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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127455951 | 12745595 | 1 | I | 20160912 | 20160915 | 20160915 | PER | PHEH2016US023204 | NOVARTIS | 0.00 | F | Y | 0.00000 | 20160915 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127455951 | 12745595 | 1 | PS | TYKERB | LAPATINIB DITOSYLATE | 1 | Oral | 250 MG, QD | 22059 | 250 | MG | QD | |||||||
| 127455951 | 12745595 | 2 | C | MEGESTROL | MEGESTROL | 1 | Unknown | 40 MG, UNK | U | 5ZP2258 | 0 | 40 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127455951 | 12745595 | 1 | Product used for unknown indication |
| 127455951 | 12745595 | 2 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127455951 | 12745595 | Diarrhoea | |
| 127455951 | 12745595 | Eating disorder | |
| 127455951 | 12745595 | Fatigue | |
| 127455951 | 12745595 | Peripheral swelling |
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 |
|---|---|---|---|---|---|---|
| 127455951 | 12745595 | 1 | 20160309 | 0 |