The following table lists adverse reactions collected from clinical trial data, and adverse events reported from post-marketing sources. The frequency of adverse reactions are as follows: Very common (≥1/10), Common (≥1/100 to <1/10), Uncommon (≥1/1000 to <1/100), Rare (≥1/10000 to <1/1000), Very rare (<1/10000), Unknown frequency (cannot be estimated from the available data). (See table.)

Reporting of suspected adverse reactions: Reporting of suspected adverse reactions after a marketing authorization has been granted to the drug is important. It allows continuous surveillance of the medicine's benefit/risk ratio. Health professionals can report any suspected adverse reaction.
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