Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4833119 | 5931324 | I | 4833119-1 | 19980901 | 20051107 | 20051117 | EXP | 2005154125 | PFIZER INC | F | N | 20051116 | UNITED STATES |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
4833119 | 1006645071 | PS | PROVERA | 1 | U | U | 11839 | ||||
4833119 | 1006671062 | SS | MEDROXYPROGESTERONE ACETATE | 1 | U | U | |||||
4833119 | 1006671064 | SS | MEDROXYPROGESTERONE | 1 | U | U | |||||
4833119 | 1006671068 | SS | PREMARIN | 1 | U | U | |||||
4833119 | 1006671079 | SS | PREMPRO | 1 | U | U |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4833119 | 1006645071 | HORMONE REPLACEMENT THERAPY |
4833119 | 1006671062 | HORMONE REPLACEMENT THERAPY |
4833119 | 1006671064 | HORMONE REPLACEMENT THERAPY |
4833119 | 1006671068 | HORMONE REPLACEMENT THERAPY |
4833119 | 1006671079 | HORMONE REPLACEMENT THERAPY |
Outcome of event
Event ID | OUTC COD |
---|---|
4833119 | OT |
Reactions reported
Event ID | PT |
---|---|
4833119 | BREAST CANCER FEMALE |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
4833119 | CSM |
Therapies reported
no results found |