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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126061941 | 12606194 | 1 | I | 20160630 | 20160701 | 20160729 | 20160729 | PER | US-TEVA-674876ACC | TEVA | 23.50 | YR | F | Y | 79.00000 | KG | 20160729 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126061941 | 12606194 | 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 |
---|---|---|---|
126061941 | 12606194 | 1 | Post coital contraception |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126061941 | 12606194 | Dysmenorrhoea | |
126061941 | 12606194 | Headache | |
126061941 | 12606194 | Insomnia | |
126061941 | 12606194 | Migraine | |
126061941 | 12606194 | Nausea | |
126061941 | 12606194 | Vaginal haemorrhage |
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 |
---|---|---|---|---|---|---|
126061941 | 12606194 | 1 | 20160625 | 20160625 | 0 |