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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
122070692 | 12207069 | 2 | F | 2010 | 20160303 | 20160324 | 20160907 | PER | US-JNJFOC-20160304724 | JANSSEN | 0.00 | A | F | Y | 39.46000 | KG | 20160907 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
122070692 | 12207069 | 1 | SS | FENTANYL TRANSDERMAL SYSTEM | FENTANYL | 1 | Transdermal | N | UNKNOWN | 0 | MATRIX PATCH | ||||||||
122070692 | 12207069 | 2 | PS | FENTANYL TRANSDERMAL SYSTEM | FENTANYL | 1 | Transdermal | N | UNKNOWN | 19813 | MATRIX PATCH |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
122070692 | 12207069 | 1 | Pain |
122070692 | 12207069 | 2 | Pain |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
122070692 | 12207069 | Abnormal loss of weight | |
122070692 | 12207069 | Activities of daily living impaired | |
122070692 | 12207069 | Condition aggravated | |
122070692 | 12207069 | Drug ineffective | |
122070692 | 12207069 | Feeding disorder |
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 |
---|---|---|---|---|---|---|
122070692 | 12207069 | 1 | 2013 | 0 | ||
122070692 | 12207069 | 2 | 2010 | 2013 | 0 |