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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126387441 | 12638744 | 1 | I | 20160720 | 20160801 | 20160809 | 20160809 | EXP | GB-MHRA-EYC 00142993 | PHHY2016GB105657 | SANDOZ | 42.00 | YR | F | Y | 83.00000 | KG | 20160809 | OT | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126387441 | 12638744 | 1 | PS | CLARITHROMYCIN. | CLARITHROMYCIN | 1 | Oral | 500 MG, UNK | GD4286 | 65136 | 500 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126387441 | 12638744 | 1 | Infected bite |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126387441 | 12638744 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126387441 | 12638744 | Diarrhoea | |
| 126387441 | 12638744 | Gastrointestinal tract irritation | |
| 126387441 | 12638744 | Nausea | |
| 126387441 | 12638744 | Reaction to drug excipients |
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 |
|---|---|---|---|---|---|---|
| 126387441 | 12638744 | 1 | 20160720 | 0 |