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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 107333274 | 10733327 | 4 | F | 201501 | 20160809 | 20150123 | 20160812 | EXP | PHHY2013CA016469 | NOVARTIS | 86.50 | YR | F | Y | 0.00000 | 20160812 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 107333274 | 10733327 | 1 | PS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Intramuscular | 10 MG, QMO (ONCE A MONTH) | U | 21008 | 10 | MG | /month | ||||||
| 107333274 | 10733327 | 2 | SS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Intramuscular | 20 MG, QMO (EVERY 4 WEEKS) | U | 21008 | 20 | MG | /month | ||||||
| 107333274 | 10733327 | 3 | SS | SANDOSTATIN | OCTREOTIDE ACETATE | 1 | Subcutaneous | 100 UG, Q12H | U | 0 | 100 | UG | Q12H | ||||||
| 107333274 | 10733327 | 4 | SS | SANDOSTATIN | OCTREOTIDE ACETATE | 1 | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 107333274 | 10733327 | 1 | Anaemia |
| 107333274 | 10733327 | 2 | Iron deficiency |
| 107333274 | 10733327 | 3 | Anaemia |
| 107333274 | 10733327 | 4 | Iron deficiency |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 107333274 | 10733327 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 107333274 | 10733327 | Blood pressure systolic increased | |
| 107333274 | 10733327 | Confusional state | |
| 107333274 | 10733327 | Fall | |
| 107333274 | 10733327 | Flatulence | |
| 107333274 | 10733327 | Heart rate decreased | |
| 107333274 | 10733327 | Hypoacusis | |
| 107333274 | 10733327 | Joint dislocation | |
| 107333274 | 10733327 | Loss of consciousness | |
| 107333274 | 10733327 | Mental impairment | |
| 107333274 | 10733327 | Movement disorder | |
| 107333274 | 10733327 | Pain | |
| 107333274 | 10733327 | Product use issue | |
| 107333274 | 10733327 | Upper limb fracture |
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 |
|---|---|---|---|---|---|---|
| 107333274 | 10733327 | 1 | 20121020 | 0 |