Junior Meltus Chesty Coughs with Catarrh

Valsts: Malta

Valoda: angļu

Klimata pārmaiņas: Medicines Authority

Nopērc to tagad

Lietošanas instrukcija Lietošanas instrukcija (PIL)
27-05-2024
Produkta apraksts Produkta apraksts (SPC)
27-05-2024

Aktīvā sastāvdaļa:

CETYLPYRIDINIUM CHLORIDE, GUAIFENESIN

Pieejams no:

Cupal Limited 103 - 105 Bath Road Slough, SL1 3UK, United Kingdom

ATĶ kods:

R05DA09

SNN (starptautisko nepatentēto nosaukumu):

CETYLPYRIDINIUM CHLORIDE 2.5 mg GUAIFENESIN 50 mg

Zāļu forma:

ORAL LIQUID

Kompozīcija:

CETYLPYRIDINIUM CHLORIDE 2.5 mg GUAIFENESIN 50 mg

Receptes veids:

OTC

Ārstniecības joma:

COUGH AND COLD PREPARATIONS

Autorizācija statuss:

Withdrawn

Autorizācija datums:

2007-07-12

Produkta apraksts

                                 
        Page 1 of 3 
 
SUMMARY OF PRODUCT CHARACTERISTICS 
 
 
1. 
NAME OF MEDICINAL PRODUCT 
 
Junior Meltus Chesty Coughs with Catarrh 
 
2. 
QUALITATIVE AND QUANTITATIVE COMPOSITION 
 
Guaiphenesin 50 mg 
Cetylpyridinium Chloride 2.5 mg 
 
3. PHARMACEUTICAL 
FORM 
 
Oral Liquid. 
 
4. CLINICAL 
PARTICULARS 
 
4.1 THERAPEUTIC 
INDICATIONS 
 
For the symptomatic relief of coughs and catarrh associated with
influenza, colds and mild 
throat infections. 
 
4.2  POSOLOGY AND METHOD OF ADMINISTRATION 
 
To be taken three to four times daily. 
_Children over 6 years_:  Two 5 ml spoonfuls 
_Children 1-6 years_: 
 
One 5 ml spoonful 
_Children under 1 year_:  Not recommended unless on medical
advice. 
 
4.3 CONTRAINDICATIONS 
 
This product is contraindicated in patients hypersensitive to any of
the ingredients. 
 
4.4  SPECIAL WARNINGS AND SPECIAL PRECAUTIONS FOR USE 
 
Children under 1 year of age - this product should only be
administered with medical advice. 
 
4.5  INTERACTION WITH OTHER MEDICAMENTS AND OTHER FORMS
OF INTERACTION 
 
Can cause transient abnormality in platelet aggregation patterns
determined one hour after 
ingestion.  
 
4.6  PREGNANCY AND LACTATION 
 
Although there are no known contra-indications, as with
all medicines caution should be 
exercised when administering to pregnant or lactating women. 
 
4.7  EFFECTS ON ABILITY TO DRIVE AND TO USE MACHINES 
 
Mild drowsiness has been reported. 
 
 
        Page 2 of 3 
 
4.8 UNDESIRABLE 
EFFECTS 
 
Some gastro-intestinal discomfort and mild drowsiness has been
reported.  Very large doses 
can cause nausea and vomiting. 
 
4.9 OVERDOSE 
 
Very large doses may cause nausea and vomiting.  It is however,
rapidly metabolised and 
excreted in the urine.  The patient should be kept
under observation and treated 
symptomatically. 
 
5. PHARMACOLOGICAL 
PROPERTIES 
 
5.1 PHARMACODYNAMIC 
PROPERTIES 
 
A cou
                                
                                Izlasiet visu dokumentu