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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 721408418 | 7214084 | 18 | F | 20160822 | 20091214 | 20160825 | EXP | PHHY2009CA21420 | NOVARTIS | 0.00 | F | Y | 0.00000 | 20160825 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 721408418 | 7214084 | 1 | PS | SANDOSTATIN LAR DEPOT | OCTREOTIDE ACETATE | 1 | Intramuscular | 20 MG, QMO | U | 21008 | 20 | MG | /month | ||||||
| 721408418 | 7214084 | 2 | SS | METOPROLOL. | METOPROLOL | 1 | Oral | UNK | U | 0 | |||||||||
| 721408418 | 7214084 | 3 | C | ADALAT | NIFEDIPINE | 1 | Unknown | U | 0 | ||||||||||
| 721408418 | 7214084 | 4 | C | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Unknown | U | 0 | ||||||||||
| 721408418 | 7214084 | 5 | C | CALCIUM | CALCIUM | 1 | Unknown | UNK | U | 0 | |||||||||
| 721408418 | 7214084 | 6 | C | PANTOLOC | PANTOPRAZOLE SODIUM | 1 | Unknown | UNK | U | 0 | |||||||||
| 721408418 | 7214084 | 7 | C | FOSAMAX | ALENDRONATE SODIUM | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 721408418 | 7214084 | 1 | Metastatic carcinoid tumour |
| 721408418 | 7214084 | 2 | Metastatic carcinoid tumour |
| 721408418 | 7214084 | 3 | Product used for unknown indication |
| 721408418 | 7214084 | 4 | Product used for unknown indication |
| 721408418 | 7214084 | 5 | Product used for unknown indication |
| 721408418 | 7214084 | 6 | Product used for unknown indication |
| 721408418 | 7214084 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 721408418 | 7214084 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 721408418 | 7214084 | Blood pressure diastolic decreased | |
| 721408418 | 7214084 | Blood pressure systolic increased | |
| 721408418 | 7214084 | Cough | |
| 721408418 | 7214084 | Heart rate decreased | |
| 721408418 | 7214084 | Product use issue |
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 |
|---|---|---|---|---|---|---|
| 721408418 | 7214084 | 1 | 20090515 | 0 |