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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125850251 | 12585025 | 1 | I | 201312 | 20160622 | 20160723 | 20160723 | PER | US-ASTRAZENECA-2016SE69408 | ASTRAZENECA | 760.00 | MON | F | Y | 63.50000 | KG | 20160723 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125850251 | 12585025 | 1 | PS | ARIMIDEX | ANASTROZOLE | 1 | Oral | 20541 | 1 | MG | TABLET | QD | |||||||
| 125850251 | 12585025 | 2 | C | PROLIA | DENOSUMAB | 1 | Intramuscular | EVERY SIX MONTHS | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125850251 | 12585025 | 1 | Breast cancer |
| 125850251 | 12585025 | 2 | Bone loss |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125850251 | 12585025 | Activities of daily living impaired | |
| 125850251 | 12585025 | Arthralgia | |
| 125850251 | 12585025 | Bone loss | |
| 125850251 | 12585025 | Pain |
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 |
|---|---|---|---|---|---|---|
| 125850251 | 12585025 | 1 | 201312 | 0 |