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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126482841 | 12648284 | 1 | I | 20160728 | 20160801 | 20160812 | 20160812 | EXP | IT-VALIDUS PHARMACEUTICALS LLC-IT-2016VAL002429 | VALIDUS | 84.00 | YR | F | Y | 0.00000 | 20160812 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126482841 | 12648284 | 1 | PS | LASIX | FUROSEMIDE | 1 | Oral | 25 MG, DAILY | U | 16273 | 25 | MG | TABLET | ||||||
| 126482841 | 12648284 | 2 | SS | COUMADIN | WARFARIN SODIUM | 1 | Oral | 5 MG, DAILY | Y | 0 | 5 | MG | TABLET | ||||||
| 126482841 | 12648284 | 3 | SS | ZOLOFT | SERTRALINE HYDROCHLORIDE | 1 | Oral | 50 MG, DAILY | U | 0 | 50 | MG | FILM-COATED TABLET | ||||||
| 126482841 | 12648284 | 4 | SS | TAVOR (LORAZEPAM) | LORAZEPAM | 1 | Oral | 1 MG, DAILY | U | 0 | 1 | MG | TABLET | ||||||
| 126482841 | 12648284 | 5 | SS | LUVION /00252501/ | CANRENONE | 1 | Oral | 50 MG, DAILY | U | 0 | 50 | MG | TABLET | ||||||
| 126482841 | 12648284 | 6 | SS | CONGESCOR | BISOPROLOL | 1 | Oral | 1.25 MG, DAILY | U | 0 | 1.25 | MG | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126482841 | 12648284 | 1 | Hypertension |
| 126482841 | 12648284 | 2 | Atrial fibrillation |
| 126482841 | 12648284 | 3 | Depression |
| 126482841 | 12648284 | 4 | Anxiety |
| 126482841 | 12648284 | 5 | Hypertension |
| 126482841 | 12648284 | 6 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126482841 | 12648284 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126482841 | 12648284 | Cerebral haemorrhage | |
| 126482841 | 12648284 | Fall |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |