Jardiance – Amputations Drug Safety Issue Remains Uncertain Due To Admitted “inherent limitations of… post hoc analyses”

Jardiance Seemingly Not Associated With Amputations Per Reexamination Of Drug Company Funded EMPA-REG OUTCOME® Trial Data

 

(Posted by Tom Lamb at DrugInjuryWatch.com)

 

In April 2016 the European Medicines Agency (EMA) warned that Invokana and Invokamet were linked to an increased risk of amputations, especially of the toes.

Ever since then we have been monitoring the medical literature concerning the risk of lower limb amputations and drugs in the sodium glucose cotransporter 2 (SGLT2) inhibitor class, such as canagliflozin (Invokana / Invokamet), empagliflozin (Jardiance / Glyxambi / Synjardy), and dapagliflozin (Farxiga / Xigduo / Qtern).

On November 13, 2017 Boehringer Ingelheim published on their website this press release, "Jardiance® reduced risk of cardiovascular death in adults with type 2 diabetes and peripheral artery disease". Therein, we found this excerpt concerning lower limb amputations:

These results, from a post-hoc analysis of the landmark EMPA-REG OUTCOME® trial, were shared as an oral presentation on behalf of Boehringer Ingelheim and Eli Lilly and Company (NYSE: LLY) at the American Heart Association® (AHA) Scientific Sessions 2017 in Anaheim, Calif. and simultaneously published online [as a Research Letter: "Cardiovascular Outcomes and Safety of [Jardiance (Empagliflozin)] in Patients With Type 2 Diabetes Mellitus and Peripheral Artery Disease: A Subanalysis of EMPA-REG OUTCOME"] in the AHA’s journal, Circulation….

Overall side effects and serious side effects were balanced between the Jardiance [(empagliflozin)] and placebo groups in adults with and without peripheral artery disease. In the group with peripheral artery disease, lower-limb amputations occurred in 5.5 percent of those treated with Jardiance and 6.3 percent of those treated with placebo. In the group without peripheral artery disease, lower-limb amputations occurred in 0.9 percent of those treated with Jardiance and 0.7 percent of those treated with placebo….

On that same date, the medical journal Diabetes Care made available online a "Publish Ahead of Print" version of this brief article, "[Jardiance (Empagliflozin)] and Assessment of Lower-Limb Amputations in the EMPA-REG OUTCOME Trial".

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It includes this apparent "soft" disclaimer about the findings of those medical researchers whose names were displayed next to the article title.

We acknowledge the inherent limitations of manually identifying [lower limb amputation (LLA)] and performing post hoc analyses. A dedicated case report form was not used in the EMPA-REG OUTCOME trial as there was no concern regarding an increased risk of amputation with [Jardiance (empagliflozin)] before or during the trial. We are confident that the reporting and systematic retrieval processes employed were thorough.

Furthermore, and perhaps significantly, at the end of this Diabetes Care article text appears the following note:

Acknowledgments. Medical writing assistance, supported financially by Boehringer Ingelheim, was provided by Elizabeth Ng of FleishmanHillard Fishburn, London, U.K., during the preparation of this paper.

We point out that there is a similar Acknowledgments note concerning the involvement of FleishmanHillard Fishburn at the end of the earlier-mentioned Circulation Research Letter, also.

A week later, on November 20, 2017, this headline caught our attention, "[Jardiance (empagliflozin)] does not increase amputation risk". This relatively short piece, published on the Healio IN THE JOURNALS PLUS website, reported on the above Diabetes Care article.

That Healio report was followed by this November 27, 2017 Medscape story, "No Signal for Amputation With [Jardiance (Empagliflozin)] in EMPA-REG" which, despite the favorable title, included this cautionary part:

[D]octors are clearly still concerned about this and whether it represents a class effect of SGLT2 inhibitors or is specific to [Invokana (canagliflozin)].

Commenting on the topic in a recent perspective for Medscape Medical News, Harpreet Bajaj of Mount Sinai Hospital, University of Toronto, Ontario, said: "To reassure us of the benefit/harm balance with [Invokana (canagliflozin)], we clinicians need more data-mining from CANVAS and additional long-term randomized controlled trials."

This Medscape story did not indicate whether Dr. Bajaj thought the Boehringer Ingelheim press release, the Diabetes Care article, or the Healio piece alleviated his own concerns, at least, about lower limb amputations possibly being associated with other SGLT2 inhibitors, like Jardiance and Farxiga.

However, that statement by Dr. Bajaj was immediately followed by this sub-headline for the next part of the November 27 Medscape story: Inherent Limitations in Manually Identifying Lower-Limb Amputations.

