Page 187 - product-manual
P. 187

TM/MC  TM/MC

               NON-MEDICINAL INGREDIENTS
               Stevia, Citric acid, Potassium sorbate, Purified water, Sodium benzoate.


                    VimForte-VM™ is manufactured under strict GMP standards and contains no dairy, yeast, corn, or wheat
                     or gluten. Does not contain animal by-products.







             PHARMACOLOGICAL ACTIVITIES - TOXICOLOGY - DRUG INTERACTIONS






                               Cholecalciferol [Vitamin D ] (C H O)
                                                               3    27  44
                               Dogs and cats may have limited ability to use UVB light for cutaneous biogenesis of vitamin
                               D (Kleiman et al., 2010). For this reason, it is important that vitamin D  be introduced directly
                                                                                             3
                               into the diet (Kleiman et al., 2010; Schenck, 2010). Vitamin D  regulates calcium:phosphorous
                                                                                     3
                               balance in the body and it stimulates the kidney’s retention of calcium, which is vitally important
                               to bone formation, nerve and muscle control. Osteomalacia occurs when insufficient calcium
                               and/or phosphorus is available for mineralization of newly formed osteoid (Ettinger & Feldman,
                               2000b).



                 Several factors, such as the chemical form (vitamin D  or Vitamin D ), species, dietary intake of calcium and
                                                                          3
                                                              2
            TOXICOLOGY  vitamin D in the diet. Most animal species appear to be able to tolerate 10 times the level of vitamin D that they
                 phosphorus, route of administration, and duration of treatment, can influence the maximum tolerable levels of
                 require for long periods of time (NRC, 1987). Intraperitoneal LD  of vitamin D  is 135.4 mg/kg of body weight
                                                                                    3
                                                                       50
                 in male mice (Hatch & Laflamme, 1989). Published human cases of vitamin D  toxicity, for which serum levels
                                                                                   3
                 and dose are known, all involve intake of > or = 40,000 IU (1,000 mcg) per day (Vieth, 1999).



                   DRUG    Due to a narrow therapeutic index, vitamin D analogs given in combination with each other or
          INTERACTIONS     with pharmacologic doses of vitamin D (calcitriol, doxercalciferol, paricalcitol) may demonstrate
                           additive  effects  resulting  in  toxicity  manifested  as  hypercalcemia,  hypercalciuria,  and
                           hyperphosphatemia  (Drugs.com).  Atorvastatin  appears  to  increase  25-hydroxycholecalciferol
                           (25[OH]D) concentrations,  whereas concurrent  vitamin D supplementation  decreases
                           concentrations  of  atorvastatin.  Use  of  thiazide  diuretics  in  combination  with  calcium  and
                           vitamin  D supplements may cause hypercalcemia  in humans or those with compromised
                           renal  function  or  hyperparathyroidism.  Insufficient  evidence  is  available  to  determine  whether
                           lipase inhibitors, antimicrobial agents, antiepileptic drugs, highly active antiretroviral agents, or H2
                           receptor antagonists alter serum 25(OH)D concentrations (Robien et al., 2013).











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