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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
123622612 | 12362261 | 2 | F | 20160424 | 20160627 | 20160512 | 20160705 | PER | US-BAYER-2016-089090 | BAYER | 26.00 | YR | A | F | Y | 0.00000 | 20160705 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
123622612 | 12362261 | 1 | PS | MIRENA | LEVONORGESTREL | 1 | Intra-uterine | 20 MCG/24HR, CONT | 21225 | 20 | UG | INTRAUTERINE DELIVERY SYSTEM | |||||||
123622612 | 12362261 | 2 | SS | MIRENA | LEVONORGESTREL | 1 | Intra-uterine | 20 MCG/24HR, CONT | 21225 | 20 | UG | INTRAUTERINE DELIVERY SYSTEM | |||||||
123622612 | 12362261 | 3 | SS | MIRENA | LEVONORGESTREL | 1 | Intra-uterine | 20 MCG/24HR, CONT | 21225 | 20 | UG | INTRAUTERINE DELIVERY SYSTEM | |||||||
123622612 | 12362261 | 4 | C | CLINDAMYCIN | CLINDAMYCINCLINDAMYCIN PHOSPHATE | 1 | Oral | 0 | |||||||||||
123622612 | 12362261 | 5 | C | PRENATAL | VITAMINS | 1 | Oral | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
123622612 | 12362261 | 1 | Contraception |
123622612 | 12362261 | 2 | Contraception |
123622612 | 12362261 | 3 | Contraception |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
123622612 | 12362261 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
123622612 | 12362261 | Complication of device insertion | |
123622612 | 12362261 | Device dislocation | |
123622612 | 12362261 | Device malfunction | |
123622612 | 12362261 | Post procedural discomfort | |
123622612 | 12362261 | Procedural pain |
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 |
---|---|---|---|---|---|---|
123622612 | 12362261 | 1 | 20160429 | 20160429 | 0 | |
123622612 | 12362261 | 2 | 20160429 | 0 | ||
123622612 | 12362261 | 3 | 20160424 | 0 |