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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125362731 | 12536273 | 1 | I | 20160620 | 20160704 | 20160707 | 20160707 | EXP | PT-INFARMED-L201606-188 | PT-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-43595PO | BOEHRINGER INGELHEIM | 83.57 | YR | F | Y | 0.00000 | 20160707 | PH | PT | PT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125362731 | 12536273 | 1 | PS | PRADAXA | DABIGATRAN ETEXILATE MESYLATE | 1 | Oral | 1 ANZ | U | 22512 | CAPSULE, HARD | QD | |||||||
| 125362731 | 12536273 | 2 | C | FUROSEMIDE. | FUROSEMIDE | 1 | Oral | 1 ANZ | 0 | QD | |||||||||
| 125362731 | 12536273 | 3 | C | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | Oral | 1 ANZ | 0 | QD | |||||||||
| 125362731 | 12536273 | 4 | C | PERINDOPRIL | PERINDOPRIL | 1 | Oral | 1 ANZ | 0 | QD | |||||||||
| 125362731 | 12536273 | 5 | C | PAROXETINE. | PAROXETINE | 1 | Oral | 1 ANZ | 0 | QD | |||||||||
| 125362731 | 12536273 | 6 | C | ALPRAZOLAM. | ALPRAZOLAM | 1 | Oral | 1 ANZ | 0 | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125362731 | 12536273 | 1 | Atrial fibrillation |
| 125362731 | 12536273 | 2 | Product used for unknown indication |
| 125362731 | 12536273 | 3 | Product used for unknown indication |
| 125362731 | 12536273 | 4 | Hypertension |
| 125362731 | 12536273 | 5 | Depression |
| 125362731 | 12536273 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125362731 | 12536273 | HO |
| 125362731 | 12536273 | LT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125362731 | 12536273 | Activated partial thromboplastin time prolonged | |
| 125362731 | 12536273 | Haemorrhage |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |