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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 112293748 | 11229374 | 8 | F | 20160705 | 20150630 | 20160711 | EXP | PHHY2015BR077903 | NOVARTIS | 0.00 | F | Y | 63.00000 | KG | 20160712 | CN | COUNTRY NOT SPECIFIED | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 112293748 | 11229374 | 1 | PS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Intramuscular | 30 MG, QMO | U | 21008 | 30 | MG | SUSPENSION | /month | |||||
| 112293748 | 11229374 | 2 | SS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Intramuscular | UNK, AFTER 20 TO 25 DAYS | U | 21008 | SUSPENSION | ||||||||
| 112293748 | 11229374 | 3 | SS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Intramuscular | UNK, APPROXIMATELY EVERY 45 DAYS | U | 21008 | SUSPENSION | ||||||||
| 112293748 | 11229374 | 4 | SS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Intramuscular | UNK, EVERY 48 DAYS | U | 21008 | SUSPENSION | ||||||||
| 112293748 | 11229374 | 5 | SS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Intramuscular | UNK, ALMOST 2 MONTHS | U | 21008 | SUSPENSION | ||||||||
| 112293748 | 11229374 | 6 | SS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Intramuscular | UNK, EVERY 45 DAYS | U | 21008 | SUSPENSION |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 112293748 | 11229374 | 1 | Neuroendocrine tumour |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 112293748 | 11229374 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 112293748 | 11229374 | Needle issue | |
| 112293748 | 11229374 | Ovarian cyst | |
| 112293748 | 11229374 | Product use issue | |
| 112293748 | 11229374 | Uterine neoplasm |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 112293748 | 11229374 | 1 | 2014 | 0 | ||
| 112293748 | 11229374 | 4 | 201601 | 0 | ||
| 112293748 | 11229374 | 5 | 201603 | 0 | ||
| 112293748 | 11229374 | 6 | 20160602 | 0 |