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No GL patients discontinued as a result of an AE.
In 26 (3.16%) cases, treatment was discontinued as a result of AEs.
The diuretic administration was never discontinued as a result of suspected adverse reactions in any patient at any time point.
Of the 19 patients who discontinued treatment, five (26·3%) discontinued as a result of a nonfatal AE.
However, these events were rarely treatment-limiting and few patients (<1%) discontinued as a result of injection-site events.
Fewer patients on maraviroc vs. efavirenz experienced treatment-related adverse events (68.9 vs. 81.7%) and discontinued as a result of any adverse event (10.6 vs. 21.3%).
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Further investigation of β-carotene for cancer prevention was discontinued as a result.
None of the rashes was accompanied by other allergic reactions, nor were any vaccinations discontinued as a result.
The incidences of lower extremity edema adverse events for etoricoxib were similar to placebo and no patient treated with etoricoxib discontinued as a result.
A total of 71 patients (13%) prematurely discontinued R-maintenance; 23% discontinued treatment due to PD (16 patients), 13% discontinued treatment as a result of treatment-related toxicity (9 patients; 1 patient received R-monotherapy as induction therapy and 8 patients received R-chemotherapy induction), and 8% of patients discontinued treatment due to death (6 patients).
Five (0.8%) patients discontinued panitumumab as a result of an adverse drug reaction or ST.
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