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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122736684 | 12273668 | 4 | F | 20110714 | 20160706 | 20160415 | 20160712 | EXP | PHHY2011CA64119 | NOVARTIS | 71.89 | YR | F | Y | 0.00000 | 20160712 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122736684 | 12273668 | 1 | PS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Intramuscular | 30 MG, QMO (EVERY 4 WEEKS) | U | S0151 | 21008 | 30 | MG | /month | |||||
| 122736684 | 12273668 | 2 | SS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Intramuscular | 30 MG, EVERY 3 WEEKS | U | S0089, S0090 | 21008 | 30 | MG | ||||||
| 122736684 | 12273668 | 3 | C | LUTETIUM (LU 177) | LUTETIUM LU-177 | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122736684 | 12273668 | 1 | Carcinoid tumour |
| 122736684 | 12273668 | 3 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 122736684 | 12273668 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122736684 | 12273668 | Anxiety | |
| 122736684 | 12273668 | Blood pressure diastolic decreased | |
| 122736684 | 12273668 | Blood pressure systolic increased | |
| 122736684 | 12273668 | Clavicle fracture | |
| 122736684 | 12273668 | Diarrhoea | |
| 122736684 | 12273668 | Dizziness | |
| 122736684 | 12273668 | Fall | |
| 122736684 | 12273668 | Fatigue | |
| 122736684 | 12273668 | Hypoglycaemia | |
| 122736684 | 12273668 | Inappropriate schedule of drug administration | |
| 122736684 | 12273668 | Incorrect product storage | |
| 122736684 | 12273668 | Laceration | |
| 122736684 | 12273668 | Malaise | |
| 122736684 | 12273668 | Needle issue | |
| 122736684 | 12273668 | Oedema peripheral | |
| 122736684 | 12273668 | Stool analysis abnormal | |
| 122736684 | 12273668 | Underdose |
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 |
|---|---|---|---|---|---|---|
| 122736684 | 12273668 | 1 | 20051209 | 0 |