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doi: 10.1098/rstb.2013.0599 237 NeumannB.BarorR.ZhaoC.SegelM.DietmannS.RawjiK
[DOI] [PMC free article] [PubMed] [Google Scholar] 132.Sojitra B, Bulani Y, Putcha UK, Kanwal A, Gupta P, Kuncha M, Banerjee SK
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The FDA first added a black-box warning label for FQs in July 2008 regarding the increased risk of tendinitis and tendon rupture
