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TM/MC  TM/MC
                                          PHARMACOLOGICAL ACTIVITIES - TOXICOLOGY - DRUG INTERACTIONS






                    Notopterygium incisum

                    Toxicity  for Radix  Notopterygii  has not been  documented in  dogs and cats  when administered  orally  in
               TOXICOLOGY  therapeutic doses. No fatalities were observed in mice following oral ingestion of aqueous extract of Radix
                    Notopterygii at 12 g/kg of body weight. Oral LD  for essential oil of Radix Notopterygii is 2.83 g/kg of body
                                                              50
                    weight (Chen & Chen, 2004).

                    Equivalent toxic dose in 20 kg dog:      56.6 g PO of Radix Notopterygii essential oil.
                    Equivalent toxic dose in 5 kg cat:       14.15 g PO of Radix Notopterygii essential oil.



                          DRUG     Validated interactions studies do not exist for Radix Notopterygii preparations. Clinical
                 INTERACTIONS      interactions with other drugs have not been reported.





                                   Rehmannia glutinosa (Rehmannia)


                                   Radix Rehmanniae Glutinosae is known in Asia as a traditional herbal medicine with anti-inflammatory
                                   properties (Sung et al., 2011). A number of chemical and pharmacological studies have been
                                   conducted on Radix Rehmanniae Glutinosae and more than 70 compounds including  iridoids,
                                   saccharides, amino acids, inorganic ions, as well as other trace elements have been identified.
                                   Studies show that Radix Rehmanniae Glutinosae and its active principles possess wide pharmacological
                                   actions on the immune system, endocrine system, cardiovascular system and the nervous system
                                   (Zhang et al., 2008). Radix Rehmanniae Glutinosae has shown strong scavenging activity against
                                   superoxide radical,  hydroxyl radical,  hydrogen peroxide, and 2,2-diphenyl-1-picrylhydrazyl
                                   (DPPH) radical (Yu et al., 2006a) and to increase the activity of antioxidant enzymes and the
                                   level of glutathione (Yu et al., 2006b).


                    Toxicity for Radix Rehmanniae Glutinosae has not been documented in dogs and cats when administered orally
                TOXICOLOGY  weight in mice (WHO, 2007). 50  >10 g PO of 70% methanol extract of Radix Rehmanniae Glutinosae.
                    in therapeutic doses. Oral LD  for 70% methanol extract of Radix Rehmanniae Glutinosae is >2.0 g/kg of body



                    Equivalent toxic dose in 20 kg dog:  >40 g PO of 70% methanol extract of Radix Rehmanniae Glutinosae.
                    Equivalent toxic dose in 5 kg cat:



                          DRUG     Validated  interactions  studies  do  not  exist  for  Radix  Rehmanniae  Glutinosae  preparations.
                 INTERACTIONS      Clinical interactions with other drugs have not been reported. However, caution should be taken
                                   when used with drugs metabolized by CYP3A4 as Radix Rehmanniae Glutinosae could activate
                                   pregnane X receptor (PXR) signalling pathway and induce CYP3A4 reporter gene (Yu et al.,
                                   2011).









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