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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5294032 | 6237206 | F | 1 | 5294032-1 | 20070330 | 20070405 | EXP | 009993 | BARR LABORATORIES | 16 | YR | F | N | 20070404 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5294032 | 1008358146 | PS | CLARAVIS | 1 | ORAL | 30 MG, BID, ORAL | U | D | 76135 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5294032 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5294032 | DRUG EXPOSURE DURING PREGNANCY |
| 5294032 | UNINTENDED PREGNANCY |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5294032 | HP |
| 5294032 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5294032 | 1008358146 | 20061107 | 20070115 |