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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127724631 | 12772463 | 1 | I | 20160913 | 20160922 | 20160922 | PER | US-PFIZER INC-2016433241 | PFIZER | 59.00 | YR | F | Y | 82.00000 | KG | 20160922 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127724631 | 12772463 | 1 | SS | ELIQUIS | APIXABAN | 1 | Oral | 5 MG, UNK | U | 0 | 5 | MG | FILM-COATED TABLET | ||||||
127724631 | 12772463 | 2 | PS | TOVIAZ | FESOTERODINE FUMARATE | 1 | Oral | 8 MG, QD | 22030 | 8 | MG | MODIFIED-RELEASE TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127724631 | 12772463 | 2 | Urge incontinence |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127724631 | 12772463 | Adverse event |
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 |
---|---|---|---|---|---|---|
127724631 | 12772463 | 2 | 20151202 | 0 |