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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4542778 | 5706564 | I | 4542778-2 | 20041223 | 20041231 | EXP | 200419807US | AVENTIS PHARMACEUTICALS, INC. | F | Y | 20041231 | PH |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4542778 | 1005546914 | PS | LOVENOX | 1 | DOSE: 30 OR 40 | UNK |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4542778 | 1005546914 | ABORTION SPONTANEOUS |
| 4542778 | 1005546914 | PROPHYLAXIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4542778 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4542778 | ABORTION SPONTANEOUS |
| 4542778 | DRUG EXPOSURE DURING PREGNANCY |
| 4542778 | INJECTION SITE HAEMORRHAGE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4542778 | HP |
Therapies reported
| no results found |