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Cetirizine Hydrochloride 5mg/5ml Oral Solution

Document: spc-doc_PL 36390-0023 change

SUMMARY OF PRODUCT CHARACTERISTICS

1    NAME OF THE MEDICINAL PRODUCT

Cetirizine Hydrochloride 5mg/5ml Oral Solution

2    QUALITATIVE AND QUANTITATIVE COMPOSITION

Cetirizine hydrochloride 5mg/5ml

For a full list of excipients, see section 6.1.

3    PHARMACEUTICAL FORM

Oral Solution.

Clear, colourless, flavoured solution.

4    CLINICAL PARTICULARS

4.1    Therapeutic indications

For the treatment of perennial rhinitis, seasonal allergic rhinitis (hay fever) and chronic idiopathic urticaria in adults and children over 6 years of age, and additionally for the symptomatic treatment of seasonal allergic rhinitis in children between the ages of 2 and 5.

4.2    Posology and method of administration

For oral use.

Adults and children over 12 years of age: 10ml once daily Children aged between 6 and 11: Either 5ml twice daily or 10ml once a day. Children aged between 2 and 5: Either 2.5ml twice daily or 5ml once a day. Not recommended for children under 2 years of age.

Elderly: The usual adult dose is recommended.

In patients with renal insufficiency, the dosage should be reduced to half that of the usual daily dose.

4.3 Contraindications

Hypersensitivity to cetirizine hydrochloride or any of the other ingredients. Lactating women.

4.4 Special warnings and precautions for use

This medicinal product contains sorbitol, sodium, glycerol, methyl and propyl parahydroxy benzoates.

When taken according to the dosage recommendations, each 10ml dose contains up to 3.5g of sorbitol. Sorbitol is broken down in the digestive system by substances called enzymes, into fructose and thus is unsuitable for patients who suffer from fructose intolerance. Sorbitol can cause stomach upset and diarrhoea.

The daily dose, 10ml, of this product contains approximately 3.2mg of sodium, and excessive consumption of sodium may be harmful to people on a low sodium diet.

Glycerol can be harmful in high doses. May cause headache, stomach upset and diarrhoea.

Methyl and Propyl parahydroxy benzoate have been known to cause urticaria, but is generally a delayed reaction, such as contact dermatitis. Rarely immediate reaction with urticaria and bronchospasm.

The elimination of cetirizine may be impaired in patients with impaired hepatic and renal function. Caution should be exercised when administering cetirizine to these patients (see section 4.2 Posology, section 4.3 Contraindications)

In some patients, long-term treatment with cetirizine may lead to an increased risk of caries due to mouth dryness. The patients should therefore be informed about the importance of oral hygiene.

4.5 Interaction with other medicinal products and other forms of interaction

Cetirizine may potentiate the effects of alcohol. It is advisable to avoid excessive alcohol consumption while taking this medicine. Caution is recommended with the concomitant use of CNS depressants.

Allergy testing - Use of cetirizine must be discontinued three days before allergy tests.

4.6 Fertility, Pregnancy and lactation

Although no adverse effects have been reported in animal studies, no information is available on the use of cetirizine hydrochloride in human pregnancy. As with all medicines therefore, its use should be avoided during pregnancy.

Contraindicated whilst breast-feeding, as cetirizine hydrochloride is excreted in breast milk.

4.7 Effects on ability to drive and use machines

Cetirizine hydrochloride does not usually cause drowsiness when taken at the recommended dose, however, patients should be warned not to drive or operate machinery if any effects are apparent.

4.8


Undesirable effects

The daily dose may be divided in patients experiencing occasional mild and transient side effects affecting the nervous and gastrointestinal systems. For adults and children over 12 years of age, this would mean taking 5 ml in the morning and 5 ml in the evening. For children aged 2 to 11, see section 4.2 (Posology).

Frequency estimates: Common (>1/100, <1/10); Uncommon (>1/1,000, <1/100); Rare (>1/10,000, <1/1,000); Very rare (<1/10,000):

Blood and lymphatic system disorders:

Very rare: thrombocytopenia

Immune system disorders:

Rare: Allergic reactions; (see Skin and subcutaneous disorders)

Very rare: Anaphylactic shock

Psychiatric disorders:

Uncommon: Agitation

Rare: Aggression, confusion, depression, hallucination, insomnia

Nervous system:

Common: Drowsiness

Uncommon: Headache, dizziness, paraesthesia.

