The following undesirable effects were observed whereas the frequency of undesirable effect is not known: The most common adverse reactions associated with oral administration are nausea, abdominal pain, dyspepsia, flatulence, constipation and diarrhoea. The reported adverse reactions are usually mild and transitory.
In the following table, adverse reactions have been grouped on the basis of "Internationally agreed Order of Importance" System Organ Class (SOC) MedDRA Classification. In each SOC, undesirable effects were classified according to their occurrence frequency. In each frequency class the undesirable effects are reported according to a decreasing order of severity. (See table.)

Cases of hypercholesterolaemia have been reported, but a causal link has not been demonstrated.
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