BOTOX (BOTULINUM TOXIN TYPE A) IM INJECTION

Nchi: Malesia

Lugha: Kiingereza

Chanzo: NPRA (National Pharmaceutical Regulatory Agency, Bahagian Regulatori Farmasi Negara)

Nunua Sasa

Shusha Taarifa za kipeperushi (PIL)
31-05-2018
Shusha Tabia za bidhaa (SPC)
16-01-2019

Viambatanisho vya kazi:

CLOSTRIDIUM BOTULINUM TOXIN TYPE A

Inapatikana kutoka:

Allergan Malaysia Sdn Bhd

INN (Jina la Kimataifa):

CLOSTRIDIUM BOTULINUM TOXIN TYPE A

Vitengo katika mfuko:

1Pieces Pieces; 1 Pieces Pieces

Viwandani na:

ALLERGAN PHARMACEUTICALS IRELAND

Taarifa za kipeperushi

                                Not Applicable
                                
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Tabia za bidhaa

                                BOTOX ® (Botulinum Toxin Type A)
Purified Neurotoxin Complex
P RESENTATION
A sterile white vacuum dried powder in a clear glass vial, for use in a single patient. One unit corresponds
to the median lethal dose (LD
50) when reconstituted BOTOX ® is injected intraperitoneally into mice under
defined conditions).
Each vial of BOTOX® 50 Units contains 50 Units of Clostridium botulinum type A neurotoxin complex
900kD, 0.25 mg of human albumin and 0.45 mg of sodium chloride in a sterile, vacuum -dried form without
a preservative.
Each vial of BOTOX® 100 Units contains 100 Units of Clostridium botulinum type A neurotoxin
complex 900kD, 0. 5 mg of human albumin and 0.9 mg of sodium chloride in a sterile, vacuum -dried form
without a preservative.
Each vial of BOTOX® 200 Units contains 200 Units of Clostridium botulinum type A neurotoxin
complex 900kD, 1.0 mg of human albumin and 1.8 mg of sodium chloride in a sterile, vacuum-dried form
without a preservative.
USES
BOTOX ® (botulinum toxin type A) purified neurotoxin complex is indicated for the following
therapeutic
indications	:
• BOTOX ® is indicated for the treatment of blepharospasm associated with dystonia, including benign
essential blepharospasm, hemifacial spasm and VIIth nerve disorders in patients 12 years or older.
• BOTOX ® is indicated for the correction of strabismus in patients 12 years of age or older.
• BOTOX ® is indicated for the treatment of spasmodic torticollis (cervical dystonia) in adults.
• BOTOX ® is indicated for the treatment of dynamic equinus foot deformity due to spasticity in
paediatric cerebral palsy patients, two years of age and older.
• BOTOX ® is indicated in the manageme nt of focal spasticity:
o including wrist and hand disability due to upper limb spasticity associated with stroke in
adults.
o Including ankle and foot disability due to lower limb spasticity associated with stroke in adult s.
Distant Spread of Toxin Effect
Postmarketing safety data from BOTOX  and other approved botulinum toxins suggest that bo
                                
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