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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123500192 | 12350019 | 2 | F | 20160804 | 20160805 | 20160510 | 20160815 | EXP | US-SA-2016SA088960 | AVENTIS | 94.00 | YR | E | F | Y | 0.00000 | 20160815 | CN | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123500192 | 12350019 | 1 | PS | CEREZYME | IMIGLUCERASE | 1 | Intravenous drip | U | UNKNOWN | 20367 | 2800 | MG | POWDER FOR SOLUTION FOR INFUSION | QOW |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123500192 | 12350019 | 1 | Gaucher's disease |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123500192 | 12350019 | DE |
| 123500192 | 12350019 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123500192 | 12350019 | Cerebrovascular accident | |
| 123500192 | 12350019 | Deafness | |
| 123500192 | 12350019 | Fall | |
| 123500192 | 12350019 | Myocardial infarction | |
| 123500192 | 12350019 | Wheelchair user | |
| 123500192 | 12350019 | Wound |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |