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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126772012 | 12677201 | 2 | F | 20160913 | 20160823 | 20160919 | PER | US-PFIZER INC-2016375700 | PFIZER | 62.00 | YR | F | Y | 65.00000 | KG | 20160919 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126772012 | 12677201 | 1 | PS | PREMARIN | ESTROGENS, CONJUGATED | 1 | Oral | 0.3 MG, 1X/DAY | N | 4782 | .3 | MG | TABLET | QD | |||||
126772012 | 12677201 | 2 | SS | PREMARIN | ESTROGENS, CONJUGATED | 1 | 0.3 UNK, UNK (3 WEEKS) | N | 4782 | .3 | MG | TABLET | QD | ||||||
126772012 | 12677201 | 3 | C | SIMVASTATIN. | SIMVASTATIN | 1 | Oral | 20 MG, 1X/DAY | 0 | 20 | MG | TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126772012 | 12677201 | 1 | Menopause |
126772012 | 12677201 | 3 | Blood cholesterol abnormal |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126772012 | 12677201 | Drug ineffective | |
126772012 | 12677201 | Irritability | |
126772012 | 12677201 | Malaise | |
126772012 | 12677201 | Mood altered |
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 |
---|---|---|---|---|---|---|
126772012 | 12677201 | 1 | 2016 | 20160802 | 0 |