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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 88860144 | 8886014 | 4 | F | 20111006 | 20160921 | 20121105 | 20160928 | EXP | JP-OTSUKA-JP-2012-15565 | OTSUKA | 62.61 | YR | M | Y | 70.00000 | KG | 20160928 | CN | JP | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 88860144 | 8886014 | 1 | PS | Pletaal OD tablets 100mg | CILOSTAZOL | 1 | Oral | 100 MG, BID | 17400 | MG | Y | 20863 | 100 | MG | ORODISPERSIBLE TABLET | BID | |||
| 88860144 | 8886014 | 2 | SS | Pletaal OD tablets 100mg | CILOSTAZOL | 1 | Oral | 100 MG, BID | 17400 | MG | Y | 20863 | 100 | MG | ORODISPERSIBLE TABLET | BID | |||
| 88860144 | 8886014 | 3 | SS | PLAVIX | CLOPIDOGREL BISULFATE | 1 | Oral | 75 MG, QD | 3525 | MG | Y | U | 0 | 75 | MG | TABLET | QD | ||
| 88860144 | 8886014 | 4 | C | BLOPRESS | CANDESARTAN CILEXETIL | 1 | Oral | 4 MG, QD | 348 | MG | 0 | 4 | MG | QD | |||||
| 88860144 | 8886014 | 5 | C | LIPITOR | ATORVASTATIN CALCIUM | 1 | Oral | 10 MG, QD | 0 | 10 | MG | QD | |||||||
| 88860144 | 8886014 | 6 | C | BAYASPIRIN | ASPIRIN | 1 | Oral | 100 MG, QD | 0 | 100 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 88860144 | 8886014 | 1 | Cerebral infarction |
| 88860144 | 8886014 | 3 | Cerebral infarction |
| 88860144 | 8886014 | 4 | Hypertension |
| 88860144 | 8886014 | 5 | Hyperlipidaemia |
| 88860144 | 8886014 | 6 | Cerebral infarction |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 88860144 | 8886014 | LT |
| 88860144 | 8886014 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 88860144 | 8886014 | Cerebral haemorrhage | |
| 88860144 | 8886014 | Subarachnoid 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 |
|---|---|---|---|---|---|---|
| 88860144 | 8886014 | 1 | 20110712 | 20111006 | 0 | |
| 88860144 | 8886014 | 2 | 20111031 | 0 | ||
| 88860144 | 8886014 | 3 | 20110821 | 20111006 | 0 | |
| 88860144 | 8886014 | 4 | 20110712 | 20111006 | 0 | |
| 88860144 | 8886014 | 5 | 20110712 | 20111006 | 0 | |
| 88860144 | 8886014 | 6 | 20110712 | 0 |