Thiocolchicoside

Please note, this OEL/ADE monograph also applies to Thiocolchicoside hydrate (CAS RN 1622135-03-8).Thiocolchicoside is a semisynthetic derivative of colchicine, a natural anti-inflammatory glycoside that originates from the flower seeds of Superba gloriosa. It is a muscle relaxant with anti-inflammatory and analgesic effects. It is used in the treatment of orthopedic, traumatic and rheumatologic disorders. It is indicated as an adjuvant drug in the treatment of painful muscle contractures and is indicated in acute spinal pathology, for adults and adolescents 16 years of age and older. Thiocolchicoside is available as tablets, capsules, syrup, and powder for oral administration and as a solution for intramuscular (IM) administration. It is also available as an ointment, cream, aerosol foam, spray, and gel for topical administration.

Affygility Solutions has an occupational exposure limit (OEL) and control band assignment for this active pharmaceutical ingredient (API). This monograph also contains the acceptable daily exposure (ADE) value.

Thiocolchicoside

CAS Registry Number:
602-41-5
Trade names:
Trade names, if needed
Brand names:
Colthiozid, Cotrax, Dyanxon, Kenfix Miorexil, Muscoril, Zyflex
Cost:
$989 USD

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Why do you need this OEL Fastrac monograph?

OEL Fastrac monographs are a cost-effective and convenient way to meet the requirements for PDEs (ADEs) contained in the EMA Guideline on setting health based exposure limits for use in risk identification in the manufacture of different medicinal products in shared facilities (EMA/CHMP/CVMP/SWP/169430/2012), as well as PIC/S and ANVISA requirements, and to obtain the following information:

  • The numerical OEL and control band assignment needed to determine the level of required engineering controls and personal protective equipment
  • A listing of all cited references utilized in the derivation of the OEL and ADE
  • An expert review and discussion with respect to the critical endpoints of concern, the rationale for the choice of endpoints, and dose that is to be used in the derivation of the ADE (PDE), as required by the EMA's Guideline on setting health-based exposure limits for use in risk identification in the manufacture of different medicinal products in shared facilities

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  • Fully documented. Over 20 pages in length, with calculations and cited references.
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  • Director of Manufacturing