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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126915831 | 12691583 | 1 | I | 2016 | 20160811 | 20160826 | 20160826 | PER | US-GLAXOSMITHKLINE-US2016116899 | GLAXOSMITHKLINE | 0.00 | A | F | Y | 0.00000 | 20160826 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126915831 | 12691583 | 1 | PS | CEFTIN | CEFUROXIME AXETIL | 1 | 2 DF (TEASPOONS), BID | UNKNOWN | 50672 | 2 | DF | ORAL SUSPENSION | BID | ||||||
| 126915831 | 12691583 | 2 | SS | CEFUROXIME. | CEFUROXIME | 1 | UNK | N | UNKNOWN | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126915831 | 12691583 | 1 | Ear infection |
| 126915831 | 12691583 | 2 | Ear infection |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126915831 | 12691583 | Drug ineffective |
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 |
|---|---|---|---|---|---|---|
| 126915831 | 12691583 | 1 | 20160801 | 0 | ||
| 126915831 | 12691583 | 2 | 20160722 | 0 |