Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124888073 | 12488807 | 3 | F | 2016 | 20160727 | 20160622 | 20160801 | EXP | GB-AMGEN-GBRSP2016080425 | AMGEN | 50.00 | YR | A | M | Y | 76.00000 | KG | 20160801 | OT | GB | GB |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124888073 | 12488807 | 1 | PS | NPLATE | ROMIPLOSTIM | 1 | Unknown | 7.5 MUG/KG, UNK | 125268 | 7.5 | UG/KG | UNKNOWN FORMULATION | |||||||
| 124888073 | 12488807 | 2 | C | MYCOPHENOLATE MOFETIL. | MYCOPHENOLATE MOFETIL | 1 | 1.5 G, BID | 0 | 1.5 | G | BID | ||||||||
| 124888073 | 12488807 | 3 | C | RITUXIMAB | RITUXIMAB | 1 | 375 MG/M2, Q4WK | 0 | 375 | MG/M**2 | |||||||||
| 124888073 | 12488807 | 4 | C | DEXAMETHASONE. | DEXAMETHASONE | 1 | 0 | ||||||||||||
| 124888073 | 12488807 | 5 | C | METHYLPREDNISOLONE. | METHYLPREDNISOLONE | 1 | Intravenous (not otherwise specified) | 0 | |||||||||||
| 124888073 | 12488807 | 6 | C | IMMUNOGLOBULIN ANTI-D (RHO) | 2 | 0 | |||||||||||||
| 124888073 | 12488807 | 7 | C | IMMUNOGLOBULIN | HUMAN IMMUNOGLOBULIN G | 1 | Intravenous (not otherwise specified) | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124888073 | 12488807 | 1 | Immune thrombocytopenic purpura |
| 124888073 | 12488807 | 2 | Immune thrombocytopenic purpura |
| 124888073 | 12488807 | 3 | Immune thrombocytopenic purpura |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124888073 | 12488807 | HO |
| 124888073 | 12488807 | DE |
| 124888073 | 12488807 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124888073 | 12488807 | Dyspnoea | |
| 124888073 | 12488807 | Haematuria | |
| 124888073 | 12488807 | Haemolysis | |
| 124888073 | 12488807 | Haemorrhage | |
| 124888073 | 12488807 | Mouth haemorrhage | |
| 124888073 | 12488807 | Platelet count decreased | |
| 124888073 | 12488807 | Platelet count increased | |
| 124888073 | 12488807 | Pulmonary embolism |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 124888073 | 12488807 | 1 | 20160410 | 0 | ||
| 124888073 | 12488807 | 2 | 20160508 | 0 |