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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127173022 | 12717302 | 2 | F | 201605 | 20160923 | 20160906 | 20160928 | PER | US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-071873 | BRISTOL MYERS SQUIBB | 74.20 | YR | F | Y | 0.00000 | 20160928 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127173022 | 12717302 | 1 | PS | COUMADIN | WARFARIN SODIUM | 1 | Unknown | N | 9218 | ||||||||||
| 127173022 | 12717302 | 2 | SS | COUMADIN | WARFARIN SODIUM | 1 | Unknown | UNK | N | 9218 | |||||||||
| 127173022 | 12717302 | 3 | SS | MYRBETRIQ | MIRABEGRON | 1 | Unknown | 50 MG, QD | 0 | 50 | MG | TABLET | QD | ||||||
| 127173022 | 12717302 | 4 | SS | DIGOXIN. | DIGOXIN | 1 | Unknown | U | 0 | ||||||||||
| 127173022 | 12717302 | 5 | C | PRAVASTATIN. | PRAVASTATIN | 1 | Unknown | 40 MG, UNK | U | 0 | 40 | MG | |||||||
| 127173022 | 12717302 | 6 | C | DILTIAZEM CD | DILTIAZEM | 1 | Unknown | 240 MG, UNK | U | 0 | 240 | MG | |||||||
| 127173022 | 12717302 | 7 | C | LISINOPRIL. | LISINOPRIL | 1 | Unknown | 5 MG, UNK | U | 0 | 5 | MG | |||||||
| 127173022 | 12717302 | 8 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | Unknown | 500 MG, UNK | U | 0 | 500 | MG | |||||||
| 127173022 | 12717302 | 9 | C | DICLOFENAC | DICLOFENAC | 1 | Unknown | 75 MG, UNK | U | 0 | 75 | MG | |||||||
| 127173022 | 12717302 | 10 | C | METOPROLOL. | METOPROLOL | 1 | Unknown | 50 MG, UNK | U | 0 | 50 | MG | |||||||
| 127173022 | 12717302 | 11 | C | PROTONIX | PANTOPRAZOLE SODIUM | 1 | Unknown | 40 MG, UNK | U | 0 | 40 | MG | |||||||
| 127173022 | 12717302 | 12 | C | RESTASIS | CYCLOSPORINE | 1 | Unknown | U | 0 | ||||||||||
| 127173022 | 12717302 | 13 | C | PATADAY | OLOPATADINE HYDROCHLORIDE | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127173022 | 12717302 | 1 | Product used for unknown indication |
| 127173022 | 12717302 | 3 | Hypertonic bladder |
| 127173022 | 12717302 | 4 | Product used for unknown indication |
| 127173022 | 12717302 | 5 | Product used for unknown indication |
| 127173022 | 12717302 | 6 | Product used for unknown indication |
| 127173022 | 12717302 | 7 | Product used for unknown indication |
| 127173022 | 12717302 | 8 | Product used for unknown indication |
| 127173022 | 12717302 | 9 | Product used for unknown indication |
| 127173022 | 12717302 | 10 | Product used for unknown indication |
| 127173022 | 12717302 | 11 | Product used for unknown indication |
| 127173022 | 12717302 | 12 | Product used for unknown indication |
| 127173022 | 12717302 | 13 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127173022 | 12717302 | International normalised ratio fluctuation |
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 |
|---|---|---|---|---|---|---|
| 127173022 | 12717302 | 3 | 201604 | 0 |