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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125299901 | 12529990 | 1 | I | 20160621 | 0 | 20160705 | 20160705 | DIR | 39.00 | YR | M | N | 250.00000 | LBS | 20160702 | N | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125299901 | 12529990 | 1 | PS | AMOXICILLIN. | AMOXICILLIN | 1 | Oral | 30 CAPSULE(S) EVERY 8 HOURS TAKEN BY MOUTH | N | D | 20170620 | 0 | 30 | DF | CAPSULE | Q8H |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125299901 | 12529990 | 1 | Tooth abscess |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125299901 | 12529990 | DS |
| 125299901 | 12529990 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125299901 | 12529990 | Back pain | |
| 125299901 | 12529990 | Chest pain | |
| 125299901 | 12529990 | Diarrhoea | |
| 125299901 | 12529990 | Dry mouth | |
| 125299901 | 12529990 | Dysphonia | |
| 125299901 | 12529990 | Hypoaesthesia oral | |
| 125299901 | 12529990 | Nausea | |
| 125299901 | 12529990 | Paraesthesia oral |
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 |
|---|---|---|---|---|---|---|
| 125299901 | 12529990 | 1 | 20160621 | 20160701 | 0 |