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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8016634 | 8317520 | I | 8016634-1 | 20111220 | 20111231 | EXP | PHHY2011JP111352 | SANDOZ,INC. | 32 | YR | F | Y | 20111231 | OT | JAPAN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8016634 | 1018419943 | SS | HYDRALAZINE HYDROCHLORIDE | 1 | INTRAVENOUS | 6 MG, UNK | |||||
| 8016634 | 1018419941 | SS | CYCLOSPORINE | 1 | ORAL | 60 MG, UNK | |||||
| 8016634 | 1018419942 | PS | HYDRALAZINE HYDROCHLORIDE | 1 | 083241 | ||||||
| 8016634 | 1018419944 | C | PREDNISOLONE | 1 | ORAL |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8016634 | 1018419941 | APLASTIC ANAEMIA |
| 8016634 | 1018419944 | APLASTIC ANAEMIA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8016634 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 8016634 | GESTATIONAL HYPERTENSION |
| 8016634 | MATERNAL EXPOSURE DURING PREGNANCY |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |