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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
120107085 | 12010708 | 5 | F | 20160128 | 20160926 | 20160205 | 20160927 | EXP | BR-JNJFOC-20160124253 | JANSSEN | 26.00 | YR | A | F | Y | 0.00000 | 20160927 | CN | BR | BR |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
120107085 | 12010708 | 1 | PS | ORTHO EVRA | ETHINYL ESTRADIOLNORELGESTROMIN | 1 | Transdermal | U | U | FFZS201;FFZS201;FFZS201;FJZSI00 | 21180 | PATCH |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
120107085 | 12010708 | 1 | Contraception |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
120107085 | 12010708 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
120107085 | 12010708 | Gastric operation | |
120107085 | 12010708 | Menorrhagia | |
120107085 | 12010708 | 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 |
---|---|---|---|---|---|---|
120107085 | 12010708 | 1 | 20151201 | 0 |