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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
113757314 | 11375731 | 4 | F | 20140310 | 20160830 | 20150813 | 20160902 | PER | US-BAYER-2015-399790 | BAYER | 30.00 | YR | A | F | Y | 0.00000 | 20160902 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
113757314 | 11375731 | 1 | PS | MIRENA | LEVONORGESTREL | 1 | Intra-uterine | 20 MCG/24HR, CONT | Y | 21225 | 20 | UG | INTRAUTERINE DELIVERY SYSTEM |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
113757314 | 11375731 | 1 | Contraception |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
113757314 | 11375731 | LT |
113757314 | 11375731 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
113757314 | 11375731 | Abdominal pain | |
113757314 | 11375731 | Device difficult to use | |
113757314 | 11375731 | General physical health deterioration | |
113757314 | 11375731 | Infection | |
113757314 | 11375731 | Injury | |
113757314 | 11375731 | Menorrhagia | |
113757314 | 11375731 | Pain | |
113757314 | 11375731 | Uterine perforation |
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 |
---|---|---|---|---|---|---|
113757314 | 11375731 | 1 | 20130108 | 20140428 | 0 |