Author: Jefferies, Sarah; Braithwaite, Irene; Walker, Steven; Weatherall, Mark; Jennings, Lance; Luck, Michelle; Barrett, Kevin; Siebers, Robert; Blackmore, Timothy; Beasley, Richard; Perrin, Kyle
Title: Randomized controlled trial of the effect of regular paracetamol on influenza infection Document date: 2015_12_6
ID: vj3m50sb_29
Snippet: One participant in the placebo group suffered a serious adverse event and withdrew from the study on Day 4. One subject in the placebo group suffered an exacerbation of asthma requiring oral prednisone. Four participants received oral antibiotics: three in the placebo group, (sinusitis (n = 2) and asthma (n = 1)), and one in the paracetamol group (tonsillitis). Oseltamivir was discontinued in 17 participants due to intolerance (7 in placebo group.....
Document: One participant in the placebo group suffered a serious adverse event and withdrew from the study on Day 4. One subject in the placebo group suffered an exacerbation of asthma requiring oral prednisone. Four participants received oral antibiotics: three in the placebo group, (sinusitis (n = 2) and asthma (n = 1)), and one in the paracetamol group (tonsillitis). Oseltamivir was discontinued in 17 participants due to intolerance (7 in placebo group, 10 in paracetamol group). The median (interquartile range) codeine use in the first 48 h was 30 mg (0-60) in both placebo and paracetamol groups.
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