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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6767571 | 7214103 | F | 6767571-1 | 20100601 | 20100614 | EXP | PHHY2009CA48783 | NOVARTIS PHARMACEUTICAL CORPORATION | YR | M | Y | 20100614 | OT | CANADA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6767571 | 1013857281 | PS | SANDOSTATIN LAR | 1 | INTRAMUSCULAR | 40 MG, EVERY 4 WEEKS | 021008 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6767571 | 1013857281 | ACROMEGALY |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6767571 | HO |
| 6767571 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6767571 | INJECTION SITE HAEMORRHAGE |
| 6767571 | INTERNATIONAL NORMALISED RATIO INCREASED |
| 6767571 | PNEUMONIA |
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 |
|---|---|---|---|---|---|
| 6767571 | 1013857281 | 19970301 | 20070620 | 3764 | DAY |