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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125516852 | 12551685 | 2 | F | 20160530 | 20160811 | 20160713 | 20160822 | EXP | PHHO2016FR009744 | NOVARTIS | 85.00 | YR | M | Y | 0.00000 | 20160822 | OT | FR | FR |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125516852 | 12551685 | 1 | PS | TRAMETINIB | TRAMETINIB | 1 | Oral | 1 MG, QD | 4 | MG | 204114 | 1 | MG | QD | |||||
125516852 | 12551685 | 2 | SS | TRAMETINIB | TRAMETINIB | 1 | Oral | UNK | 4 | MG | 204114 | ||||||||
125516852 | 12551685 | 3 | SS | DABRAFENIB | DABRAFENIB | 1 | Oral | 75 MG, BID | 600 | MG | 0 | 75 | MG | BID | |||||
125516852 | 12551685 | 4 | SS | DABRAFENIB | DABRAFENIB | 1 | Oral | UNK | 600 | MG | 0 | ||||||||
125516852 | 12551685 | 5 | SS | PREVISCAN | FLUINDIONE | 1 | Oral | 10 MG, QD | 0 | 10 | MG | QD | |||||||
125516852 | 12551685 | 6 | SS | PREVISCAN | FLUINDIONE | 1 | 0 | ||||||||||||
125516852 | 12551685 | 7 | C | AMIODARONE | AMIODARONE | 1 | Unknown | 0.5 MG, MORNING | U | 0 | .5 | MG | |||||||
125516852 | 12551685 | 8 | C | EPOETIN ALFA | ERYTHROPOIETIN | 1 | Unknown | UNK, QW | U | 0 | /wk |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125516852 | 12551685 | 1 | Malignant melanoma |
125516852 | 12551685 | 3 | Malignant melanoma |
125516852 | 12551685 | 5 | Myocardial infarction |
125516852 | 12551685 | 6 | Cardiac valve disease |
125516852 | 12551685 | 7 | Product used for unknown indication |
125516852 | 12551685 | 8 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125516852 | 12551685 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125516852 | 12551685 | General physical condition abnormal | |
125516852 | 12551685 | Overdose |
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 |
---|---|---|---|---|---|---|
125516852 | 12551685 | 1 | 20160525 | 20160528 | 0 | |
125516852 | 12551685 | 2 | 20160609 | 0 | ||
125516852 | 12551685 | 3 | 20160525 | 20160528 | 0 | |
125516852 | 12551685 | 4 | 20160609 | 0 | ||
125516852 | 12551685 | 5 | 20160530 | 0 |