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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6026599 | 6862709 | F | 1 | 6026599-X | 20081117 | 20081217 | 20081231 | EXP | 037519 | BARR LABORATORIES | 32 | YR | F | N | 20081230 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6026599 | 1010947349 | PS | CLARAVIS | 1 | ORAL | 80 MG, QD, ORAL | D | D | 76135 | ||
| 6026599 | 1010964033 | C | PLAN B | 1 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6026599 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6026599 | DEVICE BREAKAGE |
| 6026599 | DRUG EXPOSURE DURING PREGNANCY |
| 6026599 | PREGNANCY AFTER POST COITAL CONTRACEPTION |
| 6026599 | PREGNANCY WITH CONTRACEPTIVE DEVICE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6026599 | HP |
| 6026599 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6026599 | 1010947349 | 20080919 | 20081201 |