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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127014681 | 12701468 | 1 | I | 20160822 | 20160831 | 20160831 | PER | US-PFIZER INC-2016397625 | PFIZER | 58.00 | YR | F | Y | 0.00000 | 20160831 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127014681 | 12701468 | 1 | PS | PREMARIN | ESTROGENS, CONJUGATED | 1 | UNK UNK, 2X/WEEK | U | 20216 | VAGINAL CREAM | BIW |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127014681 | 12701468 | 1 | Metrorrhagia |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127014681 | 12701468 | Decreased appetite | |
127014681 | 12701468 | Fatigue | |
127014681 | 12701468 | Nausea | |
127014681 | 12701468 | Pain | |
127014681 | 12701468 | Slow response to stimuli |
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 |
---|---|---|---|---|---|---|
127014681 | 12701468 | 1 | 20160818 | 0 |