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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118222794 | 11822279 | 4 | F | 201511 | 20160719 | 20151210 | 20160722 | PER | PHEH2015US025447 | NOVARTIS | 58.22 | YR | F | Y | 0.00000 | 20160722 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118222794 | 11822279 | 1 | PS | TYKERB | LAPATINIB DITOSYLATE | 1 | Oral | 4 DF, QD | N | 5ZP1656 | 22059 | 4 | DF | TABLET | QD | ||||
| 118222794 | 11822279 | 2 | C | AMOXICILLIN. | AMOXICILLIN | 1 | Unknown | U | 0 | CAPSULE | |||||||||
| 118222794 | 11822279 | 3 | C | APAP/CODEINE | ACETAMINOPHENCODEINE PHOSPHATE | 1 | Unknown | U | 0 | TABLET | |||||||||
| 118222794 | 11822279 | 4 | C | CYCLOBENZAPRINE | CYCLOBENZAPRINE | 1 | Unknown | U | 0 | TABLET | |||||||||
| 118222794 | 11822279 | 5 | C | HYDROCODONE BITARTRATE AND ACETAMINOPHEN | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | Unknown | U | 0 | TABLET | |||||||||
| 118222794 | 11822279 | 6 | C | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | Unknown | U | 0 | TABLET | |||||||||
| 118222794 | 11822279 | 7 | C | TAMOXIFEN | TAMOXIFEN | 1 | Unknown | U | 0 | TABLET | |||||||||
| 118222794 | 11822279 | 8 | C | CALTRATE 600+D | 2 | Unknown | U | 0 | |||||||||||
| 118222794 | 11822279 | 9 | C | CETRIZINE | CETIRIZINE HYDROCHLORIDE | 1 | Unknown | U | 0 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 118222794 | 11822279 | 1 | Breast cancer female |
| 118222794 | 11822279 | 2 | Product used for unknown indication |
| 118222794 | 11822279 | 3 | Product used for unknown indication |
| 118222794 | 11822279 | 4 | Product used for unknown indication |
| 118222794 | 11822279 | 5 | Product used for unknown indication |
| 118222794 | 11822279 | 6 | Product used for unknown indication |
| 118222794 | 11822279 | 7 | Product used for unknown indication |
| 118222794 | 11822279 | 8 | Product used for unknown indication |
| 118222794 | 11822279 | 9 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 118222794 | 11822279 | Asthenia | |
| 118222794 | 11822279 | Drug ineffective | |
| 118222794 | 11822279 | Dry mouth | |
| 118222794 | 11822279 | Dysphonia | |
| 118222794 | 11822279 | Fatigue | |
| 118222794 | 11822279 | Full blood count decreased | |
| 118222794 | 11822279 | Hypoaesthesia | |
| 118222794 | 11822279 | Nausea | |
| 118222794 | 11822279 | Vomiting |
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 |
|---|---|---|---|---|---|---|
| 118222794 | 11822279 | 1 | 201511 | 0 |