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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
105875121 | 10587512 | 1 | I | 201402 | 20141107 | 20141117 | 20141117 | EXP | US-BAYER-2014-166450 | BAYER | 23.00 | YR | A | F | Y | 0.00000 | 20141117 | N | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
105875121 | 10587512 | 1 | PS | MIRENA | LEVONORGESTREL | 1 | INTRAUTERINE | 20 MCG/24HR, CONT | D | NOT AVAILABLE | 21225 | INTRAUTERINE DELIVERY SYSTEM | |||||||
105875121 | 10587512 | 2 | SS | MIRENA | LEVONORGESTREL | 1 | INTRAUTERINE | 20 MCG/24HR, CONT | D | NOT AVAILABLE | 21225 | INTRAUTERINE DELIVERY SYSTEM |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
105875121 | 10587512 | 1 | Contraception |
105875121 | 10587512 | 2 | Contraception |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
105875121 | 10587512 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
105875121 | 10587512 | Seizure | |
105875121 | 10587512 | Unintentional medical device removal | |
105875121 | 10587512 | Urinary tract infection |
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 |
---|---|---|---|---|---|---|
105875121 | 10587512 | 1 | 201310 | 201404 | 0 | |
105875121 | 10587512 | 2 | 201404 | 20141107 | 0 |