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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126870221 | 12687022 | 1 | I | 20160812 | 20160826 | 20160826 | EXP | US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-068301 | BRISTOL MYERS SQUIBB | 73.00 | YR | F | Y | 0.00000 | 20160826 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126870221 | 12687022 | 1 | PS | WARFARIN SODIUM. | WARFARIN SODIUM | 1 | Unknown | 5 MG, UNK | U | 9218 | 5 | MG | TABLET | ||||||
| 126870221 | 12687022 | 2 | C | HYDROCODONE BITARTRATE AND ACETAMINOPHEN | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | Unknown | 1 DF, UNK | U | 0 | 1 | DF | |||||||
| 126870221 | 12687022 | 3 | C | GLIPIZIDE. | GLIPIZIDE | 1 | Unknown | 5 MG, UNK | U | 0 | 5 | MG | |||||||
| 126870221 | 12687022 | 4 | C | MELOXICAM. | MELOXICAM | 1 | Unknown | 7.5 MG, UNK | U | 0 | 7.5 | MG | |||||||
| 126870221 | 12687022 | 5 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | Unknown | 20 MG, UNK | U | 0 | 20 | MG | |||||||
| 126870221 | 12687022 | 6 | C | SIMVASTATIN. | SIMVASTATIN | 1 | Unknown | 40 MG, UNK | U | 0 | 40 | MG | |||||||
| 126870221 | 12687022 | 7 | C | LISINOPRIL. | LISINOPRIL | 1 | Unknown | 10 MG, UNK | U | 0 | 10 | MG | |||||||
| 126870221 | 12687022 | 8 | C | LEVOTHYROXINE. | LEVOTHYROXINE | 1 | Unknown | 5 ?G, UNK | U | 0 | 5 | UG | |||||||
| 126870221 | 12687022 | 9 | C | OXYBUTININ ACCORD | 2 | Unknown | 5 MG, UNK | U | 0 | 5 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126870221 | 12687022 | 1 | Product used for unknown indication |
| 126870221 | 12687022 | 2 | Product used for unknown indication |
| 126870221 | 12687022 | 3 | Product used for unknown indication |
| 126870221 | 12687022 | 4 | Product used for unknown indication |
| 126870221 | 12687022 | 5 | Product used for unknown indication |
| 126870221 | 12687022 | 6 | Product used for unknown indication |
| 126870221 | 12687022 | 7 | Product used for unknown indication |
| 126870221 | 12687022 | 8 | Product used for unknown indication |
| 126870221 | 12687022 | 9 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126870221 | 12687022 | OT |
| 126870221 | 12687022 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126870221 | 12687022 | International normalised ratio increased | |
| 126870221 | 12687022 | Subdural haematoma | |
| 126870221 | 12687022 | Wrong drug administered |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |