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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6386382 | 7144036 | I | 6386382-2 | 20090926 | 20090930 | DIR | 22 | YR | F | N | 95 | KG | 20090929 | N | Y | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6386382 | 1012369949 | PS | YAZ | 1 | ORAL | 1 EVERY DAY PO | D | D | 84606A | 20091213 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6386382 | 1012369949 | CONTRACEPTION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6386382 | DS |
| 6386382 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6386382 | ABDOMINAL PAIN LOWER |
| 6386382 | ABNORMAL BEHAVIOUR |
| 6386382 | ALOPECIA |
| 6386382 | DECREASED APPETITE |
| 6386382 | DEPRESSION |
| 6386382 | DIZZINESS |
| 6386382 | FATIGUE |
| 6386382 | HEADACHE |
| 6386382 | MOOD ALTERED |
| 6386382 | NAUSEA |
| 6386382 | VISUAL IMPAIRMENT |
| 6386382 | VOMITING |
| 6386382 | WEIGHT DECREASED |
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 |
|---|---|---|---|---|---|
| 6386382 | 1012369949 | 20090612 | 20090930 |