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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125692842 | 12569284 | 2 | F | 20160707 | 20160714 | 20160719 | 20160722 | PER | US-TEVA-677741ACC | TEVA | 27.03 | YR | F | Y | 67.65000 | KG | 20160722 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125692842 | 12569284 | 1 | PS | PLAN B ONE-STEP | LEVONORGESTREL | 1 | 21998 | 1.5 | MG | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125692842 | 12569284 | 1 | Post coital contraception |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125692842 | 12569284 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125692842 | 12569284 | Exposure during pregnancy | |
| 125692842 | 12569284 | Muscle spasms | |
| 125692842 | 12569284 | Pain | |
| 125692842 | 12569284 | Pregnancy after post coital contraception | |
| 125692842 | 12569284 | Vaginal discharge | |
| 125692842 | 12569284 | Weight increased |
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 |
|---|---|---|---|---|---|---|
| 125692842 | 12569284 | 1 | 20160701 | 20160701 | 0 |