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AstraZeneca's Lokelma Receives FDA's Approval for Patients with Hyperkalaemia in Adults

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AstraZeneca's Lokelma Receives FDA's Approval for Patients with Hyperkalaemia in Adults

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  • The approval is based on five studies assessing Lokelma vs PBO in patients with hyperkalaemia
  • The study resulted in onset of action was at 1.0 hour and the median time to achieving normal potassium levels in the blood was 2.2 hours- 92% of patients achieved normal potassium level in 48 hrs. and was effective for 12 mos.
  • Lokelma insoluble- non-absorbed sodium zirconium silicate formerly known as ZS-9- and has received EU’s approval on 22 Mar-2018

Ref: AstraZeneca | Image: AstraZeneca

Click here to­ read the full press release 

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