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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120725042 | 12072504 | 2 | F | 20141218 | 20160729 | 20160212 | 20160810 | EXP | US-BAYER-2015-486543 | BAYER | 62.00 | YR | A | F | Y | 0.00000 | 20160810 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120725042 | 12072504 | 1 | SS | XARELTO | RIVAROXABAN | 1 | Oral | UNK | Y | 0 | FILM-COATED TABLET | ||||||||
| 120725042 | 12072504 | 2 | SS | XARELTO | RIVAROXABAN | 1 | Oral | 15 MG, UNK | Y | 0 | 15 | MG | FILM-COATED TABLET | ||||||
| 120725042 | 12072504 | 3 | SS | XARELTO | RIVAROXABAN | 1 | Oral | UNK | Y | 0 | FILM-COATED TABLET | ||||||||
| 120725042 | 12072504 | 4 | SS | CLOPIDOGREL | CLOPIDOGREL BISULFATE | 1 | Unknown | UNK | Y | 0 | |||||||||
| 120725042 | 12072504 | 5 | PS | ACETYLSALICYLIC ACID({=100 mg) | ASPIRIN | 1 | Unknown | UNK | U | 999999 | TABLET | ||||||||
| 120725042 | 12072504 | 6 | C | BISACODYL. | BISACODYL | 1 | Unknown | UNK | 0 | ||||||||||
| 120725042 | 12072504 | 7 | C | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | Unknown | UNK | 0 | ||||||||||
| 120725042 | 12072504 | 8 | C | PRAVASTATIN SODIUM. | PRAVASTATIN SODIUM | 1 | Unknown | UNK | 0 | ||||||||||
| 120725042 | 12072504 | 9 | C | PRAMIPEXOLE. | PRAMIPEXOLE | 1 | Unknown | UNK | 0 | ||||||||||
| 120725042 | 12072504 | 10 | C | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | Unknown | UNK | 0 | ||||||||||
| 120725042 | 12072504 | 11 | C | LEVOTHYROXIN | LEVOTHYROXINE | 1 | Unknown | UNK | 0 | ||||||||||
| 120725042 | 12072504 | 12 | C | METOPROLOL. | METOPROLOL | 1 | Unknown | UNK | 0 | ||||||||||
| 120725042 | 12072504 | 13 | C | FUROSEMIDE. | FUROSEMIDE | 1 | Unknown | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 120725042 | 12072504 | 1 | Atrial fibrillation |
| 120725042 | 12072504 | 2 | Thrombosis prophylaxis |
| 120725042 | 12072504 | 3 | Cerebrovascular accident prophylaxis |
| 120725042 | 12072504 | 4 | Product used for unknown indication |
| 120725042 | 12072504 | 5 | Product used for unknown indication |
| 120725042 | 12072504 | 6 | Product used for unknown indication |
| 120725042 | 12072504 | 7 | Product used for unknown indication |
| 120725042 | 12072504 | 8 | Product used for unknown indication |
| 120725042 | 12072504 | 9 | Product used for unknown indication |
| 120725042 | 12072504 | 10 | Product used for unknown indication |
| 120725042 | 12072504 | 11 | Product used for unknown indication |
| 120725042 | 12072504 | 12 | Product used for unknown indication |
| 120725042 | 12072504 | 13 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 120725042 | 12072504 | OT |
| 120725042 | 12072504 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 120725042 | 12072504 | Epistaxis | |
| 120725042 | 12072504 | Haemorrhagic stroke | |
| 120725042 | 12072504 | Internal 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 |
|---|---|---|---|---|---|---|
| 120725042 | 12072504 | 1 | 20141211 | 20141224 | 0 | |
| 120725042 | 12072504 | 2 | 20151219 | 2015 | 0 |