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interdental B. fragilis Capnocytophaga spp. Eikenella corrodens, Fusobacterium spp.
|Pronunciation||/ ə ˌ m ɒ k s ɪ ˈ s ɪ l ɪ n /|
|Trade names||Hundreds of names |
|Pregnancy category||AU: A US: B (No risk in non-human studies)|
|Routes of administration||By mouth, intravenous|
|Drug class||β-lactam antibiotic|
|ATC code||J01CA04 ( WHO ) QG51AA03 ( WHO )|
|Legal status||UK: POM (Prescription only) US: ℞-only|
|Bioavailability||95% by mouth|
|Metabolism||less than 30% biotransformed in liver|
|Elimination half-life||61.3 minutes|
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However, food effect studies have not been performed with the 200 mg and 500 mg formulations. o NOAC use alone: 65.66 vs rifampin: 103.14. difference, 36.90 [99% CI, 1.59- 72.22; and o NOAC use alone: 56.07 vs phenytoin : 108.52. Duration of effect The effect of this medicine lasts for an average of 1.
to 2 hours after onset of action.
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