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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7387025 | 7874629 | F | 7387025-1 | 20110329 | 20110331 | EXP | US-AMGEN-USASP2011016181 | AMGENSAFETY | 76 | YR | M | Y | 20110331 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7387025 | 1016140036 | C | CORTICOSTEROIDS | 2 | |||||||
7387025 | 1016140035 | PS | NPLATE | 1 | 500 A?G, UNK |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7387025 | 1016140035 | IDIOPATHIC THROMBOCYTOPENIC PURPURA |
Outcome of event
Event ID | OUTC COD |
---|---|
7387025 | HO |
7387025 | DE |
Reactions reported
Event ID | PT |
---|---|
7387025 | SEPSIS |
7387025 | HOSPITALISATION |
7387025 | ORGAN FAILURE |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
7387025 | 1016140035 | 20100812 | 20100921 | 41 | DAY |