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. 2015 Jun 1;2015(6):CD009566. doi: 10.1002/14651858.CD009566.pub2

1. Serious adverse events and withdrawals.

Study Serious adverse events Number withdrawn due to side effects Treatment arm from which withdrawn
Avunduk 2005 No serious adverse events reported No participants recorded to have withdrawn N/A
Azevedo 1991 No serious adverse events reported 1 participant withdrawn 1 from placebo group
Canonica 2003 No serious adverse events reported 2 participants withdrawn 1 from azelastine and 1 from placebo
Carr 2013 1 serious adverse event reported unrelated to the treatment 11 participants withdrawn 4 from bepotastine besilate and 7 from placebo
Davies 1993 No serious adverse events reported 5 participants withdrawn 2 from levocabastine group and 3 from placebo
Fujishima 2008 No serious adverse events reported No participants recorded to have withdrawn N/A
Giede‐Tuch 1998 No serious adverse events reported No participants withdrawn due to side effects N/A
Graue 1994 No serious adverse events reported 2 participants withdrawn 1 from levocabastine and 1 from placebo
Hechanova 1984 No serious adverse events reported 12 participants withdrawn 2 from cromoglycate group and 10 from placebo group
Höffling‐Lima 2001 No serious adverse events reported No participants recorded to have withdrawn N/A
James 2003 No serious adverse events reported 4 participants withdrawn due to side effects 1 from azelastine, 2 from cromoglycate, and 1 from placebo
Katelaris 2002 No serious adverse events reported 2 participants withdrawn 1 from olopatadine group, 1 from cromolyn group
Kidd 2003 4 serious adverse events: 1) persistent photophobia and 2) conjunctivitis with corneal ulcer 38 discontinued due to side effects 8 from ketotifen, 15 from levocabastine, 15 from placebo
Lanier 2001 No serious adverse events reported No participants recorded to have withdrawn N/A
Leino 1992 No serious adverse events reported 4 participants withdrawn 3 from nedocromil and 1 from cromoglycate
Lenhard 1997 No serious adverse events reported 4 participants withdrawn 2 from azelastine group and 2 from placebo group
McCabe 2012 No serious adverse events reported No participants recorded to have withdrawn N/A
Melamed 1994 No serious adverse events reported No participants recorded to have withdrawn due to side effects N/A
Melamed 2000 No serious adverse events reported No participants recorded to have withdrawn due to side effects N/A
Moller 1994 No serious adverse events reported No participants recorded to have withdrawn due to side effects N/A
Nazarov 2003 No serious adverse events reported 1 participant withdrawn due to side effects 1 participant from azelastine group
Petzold a,b,c 2002 No serious adverse events reported No participants recorded to have withdrawn due to side effects N/A
Sabbah 1998 No serious adverse events reported 1 participant withdrawn 1 participant from azelastine group
Sarker 2011 No serious adverse events reported No mention of participants withdrawing due to side effects N/A
Secchi a 2000 No serious adverse events reported 1 participant discontinued due to side effects 1 participant from emedastine
Secchi b 2000 No serious adverse events reported No mention of participants withdrawing due to side effects N/A
Trinquand 1999 No serious adverse events reported No mention of participants withdrawing due to side effects N/A
Varguez‐Rodriguez 2009 No serious adverse events reported No participants recorded to have withdrawn N/A
Verin 2001 No serious adverse events reported 3 participants withdrawn 3 participants from emedastine group
Wertheimer 1997 No serious adverse events reported No participants recorded to have withdrawn due to side effects N/A

N/A: not applicable