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Neurotoxicity is the greatest concern regarding BV, and the most frequent complication is peripheral neuropathy (PN), which often causes discontinuation of therapy.
Less than one-half of these patients discontinued minocycline or doxycycline because of side effects, suggesting that they are at least as well tolerated as other second-line RA medications, for which drug toxicity causes discontinuation in 15% of all patients [ 35].
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Overall acceptability Overall acceptability The acceptability of treatment will be defined as all-cause discontinuation, as measured by the proportion of patients who discontinued treatment (during the delivery of the intervention) up to the post-intervention time point.
We report about all adverse events causing discontinuation earlier than 180 days.
The most common side effect that caused discontinuation within 1 year was irregular bleeding.
Although adjunctive armodafinil compared with adjunctive placebo yielded a higher headache rate (15 vs 8%%), it yielded similar (generally favorably low) rates of all-cause discontinuation (16 vs 16%%), adverse event discontinuation (4 vs 5 %), nausea (6 vs 4%%), ≥7 % weight gain (2 vs 5 %), anxiety (4 vs 3 %), insomnia (3 vs 2 %), sedation/somnolence (1 vs 1 %), and hypomania (0 vs <1 %).
Anxiety and bipolar I disorder were the only AEs that caused discontinuation in >1 patient; anxiety led to treatment discontinuation in 3 (2 %) of those treated with adjunctive armodafinil and 0 treated with adjunctive placebo; 2 patients taking adjunctive armodafinil and 0 patients taking adjunctive placebo discontinued due to bipolar I disorder.
Among responders to CBZ, 27% of patients incurred in adverse events that directly caused interruption of treatment by the physician or a dosage reduction to a level that was insufficient to control pain, thus causing discontinuation, after a mean period of 8.6 months.
All-cause discontinuation was used as a measure of acceptability.
The time to all-cause discontinuation was shorter on both doses of LY2140023 than on placebo.
The association may also be confounded if manifesting symptoms cause discontinuation of vitamin D supplementation.
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