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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127077761 | 12707776 | 1 | I | 200901 | 20160824 | 20160901 | 20160901 | EXP | US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-070983 | BRISTOL MYERS SQUIBB | 65.03 | YR | M | Y | 82.50000 | KG | 20160901 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127077761 | 12707776 | 1 | PS | COUMADIN | WARFARIN SODIUM | 1 | Oral | UNK UNK, QD | U | U | 9218 | INJECTION | |||||||
| 127077761 | 12707776 | 2 | SS | ASPIRIN. | ASPIRIN | 1 | Unknown | 325 MG, UNK | U | 0 | 325 | MG | |||||||
| 127077761 | 12707776 | 3 | SS | PRADAXA | DABIGATRAN ETEXILATE MESYLATE | 1 | Unknown | UNK | Y | 0 | |||||||||
| 127077761 | 12707776 | 4 | C | CARVEDILOL. | CARVEDILOL | 1 | Unknown | 25 MG, BID | U | 0 | 25 | MG | BID | ||||||
| 127077761 | 12707776 | 5 | C | AMIODARONE | AMIODARONE | 1 | Unknown | 200 MG, QD | U | 0 | 200 | MG | QD | ||||||
| 127077761 | 12707776 | 6 | C | ATORVASTATIN | ATORVASTATIN | 1 | Unknown | 80 MG, QD | U | 0 | 80 | MG | QD | ||||||
| 127077761 | 12707776 | 7 | C | TAMSULOSIN | TAMSULOSIN | 1 | Unknown | 0.4 MG, QD | U | 0 | .4 | MG | QD | ||||||
| 127077761 | 12707776 | 8 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | Unknown | 20 MG, BID | U | 0 | 20 | MG | BID | ||||||
| 127077761 | 12707776 | 9 | C | GEMFIBROZIL. | GEMFIBROZIL | 1 | Unknown | 600 MG, BID | U | 0 | 600 | MG | BID | ||||||
| 127077761 | 12707776 | 10 | C | LEVOTHYROXINE. | LEVOTHYROXINE | 1 | Unknown | 0.175 MG, UNK | U | 0 | .175 | MG | |||||||
| 127077761 | 12707776 | 11 | C | LEVOTHYROXINE. | LEVOTHYROXINE | 1 | Unknown | 0.150 MG, UNK | U | 0 | .15 | MG | |||||||
| 127077761 | 12707776 | 12 | SS | LISINOPRIL. | LISINOPRIL | 1 | Oral | 1.25 MG, QD | U | 0 | 1.25 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127077761 | 12707776 | 1 | Deep vein thrombosis |
| 127077761 | 12707776 | 2 | Deep vein thrombosis |
| 127077761 | 12707776 | 3 | Deep vein thrombosis |
| 127077761 | 12707776 | 4 | Product used for unknown indication |
| 127077761 | 12707776 | 5 | Product used for unknown indication |
| 127077761 | 12707776 | 6 | Product used for unknown indication |
| 127077761 | 12707776 | 7 | Product used for unknown indication |
| 127077761 | 12707776 | 8 | Product used for unknown indication |
| 127077761 | 12707776 | 9 | Product used for unknown indication |
| 127077761 | 12707776 | 10 | Product used for unknown indication |
| 127077761 | 12707776 | 12 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127077761 | 12707776 | HO |
| 127077761 | 12707776 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127077761 | 12707776 | Internal haemorrhage | |
| 127077761 | 12707776 | Transfusion |
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 |
|---|---|---|---|---|---|---|
| 127077761 | 12707776 | 1 | 2001 | 0 | ||
| 127077761 | 12707776 | 2 | 200807 | 0 | ||
| 127077761 | 12707776 | 3 | 200807 | 0 |