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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126484952 | 12648495 | 2 | F | 20160318 | 20160906 | 20160812 | 20160913 | EXP | US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-51887BP | BOEHRINGER INGELHEIM | 75.00 | YR | F | Y | 0.00000 | 20160913 | PH | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126484952 | 12648495 | 1 | PS | PRADAXA | DABIGATRAN ETEXILATE MESYLATE | 1 | Oral | 300 MG | U | 22512 | 150 | MG | CAPSULE | BID | |||||
| 126484952 | 12648495 | 2 | C | ASA | ASPIRIN | 1 | Unknown | 0 | 81 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126484952 | 12648495 | 1 | Atrial fibrillation |
| 126484952 | 12648495 | 2 | Ischaemic stroke |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126484952 | 12648495 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126484952 | 12648495 | Fall | |
| 126484952 | 12648495 | Haemorrhage intracranial | |
| 126484952 | 12648495 | Subdural 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 |
|---|---|---|---|---|---|---|
| 126484952 | 12648495 | 1 | 201603 | 0 | ||
| 126484952 | 12648495 | 2 | 201602 | 0 |