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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6549565 | 7071213 | F | 3 | 6549565-4 | 20090703 | 20100105 | 20100119 | EXP | MOZO-1000230 | GENZYME | YR | M | N | 65 | KG | 20100115 | MD | NETHERLANDS |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6549565 | 1012992247 | PS | PLERIXAFOR (PLERIXAFOR) SOLUTION FOR INJECTION | 2 | SUBCUTANEOUS | 0.78 ML, SUBCUTANEOUS | U | U | 09-000446 | 20090901 | 22311 |
6549565 | 1013024715 | C | ACETAMINOPHEN | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6549565 | 1012992247 | HAEMATOPOIETIC STEM CELL MOBILISATION |
Outcome of event
Event ID | OUTC COD |
---|---|
6549565 | HO |
Reactions reported
Event ID | PT |
---|---|
6549565 | DIARRHOEA |
6549565 | DYSPNOEA |
6549565 | TACHYCARDIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
6549565 | FGN |
6549565 | HP |
6549565 | OTH |
6549565 | SDY |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
6549565 | 1012992247 | 20090703 | 20090703 |