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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
122636882 | 12263688 | 2 | F | 20120301 | 20160907 | 20160413 | 20160909 | PER | PHEH2016US008736 | NOVARTIS | 52.43 | YR | F | Y | 80.00000 | KG | 20160909 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
122636882 | 12263688 | 1 | PS | LETROZOLE. | LETROZOLE | 1 | Unknown | U | 20726 | ||||||||||
122636882 | 12263688 | 2 | SS | BENICAR | OLMESARTAN MEDOXOMIL | 1 | Oral | UNK UNK, QD | 0 | QD | |||||||||
122636882 | 12263688 | 3 | SS | ARIMIDEX | ANASTROZOLE | 1 | Unknown | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
122636882 | 12263688 | 1 | Breast cancer |
122636882 | 12263688 | 2 | Hypertension |
122636882 | 12263688 | 3 | Product used for unknown indication |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
122636882 | 12263688 | Arthralgia | |
122636882 | 12263688 | Joint stiffness |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |