Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5688585 | 6589345 | F | 5688585-9 | 20070101 | 20080321 | 20080331 | EXP | PHHY2008JP03063 | NOVARTIS PHARMACEUTICALS CORP. | 73 | YR | F | Y | 20080329 | JAPAN |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
5688585 | 1009725584 | PS | ZOMETA | 1 | INTRAVENOUS | 021223 | |||||
5688585 | 1009725585 | SS | AREDIA | 1 | INTRAVENOUS | UNK, UNK |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5688585 | 1009725584 | METASTASES TO BONE |
5688585 | 1009725585 | METASTASES TO BONE |
Outcome of event
Event ID | OUTC COD |
---|---|
5688585 | OT |
Reactions reported
Event ID | PT |
---|---|
5688585 | DENTAL OPERATION |
5688585 | GINGIVAL PAIN |
5688585 | ORAL PAIN |
5688585 | OSTEONECROSIS |
5688585 | PRIMARY SEQUESTRUM |
5688585 | TOOTH DISORDER |
5688585 | TOOTH EXTRACTION |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
5688585 | 1009725584 | 20060801 | |||
5688585 | 1009725585 | 20050501 | 20060801 |