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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123722612 | 12372261 | 2 | F | 20160706 | 20160516 | 20160715 | EXP | BR-SA-2016SA092215 | AVENTIS | 0.00 | A | F | Y | 0.00000 | 20160715 | OT | BR | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123722612 | 12372261 | 1 | PS | CLEXANE | ENOXAPARIN SODIUM | 1 | Parenteral | FOR 21 WEEKS | UNKNOWN | 20164 | 40 | MG | SOLUTION FOR INJECTION | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123722612 | 12372261 | 1 | Hypercoagulation |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123722612 | 12372261 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123722612 | 12372261 | Disability | |
| 123722612 | 12372261 | Foetal exposure timing unspecified | |
| 123722612 | 12372261 | Pain | |
| 123722612 | 12372261 | Premature separation of placenta |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |