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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 95219971 | 9521997 | 1 | I | 20111204 | 20120119 | 20120127 | 20120127 | EXP | 2012SP003488 | SCHERING PLOUGH | 21.00 | YR | F | N | 0.00000 | 20120126 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 95219971 | 9521997 | 1 | PS | NEXPLANON | 1 | SBDE | D | 21529 | 68 | MG | |||||||||
| 95219971 | 9521997 | 2 | SS | FLUCLOXACILLIN (FLUCLOXACILLIN) | 1 | ORAL | D | 0 | 250 | MG | QID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 95219971 | 9521997 | 1 | Contraception |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 95219971 | 9521997 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 95219971 | 9521997 | Abortion spontaneous | |
| 95219971 | 9521997 | Drug interaction | |
| 95219971 | 9521997 | Exposure during pregnancy | |
| 95219971 | 9521997 | Pregnancy |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | CASEID | RPSR COD |
|---|---|---|
| 95219971 | 9521997 | HP |
| 95219971 | 9521997 | FGN |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 95219971 | 9521997 | 1 | 20110916 | 20120109 | 0 | |
| 95219971 | 9521997 | 2 | 20111102 | 20111109 | 0 |