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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125925522 | 12592552 | 2 | F | 20160721 | 20160726 | 20160803 | EXP | PHHY2016BR101529 | NOVARTIS | 0.00 | F | Y | 0.00000 | 20160803 | MD | BR | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125925522 | 12592552 | 1 | PS | ACLASTA | ZOLEDRONIC ACID | 1 | Unknown | 21817 | SOLUTION FOR INJECTION | ||||||||||
125925522 | 12592552 | 2 | SS | ACLASTA | ZOLEDRONIC ACID | 1 | 21817 | SOLUTION FOR INJECTION | |||||||||||
125925522 | 12592552 | 3 | SS | ACLASTA | ZOLEDRONIC ACID | 1 | 21817 | SOLUTION FOR INJECTION |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125925522 | 12592552 | 1 | Osteoporosis |
125925522 | 12592552 | 2 | Arthritis |
125925522 | 12592552 | 3 | Osteoarthritis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125925522 | 12592552 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125925522 | 12592552 | Deafness | |
125925522 | 12592552 | Drug ineffective | |
125925522 | 12592552 | Pain |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |