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Invokana Cases Involving Diabetic Ketoacidosis And Kidney Side Effects

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According to data from IMS Health, Invokana reached 1.1 million dispensed outpatient prescriptions in the second quarter of 2015, followed by Farxiga with 411,000, and Jardiance with 136,000.

These three diabetes medicines are in a class of drugs for Type 2 diabetes that blocks the protein sodium glucose cotransporter 2 (SGLT2). In turn, this causes lower blood sugar by causing the kidneys to excrete some circulating glucose rather than returning it to circulation.

And from the ISMP QuarterWatch published January 13, 2016, with data from first and second quarters of 2015 we get this related drug safety facts about these still relatively new diabetes drugs:

Adverse drug event reports over the last 12 months increased roughly in line with patient exposure, with 5484 new cases for [Invokana (canagliflozin)], 1805 for [Farxiga (dapagliflozin)], and 455 for [Jardiance (empagliflozin)]. We observed increasing numbers of reports of metabolic acidosis–a potentially life-threatening disorder that has been the focus of two FDA Drug Safety Communications. Over the past 12 months we identified 168 possible cases for [Invokana (canagliflozin)], 80 for [Farxiga (dapagliflozin)], and 12 for [Jardiance (empagliflozin)].

In turn, this caused the January 2016 ISMP QuarterWatch publication to make this observation: “Whether the clinical benefits of these drugs outweigh the increasing evidence of their risks remains uncertain.”

We have written several times previously about Invokana, Farxiga, and Jardiance, as seen below:

Be assured that we will be watching for additional drug safety warnings about Invokana, Farxiga, Jardiance, and these other new diabetes drugs.

[Read this article in full at original source]

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