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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4204616 | 5657190 | I | 4204616-7 | 20030815 | 20030918 | 20031006 | EXP | DL2003174 | DANCO LABORATORIES, LLC | 21 | YR | F | N | 20031002 | MD |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4204616 | 1004278786 | PS | MIFEPRISTONE TABLETS, 200 MG (DANCO LABS) | 2 | ORAL | 200 MG, ORAL | D | D | 20002 | 20020331 | 20687 |
| 4204616 | 1004279849 | SS | MISOPROSTOL | 1 | VAGINAL | 800 MCG, VAGINAL | D | D | C2001748 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4204616 | 1004278786 | ABORTION INDUCED |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4204616 | HO |
| 4204616 | RI |
Reactions reported
| Event ID | PT |
|---|---|
| 4204616 | ABDOMINAL PAIN |
| 4204616 | HEART RATE INCREASED |
| 4204616 | NAUSEA |
| 4204616 | PYREXIA |
| 4204616 | UTERINE TENDERNESS |
| 4204616 | WHITE BLOOD CELL COUNT INCREASED |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4204616 | HP |
| 4204616 | SDY |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4204616 | 1004278786 | 20030812 | |||
| 4204616 | 1004279849 | 20030813 |