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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
98552443 | 9855244 | 3 | F | 201204 | 20160816 | 20140130 | 20160819 | PER | US-BAYER-2014-014234 | BAYER | 31.00 | YR | A | F | Y | 0.00000 | 20160819 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
98552443 | 9855244 | 1 | PS | MIRENA | LEVONORGESTREL | 1 | Intra-uterine | 20 MCG/24HR, CONT | 21225 | 20 | UG | INTRAUTERINE DELIVERY SYSTEM | |||||||
98552443 | 9855244 | 2 | SS | MIRENA | LEVONORGESTREL | 1 | 21225 | INTRAUTERINE DELIVERY SYSTEM |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
98552443 | 9855244 | 1 | Contraception |
98552443 | 9855244 | 2 | Menorrhagia |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
98552443 | 9855244 | LT |
98552443 | 9855244 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
98552443 | 9855244 | Abdominal pain lower | |
98552443 | 9855244 | General physical health deterioration | |
98552443 | 9855244 | Injury | |
98552443 | 9855244 | 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 |
---|---|---|---|---|---|---|
98552443 | 9855244 | 1 | 201103 | 201204 | 0 |