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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126615384 | 12661538 | 4 | F | 20160714 | 20160912 | 20160817 | 20160915 | PER | US-PFIZER INC-2016368622 | PFIZER | 69.00 | YR | M | Y | 127.91000 | KG | 20160915 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126615384 | 12661538 | 1 | PS | TOVIAZ | FESOTERODINE FUMARATE | 1 | Oral | 4 MG, 1X/DAY(ONCE DAILY IN THE MORNING ) | 60 | MG | N | 00000683 | 22030 | 4 | MG | MODIFIED-RELEASE TABLET | QD | ||
| 126615384 | 12661538 | 2 | SS | TOVIAZ | FESOTERODINE FUMARATE | 1 | 8 MG, UNK | 60 | MG | N | 0000683 | 22030 | 8 | MG | MODIFIED-RELEASE TABLET | ||||
| 126615384 | 12661538 | 3 | C | FUROSEMIDE. | FUROSEMIDE | 1 | 20 MG, UNK | 0 | 20 | MG | TABLET | ||||||||
| 126615384 | 12661538 | 4 | C | FUROSEMIDE. | FUROSEMIDE | 1 | 40 MG, 1X/DAY | 0 | 40 | MG | TABLET | ||||||||
| 126615384 | 12661538 | 5 | C | FUROSEMIDE. | FUROSEMIDE | 1 | 0 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126615384 | 12661538 | 1 | Micturition urgency |
| 126615384 | 12661538 | 2 | Urinary retention |
| 126615384 | 12661538 | 3 | Blood pressure abnormal |
| 126615384 | 12661538 | 4 | Urinary retention |
| 126615384 | 12661538 | 5 | Inflammation |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126615384 | 12661538 | Contraindicated product administered | |
| 126615384 | 12661538 | Drug effect incomplete |
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 |
|---|---|---|---|---|---|---|
| 126615384 | 12661538 | 1 | 20160714 | 20160728 | 0 | |
| 126615384 | 12661538 | 3 | 20141220 | 0 | ||
| 126615384 | 12661538 | 4 | 20150312 | 0 |