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The initial dose is continued for 2 4 weeks, and then tapered gradually (5 mg every 1 2 weeks) to a maintenance dose (5 10 mg/day).
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Methotrexate, at stable dose, was continued throughout the study.
At discharge (18 h later), this dose was continued once daily.
In the Hb target 11.0-13.0 11.0-13.0e was continued unchang/dl
Once adverse events had resolved, drug dose was increased again; if adverse events recurred, the lower dose was continued.
If recovery from such toxicities at a reduced dose was confirmed, administration at the reduced dose was continued.
The starting dose was continued for the initial 2 weeks, followed by the investigator-adjusted dose titration based on the anticholinergic side effect profile.
Following his discharge, treatment with methylprednisolone 16 mg daily on tapering dose was continued for six months along with gemcitabine and erlotinib with complete remission of polymyositis.
Dual antiplatelet therapy (ASA and clopidogrel) in maintenance dose was continued to prevent in-stent thrombosis and progression of ischemia [ 2, 3].
result in similar bronchodilatory response as measured by forced expiratory volume in 1 s (FEV1); however, when dosing is continued beyond 1 2 weeks, dose response emerges.
ZA dosing was continued on a weekly basis until 9 months of age or until the animal was moribund and sacrificed.
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