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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5080521 | 6111554 | I | 5080521-1 | 20060809 | 20060809 | EXP | 2006AL001947 | ACTAVIS ELIZABETH LLC | 24 | YR | F | N | 20060808 | OT | DENMARK |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5080521 | 1007580245 | PS | NIFEDIPINE | 1 | ORAL | 60 MG; QD; PO | U | D | 72556 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5080521 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5080521 | DRUG EXPOSURE DURING PREGNANCY |
| 5080521 | HYPOTENSION |
| 5080521 | INTRA-UTERINE DEATH |
| 5080521 | PROCEDURAL COMPLICATION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5080521 | CR |
| 5080521 | FGN |
| 5080521 | HP |
| 5080521 | OTH |
Therapies reported
| no results found |