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Therefore, this advantageous characteristic of the oral dosage form according to the current invention permits for a less expensive packaging material.
In circumstances of severe or persistent hypertension despite institution of antihypertensive therapy, take into account non permanent or permanent discontinuation of NEXAVAR see DOSAGE AND ADMINISTRATION Everlasting discontinuation as a consequence of hypertension occurred in 1 of 297 NEXAVAR-handled patients within the SHARP (HCC) research, 1 of 451 NEXAVAR-treated patients in the TARGET (RCC) examine, and 1 of 207 NEXAVAR-handled sufferers in the RESOLUTION (DTC) research.
Participation in a clinical trial involving the administration of an investigational or marketed drug inside 30 days (90 days for biologics) previous to the primary dosing or concomitant participation in an investigational examine involving no drug administration.