Our system is currently under heavy load due to increased usage. We're actively working on upgrades to improve performance. Thank you for your patience.
2017
DOI: 10.1111/jcpt.12528
|View full text |Cite
|
Sign up to set email alerts
|

Clindamycin-associated acute generalized exanthematous pustulosis

Abstract: Timely management of adverse skin reactions to antibiotics is paramount, and early identification of the culprit agent can allow for an alternative agent to be utilized. Clindamycin should be considered a potential causative agent for patients with skin reactions.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
8
0

Year Published

2017
2017
2023
2023

Publication Types

Select...
6
2

Relationship

0
8

Authors

Journals

citations
Cited by 9 publications
(8 citation statements)
references
References 9 publications
0
8
0
Order By: Relevance
“…Other Hypersensitivity Reactions Other immunologic drug reactions that have been reported include fixed drug eruptions [42]. Other rare hypersensitivity reactions to clindamycin include DRESS/DiHS [43][44][45], SDRIFE [46], AGEP [47][48][49][50][51][52][53], and acute febrile neutrophilic dermatosis or Sweet Syndrome [54][55][56]. DRESS is a rare delayed hypersensitivity reaction often occurring 2-8 weeks from drug exposure and characterized by skin eruption, fever, eosinophilia, lymphadenopathy, and internal organ (i.e., liver, kidney, lung) involvement [43][44][45].…”
Section: Ige-mediated Reactionsmentioning
confidence: 99%
See 1 more Smart Citation
“…Other Hypersensitivity Reactions Other immunologic drug reactions that have been reported include fixed drug eruptions [42]. Other rare hypersensitivity reactions to clindamycin include DRESS/DiHS [43][44][45], SDRIFE [46], AGEP [47][48][49][50][51][52][53], and acute febrile neutrophilic dermatosis or Sweet Syndrome [54][55][56]. DRESS is a rare delayed hypersensitivity reaction often occurring 2-8 weeks from drug exposure and characterized by skin eruption, fever, eosinophilia, lymphadenopathy, and internal organ (i.e., liver, kidney, lung) involvement [43][44][45].…”
Section: Ige-mediated Reactionsmentioning
confidence: 99%
“…Historically, AGEP has rarely been associated with clindamycin. There have been increasing numbers of case reports of AGEP with clindamycin in the recent literature [47][48][49][50][51][52][53].…”
Section: Ige-mediated Reactionsmentioning
confidence: 99%
“…Acute generalized exanthematous pustulosis was the most prevalent adverse event of clindamycin. Facial skin and oral mucosa were always reported as the initial site of such a lesion (Croy, Buehrle, & Austin Szwak, 2017; Karakayali et al., 2017; Sampson, Klinkova, Vitko, & Casanas, 2018), some of which sometimes occurred only in oral‐maxillofacial system (Nitta et al., 2019). Additionally, other severe cutaneous lesions attacking oral‐maxillofacial part were also investigated, such as drug reaction with eosinophilia and systemic symptoms (Miller Quidley, Bookstaver, Gainey, & Gainey, 2012; Tian, Mohan, & Stallings, 2010), hypersensitivity syndrome (Nakamura, Watamatsu, & Muto, 2013; Papakonstantinou et al., 2018), and sweet syndrome (Kandula, Burke, & Goldfarb, 2010).…”
Section: Oral‐maxillofacial Adverse Events Related To Antimlarialsmentioning
confidence: 99%
“…(1) Clindamycin-associated AGEP should in suspected in patients presenting with erythema followed by papules and pustules within 1 −3 weeks of clindamycin use [1,2]. (2) AGEP is self-limited and treatment involves discontinuation of clindamycin and supportive therapy with corticosteroids, antihistamines or antibiotics [2].…”
Section: Teaching Pointsmentioning
confidence: 99%