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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 102424112 | 10242411 | 2 | F | 20160629 | 20140617 | 20160705 | EXP | US-PFIZER INC-2014162857 | PFIZER | 87.00 | YR | F | Y | 70.00000 | KG | 20160705 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 102424112 | 10242411 | 1 | PS | PREMARIN | ESTROGENS, CONJUGATED | 1 | 0.625 MG, 1X/DAY | 4782 | .625 | MG | TABLET | QD | |||||||
| 102424112 | 10242411 | 2 | SS | PREMARIN | ESTROGENS, CONJUGATED | 1 | 4782 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 102424112 | 10242411 | 1 | Oestrogen replacement therapy |
| 102424112 | 10242411 | 2 | Hysterectomy |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 102424112 | 10242411 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 102424112 | 10242411 | Alopecia | |
| 102424112 | 10242411 | Gallbladder disorder | |
| 102424112 | 10242411 | Urinary tract infection |
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 |
|---|---|---|---|---|---|---|
| 102424112 | 10242411 | 1 | 1974 | 0 |