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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127014062 | 12701406 | 2 | F | 20160817 | 20160902 | 20160831 | 20160907 | PER | US-PFIZER INC-2016397554 | PFIZER | 91.00 | YR | F | Y | 77.00000 | KG | 20160907 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127014062 | 12701406 | 1 | PS | PREMARIN | ESTROGENS, CONJUGATED | 1 | Oral | 0.625 MG, DAILY (EVERY DAY) | U | 4782 | .625 | MG | TABLET | ||||||
| 127014062 | 12701406 | 2 | SS | PREMARIN | ESTROGENS, CONJUGATED | 1 | 0.625 MG, ALTERNATE DAY | U | 4782 | .625 | MG | TABLET | QOD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127014062 | 12701406 | 1 | Hot flush |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127014062 | 12701406 | Angiopathy | |
| 127014062 | 12701406 | Intentional product misuse | |
| 127014062 | 12701406 | Pruritus |
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 |
|---|---|---|---|---|---|---|
| 127014062 | 12701406 | 1 | 1975 | 0 |