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The mother was withdrawn from study treatments and referred to the hospital clinical team.
She was withdrawn from study with no adverse consequence to herself or her newborn.
At the completion of the protocol five achieved CR, two PR and one was withdrawn from study at investigator preference.
Patient 204 had stable disease up to course 4, but was withdrawn from study due to brain metastases.
One TACE-BEV subject developed grade 4 hyperbilirubinemia after day 8 TACE, and was withdrawn from study for liver dysfunction, having received only one dose of bevacizumab.
Participants who completed both the pre- and post-release qualitative interviews tended to be older (p = 0.027) than those that completed the pre-release interview only.> -wrap-foot> a1 participant was withdrawn from study prior to collection of baseline data.
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will be withdrawn from study drugs one week later.
Patients with major hypersensitivity were withdrawn from study treatment.
Any patient requiring > 2 reductions due to toxicity was to be withdrawn from study therapy.
Women who were withdrawn from study medication continued to attend follow-up.
Following completion of the treatment phase, subjects were withdrawn from study medication while continuing their SRIs.
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