Ondansetron 8mg tablets

国家: 英国

语言: 英文

来源: MHRA (Medicines & Healthcare Products Regulatory Agency)

现在购买

资料单张 资料单张 (PIL)
22-10-2021
产品特点 产品特点 (SPC)
19-03-2020
公众评估报告 公众评估报告 (PAR)
30-11--0001

有效成分:

Ondansetron hydrochloride dihydrate

可用日期:

Ennogen Healthcare Ltd

ATC代码:

A04AA01

INN(国际名称):

Ondansetron hydrochloride dihydrate

剂量:

8mg

药物剂型:

Oral tablet

给药途径:

Oral

类:

No Controlled Drug Status

处方类型:

Valid as a prescribable product

產品總結:

BNF: 04060000; GTIN: 05060254923000

资料单张

                                Page 1 of 1
PRODUCT
SUPERSEDED ITEM CODE NO. :
VERSION :
REASON FOR ISSUE :
ITEM CODE
SUBSTRATE:
MARKET
COLOR :
MFG. LOCATION
DIMENSION
PHARMA CODE :
COMPONENT
CHANGE PART LAYOUT:
NO. OF. COLORS :
Ondansetron 4 mg & 8 mg tablets
OETB30564
Dholka
Export (Ennogen UK)
leaflet-Front Side
240 x 400 mm
NA
28 gsm Bible Paper Pack Insert ( Folding size : 120 x 25 )
OETB20564
Pantone P Black
01
3195
03
Text matter changed
C A D IL A P H A R MA C E U T IC A L S LT D .
BS-13/02/19-V01
Page 1 of 1
PRODUCT
SUPERSEDED ITEM CODE NO. :
VERSION :
REASON FOR ISSUE :
ITEM CODE
SUBSTRATE:
MARKET
COLOR :
MFG. LOCATION
DIMENSION
PHARMA CODE :
COMPONENT
CHANGE PART LAYOUT:
NO. OF. COLORS :
OETB30564
Bhavin
Kalola
Digitally signed
by Bhavin Kalola
Date: 2020.12.21
10:35:33 Z
                                
                                阅读完整的文件
                                
                            

产品特点

                                SUMMARY OF PRODUCT CHARACTERISTICS
1
NAME OF THE MEDICINAL PRODUCT
Ondansetron 8mg Orodispersible Tablets
2
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each orodispersible tablet contains ondansetron 8mg.
Excipient with known effect
Each orodispersible tablet contains 6mg aspartame.
For the full list of excipients, see section 6.1.
3
PHARMACEUTICAL FORM
Orodispersible tablets.
Round, white to off-white, flat, bevelled edged, tablets plain on both
the surfaces,
having strawberry odour.
4
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
_Adults: _
Ondansetron orodispersible tablets are indicated for the management of
nausea and
vomiting induced by cytotoxic chemotherapy and radiotherapy.
Ondansetron orodispersible tablets are indicated for the prevention of
post-operative
nausea and vomiting (PONV).
For treatment of established PONV, administration by injection is
recommended.
_Paediatric Population:_
_ _
Ondansetron is indicated for the management of chemotherapy-induced
nausea and
vomiting (CINV) in children aged
≥
6 months.
No studies have been conducted on the use of orally administered
ondansetron in the
prevention and treatment of PONV in children aged
≥
1 month, administration by IV
injection is recommended for this purpose.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
Chemotherapy and radiotherapy induced nausea and vomiting:
_Adults: _
The emetogenic potential of cancer treatment varies according to the
doses and
combinations of chemotherapy and radiotherapy regimens used. The
selection of dose
regimen should be determined by the severity of the emetogenic
challenge.
_ _
_Emetogenic chemotherapy and radiotherapy:_ Ondansetron can be given
either by
rectal, oral (as orodispersible tablet, tablets or syrup) intravenous
or intramuscular
administration.
For oral administration: 8 mg taken 1 to 2 hours before chemotherapy
or radiation
treatment, followed by 8 mg every 12 hours for a maximum of 5 days to
protect
against delayed or prolonged emesis.
_For highly emetogenic chemotherapy_: a single dose of up
                                
                                阅读完整的文件