Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7790311 | 8154550 | F | 7790311-4 | 20110920 | 20110930 | 20110930 | PER | US-TEVA-302081USA | TEVA | 19 | YR | F | Y | 56.75 | KG | 20110930 | CN | UNITED STATES |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7790311 | 1017681497 | PS | PLAN B ONE-STEP | 1 | ORAL | 1.5 MILLIGRAM; | 021998 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7790311 | 1017681497 | POST COITAL CONTRACEPTION |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 7790311 | MENSTRUATION IRREGULAR |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 7790311 | 1017681497 | 20110915 | 20110915 |