FDA Tracks Invokana
FDA Tracks Invokana
Introduction
Invokana, (a diabetic medication and SGLT2 inhibitor) was also in the news as the FDA now requires a serious boxed warning to be highlighted in the labels about the increased risk of leg and foot amputations. This decision is bagged by the results of two interim clinical trials and is applicable to all the canagliflozin drug labels. Previously, a safety warning about the increased risk of acute kidney injury and kidney failure, followed by a warning of increased risk of ketoacidosis was ordered by the FDA to be a part of the label.
Invokana Multidistrict Litigation (MDL) is filed before U.S. District Judge Brian Martinotti in the District of New Jersey. Cases have also come forward, wherein plaintiffs have further alleged that the use of Invokana resulted in an increased risk of ischemic stroke along with Urosepsis which is a dangerous type of urinary tract infection. The number of litigation filed is expected to rise as more research results are brought forth.
Latest News
Study Links Roundup Chemical to Long-Term Brain Damage
A recent study suggests that exposure to the widely used herbicide Roundup, which contains the active ingredient glyphosate, may be…
Zimmer Biomet Gets FDA Approval for Cementless Partial Knee
Zimmer Biomet announced it has received supplemental FDA premarket approval (PMA) for the Oxford Cementless Partial…
Court Names Special Masters for Bard Mesh Claim Settlements
The U.S. District Judge overseeing the federal litigation involving Bard hernia mesh lawsuits has appointed two…