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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 96579532 | 9657953 | 2 | F | 20131024 | 20131029 | 20131104 | EXP | VAL_02785_2013 | VALIDUS | 34.00 | YR | F | N | 0.00000 | 20131101 | PH | JP |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 96579532 | 9657953 | 1 | PS | METHERGINE | METHYLERGONOVINE MALEATE | 1 | ORAL | 6035 | 0.375 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 96579532 | 9657953 | 1 | Post abortion haemorrhage |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 96579532 | 9657953 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 96579532 | 9657953 | No therapeutic response | |
| 96579532 | 9657953 | Uterine haemorrhage |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | CASEID | RPSR COD |
|---|---|---|
| 96579532 | 9657953 | FGN |
| 96579532 | 9657953 | HP |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 96579532 | 9657953 | 1 | 2 | MON | ||
| 96579532 | 9657953 | 1 | 2 | WK | ||
| 96579532 | 9657953 | 1 | 30 | DAY |