The prescription drugs Invokana® (canagliflozin) and Invokamet® (canagliflozin and metformin) are used to treat Type 2 diabetes. However, they have been linked to an increased risk of serious complications, including leg and foot amputations and ketoacidosis, a potentially fatal medical condition that results in the body releasing dangerous acids into the bloodstream.
If you or your loved one took Invokana or Invokamet and underwent leg or foot amputation or experienced ketoacidosis, you may be entitled to compensation. Contact our drug injury lawyers now to see how we can help.
Side Effects of Invokana® and Invokamet®
An increased risk of the following dangerous conditions and side effects has been linked to Invokana and Invokamet:
- Leg and foot amputations
- Hyperkalemia (too much potassium in the blood)
- Hypoglycemia (low blood sugar)
- Kidney failure
- Fluid buildup in the brain (cerebral edema)
- Hypotension (low blood pressure)
- Death of bowel tissue due to low blood pressure
If you or a loved one took Invokana or Invokamet and experienced any of these side effects, contact us immediately. Our drug injury lawyers may be able to help you recover compensation.
Lawyers Helping Invokana® Amputation Patients
In May 2017, the U.S. Food and Drug Administration (FDA) released a Drug Safety Communication warning patients that taking Invokana, Invokamet, and Invokamet XR causes an increased risk of leg and foot amputations. Two large clinical trials showed that amputations of the toe and middle of the foot were most common, but amputations above and below the knee also occurred.
Invokana® and Invokamet® Ketoacidosis Risk
Invokana and Invokamet are classified as SGLT2 inhibitors, a class of drugs prescribed to treat patients with Type 2 diabetes. Ketoacidosis is a serious medical condition normally associated with patients with Type 1 diabetes.
Since March 2013, the FDA has received more than 70 reports of acidosis—including diabetic ketoacidosis (DKA) and ketosis—among Type 2 diabetics treated with SGLT2 inhibitors, such as Invokana and Invokamet. Life-threatening blood infections that started as urinary tract infections were also reported.
In December 2015, the FDA announced the addition of new warnings to all SGLT2 inhibitor labels to address the risk of ketoacidosis and serious urinary tract infections.
What Triggers Ketoacidosis?
The FDA reports that three factors may potentially trigger ketoacidosis in patients taking drugs such as Invokana and Invokamet:
- Major illness
- Reduced food and fluid intake
- Reduced insulin dose
Symptoms of Diabetic Ketoacidosis (DKA)
Ketoacidosis occurs when the body cannot break down sugars in the blood due to a lack of insulin. The body then begins to break down fats for energy, which releases acids (called ketones) into the bloodstream. If left untreated, ketoacidosis can be fatal.
Symptoms of Ketoacidosis can include:
- Difficulty breathing
- Fatigue or sleepiness
- Fruity breath
- Flushed face
- Abdominal pain
If you or a loved one with diabetes experience any of these symptoms after taking Invokana, Invokamet, or another SGLT2 inhibitor, seek medical care immediately.
Our Invokana® Lawyers Want to Help
If you or someone you love took Invokana or Invokamet and suffered ketoacidosis or underwent a leg or foot amputation, our lawyers want to help. There are strict deadlines for filing drug injury lawsuits, so contact us immediately. Our experienced legal team is standing by to answer your questions.
Invokana® and Invokamet® are trademarks of Johnson & Johnson Corporation and are used here only to identify the products in question. This law firm is not associated with, sponsored by, or affiliated with Johnson & Johnson Corporation or the U.S. Food and Drug Administration.