Now, we take you back to this past June and an article, "Invokana Shown to Have Heart Benefits, but Elevated Amputation Risks", which was posted on our Drug Safety Developments blog. Only five months ago a leading expert in diabetes medicine made this observation:

John Buse, the chief of endocrinology at UNC – Chapel Hill provided his opinion on the matter, "Personally, I would much rather have a small heart attack than lose a toe…  And I think I would much rather have a big heart attack than lose a leg.” He anticipates a significant debate, saying that the benefits and harms are most likely "over- and under-estimated in each study." [emphasis added]

In closing, it appears there needs to more medical research done on the risk of lower limb amputations for patients who use the increasing popular diabetes medicines in this SGLT2 inhibitors drug class, which includes Invokana and Jardiance as well as Farxiga.


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6 responses to “Jardiance – Amputations Drug Safety Issue Remains Uncertain Due To Admitted “inherent limitations of… post hoc analyses””

  1. Charlene Avatar
    Charlene

    I have been taking both Januvia and Jardiance for several years now and
    sometime after being prescribed the two of them I suddenly had a “dropped
    toe” the large toe on my left foot. The Doctor, upon having it drawn to his
    attention, determined that it was caused by a back problem and consequently sent me to a surgeon whooperated on my lower back. I had NOT been having a great deal of pain in my back and what pain I had I concluded was brought on by arthritis as I had been told that I had that in my neck. Now I am reading that the “Dropped Toe” may well have been caused by the medications that I have been prescribed so I mentioned that to my Doctor only to be completely ignored. When I asked of the ultimate fate of the toe the reply was, ” oh you will probably injure it at some time or another or it will be bothersome and you will have to have it amputated.” The nonchalance of the response was chilling to me! So I guess what I really want to know is should I continue with either or both of these medications and if I do am I putting my other digits and joints at risk? (I have already had to have a hip joint replacement! and am having pain in my left ankle and my right knee. I am worried. Charlene

  2. Charlene Avatar
    Charlene

    I have been taking both Januvia and Jardiance for several years now and
    sometime after being prescribed the two of them I suddenly had a “dropped
    toe” the large toe on my left foot. The Doctor, upon having it drawn to his
    attention, determined that it was caused by a back problem and consequently sent me to a surgeon whooperated on my lower back. I had NOT been having a great deal of pain in my back and what pain I had I concluded was brought on by arthritis as I had been told that I had that in my neck. Now I am reading that the “Dropped Toe” may well have been caused by the medications that I have been prescribed so I mentioned that to my Doctor only to be completely ignored. When I asked of the ultimate fate of the toe the reply was, ” oh you will probably injure it at some time or another or it will be bothersome and you will have to have it amputated.” The nonchalance of the response was chilling to me! So I guess what I really want to know is should I continue with either or both of these medications and if I do am I putting my other digits and joints at risk? (I have already had to have a hip joint replacement! and am having pain in my left ankle and my right knee. I am worried. Charlene

  3. KR Avatar
    KR

    Charlene,
    First let me say I’m sorry to hear that you are going through these problems. Connecting the dots between reported clinical adverse events (AE’s) and your specific issues is complicated to do. However, it may be useful to begin ruling out your specific clinical issues with the medications. Your healthcare provider should help you do that and then a shared decision between the both of you can begin. A patient with diabetes especially long standing diabetes I’d want to know how long have you had this diagnosis, what your blood sugars are on average. Do you have diagnoses like neuropathy, peripheral vascular disease, cardiovascular disease, have you had any amputations in the past, have you had an ankle brachial index score/test done? Do you have foot ulcers, gangrene or infections? Does your provider do routine foot exams and have you been taught to examine your own feet and educated on what to look for and report? Do your feet look pale and is the feeling in your feet/toes becoming less sensitive? These exams must be performed by your practitioner very thoroughly. What is problematic when a patient is scared of the drug that greatly minimizes your risk for heart attack, stroke and death and other complications to diabetes is that you trade off taking the drug that can potentially save your life/improve your life with being left with very few other clinical options. Sometimes that risk becomes great. If diabetes is left uncontrolled than the risk of amputation is much greater than any medication adverse affect. If a provider and you pay attention to your eyes, feet, kidneys, heart, etc. your likelihood of amputation via any source is minimized exponentially. Make sure you are happy and have a good relationship with your provider and do what they tell you with lifestyle changes religiously! I hope that helps. It’s good to hear you are in tune to your body and engaged in your health.

