Kaimax 100 Units

Kaimax 100 Units

Introducing Kaimax 100 Units. Product Description in Depth:

[COMPOSITION] 1 vial includes

Clostridium botulinum toxin type A (in-house)

0.5mg human serum albumin (EP)

USP sodium chloride……0.9mg

DESCRIPTION

When diluted with normal saline, the white or light-yellow dried powder in a colourless and clear glass vial should turn into a colourless transparent or light-yellow liquid.

INDICATIONS AND APPLICATIONS

Kaimax 100 Units (botulinum toxin type A injection) is approved in adult patients aged 19 to 65 years for the temporary improvement in the appearance of moderate to severe glabellar lines associated with corrugator muscle and/or procerus muscle activity.

ADMINISTRATION AND DOSE

DILUTION AND PREPARATION METHODS

Dilute with sterile, preservative-free 0.9% sodium chloride injection to 100U/2.5ml (4U/0.1 ml).

Method of dilution:

Each Kaimax 100 Units vial must be reconstituted with sterile, preservative-free saline. The diluent of choice is 0.9% sodium chloride injection. Fill a syringe with the required amount of diluent. Slowly inject the diluent into the vial because this medicine will be denatured if there is froth or other agitation. If the vial was not filled with diluent while under vacuum, discard it.

On the label, write the date and time of dissolution, and allow it to be administered within 24 hours of dissolution. Kaimax should be stored in a refrigerator at 2-8°C after reconstitution. When Kaimax is dissolved, it should be colourless and transparent, with no foreign substance present. Prior to delivery, parenteral formulations should be checked for foreign contaminants and discolouration. Because this medicine and diluent include no preservatives, it is not recommended to utilise a single vial for more than one patient.