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Tajima's D [ 48] and Fu's F S [ 49] were estimated and a mismatch distribution test was administered with reference to the method of Schneider et al. [ 50].
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Normal and ulcer control received carboxymethycellulose (5 mL/kg) orally, positive control was administered with 20 mg/kg omeprazole (reference drug) and 2 groups were received 250 mg/kg and 500 mg/kg of the leaf extract, respectively.
The reference group was administered with a dose of 50 mg/kg of the suspension of diclofenac sodium (standard).
Another group of rats was orally administered with 1 mg/kg of mianserin as a standard reference.
When administered with the other OADs, the Cmax, AUC0 24h, and AUCinf of luseogliflozin and the OADs were within the reference range for bioequivalence.
When glimepiride, metformin, sitagliptin, and miglitol were administered with luseogliflozin, the GMRs and 90% CIs for Cmax, AUC0 24h, and AUCinf of each OAD were within the reference range for bioequivalence.
Pegfilgrastim was administered with each cycle.
Animals were orally administered with CXT.
Behavioral abnormalities were improved in mice administered with nilotinib.
Sevoflurane was administered with the MirusTM system.
Flumazenil could be safely administered with ECT.
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