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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6524175 | 7235367 | I | 6524175-3 | 20090601 | 20091221 | 20091231 | EXP | US-GENENTECH-296196 | GNEFDAAERSPRD | 13 | M | Y | 36.4 | KG | 20091231 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6524175 | 1012889286 | PS | NUTROPIN | 1 | SUBCUTANEOUS | 1.4 MG, QD | 778443 | 019676 | |||
| 6524175 | 1012889287 | SS | NUTROPIN | 1 | SUBCUTANEOUS | 2.0 MG, QD | NOT REPORTED | 019676 | |||
| 6524175 | 1012889288 | SS | NUTROPIN | 1 | SUBCUTANEOUS | 2.4 MG, QD | NOT REPORTED | 019676 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6524175 | 1012889286 | GROWTH HORMONE DEFICIENCY |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6524175 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6524175 | ARTERIOVENOUS MALFORMATION |
| 6524175 | HAEMANGIOMA |
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 |
|---|---|---|---|---|---|
| 6524175 | 1012889286 | 20090212 | |||
| 6524175 | 1012889287 | 20090601 | |||
| 6524175 | 1012889288 | 20091008 | 20091210 | 64 | DAY |