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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125379131 | 12537913 | 1 | I | 20160530 | 20160706 | 20160707 | 20160707 | EXP | SI-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-44603SL | BOEHRINGER INGELHEIM | 88.00 | YR | F | Y | 0.00000 | 20160707 | MD | SK | SI |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125379131 | 12537913 | 1 | PS | PRADAXA | DABIGATRAN ETEXILATE MESYLATE | 1 | Unknown | 220 MG | 22512 | 220 | MG | QD | |||||||
| 125379131 | 12537913 | 2 | C | MICARDIS | TELMISARTAN | 1 | Unknown | 0 | |||||||||||
| 125379131 | 12537913 | 3 | C | CORDARONE | AMIODARONE HYDROCHLORIDE | 1 | Unknown | 0 | |||||||||||
| 125379131 | 12537913 | 4 | C | LASIX | FUROSEMIDE | 1 | Unknown | 0 | |||||||||||
| 125379131 | 12537913 | 5 | C | ATORIS | ATORVASTATIN CALCIUM | 1 | Unknown | 0 | |||||||||||
| 125379131 | 12537913 | 6 | C | ACIPAN | PANTOPRAZOLE SODIUM | 1 | Unknown | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125379131 | 12537913 | 1 | Atrial fibrillation |
| 125379131 | 12537913 | 2 | Product used for unknown indication |
| 125379131 | 12537913 | 3 | Product used for unknown indication |
| 125379131 | 12537913 | 4 | Product used for unknown indication |
| 125379131 | 12537913 | 5 | Product used for unknown indication |
| 125379131 | 12537913 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125379131 | 12537913 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125379131 | 12537913 | Cerebral haemorrhage |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |