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In terms of the severity of infusion-related adverse events, severe events were not observed.
For example, use of pharmacogenomics of warfarin decreases risk of adverse events (severe hemorrhage) and increases efficacy [1 3].
Secondary outcomes were any adverse event, severe adverse event, relapse, relapse free survival, event free survival and quality of life.
There was no significant variation in the rates of adverse and severe adverse events between the two treatment groups.
There were no significant adverse events, severe infections, or infusion-related reactions.
No severe adverse events were reported and no adverse event was dose-limiting.
Patients and healthcare professionals reported relatively more preventable and severe adverse events compared to less preventable and severe adverse events.
No severe adverse reactions were observed.
No severe adverse event occurred.
No serious or severe adverse events were reported.
Such errors can have severe adverse effects on patients.
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