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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126643422 | 12664342 | 2 | F | 2009 | 20160916 | 20160818 | 20160920 | EXP | US-JNJFOC-20160811050 | JANSSEN | 59.73 | YR | A | F | Y | 83.92000 | KG | 20160920 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126643422 | 12664342 | 1 | PS | DURAGESIC | FENTANYL | 1 | Transdermal | N | 1509761P1 | 19813 | UNSPECIFIED |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126643422 | 12664342 | 1 | Pain management |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126643422 | 12664342 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126643422 | 12664342 | Amnesia | |
126643422 | 12664342 | Gallbladder operation | |
126643422 | 12664342 | Hypertension | |
126643422 | 12664342 | Ligament operation | |
126643422 | 12664342 | Medical device implantation | |
126643422 | 12664342 | Product adhesion issue | |
126643422 | 12664342 | Rotator cuff repair | |
126643422 | 12664342 | Spinal osteoarthritis | |
126643422 | 12664342 | Type 2 diabetes mellitus | |
126643422 | 12664342 | Withdrawal syndrome | |
126643422 | 12664342 | Wrong technique in product usage process |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |