Zolmitriptan Sandoz tablet 5 mg, filmomhulde tabletten

Land: Holland

Sprog: hollandsk

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

Aktiv bestanddel:

ZOLMITRIPTAN 5 mg/stuk

Tilgængelig fra:

Sandoz B.V. Veluwezoom 22 1327 AH ALMERE

ATC-kode:

N02CC03

INN (International Name):

ZOLMITRIPTAN 5 mg/stuk

Lægemiddelform:

Filmomhulde tablet

Sammensætning:

CELLULOSE, MICROKRISTALLIJN (E 460(i)) ; CROSPOVIDON (E 1202) ; HYPROLOSE (E 463) ; HYPROMELLOSE (E 464) ; IJZEROXIDE GEEL (E 172) ; IJZEROXIDE ROOD (E 172) ; LACTOSE 0-WATER ; MACROGOL 400 ; MAGNESIUMSTEARAAT (E 470b) ; SILICIUMDIOXIDE (E 551) ; TALK (E 553 B) ; TITAANDIOXIDE (E 171), CELLULOSE, MICROKRISTALLIJN (E 460) ; CROSPOVIDON (E 1202) ; HYPROLOSE (E 463) ; HYPROMELLOSE (E 464) ; IJZEROXIDE GEEL (E 172) ; IJZEROXIDE ROOD (E 172) ; LACTOSE 0-WATER ; MACROGOL 400 ; MAGNESIUMSTEARAAT (E 470b) ; SILICIUMDIOXIDE (E 551) ; TALK (E 553 B) ; TITAANDIOXIDE (E 171),

Indgivelsesvej:

Oraal gebruik

Terapeutisk område:

Zolmitriptan

Produkt oversigt:

Hulpstoffen: CELLULOSE, MICROKRISTALLIJN (E 460); CROSPOVIDON (E 1202); HYPROLOSE (E 463); HYPROMELLOSE (E 464); IJZEROXIDE GEEL (E 172); IJZEROXIDE ROOD (E 172); LACTOSE 0-WATER; MACROGOL 400; MAGNESIUMSTEARAAT (E 470b); SILICIUMDIOXIDE (E 551); TALK (E 553 B); TITAANDIOXIDE (E 171);

Autorisation dato:

1900-01-01

Indlægsseddel

Sandoz B.V.
Page 1/8
Zolmitriptan Sandoz tablet 2,5 mg, 5 mg filmomhulde tabletten
RVG 106557-8
1313-V3
1.3.1.3 Package Leaflet
June 2021
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
ZOLMITRIPTAN SANDOZ TABLET 2,5 MG, FILMOMHULDE TABLETTEN
ZOLMITRIPTAN SANDOZ TABLET 5 MG, FILMOMHULDE TABLETTEN
zolmitriptan
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 [Nationally completed name] is and what it is used for
2.
What you need to know before you take [Nationally completed name]
3.
How to take [Nationally completed name]
4.
Possible side effects
5.
How to store [Nationally completed name]
6.
Contents of the pack and other information
1.
WHAT [NATIONALLY COMPLETED NAME] IS AND WHAT IT IS USED FOR
[Nationally completed name] contains zolmitriptan and belongs to a
group of medicines called triptans.
[NATIONALLY COMPLETED NAME] IS USED TO TREAT MIGRAINE HEADACHE
IN ADULTS AGED 18 YEARS AND OLDER
.
•
Migraine symptoms may be caused by the widening of blood vessels in
the head. [Nationally
completed name] is thought to reduce the widening of these blood
vessels. This helps to take away the
headache and other symptoms of a migraine attack, such as feeling or
being sick (nausea or vomiting)
and being sensitive to light and sound.
•
[Nationally completed name] works only when a migraine attack has
started. It will not stop you from
getting an attack.
Sandoz B.V.
Page 2/8
Zolmitriptan Sandoz tablet 2,5 mg, 5 mg filmomhulde tabletten
RVG 106557-8
1313-V3
1.3.1.3 Package Leaflet
June 2021
2.
WHAT YOU NEED T

Produktets egenskaber

Sandoz B.V.
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Zomitriptan Sandoz tablet 2,5+5 mg
RVG 106557-106558
1311-v3
1.3.1.1 Samenvatting van de Productkenmerken
Juni 2021
SUMMARY OF PRODUCT CHARACTERISTICS
1.
NAME OF THE MEDICINAL PRODUCT
Zolmitriptan Sandoz tablet 2,5 mg, filmomhulde tabletten
Zolmitriptan Sandoz tablet 5 mg, filmomhulde tabletten
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each film-coated tablet contains 2.5 mg of zolmitriptan.
Excipient with known effect
Each film-coated tablet contains 83 mg of lactose.
Each film-coated tablet contains 5 mg of zolmitriptan.
_ _
Excipient with known effect
Each film-coated tablet contains 167 mg of lactose.
_ _
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet.
_2.5 mg _
Yellow, round, biconvex, film-coated tablet with ‘ZMT 2.5’
debossed on one side.
_5 mg _
Pink, round, biconvex, film-coated tablet with ‘ZMT 5’ debossed on
one side.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
[Nationally completed name] is indicated in adults aged 18 years and
older for acute treatment of
migraine headache with or without aura.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
The recommended dose of [Nationally completed name] film-coated
tablets to treat a migraine attack
is 2.5 mg. It is advisable that [Nationally completed name] is taken
as early as possible after the onset
of migraine headache but it is also effective if taken at a later
stage.
If symptoms of migraine should recur within 24 hours following an
initial response, a second dose
may be taken. If a second dose is required, it should not be taken
within 2 hours of the initial dose. If a
Sandoz B.V.
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Zomitriptan Sandoz tablet 2,5+5 mg
RVG 106557-106558
1311-v3
1.3.1.1 Samenvatting van de Productkenmerken
Juni 2021
patient does not respond to the first dose, it is unlikely that a
second dose will be of benefit in the same
attack.
If a patient does not achieve satisfactory relief with 2.5 mg doses,
for subsequent attacks 5 mg doses
of [Nationally completed name] could be conside