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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127191781 | 12719178 | 1 | I | 201605 | 20160705 | 20160907 | 20160907 | PER | US-JNJFOC-20160704515 | JANSSEN | 54.36 | YR | A | F | Y | 81.65000 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127191781 | 12719178 | 1 | PS | DURAGESIC | FENTANYL | 1 | Transdermal | 25 MCG/ HR AND 12.5 MCG/ HR PATCH USED AT THE SAME TIME | N | 1509823P1;1415597P1 | 19813 | MATRIX PATCH | |||||||
127191781 | 12719178 | 2 | C | NORCO | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | Unknown | DOSE: 10/325MG | 0 | UNSPECIFIED |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127191781 | 12719178 | 1 | Arthritis |
127191781 | 12719178 | 2 | Pain |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127191781 | 12719178 | Pain | |
127191781 | 12719178 | Product quality issue |
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 |
---|---|---|---|---|---|---|
127191781 | 12719178 | 1 | 201605 | 0 | ||
127191781 | 12719178 | 2 | 201604 | 0 |