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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1023502614 | 10235026 | 14 | F | 20130929 | 20151227 | 20140613 | 20151231 | EXP | PHHY2011CA80563 | NOVARTIS | 77.14 | YR | M | Y | 0.00000 | 20160101 | MD | CA | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1023502614 | 10235026 | 1 | PS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Intramuscular | 30 MG, QMO (EVERY 4 WEEKS) | 21008 | 30 | MG | /month | |||||||
| 1023502614 | 10235026 | 2 | SS | SANDOSTATIN | OCTREOTIDE ACETATE | 1 | Subcutaneous | UNKNOWN TEST DOSE | 0 | ||||||||||
| 1023502614 | 10235026 | 3 | C | ALLOPURINOL. | ALLOPURINOL | 1 | Subcutaneous | 0 | |||||||||||
| 1023502614 | 10235026 | 4 | C | CRESTOR | ROSUVASTATIN CALCIUM | 1 | Unknown | 0 | |||||||||||
| 1023502614 | 10235026 | 5 | C | ATACAND | CANDESARTAN CILEXETIL | 1 | Unknown | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 1023502614 | 10235026 | 1 | Pancreatic neuroendocrine tumour |
| 1023502614 | 10235026 | 2 | Pancreatic neuroendocrine tumour |
| 1023502614 | 10235026 | 3 | Product used for unknown indication |
| 1023502614 | 10235026 | 4 | Product used for unknown indication |
| 1023502614 | 10235026 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 1023502614 | 10235026 | DE |
| 1023502614 | 10235026 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 1023502614 | 10235026 | Anorectal discomfort | |
| 1023502614 | 10235026 | Arthralgia | |
| 1023502614 | 10235026 | Back pain | |
| 1023502614 | 10235026 | Blood glucose increased | |
| 1023502614 | 10235026 | Blood pressure increased | |
| 1023502614 | 10235026 | Circulatory collapse | |
| 1023502614 | 10235026 | Constipation | |
| 1023502614 | 10235026 | Contusion | |
| 1023502614 | 10235026 | Death | |
| 1023502614 | 10235026 | Diarrhoea | |
| 1023502614 | 10235026 | Epistaxis | |
| 1023502614 | 10235026 | Fall | |
| 1023502614 | 10235026 | Gait disturbance | |
| 1023502614 | 10235026 | Headache | |
| 1023502614 | 10235026 | Hip fracture | |
| 1023502614 | 10235026 | Hypotension | |
| 1023502614 | 10235026 | Injury | |
| 1023502614 | 10235026 | Muscle strain | |
| 1023502614 | 10235026 | Pain | |
| 1023502614 | 10235026 | Pain in extremity | |
| 1023502614 | 10235026 | Syncope |
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 |
|---|---|---|---|---|---|---|
| 1023502614 | 10235026 | 1 | 20110117 | 0 | ||
| 1023502614 | 10235026 | 2 | 20110106 | 20110106 | 0 |