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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120777414 | 12077741 | 4 | F | 20160727 | 20160215 | 20160801 | EXP | PHHY2016CA017165 | NOVARTIS | 0.00 | M | Y | 0.00000 | 20160801 | CN | COUNTRY NOT SPECIFIED | CA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120777414 | 12077741 | 1 | PS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Intramuscular | 30 MG, QMO (EVERY 28 DAYS) | 21008 | 30 | MG | /month | |||||||
| 120777414 | 12077741 | 2 | SS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Intramuscular | 30 MG, TIW (EVERY 3 WEEKS) | 21008 | 30 | MG | Q3W | |||||||
| 120777414 | 12077741 | 3 | SS | SANDOSTATIN | OCTREOTIDE ACETATE | 1 | Subcutaneous | 100 UG, TID | 0 | 100 | UG | TID | |||||||
| 120777414 | 12077741 | 4 | SS | SANDOSTATIN | OCTREOTIDE ACETATE | 1 | Subcutaneous | 100 UG, QD | 0 | 100 | UG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 120777414 | 12077741 | 1 | Neuroendocrine tumour |
| 120777414 | 12077741 | 3 | Neuroendocrine tumour |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 120777414 | 12077741 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 120777414 | 12077741 | Blood pressure diastolic increased | |
| 120777414 | 12077741 | Hepatic neoplasm | |
| 120777414 | 12077741 | Inappropriate schedule of drug administration | |
| 120777414 | 12077741 | Injection site pain | |
| 120777414 | 12077741 | Weight increased |
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 |
|---|---|---|---|---|---|---|
| 120777414 | 12077741 | 1 | 20150922 | 0 | ||
| 120777414 | 12077741 | 3 | 20150605 | 201506 | 0 | |
| 120777414 | 12077741 | 4 | 20150630 | 2015 | 0 |