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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127169651 | 12716965 | 1 | I | 20160830 | 20160906 | 20160906 | EXP | PHHY2016BR121975 | NOVARTIS | 0.00 | M | Y | 0.00000 | 20160906 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127169651 | 12716965 | 1 | PS | ZOMETA | ZOLEDRONIC ACID | 1 | Unknown | UNK UNK, QMO | 21223 | /month |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127169651 | 12716965 | 1 | Metastases to bone |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127169651 | 12716965 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127169651 | 12716965 | Impaired healing | |
127169651 | 12716965 | Osteonecrosis of jaw | |
127169651 | 12716965 | Pain | |
127169651 | 12716965 | Procedural complication | |
127169651 | 12716965 | Pulpitis dental | |
127169651 | 12716965 | Suture rupture | |
127169651 | 12716965 | Swelling |
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 |
---|---|---|---|---|---|---|
127169651 | 12716965 | 1 | 201501 | 0 |