LORATADINE
Generic: LORATADINE
YYBA CORPManufacturer
ORALRoute
LORATADINEActive Substance
2018-04-16Original Approval
LORATADINE is FDA application ANDA208314, sponsored by AUROBINDO PHARMA LTD. Any recalls listed below come from FDA drug enforcement reports, and reaction counts are the number of FAERS adverse event reports that mention the drug and that reaction; a report does not prove the drug caused it.
Top Reported Reactions
1
FATIGUE
8,799 reports
2
DRUG INEFFECTIVE
8,737 reports
3
HEADACHE
7,678 reports
4
OFF LABEL USE
7,233 reports
5
NAUSEA
7,161 reports
6
PAIN
6,734 reports
7
DYSPNOEA
6,721 reports
8
DIARRHOEA
5,787 reports
9
ARTHRALGIA
5,297 reports
10
PNEUMONIA
5,120 reports