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One patient developed a severe injection site reaction, which took several weeks to heal and this patient withdrew from the study.
A third cycle was applied, but required severe injection conditions and provided only incremental improvement.
Both codes predict substantial salt deposition close to the injection point, with associated severe injection impairment.
Topical drops were begun: prednisolone acetate 1% ophthalmic suspension and moxifloxacin ophthalmic every 30 min. On the next day, she developed worsening left eye pain and continued severe injection.
Three subjects (7.5%) in the VAX 102 + TIV arm had severe injection pain.
The reaction was characterized by severe injection site erythema, edema and induration.
Similar(45)
No patients treated with ExBID reported severe injection-site AEs.
There were no moderate or severe injection-site reactions (Table II).
Most events in either group were mild in intensity, with only a single patient treated with ExQW experiencing a severe injection-site adverse event.
Isolated cases of severe injection-site reactions involving infection or necrosis as well as severe cases of acute liver failure and pancreatitis have been reported.
This purer and more consistent extract did not result in such severe injection-site reactions, highlighting the importance of obtaining as pure an extract as possible.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com