  4. KR Avatar
    KR

    Charlene,
    First let me say I’m sorry to hear that you are going through these problems. Connecting the dots between reported clinical adverse events (AE’s) and your specific issues is complicated to do. However, it may be useful to begin ruling out your specific clinical issues with the medications. Your healthcare provider should help you do that and then a shared decision between the both of you can begin. A patient with diabetes especially long standing diabetes I’d want to know how long have you had this diagnosis, what your blood sugars are on average. Do you have diagnoses like neuropathy, peripheral vascular disease, cardiovascular disease, have you had any amputations in the past, have you had an ankle brachial index score/test done? Do you have foot ulcers, gangrene or infections? Does your provider do routine foot exams and have you been taught to examine your own feet and educated on what to look for and report? Do your feet look pale and is the feeling in your feet/toes becoming less sensitive? These exams must be performed by your practitioner very thoroughly. What is problematic when a patient is scared of the drug that greatly minimizes your risk for heart attack, stroke and death and other complications to diabetes is that you trade off taking the drug that can potentially save your life/improve your life with being left with very few other clinical options. Sometimes that risk becomes great. If diabetes is left uncontrolled than the risk of amputation is much greater than any medication adverse affect. If a provider and you pay attention to your eyes, feet, kidneys, heart, etc. your likelihood of amputation via any source is minimized exponentially. Make sure you are happy and have a good relationship with your provider and do what they tell you with lifestyle changes religiously! I hope that helps. It’s good to hear you are in tune to your body and engaged in your health.

  5. Karen Reighert Avatar

    I started Jardience when it first came out and my doctor was very insistent this is the drug I needed for my diabetes. I started on the low dose and then last year she increased to 25 mg. I was so dehydrated I could not even talk with out taking a drink between a few words. My family and others looked at me like what is wrong with you. I had some dry mouth with other meds I had been on for years but nothing like the dry mouth from the Jardience.I began to have teeth that were needing pulled due to the dry mouth that was caused from the Jardience. My dental insurance will not cover a new partial upper and lower due to all the extractions. I still have one more needing pulled and waiting to see oral surgeon again. I have a root canal tomorrow and I pray I do not lose a front tooth. I had a new bridge break at the gum line and had to have the oral surgeon excise. Had I know that this medication was going to cause me to have dry moth and loss of precious teeth I never would have started taking it. Presently I’m not taking Jardience and what a difference to have saliva agian in my mouth. Not only did the Jardience cause dry mouth I constantly was sore and irritated with open areas of the peri area, yeast infection vaginally almost always. Oral surgeon gave me Nyastin for oral thrush and dentist prescribed nystatin cream for corners of my mouth. Since stopping Jardience this has resolved. I so wish losing precious teeht could be so easy to resolve. When I also found out that while on Jardience your chances of a lower extremity amputation’s increases by 50% why would a medical doctor even prescribe this medication. Also my HgbA1c never decreased, just increased by a point. I hope they take this drug and others in the same category off the market or make the doctors give a complete disclosure on the possible side effects that are life changing and not for the better. Sad part is the NP at the office wanted to get me off the drug due to the severe dehydration and the irritation from yeast; however the day i was to see her the doctor saw me instead and increased the dose. I mentioned that the NP wanted to get me off of the drug and she said your kidney functions are fine lets increase the dosage. The NO felt bad that I could not hardly talk do to the dry mouth. I’m so emotionally and mentally stressed over what happened and do not see a resolution to the damage it caused.

  6. Karen Reighert Avatar

    I started Jardience when it first came out and my doctor was very insistent this is the drug I needed for my diabetes. I started on the low dose and then last year she increased to 25 mg. I was so dehydrated I could not even talk with out taking a drink between a few words. My family and others looked at me like what is wrong with you. I had some dry mouth with other meds I had been on for years but nothing like the dry mouth from the Jardience.I began to have teeth that were needing pulled due to the dry mouth that was caused from the Jardience. My dental insurance will not cover a new partial upper and lower due to all the extractions. I still have one more needing pulled and waiting to see oral surgeon again. I have a root canal tomorrow and I pray I do not lose a front tooth. I had a new bridge break at the gum line and had to have the oral surgeon excise. Had I know that this medication was going to cause me to have dry moth and loss of precious teeth I never would have started taking it. Presently I’m not taking Jardience and what a difference to have saliva agian in my mouth. Not only did the Jardience cause dry mouth I constantly was sore and irritated with open areas of the peri area, yeast infection vaginally almost always. Oral surgeon gave me Nyastin for oral thrush and dentist prescribed nystatin cream for corners of my mouth. Since stopping Jardience this has resolved. I so wish losing precious teeht could be so easy to resolve. When I also found out that while on Jardience your chances of a lower extremity amputation’s increases by 50% why would a medical doctor even prescribe this medication. Also my HgbA1c never decreased, just increased by a point. I hope they take this drug and others in the same category off the market or make the doctors give a complete disclosure on the possible side effects that are life changing and not for the better. Sad part is the NP at the office wanted to get me off the drug due to the severe dehydration and the irritation from yeast; however the day i was to see her the doctor saw me instead and increased the dose. I mentioned that the NP wanted to get me off of the drug and she said your kidney functions are fine lets increase the dosage. The NO felt bad that I could not hardly talk do to the dry mouth. I’m so emotionally and mentally stressed over what happened and do not see a resolution to the damage it caused.

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