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                                          PHARMACOLOGICAL ACTIVITIES - TOXICOLOGY - DRUG INTERACTIONS







                TOXICOLOGY  Arctostaphylos uva-ursi


                    Toxicity for Folium Uvae Ursi has not been documented in dogs and cats when administered orally in therapeutic
                    doses. No data on single or repeated dose toxicity has been reported for Folium Uvae Ursi extract (EMEA, 2011).




                       DRUG    Validated interactions studies do not exist for Folium Uvae Ursi preparations. Clinical interactions
              INTERACTIONS     with other drugs have not been reported.






            Tribulus terrestris (Puncture Vine)


            In traditional medicine, Fructus Tribuli is used in the treatment of urolithiasis. It is also used
            as a diuretic (WHO, 2009). Extract of Fructus Tribuli has exhibited a concentration dependent
            inhibition of nucleation and the growth of calcium oxalate crystals (Aggarwal et al., 2010).
            Ethanol extract of Fructus Tribuli showed significant dose dependent protection against uroliths
            induced by glass bead implantation in albino rats. The extract provided significant protection
            against deposition of calculogenic material around the glass bead. It also protected against
            leukocytosis and elevation of serum urea levels (Anand et al., 1994). In a study, aqueous extract
            of Fructus Tribuli elicited a positive diuresis, which was slightly more than that of furosemide.
            The  diuretic  and  contractile  effects  of  Fructus  Tribuli  indicate  that  it  has  the  potential  of
            propelling urinary stones (Al-Ali et al., 2003). A dried extract of Fructus Tribuli induced diuresis
            and increased creatinine clearance in anaesthetized dogs (Van Valkenburg & Bunyapraphatsara,
            2003). Oral administration of Fructus Tribuli extract provided protection against the mercuric
            chloride induced toxicity in mice kidney tissue (Kavitha & Jagadeesan, 2006) and reduced
            hyperoxaluria-caused  oxidative  stress,  and  restored  antioxidant  enzyme  activity  and  their
            expression profile in kidney tissue (Kamboj et al., 2011).



                    Toxicity for Fructus Tribuli has not been documented in dogs and cats when administered orally in therapeutic
               TOXICOLOGY  (Arcasoy et al., 1998).   50
                    doses. Intraperitoneal LD  of lyophilized saponin mixture of Fructus Tribuli is 813 mg/kg of body weight in mice



                    Equivalent toxic dose in 20 kg dog:   16,260 mg IP of lyophilized saponin mixture of Fructus Tribuli.
                    Equivalent toxic dose in 5 kg cat:    4,065 mg IP of lyophilized saponin mixture of Fructus Tribuli.



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






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