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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125542322 | 12554232 | 2 | F | 20160712 | 20160713 | 20160808 | PER | US-PFIZER INC-2016316429 | PFIZER | 62.00 | YR | F | Y | 0.00000 | 20160808 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125542322 | 12554232 | 1 | PS | PREMARIN | ESTROGENS, CONJUGATED | 1 | 1 DF, 3X/DAY | 4782 | 1 | DF | TABLET | TID |
Indications of drugs used
no results found |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125542322 | 12554232 | Fatigue | |
125542322 | 12554232 | Hyperhidrosis | |
125542322 | 12554232 | Insomnia | |
125542322 | 12554232 | Mood altered |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |