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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
113460186 | 11346018 | 6 | F | 200906 | 20160810 | 20150806 | 20160812 | PER | US-BAYER-2015-394331 | BAYER | 18.00 | YR | A | F | Y | 90.70000 | KG | 20160812 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
113460186 | 11346018 | 1 | PS | MIRENA | LEVONORGESTREL | 1 | Intra-uterine | 20 MCG/24HR, CONT | TU0014F | 21225 | 20 | UG | INTRAUTERINE DELIVERY SYSTEM | ||||||
113460186 | 11346018 | 2 | C | FERROUS SULFATE. | FERROUS SULFATE | 1 | Oral | 325 MG, UNK | 0 | 325 | MG | ||||||||
113460186 | 11346018 | 3 | C | PROMETRIUM | PROGESTERONE | 1 | Oral | 200 MG, UNK | 0 | 200 | MG |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
113460186 | 11346018 | OT |
113460186 | 11346018 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
113460186 | 11346018 | Device failure | |
113460186 | 11346018 | Device issue | |
113460186 | 11346018 | Drug ineffective | |
113460186 | 11346018 | Embedded device | |
113460186 | 11346018 | Pregnancy with contraceptive device |
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 |
---|---|---|---|---|---|---|
113460186 | 11346018 | 1 | 200906 | 20130321 | 0 |