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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
119494503 | 11949450 | 3 | F | 20120606 | 20160629 | 20160125 | 20160707 | EXP | US-BAYER-2016-012737 | BAYER | 24.00 | YR | A | F | Y | 95.24000 | KG | 20160707 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
119494503 | 11949450 | 1 | PS | MIRENA | LEVONORGESTREL | 1 | Intra-uterine | 20 MCG/24HR, CONT | 21225 | 20 | UG | INTRAUTERINE DELIVERY SYSTEM |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
119494503 | 11949450 | 1 | Contraception |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
119494503 | 11949450 | OT |
119494503 | 11949450 | LT |
119494503 | 11949450 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
119494503 | 11949450 | Abdominal pain | |
119494503 | 11949450 | Device issue | |
119494503 | 11949450 | Medical device discomfort | |
119494503 | 11949450 | Menorrhagia | |
119494503 | 11949450 | Pelvic organ injury | |
119494503 | 11949450 | Scar | |
119494503 | 11949450 | 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 |
---|---|---|---|---|---|---|
119494503 | 11949450 | 1 | 20120210 | 20120608 | 0 |