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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125770861 | 12577086 | 1 | I | 20160617 | 20160715 | 20160720 | 20160720 | EXP | TR-SA-2016SA131040 | AVENTIS | 44.00 | YR | A | F | Y | 82.00000 | KG | 20160720 | CN | TR | TR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125770861 | 12577086 | 1 | PS | CLEXANE | ENOXAPARIN SODIUM | 1 | Subcutaneous | U | UNKNOWN | 20164 | 2 | DF | SOLUTION FOR INJECTION | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125770861 | 12577086 | 1 | Venous thrombosis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125770861 | 12577086 | LT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125770861 | 12577086 | Burning sensation | |
| 125770861 | 12577086 | Lip pruritus | |
| 125770861 | 12577086 | Lip swelling |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |