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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124679204 | 12467920 | 4 | F | 20160722 | 20160615 | 20160726 | PER | US-PFIZER INC-2016286447 | PFIZER | 0.00 | M | Y | 0.00000 | 20160726 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124679204 | 12467920 | 1 | PS | TOVIAZ | FESOTERODINE FUMARATE | 1 | 4 MG, UNK | 22030 | 4 | MG | MODIFIED-RELEASE TABLET | ||||||||
124679204 | 12467920 | 2 | SS | TOVIAZ | FESOTERODINE FUMARATE | 1 | 8 MG, 1X/DAY (AT BED TIME) | 22030 | 8 | MG | MODIFIED-RELEASE TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
124679204 | 12467920 | 1 | Micturition urgency |
124679204 | 12467920 | 2 | Hypertonic bladder |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124679204 | 12467920 | Drug ineffective | |
124679204 | 12467920 | Pollakiuria |
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 |
---|---|---|---|---|---|---|
124679204 | 12467920 | 1 | 20160602 | 0 |