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TABLE 1. Botulinum Toxin Manufacturer Recommendations on Supply, Dilution, and Storage

OnabotulinumtoxinA AbobotulinumtoxinA BONTA

BONTA

IncobotulinumtoxinA RimabotulinumtoxinB

Company

Allergan, Inc.

Ipsen Inc./Medicis

Inc.

Lanzhou

Medy-Tox Inc.,

South Korea

Merz Pharmaceuti-

cals

Solstice Neuro-

sciences Inc./Eisai

Co., Ltd.

Commercial

names

Botox, Botox cos

metic, Vistabel,

Vistabex

Dysport, Reloxin,

Azzalure

Prosigne

Lantox, Redux

Neuronox,

Meditoxin

Botulift

Xeomin, Bocoture

Myobloc, Neurobloc

Approvals

Worldwide, includ-

ing United States

and Canada

In more than 65

countries, includ-

ing United States

and Canada

4

10 countries

including China

Korea, India,

Latin South

America

Germany, other

European coun-

tries, Mexico,

Argentina, Brazil

United States, some

European coun-

tries

Type

Type A-Hall strain Type A (NCTC 2916

strain)

A

A

Type A-Hall strain B

Active sub-

stance

Botulinum toxin type

A complex

(900 kDa)

Botulinum toxin

type A complex

(400 kDa)

Botulinum toxin

type A

(900 kDa)

y

Botulinum

toxin type A

(940 kDa)

Botulinum toxin

type A, free from

complexing pro-

teins (150 kDa)

Botulinum toxin type

B (700 kDa)

Indications

Blepharospasm,

cervical dystonia,

glabellar lines,

hyperhidrosis,

chronic migraine

Blepharospasm,

cervical dystonia,

glabellar lines

Blepharospasm,

cervical dysto-

nia, glabellar

lines, hyper-

hidrosis

Blepharospasm Blepharospasm,

cervical dystonia,

cosmetic use in

some countries

Cervical dystonia

Mode of action SNAP 25/SV2

SNAP 25/SV2

SNAP 25

SNAP 25

SNAP 25

Vesicle associated

membrane protein

U/vial

100 or 200

300 or 500

100 or 50

100

100 or 50

2,500, 5,000, or

10,000

Pharmaceutical

form

Powder dissolved in

solution for injec-

tion

Powder dissolved in

solution for injec-

tion

Powder dis-

solved in solu-

tion for

injection

Powder dis-

solved in

solution for

injection

Powder dissolved in

solution for injec-

tion

Solution

Excipients

500

m

g HSA

0.9mg NaCl

125

m

g HSA

2.5mg lactose

5mg gelatin

25mg dextran

25mg sucrose

500

m

g HSA

0.9mg NaCl

1,000

m

g HSA

4.7mg sucrose

500

m

g/mL HSA

NaCl 0.1M

Disodium succinate

0.01MHCl (to adjust

pH)

Water for injection

Transportation

and storage

before dilu-

tion

2–8

1

C

2–8

1

C

2–8

1

C

2–8

1

C

o

25

1

C

2–8

1

C

3 7 : 1 1 : NOVEMBER 2 0 1 1

TR I NDADE DE ALME I DA ET AL