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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6666847 | 7357830 | F | 1 | 6666847-6 | 20090201 | 20100322 | 20100331 | EXP | 288120 | NOVOPROD | 57 | YR | M | N | 142.5 | KG | 20100401 | MD | GERMANY |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6666847 | 1013442033 | PS | NORDITROPIN NORDIFLEX | 1 | SUBCUTANEOUS | 0.2 MG, QD, SUBCUTANEOUS | 21148 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6666847 | 1013442033 | HYPOPITUITARISM |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6666847 | OT |
| 6666847 | RI |
Reactions reported
| Event ID | PT |
|---|---|
| 6666847 | NEOPLASM PROGRESSION |
| 6666847 | PITUITARY TUMOUR |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6666847 | FGN |
| 6666847 | HP |
| 6666847 | OTH |
| 6666847 | SDY |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6666847 | 1013442033 | 20060201 | 20090212 |