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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118789753 | 11878975 | 3 | F | 201505 | 20160801 | 20151230 | 20160804 | EXP | PHHY2015CA115343 | NOVARTIS | 47.26 | YR | F | Y | 36.28000 | KG | 20160804 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118789753 | 11878975 | 1 | PS | SANDOSTATIN | OCTREOTIDE ACETATE | 1 | Subcutaneous | 100 UG, QD (ONCE A DAY) | U | 19667 | 100 | UG | QD | ||||||
| 118789753 | 11878975 | 2 | SS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Intramuscular | 10 MG, QMO (ONCE A MONTH) | U | 0 | 10 | MG | /month | ||||||
| 118789753 | 11878975 | 3 | SS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Intramuscular | 40 MG, QMO | U | 0 | 40 | MG | /month | ||||||
| 118789753 | 11878975 | 4 | SS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Intramuscular | 30 MG, QMO | U | 0 | 30 | MG | /month | ||||||
| 118789753 | 11878975 | 5 | C | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | UNK, BIW | U | 0 | QOW |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 118789753 | 11878975 | 1 | Diarrhoea |
| 118789753 | 11878975 | 2 | Diarrhoea |
| 118789753 | 11878975 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 118789753 | 11878975 | HO |
| 118789753 | 11878975 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 118789753 | 11878975 | Blood pressure decreased | |
| 118789753 | 11878975 | Body temperature decreased | |
| 118789753 | 11878975 | Dehydration | |
| 118789753 | 11878975 | Dizziness | |
| 118789753 | 11878975 | Ear discomfort | |
| 118789753 | 11878975 | Gastrointestinal stoma complication | |
| 118789753 | 11878975 | Lung infection | |
| 118789753 | 11878975 | Migraine | |
| 118789753 | 11878975 | Multiple sclerosis | |
| 118789753 | 11878975 | Nausea | |
| 118789753 | 11878975 | Pneumonia | |
| 118789753 | 11878975 | Product use issue | |
| 118789753 | 11878975 | Weight decreased | |
| 118789753 | 11878975 | Weight fluctuation |
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 |
|---|---|---|---|---|---|---|
| 118789753 | 11878975 | 1 | 201505 | 0 | ||
| 118789753 | 11878975 | 2 | 20150921 | 20160226 | 0 | |
| 118789753 | 11878975 | 3 | 20160309 | 20160408 | 0 | |
| 118789753 | 11878975 | 4 | 20160506 | 0 |