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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7488572 | 7812163 | F | 7488572-4 | 20080301 | 20110411 | 20110518 | EXP | US-BAYER-2011-013512 | BAYER HEALTHCARE PHARMACEUTICALS INC. | 24 | YR | F | Y | 68.027 | KG | 20110518 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7488572 | 1016530342 | PS | YASMIN | 1 | UNK | 021098 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7488572 | 1016530342 | CONTRACEPTION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7488572 | HO |
| 7488572 | OT |
| 7488572 | LT |
Reactions reported
| Event ID | PT |
|---|---|
| 7488572 | ANXIETY |
| 7488572 | PAIN |
| 7488572 | CHOLECYSTITIS |
| 7488572 | CHOLELITHIASIS |
| 7488572 | BILE DUCT STONE |
| 7488572 | LIVER DISORDER |
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 |
|---|---|---|---|---|---|
| 7488572 | 1016530342 | 20040401 | 20081201 |