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Meloxicam‐Induced Thrombocytopenia
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Immune thrombocytopenia can have several causes including the use of certain drugs. Thrombocytopenia has been documented as a rare adverse effect of some nonsteroidal antiinflammatory drugs (NSAIDs) including diclofenac, naproxen, and ibuprofen. However, only one previously documented case of meloxicam‐associated thrombocytopenia has been reported in the literature. We describe an 84‐year‐old woman who developed a case of immune‐mediated thrombocytopenia that was attributed to meloxicam therapy. The patient's platelet count decreased from a baseline of 267 × 103/mm3 to 2 × 103/mm3 1 week after she received her first lifetime dose of meloxicam. She also experienced black stools and bruising that coincided with the meloxicam administration. The almost immediate onset of thrombocytopenia and symptoms after initiation of meloxicam, as well as the marked reduction in her platelet count, suggest an idiosyncratic reaction. According to the Hill criteria for assessing causality of adverse drug events, it is plausible that this reaction was due to meloxicam. Health care providers should be aware of the possibility of thrombocytopenia secondary to NSAID therapy including meloxicam. Immune thrombocytopenia can be life threatening if it is not identified and treated promptly. A thorough medication history is particularly important when patients present with unusual symptoms, with a focus on those drugs that have been recently initiated. Although thrombocytopenia is a rare adverse effect of NSAID therapy, it should be considered a potential cause in patients receiving these drugs who have signs and symptoms consistent with this blood dyscrasia.
Title: Meloxicam‐Induced Thrombocytopenia
Description:
Immune thrombocytopenia can have several causes including the use of certain drugs.
Thrombocytopenia has been documented as a rare adverse effect of some nonsteroidal antiinflammatory drugs (NSAIDs) including diclofenac, naproxen, and ibuprofen.
However, only one previously documented case of meloxicam‐associated thrombocytopenia has been reported in the literature.
We describe an 84‐year‐old woman who developed a case of immune‐mediated thrombocytopenia that was attributed to meloxicam therapy.
The patient's platelet count decreased from a baseline of 267 × 103/mm3 to 2 × 103/mm3 1 week after she received her first lifetime dose of meloxicam.
She also experienced black stools and bruising that coincided with the meloxicam administration.
The almost immediate onset of thrombocytopenia and symptoms after initiation of meloxicam, as well as the marked reduction in her platelet count, suggest an idiosyncratic reaction.
According to the Hill criteria for assessing causality of adverse drug events, it is plausible that this reaction was due to meloxicam.
Health care providers should be aware of the possibility of thrombocytopenia secondary to NSAID therapy including meloxicam.
Immune thrombocytopenia can be life threatening if it is not identified and treated promptly.
A thorough medication history is particularly important when patients present with unusual symptoms, with a focus on those drugs that have been recently initiated.
Although thrombocytopenia is a rare adverse effect of NSAID therapy, it should be considered a potential cause in patients receiving these drugs who have signs and symptoms consistent with this blood dyscrasia.
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