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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126897492 | 12689749 | 2 | F | 20100521 | 20160817 | 20160826 | 20160826 | EXP | PL-SANOFI-AVENTIS-2013SA076263 | AVENTIS | 60.00 | YR | A | M | Y | 66.30000 | KG | 20160826 | CN | PL | PL |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126897492 | 12689749 | 1 | PS | ENOXAPARIN SODIUM. | ENOXAPARIN SODIUM | 1 | Subcutaneous | Y | UNKNOWN | 20164 | 80 | MG | BID | ||||||
| 126897492 | 12689749 | 2 | SS | CLOPIDOGREL BISULFATE. | CLOPIDOGREL BISULFATE | 1 | Oral | UNKNOWN | 20839 | 75 | MG | QD | |||||||
| 126897492 | 12689749 | 3 | SS | ACETYLSALICYLIC ACID | ASPIRIN | 1 | Oral | Y | UNKNOWN | 0 | 75 | MG | QD | ||||||
| 126897492 | 12689749 | 4 | C | FUROSEMIDE. | FUROSEMIDE | 1 | 0 | ||||||||||||
| 126897492 | 12689749 | 5 | C | ASPIRIN. | ASPIRIN | 1 | Oral | EFFERVESCENT TABLET | UNKNOWN | 0 | 75 | MG | QD | ||||||
| 126897492 | 12689749 | 6 | C | BLINDED THERAPY | INVESTIGATIONAL PRODUCT | 1 | Intravenous (not otherwise specified) | 0 | 10 | ML | /hr |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126897492 | 12689749 | 1 | Product used for unknown indication |
| 126897492 | 12689749 | 2 | Product used for unknown indication |
| 126897492 | 12689749 | 3 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126897492 | 12689749 | HO |
| 126897492 | 12689749 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126897492 | 12689749 | Myocardial infarction | |
| 126897492 | 12689749 | Off label use | |
| 126897492 | 12689749 | Post procedural haemorrhage |
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 |
|---|---|---|---|---|---|---|
| 126897492 | 12689749 | 1 | 20100521 | 20100528 | 0 | |
| 126897492 | 12689749 | 2 | 20100521 | 20100524 | 0 | |
| 126897492 | 12689749 | 3 | 20100521 | 20100528 | 0 | |
| 126897492 | 12689749 | 5 | 20100521 | 20100528 | 0 | |
| 126897492 | 12689749 | 6 | 20100521 | 20100523 | 0 |