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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126013541 | 12601354 | 1 | I | 20160628 | 20160728 | 20160728 | PER | US-TEVA-673034ACC | TEVA | 0.00 | F | Y | 0.00000 | 20160728 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126013541 | 12601354 | 1 | PS | PLAN B ONE-STEP | LEVONORGESTREL | 1 | 21998 | 1.5 | MG | TABLET | |||||||||
| 126013541 | 12601354 | 2 | SS | PLAN B ONE-STEP | LEVONORGESTREL | 1 | 21998 | 1.5 | MG | TABLET | |||||||||
| 126013541 | 12601354 | 3 | SS | PLAN B ONE-STEP | LEVONORGESTREL | 1 | 21998 | 1.5 | MG | TABLET | |||||||||
| 126013541 | 12601354 | 4 | SS | PLAN B ONE-STEP | LEVONORGESTREL | 1 | 21998 | 1.5 | MG | TABLET | |||||||||
| 126013541 | 12601354 | 5 | SS | PLAN B ONE-STEP | LEVONORGESTREL | 1 | 21998 | 1.5 | MG | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126013541 | 12601354 | 1 | Post coital contraception |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126013541 | 12601354 | Abdominal pain lower | |
| 126013541 | 12601354 | Headache | |
| 126013541 | 12601354 | Intentional product misuse | |
| 126013541 | 12601354 | Nausea |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |