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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 100288875 | 10028887 | 5 | F | 20070201 | 20150619 | 20140321 | 20150630 | EXP | US-SANOFI-AVENTIS-2012SA066400 | AVENTIS | 68.00 | YR | E | F | Y | 0.00000 | 20150630 | N | MD | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 100288875 | 10028887 | 1 | PS | PLAVIX | CLOPIDOGREL BISULFATE | 1 | Oral | D | UNKNOWN | 20839 | 75 | MG | FILM-COATED TABLET | QD | |||||
| 100288875 | 10028887 | 2 | SS | PLAVIX | CLOPIDOGREL BISULFATE | 1 | Oral | D | UNKNOWN | 20839 | 75 | MG | FILM-COATED TABLET | QD | |||||
| 100288875 | 10028887 | 3 | C | DARVOCET | ACETAMINOPHENPROPOXYPHENE HYDROCHLORIDE | 1 | D | 0 | |||||||||||
| 100288875 | 10028887 | 4 | C | LIPITOR | ATORVASTATIN CALCIUM | 1 | Oral | D | 0 | 40 | MG | QD | |||||||
| 100288875 | 10028887 | 5 | C | TRICOR | FENOFIBRATE | 1 | Oral | D | 0 | 160 | MG | QD | |||||||
| 100288875 | 10028887 | 6 | C | TOPROL XL | METOPROLOL SUCCINATE | 1 | Oral | D | 0 | 50 | MG | QD | |||||||
| 100288875 | 10028887 | 7 | C | ACTOS | PIOGLITAZONE HYDROCHLORIDE | 1 | Oral | D | 0 | 30 | MG | QD | |||||||
| 100288875 | 10028887 | 8 | C | INSULIN | INSULIN NOS | 1 | DOSE:15 UNIT(S) | D | 0 | BID | |||||||||
| 100288875 | 10028887 | 9 | C | ASPIRIN. | ASPIRIN | 1 | D | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 100288875 | 10028887 | 1 | Acute coronary syndrome |
| 100288875 | 10028887 | 2 | Myocardial infarction |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 100288875 | 10028887 | OT |
| 100288875 | 10028887 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 100288875 | 10028887 | Gastrointestinal haemorrhage | |
| 100288875 | 10028887 | Multiple injuries | |
| 100288875 | 10028887 | Ulcer |
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 |
|---|---|---|---|---|---|---|
| 100288875 | 10028887 | 1 | 200305 | 200703 | 0 | |
| 100288875 | 10028887 | 2 | 200305 | 200703 | 0 |