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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5587768 | 6527555 | I | 5587768-6 | 20071210 | 20071219 | 20071231 | EXP | WSDF_00696 | CANGENE CORPORATION | 23 | YR | F | N | 20071221 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5587768 | 1009383507 | PS | WINRHO SDF | 1 | D | D |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5587768 | 1009383507 | IDIOPATHIC THROMBOCYTOPENIC PURPURA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5587768 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5587768 | CONDITION AGGRAVATED |
| 5587768 | DIZZINESS |
| 5587768 | HAEMOGLOBIN DECREASED |
| 5587768 | HEADACHE |
| 5587768 | IDIOPATHIC THROMBOCYTOPENIC PURPURA |
| 5587768 | SINUS HEADACHE |
| 5587768 | SINUSITIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5587768 | CSM |
| 5587768 | DT |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5587768 | 1009383507 | 20071207 | 20071207 |