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Taltz ® (ixekizumab)
This information is intended for UK registered healthcare professionals only as a scientific exchange in response to your search for information. Please refer to the link for full prescribing information:
Taltz Summary of Product Characteristics (SmPC)
Taltz® (ixekizumab): Management of Overdose
In the event of ixekizumab overdosage, monitor the patient for any signs or symptoms of adverse reactions and institute appropriate symptomatic treatment immediately.
summary contains discussion of doses that are inconsistent with the
approved dose of ixekizumab. Please refer to Taltz summary of product
characteristics for full prescribing information.1
up to 180 mg have been administered subcutaneously in clinical trials
in adults without dose-limiting toxicity. Overdoses up to 240 mg,
subcutaneously in adults, have been reported without any serious
the event of overdosage, it is recommended that the patient be
monitored for any signs or symptoms of adverse reactions and
appropriate symptomatic treatment be instituted immediately.1
Taltz [summary of product characteristics]. Eli Lilly Nederland
B.V., The Netherlands.
Data on file, Eli Lilly and Company and/or one of its subsidiaries.
Date of Last Review:March 09, 2020
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