Rare: Convulsions, movement disorders Very rare: Dysgeusia, syncope

Eye disorders:

Very rare: Accommodation disorder, blurred vision

Cardiac disorders:

Rare: Tachycardia

Gastrointestinal disorders:

Common: dry mouth

Uncommon: gastrointestinal disorders (nausea, diarrhoea, abdominal pain, dyspepsia)

Hepatobiliary disorders

Rare: Abnormal hepatic function (increased transaminases, alkaline phosphatase, gamma-GT, bilirubin)

Skin and subcutaneous tissue disorders:

Uncommon: Skin rash, pruritus Rare: Urticaria

Very rare: Angioedema, erythema multiforme

Renal and urinary disorders:

Very rare: Dysuria, enuresis, micturition difficulties

General disorders

Uncommon: asthenia, malaise Rare: Oedema, weight increase

4.9 Overdose

There is limited experience of overdosing. 20 mg to a 2-year-old, 30 mg to a 3-year-old and 40 mg to an 11-year-old did not give any symptoms. 60 mg to a 4-year-old gave mild intoxication, 400 mg to a 14-year-old gave mild symptoms, while 400 to 500 mg to an adult gave no symptoms at all.

a)    Symptoms

Cetirizine has a low sedative and anticholinergic effect. Adverse events reported after intake of at least five times the recommended daily dose are confusion, diarrhoea, dizziness, fatigue, headache, malaise, mydriasis, pruritus. Restlessness, sedation, somnolence, stupor, tachycardia, tremor and urinary retention.

b)    Management

Should overdose occur, symptomatic or supportive measures are recommended. The patient should be kept under clinical observation for at least four hours after ingestion, and the blood pressure, heart rate and vital signs monitored until stable. In symptomatic cases, ECG should be performed.

The benefit of gastric lavage is uncertain. Oral activated charcoal (50 g for an adult, 10-15 g for a child) should be considered if more than 2.5 mg/kg cetirizine has been ingested within one hour,

There is no specific antidote.

Cetririzine is not effectively removed by dialysis.

5 PHARMACOLOGICAL PROPERTIES

5.1 Pharmacodynamic properties

ATC Code: R06A E07

Cetirizine hydrochloride is a piperizine derivative and metabolite of hydroxyzine. It is a potent antihistamine with a low potential for drowsiness at the usual doses, and with additional anti-allergic properties. It is a selective H1 antagonist with negligible effects on other receptors and is therefore virtually free from anti-cholinergic and anti-serotonin effects.

5.2 Pharmacokinetic properties

Cetirizine hydrochloride is rapidly absorbed from the gastro-intestinal tract after oral administration, with peak plasma concentrations occurring in 30 - 60 minutes. It is highly bound to plasma proteins and has an elimination half-life of about 10 hours in adults, and about 6 hours in children. It is excreted primarily in the urine mainly as unchanged drug. It is detected in breast milk.

5.3 Preclinical safety data

No data of relevance which is additional to that already included in other sections of the SPC.

6 PHARMACEUTICAL PARTICULARS

6.1 List of excipients

Methyl parahydroxybenzoate (E218) Propyl parahydroxybenzoate (E216) Sorbitol solution (70%)

Glycerol

Sodium Citrate

Citric acid

Propylene glycol

Monoammonium Glycyrrhizinate

Purified water

Flavours

Pineapple Singapore flavour (flavouring agent and propylene glycol) Sweet orange No. 1(flavouring agent and propylene glycol)

6.2 Incompatibilities

Not applicable.

6.3 Shelf life

Unopened: 3 years After opening: 6 months

6.4 Special precautions for storage

No special precautions for storage.

6.5 Nature and contents of container

Pack size: 200ml bottle.

Packaging: Type III amber glass bottle with Tamper proof polypropylene closure and Polyethylene Terepthalate (PET) amber bottle with Tamper proof polypropylene closure.

6.6 Special precautions for disposal

Not applicable.

7. MARKETING AUTHORISATION HOLDER

Cipla (EU) Limited Hillbrow House Hillbrow Road Esher Surrey

8    MARKETING AUTHORISATION NUMBER(S)

PL 36390/0023

9    DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION

03/11/2011

10    DATE OF REVISION OF THE TEXT

22/11/2013