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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125378801 | 12537880 | 1 | I | 201407 | 20160622 | 20160707 | 20160707 | EXP | CA-VALIDUS PHARMACEUTICALS LLC-CA-2016VAL002221 | VALIDUS | 0.00 | Y | 0.00000 | 20160707 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125378801 | 12537880 | 1 | PS | METOPROLOL TARTRATE. | METOPROLOL TARTRATE | 1 | Oral | 75 MG, BID | U | 17963 | 75 | MG | |||||||
| 125378801 | 12537880 | 2 | SS | SANDOSTATIN | OCTREOTIDE ACETATE | 1 | Intramuscular | 20 MG, QMO (ONCE A MONTH); SANDOSTATIN LAR | U | 0 | 20 | MG | |||||||
| 125378801 | 12537880 | 3 | SS | SANDOSTATIN | OCTREOTIDE ACETATE | 1 | Subcutaneous | UNK, BID | 0 | ||||||||||
| 125378801 | 12537880 | 4 | SS | SANDOSTATIN | OCTREOTIDE ACETATE | 1 | Subcutaneous | UNK, QD | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125378801 | 12537880 | 1 | Product used for unknown indication |
| 125378801 | 12537880 | 2 | Iron deficiency anaemia |
| 125378801 | 12537880 | 3 | Iron deficiency anaemia |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125378801 | 12537880 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125378801 | 12537880 | Blood pressure systolic increased | |
| 125378801 | 12537880 | Decreased appetite | |
| 125378801 | 12537880 | Diarrhoea | |
| 125378801 | 12537880 | Fatigue | |
| 125378801 | 12537880 | Frequent bowel movements | |
| 125378801 | 12537880 | Heart rate decreased | |
| 125378801 | 12537880 | Product use issue | |
| 125378801 | 12537880 | 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 |
|---|---|---|---|---|---|---|
| 125378801 | 12537880 | 2 | 20151030 | 0 | ||
| 125378801 | 12537880 | 3 | 201407 | 20150514 | 0 | |
| 125378801 | 12537880 | 4 | 20151001 | 20151008 | 0 |