Lopresor SR 200mg tablets

Negara: Inggris

Bahasa: Inggris

Sumber: MHRA (Medicines & Healthcare Products Regulatory Agency)

Beli Sekarang

Unduh Selebaran informasi (PIL)
30-11--0001
Unduh Karakteristik produk (SPC)
20-04-2020

Bahan aktif:

Metoprolol tartrate

Tersedia dari:

Mawdsley-Brooks & Company Ltd

Kode ATC:

C07AB02

INN (Nama Internasional):

Metoprolol tartrate

Dosis:

200mg

Bentuk farmasi:

Modified-release tablet

Rute administrasi :

Oral

Kelas:

No Controlled Drug Status

Jenis Resep:

Valid as a prescribable product

Ringkasan produk:

BNF: 02040000

Selebaran informasi

                                LOPRESOR
® SR 200MG TABLETS
(metoprolol tartrate)
PATIENT INFORMATION LEAFLET
WHAT YOU NEED TO KNOW ABOUT LOPRESOR SR TABLETS
Your doctor has decided that you need this medicine to help
treat your condition.
PLEASE READ THIS LEAFLET CAREFULLY BEFORE YOU START TO TAKE
YOUR MEDICINE. 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 Lopresor SR tablets are and what they are used for
2. Things to consider before you start to take Lopresor SR
tablets
3. How to take Lopresor SR tablets
4. Possible side effects
5. How to store Lopresor SR tablets
6. Further information
1. WHAT LOPRESOR SR TABLETS ARE AND WHAT THEY
ARE USED FOR
Metoprolol tartrate, the active ingredient in Lopresor SR
tablets, is one of a group of medicines called beta-blockers.
Beta-blockers slow the heart beat, lessen the force with
which the heart muscle contracts and reduce blood vessel
contraction in the heart, brain, and throughout the body.
Lopresor SR tablets are specially formulated to release the
active ingredient slowly.
They are used to treat high blood pressure and angina
(chest pain).
They can also be taken to help prevent migraine attacks.
2
.
THINGS TO CONSIDER BEFORE YOU START TO TAKE
LOPRESOR SR TABLETS
SOME PEOPLE MUST NOT TAKE LOPRESOR SR TABLETS. TALK
TO YOUR DOCTOR IF:
•
you think you may be allergic to metoprolol or to any of
the other ingredients of Lopresor SR tablets, (These are
listed at the end of the leaflet.)
•
you are allergic to any other beta-blocker drugs,
•
you have severe asthma or severe attacks of wheezing
                                
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Karakteristik produk

                                PRODUCT SUMMARY
1.
NAME OF THE MEDICINAL PRODUCT
Not applicable
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Not applicable
3.
PHARMACEUTICAL FORM
Not applicable
4.
CLINICAL PARTICULARS
4.1.
THERAPEUTIC INDICATIONS
Not applicable
4.2.
POSOLOGY AND METHOD OF ADMINISTRATION
Not applicable
4.3.
CONTRAINDICATIONS
Not applicable
4.4.
SPECIAL WARNINGS AND PRECAUTIONS FOR USE
Not applicable
4.5.
INTERACTIONS WITH OTHER MEDICINAL PRODUCTS 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
5.
PHARMACOLOGICAL PROPERTIES
5.1.
PHARMACODYNAMIC PROPERTIES
Not applicable
5.2.
PHARMACOKINETIC PROPERTIES
Not applicable
5.3.
PRECLINICAL SAFETY DATA
Not applicable
6.
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 AND HANDLING (, AND DISPOSAL)
Not applicable
No Data Held
ADMINISTRATIVE DATA
7.
MARKETING AUTHORISATION HOLDER
Not applicable
8.
MARKETING AUTHORISATION NUMBER
Not applicable
9.
DATE OF FIRST AUTHORISATION/RENEWAL OF THE
AUTHORISATION
Not applicable
10.
DATE OF REVISION OF THE TEXT
Not applicable
                                
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