LORATADINE 10 MG
Generic: LORATADINE TABLETS USP, 10 MG, LORATADINE 10MG
TIME CAP LABORATORIESManufacturer
ORALRoute
LORATADINEActive Substance
2024-11-21Original Approval
LORATADINE 10 MG is FDA application ANDA219223, sponsored by PHARMAZONE. 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
DRUG INEFFECTIVE
3,618 reports
2
FATIGUE
3,297 reports
3
NAUSEA
2,750 reports
4
DYSPNOEA
2,494 reports
5
HEADACHE
2,461 reports
6
DIARRHOEA
2,428 reports
7
OFF LABEL USE
2,283 reports
8
DIZZINESS
2,116 reports
9
PAIN
2,019 reports
10
RASH
1,650 reports