clearance below 10 ml/min); - if you are allergic to cetirizine dihydrochloride, to any of the other ingredients (listed in section 6), to hydroxyzine or to piperazine derivatives (closely related active ingredients of other medicines).
Warning and precautions
Ask your doctor or pharmacist for advice before taking Zyrtec. If you are a patient with renal insufficiency, please ask your doctor for advice; if necessary, you will take a lower dose. The new dose will be determined by your doctor. If you have problems passing urine (like spinal cord problems or prostate or bladder problems), please ask your doctor for advice. If you are an epileptic patient or a patient at risk of convulsions, you should ask your doctor for advice. No clinically significant interactions have been observed between alcohol (at the blood level of 0.5 per mille (g/l) corresponding to one glass of wine) and cetirizine used at the recommended doses. However, there are no data available on the safety when higher doses of cetirizine and alcohol are taken together. Therefore, as it is the case with all antihistamines, it is recommended to avoid taking Zyrtec with alcohol. If you are scheduled for allergy testing, ask your doctor if you should stop taking Zyrtec for several days before testing. This medicine may affect your allergy test results.
Children
Do not give this medicine to children below the age of 6 years because the tablet formulation does not allow the necessary dose adjustments.
Other medicines and Zyrtec
Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.
Zyrtec with food and drink
Food does not affect absorption of Zyrtec.
Pregnancy and breast-feeding
If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor for advice before taking this medicine. Zyrtec should be avoided in pregnant women. Accidental use of the drug by a pregnant woman should not produce any harmful effects on the foetus. Nevertheless, the medicine should only be administered if necessary and after medical advice. Cetirizine passes into breast milk. Therefore, you should not take Zyrtec during breast-feeding unless you have contacted a doctor.
Driving and using machines
Clinical studies have produced no evidence of impaired attention, alertness and driving capabilities after taking Zyrtec at the recommended dose. You should closely observe your response to the drug after you have taken Zyrtec if you are intending to drive, engage in potentially hazardous activities or operate machinery. You should not exceed the recommended dose. Zyrtec film-coated tablets contains lactose; if you have been told by your doctor that you have an intolerance to some sugars, please contact your doctor before taking this medicinal product.
3. How to take Zyrtec
Always take this medicine exactly as described in this leaflet or as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are not sure. The tablets need to be swallowed with a glass of liquid. The tablet can be divided into 2 equal doses.
Adults and adolescents above 12 years old:
The recommended dose is 10 mg once daily as 1 tablet.
Use in children between 6 and 12 years old:
The recommended dose is 5 mg twice daily as a half tablet twice daily.
Patients with renal impairment
Patients with moderate renal impairment are recommended to take 5 mg once daily. If you suffer from severe kidney disease, please contact your doctor or pharmacist who may adjust the dose accordingly. If your child suffers from kidney disease, please contact your doctor or pharmacist who may adjust the dose according to your child’s needs. If you feel that the effect of Zyrtec is too weak or too strong, please consult your doctor.
Duration of treatment
The duration of treatment depends on the type, duration and course of your complaints. Please ask your doctor or pharmacist for advice.
If you take more Zyrtec than you should
If you think you have taken an overdose of Zyrtec please inform your doctor. Your doctor will then decide what measures, if any, should be taken. After an overdose, the side effects described below may occur with increased intensity. Adverse effects such as confusion, diarrhoea, dizziness, tiredness, headache, ailing, dilating of pupil, itching, restlessness, sedation, somnolence, stupor, abnormal rapid heart rate, tremors and urinary retention have been reported.
If you forget to take Zyrtec
Do not take a double dose to make up for a forgotten dose.
If you stop taking Zyrtec
Rarely, pruritus (intense itching) and/or urticaria may return if you stop taking Zyrtec. If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
4. Possible side effects
Like all medicines, this medicine can cause side effects, although not everybody gets them.
The following side effects are rare or very rare, but you must stop taking the medicine and speak to your doctor straight away if you notice them:
- Allergic reactions, including severe reactions and angioedema (serious allergic reaction which causes swelling of the face or throat). These reactions may start soon after you first take the medicine, or it might start later. Common side effects (may affect up to 1 in 10 patients) - Somnolence (sleepiness) - Dizziness, headache - Pharyngitis, rhinitis (in children) - Diarrhea, nausea, dry mouth - Fatigue Uncommon side effects (may affect up to 1 in 100 patients) - Agitation - Paresthesia (abnormal feelings of the skin) - Abdominal pain - Pruritus (itchy skin), rash - Asthenia (extreme fatigue), malaise Rare side effects (may affect up to 1 in 1,000 patients) - Allergic reactions, some severe (very rare) - Depression, hallucination, aggression, confusion, insomnia - Convulsions - Tachycardia (heart beating too fast) - Liver function abnormal - Urticaria (hives) - Oedema (swelling) - Weight increased Very rare side effects (may affect up to 1 in 10,000 patients) - Thrombocytopenia (low levels of blood platelets) - Tics (habit spasm) - Syncope, dyskinesia (involuntary movements), dystonia (abnormal prolonged muscular contractions), tremor, dysgeusia (altered taste) - Blurred vision, accommodation disorder (difficulty focusing), oculogyration (eyes having uncontrolled circular movements) - Angioedema (serious allergic reaction which causes swelling of the face or throat), fixed drug eruption - Abnormal elimination of urine (bed wetting, pain and/or difficulty passing water) Not known frequency of side effects (frequency cannot be estimated from the available data) - Increased appetite - Suicidal ideation (recurring thoughts of or preoccupation with suicide), nightmares - Amnesia, memory impairment - Vertigo (sensation of rotation or movement) - Urinary retention (inability to completely empty the urinary bladder) - Pruritus (intense itching) and/or urticaria upon discontinuation - Joint pain - Pustular rash - Hepatitis (inflammation of the liver).
Reporting of side effects
If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly viawww.ravimiamet.ee. By reporting side effects you can help provide more information on the safety of this medicine.
5. How to store Zyrtec
Keep this medicine out of the sight and reach of children. Do not use this medicine after the expiry date which is stated on the box and blister. The expiry date refers to the last day of that month. This medicine does not require any special storage conditions.
6. Contents of the pack and other information
What Zyrtec contains
- The active substance is cetirizine dihydrochloride. One film-coated tablet contains 10 mg cetirizine dihydrochloride. - The other ingredients are microcrystalline cellulose, lactose-monohydrate, colloidal anhydrous silica, magnesium stearate, Opadry Y-1-7000 (hydroxypropylmethylcellulose (E 464), titanium dioxide (E 171), macrogol 400).
What Zyrtec looks like and contents of the pack
White, oblong, film-coated tablet, with breakline and Y-Y logo. Pack with 1, 4, 5, 7, and 10 tablets. Not all pack sizes may be marketed
Marketing Authorisation Holder and Manufacturer
Marketing Authorisation Holder: UCB Pharma Oy Finland Bertel Jungin aukio 5 02600 Espoo Finland Manufacturers: Aesica Pharmaceuticals S.r.l., Via Praglia 15, I-10044 Pianezza (TO), Italy UCB Pharma Limited, 208 Bath Road, Slough, Berkshire, SL1 3WE, United Kingdom Phoenix Pharma Polska Sp. z o.o., ul. Oplotek 26, 01-940 Warsaw, Poland ExtractumPharma Co. Ltd., 6413 Kunfeherto, IV. körzet 6., Hungary Movianto Polska Sp. z o.o, ul. Artura i Franciszka Radziwillow 5, 05-850 Ozarow Mazowiecki, Poland
This medicinal product is authorised in the Member States of the EEA under the following names: