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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126869201 | 12686920 | 1 | I | 20160727 | 20160729 | 20160826 | 20160826 | PER | US-TEVA-682041ACC | TEVA | 22.21 | YR | F | Y | 81.72000 | KG | 20160826 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126869201 | 12686920 | 1 | PS | PLAN B ONE-STEP | LEVONORGESTREL | 1 | 21998 | 1.5 | MOL | TABLET | |||||||||
126869201 | 12686920 | 2 | C | JOLESSA | ETHINYL ESTRADIOLLEVONORGESTREL | 1 | 0 | ||||||||||||
126869201 | 12686920 | 3 | C | TOPIRAMATE. | TOPIRAMATE | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126869201 | 12686920 | 1 | Post coital contraception |
126869201 | 12686920 | 2 | Contraception |
126869201 | 12686920 | 3 | Migraine |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126869201 | 12686920 | Abdominal distension | |
126869201 | 12686920 | Abdominal pain upper | |
126869201 | 12686920 | Diarrhoea | |
126869201 | 12686920 | Dysmenorrhoea | |
126869201 | 12686920 | Nausea | |
126869201 | 12686920 | Vaginal discharge |
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 |
---|---|---|---|---|---|---|
126869201 | 12686920 | 1 | 20160714 | 20160714 | 0 |