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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127014451 | 12701445 | 1 | I | 2016 | 20160825 | 20160831 | 20160831 | PER | US-PFIZER INC-2016404032 | PFIZER | 77.00 | YR | F | Y | 0.00000 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127014451 | 12701445 | 1 | PS | AROMASIN | EXEMESTANE | 1 | Oral | 25 MG, 1X/DAY | Y | 708BH | 20753 | 25 | MG | COATED TABLET | QD |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127014451 | 12701445 | Asthenia | |
| 127014451 | 12701445 | Decreased appetite | |
| 127014451 | 12701445 | Dyspnoea | |
| 127014451 | 12701445 | Impaired self-care | |
| 127014451 | 12701445 | Retching | |
| 127014451 | 12701445 | Stress urinary incontinence | |
| 127014451 | 12701445 | Urinary incontinence | |
| 127014451 | 12701445 | Vomiting | |
| 127014451 | 12701445 | Weight decreased |
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 |
|---|---|---|---|---|---|---|
| 127014451 | 12701445 | 1 | 20160526 | 20160818 | 0 |