cefonicid

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Reactions 892 - 9 Mar 2002 S Cefonicid First report of eosinophilic hepatitis in an elderly patient: case report Treatment with cefonicid for community-acquired pneumonia was associated with the development of eosinophilic hepatitis in a 67-year-old man. The man had been receiving IM cefonicid 1 g/day for 1 week when he reported the transient appearance of a pruritic, erythematous papular rash involving his chest, forehead and back. He had also been receiving salmeterol and fluticasone propionate. One week later, he presented with nausea, vomiting, anorexia, fatigue and abdominal discomfort. His AST and ALT levels were 160 U/L (normal 10–36) and 312 U/L (6–40), respectively, his γ-glutamyl transferase level was 453 U/L (7–49), his alkaline phosphatase level was 563 U/l (91–258) and his peripheral eosinophil count was 700/mm 3 . Investigations revealed a fatty, enlarged liver. Treatment with cefonicid was stopped, and the man’s symptoms resolved after 4 days. At discharge on hospital day 8, his liver enzyme levels and eosinophil count had decreased, and they had normalised within 7 weeks of cefonicid discontinuation. During 6 months’ follow-up, he remained symptom-free with normal liver function. Author comment: ‘The temporal relationship in our patient linking the institution of cefonicid therapy with the development of rash, peripheral eosinophilia, and hepatitis implicates a hypersensitivity-like liver injury, which reflects an immune mechanism triggered by the drug.’ Famularo G, et al. Eosinophillic hepatitis associated with cefonicid therapy. Annals of Pharmacotherapy 35: 1669-1671, Dec 2001 - Italy 800900209 » Editorial comment: A search of AdisBase and Medline did not reveal any previous case reports of hepatitis or eosinophilia associated with cefonicid. The WHO Adverse Drug Reactions database contained 2 reports of hepatitis, and 1 report of eosinophilia, associated with cefonicid. 1 Reactions 9 Mar 2002 No. 892 0114-9954/10/0892-0001/$14.95 Adis © 2010 Springer International Publishing AG. All rights reserved

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Page 1: Cefonicid

Reactions 892 - 9 Mar 2002

★ SCefonicid

First report of eosinophilic hepatitis in an elderlypatient: case report

Treatment with cefonicid for community-acquiredpneumonia was associated with the development ofeosinophilic hepatitis in a 67-year-old man.

The man had been receiving IM cefonicid 1 g/day for 1 weekwhen he reported the transient appearance of a pruritic,erythematous papular rash involving his chest, forehead andback. He had also been receiving salmeterol and fluticasonepropionate. One week later, he presented with nausea,vomiting, anorexia, fatigue and abdominal discomfort. His ASTand ALT levels were 160 U/L (normal 10–36) and 312 U/L(6–40), respectively, his γ-glutamyl transferase level was 453U/L (7–49), his alkaline phosphatase level was 563 U/l(91–258) and his peripheral eosinophil count was 700/mm3.Investigations revealed a fatty, enlarged liver.

Treatment with cefonicid was stopped, and the man’ssymptoms resolved after 4 days. At discharge on hospital day8, his liver enzyme levels and eosinophil count had decreased,and they had normalised within 7 weeks of cefoniciddiscontinuation. During 6 months’ follow-up, he remainedsymptom-free with normal liver function.

Author comment: ‘The temporal relationship in our patientlinking the institution of cefonicid therapy with thedevelopment of rash, peripheral eosinophilia, and hepatitisimplicates a hypersensitivity-like liver injury, which reflects animmune mechanism triggered by the drug.’Famularo G, et al. Eosinophillic hepatitis associated with cefonicid therapy. Annalsof Pharmacotherapy 35: 1669-1671, Dec 2001 - Italy 800900209

» Editorial comment: A search of AdisBase and Medline didnot reveal any previous case reports of hepatitis or eosinophiliaassociated with cefonicid. The WHO Adverse Drug Reactionsdatabase contained 2 reports of hepatitis, and 1 report ofeosinophilia, associated with cefonicid.

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Reactions 9 Mar 2002 No. 8920114-9954/10/0892-0001/$14.95 Adis © 2010 Springer International Publishing AG. All rights reserved