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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124893663 | 12489366 | 3 | F | 20160617 | 20160622 | 20160912 | EXP | PH-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-39411RP | BOEHRINGER INGELHEIM | 50.00 | YR | M | Y | 0.00000 | 20160912 | MD | PH | PH |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124893663 | 12489366 | 1 | PS | PRADAXA | DABIGATRAN ETEXILATE MESYLATE | 1 | Oral | 300 MG | U | 22512 | 150 | MG | CAPSULE | BID | |||||
| 124893663 | 12489366 | 2 | SS | PRADAXA | DABIGATRAN ETEXILATE MESYLATE | 1 | U | 22512 | |||||||||||
| 124893663 | 12489366 | 3 | C | LOSARTAN. | LOSARTAN | 1 | Unknown | 0 | |||||||||||
| 124893663 | 12489366 | 4 | C | ROSUVASTATIN. | ROSUVASTATIN | 1 | Unknown | 0 | |||||||||||
| 124893663 | 12489366 | 5 | C | LANOXIN | DIGOXIN | 1 | Unknown | 0 | |||||||||||
| 124893663 | 12489366 | 6 | C | VASTAREL | TRIMETAZIDINE DIHYDROCHLORIDE | 1 | Unknown | 0 | |||||||||||
| 124893663 | 12489366 | 7 | C | FUROSOMIDE | 2 | Unknown | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124893663 | 12489366 | 1 | Cerebrovascular accident prophylaxis |
| 124893663 | 12489366 | 2 | Atrial fibrillation |
| 124893663 | 12489366 | 3 | Product used for unknown indication |
| 124893663 | 12489366 | 4 | Product used for unknown indication |
| 124893663 | 12489366 | 5 | Product used for unknown indication |
| 124893663 | 12489366 | 6 | Product used for unknown indication |
| 124893663 | 12489366 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124893663 | 12489366 | HO |
| 124893663 | 12489366 | DE |
| 124893663 | 12489366 | LT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124893663 | 12489366 | Cerebral haemorrhage | |
| 124893663 | 12489366 | Cerebral infarction |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |