Person who experienced the adverse event (patient)
Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125731891 | 12573189 | 1 | I | 20160711 | 20160713 | 20160720 | 20160720 | PER | US-BAYER-2016-137931 | BAYER | 94.00 | YR | E | F | Y | 52.61000 | KG | 20160720 | CN | US | US |
Drug(s) used by person
Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125731891 | 12573189 | 1 | PS | CLARITIN | LORATADINE | 1 | Oral | 1 DF, QD | CVM01Z8 | 19658 | 1 | DF | TABLET | QD | |||||
125731891 | 12573189 | 2 | C | AMOXICILLIN. | AMOXICILLIN | 1 | UNK | 0 | QD |
Indications of drugs used
no results found |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125731891 | 12573189 | Drug ineffective | |
125731891 | 12573189 | Product use issue | |
125731891 | 12573189 | Somnolence |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
125731891 | 12573189 | 1 | 20160711 | 0 |