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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
122789182 | 12278918 | 2 | F | 20160714 | 20160418 | 20160715 | EXP | PHHY2016NL051506 | NOVARTIS | 0.00 | M | Y | 0.00000 | 20160715 | CN | COUNTRY NOT SPECIFIED | NL |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
122789182 | 12278918 | 1 | PS | ACLASTA | ZOLEDRONIC ACID | 1 | Intravenous (not otherwise specified) | 0.5 MG, Q12MO (ONCE EVERY 52 WEEKS) | 16HB0109A | 21817 | .5 | MG | SOLUTION FOR INJECTION | ||||||
122789182 | 12278918 | 2 | SS | ACLASTA | ZOLEDRONIC ACID | 1 | 21817 | SOLUTION FOR INJECTION | |||||||||||
122789182 | 12278918 | 3 | C | ACENOCOUMAROL | ACENOCOUMAROL | 1 | Unknown | UNK | 0 | ||||||||||
122789182 | 12278918 | 4 | C | ATORVASTATIN | ATORVASTATIN | 1 | Unknown | 0 | |||||||||||
122789182 | 12278918 | 5 | C | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | Unknown | 0 | |||||||||||
122789182 | 12278918 | 6 | C | LEUPRORELIN | LEUPROLIDE ACETATE | 1 | Unknown | 0 | |||||||||||
122789182 | 12278918 | 7 | C | CALCIUM | CALCIUM | 1 | Unknown | 0 | |||||||||||
122789182 | 12278918 | 8 | C | VITAMIN D | CHOLECALCIFEROL | 1 | Unknown | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
122789182 | 12278918 | 1 | Prostate cancer |
122789182 | 12278918 | 2 | Osteoporosis |
122789182 | 12278918 | 3 | Product used for unknown indication |
122789182 | 12278918 | 4 | Product used for unknown indication |
122789182 | 12278918 | 5 | Product used for unknown indication |
122789182 | 12278918 | 6 | Product used for unknown indication |
122789182 | 12278918 | 7 | Product used for unknown indication |
122789182 | 12278918 | 8 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
122789182 | 12278918 | DE |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
122789182 | 12278918 | Death | |
122789182 | 12278918 | 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 |
---|---|---|---|---|---|---|
122789182 | 12278918 | 1 | 20150605 | 0 |