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SILICEA PILLULES 4X-60X 2C-200C & 2K-100000K INCLUSIVE

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SUMMARY OF PRODUCT CHARACTERISTICS

1

NAME OF THE MEDICINAL PRODUCT
Not required for products registered under Article 14 of Directive 2001/83 EC as
amended ‘The Simplified Homeopathic Registration Scheme’

2

QUALITATIVE AND QUANTITATIVE COMPOSITION
Not required for products registered under Article 14 of Directive 2001/83 EC as
amended ‘The Simplified Homeopathic Registration Scheme’

3

PHARMACEUTICAL FORM
Not required for products registered under Article 14 of Directive 2001/83 EC as
amended ‘The Simplified Homeopathic Registration Scheme’

4

CLINICAL PARTICULARS

4.1

Therapeutic indications
Not required for products registered under Article 14 of Directive 2001/83 EC as
amended ‘The Simplified Homeopathic Registration Scheme’

4.2

Posology and method of administration
Not required for products registered under Article 14 of Directive 2001/83 EC as
amended ‘The Simplified Homeopathic Registration Scheme’

4.3

Contraindications
Not required for products registered under Article 14 of Directive 2001/83 EC as
amended ‘The Simplified Homeopathic Registration Scheme’

4.4

Special warnings and precautions for use
Not required for products registered under Article 14 of Directive 2001/83 EC as
amended ‘The Simplified Homeopathic Registration Scheme’

4.5

Interaction with other medicinal products and other forms of interaction
Not required for products registered under Article 14 of Directive 2001/83 EC as
amended ‘The Simplified Homeopathic Registration Scheme’

4.6

Pregnancy and lactation
Not required for products registered under Article 14 of Directive 2001/83 EC as
amended ‘The Simplified Homeopathic Registration Scheme’

4.7

Effects on ability to drive and use machines
Not required for products registered under Article 14 of Directive 2001/83 EC as
amended ‘The Simplified Homeopathic Registration Scheme’

4.8

Undesirable effects
Not required for products registered under Article 14 of Directive 2001/83 EC as
amended ‘The Simplified Homeopathic Registration Scheme’

4.9

Overdose
Not required for products registered under Article 14 of Directive 2001/83 EC as
amended ‘The Simplified Homeopathic Registration Scheme’

5

PHARMACOLOGICAL PROPERTIES

5.1

Pharmacodynamic properties
Not required for products registered under Article 14 of Directive 2001/83 EC as
amended ‘The Simplified Homeopathic Registration Scheme’

5.2

Pharmacokinetic properties
Not required for products registered under Article 14 of Directive 2001/83 EC as
amended ‘The Simplified Homeopathic Registration Scheme’

5.3

Preclinical safety data
Not required for products registered under Article 14 of Directive 2001/83 EC as
amended ‘The Simplified Homeopathic Registration Scheme’

6

PHARMACEUTICAL PARTICULARS

6.1

List of excipients
Not required for products registered under Article 14 of Directive 2001/83 EC as
amended ‘The Simplified Homeopathic Registration Scheme’

6.2

Incompatibilities
Not required for products registered under Article 14 of Directive 2001/83 EC as
amended ‘The Simplified Homeopathic Registration Scheme’

6.3

Shelf life
Not required for products registered under Article 14 of Directive 2001/83 EC as
amended ‘The Simplified Homeopathic Registration Scheme’

6.4

Special precautions for storage
Not required for products registered under Article 14 of Directive 2001/83 EC as
amended ‘The Simplified Homeopathic Registration Scheme’

6.5

Nature and contents of container
Not required for products registered under Article 14 of Directive 2001/83 EC as
amended ‘The Simplified Homeopathic Registration Scheme’

6.6

Special precautions for disposal
Not required for products registered under Article 14 of Directive 2001/83 EC as
amended ‘The Simplified Homeopathic Registration Scheme’

7

MARKETING AUTHORISATION HOLDER
Not required for products registered under Article 14 of Directive 2001/83 EC as
amended ‘The Simplified Homeopathic Registration Scheme’

8

MARKETING AUTHORISATION NUMBER(S)
Not required for products registered under Article 14 of Directive 2001/83 EC as
amended ‘The Simplified Homeopathic Registration Scheme’

9

DATE OF FIRST AUTHORISATION/RENEWAL OF THE
AUTHORISATION
02/11/2010

10

DATE OF REVISION OF THE TEXT
02/11/2010

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Source: Medicines and Healthcare Products Regulatory Agency

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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