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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126280871 | 12628087 | 1 | I | 20160501 | 20160725 | 20160808 | 20160808 | EXP | IT-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-061475 | BRISTOL MYERS SQUIBB | 88.94 | YR | F | Y | 0.00000 | 20160808 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126280871 | 12628087 | 1 | PS | COUMADIN | WARFARIN SODIUM | 1 | Oral | 5 MG, PRN | 9218 | 5 | MG | TABLET | |||||||
| 126280871 | 12628087 | 2 | C | ALLOPURINOL. | ALLOPURINOL | 1 | Oral | 1 UNIT, UNK | U | 0 | 1 | DF | |||||||
| 126280871 | 12628087 | 3 | C | MODURETIC 5-50 | AMILORIDE HYDROCHLORIDEHYDROCHLOROTHIAZIDE | 1 | Oral | 0.5 UNIT, UNK | U | 0 | .5 | DF | |||||||
| 126280871 | 12628087 | 4 | C | SERENASE /00027401/ | HALOPERIDOL | 1 | Oral | 1 DF, QD | U | 0 | 1 | DF | QD | ||||||
| 126280871 | 12628087 | 5 | C | MINIAS | LORMETAZEPAM | 1 | Oral | 2 MG, QD | U | 0 | 2 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126280871 | 12628087 | 1 | Atrial fibrillation |
| 126280871 | 12628087 | 2 | Product used for unknown indication |
| 126280871 | 12628087 | 3 | Hypertension |
| 126280871 | 12628087 | 4 | Product used for unknown indication |
| 126280871 | 12628087 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126280871 | 12628087 | OT |
| 126280871 | 12628087 | DE |
| 126280871 | 12628087 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126280871 | 12628087 | Cerebral haemorrhage | |
| 126280871 | 12628087 | Gastrointestinal tube insertion | |
| 126280871 | 12628087 | Head injury |
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 |
|---|---|---|---|---|---|---|
| 126280871 | 12628087 | 1 | 20150101 | 20160501 | 0 |