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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126596012 | 12659601 | 2 | F | 20160114 | 20160808 | 20160817 | 20160822 | EXP | FR-PFIZER INC-2016378741 | PFIZER | 73.00 | YR | F | Y | 0.00000 | 20160822 | OT | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126596012 | 12659601 | 1 | PS | Amlor | AMLODIPINE BESYLATE | 1 | 5 MG, 2X/DAY | U | 19787 | 5 | MG | CAPSULE, HARD | BID | ||||||
| 126596012 | 12659601 | 2 | SS | Discotrine | NITROGLYCERIN | 1 | Transdermal | 1 DF, DAILY | U | 21134 | 1 | DF | TRANSDERMAL PATCH | ||||||
| 126596012 | 12659601 | 3 | SS | XARELTO | RIVAROXABAN | 1 | Oral | 20 MG, 1X/DAY (AT NOON) | Y | 0 | 20 | MG | FILM-COATED TABLET | QD | |||||
| 126596012 | 12659601 | 4 | SS | APROVEL | IRBESARTAN | 1 | 75 MG, 1X/DAY (EVENING) | U | 0 | 75 | MG | QD | |||||||
| 126596012 | 12659601 | 5 | SS | LEXOMIL | BROMAZEPAM | 1 | 0.5 DF, 1X/DAY (EVENING) | U | 0 | .5 | DF | QD | |||||||
| 126596012 | 12659601 | 6 | SS | IMOVANE | ZOPICLONE | 1 | Oral | 7.5 MG, 1X/DAY (EVENING) | U | 0 | 7.5 | MG | FILM-COATED TABLET | QD | |||||
| 126596012 | 12659601 | 7 | SS | DIFFU-K | POTASSIUM CHLORIDE | 1 | Oral | 1 DF, 1X/DAY AT NOON | U | 0 | 1 | DF | CAPSULE | QD | |||||
| 126596012 | 12659601 | 8 | C | CERIS | TROSPIUM CHLORIDE | 1 | 20 MG, 1X/DAY (AT NOON) | 0 | 20 | MG | FILM-COATED TABLET | QD | |||||||
| 126596012 | 12659601 | 9 | C | LASILIX /00032601/ | FUROSEMIDE | 1 | 20 MG, 1X/DAY (AT NOON) | 0 | 20 | MG | QD | ||||||||
| 126596012 | 12659601 | 10 | C | DEROXAT | PAROXETINE HYDROCHLORIDE | 1 | Oral | 20 MG, 1X/DAY (IN THE MORNING) | 0 | 20 | MG | FILM-COATED TABLET | QD |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126596012 | 12659601 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126596012 | 12659601 | Subdural haematoma |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |