Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8016623 | 8317513 | I | 8016623-7 | 20111202 | 20111223 | 20111231 | EXP | PHHY2011DK111699 | SANDOZ,INC. | 76 | YR | M | Y | 20111231 | OT | DENMARK |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
8016623 | 1018419897 | PS | FLUCONAZOLE | 1 | 076086 | ||||||
8016623 | 1018419898 | I | PRADAXA | 1 | ORAL | 110 MG, BID |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
8016623 | 1018419898 | ATRIAL FIBRILLATION |
Outcome of event
Event ID | OUTC COD |
---|---|
8016623 | OT |
Reactions reported
Event ID | PT |
---|---|
8016623 | DRUG INTERACTION |
8016623 | HAEMOGLOBIN DECREASED |
8016623 | MELAENA |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
8016623 | 1018419898 | 20111122 | 20111212 | 20 | DAY |