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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117493376 | 11749337 | 6 | F | 20130814 | 20160919 | 20151118 | 20160922 | EXP | PHHY2013CA090619 | NOVARTIS | 64.66 | YR | M | Y | 99.00000 | KG | 20160922 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117493376 | 11749337 | 1 | PS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Intramuscular | 30 MG, QMO | U | 21008 | 30 | MG | /month | ||||||
| 117493376 | 11749337 | 2 | SS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Intramuscular | 40 MG, QMO (EVERY 4 WEEKS) | U | 21008 | 40 | MG | /month | ||||||
| 117493376 | 11749337 | 3 | C | TIAZAC | DILTIAZEM HYDROCHLORIDE | 1 | Unknown | U | 0 | ||||||||||
| 117493376 | 11749337 | 4 | C | CRESTOR | ROSUVASTATIN CALCIUM | 1 | Unknown | U | 0 | ||||||||||
| 117493376 | 11749337 | 5 | C | BISOPROLOL | BISOPROLOL | 1 | Oral | 10 MG, QD | U | 0 | 10 | MG | QD | ||||||
| 117493376 | 11749337 | 6 | C | ATACAND | CANDESARTAN CILEXETIL | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 117493376 | 11749337 | 1 | Neuroendocrine tumour |
| 117493376 | 11749337 | 3 | Product used for unknown indication |
| 117493376 | 11749337 | 4 | Product used for unknown indication |
| 117493376 | 11749337 | 5 | Product used for unknown indication |
| 117493376 | 11749337 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 117493376 | 11749337 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 117493376 | 11749337 | Abdominal pain | |
| 117493376 | 11749337 | Anger | |
| 117493376 | 11749337 | Anxiety | |
| 117493376 | 11749337 | Blood pressure diastolic decreased | |
| 117493376 | 11749337 | Blood pressure fluctuation | |
| 117493376 | 11749337 | Blood pressure increased | |
| 117493376 | 11749337 | Blood pressure systolic increased | |
| 117493376 | 11749337 | Body temperature decreased | |
| 117493376 | 11749337 | Decreased appetite | |
| 117493376 | 11749337 | Feeling cold | |
| 117493376 | 11749337 | Gastric ulcer | |
| 117493376 | 11749337 | Lethargy | |
| 117493376 | 11749337 | Nervousness | |
| 117493376 | 11749337 | Oesophageal pain | |
| 117493376 | 11749337 | Sleep disorder | |
| 117493376 | 11749337 | Weight decreased |
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 |
|---|---|---|---|---|---|---|
| 117493376 | 11749337 | 2 | 20100721 | 0 |