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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126927981 | 12692798 | 1 | I | 20160818 | 20160829 | 20160829 | EXP | US-PFIZER INC-2016394768 | PFIZER | 71.00 | YR | F | Y | 0.00000 | 20160829 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126927981 | 12692798 | 1 | PS | IBRANCE | PALBOCICLIB | 1 | 100 MG, UNK | U | 207103 | 100 | MG | CAPSULE | |||||||
| 126927981 | 12692798 | 2 | SS | FASLODEX | FULVESTRANT | 1 | UNK | U | 0 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126927981 | 12692798 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126927981 | 12692798 | Asthenia | |
| 126927981 | 12692798 | Contusion | |
| 126927981 | 12692798 | Haemorrhage | |
| 126927981 | 12692798 | Laceration | |
| 126927981 | 12692798 | Nausea | |
| 126927981 | 12692798 | Tremor |
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 |
|---|---|---|---|---|---|---|
| 126927981 | 12692798 | 1 | 20160807 | 0 |