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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 103646314 | 10364631 | 4 | F | 201405 | 20160921 | 20140806 | 20160928 | EXP | PHHY2014BR066863 | NOVARTIS | 39.18 | YR | F | Y | 87.00000 | KG | 20160928 | CN | COUNTRY NOT SPECIFIED | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 103646314 | 10364631 | 1 | PS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Unknown | 20 MG, UNK | Y | 21008 | 20 | MG | VIAL | ||||||
| 103646314 | 10364631 | 2 | SS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Unknown | 30 MG, UNK | Y | S0237 | 21008 | 30 | MG | VIAL | |||||
| 103646314 | 10364631 | 3 | SS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Unknown | 20 MG, UNK | Y | 21008 | 20 | MG | VIAL | ||||||
| 103646314 | 10364631 | 4 | SS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Unknown | 30 MG, EVERY 28 DAYS | Y | S0237 | 21008 | 30 | MG | VIAL | |||||
| 103646314 | 10364631 | 5 | SS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Unknown | 20 MG, UNK | Y | 21008 | 20 | MG | VIAL | ||||||
| 103646314 | 10364631 | 6 | SS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Unknown | 30 MG, UNK | Y | 21008 | 30 | MG | VIAL | ||||||
| 103646314 | 10364631 | 7 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | Unknown | 1 DF, DAILY | 0 | 1 | DF | TABLET | |||||||
| 103646314 | 10364631 | 8 | C | FLUVASTATIN | FLUVASTATIN SODIUM | 1 | Unknown | 1 DF, AT NIGHT | 0 | 1 | DF | TABLET | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 103646314 | 10364631 | 1 | Acromegaly |
| 103646314 | 10364631 | 7 | Diabetes mellitus |
| 103646314 | 10364631 | 8 | Crying |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 103646314 | 10364631 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 103646314 | 10364631 | Cardiomegaly | |
| 103646314 | 10364631 | Headache | |
| 103646314 | 10364631 | Hyperglycaemia | |
| 103646314 | 10364631 | Hypoaesthesia | |
| 103646314 | 10364631 | Malaise | |
| 103646314 | 10364631 | Peripheral swelling | |
| 103646314 | 10364631 | Therapeutic response unexpected |
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 |
|---|---|---|---|---|---|---|
| 103646314 | 10364631 | 1 | 2002 | 0 |