Probable tacrolimus toxicity from tibolone co-administration in a woman: a case report
<p>Abstract</p> <p>Introduction</p> <p>Tibolone is a synthetic steroid, used with increasing frequency to treat symptoms of menopause, including patients with solid-organ transplants who are taking concurrent immune suppression. To the best of our knowledge, there are n...
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doaj-0cd00ad9aeb543a79a6af1d83fe4cf2d2020-11-25T00:09:55ZengBMCJournal of Medical Case Reports1752-19472010-08-014127610.1186/1752-1947-4-276Probable tacrolimus toxicity from tibolone co-administration in a woman: a case reportClark Carolyn JHawley Carmel MMudge David W<p>Abstract</p> <p>Introduction</p> <p>Tibolone is a synthetic steroid, used with increasing frequency to treat symptoms of menopause, including patients with solid-organ transplants who are taking concurrent immune suppression. To the best of our knowledge, there are no reported drug interactions between tibolone and tacrolimus, one of the principal immune suppressants used in kidney transplantation.</p> <p>Case presentation</p> <p>We report the case of a 49-year-old Caucasian woman who had received a kidney transplant and who developed acute kidney injury secondary to tacrolimus toxicity 10 days after starting tibolone therapy. No alternative causes were found. Tibolone is known to be a weak competitive inhibitor of CYP3A4, which is involved in tacrolimus metabolism.</p> <p>Conclusions</p> <p>Despite a careful evaluation, no alternative reason was found for the acute kidney injury, and her kidney function returned to the previous baseline within several days of cessation of the medication, and with no other specific treatment. Using the Drug Interaction Probability Scale we conclude that she experienced a probable drug interaction. We believe that transplant clinicians should utilise frequent therapeutic drug monitoring of tacrolimus in patients starting or stopping tibolone therapy.</p> http://www.jmedicalcasereports.com/content/4/1/276 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Clark Carolyn J Hawley Carmel M Mudge David W |
spellingShingle |
Clark Carolyn J Hawley Carmel M Mudge David W Probable tacrolimus toxicity from tibolone co-administration in a woman: a case report Journal of Medical Case Reports |
author_facet |
Clark Carolyn J Hawley Carmel M Mudge David W |
author_sort |
Clark Carolyn J |
title |
Probable tacrolimus toxicity from tibolone co-administration in a woman: a case report |
title_short |
Probable tacrolimus toxicity from tibolone co-administration in a woman: a case report |
title_full |
Probable tacrolimus toxicity from tibolone co-administration in a woman: a case report |
title_fullStr |
Probable tacrolimus toxicity from tibolone co-administration in a woman: a case report |
title_full_unstemmed |
Probable tacrolimus toxicity from tibolone co-administration in a woman: a case report |
title_sort |
probable tacrolimus toxicity from tibolone co-administration in a woman: a case report |
publisher |
BMC |
series |
Journal of Medical Case Reports |
issn |
1752-1947 |
publishDate |
2010-08-01 |
description |
<p>Abstract</p> <p>Introduction</p> <p>Tibolone is a synthetic steroid, used with increasing frequency to treat symptoms of menopause, including patients with solid-organ transplants who are taking concurrent immune suppression. To the best of our knowledge, there are no reported drug interactions between tibolone and tacrolimus, one of the principal immune suppressants used in kidney transplantation.</p> <p>Case presentation</p> <p>We report the case of a 49-year-old Caucasian woman who had received a kidney transplant and who developed acute kidney injury secondary to tacrolimus toxicity 10 days after starting tibolone therapy. No alternative causes were found. Tibolone is known to be a weak competitive inhibitor of CYP3A4, which is involved in tacrolimus metabolism.</p> <p>Conclusions</p> <p>Despite a careful evaluation, no alternative reason was found for the acute kidney injury, and her kidney function returned to the previous baseline within several days of cessation of the medication, and with no other specific treatment. Using the Drug Interaction Probability Scale we conclude that she experienced a probable drug interaction. We believe that transplant clinicians should utilise frequent therapeutic drug monitoring of tacrolimus in patients starting or stopping tibolone therapy.</p> |
url |
http://www.jmedicalcasereports.com/content/4/1/276 |
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