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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
123399313 | 12339931 | 3 | F | 20160327 | 20160722 | 20160506 | 20160802 | EXP | IT-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-032968 | BRISTOL MYERS SQUIBB | 85.48 | YR | M | Y | 0.00000 | 20160802 | CN | IT | IT |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
123399313 | 12339931 | 1 | PS | COUMADIN | WARFARIN SODIUM | 1 | Unknown | UNK | U | 9218 | TABLET | ||||||||
123399313 | 12339931 | 2 | C | CARVEDILOL. | CARVEDILOL | 1 | Oral | 6.25 MG, UNK | U | 0 | 6.25 | MG | |||||||
123399313 | 12339931 | 3 | C | ALLOPURINOL. | ALLOPURINOL | 1 | Oral | 300 MG, UNK | U | 0 | 300 | MG | |||||||
123399313 | 12339931 | 4 | C | LASIX | FUROSEMIDE | 1 | Oral | 125 MG, UNK | U | 0 | 125 | MG | TABLET | ||||||
123399313 | 12339931 | 5 | C | LASIX | FUROSEMIDE | 1 | Oral | 175 UNK, UNK | U | 0 | 175 | MG | TABLET | ||||||
123399313 | 12339931 | 6 | C | LASIX | FUROSEMIDE | 1 | Oral | 50 MG, UNK | U | 0 | 50 | MG | TABLET | ||||||
123399313 | 12339931 | 7 | C | ZAROXOLYN | METOLAZONE | 1 | Oral | 0.5 TAB, UNK | U | 0 | .5 | DF | TABLET | ||||||
123399313 | 12339931 | 8 | C | PRADIF | TAMSULOSIN HYDROCHLORIDE | 1 | Oral | 0.4 MG, UNK | U | 0 | .4 | MG | CAPSULE | ||||||
123399313 | 12339931 | 9 | C | PANTORC | PANTOPRAZOLE SODIUM | 1 | Oral | 20 MG, UNK | U | 0 | 20 | MG | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
123399313 | 12339931 | 1 | Atrial fibrillation |
123399313 | 12339931 | 2 | Product used for unknown indication |
123399313 | 12339931 | 3 | Product used for unknown indication |
123399313 | 12339931 | 4 | Product used for unknown indication |
123399313 | 12339931 | 6 | Product used for unknown indication |
123399313 | 12339931 | 7 | Constipation |
123399313 | 12339931 | 8 | Product used for unknown indication |
123399313 | 12339931 | 9 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
123399313 | 12339931 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
123399313 | 12339931 | Asthenia | |
123399313 | 12339931 | Haemoptysis | |
123399313 | 12339931 | Malaise |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |