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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122464753 | 12246475 | 3 | F | 201604 | 20160818 | 20160407 | 20160831 | PER | US-PFIZER INC-2016157597 | PFIZER | 74.00 | YR | F | Y | 67.13000 | KG | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122464753 | 12246475 | 1 | PS | PREMARIN | ESTROGENS, CONJUGATED | 1 | Oral | 0.9 MG, 1X/DAY | 4782 | .9 | MG | TABLET | QD | ||||||
| 122464753 | 12246475 | 2 | C | ARTHROTEC | DICLOFENAC SODIUMMISOPROSTOL | 1 | 50/200 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122464753 | 12246475 | 1 | Hormone replacement therapy |
| 122464753 | 12246475 | 2 | Arthralgia |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122464753 | 12246475 | Intentional product misuse | |
| 122464753 | 12246475 | Malaise | |
| 122464753 | 12246475 | Weight increased |
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 |
|---|---|---|---|---|---|---|
| 122464753 | 12246475 | 1 | 1985 | 201604 | 0 |