Zolpidemtartraat ratiopharm 10 mg, tabletten

国家: 荷兰

语言: 荷兰文

来源: CBG-MEB (College ter Beoordeling van Geneesmiddelen)

有效成分:

ZOLPIDEMTARTRAAT 10 mg/stuk

可用日期:

Ratiopharm GmbH Graf-Arco-Strasse 3 89079 ULM (DUITSLAND)

ATC代码:

N05CF02

INN（国际名称）:

ZOLPIDEMTARTRAAT 10 mg/stuk

药物剂型:

Filmomhulde tablet

组成:

CELLULOSE, MICROKRISTALLIJN (E 460(i)) ; HYPROMELLOSE (E 464) ; LACTOSE 1-WATER ; MAGNESIUMSTEARAAT (E 470b) ; NATRIUMZETMEELGLYCOLAAT ; POLYETHYLEENGLYCOL (E 1521) ; TITAANDIOXIDE (E 171), CELLULOSE, MICROKRISTALLIJN (E 460) ; HYPROMELLOSE (E 464) ; LACTOSE 1-WATER ; MAGNESIUMSTEARAAT (E 470b) ; NATRIUMZETMEELGLYCOLAAT ; POLYETHYLEENGLYCOL (E 1521) ; TITAANDIOXIDE (E 171), CELLULOSE, MICROKRISTALLIJN (E 460) ; HYPROMELLOSE (E 464) ; LACTOSE 1-WATER ; MAGNESIUMSTEARAAT (E 470b) ; NATRIUMZETMEELGLYCOLAAT (E468) ; POLYETHYLEENGLYCOL (E 1521) ; TITAANDIOXIDE (E 171),

给药途径:

Oraal gebruik

治疗领域:

Zolpidem

產品總結:

Hulpstoffen: CELLULOSE, MICROKRISTALLIJN (E 460); HYPROMELLOSE (E 464); LACTOSE 1-WATER; MAGNESIUMSTEARAAT (E 470b); NATRIUMZETMEELGLYCOLAAT (E468); POLYETHYLEENGLYCOL (E 1521); TITAANDIOXIDE (E 171);

授权日期:

1900-01-01

资料单张

1
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PACKAGE LEAFLET: INFORMATION FOR THE USER
ZOLPIDEMTARTRAAT RATIOPHARM 5 MG, TABLETTEN
ZOLPIDEMTARTRAAT RATIOPHARM 10 MG, TABLETTEN
zolpidem tartrate
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START TAKING THIS
MEDICINE BECAUSE IT CONTAINS IMPORTANT
INFORMATION FOR YOU.
-
Keep this leaflet. You may need to read it again.
-
If you have any further questions, ask your doctor or pharmacist.
-
This medicine has been prescribed for you only. Do not pass it on to
others. It may harm them, even if
their signs of illness are the same as yours.
-
If you get any side effects, talk to your doctor or pharmacist. This
includes any possible side effects
not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What is and what it is used for
2.
What you need to know before you take
3.
How to take
4.
Possible side effects
5.
How to store
6.
Contents of the pack and other information
1.
WHAT IS AND WHAT IT IS USED FOR
is a sleeping tablet belonging to a group of medicines
known as benzodiazepine-like agents.
It is used for the short-term treatment of sleep disturbances in
adults.
is only prescribed for sleep disturbances that are
severe, disabling or cause extreme distress.
2.
WHAT YOU NEED TO KNOW BEFORE YOU TAKE
DO NOT TAKE :
•
if you are ALLERGIC TO ZOLPIDEM OR ANY OF THE OTHER INGREDIENTS of
this medicine (listed in section 6).
Signs of an allergic reaction include: rash, swallowing or breathing
problems, swelling of your lips, face,
throat or tongue.
•
if you have ever experienced sleep walking or other behaviours which
are unusual while sleeping, (such as
driving, eating, making a phone call or having sex etc.) while not
being fully awake after taking or other medicines containing zolpidem.
•
if you suffer from severe muscle weakness (MYASTHENIA GRAVIS).
•
if your breathing stops for short periods while you ar

产品特点

rvg 25110_1 EU SPC II-047 met NL info clean
SUMMARY OF PRODUCT CHARACTERISTICS
1.
NAAM VAN HET GENEESMIDDEL
Zolpidemtartraat ratiopharm 5 mg, tabletten
Zolpidemtartraat ratiopharm 10 mg, tabletten
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
_˂Product name˃ 5 mg film-coated tablets _
One film-coated tablet contains 5 mg zolpidem tartrate.
Excipient with known effect: 43 mg lactose/film-coated tablet
_˂Product name˃ 10 mg film-coated tablets _
One film-coated tablet contains 10 mg zolpidem tartrate.
Excipient with known effect: 86 mg lactose/film-coated tablet
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet.
_˂Product name˃ 5 mg film-coated tablets _
White, oval, biconvex, film-coated tablet, embossed with "ZIM" on one
side and "5" on the other side_._
_˂Product name˃ 10 mg film-coated tablets _
White, oval, biconvex, film-coated tablet, scored on both sides and
embossed with "ZIM" and "10" on
one side_. _The tablet can be divided into equal doses.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Short term treatment of insomnia in adults.
Benzodiazepines or benzodiazepine-like agents are only indicated when
the disorder is severe,
disabling or subjecting the individual to extreme distress.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
POSOLOGY
Treatment should be as short as possible. Generally the duration of
treatment varies from a few days to
two weeks with a maximum, including the tapering off process, of four
weeks. The tapering off
process should be tailored to the individual.
In certain cases extension beyond the maximum treatment period may be
necessary; if so, it should not
take place without re-evaluation of the patient's status since the
risk of abuse and dependence increases
with the duration of treatment (see section 4.4).
The treatment should be taken in a single intake and not be
re-administered during the same night.
rvg 25110_1 EU SPC II-047 met NL info clean
Adults
The recommended daily dose for adults is 10 mg to be taken immediately
at bedtime.