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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 88116116 | 8811611 | 6 | F | 201603 | 20160919 | 20120927 | 20160922 | EXP | PHHY2012CA078127 | NOVARTIS | 56.09 | YR | F | Y | 0.00000 | 20160922 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 88116116 | 8811611 | 1 | PS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Intramuscular | 20 MG, QMO (EVERY 4 WEEKS) | U | 21008 | 20 | MG | /month | ||||||
| 88116116 | 8811611 | 2 | SS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Intramuscular | 20 MG, EVERY 6 WEEKS | U | 21008 | 20 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 88116116 | 8811611 | 1 | Acromegaly |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 88116116 | 8811611 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 88116116 | 8811611 | Blood glucose decreased | |
| 88116116 | 8811611 | Blood pressure increased | |
| 88116116 | 8811611 | Blood pressure systolic increased | |
| 88116116 | 8811611 | Chest pain | |
| 88116116 | 8811611 | Disturbance in attention | |
| 88116116 | 8811611 | Hypophagia | |
| 88116116 | 8811611 | Influenza like illness | |
| 88116116 | 8811611 | Malaise | |
| 88116116 | 8811611 | Memory impairment | |
| 88116116 | 8811611 | Musculoskeletal chest pain | |
| 88116116 | 8811611 | Nausea | |
| 88116116 | 8811611 | Product use issue | |
| 88116116 | 8811611 | Viral infection |
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 |
|---|---|---|---|---|---|---|
| 88116116 | 8811611 | 1 | 20041020 | 0 |