Diclofenac 100mg suppositories

Maa: Yhdistynyt kuningaskunta

Kieli: englanti

Lähde: MHRA (Medicines & Healthcare Products Regulatory Agency)

Osta se nyt

Pakkausseloste Pakkausseloste (PIL)
03-12-2019
Valmisteyhteenveto Valmisteyhteenveto (SPC)
20-04-2020

Aktiivinen ainesosa:

Diclofenac sodium

Saatavilla:

Kent Pharma (UK) Ltd

ATC-koodi:

M01AB05

INN (Kansainvälinen yleisnimi):

Diclofenac sodium

Annos:

100mg

Lääkemuoto:

Suppository

Antoreitti:

Rectal

luokka:

No Controlled Drug Status

Prescription tyyppi:

Valid as a prescribable product

Tuoteyhteenveto:

BNF: 10010100

Pakkausseloste

                                _S423 LEAFLET Voltarol 20191203_
_ _
PATIENT INFORMATION LEAFLET
VOLTAROL

100MG SUPPOSITORIES
(diclofenac sodium)
Your medicine is known as Voltarol

100mg suppositories but will
be referred to as Voltarol Suppositories throughout the following
patient information leaflet.
Information for other strengths of Voltarol Suppositories i.e. 12.5mg,
25mg and 50mg also may be present in this leaflet.
WHAT YOU NEED TO KNOW ABOUT VOLTAROL SUPPOSITORIES
Your doctor has decided that you need this medicine to help treat
your condition.
PLEASE READ THIS LEAFLET CAREFULLY BEFORE YOU START TO USE THESE
SUPPOSITORIES. IT CONTAINS IMPORTANT INFORMATION. Keep the
leaflet in a safe place because you may want to read it again.
If you have any other questions, or if there is something you don’t
understand, please ask your doctor or pharmacist.
This medicine has been prescribed for you. Never give it to
someone else. It may not be the right medicine for them even if
their symptoms seem to be the same as yours.
If any of the side effects gets serious, or if you notice any side
effects not listed in this leaflet, please tell your doctor or
pharmacist.
IN THIS LEAFLET:
1.
What Voltarol Suppositories are, and what they are used for
2.
Things to consider before you start to use Voltarol
Suppositories
3.
How to use Voltarol Suppositories
4.
Possible side effects
5.
How to store Voltarol Suppositories
6.
Further information
1.
WHAT VOLTAROL SUPPOSITORIES ARE AND WHAT
THEY ARE USED FOR
Diclofenac sodium, the active ingredient in Voltarol Suppositories, is
one of a group of medicines called non-steroidal anti
‑
inflammatory
drugs (NSAIDs). NSAIDs reduce pain and inflammation.

Voltarol Suppositories relieve pain, reduce swelling and ease
inflammation in conditions affecting the joints, muscles and
tendons including:
–
Rheumatoid arthritis, osteoarthritis, acute gout, ankylosing
spondylitis
–
Backache, sprains and strains, soft tissue sports injuries,
frozen shoulder, dislocations and fractures
–
Tendonitis, tenosynovitis, bu
                                
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Valmisteyhteenveto

                                PRODUCT SUMMARY
1.
Trade Name of the Medicinal Product
Not applicable
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Not applicable
3.
PHARMACEUTICAL FORM
Not applicable
CLINICAL PARTICULARS
4.1.
Therapeutic Indications
Not applicable
4.2.
POSOLOGY AND METHOD OF ADMINISTRATION
Not applicable
4.3.
CONTRA-INDICATIONS
Not applicable
4.4.
SPECIAL WARNINGS AND PRECAUTIONS FOR USE
Not applicable
4.5.
INTERACTIONS WITH OTHER MEDICAMENTS AND OTHER FORMS OF INTERACTION
Not applicable
4.6.
PREGNANCY AND LACTATION
Not applicable
4.7.
EFFECTS ON ABILITY TO DRIVE AND USE MACHINES
Not applicable
4.8.
UNDESIRABLE EFFECTS
Not applicable
4.9.
OVERDOSE
Not applicable
PHARMACOLOGICAL PROPERTIES
5.1.
Pharmacodynamic Properties
Not applicable
5.2.
PHARMACOKINETIC PROPERTIES
Not applicable
5.3.
PRECLINICAL SAFETY DATA
Not applicable
PHARMACEUTICAL PARTICULARS
6.1.
List of Excipients
Not applicable
6.2.
INCOMPATIBILITIES
Not applicable
6.3.
SHELF LIFE
Not applicable
6.4.
SPECIAL PRECAUTIONS FOR STORAGE
Not applicable
6.5.
NATURE AND CONTENTS OF CONTAINER
Not applicable
6.6.
INSTRUCTION FOR USE/HANDLING
Not applicable
ADMINISTRATIVE DATA
7.
Marketing Authorisation Holder
Not applicable
8.
MARKETING AUTHORIZATION NUMBER
Not applicable
9.
DATE OF FIRST AUTHORISATION/RENEWAL OF AUTHORISATION
Not applicable
10.
DATE OF (PARTIAL) REVISION OF THE TEXT
Not applicable
                                
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